Timing of development of arrhythmias with central line.
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",isbn:"978-1-83768-132-7",printIsbn:"978-1-83768-131-0",pdfIsbn:"978-1-83768-133-4",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!0,isSalesforceBook:!1,isNomenclature:!1,hash:"8e41aab8223c29ce69c00e8c8f6f560d",bookSignature:"Prof. Vlassios Hrissanthou and Assistant Prof. Vasilis Bellos",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/12059.jpg",keywords:"Reservoir, Check Dam, River Flow, River Sediment Transport, Stilling Basin, Weir, Bridge Pier, Scouring, Reservoir Volume Capacity, Dimensioning Flood, Dimensioning Hydrograph, Length of Spillway",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"May 20th 2022",dateEndSecondStepPublish:"July 21st 2022",dateEndThirdStepPublish:"September 19th 2022",dateEndFourthStepPublish:"December 8th 2022",dateEndFifthStepPublish:"February 6th 2023",dateConfirmationOfParticipation:null,remainingDaysToSecondStep:"15 days",secondStepPassed:!1,areRegistrationsClosed:!1,currentStepOfPublishingProcess:2,editedByType:null,kuFlag:!1,biosketch:"Prof. Hrissanthou is the author and co-author of 48 publications in scientific journals, 88 publications in conference proceedings, and 12 book chapters published in English, Greek, and German. He is a member of the Hellenic Hydrotechical Association, the Deutsche Vereinigung fur Wasserwirtschaft, the European Water Resources Association (EWRA), the International Association of Hydrological Sciences (IAHS), and the International Association for Hydro-Environment Engineering and Research (IAHR).",coeditorOneBiosketch:"Dr. Vasilis Bellos is an Assistant Professor at the Department of Environmental Engineering, Democritus University of Thrace, Xanthi, Greece. Dr. Bello's research interest includes integrated water resources management focusing on the design and the environmental management of hydraulic works.",coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"37707",title:"Prof.",name:"Vlassios",middleName:null,surname:"Hrissanthou",slug:"vlassios-hrissanthou",fullName:"Vlassios Hrissanthou",profilePictureURL:"https://mts.intechopen.com/storage/users/37707/images/system/37707.png",biography:"Dr.-Ing. Vlassios Hrissanthou is an Emeritus Professor at the Civil Engineering Department of Democritus University of Thrace (DUTH), Xanthi, Greece. He studied Civil Engineering at the Aristotle University of Thessaloniki (AUTH), Greece, obtaining the diploma of Civil Engineer in 1972. He then undertook postgraduate and doctoral studies on Hydrology and Hydraulic Structures at the University of Karlsruhe (KIT), Germany. Subsequently, he completed a postdoctoral study on Hydraulics and Hydraulic Structures at the University of the Armed Forces Munich (UniBw München), Germany. His teaching work includes the following graduate and postgraduate study courses: Fluid Mechanics, Hydraulics, Engineering Hydrology, River Engineering, Hydropower Engineering, Water Resources Management, Open Channel Hydraulics, Hydrology of Groundwater, Advanced Engineering Hydrology, Sediment Transport, Reservoir Design, Time Series Analysis, Selected Chapters of Hydropower Engineering, and Hydraulics of Stratified Flows. He has supervised a plethora of diploma, postgraduate and doctoral dissertations. He has participated as principal investigator in several competitive international, german and greek research projects, dealing amongst others with soil erosion and sediment transport. Professor Hrissanthou is the author and co-author of 48 publications in scientific journals, 88 publications in conference proceedings, as well as 12 publications in book chapters in English, Greek and German. 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It forms the vital part of the ongoing management of preterm and sick term neonates. Though this has many advantages, it is not uncommon to encounter complications associated with the central lines. The main advantages of PICC lines include attainment of minimal handling, a long-term intravenous access for parenteral nutrition, the ability to transfuse hyperosmolar fluids, the opportunity to inject important drugs with PH less than 6 (e.g., vancomycin) or more than 8 (e.g., phenytoin) and continuous infusions like prostaglandins, irritants (calcium gluconate) and extended antibiotic therapy [1, 2, 11, 12]. These PICC lines are made of silicone or polyurethane. The preferred site of insertion is from the antecubital vein, cephalic vein, basilic vein or the long saphenous vein. The goal is to place the catheter tip at the level of superior vena cava (SVC) or inferior vena cava (IVC). The optimal placement of PICC lines in SVC should be 0.5–1 cm away from the cardiac silhouette in preterm and 1–2 cm away from the cardiac silhouette in term neonates [1]. This could help us in reducing the dreadful cardiac complications induced by PICC lines. All neonatal intensivists involved in taking decisions for insertion of central venous catheterization such as PICC or umbilical venous catheterization (UVC) should be aware of potential risk factors for complications. This helps to prevent or minimize the complication rate.
The aim of the chapter is to describe the common complications of central venous catheter with focus on arrhythmic complications. The timing and proposed mechanisms of malpositioned intracardiac catheter-induced arrhythmias are also explained. Common types of arrhythmias (atrial flutter and supraventricular tachycardia) secondary to the intracardiac catheters are explained with an outline of its basic management. Finally, practical tips are discussed to minimize the arrhythmic complications of central venous catheters.
Any venous catheters tip placed in the lower half or lower one-third of SVC/at or above the level of the diaphragm in IVC is called as centrally placed venous catheters, which commonly includes PICC line/umbilical venous catheter.
Above are the X-rays showing PICC line in an accepted position (Figure 1), PICC line in the right atrium (Figure 2), and PICC line looping within the cardiac chamber (Figure 3).
PICC line—optimal position. Chest X-ray showing right PICC line in SVC—0.5 cm away from the cardiac silhouette an optimal position.
PICC line in the right atrium. Chest X-ray showing right PICC line in the right atrium.
PICC line with intracardiac looping. Chest X-ray shows left PICC line passed superior vena cava, got looped in right atrium.
Although it is a common procedure in the neonatal critical care unit, it is not uncommon to have complications related to it. Due to the smaller size of the heart in neonates and premature infants, the usual anatomic landmark and distance from the insertion site may not be accurate. As they are commonly performed at bedside, fluoroscopic guidance would not be possible.
There are only a few randomized control clinical trials for PICC line use in neonates. The precise rate of complications of central venous catheters in neonates is unclear due to underreporting [5]. The reported incidence of PICC line induced complications from a compilation of various case reports varies from 0 to 33% [3]. Complications can be due to mechanical, vascular, cardiac and/or miscellaneous reasons. The most common mechanical complications are occlusion (reported as 30%), which can be minimized by inserting the smallest catheters into the larger veins. Vascular complications include phlebitis, bleeding from the insertion site, extravasation, and catheter-related venous thrombosis. It can be reduced through the atraumatic catheter insertion technique (slow and controlled technique), good compression immediately after insertion and accurate placement of the catheter in the vena cava [3, 5]. Migration of a properly placed catheter is not unusual to encounter and it may precipitate significant arrhythmias. A prospective study of 100 PICCs where catheter tip was evaluated at 24 h of post insertion revealed that 32.6% of catheters are migrated toward the heart and migration is more common in upper extremity PICC lines (47%) [4]. Peripheral dislodgement of catheters, catheter damage, catheter leakage/breakage and catheter fractures can occur. The above complications can be decreased with proper, transparent fixation of catheter end and more importantly fixation of its extension set [3]. Cardiac tamponade, myocardial perforation, and valve injury are commonly associated with curved or kinked intracardiac placement of centrally placed catheters. These complications can be minimized by making sure that the catheter tip is straight before insertion and most importantly adjusting the catheter position outside the cardiac shadow immediately after taking X-ray. After adjustment of the catheter tip, confirmatory X-ray is mandatory. Massive pleural effusion and pericardial effusion has been reported following an inappropriately placed PICC lines [1, 14].
The innate properties of neonatal myocardium predispose to different types of arrhythmia. Cardiac arrhythmias are rare but potentially life-threatening. Hence, should be identified and intervened immediately by the bedside neonatologist, especially when it occurs with an indwelling central venous catheter. Even though many neonatal literature mentions about the risk of arrhythmias with centrally placed catheters in neonates, the incidence is less known. Until now 16 cases of central venous catheter-induced arrhythmias are reported, with tachyarrhythmias being the commonest form. The most common arrhythmias reported so far are atrial flutter (8/16) and supraventricular tachycardia (7/16) [6, 7].
Arrhythmias may occur anytime, from the time of insertion of central catheters till the time of withdrawal (Table 1).
Procedural phase: due to advancement beyond SVC. It commonly happens due to improper measurement. Willful over advancement of the catheter into the intracardiac chamber with the hope to withdraw the catheter after radiographic confirmation is one of the common practices which should be forbidden.
Securing phase—migration to the intracardiac chamber can occur due to handling during the time of fixation.
Anytime at the indwelling phase due to migration/dislodgement of central venous catheters.
Cases were documented from within few minutes after insertion till 47 days post insertion of central venous catheter (CVC) [16, 17].
Serial number | Time phase | Possible reason |
---|---|---|
1 | Procedural phase |
|
2 | Secure phase | Migration of catheters can happen due to handling at the time of fixation |
3 | Indwelling phase | Migration and dislodgement |
Timing of development of arrhythmias with central line.
Typically the etiology lies on inappropriately placed intracardiac catheters in all the cases.
The possible mechanisms are
Malpositioned, migrated or inappropriately placed central venous catheter can cause a wide range of arrhythmias ranging from tachyarrhythmias to bradyarrhythmias as mentioned in Figure 4.
Types of Cardiac arrhythmias induced by centra lines.
Tachyarrhythmias are abnormal fast rhythms originating from atria or from ventricles of the heart. With intracardiac indwelling catheters, tachyarrhythmias are more common than bradyarrhythmias. Recognition of tachyarrhythmia is crucial for any intensivist. If not identified in time, it may end up with congestive cardiac failure due to significantly compromised cardiac output due to incessant tachycardia. Cardiogenic shock may happen due to prolonged myocardial hypoxia. It manifests as effortless tachypnoea, tachycardia (earliest sign), poor perfusion, prolonged capillary refill time, bilateral crepitations and hypotension (late sign).
Knowledge of normal heart rate is essential before diagnosing any tachyarrhythmia. Normal heart rate varies in newborn widely (Table 2).
Age | Awake rate (bpm) | Mean | Sleeping rate |
---|---|---|---|
Newborn to 3 months | 85–205 | 140 | 80–160 |
Normal heart rate variations in neonates.
Tachyarrhythmia is classified into supraventricular tachycardia/atrial tachyarrhythmia, junctional tachycardia and ventricular tachycardia depending on where the arrhythmic impulses emanate from (Figure 5). Any of the mentioned tachyarrhythmia depicted in Figure 5 can occur due to above-mentioned mechanisms.
Types of Tachyarrhytmias.
For clinical purpose, tachyarrhythmias are classified based on QRS complex in the ECG (Table 3).
The essential part of treating any tachyarrhythmia is based on differentiating different types of tachyarrhythmia like sinus tachycardia, supraventricular tachycardia, atrial flutter and ventricular tachycardia. The management is different for each type of tachyarrhythmia. Important arrhythmias induced by central lines are described here, explaining other rare forms are out of the scope of this chapter.
Sinus tachycardia can arise at the rate of 180–220 bpm. It arises due to stimulation of SA node typically due to body’s response to the need of increased cardiac output. It can arise in response to any stress, pain, hyperthermia, anemia, commonly used drugs like caffeine and more. It must be differentiated from other pathological causes by means of Normal P waves, variable R-R interval, constant PR interval, precipitating factors like fever, sepsis, and failure to respond with vagal maneuvers.
Atrial tachycardia arises when the impulses emanate from the atrium, specifically the right atrium. Atrial excitations have a very low threshold potential in preterm infants. Thereby whenever irritated by any mechanical stimuli, for example, a central venous catheter, atrial tachyarrhythmia occurs more often. The true two forms of atrial tachycardia are atrial flutter and atrial ectopy.
Atrial flutter is the common rhythm induced by the intracardiac position of PICC line and an awareness of this pattern is crucial for a neonatologist. Atrial flutter is best described by regular rapid atrial rates of 240–360 beats/min. The electrocardiogram (ECG) will show a regular rhythm with a sawtooth pattern of P waves otherwise known as the typical flutter waves. It is best seen in lead II, lead III and aVF leads with a long strip ECG. The QRS complex will be narrow if there is no aberrant pathway (Figure 6).
Atrial flutter. Lead II ECG: sawtooth flutter waves.
In neonates, atrial flutter commonly causes 2:1 AV conduction block. It may also cause various degrees of AV block. Atrial flutter in a non-catheter related context is less common than SVT. So it is potentially prone to under-recognition. A 12-h time of incessant tachycardia is enough to decompensate the hemodynamic status of a neonate. The chances of developing cardiac failure depend on the duration of arrhythmia, structural nature of the heart and gestational age rather than the rate alone. One has to quickly recognize atrial flutter and able to differentiate from SVT as the treatment option varies for both, with synchronized cardioversion for atrial flutter and adenosine for SVT [7, 8, 17].
Management depends on proper identification of atrial flutter, assessing the hemodynamic status of the neonate and recognition of treatable causes. As the arrhythmia occurred secondary to the malposition of the catheter, the first step of management should be to pull back or even remove the catheter. If the neonate is hemodynamically unstable, the best treatment option will be synchronized cardioversion with a dose of 0.5 J/kg. If the neonate is hemodynamically stable, digoxin therapy can be used as a first line management. The response rate for digoxin is roughly around 33%. Many times atrial flutter needs permanent reversion to DC cardioversion. Intravenous adenosine can be used to terminate the arrhythmia which uncovers a flutter in SVT. Occasionally esophageal overdrive pacing may be required [7, 8, 17].
Narrow complex SVT is the most common type of hemodynamically significant arrhythmia in neonates. With better modes of detection and high index of suspicion, the incidence of SVT is now estimated to be 1 in 200–250 neonates. In SVT the impulses are originating proximal to the bundle of His. The typical infant who has SVT has a regular R-R interval, with rates often greater than 230 beats/min and commonly 260–300 beats/min. The atrial and ventricular rates are equal. They are further sub-classified by the inducing mechanisms into either automatic or re-entry. Most SVTs are re-entry type atrioventricular SVTs utilizing an accessory pathway. Commonly the impulses travel down the AV node and retrogradely up the accessory pathway (Figure 7) [15, 16].
Supra ventricular tachycardia. Lead II ECG: absent P wave, narrow QRS complex and constant R-R interval.
Management depends on the hemodynamic status of the neonate. As the arrhythmia occurred secondary to the malposition of the catheter, the first step of management should be to pull back or even remove the catheter. If the neonate is relatively stable, the next step is to stop the re-entry loop (as most of the neonates with SVT have atrioventricular re-entry tachycardia) by inducing vagal maneuvers. One can perform vagal maneuvers like keeping crushed ice inside two plastic bags and place the ice pack over the face carefully for few minutes. Oropharyngeal suction can be used to stimulate the vagus. The use of vagal maneuvers in neonates are controversial, but still one can use for buying time of adenosine preparation. Pressure on eyeballs and carotid sinus massage should not be attempted in neonates, as this may cause retinal detachment and cerebral ischemia [6, 15, 16]. If tachycardia persists, the initial step of management is stabilizing the neonate (intubation/assisted ventilation/check the blood pressure and do ABG) followed by administration of intravenous adenosine. Adenosine can be given in a starting dose of 0.05 mg/kg and can be increased by 0.05 mg/kg up to 0.25 mg/kg. The dosage can be increased up to 0.3 mg/kg for recalcitrant cases with a cardiologist approval. Recent literature suggests the starting dose of adenosine as 0.1 mg/kg with the maximum of 0.5 mg/kg [8, 9].
Adenosine is an endogenously available purine nucleoside.
It is a rapidly acting (onset within 20 s) drug with a short half-life of less than 10 s as it is metabolized rapidly by adenosine deaminase.
It slows the conduction through atrioventricular node and thereby interrupts AV re-entry pathways and restores normal sinus rhythm within 20 s of its administration.
Before giving adenosine place the neonate in mild reverse Trendelenburg position with continuous ECG monitoring.
Adenosine must be given as a rapid injection (within 3 s) by peripheral intravenous route directly to the vein. Select the vein which is more proximal to the patient. Injection should be followed by rapid normal saline flush (5 ml or more).
After conversion of sinus rhythm by adenosine, always save and check the ECG strip for concealed pre-excitation.
If the correct technique is followed, adenosine will terminate 85–93% of SVTs caused by a re-entry mechanism.
Adenosine is a safe and effective drug with minimal transient side effects. The side effects include flushing (18%), changes in respiration, rarely short bradycardia, hypotension, and sweating may occur. Very rarely, short complete AV block can occur.
Adenosine will not terminate the atrial tachycardia. However, it produces transient AV block which may help to detect atrial flutter (Table 4) [8, 9].
Narrow QRS complex (≤80 ms) | Wide QRS complex (>80 ms) |
---|---|
|
|
Clinical classification of tachyarrhythmias.
Fetal period | SVT and atrial flutter |
---|---|
Neonatal period (generally, they are benign) | Premature atrial complexes (PAC) |
Neonatal period (pathological cause) | Narrow complex SVT |
Indwelling catheter in situ | Atrial flutter |
Commonly encountered tachyarrhythmia in fetal/neonatal period.
As depicted in Figure 8, bradyarrhythmias may occur either due to contact/injury to the sinoatrial node (SA node) or the atrioventricular node (AV node). So far bradyarrhythmias as complications of central venous catheters are not reported but can happen.
Types of Bradyarrhythmias.
Bradyarrhythmia can occur as a result of SA node dysfunction due to direct injury by the catheter and it can cause complications ranging from first-degree block to sinus arrest. Bradyarrhythmias can be benign but however, acutely unstable bradycardia can lead to cardiac arrest. Management includes identification and correction of reversible causes, pharmacotherapy, and rarely cardiac pacing.
AV nodal conduction disturbances can occur due to endocardial irritation by the catheters. It can lead to bradycardia ranging from first degree to third degree AV block.
Measure the length of intravascular placement of a catheter for each neonate and document it properly in the case record. If possible, double check it with another physician.
Traditional measurements for PICC line insertion length are based on straight line measurements with bony points using inch tape. These measurements are commonly overestimated, which leads to more advancement of PICC line. This can be avoided by using rope method of measurements (can use a nasogastric tube or any flexible tubes) along the course of veins applicable to lower and upper extremity veins.
Before insertion, make sure the catheter tip is not bent or curved, which is proposed to cause more damage to the vessel wall and vascular erosion. If the catheter is inappropriately placed in the intracardiac position, it can cause pericardial tamponade and pleural effusion secondary to the curved catheter.
Central venous catheter insertion should be done under strict cardiac monitoring with properly placed ECG leads. Performing physician should monitor the ECG wave patterns carefully especially while introducing the catheter beyond brachiocephalic vein. If any mild changes are observed in the ECG, the catheter should be withdrawn immediately.
If the introducer feels the cardiac pulsations in the catheter or the slightest resistance during the pathway, the catheter should be withdrawn immediately.
Fix the catheter with the exact measurement. One should avoid increasing 1 or 2 cm more, assuming that can later withdraw it after confirming the position with X-ray.
Confirmation of catheter positioning with radiography should be done immediately after the insertion of catheters. Optimizing a good position of the neonate is mandatory (Table 5).
The interaction between the neonatal posture, and radiological catheter position is well explained in advances in neonatal care.
Always aim to place the catheter in an optimal position. The ideal position is 0.5–1 cm away from the cardiac outline in preterm and 1–2 cm away from the cardiac outline in term neonates. Confirmation by ultrasound is upcoming and it is welcoming advancement in neonatal care [15]. Real-time ultrasound has been shown to have good diagnostic utility in comparison with X-ray with sensitivity of 95–96.5% and specificity of 100% in neonates [18–20].
Know the catheter tip position. Identify it in each X-ray and if it needs adjustments, perform the amendments. Do not ever forget to document it.
Prevention of catheter migration is at most important by application of the secure transparent dressing. Secure it with proper measurement and document the external catheter length. External length needs to be verified in each shift. Proper hand over by the concerned staff nurse is mandatory to notify the migration early. Repeated pump occlusion alarms could be a sign of migration [13].
Arrhythmic complications can occur anytime from the time of insertion to the time of removal of catheters. Any neonate with the catheter in situ developed arrhythmia could be due to the migration of catheter until proved otherwise. So check for migration, verify the external length and immediately withdraw the catheter. Confirm the position with an X-ray, check for kinking, curving and looping which is potentially dangerous as it can induce pericardial tamponade.
Vigilantly look for catheter migration whenever the critical neonates are on high-frequency ventilation.
Take precautions while handling for ultrasonography, daily weight check, the neonatal transfer for any cause, pre and post-operative periods and any invasive procedures which need more manipulation of neonates.
Ultrasound-guided insertion of central lines (PICC or UVC) is more reliable, safe and effective when compared with the blind procedure.
While inserting the PICC line turn the head of the neonate toward the ipsilateral side of insertion as it prevents the entry of PICC line into the jugular veins.
Upper extremity X-ray | Keep both arms and forearms straight Over the sides of the neonate |
Lower extremity X-ray | Keep both legs straight |
Ideal positions for X-rays pertaining to different sites of PICC line [10].
Central line insertion is a very common bedside procedure in NICU setup, it is not uncommon to encounter complications. Although there are various complications related to PICC line insertion, arrhythmic complications are preventable by exact measurements along the venous course, avoidance of willful over advancement of the catheter, prevention of migration and early detection of migration and adjusting the catheter tip properly. Ultrasound-guided insertion of catheter and placement of catheter tip using real-time ultrasonography is a welcoming advancement to minimize arrhythmic complications. Worldwide, the reported incidence of arrhythmic complications published in the literatures are few.
CVC | central venous catheter |
PICC | peripherally inserted central catheter |
UVC | umbilical venous catheter |
AF | atrial flutter |
SVT | supraventricular tachycardia |
NICU | neonatal intensive care unit |
IVC | inferior vena cava |
SVC | superior vena cava |
PAC | premature atrial complexes |
SA node | sinoatrial node |
AV node | atrioventricular node |
ECG | electrocardiogram |
Bioprocesses, which are consisted of a series of enzymatically catalyzed biochemical reactions in all living things, are necessary for survival. They have a high potential in terms of material synthesis, which has recently been performed by chemical techniques [1]. Furthermore, the advancement of heterologous production systems and genetic engineering techniques has resulted in pioneering initiatives to manufacture usable biomaterials [2]. These advancements also enabled the successful generation of primary and secondary metabolic pathway products in physiologically and genetically well-defined hosts, such as
NRPs are secondary metabolites that are synthesized outside of the ribosomal machinery and have a variety of properties such as cytostatics, immunosuppressants or anticancer agents, antibiotics, pigments, siderophores, toxins [3, 5, 6]. NRPs are typically produced by marine microorganisms and invertebrates, as well as soil-inhabiting microorganisms [5, 7, 8]. The majority of natural products produced by sponges, bryozoans, mollusks, and tunicates are members of the NRP or mixed polyketide–NRP families. Several of NRPs are being used in the development of new medicines for inflammatory, cancer, neurological diseases, and infectious disease nowadays [7].
Non-ribosomal peptide synthetases (NRPSs) enzymes are poly-functional mega-synthases that biosynthesize NRPs [7, 9, 10]. NRPSs, multi-modular enzyme or enzyme complexes from common bacteria, less common eukarya, and rare archaea, are capable of producing a wide range of natural pharmaceutical products (Bacitracin, antibiotics for skin infections; Bleomycin antitumor; Cyclosporin, antifungal, and immunosuppressive drugs; Daptomycin, antibiotics) [5, 7, 11]. NRPSs use both proteinogenic and nonproteinogenic amino acids (not encoded by DNA) as building blocks for the growing peptide chain [1, 7, 11, 12]. They catalyze multiple biosynthetic processes, each of which is responsible for particular one amino acid elongation on the growing peptide chain [10]. This chapter looks at the structure, function, and synthesis of NRPs, as well as producer microorganisms and their various applications.
NRPSs are responsible for nonribosomal peptide (NRP) synthesis. These are large multi-enzyme complexes that are modularly organized and serve as biosynthetic machinery and templates [5, 11, 12, 13, 14]. For example, a single NRPS of 1.6 MDa synthesizes the Cyclosporine A (7). In fungal systems, such as in the case of cyclosporine A (7), a single NRPS synthesizes peptides, whereas bacteria frequently use numerous NRPSs with genes grouped in an operon. NRPSs have a modular structure [14, 15].
In a genome mining research of 2699 genomes, Wang et al. found that more than half of the NRPS enzymes were non-modular NRPS enzymes [16]. Nonmodular NRPS enzymes can be found in siderophore biosynthesis pathways, such as EntE and VibH in enterobactin and VibE in vibriobactin, or as a standalone peptidyl carrier protein, such as BlmI from the bleomycin gene cluster. NRPS enzymes are found frequently in bacteria, less frequently in eukaryotes, and infrequently in archaea. Actinobacteria, Cyanobacteria, Firmicutes, and Proteobacteria were the phyla with the greatest number of these enzymes in the bacterial domain. There was a correlation between genome size and the number of NRPS clusters [5, 17].
A module is a part of the NRPS polypeptide chain that is in charge of integrating one amino acid into the final product. Modules can further be separated into domains (Figure 1), which represent enzyme units that catalyze distinct steps of NRP synthesis. On the protein level, domains are defined by distinctive, greatly conserved order of patterns known as “core motifs.” In certain instances, biochemical and structural data were used to confirm the involvement of greatly conserved residues in domain function (Table 1) [14].
Catalyzed reactions by various NRPS-domains [
A1 L(TS)YxEL A2 LKAGxAYL(VL)P(LI)D A3 LAYxxYTSG(ST)TGxPKG A4 FDxS A5 NxYGPTE A6 GELxJGx(VL)ARGYL A7 Y(RK)TGDL A8 GRxPxQVKIRGxRIELGEIE A9 LPxYM(IV)P A10 NGK(VL)DR | T LGG(DH)SL |
C1 SxAQxR(LM)(WY)xL C2 RHExLRTxF C3 MHHxISDG(WV)S C4 YxD(FY)AVW C5 (IV)GxFVNT(QL)(CA)xR C6 HN)QD(YD)PFE C7 RDxSRNPL | Te GxSxG |
E1 PIQxWF E2 HHxISDG(WV)S E3 DxLLxAxG E4 EGHGRE E5 RTVGWFTxxYP(YV)PFE E6 PxxGxGYG E7 FNYLG(QR) | Cy1 FPL(TS)xxQxAYxxGR Cy2 RHx(IM)L(PAL)x(ND)GxQ C3 D(NLI)xDxxS Cy3 LPxxPxLPLxxxP Cy4 (TS)(PA)3x(LAF)6x(IVT)LxxW Cy5 (GA)DFTxLxLL Cy6 PVVFTSxL Cy7 (ST)(QR)TPQVx(LI)D13xWD |
Ox1 KYxYxSxGxxY(PG)VQ Ox2 GxxxG(LV)xxGxYYY(HD)P Ox3 IxxxYG | M1 VL(DE)xGxGxG M2 NELSxYRYxAV M3 VExSxARQxGxLD |
R1 V(L)(L)TG(A)TG(F)(L)GxxLL R2 Vx(L)(L)VR(A) R3 GPL(G)x(P)x(L)GL R4 V(Y)PYxYLxx(P)NVxxT R5 GYxxSKW(A)(A)E R6 R(P)G R7 YxxxxG(LF)LxxP |
NPRS-domains’ core-motifs [14].
There are three domains in a module. These are 1) the adenylation (A) domain, 2) the peptidyl carrier protein (PCP) or thiolation (T) domain, and 3) the condensation (C) domain, all of which are responsible for the synthesis of NRPs. A module may include additional tailoring or altering domains incorporating epimerization (E), methylation and oxidation domains or a heterocyclization (Cy) domain in place of a C-domain. Finally, most NRPS termination modules have a TE-domain, which is in charge of releasing linear, cyclic, or branching cyclic peptides [5, 9, 10, 11, 15, 18, 19, 20, 21].
The order of the modules is frequently aligned with the sequences of the resulting peptides. NRP synthesis begins at the N-terminus and ends at the C-terminus, yielding peptides that are typically 3–15 amino acids long. The released peptides contain amino acids, that is, imino acids or ornithine and their structures are linear, cyclic-macrocyclic, branched-cyclic, branched-macrocyclic, dimers or trimers of identical structural elements [5].
The A-domain is responsible for the first step in biosynthesis, which involves recognizing and activating the amino acid substrate via adenylation with Mg-ATP, resulting in an aminoacyl adenylated intermediate. Around 550 amino acids make up domain A. It has 10 amino acid residues that serve as NRPS enzyme “codons” and are essential for substrate specificity. The D and L forms of the 20 amino acids used in ribosomal protein synthesis, as well as non-proteinogenic amino acids like imino acids, ornithine, and hydroxy acids like β-butyric acids and α-aminoadipic, are substrates recognized by the A-domain. The PCP-domain, which consists of about 80 amino acids and covalently attaches the activated amino acid to their cofactor 4′-phosphopantetheine (PP) arm via a thioester bond, completes the second step. And also, the active substrate and elongation intermediates are transferred to the C-domain via this domain. In the last step, C-domain, which contains approximately 450 amino acids, catalyzes the formation of peptide bonds between the carboxyl group of the incipiently synthesized peptide and the amino acid transported by the side module [5, 22]. Furthermore, this domain allows the expanding chain to be translocated to the next module. Following this step, the linear intermediate peptide is liberated in bacteria via internal cyclization or hydrolysis with the help of the Thioesterase (TE) domain. On the other hand, it appears less commonly in fungi’s NRPSs. Fungi use a variety of ways to release chains. The first is a thioesterase NADP(H)-dependent reductase domain (R), which catalyzes NADPH reduction to create an aldehyde and the second is a terminal C domain, which catalyzes release by forming intermolecular or intramolecular amide bonds. By N-, C-, and O-methylation, halogenation, acylation, hydroxylation, glycosylation, or heterocyclic ring formation, the primary product of this synthesis can be changed post-synthetically to reach its mature form by additional tailoring enzymes that are not part of the NRPS. The structural diversity of NRPs is formed in part by these enzymes and their reactions [5].
Because of their extensive multidomain organization, NRPS genes are easier to identify using recent genome mining technologies, and they are also relatively easy to detect. Secondary metabolites production genes are frequently found in bacterial and fungal gene clusters. The clusters’ core is thought to be NRPS genes. Nevertheless, they are linked to genes involved in building blocks synthesis, product ornamentation, self-resistance, and peptide export. For the purpose of analyzing and in silico exploration of NRPS pathways, advanced genome sequencing techniques have made genome mining methodologies available, which are assisted by a variety of bioinformatics tools, such as AntiSMASH, PRISM, and SMURF [23].
Nowadays, known NRP structures are divided into various categories, each with its own structural characteristics. Lipocyclopeptides with varied linkage patterns, such as fengycin, iturin, surfactin, and head-to-tail-cyclized peptides of varying ring sizes, such as cyclosporine, gramicidin S, maybe the largest group. There are also a lot of linear peptide configurations. They include tripeptides (such as sevadicin and bialaphos) as well as 20-mer peptides (e.g., alamethicin, peptaibols). The current highest size limit for NRPs is syringopeptin 25A, which has 25 amino acids (syringopeptin 25A). Tailoring enzymes modify the structure of some NRPs. The most structurally complicated molecules are probably bleomycins, ergopeptides, glycopeptide antibiotics, and β-lactams [23].
Figure 2 shows some NRPs with diverse structures and a wide spectrum of activities. ACV-tripeptide (6), for example, is a precursor to antibiotics of the penicillin and cephalosporin families. Gramicidin S (4), tyrocidine A (1), and vancomycin (5) are three other antibiotic-active substances. Cyclosporin A (7), an immunosuppressive drug, is used in the post-transplantation care of patients. Cancer is treated with cytostatic agents, such as bleomycin A2 (8) and epothilone (9). Enterobactin (10), bacillibactin (11), mixochelin A (12), yersiniabactin (13), and vibriobactin (14) are examples of iron chelating agents. These compounds, known as siderophores, are created in iron-deficient environments to provide bacteria with an iron source. Figure 2 also depicts the structures of pigments like indigodin (15), toxins like thaxtomin A (17), and peptides with uncertain functions like anabaenopeptilide 90-A (18) [14].
Some NRPs with structural diversity [
NRPs have a number of structural characteristics that distinguish them from ribosomal peptides. For example, non-proteinogenic amino acids, such as ornithine in 1, 2, and 4, hydroxyphenyl or dihydroxyphenyl-glycine in 5 and (4R)-4-[(E)-2-butenyl]-4-methyl-L. -threonine (Bmt) in 7, are included. Furthermore, the structures are frequently macrocyclic (1), branched macrocyclic (2), or dimers of two (4) or trimers of three (10, 11) structural components. Smaller heterocyclic rings, such as thiazole in 9, thiazoline in 13, or oxazoline in 14, are common structural properties of nonribosomal peptides. In addition, fatty acids (3), glycosylations (5), N-methylations (7), and N-formylations (18) may also be present, as well as the addition of propionate units (8) or acetate [14].
NRPs are typically produced by marine microorganisms, soil-inhabiting microorganisms, including
Novel peptide products’ biological functions are strictly associated with their chemical structure, which is constrained by a peptide sequence that ensures specific interaction with a specific molecular target. Chemical alterations, such as the incorporation of fatty acid chains, D-amino acids, glycosylated amino acids, and heterocyclic rings, as well as cyclization or oxidative cross-linking of side chains, add a lot to these unique interactions. Bacitracin, fengycin, pristinamycin, surfactin, tyrocidine, and vancomycin are examples of novel peptides with antibacterial and antifungal properties [25].
When the ribosomal code was deciphered in the 1960s, Tatum and coworkers discovered that ribosomes had no effect on cell-based tyrocidine production [23, 26]. The first NRPs agent is tyrocidine, a cyclic decapeptide that is biosynthesized outside of the
Compound | Biosynthetic class of agent | Source | Disease/Molecular target |
---|---|---|---|
Bacitracin | Cyclic peptide | Antibiotic/dephosphorylation of C55-isoprenyl pyrophosphate | |
Bleomycin | Hybrid peptide | Antibiotic/inhibition of DNA synthesis | |
Capreomycin | Cyclicpeptide | Antibiotic/protein synthesis inhibitor | |
Carbapenems | Synthetic thienamycin | Antibacterial (multidrug resistant)/bacterial cell-wall biosynthesis (peptidoglycan;β-lactamase inhibition) | |
Cephalosporin | Antibiotic/Alters bacterial outer membrane | ||
Chlorampheniol | Synthetic;further derivatives: thiamphenicol [c], florfenicol | Antibacterial/inhibition of ribosomal protein synthesis | |
Colistin (Polymyxin E) | — | Antibacterial/binding to lipopolysaccharide (outer membrane), interaction with the cytoplasmic membrane | |
Dalbavancin | Semisynthetic teicoplanin derivative | — | Antibacterial (Gram-positive)/membrane anchoring; disruption of cell membrane and inhibition of bacterial cell wall biosynthesis |
Daptomycin | Lipopeptide | Antibiotic (Gram-positive)/disrupts the cell membrane | |
Gramicidin | Linear pentadecapeptide | Antibiotic/ion-channel formation, increasing the permeability of the membrane | |
Lincomycin | — | Antibacterial (patients allergic to penicillin) inhibition of the ribosomal protein synthesis (50S-subunit, dissociation of peptidyl-tRNA from the ribosome) | |
Monobactams | — | Antibacterial (Gram-negative)/bacterial cell-wall biosynthesis | |
Oritavancin | — | Semi synthetic | Antibiotic/disrupts the cell membrane |
Polymyxin B | Polypeptides | Antibacterial (Gram-negative)/binding to lipopolysaccharide (outer membrane), interaction with cytoplasmic membrane | |
Pristinamycin | Depsipeptide | Antibacterial (Gram-positive)/ribosomal biosynthesis (50S-subunit, peptidyl transfer, and elongation of protein synthesis) | |
Teicoplanin | Glycopeptide | Antibiotic/inhibit cell wall synthesis | |
Telavancin | — | Antibacterial (Gram-positive) disruption of cell membrane and inhibition of bacterial cell-wall biosynthesis | |
Tyrothricin | — | Antibacterial (Gram-positive)/disruption of cell membrane | |
Vancomycin | Glycopeptide | Antibiotic/inhibit cell wall synthesis | |
Virginiamycin | — | Antibacterial/ribosomal biosynthesis (50S-subunit, peptidyl transfer, and elongation of protein synthesis) |
As demonstrated in Table 2, systemic and topical antibacterials are the most often used NRPs-based drugs, accounting for billions of dollars in the chemical and pharmaceutical industry sales. Table 3 lists their other applications, which include anticancer agents, antifungals, animal feed additives, immunosuppressants (cyclosporine), obstetrics (ergometrine), and pain management (ergotamine).
Agent | Origin | Properties and area of application |
---|---|---|
Actinomycin D (Dactinomycin) | Antitumor/DNA intercalator, inhibition of transcription | |
Bialaphos | Herbicide/tripeptide prodrug, inhibitor of glutamine synthetase | |
Bleomycin A2, B2 | Antitumor/metal-dependent oxidative cleavage of DNA in presence of molecular oxygen | |
Capreomycin | Antituberculous/ inhibition of the ribosomal protein synthesis (16S and 23S-rRNA) | |
Carfilzomib | Synthetic derivative of epoxomycin ( | Anticancer/proteasome inhibitor |
Caspofungin | Antifungal (candidiasis, aspergillosis) fungal cell-wall integrity ((1-3)-β-D-glucan synthase) | |
Cyclosporine A | Immunosuppressant/cyclophilin binding, inhibition of IL-2 expression (inhibition of T-cell activation) | |
Emodepside | Anthelmintic/Slo-1 receptor (K+ channel) | |
Enduracidin (Enramycin) | Antibacterial, food additive/inhibition of MurG (essential for cell-wall biosynthesis in Gram positive bacteria), inhibition of the transglycosylation step of peptidoglycan biosynthesis | |
Enniatins (fusafungine) | Antibacterial (topical), antifungal, anti-inflammatory/ ionophore (NH4+) membrane depolarization | |
Ergometrine (ergonovine) | Obstetrics/interaction with a-adrenergic, dopaminergic and serotonin receptors | |
Ergotamine | Migraine vasoconstrictive (5-HT1B receptor, but also dopamine and noradrenaline receptors) | |
Romidepsin | Antitumor/histone deacetylase inhibitor (inducing apoptosis) | |
Trabectedin | Bacterial symbiont of | Antitumor (antiproliferative, treatment of soft tissue sarcoma) DNA binder, blocks binding of transcription factors |
Marketed-NRPs agents [23].
In the medical field, NRP-based marketed drugs, such as Cyclosporin A and Bleomycin A2, have high selling prices. The cost of these medicines is $107 for 25 mg of Cyclosporine A (98% purity) obtained from
The 70% discovery of NRPs with antibacterial, antiviral, cytostatic, immunosuppressive, antimalarial, antiparasitic, animal growth promoters, and natural insecticides activity is mostly attributed to marine organisms [13]. NRPs obtained from marine organisms (sponges, tunicates, and their associated phyla, such as Acidobacteria, Actinobacteria, Bacteriodetes, Chloroflexi, Cyanobacteria, Nitrospira, Planctomycetes, Poribacteria, Proteobacteria, Verrucomicrobia, and Archaea) have excellent binding properties, low off-target toxicity, and high stability and these properties make them a promising molecule for the development of new therapeutics pharmacologically active in many clinical searches. Table 4 shows the chemical structure and source of various NRPs isolated from marine sponges and tunicates.
NRPs agents | Chemical class | Origin | Target |
---|---|---|---|
Miraziridine A | Linear pentapeptide | Cancer/inhibit protease cathepsin B | |
Haligramides A-B | Cyclic hexapeptides | Cancer/A-549 (lung), HCT-15 (colon), SF-539 (CNS), SNB-19 (CNS) | |
Prepatellamide A | Cyclic peptide | Cancer/P388 murine leukemia cell lines | |
Tamandarins A-B | Depsipeptides | Cancer/pancreatic carcinoma BX-PC3, prostatic cancer DU-145, head and neck carcinoma UMSCC10b | |
Microsclerodermins F–I | Cyclic peptides | Cancer/HCT-116 cell line | |
Wainunuamide | Cyclic hexapeptide | Cancer/A2780 ovarian, K562 leukemia cancer cells | |
Leucamide A | Cyclic hexapeptide | Cancer/Tumor cell lines HM02, HepG2, Huh7 | |
Axinellin C | Cyclic octapeptide | Cancer/A2780 ovarian, K562 leukemia cancer cells | |
Milnamide D | Linearpeptide | Cancer/HCT-116 cells | |
Kapakahines E–G | — | Cancer/P388 murine leukemia cells | |
Didmolamides A-B | Cyclic hexapeptides | Cancer Tumor cell lines (A549, HT29 and MEL28) | |
Bistratamides E–J | Cyclic hexapeptides | Cancer/Human colon tumor (HCT-116) cell line | |
Milnamide C | — | Cancer/MDA-MB-435cancer cells | |
Scleritodermin A | Cyclic peptide | Cancer | |
Microcionamids A-B | — | Cancer/Human breast tumor cell lines MCF-7 and SKBR-3 | |
Kendarimide A | Linear peptide | Cancer/KB-C2 cells | |
Phakellistatin 14 | Cyclo heptapeptide | Cancer/Murine lymphocytic leukemia P388 cell line | |
Polytheonamides A-B | Polypeptides | Cancer/P388 murine leukemia cells | |
Neopetrosiamides A-B | Tricyclic peptides | Cancer | |
Seragamides A–F | Depsipeptides | Cancer | |
Theopapuamide | Cyclic depsipeptide | Cancer/CEM-TART, HCT-116 cell lines | |
Azumamide A-E | Cyclo tetrapeptides | Cancer | |
Callyaerin G | Cyclic peptide | Cancer/Mouselymphoma cell line (L5178Y) and HeLa cells | |
Stylopeptide 2 | Cyclo decapeptide | Cancer/BT-549 and HS578T breast cancer cell lines | |
Ciliatamides A-C | Lipopeptides | Cancer/HeLa cells | |
Diazonamides C–E | Macrocyclic peptides | Cancer/Human tumor cell lines (A549, HT29, MDA-MB231) | |
Rolloamide A-B | Cyclic heptapeptides | Cancer | |
Euryjanicin A | Cycloheptapeptide | Cancer | |
Callyaerin A–F and H | Cyclic peptides | Cancer/L5178Y cell line | |
Papuamides E-F | Depsipeptides | Cancer/Brine shrimp | |
Stylissamide X | Octapeptide | Cancer/HeLa cells | |
Gombamide A | Hexapeptide | Cancer/K562 and A549 cell lines | |
Microspinosamide | Cyclic depsipeptide | HIV | |
Neamphamide A | Cyclic depsipeptide | HIV | |
Mirabamides A-D | Cyclic depsipeptide | HIV | |
Homophymine A | Cyclodepsipeptide | HIV/PBMC cell line | |
Celebeside A-C | Depsipeptides | HIV/Colon carcinoma (HCT-116) cells | |
Theopapuamides B–D, Mutremdamide A, Koshikamides C-H | Cyclic depsipeptide | HIV | |
Ceratospongamide | Cyclic heptapeptide | Inflammation | |
Halipeptin A-B | Cyclic depsipeptide | Inflammation | |
Perthamide C-D | Cyclopeptide | Inflammation | |
Solomonamide A- B | Cyclic peptide | Inflammation | |
Stylissatin A | Cyclic peptide | Murine macrophage RAW264.7 | |
Dicynthaurin | — | Antimicrobial | |
Nagahamide A | Depsipeptide | Antibacterial | |
Plicatamide | Octapeptide | Antimicrobial | |
Callipeltins | — | ||
Citronamides A- B | — | ||
Renieramide | Cyclic tripeptide | — | |
Phoriospongins A-B | Depsipeptide | Nematocidal/ |
Agents produced from marine sponges and tunicates which are based on NRPs [7].
In the NCBI database, there are currently about 1.164 distinct non-ribosomal peptides that form over 500 different monomers including both proteinogenic and non-proteinogenic L- and D-amino acids, as well as amines and carboxylic acids. These complex secondary metabolites’ linear, cyclic, branching, or other complicated primary structures are frequently altered to enhance clinical qualities and/or bypass resistance mechanisms. Indeed, the nucleotide sequence modification of a native NRPS gene or mixing modules from multiple NRPSs makes them more efficient with pharmacological properties. Several bioengineering and molecular techniques have been developed during the last few decades to produce modified NRPs with improved physicochemical characteristics and bioactivity [13].
In this chapter, we discussed the significance, synthesis, and application areas of NRPs-based agents, which have received a lot of interest as a new source of pharmaceutical agents. NRPs with unique chemical structures and diverse biological actions, such as antibacterials (penicillin, vancomycin), anticancer compounds (bleomycin), and immunosuppressants (cyclosporine), have been researched as novel compounds for new drug discovery and development throughout the last several decades.
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\\n\\nNothing in this Publication Agreement shall have the effect of excluding or limiting any liability for death or personal injury caused by negligence or any other liability that cannot be excluded or limited by applicable law.
\\n\\nTERMINATION
\\n\\nIntechOpen has the right to terminate this Publication Agreement for quality, program, technical or other reasons with immediate effect, including without limitation (i) if the Author and/or any Co-Author commits a material breach of this Publication Agreement; (ii) if the Author and/or any Co-Author (being a private individual) is the subject of a bankruptcy petition, application or order; or (iii) if the Author and/or any Co-Author (as a corporate entity) commences negotiations with all or any class of its creditors with a view to rescheduling any of its debts, or makes a proposal for, or enters into, any compromise or arrangement with any of its creditors.
\\n\\nIn the event of termination, IntechOpen will notify the Author of the decision in writing.
\\n\\nIntechOpen’s DUTIES AND RIGHTS
\\n\\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen, at its discretion, agrees to publish the Work attributing it to the Author and Co-Authors.
\\n\\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen agrees to provide publishing services which include: managing editing (editorial and publishing process coordination, Author assistance); publishing software technology; language copyediting; typesetting; online publishing; hosting and web management; and abstracting and indexing services.
\\n\\nIntechOpen agrees to offer free online access to readers and use reasonable efforts to promote the Publication to relevant audiences.
\\n\\nIntechOpen is granted the authority to enforce the rights from this Publication Agreement on behalf of the Author and Co-Authors against third parties, for example in cases of plagiarism or copyright infringements. In respect of any such infringement or suspected infringement of the copyright in the Work, IntechOpen shall have absolute discretion in addressing any such infringement that is likely to affect IntechOpen's rights under this Publication Agreement, including issuing and conducting proceedings against the suspected infringer.
\\n\\nIntechOpen has the right to include/use the Author and Co-Authors names and likeness in connection with scientific dissemination, retrieval, archiving, web hosting and promotion and marketing of the Work and has the right to contact the Author and Co-Authors until the Work is publicly available on any platform owned and/or operated by IntechOpen.
\\n\\nMISCELLANEOUS
\\n\\nFurther Assurance: The Author shall ensure that any relevant third party, including any Co-Author, shall execute and deliver whatever further documents or deeds and perform such acts as IntechOpen reasonably requires from time to time for the purpose of giving IntechOpen the full benefit of the provisions of this Publication Agreement.
\\n\\nThird Party Rights: A person who is not a party to this Publication Agreement may not enforce any of its provisions under the Contracts (Rights of Third Parties) Act 1999.
\\n\\nEntire Agreement: This Publication Agreement constitutes the entire agreement between the parties in relation to its subject matter. It replaces all prior agreements, draft agreements, arrangements, collateral warranties, collateral contracts, statements, assurances, representations and undertakings of any nature made by, or on behalf of, the parties, whether oral or written, in relation to that subject matter. Each party acknowledges that in entering into this Publication Agreement it has not relied upon any oral or written statements, collateral or other warranties, assurances, representations or undertakings which were made by or on behalf of the other party in relation to the subject matter of this Publication Agreement at any time before its signature (known as the "Pre-Contractual Statements"), other than those which are set out in this Publication Agreement. Each party hereby waives all rights and remedies which might otherwise be available to it in relation to such Pre-Contractual Statements. Nothing in this clause shall exclude or restrict the liability of either party arising out of any fraudulent pre-contract misrepresentation or concealment.
\\n\\nWaiver: No failure or delay by a party to exercise any right or remedy provided under this Publication Agreement or by law shall constitute a waiver of that or any other right or remedy, nor shall it preclude or restrict the further exercise of that or any other right or remedy. No single or partial exercise of such right or remedy shall preclude or restrict the further exercise of that or any other right or remedy.
\\n\\nVariation: No variation of this Publication Agreement shall have effect unless it is in writing and signed by the parties, or their duly authorized representatives.
\\n\\nSeverance: If any provision, or part-provision, of this Publication Agreement is, or becomes invalid, illegal or unenforceable, it shall be deemed modified to the minimum extent necessary to make it valid, legal and enforceable. If such modification is not possible, the relevant provision or part-provision shall be deemed deleted. Any modification to, or deletion of, a provision or part-provision under this clause shall not affect the validity and enforceability of the rest of this Publication Agreement.
\\n\\nNo partnership: Nothing in this Publication Agreement is intended to, or shall be deemed to, establish or create any partnership or joint venture or the relationship of principal and agent or employer and employee between IntechOpen and the Author or any Co-Author, nor authorize any party to make or enter into any commitments for, or on behalf of, any other party.
\\n\\nGoverning law: This Publication Agreement and any dispute or claim, including non-contractual disputes or claims arising out of, or in connection with it, or its subject matter or formation, shall be governed by and construed in accordance with the law of England and Wales. The parties submit to the exclusive jurisdiction of the English courts to settle any dispute or claim arising out of, or in connection with, this Publication Agreement, including any non-contractual disputes or claims.
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\n\nCORRESPONDING AUTHOR'S GRANT OF RIGHTS
\n\nSubject to the following Article, the Author grants to IntechOpen, during the full term of copyright, and any extensions or renewals of that term, the following:
\n\nThe foregoing licenses shall survive the expiry or termination of this Publication Agreement for any reason.
\n\nThe Author, on his or her own behalf and on behalf of any of the Co-Authors, reserves the following rights in the Work but agrees not to exercise them in such a way as to adversely affect IntechOpen's ability to utilize the full benefit of this Publication Agreement: (i) reprographic rights worldwide, other than those which subsist in the typographical arrangement of the Work as published by IntechOpen; and (ii) public lending rights arising under the Public Lending Right Act 1979, as amended from time to time, and any similar rights arising in any part of the world.
\n\nThe Author, and any Co-Author, confirms that they are, and will remain, a member of any applicable licensing and collecting society and any successor to that body responsible for administering royalties for the reprographic reproduction of copyright works.
\n\nSubject to the license granted above, copyright in the Work and all versions of it created during IntechOpen's editing process, including all published versions, is retained by the Author and any Co-Authors.
\n\nSubject to the license granted above, the Author and Co-Authors retain patent, trademark and other intellectual property rights to the Work.
\n\nAll rights granted to IntechOpen in this Article are assignable, sublicensable or otherwise transferrable to third parties without the specific approval of the Author or Co-Authors.
\n\nThe Author, on his/her own behalf and on behalf of the Co-Authors, will not assert any rights under the Copyright, Designs and Patents Act 1988 to object to derogatory treatment of the Work as a consequence of IntechOpen's changes to the Work arising from the translation of it, corrections and edits for house style, removal of problematic material and other reasonable edits as determined by IntechOpen.
\n\nAUTHOR'S DUTIES
\n\nWhen distributing or re-publishing the Work, the Author agrees to credit the Monograph/Compacts as the source of first publication, as well as IntechOpen. The Author guarantees that Co-Authors will also credit the Monograph/Compacts as the source of first publication, as well as IntechOpen, when they are distributing or re-publishing the Work.
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\n\nAll payments shall be due 30 days from the date of issue of the invoice. The Author or whoever is paying on behalf of the Author and Co-Authors will bear all banking and similar charges incurred.
\n\nThe Author shall obtain in writing all consents necessary for the reproduction of any material in which a third-party right exists, including quotations, photographs and illustrations, in all editions of the Work worldwide for the full term of the above licenses, and shall provide to IntechOpen, at its request, the original copies of such consents for inspection or the photocopies of such consents.
\n\nThe Author shall obtain written informed consent for publication from those who might recognize themselves or be identified by others, for example from case reports or photographs.
\n\nThe Author shall respect confidentiality during and after the termination of this Agreement. The information contained in all correspondence and documents as part of the publishing activity between IntechOpen and the Author and Co-Authors are confidential and are intended only for the recipients. The contents of any communication may not be disclosed publicly and are not intended for unauthorized use or distribution. Any use, disclosure, copying, or distribution is prohibited and may be unlawful.
\n\nAUTHOR'S WARRANTY
\n\nThe Author and Co-Authors confirm and warrant that the Work does not and will not breach any applicable law or the rights of any third party and, specifically, that the Work contains no matter that is defamatory or that infringes any literary or proprietary rights, intellectual property rights, or any rights of privacy.
\n\nThe Author and Co-Authors confirm that: (i) the Work is their original work and is not copied wholly or substantially from any other work or material or any other source; (ii) the Work has not been formally published in any other peer-reviewed journal or in a book or edited collection, and is not under consideration for any such publication; (iii) Authors and any applicable Co-Authors are qualifying persons under section 154 of the Copyright, Designs and Patents Act 1988; (iv) Authors and any applicable Co-Authors have not assigned, and will not during the term of this Publication Agreement purport to assign, any of the rights granted to IntechOpen under this Publication Agreement; and (v) the rights granted by this Publication Agreement are free from any security interest, option, mortgage, charge or lien.
\n\nThe Author and Co-Authors also confirm and warrant that: (i) he/she has the power to enter into this Publication Agreement on his or her own behalf and on behalf of each Co-Author; and (ii) has the necessary rights and/or title in and to the Work to grant IntechOpen, on behalf of themselves and any Co-Author, the rights and licences in this Publication Agreement. If the Work was prepared jointly by the Author and Co-Authors, the Author confirms that: (i) all Co-Authors agree to the submission, license and publication of the Work on the terms of this Publication Agreement; and (ii) the Author has the authority to enter into this biding Publication Agreement on behalf of each Co-Author. The Author shall: (i) ensure each Co-Author complies with all relevant provisions of this Publication Agreement, including those relating to confidentiality, performance and standards, as if a party to this Publication Agreement; and (ii) remain primarily liable for all acts and/or omissions of each Co-Author.
\n\nThe Author agrees to indemnify IntechOpen harmless against all liabilities, costs, expenses, damages and losses, as well as all reasonable legal costs and expenses suffered or incurred by IntechOpen arising out of, or in connection with, any breach of the agreed confirmations and warranties. This indemnity shall not apply in a situation in which a claim results from IntechOpen's negligence or willful misconduct.
\n\nNothing in this Publication Agreement shall have the effect of excluding or limiting any liability for death or personal injury caused by negligence or any other liability that cannot be excluded or limited by applicable law.
\n\nTERMINATION
\n\nIntechOpen has the right to terminate this Publication Agreement for quality, program, technical or other reasons with immediate effect, including without limitation (i) if the Author and/or any Co-Author commits a material breach of this Publication Agreement; (ii) if the Author and/or any Co-Author (being a private individual) is the subject of a bankruptcy petition, application or order; or (iii) if the Author and/or any Co-Author (as a corporate entity) commences negotiations with all or any class of its creditors with a view to rescheduling any of its debts, or makes a proposal for, or enters into, any compromise or arrangement with any of its creditors.
\n\nIn the event of termination, IntechOpen will notify the Author of the decision in writing.
\n\nIntechOpen’s DUTIES AND RIGHTS
\n\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen, at its discretion, agrees to publish the Work attributing it to the Author and Co-Authors.
\n\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen agrees to provide publishing services which include: managing editing (editorial and publishing process coordination, Author assistance); publishing software technology; language copyediting; typesetting; online publishing; hosting and web management; and abstracting and indexing services.
\n\nIntechOpen agrees to offer free online access to readers and use reasonable efforts to promote the Publication to relevant audiences.
\n\nIntechOpen is granted the authority to enforce the rights from this Publication Agreement on behalf of the Author and Co-Authors against third parties, for example in cases of plagiarism or copyright infringements. In respect of any such infringement or suspected infringement of the copyright in the Work, IntechOpen shall have absolute discretion in addressing any such infringement that is likely to affect IntechOpen's rights under this Publication Agreement, including issuing and conducting proceedings against the suspected infringer.
\n\nIntechOpen has the right to include/use the Author and Co-Authors names and likeness in connection with scientific dissemination, retrieval, archiving, web hosting and promotion and marketing of the Work and has the right to contact the Author and Co-Authors until the Work is publicly available on any platform owned and/or operated by IntechOpen.
\n\nMISCELLANEOUS
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\n\nThird Party Rights: A person who is not a party to this Publication Agreement may not enforce any of its provisions under the Contracts (Rights of Third Parties) Act 1999.
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\n\nWaiver: No failure or delay by a party to exercise any right or remedy provided under this Publication Agreement or by law shall constitute a waiver of that or any other right or remedy, nor shall it preclude or restrict the further exercise of that or any other right or remedy. No single or partial exercise of such right or remedy shall preclude or restrict the further exercise of that or any other right or remedy.
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\n\nSeverance: If any provision, or part-provision, of this Publication Agreement is, or becomes invalid, illegal or unenforceable, it shall be deemed modified to the minimum extent necessary to make it valid, legal and enforceable. If such modification is not possible, the relevant provision or part-provision shall be deemed deleted. Any modification to, or deletion of, a provision or part-provision under this clause shall not affect the validity and enforceability of the rest of this Publication Agreement.
\n\nNo partnership: Nothing in this Publication Agreement is intended to, or shall be deemed to, establish or create any partnership or joint venture or the relationship of principal and agent or employer and employee between IntechOpen and the Author or any Co-Author, nor authorize any party to make or enter into any commitments for, or on behalf of, any other party.
\n\nGoverning law: This Publication Agreement and any dispute or claim, including non-contractual disputes or claims arising out of, or in connection with it, or its subject matter or formation, shall be governed by and construed in accordance with the law of England and Wales. The parties submit to the exclusive jurisdiction of the English courts to settle any dispute or claim arising out of, or in connection with, this Publication Agreement, including any non-contractual disputes or claims.
\n\nPolicy last updated: 2018-09-11
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On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. 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Those nanoparticles with small size to large surface area (1–100 nm) have several potential functions. These days, sustainable agriculture is needed. The development of nanochemicals has appeared as promising agents for the plant growth, fertilizers and pesticides. In recent years, the use of nanomaterials has been considered as an alternative solution to control plant pests including insects, fungi and weeds. Several nanomaterials are used as antimicrobial agents in food packing in which several nanoparticles such as silver nanomaterials are in great interest. Many nanoparticles (Ag, Fe, Cu, Si, Al, Zn, ZnO, TiO2, CeO2, Al2O3 and carbon nanotubes) have been reported to have some adverse effects on plant growth apart from the antimicrobial properties. In food industries, nanoparticles are leading in forming the food with high quality and good nutritive value.",book:{id:"9012",slug:"applications-of-nanobiotechnology",title:"Applications of Nanobiotechnology",fullTitle:"Applications of Nanobiotechnology"},signatures:"Alaa Y. Ghidan and Tawfiq M. Al Antary",authors:null},{id:"68760",doi:"10.5772/intechopen.88744",title:"Nanofibrous Scaffolds for Skin Tissue Engineering and Wound Healing Based on Synthetic Polymers",slug:"nanofibrous-scaffolds-for-skin-tissue-engineering-and-wound-healing-based-on-synthetic-polymers",totalDownloads:1278,totalCrossrefCites:5,totalDimensionsCites:15,abstract:"Nanofibrous scaffolds are popular materials in all areas of tissue engineering, because they mimic the fibrous component of the natural extracellular matrix. In this chapter, we focused on the application of nanofibers in skin tissue engineering and wound healing, because the skin is an organ with several vitally important functions, particularly barrier, thermoregulatory, and sensory functions. Nanofibrous meshes not only serve as carriers for skin cells but also can prevent the penetration of microbes into wounds and can keep appropriate moisture in the damaged skin. The nanofibrous meshes have been prepared from a wide range of synthetic and nature-derived polymers. This review is concentrated on synthetic non-degradable and degradable polymers, which have been explored for skin tissue engineering and wound healing. These synthetic polymers were often combined with natural polymers of the protein or polysaccharide nature, which improved their attractiveness for cell colonization. The nanofibrous scaffolds can also be loaded with various bioactive molecules, such as growth factors, hormones, vitamins, antioxidants, antimicrobial, and antitumor agents. In advanced tissue engineering approaches, the cells on the nanofibrous scaffolds are cultured in dynamic bioreactors enabling appropriate mechanical stimulation of cells and at air-liquid interface. This chapter summarizes recent results achieved in the field of nanofiber-based skin tissue engineering, including results of our research group.",book:{id:"9012",slug:"applications-of-nanobiotechnology",title:"Applications of Nanobiotechnology",fullTitle:"Applications of Nanobiotechnology"},signatures:"Lucie Bacakova, Marketa Zikmundova, Julia Pajorova, Antonin Broz, Elena Filova, Andreu Blanquer, Roman Matejka, Jana Stepanovska, Petr Mikes, Vera Jencova, Eva Kuzelova Kostakova and Alla Sinica",authors:null},{id:"52066",doi:"10.5772/64394",title:"Supported Gold Nanoparticles as Promising Catalysts",slug:"supported-gold-nanoparticles-as-promising-catalysts",totalDownloads:3094,totalCrossrefCites:5,totalDimensionsCites:11,abstract:"In recent times, gold nanoparticles (AuNPs) either in the form of colloids or as supported nanoparticles are being extensively used as efficient redox catalyst materials. Catalysis particularly using supported gold nanoparticles (AuNPs) has attracted immense research interest due to their unique properties and greater potentiality that is directly related to their particle size. The primary objective of this chapter is to provide comprehensive overview about gold metal nanoparticles (AuNPs) and their application as promising catalysts. This chapter contains six sections in total. Section 1 starts with a general introduction, recent progress, and brief summary of the application of supported AuNPs as promising catalysts for different applications. Section 2 briefs the properties and stability of gold nanoparticles. Section 3 reviews the preparation methods of supported AuNPs for a wide range of catalytic applications. Section 4 describes briefly some of the most commonly reported supported AuNPs for different applications. Section 5 concentrates on our own results related to the application of supported AuNPs in heterogeneous catalysis. In this section, the oxidation of cyclohexane (CH) and benzyl alcohol (BA) to adipic acid (AA), benzaldehyde (BAl), and ammoxidation of 2-methylpyrazine to 2-cyanopyrazine are discussed. Finally, Section 6 describes, main points and outlook are summarized.",book:{id:"5310",slug:"catalytic-application-of-nano-gold-catalysts",title:"Catalytic Application of Nano-Gold Catalysts",fullTitle:"Catalytic Application of Nano-Gold Catalysts"},signatures:"Ahmad Alshammari and Venkata Narayana Kalevaru",authors:[{id:"178547",title:"Dr.",name:"Ahmad",middleName:null,surname:"Alshammari",slug:"ahmad-alshammari",fullName:"Ahmad Alshammari"},{id:"180753",title:"Dr.",name:"V. Narayana",middleName:null,surname:"Kalevaru",slug:"v.-narayana-kalevaru",fullName:"V. Narayana Kalevaru"}]},{id:"50852",doi:"10.5772/63729",title:"Synthesis of Gold Nanoparticles Using Amino Acids by Light Irradiation",slug:"synthesis-of-gold-nanoparticles-using-amino-acids-by-light-irradiation",totalDownloads:3602,totalCrossrefCites:3,totalDimensionsCites:10,abstract:"The synthesis of nanoparticles is generally carried out by chemical reduction, which is effective but uses a number of toxic substances, making the process potentially harmful to the environment. Thus, as part of the search for environmentally friendly or green synthetic methods, this chapter aimed to present the synthesis of gold nanoparticles (AuNPs) using only HAuCl4, Milli-Q water, white light from a xenon lamp, and amino acids. A total of 21 amino acids were studied, and the shapes and sizes of the resultant nanoparticles were evaluated. The products were characterized by ultraviolet-visible (UV-Vis) and fluorescence spectroscopy, zeta potential measurements, and transmission electron microscopy. The synthesis of the AuNPs was successful with 18 amino acids, and the best results were obtained with aspartic acid, arginine, threonine, tryptophan, and valine. The nanoparticles were spherical and their sizes ranged from 5 to 100 nm. Changes in pH were required to improve the stability of the colloidal suspensions.",book:{id:"5310",slug:"catalytic-application-of-nano-gold-catalysts",title:"Catalytic Application of Nano-Gold Catalysts",fullTitle:"Catalytic Application of Nano-Gold Catalysts"},signatures:"Lilia Coronato Courrol and Ricardo Almeida de Matos",authors:[{id:"183894",title:"Ph.D.",name:"Lilia",middleName:null,surname:"Courrol",slug:"lilia-courrol",fullName:"Lilia Courrol"},{id:"185446",title:"MSc.",name:"Ricardo",middleName:null,surname:"Matos",slug:"ricardo-matos",fullName:"Ricardo Matos"}]},{id:"51091",doi:"10.5772/64081",title:"Nanoporous Gold Films as Catalyst",slug:"nanoporous-gold-films-as-catalyst",totalDownloads:2029,totalCrossrefCites:2,totalDimensionsCites:6,abstract:"Nanoporous gold (NPG) is reviewed as a catalyst. Various preparation methods were first reviewed for NPG and its structure. Applications of this catalyst in CO oxidation, hydrogen oxidation, hydrogen production are discussed. Regarding CO oxidation, detailed studies on reaction mechanism and density functional theory (DFT) calculations were also reviewed. Not only as a model reaction but also practical aspects of removing CO residue in hydrogen stream are discussed. Beyond those simple reactions, the application of NPG to more complicated reactions such as alcohol oxidation is reviewed. Selective aerobic oxidation of gas‐phase alcohols is first reviewed and reactions in liquid phase are discussed. Finally, future prospects of NPG as a catalyst for more complicated reactions such as organic synthesis are briefly discussed.",book:{id:"5310",slug:"catalytic-application-of-nano-gold-catalysts",title:"Catalytic Application of Nano-Gold Catalysts",fullTitle:"Catalytic Application of Nano-Gold Catalysts"},signatures:"Sang Hoon Kim",authors:[{id:"183817",title:"Dr.",name:"Sang Hoon",middleName:null,surname:"Kim",slug:"sang-hoon-kim",fullName:"Sang Hoon Kim"}]}],mostDownloadedChaptersLast30Days:[{id:"68970",title:"Applications of Nanotechnology in Agriculture",slug:"applications-of-nanotechnology-in-agriculture",totalDownloads:3459,totalCrossrefCites:7,totalDimensionsCites:19,abstract:"Nanotechnology has gained intense attention in the recent years due to its wide applications in several areas like medicine, medical drugs, catalysis, energy and materials. Those nanoparticles with small size to large surface area (1–100 nm) have several potential functions. These days, sustainable agriculture is needed. The development of nanochemicals has appeared as promising agents for the plant growth, fertilizers and pesticides. In recent years, the use of nanomaterials has been considered as an alternative solution to control plant pests including insects, fungi and weeds. Several nanomaterials are used as antimicrobial agents in food packing in which several nanoparticles such as silver nanomaterials are in great interest. Many nanoparticles (Ag, Fe, Cu, Si, Al, Zn, ZnO, TiO2, CeO2, Al2O3 and carbon nanotubes) have been reported to have some adverse effects on plant growth apart from the antimicrobial properties. In food industries, nanoparticles are leading in forming the food with high quality and good nutritive value.",book:{id:"9012",slug:"applications-of-nanobiotechnology",title:"Applications of Nanobiotechnology",fullTitle:"Applications of Nanobiotechnology"},signatures:"Alaa Y. Ghidan and Tawfiq M. Al Antary",authors:null},{id:"72461",title:"Role of Nanobiotechnology in Drug Discovery, Development and Molecular Diagnostic",slug:"role-of-nanobiotechnology-in-drug-discovery-development-and-molecular-diagnostic",totalDownloads:1028,totalCrossrefCites:2,totalDimensionsCites:6,abstract:"Nano-biotechnology has already tested its magnitude in a number of sections of existence science and biotechnology field. It is no longer hyperbole to say that in future, nano-scale method would in reality take the associated science area to the subsequent level. Since, there are technical hurdles present; despite the fact that scientists are giving their great to overcome such problems. Applications of nano-biotechnology have already been discussed in this chapter. Future potential are really associated with innovative amendment of such applications. Despite of some impedance, this technology presents giant hope in the future. It performs most important position in distinct sorts of biomedical application such as shipping of drug, gene therapy, biosensors, biomarkers and molecular imaging. It additionally leads to innovations in this field. The fundamental lookup goal of this discipline would be the innovation of early analysis approach and cure with target-specific remedy therapy. Although there would possibly be some safety worries with admire to the in vivo use of nanoparticles, research are in region to decide the nature and extent of adverse events.",book:{id:"9012",slug:"applications-of-nanobiotechnology",title:"Applications of Nanobiotechnology",fullTitle:"Applications of Nanobiotechnology"},signatures:"Deepak Kumar Dash, Rajni Kant Panik, Anil Kumar Sahu and Vaibhav Tripathi",authors:[{id:"204256",title:"Dr.",name:"Anil",middleName:"Kumar",surname:"Kumar Sahu",slug:"anil-kumar-sahu",fullName:"Anil Kumar Sahu"},{id:"250558",title:"Dr.",name:"Deepak Kumar",middleName:null,surname:"Dash",slug:"deepak-kumar-dash",fullName:"Deepak Kumar Dash"},{id:"314683",title:"Dr.",name:"Rajnikant",middleName:null,surname:"Panik",slug:"rajnikant-panik",fullName:"Rajnikant Panik"},{id:"316679",title:"Dr.",name:"Vaibhav",middleName:null,surname:"Tripathi",slug:"vaibhav-tripathi",fullName:"Vaibhav Tripathi"}]},{id:"51930",title:"Gold-Catalysed Reactions",slug:"gold-catalysed-reactions",totalDownloads:1934,totalCrossrefCites:0,totalDimensionsCites:1,abstract:"In recent years, there have been three significant pieces of research which helped propel gold catalysis research into the forefront: the discoveries that gold/silica can catalyse the hydrogenation of pentene, that gold on carbon can be used in the hydrochlorination of acetylene and that deposition-precipitation (DP) methods can be used to prepare nanogold on titania capable of enabling the oxidation of CO at very low temperatures. The synthesis of small gold particles, their characterisation and peculiar properties are considered together with their behaviour as heterogeneous catalysts for a variety of reactions. Some of the issues concerning the practical application of gold catalysts are also discussed.",book:{id:"5310",slug:"catalytic-application-of-nano-gold-catalysts",title:"Catalytic Application of Nano-Gold Catalysts",fullTitle:"Catalytic Application of Nano-Gold Catalysts"},signatures:"J.A. Moma, T.A. Ntho and Michael Scurrell",authors:[{id:"179872",title:"Prof.",name:"Mike",middleName:null,surname:"Scurrell",slug:"mike-scurrell",fullName:"Mike Scurrell"},{id:"183973",title:"Dr.",name:"John",middleName:null,surname:"Moma",slug:"john-moma",fullName:"John Moma"},{id:"183974",title:"Dr.",name:"Thabang",middleName:"Abraham",surname:"Ntho",slug:"thabang-ntho",fullName:"Thabang Ntho"}]},{id:"52066",title:"Supported Gold Nanoparticles as Promising Catalysts",slug:"supported-gold-nanoparticles-as-promising-catalysts",totalDownloads:3092,totalCrossrefCites:5,totalDimensionsCites:11,abstract:"In recent times, gold nanoparticles (AuNPs) either in the form of colloids or as supported nanoparticles are being extensively used as efficient redox catalyst materials. Catalysis particularly using supported gold nanoparticles (AuNPs) has attracted immense research interest due to their unique properties and greater potentiality that is directly related to their particle size. The primary objective of this chapter is to provide comprehensive overview about gold metal nanoparticles (AuNPs) and their application as promising catalysts. This chapter contains six sections in total. Section 1 starts with a general introduction, recent progress, and brief summary of the application of supported AuNPs as promising catalysts for different applications. Section 2 briefs the properties and stability of gold nanoparticles. Section 3 reviews the preparation methods of supported AuNPs for a wide range of catalytic applications. Section 4 describes briefly some of the most commonly reported supported AuNPs for different applications. Section 5 concentrates on our own results related to the application of supported AuNPs in heterogeneous catalysis. In this section, the oxidation of cyclohexane (CH) and benzyl alcohol (BA) to adipic acid (AA), benzaldehyde (BAl), and ammoxidation of 2-methylpyrazine to 2-cyanopyrazine are discussed. Finally, Section 6 describes, main points and outlook are summarized.",book:{id:"5310",slug:"catalytic-application-of-nano-gold-catalysts",title:"Catalytic Application of Nano-Gold Catalysts",fullTitle:"Catalytic Application of Nano-Gold Catalysts"},signatures:"Ahmad Alshammari and Venkata Narayana Kalevaru",authors:[{id:"178547",title:"Dr.",name:"Ahmad",middleName:null,surname:"Alshammari",slug:"ahmad-alshammari",fullName:"Ahmad Alshammari"},{id:"180753",title:"Dr.",name:"V. Narayana",middleName:null,surname:"Kalevaru",slug:"v.-narayana-kalevaru",fullName:"V. Narayana Kalevaru"}]},{id:"50852",title:"Synthesis of Gold Nanoparticles Using Amino Acids by Light Irradiation",slug:"synthesis-of-gold-nanoparticles-using-amino-acids-by-light-irradiation",totalDownloads:3602,totalCrossrefCites:3,totalDimensionsCites:9,abstract:"The synthesis of nanoparticles is generally carried out by chemical reduction, which is effective but uses a number of toxic substances, making the process potentially harmful to the environment. Thus, as part of the search for environmentally friendly or green synthetic methods, this chapter aimed to present the synthesis of gold nanoparticles (AuNPs) using only HAuCl4, Milli-Q water, white light from a xenon lamp, and amino acids. A total of 21 amino acids were studied, and the shapes and sizes of the resultant nanoparticles were evaluated. The products were characterized by ultraviolet-visible (UV-Vis) and fluorescence spectroscopy, zeta potential measurements, and transmission electron microscopy. The synthesis of the AuNPs was successful with 18 amino acids, and the best results were obtained with aspartic acid, arginine, threonine, tryptophan, and valine. The nanoparticles were spherical and their sizes ranged from 5 to 100 nm. Changes in pH were required to improve the stability of the colloidal suspensions.",book:{id:"5310",slug:"catalytic-application-of-nano-gold-catalysts",title:"Catalytic Application of Nano-Gold Catalysts",fullTitle:"Catalytic Application of Nano-Gold Catalysts"},signatures:"Lilia Coronato Courrol and Ricardo Almeida de Matos",authors:[{id:"183894",title:"Ph.D.",name:"Lilia",middleName:null,surname:"Courrol",slug:"lilia-courrol",fullName:"Lilia Courrol"},{id:"185446",title:"MSc.",name:"Ricardo",middleName:null,surname:"Matos",slug:"ricardo-matos",fullName:"Ricardo Matos"}]}],onlineFirstChaptersFilter:{topicId:"44",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:90,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:104,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:32,numberOfPublishedChapters:320,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:12,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:141,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:133,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:113,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:107,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:5,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:16,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. 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Topics will include general overviews of infections, immunopathology, diagnosis, treatment, epidemiology, etiology, and current clinical recommendations for managing infectious diseases. Ongoing issues, recent advances, and future diagnostic approaches and therapeutic strategies will also be discussed. This book series will focus on various aspects and properties of infectious diseases whose deep understanding is essential for safeguarding the human race from losing resources and economies due to pathogens.",coverUrl:"https://cdn.intechopen.com/series/covers/6.jpg",latestPublicationDate:"June 25th, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:13,editor:{id:"131400",title:"Prof.",name:"Alfonso J.",middleName:null,surname:"Rodriguez-Morales",slug:"alfonso-j.-rodriguez-morales",fullName:"Alfonso J. 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He is an External Professor, Master in Research on Tropical Medicine and International Health, Universitat de Barcelona, Spain. He is also a professor at the Master in Clinical Epidemiology and Biostatistics, Universidad Científica del Sur, Lima, Peru. In 2021 he has been awarded the “Raul Isturiz Award” Medal of the API. Also, in 2021, he was awarded with the “Jose Felix Patiño” Asclepius Staff Medal of the Colombian Medical College, due to his scientific contributions to COVID-19 during the pandemic. He is currently the Editor in Chief of the journal Travel Medicine and Infectious Diseases. 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He completed a one-year Post-Doctoral Fellowship awarded by the DFAIT (Foreign Affairs and International Trade Canada) at the Institute of Biomedical Engineering of the University of New Brunswick (Canada) in 2010. Currently, he is Professor in the Faculty of Electrical Engineering (UFU). He has authored and co-authored more than 200 peer-reviewed publications in Biomedical Engineering. He has been a researcher of The National Council for Scientific and Technological Development (CNPq-Brazil) since 2009. He has served as an ad-hoc consultant for CNPq, CAPES (Coordination for the Improvement of Higher Education Personnel), FINEP (Brazilian Innovation Agency), and other funding bodies on several occasions. He was the Secretary of the Brazilian Society of Biomedical Engineering (SBEB) from 2015 to 2016, President of SBEB (2017-2018) and Vice-President of SBEB (2019-2020). He was the head of the undergraduate program in Biomedical Engineering of the Federal University of Uberlândia (2015 - June/2019) and the head of the Centre for Innovation and Technology Assessment in Health (NIATS/UFU) since 2010. He is the head of the Postgraduate Program in Biomedical Engineering (UFU, July/2019 - to date). He was the secretary of the Parkinson's Disease Association of Uberlândia (2018-2019). Dr. Andrade's primary area of research is focused towards getting information from the neuromuscular system to understand its strategies of organization, adaptation and controlling in the context of motor neuron diseases. 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For 20 years, he has studied the analysis and processing of biomedical images, emphasizing the full automation of measurement for a large inter-individual variability of patients. Dr. Koprowski has authored more than a hundred research papers with dozens in impact factor (IF) journals and has authored or co-authored six books. Additionally, he is the author of several national and international patents in the field of biomedical devices and imaging. 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His fields of interest are anterior segment disease, keratoconus, glaucoma, corneal dystrophies, and cataracts. His research topics include\nintraocular lens power calculation, eye modification induced by refractive surgery, glaucoma progression, and validation of new diagnostic devices in ophthalmology. \nHe has published more than 100 papers in international and Italian scientific journals, more than 60 in journals with impact factors, and chapters in international and Italian books. He has also edited two international books and authored more than 150 communications or posters for the most important international and Italian ophthalmology conferences.",institutionString:'University of Campania "Luigi Vanvitelli"',institution:{name:'University of Campania "Luigi Vanvitelli"',institutionURL:null,country:{name:"Italy"}}}]},{type:"book",id:"7560",title:"Non-Invasive Diagnostic Methods",subtitle:"Image Processing",coverURL:"https://cdn.intechopen.com/books/images_new/7560.jpg",slug:"non-invasive-diagnostic-methods-image-processing",publishedDate:"December 19th 2018",editedByType:"Edited by",bookSignature:"Mariusz Marzec and Robert Koprowski",hash:"d92fd8cf5a90a47f2b8a310837a5600e",volumeInSeries:3,fullTitle:"Non-Invasive Diagnostic Methods - Image Processing",editors:[{id:"253468",title:"Dr.",name:"Mariusz",middleName:null,surname:"Marzec",slug:"mariusz-marzec",fullName:"Mariusz Marzec",profilePictureURL:"https://mts.intechopen.com/storage/users/253468/images/system/253468.png",biography:"An assistant professor at Department of Biomedical Computer Systems, at Institute of Computer Science, Silesian University in Katowice. 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He is an author and co-author of scientific publications covering analysis and processing of biomedical images and development of database systems.",institutionString:"University of Silesia",institution:null}]},{type:"book",id:"6843",title:"Biomechanics",subtitle:null,coverURL:"https://cdn.intechopen.com/books/images_new/6843.jpg",slug:"biomechanics",publishedDate:"January 30th 2019",editedByType:"Edited by",bookSignature:"Hadi Mohammadi",hash:"85132976010be1d7f3dbd88662b785e5",volumeInSeries:4,fullTitle:"Biomechanics",editors:[{id:"212432",title:"Prof.",name:"Hadi",middleName:null,surname:"Mohammadi",slug:"hadi-mohammadi",fullName:"Hadi Mohammadi",profilePictureURL:"https://mts.intechopen.com/storage/users/212432/images/system/212432.jpeg",biography:"Dr. Hadi Mohammadi is a biomedical engineer with hands-on experience in the design and development of many engineering structures and medical devices through various projects that he has been involved in over the past twenty years. 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The preliminary objectives of the study are to understand and develop the evidence-based tools and interventions for the control and prevention of malaria in different sites of the INDIA. Alongside, with the help of next-generation genomics study, the team has studied the antimalarial drug resistance in India. Further, he has extended his research in the development of Humanized mice for the study of liver-stage malaria and identification of molecular marker(s) for the Artemisinin resistance. At present, his research focuses on understanding the role of B cells in the activation of CD8+ T cells in malaria. Received the CSIR-SRF (Senior Research Fellow) award-2018, FIMSA (Federation of Immunological Societies of Asia-Oceania) Travel Bursary award to attend the IUIS-IIS-FIMSA Immunology course-2019',institutionString:"Nirma University",institution:{name:"Nirma University",country:{name:"India"}}},{id:"334383",title:"Ph.D.",name:"Simone",middleName:"Ulrich",surname:"Ulrich Picoli",slug:"simone-ulrich-picoli",fullName:"Simone Ulrich Picoli",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/334383/images/15919_n.jpg",biography:"Graduated in Pharmacy from Universidade Luterana do Brasil (1999), Master in Agricultural and Environmental Microbiology from Federal University of Rio Grande do Sul (2002), Specialization in Clinical Microbiology from Universidade de São Paulo, USP (2007) and PhD in Sciences in Gastroenterology and Hepatology (2012). She is currently an Adjunct Professor at Feevale University in Medicine and Biomedicine courses and a permanent professor of the Academic Master\\'s Degree in Virology. She has experience in the field of Microbiology, with an emphasis on Bacteriology, working mainly on the following topics: bacteriophages, bacterial resistance, clinical microbiology and food microbiology.",institutionString:null,institution:{name:"Universidade Feevale",country:{name:"Brazil"}}},{id:"229220",title:"Dr.",name:"Amjad",middleName:"Islam",surname:"Aqib",slug:"amjad-aqib",fullName:"Amjad Aqib",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229220/images/system/229220.png",biography:"Dr. Amjad Islam Aqib obtained a DVM and MSc (Hons) from University of Agriculture Faisalabad (UAF), Pakistan, and a PhD from the University of Veterinary and Animal Sciences Lahore, Pakistan. Dr. Aqib joined the Department of Clinical Medicine and Surgery at UAF for one year as an assistant professor where he developed a research laboratory designated for pathogenic bacteria. Since 2018, he has been Assistant Professor/Officer in-charge, Department of Medicine, Manager Research Operations and Development-ORIC, and President One Health Club at Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan. He has nearly 100 publications to his credit. His research interests include epidemiological patterns and molecular analysis of antimicrobial resistance and modulation and vaccine development against animal pathogens of public health concern.",institutionString:"Cholistan University of Veterinary and Animal Sciences",institution:null},{id:"62900",title:"Prof.",name:"Fethi",middleName:null,surname:"Derbel",slug:"fethi-derbel",fullName:"Fethi Derbel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/62900/images/system/62900.jpeg",biography:"Professor Fethi Derbel was born in 1960 in Tunisia. He received his medical degree from the Sousse Faculty of Medicine at Sousse, University of Sousse, Tunisia. He completed his surgical residency in General Surgery at the University Hospital Farhat Hached of Sousse and was a member of the Unit of Liver Transplantation in the University of Rennes, France. He then worked in the Department of Surgery at the Sahloul University Hospital in Sousse. Professor Derbel is presently working at the Clinique les Oliviers, Sousse, Tunisia. His hospital activities are mostly concerned with laparoscopic, colorectal, pancreatic, hepatobiliary, and gastric surgery. He is also very interested in hernia surgery and performs ventral hernia repairs and inguinal hernia repairs. He has been a member of the GREPA and Tunisian Hernia Society (THS). During his residency, he managed patients suffering from diabetic foot, and he was very interested in this pathology. For this reason, he decided to coordinate a book project dealing with the diabetic foot. Professor Derbel has published many articles in journals and collaborates intensively with IntechOpen Access Publisher as an editor.",institutionString:"Clinique les Oliviers",institution:null},{id:"300144",title:"Dr.",name:"Meriem",middleName:null,surname:"Braiki",slug:"meriem-braiki",fullName:"Meriem Braiki",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/300144/images/system/300144.jpg",biography:"Dr. Meriem Braiki is a specialist in pediatric surgeon from Tunisia. She was born in 1985. She received her medical degree from the University of Medicine at Sousse, Tunisia. She achieved her surgical residency training periods in Pediatric Surgery departments at University Hospitals in Monastir, Tunis and France.\r\nShe is currently working at the Pediatric surgery department, Sidi Bouzid Hospital, Tunisia. Her hospital activities are mostly concerned with laparoscopic, parietal, urological and digestive surgery. She has published several articles in diffrent journals.",institutionString:"Sidi Bouzid Regional Hospital",institution:null},{id:"229481",title:"Dr.",name:"Erika M.",middleName:"Martins",surname:"de Carvalho",slug:"erika-m.-de-carvalho",fullName:"Erika M. de Carvalho",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229481/images/6397_n.jpg",biography:null,institutionString:null,institution:{name:"Oswaldo Cruz Foundation",country:{name:"Brazil"}}},{id:"186537",title:"Prof.",name:"Tonay",middleName:null,surname:"Inceboz",slug:"tonay-inceboz",fullName:"Tonay Inceboz",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/186537/images/system/186537.jfif",biography:"I was graduated from Ege University of Medical Faculty (Turkey) in 1988 and completed his Med. PhD degree in Medical Parasitology at the same university. I became an Associate Professor in 2008 and Professor in 2014. I am currently working as a Professor at the Department of Medical Parasitology at Dokuz Eylul University, Izmir, Turkey.\n\nI have given many lectures, presentations in different academic meetings. I have more than 60 articles in peer-reviewed journals, 18 book chapters, 1 book editorship.\n\nMy research interests are Echinococcus granulosus, Echinococcus multilocularis (diagnosis, life cycle, in vitro and in vivo cultivation), and Trichomonas vaginalis (diagnosis, PCR, and in vitro cultivation).",institutionString:"Dokuz Eylül University",institution:{name:"Dokuz Eylül University",country:{name:"Turkey"}}},{id:"71812",title:"Prof.",name:"Hanem Fathy",middleName:"Fathy",surname:"Khater",slug:"hanem-fathy-khater",fullName:"Hanem Fathy Khater",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/71812/images/1167_n.jpg",biography:"Prof. Khater is a Professor of Parasitology at Benha University, Egypt. She studied for her doctoral degree, at the Department of Entomology, College of Agriculture, Food and Natural Resources, University of Missouri, Columbia, USA. She has completed her Ph.D. degrees in Parasitology in Egypt, from where she got the award for “the best scientific Ph.D. dissertation”. She worked at the School of Biological Sciences, Bristol, England, the UK in controlling insects of medical and veterinary importance as a grant from Newton Mosharafa, the British Council. Her research is focused on searching of pesticides against mosquitoes, house flies, lice, green bottle fly, camel nasal botfly, soft and hard ticks, mites, and the diamondback moth as well as control of several parasites using safe and natural materials to avoid drug resistances and environmental contamination.",institutionString:null,institution:{name:"Banha University",country:{name:"Egypt"}}},{id:"99780",title:"Prof.",name:"Omolade",middleName:"Olayinka",surname:"Okwa",slug:"omolade-okwa",fullName:"Omolade Okwa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/99780/images/system/99780.jpg",biography:"Omolade Olayinka Okwa is presently a Professor of Parasitology at Lagos State University, Nigeria. She has a PhD in Parasitology (1997), an MSc in Cellular Parasitology (1992), and a BSc (Hons) Zoology (1990) all from the University of Ibadan, Nigeria. She teaches parasitology at the undergraduate and postgraduate levels. She was a recipient of a Commonwealth fellowship supported by British Council tenable at the Centre for Entomology and Parasitology (CAEP), Keele University, United Kingdom between 2004 and 2005. She was awarded an Honorary Visiting Research Fellow at the same university from 2005 to 2007. \nShe has been an external examiner to the Department of Veterinary Microbiology and Parasitology, University of Ibadan, MSc programme between 2010 and 2012. She is a member of the Nigerian Society of Experimental Biology (NISEB), Parasitology and Public Health Society of Nigeria (PPSN), Science Association of Nigeria (SAN), Zoological Society of Nigeria (ZSN), and is Vice Chairperson of the Organisation of Women in Science (OWSG), LASU chapter. She served as Head of Department of Zoology and Environmental Biology, Lagos State University from 2007 to 2010 and 2014 to 2016. She is a reviewer for several local and international journals such as Unilag Journal of Science, Libyan Journal of Medicine, Journal of Medicine and Medical Sciences, and Annual Research and Review in Science. \nShe has authored 45 scientific research publications in local and international journals, 8 scientific reviews, 4 books, and 3 book chapters, which includes the books “Malaria Parasites” and “Malaria” which are IntechOpen access publications.",institutionString:"Lagos State University",institution:{name:"Lagos State University",country:{name:"Nigeria"}}},{id:"273100",title:"Dr.",name:"Vijay",middleName:null,surname:"Gayam",slug:"vijay-gayam",fullName:"Vijay Gayam",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/273100/images/system/273100.jpeg",biography:"Dr. Vijay Bhaskar Reddy Gayam is currently practicing as an internist at Interfaith Medical Center in Brooklyn, New York, USA. He is also a Clinical Assistant Professor at the SUNY Downstate University Hospital and Adjunct Professor of Medicine at the American University of Antigua. He is a holder of an M.B.B.S. degree bestowed to him by Osmania Medical College and received his M.D. at Interfaith Medical Center. His career goals thus far have heavily focused on direct patient care, medical education, and clinical research. He currently serves in two leadership capacities; Assistant Program Director of Medicine at Interfaith Medical Center and as a Councilor for the American\r\nFederation for Medical Research. As a true academician and researcher, he has more than 50 papers indexed in international peer-reviewed journals. He has also presented numerous papers in multiple national and international scientific conferences. His areas of research interest include general internal medicine, gastroenterology and hepatology. He serves as an editor, editorial board member and reviewer for multiple international journals. His research on Hepatitis C has been very successful and has led to multiple research awards, including the 'Equity in Prevention and Treatment Award” from the New York Department of Health Viral Hepatitis Symposium (2018) and the 'Presidential Poster Award” awarded to him by the American College of Gastroenterology (2018). He was also awarded 'Outstanding Clinician in General Medicine” by Venus International Foundation for his extensive research expertise and services, perform over and above the standard expected in the advancement of healthcare, patient safety and quality of care.",institutionString:"Interfaith Medical Center",institution:{name:"Interfaith Medical Center",country:{name:"United States of America"}}},{id:"93517",title:"Dr.",name:"Clement",middleName:"Adebajo",surname:"Meseko",slug:"clement-meseko",fullName:"Clement Meseko",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/93517/images/system/93517.jpg",biography:"Dr. Clement Meseko obtained DVM and PhD degree in Veterinary Medicine and Virology respectively. He has worked for over 20 years in both private and public sectors including the academia, contributing to knowledge and control of infectious disease. Through the application of epidemiological skill, classical and molecular virological skills, he investigates viruses of economic and public health importance for the mitigation of the negative impact on people, animal and the environment in the context of Onehealth. \r\nDr. Meseko’s field experience on animal and zoonotic diseases and pathogen dynamics at the human-animal interface over the years shaped his carrier in research and scientific inquiries. He has been part of the investigation of Highly Pathogenic Avian Influenza incursions in sub Saharan Africa and monitors swine Influenza (Pandemic influenza Virus) agro-ecology and potential for interspecies transmission. He has authored and reviewed a number of journal articles and book chapters.",institutionString:"National Veterinary Research Institute",institution:{name:"National Veterinary Research Institute",country:{name:"Nigeria"}}},{id:"158026",title:"Prof.",name:"Shailendra K.",middleName:null,surname:"Saxena",slug:"shailendra-k.-saxena",fullName:"Shailendra K. Saxena",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRET3QAO/Profile_Picture_2022-05-10T10:10:26.jpeg",biography:"Professor Dr. Shailendra K. Saxena is a vice dean and professor at King George's Medical University, Lucknow, India. His research interests involve understanding the molecular mechanisms of host defense during human viral infections and developing new predictive, preventive, and therapeutic strategies for them using Japanese encephalitis virus (JEV), HIV, and emerging viruses as a model via stem cell and cell culture technologies. His research work has been published in various high-impact factor journals (Science, PNAS, Nature Medicine) with a high number of citations. He has received many awards and honors in India and abroad including various Young Scientist Awards, BBSRC India Partnering Award, and Dr. JC Bose National Award of Department of Biotechnology, Min. of Science and Technology, Govt. of India. Dr. Saxena is a fellow of various international societies/academies including the Royal College of Pathologists, United Kingdom; Royal Society of Medicine, London; Royal Society of Biology, United Kingdom; Royal Society of Chemistry, London; and Academy of Translational Medicine Professionals, Austria. He was named a Global Leader in Science by The Scientist. He is also an international opinion leader/expert in vaccination for Japanese encephalitis by IPIC (UK).",institutionString:"King George's Medical University",institution:{name:"King George's Medical University",country:{name:"India"}}},{id:"94928",title:"Dr.",name:"Takuo",middleName:null,surname:"Mizukami",slug:"takuo-mizukami",fullName:"Takuo Mizukami",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94928/images/6402_n.jpg",biography:null,institutionString:null,institution:{name:"National Institute of Infectious Diseases",country:{name:"Japan"}}},{id:"233433",title:"Dr.",name:"Yulia",middleName:null,surname:"Desheva",slug:"yulia-desheva",fullName:"Yulia Desheva",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/233433/images/system/233433.png",biography:"Dr. Yulia Desheva is a leading researcher at the Institute of Experimental Medicine, St. Petersburg, Russia. She is a professor in the Stomatology Faculty, St. Petersburg State University. She has expertise in the development and evaluation of a wide range of live mucosal vaccines against influenza and bacterial complications. Her research interests include immunity against influenza and COVID-19 and the development of immunization schemes for high-risk individuals.",institutionString:'Federal State Budgetary Scientific Institution "Institute of Experimental Medicine"',institution:null},{id:"238958",title:"Mr.",name:"Atamjit",middleName:null,surname:"Singh",slug:"atamjit-singh",fullName:"Atamjit Singh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/238958/images/6575_n.jpg",biography:null,institutionString:null,institution:null},{id:"333753",title:"Dr.",name:"Rais",middleName:null,surname:"Ahmed",slug:"rais-ahmed",fullName:"Rais Ahmed",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/333753/images/20168_n.jpg",biography:null,institutionString:null,institution:null},{id:"252058",title:"M.Sc.",name:"Juan",middleName:null,surname:"Sulca",slug:"juan-sulca",fullName:"Juan Sulca",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/252058/images/12834_n.jpg",biography:null,institutionString:null,institution:null},{id:"191392",title:"Dr.",name:"Marimuthu",middleName:null,surname:"Govindarajan",slug:"marimuthu-govindarajan",fullName:"Marimuthu Govindarajan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/191392/images/5828_n.jpg",biography:"Dr. M. Govindarajan completed his BSc degree in Zoology at Government Arts College (Autonomous), Kumbakonam, and MSc, MPhil, and PhD degrees at Annamalai University, Annamalai Nagar, Tamil Nadu, India. He is serving as an assistant professor at the Department of Zoology, Annamalai University. His research interests include isolation, identification, and characterization of biologically active molecules from plants and microbes. He has identified more than 20 pure compounds with high mosquitocidal activity and also conducted high-quality research on photochemistry and nanosynthesis. He has published more than 150 studies in journals with impact factor and 2 books in Lambert Academic Publishing, Germany. He serves as an editorial board member in various national and international scientific journals.",institutionString:null,institution:null},{id:"274660",title:"Dr.",name:"Damodar",middleName:null,surname:"Paudel",slug:"damodar-paudel",fullName:"Damodar Paudel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/274660/images/8176_n.jpg",biography:"I am DrDamodar Paudel,currently working as consultant Physician in Nepal police Hospital.",institutionString:null,institution:null},{id:"241562",title:"Dr.",name:"Melvin",middleName:null,surname:"Sanicas",slug:"melvin-sanicas",fullName:"Melvin Sanicas",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/241562/images/6699_n.jpg",biography:null,institutionString:null,institution:null},{id:"337446",title:"Dr.",name:"Maria",middleName:null,surname:"Zavala-Colon",slug:"maria-zavala-colon",fullName:"Maria Zavala-Colon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Puerto Rico, Medical Sciences Campus",country:{name:"United States of America"}}},{id:"338856",title:"Mrs.",name:"Nur Alvira",middleName:null,surname:"Pascawati",slug:"nur-alvira-pascawati",fullName:"Nur Alvira Pascawati",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Universitas Respati Yogyakarta",country:{name:"Indonesia"}}},{id:"441116",title:"Dr.",name:"Jovanka M.",middleName:null,surname:"Voyich",slug:"jovanka-m.-voyich",fullName:"Jovanka M. Voyich",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Montana State University",country:{name:"United States of America"}}},{id:"330412",title:"Dr.",name:"Muhammad",middleName:null,surname:"Farhab",slug:"muhammad-farhab",fullName:"Muhammad Farhab",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Agriculture Faisalabad",country:{name:"Pakistan"}}},{id:"349495",title:"Dr.",name:"Muhammad",middleName:null,surname:"Ijaz",slug:"muhammad-ijaz",fullName:"Muhammad Ijaz",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Veterinary and Animal Sciences",country:{name:"Pakistan"}}}]}},subseries:{item:{id:"5",type:"subseries",title:"Parasitic Infectious Diseases",keywords:"Blood Borne Parasites, Intestinal Parasites, Protozoa, Helminths, Arthropods, Water Born Parasites, Epidemiology, Molecular Biology, Systematics, Genomics, Proteomics, Ecology",scope:"Parasitic diseases have evolved alongside their human hosts. In many cases, these diseases have adapted so well that they have developed efficient resilience methods in the human host and can live in the host for years. Others, particularly some blood parasites, can cause very acute diseases and are responsible for millions of deaths yearly. Many parasitic diseases are classified as neglected tropical diseases because they have received minimal funding over recent years and, in many cases, are under-reported despite the critical role they play in morbidity and mortality among human and animal hosts. The current topic, Parasitic Infectious Diseases, in the Infectious Diseases Series aims to publish studies on the systematics, epidemiology, molecular biology, genomics, pathogenesis, genetics, and clinical significance of parasitic diseases from blood borne to intestinal parasites as well as zoonotic parasites. We hope to cover all aspects of parasitic diseases to provide current and relevant research data on these very important diseases. In the current atmosphere of the Coronavirus pandemic, communities around the world, particularly those in different underdeveloped areas, are faced with the growing challenges of the high burden of parasitic diseases. At the same time, they are faced with the Covid-19 pandemic leading to what some authors have called potential syndemics that might worsen the outcome of such infections. Therefore, it is important to conduct studies that examine parasitic infections in the context of the coronavirus pandemic for the benefit of all communities to help foster more informed decisions for the betterment of human and animal health.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/5.jpg",hasOnlineFirst:!0,hasPublishedBooks:!0,annualVolume:11401,editor:{id:"67907",title:"Dr.",name:"Amidou",middleName:null,surname:"Samie",slug:"amidou-samie",fullName:"Amidou Samie",profilePictureURL:"https://mts.intechopen.com/storage/users/67907/images/system/67907.jpg",biography:"Dr. Amidou Samie is an Associate Professor of Microbiology at the University of Venda, in South Africa, where he graduated for his PhD in May 2008. He joined the Department of Microbiology the same year and has been giving lectures on topics covering parasitology, immunology, molecular biology and industrial microbiology. He is currently a rated researcher by the National Research Foundation of South Africa at category C2. He has published widely in the field of infectious diseases and has overseen several MSc’s and PhDs. His research activities mostly cover topics on infectious diseases from epidemiology to control. His particular interest lies in the study of intestinal protozoan parasites and opportunistic infections among HIV patients as well as the potential impact of childhood diarrhoea on growth and child development. He also conducts research on water-borne diseases and water quality and is involved in the evaluation of point-of-use water treatment technologies using silver and copper nanoparticles in collaboration with the University of Virginia, USA. He also studies the use of medicinal plants for the control of infectious diseases as well as antimicrobial drug resistance.",institutionString:null,institution:{name:"University of Venda",institutionURL:null,country:{name:"South Africa"}}},editorTwo:null,editorThree:null,series:{id:"6",title:"Infectious Diseases",doi:"10.5772/intechopen.71852",issn:"2631-6188"},editorialBoard:[{id:"188881",title:"Dr.",name:"Fernando José",middleName:null,surname:"Andrade-Narváez",slug:"fernando-jose-andrade-narvaez",fullName:"Fernando José Andrade-Narváez",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRIV7QAO/Profile_Picture_1628834308121",institutionString:null,institution:{name:"Autonomous University of Yucatán",institutionURL:null,country:{name:"Mexico"}}},{id:"269120",title:"Dr.",name:"Rajeev",middleName:"K.",surname:"Tyagi",slug:"rajeev-tyagi",fullName:"Rajeev Tyagi",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRaBqQAK/Profile_Picture_1644331884726",institutionString:"CSIR - Institute of Microbial Technology, India",institution:null},{id:"336849",title:"Prof.",name:"Ricardo",middleName:null,surname:"Izurieta",slug:"ricardo-izurieta",fullName:"Ricardo Izurieta",profilePictureURL:"https://mts.intechopen.com/storage/users/293169/images/system/293169.png",institutionString:null,institution:{name:"University of South Florida",institutionURL:null,country:{name:"United States of America"}}}]},onlineFirstChapters:{paginationCount:14,paginationItems:[{id:"82457",title:"Canine Hearing Management",doi:"10.5772/intechopen.105515",signatures:"Peter M. 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Topics include, but are not limited to: Advanced techniques of cellular and molecular biology (Molecular methodologies, imaging techniques, and bioinformatics); Biological activities at the molecular level; Biological processes of cell functions, cell division, senescence, maintenance, and cell death; Biomolecules interactions; Cancer; Cell biology; Chemical biology; Computational biology; Cytochemistry; Developmental biology; Disease mechanisms and therapeutics; DNA, and RNA metabolism; Gene functions, genetics, and genomics; Genetics; Immunology; Medical microbiology; Molecular biology; Molecular genetics; Molecular processes of cell and organelle dynamics; Neuroscience; Protein biosynthesis, degradation, and functions; Regulation of molecular interactions in a cell; Signalling networks and system biology; Structural biology; Virology and microbiology.",annualVolume:11410,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"79367",title:"Dr.",name:"Ana Isabel",middleName:null,surname:"Flores",fullName:"Ana Isabel Flores",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRpIOQA0/Profile_Picture_1632418099564",institutionString:null,institution:{name:"Hospital Universitario 12 De Octubre",institutionURL:null,country:{name:"Spain"}}},{id:"328234",title:"Ph.D.",name:"Christian",middleName:null,surname:"Palavecino",fullName:"Christian Palavecino",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000030DhEhQAK/Profile_Picture_1628835318625",institutionString:null,institution:{name:"Central University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",fullName:"Francisco Javier Martin-Romero",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",institutionString:null,institution:{name:"University of Extremadura",institutionURL:null,country:{name:"Spain"}}}]},{id:"15",title:"Chemical Biology",keywords:"Phenolic Compounds, Essential Oils, Modification of Biomolecules, Glycobiology, Combinatorial Chemistry, Therapeutic peptides, Enzyme Inhibitors",scope:"Chemical biology spans the fields of chemistry and biology involving the application of biological and chemical molecules and techniques. In recent years, the application of chemistry to biological molecules has gained significant interest in medicinal and pharmacological studies. This topic will be devoted to understanding the interplay between biomolecules and chemical compounds, their structure and function, and their potential applications in related fields. Being a part of the biochemistry discipline, the ideas and concepts that have emerged from Chemical Biology have affected other related areas. This topic will closely deal with all emerging trends in this discipline.",annualVolume:11411,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null,editorialBoard:[{id:"219081",title:"Dr.",name:"Abdulsamed",middleName:null,surname:"Kükürt",fullName:"Abdulsamed Kükürt",profilePictureURL:"https://mts.intechopen.com/storage/users/219081/images/system/219081.png",institutionString:null,institution:{name:"Kafkas University",institutionURL:null,country:{name:"Turkey"}}},{id:"241413",title:"Dr.",name:"Azhar",middleName:null,surname:"Rasul",fullName:"Azhar Rasul",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRT1oQAG/Profile_Picture_1635251978933",institutionString:null,institution:{name:"Government College University, Faisalabad",institutionURL:null,country:{name:"Pakistan"}}},{id:"178316",title:"Ph.D.",name:"Sergey",middleName:null,surname:"Sedykh",fullName:"Sergey Sedykh",profilePictureURL:"https://mts.intechopen.com/storage/users/178316/images/system/178316.jfif",institutionString:null,institution:{name:"Novosibirsk State University",institutionURL:null,country:{name:"Russia"}}}]},{id:"17",title:"Metabolism",keywords:"Biomolecules Metabolism, Energy Metabolism, Metabolic Pathways, Key Metabolic Enzymes, Metabolic Adaptation",scope:"Metabolism is frequently defined in biochemistry textbooks as the overall process that allows living systems to acquire and use the free energy they need for their vital functions or the chemical processes that occur within a living organism to maintain life. Behind these definitions are hidden all the aspects of normal and pathological functioning of all processes that the topic ‘Metabolism’ will cover within the Biochemistry Series. Thus all studies on metabolism will be considered for publication.",annualVolume:11413,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"243049",title:"Dr.",name:"Anca",middleName:null,surname:"Pantea Stoian",fullName:"Anca Pantea Stoian",profilePictureURL:"https://mts.intechopen.com/storage/users/243049/images/system/243049.jpg",institutionString:null,institution:{name:"Carol Davila University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"203824",title:"Dr.",name:"Attilio",middleName:null,surname:"Rigotti",fullName:"Attilio Rigotti",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institutionString:null,institution:{name:"Pontifical Catholic University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"300470",title:"Dr.",name:"Yanfei (Jacob)",middleName:null,surname:"Qi",fullName:"Yanfei (Jacob) Qi",profilePictureURL:"https://mts.intechopen.com/storage/users/300470/images/system/300470.jpg",institutionString:null,institution:{name:"Centenary Institute of Cancer Medicine and Cell Biology",institutionURL:null,country:{name:"Australia"}}}]},{id:"18",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",annualVolume:11414,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",fullName:"Shymaa Enany",profilePictureURL:"https://mts.intechopen.com/storage/users/81926/images/system/81926.png",institutionString:"Suez Canal University",institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"chapter.detail",path:"/chapters/60324",hash:"",query:{},params:{id:"60324"},fullPath:"/chapters/60324",meta:{},from:{name:null,path:"/",hash:"",query:{},params:{},fullPath:"/",meta:{}}}},function(){var e;(e=document.currentScript||document.scripts[document.scripts.length-1]).parentNode.removeChild(e)}()