Characterization of PVC samples.
\r\n\t
",isbn:"978-1-80356-552-1",printIsbn:"978-1-80356-551-4",pdfIsbn:"978-1-80356-553-8",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!0,isSalesforceBook:!1,isNomenclature:!1,hash:"4c2e03f295fbc697350f0bf3bf89a14f",bookSignature:"Associate Prof. Murat Eyvaz, Dr. Ahmed Albahnasawi, M.Sc. Ercan Gürbulak and MSc. Mesut Tekbaş",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/11840.jpg",keywords:"Aridity and Drought, Precipitation and Evapotranspiration, Land Use, Human Activity, Desertification, Desert, Soil Structure, Water Treatment, Water Scarcity, Irrigated Agriculture, Remote Sensing, Climate Change",numberOfDownloads:50,numberOfWosCitations:0,numberOfCrossrefCitations:0,numberOfDimensionsCitations:0,numberOfTotalCitations:0,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"March 10th 2022",dateEndSecondStepPublish:"May 11th 2022",dateEndThirdStepPublish:"July 10th 2022",dateEndFourthStepPublish:"September 28th 2022",dateEndFifthStepPublish:"November 27th 2022",dateConfirmationOfParticipation:null,remainingDaysToSecondStep:"2 months",secondStepPassed:!0,areRegistrationsClosed:!1,currentStepOfPublishingProcess:3,editedByType:null,kuFlag:!1,biosketch:"Dr. Murat Eyvaz has co-authored many journal articles and conference papers and has taken part in many national projects. 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His research interests are the application and designing of supercritical water oxidation processes for wastewater treatment/solid waste management and electrochemical analyses.",coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"170083",title:"Associate Prof.",name:"Murat",middleName:null,surname:"Eyvaz",slug:"murat-eyvaz",fullName:"Murat Eyvaz",profilePictureURL:"https://mts.intechopen.com/storage/users/170083/images/system/170083.png",biography:"Dr. Murat Eyvaz is an associate professor in the Environmental Engineering Department, Gebze Technical University, Turkey. 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Based on his Ph.D. research, Dr. Albahnasawi published three journal articles and participated in three international conferences. His research interests include the application and design of a microbial fuel cell integrated with Fenton oxidation for industrial wastewater treatment/solid waste management and monitoring of organic micropollutants by both chromatographic and spectrophotometric analyses.",institutionString:"Gebze Technical University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"0",totalChapterViews:"0",totalEditedBooks:"0",institution:{name:"Gebze Technical University",institutionURL:null,country:{name:"Turkey"}}},coeditorTwo:{id:"176699",title:"Dr.",name:"Ercan",middleName:null,surname:"Gürbulak",slug:"ercan-gurbulak",fullName:"Ercan Gürbulak",profilePictureURL:"https://mts.intechopen.com/storage/users/176699/images/system/176699.png",biography:"Dr. Ercan Gürbulak is a research associate in the Environmental Engineering Department, Gebze Technical University, Turkey. He received his bachelor’s degree in Environmental Engineering from Marmara University, Turkey, in 2005. 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Theophanides",coverURL:"https://cdn.intechopen.com/books/images_new/1591.jpg",editedByType:"Edited by",editors:[{id:"37194",title:"Dr.",name:"Theophile",surname:"Theophanides",slug:"theophile-theophanides",fullName:"Theophile Theophanides"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3161",title:"Frontiers in Guided Wave Optics and Optoelectronics",subtitle:null,isOpenForSubmission:!1,hash:"deb44e9c99f82bbce1083abea743146c",slug:"frontiers-in-guided-wave-optics-and-optoelectronics",bookSignature:"Bishnu Pal",coverURL:"https://cdn.intechopen.com/books/images_new/3161.jpg",editedByType:"Edited by",editors:[{id:"4782",title:"Prof.",name:"Bishnu",surname:"Pal",slug:"bishnu-pal",fullName:"Bishnu Pal"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3092",title:"Anopheles mosquitoes",subtitle:"New insights into malaria vectors",isOpenForSubmission:!1,hash:"c9e622485316d5e296288bf24d2b0d64",slug:"anopheles-mosquitoes-new-insights-into-malaria-vectors",bookSignature:"Sylvie Manguin",coverURL:"https://cdn.intechopen.com/books/images_new/3092.jpg",editedByType:"Edited by",editors:[{id:"50017",title:"Prof.",name:"Sylvie",surname:"Manguin",slug:"sylvie-manguin",fullName:"Sylvie Manguin"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}]},chapter:{item:{type:"chapter",id:"70781",title:"Solubility, Discoloration, and Solid-State 13C NMR Spectra of Stereoregular Poly(Vinyl Chloride) Prepared by Urea Clathrate Polymerization at Low Temperatures",doi:"10.5772/intechopen.90784",slug:"solubility-discoloration-and-solid-state-sup-13-sup-c-nmr-spectra-of-stereoregular-poly-vinyl-chlori",body:'\nSolid-state polymerization is a unique polymer synthetic method in Polymer Science. The most famous example is probably a urea clathrate polymerization of vinyl chloride (VC) as described here. That is, VC monomers are packed regularly in one-dimensional narrow urea canal under low temperatures (canal complex or inclusion complex). When strong γ-irradiation or electron beam one will be made, polymerization takes place, and highly stereoregular poly(vinyl chloride) (PVC) is obtained.
\nThe first research in this area was carried out by Brown and White, researchers of GE company (USA) [1, 2]. They showed that urea canal-polymerized polymers have a remarkable difference in its physical properties. Particularly, not only ordinary urea but also thiourea does the canal complex at low temperature, and their difference is an inner diameter of cavity (5A or 6A). The structures and properties of the resulting polymers are well described by a limited number of instruments including solubility measurements, etc. Although the described time period is old, their valuable finding and observation have still a brilliant light in Polymer Science even at the present time.
\nStereoregular PVC was investigated by Krimm et al. by using IR spectroscopy [3, 4]. Their first paper on stereoregular PVC was only one page, but its IR spectra were printed and published in all the textbooks and professional ones in the world (see \nFigure 1\n). In the IR spectra, structural difference appeared in the 700–600 cm−1 region. One can notice that only two peaks are clearly seen in the urea canal PVC in contrast with three peaks in free radical one. Lack of the left-hand side band (690 cm−1, assigned to be isotactic) strongly suggests that stereoregular PVC is highly syndiotactic.
\nKrimm’s data [
In Japan, a detailed IR study of PVC including stereoregular one was carried out by Shimanouchi and Tasumi in the University of Tokyo [5, 6]. Their standpoint of view was purely scientific, and direct application to industrial field appeared to be relatively small. However, their effort was greatly helpful for the improvement of commercial PVC products in Japan. They synthesized various model compounds and confirmed IR assignment of PVC, for example, the effects of C-Cl position on IR spectra and related problems are typical examples. Their collaborative work has been summarized and published in Ref. [7].
\n\n\nFigure 2\n shows the principle of urea canal polymerization [8, 9, 10]. When organic monomers are mixed with fine urea and the mixture is kept at low temperatures (−78°C), a canal complex is formed spontaneously. This is a typical inclusion phenomenon, and the resulting canal complex is called
Principle of urea canal polymerization.
The geometrical shape and size of the complex are quite different according to the type of monomers [9, 10]. An ideal complex is n-paraffin/urea system (\nFigure 2\n, right). A well-known fact is that started from ethylene/urea system, linear polyethylene with no branching is obtained.
\nIn the case of polar vinyl monomers, inclusion structure is quite different according to the type of monomers, e.g.,
The shape and size of canal complex.
Canal PVC was a white powder and was totally insoluble to organic solvent such as N,N-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO).
Type | \nSymbol | \nCode | \nForm | \nColor | \nSolubility\n4\n\n | \n
---|---|---|---|---|---|
Canal\n1\n\n | \n\n | \nγ-Ray | \nPowder | \nWhite | \n× | \n
Radical\n2\n\n | \n\n | \nZeon 103 | \nParticle | \nWhite | \n○ | \n
Radical\n3\n\n | \n\n | \n#038 | \nPowder | \nWhite | \n○ | \n
Characterization of PVC samples.
Prepared in JAERI, Takasaki by urea canal polymerization as described in the text.
Supplied from production company, Japan Zeon Co. Ltd. This polymer was a homopolymer.
Supplied from the Scientific Polymer Products (USA). This was a high molecular weight homopolymer.
Solubility into DMF at room temperature. (0), soluble, (x) insoluble.
Various measurements were carried out by using instrumental analyses such as solid-state NMR, FT-IR (KBr method), WAXD, TG, solid-state ESR, etc. under carefully controlled conditions. For example, typical NMR conditions in \nFigure 7\n were as follows: spectrometer, JEOL JNM GX-270; nucleus, 13C; PW2 contact time, 8 ms; PW1 pulse width (90° pulse), 4.5 μs; PD repetition time, 5000 s; number of scans, 150,000; probe, Doty’s ceramic probe (7 mm
\n\nFigure 4\n shows IR spectra [12]. There was a distinct difference in the band below 700 cm−1 region. Only two peeks are clearly observed in sample A. Lack of the left-hand side band (690 cm−1: assigned to be isotactic in amorphous region) suggests that the urea canal PVC has syndiotactic configuration. It is apparent that Krimm’s novel finding was confirmed in this way.
\nComparison of IR spectra of two kinds of PVC.
A small difference was also observed in 2900 cm−1 region. A new band (2933 cm−1) appeared especially in the urea canal PVC (\nFigure 5\n). This band may be correlated with some stereochemical structural factors including
FT-IR spectra of νCH2 region (diffuse reflection, KBr).
\n\nFigure 6\n shows the WAXD results. The existence of many coaxial Debye-Scherrer rings in the sample A is apparent. Careful observation revealed sixth diffraction rings can be counted. With regard to WAXD measurements,
\nComparison of WAXD of three kinds of PVC (negative film).
Sakurada et al. already observed sixth diffraction rings in γ-ray PVC (consists of three components indicating partial dissolution into DMF solvent) [14], but they didn’t show a WAXD photograph. Even in our experiments, it was very difficult to show rings by ordinary WAXD photograph technically; therefore, we preferred to the direct observation of negative film. By this method, the number of higher order of reflected rings can be counted. Further, very thin but distinct coaxial rings in sample B (commercial one) are obvious.
\n\n\nFigure 7\n shows the solid-state NMR spectra. (Since this polymer didn’t dissolve in any organic solvent, high-resolution NMR spectra couldn’t be obtained.) In comparison with that of free radical PVC (sample B), there was a distinct difference in the NMR spectra. PVC shows two 13C NMR peaks deriving from CH and CH2 groups on a polymer backbone. Their relative height was almost equal in
Comparison of solid-state 13C NMR spectra of two kinds of PVC.
Microtacticity of γ-ray PVC couldn’t be determined by solid-state NMR in this way, although quite different NMR peak shape was obtained.
\n\n\nFigure 8\n shows the solubility results of PVC. Free radical PVC (
Solubility of PVC in DMF solvent.
Results are given in \nFigures 9\n and \n10\n. In
FT-IR of PVC suspension heated in DMF 1080 cm−1 at 120 °C: a: original, b: 1 h, and c: 19 h.
FT-IR of PVC solution heated in DMF 1080 cm−1 at 120°C: d, 1 hour; e, 10 hours; and f, 19 hours.
A small band appeared at 1080 cm−1, which can be assigned to be trans-type of double bond [16]. In
Variation of IR intensity of trans-type double bond.
\n\nFigure 12\n shows the solid-state NMR spectra [17]. In sample A, spectral change was small. In contrast, in sample B, it was large. The appearance of broad peak at about 125–130 ppm is probably due to the formation of double bond, –(CH=CH)n\n−. In fact, various rubberlike materials having double bond in its molecular structure have strong peak in this region [18]. NMR results were as a whole in good agreement with those of FT-IR (\nFigures 9\n and \n10\n).
\nComparison of solid-state 13C NMR spectra of heated PVC.
\n\nFigure 13\n shows a photograph of heated PVC samples [12]. Canal PVC turns in its color from white (RT) to pale purple (160°C), deep purple (200°C), and then black (~280°C). It is very easy in discoloration. In contrast, free radical one is very hard in its discoloration. One can understand this when compared with the color of two PVC specimens heated up to 200°C (indicated by an arrow). Canal PVC is very deep purple (left), whereas free radical one is only slightly pale orange (right side). Easy discoloration of sample A is probably inherent characteristics of urea canal polymer due to the absence of termination reaction. Because of these characteristics, end radicals are generally living, which would act as a trigger of an elimination reaction (HCl) via a well-known β-elimination mechanism at higher temperatures.
\nComparison of a photograph of heated PVC.
\n\nFigure 14\n shows solid-state ESR results for sample A under the dynamic heating conditions. Pay attention to the central signal indicated by an asterisk (*), which is derived from the PVC power. Outer several peaks are due to the one from MnO+2 inserted as an ESR marker. One can notice that peak intensity increased with the elevation of temperature.
\nSolid-state ESR spectra under dynamic heating conditions.
As summarized in \nFigure 15\n, signal intensification is started at about 160°C, which corresponds to the onset of color changing from white to pale purple (see a photograph in \nFigure 13\n). Smooth increase of signal intensity means that elimination reaction proceeds zipper-like (autocatalytically), but its intensity stopped apparently in two regions (
ESR intensity and TG derivative curve.
It is worth while noting that
\n\nFigure 16\n shows solid-state NMR spectra. The original structure has retained considerably in sample A, since CH2 and CH peaks are clearly present. In contrast, in sample B, the original structural peaks have lost and new broad peak appeared at 130 ppm region. This spectral change in NMR is basically very close to those of FT-IR spectra in \nFigures 9\n and \n10\n (heat treatment in the solution or suspension state). In NMR measurements, it should be noted that the peak area is directly proportional to the concentration of functional groups in question; therefore, from both the position (chemical shift) and the peak shape (area), one can understand the mechanism wholly or intuitively.
\nComparison of solid-state 13C NMR spectra.
\n
The principle of urea clathrate polymerization at low temperatures was described from a purely experimental point of view. The basis lies on the canal complex formation of urea at low temperatures. Geometrical shape and size of the canal complex were described.
Characterization of bulk PVC sample was carried out by using FT-IR, WAXD, and solid-state NMR spectra. Lack of isotactic sequence was confirmed by IR spectra of 700–600 cm−1 region. Presence of well-ordered region was suggested by FT-IR characteristic band (2933 cm−1), WAXD rings, and solid-state NMR.
Solubility into DMF was studied. Free radical sample showed perfect solubility in DMF, while canal sample didn’t. Suspension was obtained. Heat treatment caused an elimination reaction followed by formation of trans-type of double bond. The reaction rate of sample A was small.
Discoloration by heat treatment was described. Canal PVC showed easy discoloration but rather delay in the TG degradation. The lack of termination reaction is related to the easy discoloration (β-elimination). Slow degradation will be attributed to the stiffness of molecular chain.
Solid-state ESR measurements were made. Signal intensity increased exponentially with temperature, but two abrupt stopping regions appeared. The existence of some modification of the mechanism (zipper-like autocatalytic elimination) under uniform heating conditions became apparent.
Solid-state NMR was used in various steps such as the characterization of original PVC and thermally degraded samples. Structural change can be visually understood by the appearance of a new peak. Since the peak area is directly proportional to the amount of functional group, a whole understanding of the extent of the progress of degradation is greatly of help.
We wish to express our hearty thanks to Mr. H. Sugisawa (JEOL), Prof. Y. Nozawa (Tohoku University), and Mr. T. Katoh (Yamagata University) for NMR measurements. Thanks are also expressed to Prof. M. Matsuda, Prof. T. Miyashita, and Dr. F. Bae (Tohoku University) for many conveniences in solid-state ESR measurements. The valuable discussion on IR spectroscopic data with Prof. M. Tasumi (University of Tokyo) is also greatly acknowledged.
\nArsenic (As) is the one the most toxic element present in earth which poses a serious health hazard to animal and human health. Generally arsenic is present in the earth crust in the form minerals, especially associated with iron pyrite and zinc ores. Arsenic contamination occurs through both by natural as well as anthropogenic processes [1]. Unlike other toxic heavy metals (Cadmium, mercury and chromium) arsenic contamination in environment predominately occurs through natural biogeochemical process [2] and some manmade activities play important role (triggering the process) in that process. Anthropogenic activities such as coal mining and burning smelting of As containing metal ores and other industrial activities are also responsible for distribution of arsenic in the environment [3]. Arsenic contamination of drinking water in South and Southeast Asia reported one of the most threatening problems that causes serious health hazard of millions of people of India and Bangladesh [4]. The source of As contamination in water in those countries were due to two different natural processes; oxidation of arsenopyrite minerals lies below ground water table due to water mining process and reduction of As containing iron hydroxides [5]. Arsenic exists in the nature in −3, 0, +3 and + 5 oxidation states and environmental forms include arsenious acids, arsenic acids, arsenites, arsenates, methylarsenic acid, dimethylarsinic acid, arsine, etc. Two inorganic forms are very common in natural waters: arsenite (AsO33−) and arsenate (AsO43−), referred to as arsenic (III) and arsenic (V). Pentavalent (+5) or arsenate species are AsO43−, HAsO42−, H2AsO4− while trivalent (+3) arsenites include As(OH)3, As(OH)4−, AsO2OH2− and AsO33−. The solubility of inorganic species depends on pH and redox potential of the environment and arsenite (As3+) is the most soluble form inorganic As. Pentavalent species or arsenate (As5+) predominate in oxygen rich aerobic environments, where as trivalent arsenites (As3+) dominant in moderately reducing anaerobic environments such as groundwater [4].
Arsenic concentration in drinking water reported more than 50 μg L−1 in many areas in the world [6], whereas maximum permissible limit set by World Health Organization (WHO) is 10 μg L−1. The use of arsenic contaminated ground water for irrigation purpose causes build up of As in soil and leads to entry of As in food crops, especially in rice and vegetables [7, 8]. This causes serious health hazard, in those As containing areas. In Southeast Asian countries like Bangladesh, Eastern parts of India (West Bengal and Bihar) and Vietnam, rice is consumed as major staple food and is very efficient in As translocation in grains [9]. Thus rice crop play a major pathway for As entry in human body living in those contaminated areas apart from drinking water. Thus remediation of arsenic contaminated water is important for environmental point of view. Various technologies are for remediation of arsenic contaminated water like ion exchange, electro dialysis, membrane filtration, adsorption and coagulation-flocculation generates lot of arsenic enriched waste. That waste material generally dumped or disposed in nearby surroundings, from where arsenic can also come back to soil and water by leaching thus making system susceptible to arsenic contamination. Along with above mentioned problem, huge cost is involved in this existing arsenic remediation technology. That necessitates finding out an alternate low cost technology which can take care of arsenic contaminated water.
Phytoremediation is an alternate and low cost technology that utilizes green plant to extract arsenic from water and store it vegetative cells. Phytoremediation process includes phytoextraction, phytostabilization, phytovolatilization, phytotransformation, and rhizofiltration [10]. Researchers find out that plants uptake arsenic by roots through phosphate uptake pathway and transfer it their above ground parts (shoot and leave). But how much amount of arsenic translocated from source (water) to sink (plant parts) depends on phytoremediation efficiency of the plant concern. However, more than 90% of total arsenic accumulated into the plant is stored in roots.
The plants utilized for phytoremediation have some criteria like (1) plant have higher specific growth rate under contaminated environment, (2) higher translocation capability of the toxic element concerned [11]. Metal translocation capability depends on factors like (1) bio concentration factor (BCF) and (2) translocation factor (TF). Plants having BCF >1 are ideal for Phytoremediation. Chinese brake fern (
The terminology “Phytoremediation” consists of two words, “Phyto” means “green plants” and “remediation” means “curative measures or restoration”. The word “phytoremediation” was first given by Chaney [18]. In phytoremediation process, generally green plants are used which uptake toxic chemical substances (such as heavy metals and metalloids, pesticide residues etc.) from contaminated sites (soil and water) by various mechanisms and remove them from environment. Various crop and weed plants are found to be suitable for phytoremediation purpose. But research results indicated that weed flora had higher phytoremediation potential than cultivated crops (Example- Brassica sp). There are various pathways of phytoremediation process such as, rhizofiltration, phytoaccumulation or phytoextraction, phytostabilization, phytodegradation or phytotransformation and phytovolatilization etc.
Rhizofiltration: Plants uptake toxics substances by their roots through adsorption or absorption process and sequester in their root system. Aquatic plants mainly exhibited this process.
Phytoaccumulation or phytoextraction: Plants uptake toxic substances by their root system and translocated to other plant parts such as stem and leave or other modified plant parts. This mechanism mainly exhibited this process are suitable for remediation of contaminated soil.
Phytostabilization: In this process, plants restrict movement of toxic substances in soil or water, thus reduced their availability to plants. In this method, plants do not uptake toxic substances from environment. Rather, plants secrets some root exudates or photochemicals which form stable chemical bond with toxic substances and increases its stability in environments.
Phytodegradation or Phytotransformation: In this process, plants uptake toxic substance from soil or water and degrade these primary toxic substances into nontoxic forms. A large number of metabolic and physiological factors are involved in this process.
Phytovolatilization: Plant uptake toxic substances by their root system and translocated to their aerial plant parts especially in leaves; and release toxic substances in the form of vapor which may not be toxic as their primary source.
Apart from this there are some other terminologies often used in phytoremediation process are bioconcentration factor (BCF) and translocation factor (TF).
BCF = toxic substance uptake by plant/toxic substance present in environment (soil or water).
TF = toxic substance present in shoot or stem/toxic substance present in roots or.
Toxic substance present in leaves/Toxic present in shoot or stem.
For, Hyper accumulator plants both BCF and TF is >1 is desired. In other words, plants suitable for phytoremediation, BCF >1 is always desirable. But for aquatic weeds, as their dominant pathways is rhizofiltration; their toxic substances BCF >1 but TF for root to shoot or shoot to leaves is <1.
The capability of removing arsenic from contaminated water was earlier observed by Misbahuddin and Fariduddin [20] and they observed that water hyacinth can removes arsenic from water within 3–6 hr. exposure time. Amount of arsenic removed depends on number of the plant used, exposure time, presence of air and sunlight. They concluded that whole plants were more effective than fibruous roots alone. It was observed that dried roots of water hyacinth can rapidly reduces As content in contaminated water within below WHO recommended critical level (<10 μg Lg−1) [21]. A fine powder was prepared from dried roots of water hyacinth plants (obtained from Dhaka, Bangladesh) removed more than 93% arsenite and 95% of arsenate from a solution containing As @ 200 μg L−1 within 1 hr. exposure time [21]. Higher biomass production ability of water hyacinth allow it to remove As at higher rate (600 mg As ha−1 day−1) and greater efficiency (17%) compared to lower biomass producing aquatic macrophytes such as lesser duck weed (
However nutrients like phosphate addition may suppressed As uptake by duckweeds as both phosphorus and arsenic belongs same group-V(b) element family in periodic table [33]. In most of the phytoremediation study carried out in laboratory condition, As is provided either in the form of arsenite (As3+) or arsenate (As5+). But some studies included dimethyl arsenic acid (DMAA), an organic form of arsenic for evaluation of As phytoremediation potential of duckweed species. In a lab study,
Arsenic uptake pattern in different Azolla sp. (adapted from Zhang et al., 2009).
Some semi aquatic weed such as
Among the submerged aquatic weeds
In natural conditions, submerged weeds grow in water bodies in association with floating macrophytes. Use of Combinations of submerged and floating weeds found more effective for phytoremediation purpose than submerged and floating weeds alone. Research work carried out using Hydrilla, Certophyllum, lemna and Wolfia at various combinations showed that Ceratophyllum + lemna combination (3326 μg) combination removed maximum total As followed by
Arsenic uptake comparison between various weed plants (Hydrilla, Ceratophyllum, Wolffia, Lemna and Eicchornia) grown in singly or in various combinations upon arsenic exposure for 30 days (adapted from Srivastava et al., 2014).
Name of the plants | Key findings | Reference |
---|---|---|
Removed 600 mg As ha−1 day−1 within 21 days with 18% removal efficiency when As was applied @ 0.15 mg L−1 | [13] | |
Removal rate 140 mg As ha−1 day−1 within 21 days with 5% removal efficiency when As was applied @ 0.15 mg L−1 | [13] | |
Removed relatively higher As3+ (17408 μg g−1) and lower As5+ (8674 μg g−1As) from As containing solutions (64 μM As each) | [35] | |
Accumulates 1120 μg g−1 As in | [31] | |
Accumulates 50 μg g−1 As in roots | [41] | |
Removed sum total 8546 μg (348 μg g−1) of As from contaminated water (As concentration 1500 μg L−1) | [49] | |
Accumulates 525 μg g−1 (dry weight baisis) from 250 μM As5+ solution for 7 days | [22] | |
Accumulates 1000 mg kg−1 (dry weight basis) from As contaminated environment | [52] | |
Accumulates 1000 mg kg−1 (dry weight basis) from As contaminated environment | [52] | |
Vallisnaria natans | Accumulates 1000 mg kg−1 (dry weight basis) from As contaminated environment | [52] |
Extract 12.94 mg kg−1 total As (dry weight basis) from pulp paper industry effluents | [61] | |
Accumulates As at the rate 9 mg kg−1 with TF = 4.93 and BF = 15.00 for the arsenic containing solution 600 μg L−1. | [16] | |
Phragnites austratlis | Accumulates 32.5 mg kg−1 As in root | [62] |
Phytoremediation ability of various aquatic and semi aquatic weeds.
Three pathways for arsenic uptake in marine macrophytes have been described – (i) active uptake through phosphate uptake transporters, (ii) passive uptake through aquaglyceroporins, and (iii) physicochemical adsorption on root surfaces. Plants mainly uptake As(V) through phosphate uptake transporters [63, 64]. As(III), DMAA and MMAA gets into the plants by passive mechanism through the aquaglyceroporin channels [64].
As(V) and phosphate are chemical analogs, and compete for uptake carriers in the plasmalemma [65]. As a result, as the phosphate content rises, more As (V) is required to be desorbed in the solution. Mkandawire and Dudel. [32] and Rahman et al. [33] showed that As (V) is taken up by aquatic plants through the phosphate uptake pathway, it competes with phosphate for uptake in tissues of
Physiological studies indicate that these arsenic species are transported in rice through aquaporins /aquaglyceroporins via passive uptake mechanisms [66, 67]. Molecular studies revealed that Nodulin26-like intrinsic membrane proteins (NIPs), one of the major subfamilies of aquaporins transporters that promote the transport of neutral molecules like water, glycerol, and urea, are responsible for transporting As(III) into rice roots [68]. Aquaporins and aquaglyceroporins are two of three subfamilies of water channel proteins (WCPs), the transmembrane proteins that have a specific three-dimensional structure with a pore that permeates water molecules [69], which are permeable to water, glycerol, and/or other small, neutral molecules. Glycerol and As(III) compete for uptake in rice (
Arsenic is adsorbing and accumulating on the surfaces of aquatic plants due to suspended iron oxides (Fe-plaque). Robinson et al. [70] discovered a strong association between arsenic and iron concentrations in aquatic plants, which is believed to be due to arsenic adsorption on plant surfaces’ iron oxides. Rahman et al. [14] investigated arsenic species adsorption on precipitated iron oxides on
Arsenic occurs primarily as As (V) in an oxic environment and as As (III) in a reduced environment [64]. In plants, As (V) and phosphate share the same transporter, while As(III) enters plant cells through NIPs’aquaporins [57, 64]. Because of their distinct molecular properties, these two types of arsenic elicit different biochemical responses in aquatic plants [71]. As (V) has no affinity for thiol ligands, while As(III) has a strong affinity for peptides with sulfhydryl (-SH) groups, such as glutathione (GSH) and phytochelatins (PCs) [64, 72]. Even though plants had been exposed to As, arsenic speciation in plant tissues indicates that arsenic is primarily present in the As(III) oxidation state (V).This suggests that As(V) is effectively reduced to As(III) in plant cells after uptake, and that most plants have high As(V) reduction competence [64]. The reduction of As(V) to As(III) is mediated by GSH [73] and by enzyme [74], which is thought to be a detoxification mechanism of the plants. As(V) and As(III) have been shown to generate reactive oxygen species (ROS) within cells when they are taken up [75], and plants counteract the generation of ROS by various enzymes and cellular compounds [76]. The GSH can act as an antioxidant and is required for the synthesis of Phytochelatins which are required for metalloid chelation [71].
The mechanism of arsenic accumulation and detoxification was studied by many others in aquatic plant
Plants have been utilized for phytoremediation of toxic metals and metalloids, however due to heavy metal phytotoxicity to plants; this process has been slow and largely rendered ineffective [77]. Natural heavy metal hyperaccumulators are also available, however, they are limited to specific geo-climatic conditions and also lack the crucial biomass required for efficient phytoremediation. Phytoremediation has a lot of potential using genetic engineering technologies to improve plant tolerance and heavy metal accumulation. Furthermore, various new studies using omics technologies such as genomics, transcriptomics, proteomics, and metabolomics to elucidate the genetic determinants and pathways involved in heavy metal and metalloid tolerance in plants have been identified. Presently there are three main biotechnological approaches for the phytoremediation of heavy metals and metalloids are currently being used to engineer plants for phytoremediation of heavy metals and metalloids: (1) manipulating metal/metalloid transporter genes and uptake systems; (2) enhancing metal and metalloid ligand production; (3) conversion of metals and metalloids to less toxic and volatile forms [78] (Figure 3).
Potential biotechnological strategies for phytoremediation. Heavy/toxic metals can be mobilized and transported (influx) into roots through plasma membrane transporters. They can then be transported (efflux) out of the roots into the xylem and translocated into the shoots. At this stage, plant tolerance to toxic elements may be enhanced through manipulation of influx/efflux transporters or by increasing the levels of ligands/chelators. Volatilization of the toxic elements can be achieved through enzymes that modify these toxic elements. Chelators or efflux transporters can also be used to export the toxic elements out of the cytosol and into vacuoles or the cell wall. Adapted from Dhankher et al. (2011).
Enhanced heavy metal tolerance and bioaccumulation has been attained in different plant species by genetic manipulation of metal transporter genes. For example, the overexpression of full length
Recent research findings have revealed arsenite is transported in plants by proteins belonging to the aquaporins [83, 84]. It is observed that in efficient arsenic hyperaccumulators such as
Genome-wide gene expression analysis in
Complexation of Arsenic with phytochelatins (PCs), or metallothionein (MTs) or glutathione (GSH) is an proficient way to detoxify As(III), since these complexes are sequestered in the vacuoles, this process is catalyzed by the homologs of multidrug resistance proteins (MRPs) [92, 93]. Enhancing the accumulation or synthesis of PCs and/or GSH and/or MTs may be one way to increase phytoremediation of arsenic. The overexpression of
Arsenic (As) tolerance in plants can also be increased by modifying GSH and PCs. Dhankher et al. [96] transferred and co-expressed two bacterial genes,
The
There are several reports for developing phytoremediation strategies for heavy metals with the help of biotechnological interventions by conversion of these metals to less toxic and volatile forms. It is observed that many organisms, including bacteria, fungi, and animals, methylate arsenic. Methylated arsenic have been discovered in several plant species, including rice grain [100, 101], and suggest that this is the process is a result of endogenous methylation by the plants themselves. The final product of this pathway is the gas trimethylarsine (TMAs(III)), that can be volatilized from the plant. Qin et al. [102] have cloned a gene encoding an As(III)-S-adenosylmethionine methyltransferase (arsM) from the soil bacterium
Contamination of soils and water by arsenic is one the serious threat for food security and human health in throughout the world. Some severe skin and other diseases occur due to continuous consumption of As contaminated foods and water. This necessitates a suitable technology to handle arsenic contaminated water carefully, so that above mentions points can be satisfied. Phytoremediation of arsenic contaminated water by aquatic and semi aquatic weeds offers low cost, economically feasible and eco-friendly technology to remove arsenic from contaminated water for long term. Some weeds have tremendous potential to accumulate higher amount of arsenic in their plant parts such as Eichhornia crassipes, Hydrilla verticillata, Spirodella polyrhiza, Arundo donax and Vetivaria spp. More specifically semi aquatic weeds like Arundo donax and Vetivaria sp. (perennial) can be used with in combination with Eicchornia, Spirodella and Hydrilla to remove arsenic more efficiently from treatment tanks or constructed wetland system. Although management of plant biomass will be another concern for disposal, but these plant materials can be used for making fiber (water hyacinth), handcraft items (Arundo and Typha stems) and biofuel purpose. Moreover, with advancement of molecular genetics in future As tolerance genes can be transferred to food crops (specially rice) which can store huge amount of As in their roots or very low transfer co-efficient from root to grain so that transgenic rice crops will able to grow using As contaminated water and contribute in food security in upcoming days.
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Jane Grande-Allen"}]},{id:"59778",doi:"10.5772/intechopen.74768",title:"Epidemiology of Myocardial Infarction",slug:"epidemiology-of-myocardial-infarction",totalDownloads:4515,totalCrossrefCites:12,totalDimensionsCites:24,abstract:"Coronary heart disease (CHD) is the leading cause of morbidity and mortality throughout the world. The most common form of CHD is the myocardial infarction. It is responsible for over 15% of mortality each year, among the vast majority of people suffering from non-ST-segment elevation myocardial infarction (NSTEMI) than ST-segment elevation myocardial infarction (STEMI). The prevalence of myocardial infarction (MI) is higher in men in all age-specific groups than women. Although the incidence of MI is decreased in the industrialized nations partly because of improved health systems and implementation of effective public health strategies, nevertheless the rates are surging in the developing countries such as South Asia, parts of Latin America, and Eastern Europe. The modifiable risk factors represent over 90% of the risk for acute MI. The risk factors such as dyslipidemia, smoking, psychosocial stressors, diabetes mellitus, hypertension, obesity, alcohol consumption, physical inactivity, and a diet low in fruits and vegetables were strongly associated with acute MI.",book:{id:"6373",slug:"myocardial-infarction",title:"Myocardial Infarction",fullTitle:"Myocardial Infarction"},signatures:"Joshua Chadwick Jayaraj, Karapet Davatyan, S.S. Subramanian and Jemmi Priya",authors:[{id:"223196",title:"Dr.",name:"Joshua",middleName:null,surname:"Chadwick",slug:"joshua-chadwick",fullName:"Joshua Chadwick"},{id:"231054",title:"Dr.",name:"Karapet",middleName:null,surname:"Davatyan",slug:"karapet-davatyan",fullName:"Karapet Davatyan"},{id:"231055",title:"Ms.",name:"Jemmi",middleName:null,surname:"Priya",slug:"jemmi-priya",fullName:"Jemmi Priya"},{id:"244487",title:"Dr.",name:"S.S.",middleName:null,surname:"Subramanian",slug:"s.s.-subramanian",fullName:"S.S. Subramanian"}]}],mostDownloadedChaptersLast30Days:[{id:"80213",title:"Evolution of Heart Transplantation Surgical Techniques",slug:"evolution-of-heart-transplantation-surgical-techniques",totalDownloads:241,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Organ transplantation has kindled the human imagination since the beginning of time. Prehistorically, transplantation appeared as mythological stories: from creatures with body parts from different species, the heart transplant between two Chinese soldiers by Pien Ch’iao, to the leg transplant by physician Saints Cosmas and Damian. By 19th century, the transplantation concept become possible by extensive contributions from scientists and clinicians whose works had taken generations. Although Alexis Carrel is known as the founding father of experimental organ transplantation, many legendary names had contributed to the experimental works of heart transplantation, including Guthrie, Mann, and Demikhov. The major contribution to experimental heart transplantation before the clinical era were made by a team lead by Richard Lower and Norman Shumway at Stanford University in the early 1960s. They played the vital role in developing experimental and clinical heart transplantation as it is known today. Using Shumway biatrial technique Christiaan Barnard started a new era of clinical heart transplantation, by performing the first in man human-to-human heart transplantation in 1967. The techniques of heart transplant have evolved since the first heart transplant. This chapter will summarize the techniques that have been used in clinical heart transplantation.",book:{id:"11236",slug:null,title:"Heart Transplantation - New Insights in Therapeutic Strategies",fullTitle:"Heart Transplantation - New Insights in Therapeutic Strategies"},signatures:"Samuel Jacob, Anthony N. Pham and Si M. Pham",authors:null},{id:"65757",title:"Prevalence of Dyslipidemia and Goal Attainment with Lipid-Lowering Therapy: Insights from Thai Multicenter Study and Overview of the Major Guidelines",slug:"prevalence-of-dyslipidemia-and-goal-attainment-with-lipid-lowering-therapy-insights-from-thai-multic",totalDownloads:2359,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Background Since the release in Thailand in 2001 of the Third Guidelines by the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation and Treatment of High Blood Cholesterol in Adults or the Adult Treatment Panel (ATP III), there have been no nationwide studies on the proportion of dyslipidaemic patients who have achieved the low-density lipoprotein cholesterol (LDL-C) goals. The authors therefore aimed to estimate the percentage achievement of LDL-C goals based on the modified NCEP ATP III guidelines in intermediate- to high-risk patients. Methods The authors conducted a hospital-based, cross-sectional, epidemiological survey. Patients (1240) were selected consecutively from 50 hospitals across Thailand. Patients were included if they had been treated with statins for at least 3 months. Results Two-thirds were female, and the mean age was 61.7+69.5 years. The median duration of statin treatment was 21 months. Half (633/1240) of the patients achieved the LDL-C goal levels as defined by the NCEP guidelines (51.1%, 95% CI 48.3% to 53.8%). The very high-risk group had the lowest percentage achievement (11.6%; 95% CI 1.6% to 21.6%), compared with 54.2% (95% CI 50.9% to 57.4%) for the high-risk group and 47.0% (95% CI 41.1% to 52.8%) for the moderate-risk group. More males achieved the LDL-C goals than females (55.6% vs. 48.9%; P = 0.029). Conclusions Overall, 51.1% of the patients with cardiovascular risk, on statins treatment, achieved the NCEP ATP III LDL-C goal levels.",book:{id:"7556",slug:"dyslipidemia",title:"Dyslipidemia",fullTitle:"Dyslipidemia"},signatures:"Songkwan Silaruks, Charn Sriratanasathavorn, Petch Rawdaree, Rapeephon Kunjara-Na-Ayudhaya, Bandit Thinkhamrop and Piyamitr Sritara",authors:[{id:"256769",title:"Prof.",name:"Songkwan",middleName:null,surname:"Silaruks",slug:"songkwan-silaruks",fullName:"Songkwan Silaruks"},{id:"283455",title:"Dr.",name:"Charn",middleName:null,surname:"Sriratanasathavorn",slug:"charn-sriratanasathavorn",fullName:"Charn Sriratanasathavorn"},{id:"283456",title:"Dr.",name:"Petch",middleName:null,surname:"Rawdaree",slug:"petch-rawdaree",fullName:"Petch Rawdaree"},{id:"283457",title:"Dr.",name:"Rapeephon",middleName:null,surname:"Kunjara-Na-Ayudhaya",slug:"rapeephon-kunjara-na-ayudhaya",fullName:"Rapeephon Kunjara-Na-Ayudhaya"},{id:"283458",title:"Dr.",name:"Bandit",middleName:null,surname:"Thinkhamrop",slug:"bandit-thinkhamrop",fullName:"Bandit Thinkhamrop"},{id:"283459",title:"Prof.",name:"Piyamitr",middleName:null,surname:"Sritara",slug:"piyamitr-sritara",fullName:"Piyamitr Sritara"}]},{id:"59778",title:"Epidemiology of Myocardial Infarction",slug:"epidemiology-of-myocardial-infarction",totalDownloads:4507,totalCrossrefCites:11,totalDimensionsCites:24,abstract:"Coronary heart disease (CHD) is the leading cause of morbidity and mortality throughout the world. The most common form of CHD is the myocardial infarction. It is responsible for over 15% of mortality each year, among the vast majority of people suffering from non-ST-segment elevation myocardial infarction (NSTEMI) than ST-segment elevation myocardial infarction (STEMI). The prevalence of myocardial infarction (MI) is higher in men in all age-specific groups than women. Although the incidence of MI is decreased in the industrialized nations partly because of improved health systems and implementation of effective public health strategies, nevertheless the rates are surging in the developing countries such as South Asia, parts of Latin America, and Eastern Europe. The modifiable risk factors represent over 90% of the risk for acute MI. The risk factors such as dyslipidemia, smoking, psychosocial stressors, diabetes mellitus, hypertension, obesity, alcohol consumption, physical inactivity, and a diet low in fruits and vegetables were strongly associated with acute MI.",book:{id:"6373",slug:"myocardial-infarction",title:"Myocardial Infarction",fullTitle:"Myocardial Infarction"},signatures:"Joshua Chadwick Jayaraj, Karapet Davatyan, S.S. Subramanian and Jemmi Priya",authors:[{id:"223196",title:"Dr.",name:"Joshua",middleName:null,surname:"Chadwick",slug:"joshua-chadwick",fullName:"Joshua Chadwick"},{id:"231054",title:"Dr.",name:"Karapet",middleName:null,surname:"Davatyan",slug:"karapet-davatyan",fullName:"Karapet Davatyan"},{id:"231055",title:"Ms.",name:"Jemmi",middleName:null,surname:"Priya",slug:"jemmi-priya",fullName:"Jemmi Priya"},{id:"244487",title:"Dr.",name:"S.S.",middleName:null,surname:"Subramanian",slug:"s.s.-subramanian",fullName:"S.S. Subramanian"}]},{id:"70032",title:"Coronary Artery Bypass Grafting: Surgical Anastomosis: Tips and Tricks",slug:"coronary-artery-bypass-grafting-surgical-anastomosis-tips-and-tricks",totalDownloads:1363,totalCrossrefCites:0,totalDimensionsCites:2,abstract:"The definite feature of coronary artery disease is the focal narrowing in the vascular endothelium, and this leads to the decrease in the flow of blood to the myocardium. Atherosclerotic plaque is the main lesion. These patients can present with chest pain (angina or myocardial infarction) and need further workup noninvasively and invasively for the management. The main reasons for myocardial revascularization can be: (1) relief from symptoms of myocardial ischemia; (2) reduce the risks of future mortality; (3) to treat or prevent morbidities such as myocardial infarction, arrhythmias, or heart failure. Coronary artery bypass grafting (CABG) is the surgical technique of cardiac revascularization. In 1910, Dr. Alexis Carrel described a series of canine experiments in which he devised means to treat CAD by creating a “complementary circulation” for the diseased native coronary arteries. No clinical translation occurred at the time, but he was awarded the Nobel Prize in Medicine. Experimental refinements of coronary arterial revascularization, including the use of internal thoracic artery (ITA) grafts, were later reported by Murray and colleagues, Demikhov, and Goetz and colleagues in the 1950s and early 1960s. Dr. Rene Favaloro performed his first coronary bypass operation in May 1967 with an interposed saphenous vein graft (SVG) and shortly thereafter used aortocoronary bypasses sutured proximally to the ascending aorta. The stenosed segment is bypassed using an arterial or venous graft. Left internal thoracic artery is the most commonly used artery, and long saphenous vein is the most commonly used vein for the coronary artery grafting to reestablish the blood flow to the compromised myocardium. This can be performed with or without the help of cardiopulmonary bypass machine and also with or without arresting the heart. These techniques are called as on-pump beating or on-pump arrested and off-pump beating coronary artery bypass grafting surgery. Distal and proximal anastomoses are usually performed in an end-to-side manner, but in the case of doing sequential grafting, side-to-side anastomosis is also performed proximal to the end-to-side anastomosis. In this chapter we are going to discuss the coronary artery bypass grafting tips and tricks in details.",book:{id:"9060",slug:"the-current-perspectives-on-coronary-artery-bypass-grafting",title:"The Current Perspectives on Coronary Artery Bypass Grafting",fullTitle:"The Current Perspectives on Coronary Artery Bypass Grafting"},signatures:"Mohd. Shahbaaz Khan",authors:[{id:"278633",title:"Dr.",name:"Mohd. Shahbaaz",middleName:null,surname:"Khan",slug:"mohd.-shahbaaz-khan",fullName:"Mohd. Shahbaaz Khan"}]},{id:"53810",title:"Angiography and Endovascular Therapy for Below-the-Knee Artery Disease",slug:"angiography-and-endovascular-therapy-for-below-the-knee-artery-disease",totalDownloads:3130,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"Critical limb ischemia (CLI) is growing in global prevalence and is associated with high rates of limb loss and mortality. “Endovascular-first” approach is considered to be the current standard care for symptomatic infrainguinal atherosclerotic disease. Given the facts that many CLI patients have severe comorbidities and endovascular-first approach is a common practice and may reduce the magnitude of the surgical trauma and systemic complications. In this chapter, updated angiographic approach for below-the-knee disease is described with endovascular technique.",book:{id:"5596",slug:"angiography-and-endovascular-therapy-for-peripheral-artery-disease",title:"Angiography and Endovascular Therapy for Peripheral Artery Disease",fullTitle:"Angiography and Endovascular Therapy for Peripheral Artery Disease"},signatures:"Akihiro Higashimori",authors:[{id:"195500",title:"Dr.",name:"Akihiro",middleName:null,surname:"Higashimori",slug:"akihiro-higashimori",fullName:"Akihiro Higashimori"}]}],onlineFirstChaptersFilter:{topicId:"170",limit:6,offset:0},onlineFirstChaptersCollection:[{id:"81437",title:"Pediatric Heart Transplantation",slug:"pediatric-heart-transplantation",totalDownloads:17,totalDimensionsCites:0,doi:"10.5772/intechopen.104518",abstract:"Despite advances in medical management, patients submitted for heart transplantation procedures still are at risk to development of complications. This chapter will discuss some specific topics of pediatric heart transplantation, focusing on perioperative care: (i) recipient management, (ii) donor evaluation, (iii) immunosuppression, (iv) early postoperative management, (v) complications, and (vi) conclusions.",book:{id:"11236",title:"Heart Transplantation - New Insights in Therapeutic Strategies",coverURL:"https://cdn.intechopen.com/books/images_new/11236.jpg"},signatures:"Estela Azeka"},{id:"81451",title:"Donor Assessment and Management for Heart Transplantation",slug:"donor-assessment-and-management-for-heart-transplantation",totalDownloads:20,totalDimensionsCites:0,doi:"10.5772/intechopen.104504",abstract:"For many years, heart transplantation has been an established procedure for patients with end-stage heart failure using the so-called “Standard Criteria” for an optimal heart donor. However, annually listed patients for heart transplantation greatly increased worldwide, and the use of extended criteria donor hearts has been utilized as many as possible in many countries. In this chapter, firstly, pathophysiology of brain death is explained. Secondly, donor assessment and issues of extended criteria donors are introduced. Then, donor management to maximize the heart graft availability, and the Japanese donor assessment and evaluation system and its outcome are reviewed.",book:{id:"11236",title:"Heart Transplantation - New Insights in Therapeutic Strategies",coverURL:"https://cdn.intechopen.com/books/images_new/11236.jpg"},signatures:"Norihide Fukushima"},{id:"81057",title:"Induction Therapy in the Current Immunosuppressive Therapy",slug:"induction-therapy-in-the-current-immunosuppressive-therapy",totalDownloads:18,totalDimensionsCites:0,doi:"10.5772/intechopen.103746",abstract:"The current immunosuppressive therapy including calcineurin inhibitors, mycophenolate mofetil, and steroids, has substantially suppress rejections and improved clinical outcomes in heart transplant (HTx) recipients. Nevertheless, the management of drug-related nephrotoxicity, fatal acute cellular rejection (ACR), antibody-mediated rejection and infections remains challenging. Although previous some studies suggested that perioperative induction immunosuppressive therapy may be effective for the suppressing ACR and deterioration of renal function, increased incidence of infection and malignancy was concerned in recipients with induction immunosuppressive therapy. The international society of heart and lung transplantation (ISHLT) guidelines for the care of heart transplant recipients do not recommend routine use of induction immunosuppressive therapy, except for the patients with high risk of acute rejection or renal dysfunction, however, appropriate therapeutic regimen and indication of induction immunosuppressive therapy remains unclear in HTx recipients. We review current evidence of induction immunosuppressive therapy in HTx recipients, and discuss the appropriate therapeutic regimen and indication of induction therapy.",book:{id:"11236",title:"Heart Transplantation - New Insights in Therapeutic Strategies",coverURL:"https://cdn.intechopen.com/books/images_new/11236.jpg"},signatures:"Takuya Watanabe, Yasumasa Tsukamoto, Hiroki Mochizuki, Masaya Shimojima, Tasuku Hada, Satsuki Fukushima, Tomoyuki Fujita and Osamu Seguchi"},{id:"80305",title:"Hepatic and Endocrine Aspects of Heart Transplantation",slug:"hepatic-and-endocrine-aspects-of-heart-transplantation",totalDownloads:14,totalDimensionsCites:0,doi:"10.5772/intechopen.102418",abstract:"End-organ dysfunction is a progression that can often develop in patients with end-stage heart failure. Hepatic abnormalities in advanced systolic heart failure may affect several aspects of the liver function. Hepatic function is dependent on age, nutrition, previous hepatic diseases, and drugs. The hepatic dysfunction can have metabolic, synthetic, and vascular consequences, which strongly influence the short- and long-term results of the transplantation. In this chapter, the diagnostic and treatment modalities of the transplanted patient will be discussed. On the other hand, endocrine abnormalities, particularly thyroid dysfunction, are also frequently detected in patients on the waiting list. Endocrine supplementation during donor management after brain death is crucial. Inappropriate management of central diabetes insipidus, hyperglycemia, or adrenal insufficiency can lead to circulatory failure and graft dysfunction during procurement. Thyroid dysfunction in donors and recipients is conversely discussed.",book:{id:"11236",title:"Heart Transplantation - New Insights in Therapeutic Strategies",coverURL:"https://cdn.intechopen.com/books/images_new/11236.jpg"},signatures:"Andrea Székely, András Szabó and Balázs Szécsi"},{id:"79970",title:"The Role of Large Impella Devices in Temporary Mechanical Circulatory Support for Patients Undergoing Heart Transplantation",slug:"the-role-of-large-impella-devices-in-temporary-mechanical-circulatory-support-for-patients-undergoin",totalDownloads:17,totalDimensionsCites:0,doi:"10.5772/intechopen.101680",abstract:"Large microaxial pump systems (Impella 5.0, or Impella 5.5; i.e., Impella 5+) (Abiomed Inc., Danvers, MA, USA) have gained increasing levels of attendance as valuable tools of mechanical circulatory support (MCS). Patients undergoing heart transplantation (HTX) often need temporary MCS in the perioperative course, either as a preoperative bridge or occasionally in the early post-transplant period. Here we present our experience using Impella 5+ support for patients designated to undergo HTX, describe technical aspects of implantation and removal, and further analyze factors influencing the overall patient outcome. Significant factors are discussed in front of the background of contemporary international literature, and current scientific questions are highlighted.",book:{id:"11236",title:"Heart Transplantation - New Insights in Therapeutic Strategies",coverURL:"https://cdn.intechopen.com/books/images_new/11236.jpg"},signatures:"Yukiharu Sugimura, Sebastian Bauer, Moritz Benjamin Immohr, Arash Mehdiani, Hug Aubin, Ralf Westenfeld, Udo Boeken, Artur Lichtenberg and Payam Akhyari"},{id:"80721",title:"Gene Therapy for Cardiac Transplantation",slug:"gene-therapy-for-cardiac-transplantation",totalDownloads:85,totalDimensionsCites:0,doi:"10.5772/intechopen.102865",abstract:"Gene therapy is an advanced treatment approach that alters the genetic composition of cells to confer therapeutic protein or RNA expression to the target organ. It has been successfully introduced into clinical practice for the treatment of various diseases. Cardiac transplantation stands to benefit from applications of gene therapy to prevent the onset of post-transplantation complications, such as primary graft dysfunction, cardiac allograft vasculopathy, and rejection. Additionally, gene therapy can be used to minimize or potentially eliminate the need for immunosuppression post-transplantation. Several animal models and delivery strategies have been developed over the years with the goal of achieving robust gene expression in the heart. However, a method for doing this has yet to be successfully translated into clinical practice. The recent advances in ex vivo perfusion for organ preservation provide potential ways to overcome several barriers to achieving gene therapy for cardiac transplantation into clinical practice. Optimizing the selection of the gene-carrying vector for gene delivery and selection of the therapeutic gene to be conferred is also crucial for being able to implement gene therapy in cardiac transplantation. Here, we discuss the history and current state of research on gene therapy for cardiac transplantation.",book:{id:"11236",title:"Heart Transplantation - New Insights in Therapeutic Strategies",coverURL:"https://cdn.intechopen.com/books/images_new/11236.jpg"},signatures:"Michelle Mendiola Pla, Yuting Chiang, Jun-Neng Roan and Dawn E. Bowles"}],onlineFirstChaptersTotal:19},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:89,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:318,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:129,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:106,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:15,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. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}}]},series:{item:{id:"11",title:"Biochemistry",doi:"10.5772/intechopen.72877",issn:"2632-0983",scope:"Biochemistry, the study of chemical transformations occurring within living organisms, impacts all areas of life sciences, from molecular crystallography and genetics to ecology, medicine, and population biology. Biochemistry examines macromolecules - proteins, nucleic acids, carbohydrates, and lipids – and their building blocks, structures, functions, and interactions. Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. This Biochemistry Series will address the current research on biomolecules and the emerging trends with great promise.",coverUrl:"https://cdn.intechopen.com/series/covers/11.jpg",latestPublicationDate:"June 29th, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:32,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"Blumenberg",slug:"miroslav-blumenberg",fullName:"Miroslav Blumenberg",profilePictureURL:"https://mts.intechopen.com/storage/users/31610/images/system/31610.jpg",biography:"Miroslav Blumenberg, Ph.D., was born in Subotica and received his BSc in Belgrade, Yugoslavia. He completed his Ph.D. at MIT in Organic Chemistry; he followed up his Ph.D. with two postdoctoral study periods at Stanford University. Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. He has published more than 100 peer-reviewed research articles and graduated numerous Ph.D. and postdoctoral students.",institutionString:null,institution:{name:"New York University Langone Medical Center",institutionURL:null,country:{name:"United States of America"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"3",title:"Bacterial Infectious Diseases",coverUrl:"https://cdn.intechopen.com/series_topics/covers/3.jpg",isOpenForSubmission:!1,editor:null,editorTwo:null,editorThree:null},{id:"4",title:"Fungal Infectious Diseases",coverUrl:"https://cdn.intechopen.com/series_topics/covers/4.jpg",isOpenForSubmission:!0,editor:{id:"174134",title:"Dr.",name:"Yuping",middleName:null,surname:"Ran",slug:"yuping-ran",fullName:"Yuping Ran",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bS9d6QAC/Profile_Picture_1630330675373",biography:"Dr. Yuping Ran, Professor, Department of Dermatology, West China Hospital, Sichuan University, Chengdu, China. 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He is also a faculty member in the Molecular Oncology Program. He obtained his MSc and Ph.D. at Oregon State University and Texas Tech University, respectively. He pursued his postdoctoral studies at Rutgers University Medical School and the National Institutes of Health (NIH/NIDDK), USA. His research focuses on biochemistry, biophysics, genetics, molecular biology, and molecular medicine with specialization in the fields of drug design, protein structure-function, protein folding, prions, microRNA, pseudogenes, molecular cancer, epigenetics, metabolites, proteomics, genomics, protein expression, and characterization by spectroscopic and calorimetric methods.",institutionString:"University of Health Sciences",institution:null},{id:"180528",title:"Dr.",name:"Hiroyuki",middleName:null,surname:"Kagechika",slug:"hiroyuki-kagechika",fullName:"Hiroyuki Kagechika",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/180528/images/system/180528.jpg",biography:"Hiroyuki Kagechika received his bachelor’s degree and Ph.D. in Pharmaceutical Sciences from the University of Tokyo, Japan, where he served as an associate professor until 2004. He is currently a professor at the Institute of Biomaterials and Bioengineering (IBB), Tokyo Medical and Dental University (TMDU). From 2010 to 2012, he was the dean of the Graduate School of Biomedical Science. Since 2012, he has served as the vice dean of the Graduate School of Medical and Dental Sciences. He has been the director of the IBB since 2020. Dr. Kagechika’s major research interests are the medicinal chemistry of retinoids, vitamins D/K, and nuclear receptors. He has developed various compounds including a drug for acute promyelocytic leukemia.",institutionString:"Tokyo Medical and Dental University",institution:{name:"Tokyo Medical and Dental University",country:{name:"Japan"}}},{id:"94311",title:"Prof.",name:"Martins",middleName:"Ochubiojo",surname:"Ochubiojo Emeje",slug:"martins-ochubiojo-emeje",fullName:"Martins Ochubiojo Emeje",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94311/images/system/94311.jpeg",biography:"Martins Emeje obtained a BPharm with distinction from Ahmadu Bello University, Nigeria, and an MPharm and Ph.D. from the University of Nigeria (UNN), where he received the best Ph.D. award and was enlisted as UNN’s “Face of Research.” He established the first nanomedicine center in Nigeria and was the pioneer head of the intellectual property and technology transfer as well as the technology innovation and support center. Prof. Emeje’s several international fellowships include the prestigious Raman fellowship. He has published more than 150 articles and patents. He is also the head of R&D at NIPRD and holds a visiting professor position at Nnamdi Azikiwe University, Nigeria. He has a postgraduate certificate in Project Management from Walden University, Minnesota, as well as a professional teaching certificate and a World Bank certification in Public Procurement. Prof. Emeje was a national chairman of academic pharmacists in Nigeria and the 2021 winner of the May & Baker Nigeria Plc–sponsored prize for professional service in research and innovation.",institutionString:"National Institute for Pharmaceutical Research and Development",institution:{name:"National Institute for Pharmaceutical Research and Development",country:{name:"Nigeria"}}},{id:"268659",title:"Ms.",name:"Xianquan",middleName:null,surname:"Zhan",slug:"xianquan-zhan",fullName:"Xianquan Zhan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/268659/images/8143_n.jpg",biography:"Dr. Zhan received his undergraduate and graduate training in the fields of preventive medicine and epidemiology and statistics at the West China University of Medical Sciences in China during 1989 to 1999. He received his post-doctoral training in oncology and cancer proteomics for two years at the Cancer Research Institute of Human Medical University in China. In 2001, he went to the University of Tennessee Health Science Center (UTHSC) in USA, where he was a post-doctoral researcher and focused on mass spectrometry and cancer proteomics. Then, he was appointed as an Assistant Professor of Neurology, UTHSC in 2005. He moved to the Cleveland Clinic in USA as a Project Scientist/Staff in 2006 where he focused on the studies of eye disease proteomics and biomarkers. He returned to UTHSC as an Assistant Professor of Neurology in the end of 2007, engaging in proteomics and biomarker studies of lung diseases and brain tumors, and initiating the studies of predictive, preventive, and personalized medicine (PPPM) in cancer. In 2010, he was promoted to Associate Professor of Neurology, UTHSC. Currently, he is a Professor at Xiangya Hospital of Central South University in China, Fellow of Royal Society of Medicine (FRSM), the European EPMA National Representative in China, Regular Member of American Association for the Advancement of Science (AAAS), European Cooperation of Science and Technology (e-COST) grant evaluator, Associate Editors of BMC Genomics, BMC Medical Genomics, EPMA Journal, and Frontiers in Endocrinology, Executive Editor-in-Chief of Med One. He has\npublished 116 peer-reviewed research articles, 16 book chapters, 2 books, and 2 US patents. His current main research interest focuses on the studies of cancer proteomics and biomarkers, and the use of modern omics techniques and systems biology for PPPM in cancer, and on the development and use of 2DE-LC/MS for the large-scale study of human proteoforms.",institutionString:null,institution:{name:"Xiangya Hospital Central South University",country:{name:"China"}}},{id:"40482",title:null,name:"Rizwan",middleName:null,surname:"Ahmad",slug:"rizwan-ahmad",fullName:"Rizwan Ahmad",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/40482/images/system/40482.jpeg",biography:"Dr. Rizwan Ahmad is a University Professor and Coordinator, Quality and Development, College of Medicine, Imam Abdulrahman bin Faisal University, Saudi Arabia. Previously, he was Associate Professor of Human Function, Oman Medical College, Oman, and SBS University, Dehradun. Dr. Ahmad completed his education at Aligarh Muslim University, Aligarh. He has published several articles in peer-reviewed journals, chapters, and edited books. His area of specialization is free radical biochemistry and autoimmune diseases.",institutionString:"Imam Abdulrahman Bin Faisal University",institution:{name:"Imam Abdulrahman Bin Faisal University",country:{name:"Saudi Arabia"}}},{id:"41865",title:"Prof.",name:"Farid A.",middleName:null,surname:"Badria",slug:"farid-a.-badria",fullName:"Farid A. Badria",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/41865/images/system/41865.jpg",biography:"Farid A. Badria, Ph.D., is the recipient of several awards, including The World Academy of Sciences (TWAS) Prize for Public Understanding of Science; the World Intellectual Property Organization (WIPO) Gold Medal for best invention; Outstanding Arab Scholar, Kuwait; and the Khwarizmi International Award, Iran. He has 250 publications, 12 books, 20 patents, and several marketed pharmaceutical products to his credit. He continues to lead research projects on developing new therapies for liver, skin disorders, and cancer. Dr. Badria was listed among the world’s top 2% of scientists in medicinal and biomolecular chemistry in 2019 and 2020. He is a member of the Arab Development Fund, Kuwait; International Cell Research Organization–United Nations Educational, Scientific and Cultural Organization (ICRO–UNESCO), Chile; and UNESCO Biotechnology France",institutionString:"Mansoura University",institution:{name:"Mansoura University",country:{name:"Egypt"}}},{id:"329385",title:"Dr.",name:"Rajesh K.",middleName:"Kumar",surname:"Singh",slug:"rajesh-k.-singh",fullName:"Rajesh K. Singh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/329385/images/system/329385.png",biography:"Dr. Singh received a BPharm (2003) and MPharm (2005) from Panjab University, Chandigarh, India, and a Ph.D. (2013) from Punjab Technical University (PTU), Jalandhar, India. He has more than sixteen years of teaching experience and has supervised numerous postgraduate and Ph.D. students. He has to his credit more than seventy papers in SCI- and SCOPUS-indexed journals, fifty-five conference proceedings, four books, six Best Paper Awards, and five projects from different government agencies. He is currently an editorial board member of eight international journals and a reviewer for more than fifty scientific journals. He received Top Reviewer and Excellent Peer Reviewer Awards from Publons in 2016 and 2017, respectively. He is also on the panel of The International Reviewer for reviewing research proposals for grants from the Royal Society. He also serves as a Publons Academy mentor and Bentham brand ambassador.",institutionString:"Punjab Technical University",institution:{name:"Punjab Technical University",country:{name:"India"}}},{id:"142388",title:"Dr.",name:"Thiago",middleName:"Gomes",surname:"Gomes Heck",slug:"thiago-gomes-heck",fullName:"Thiago Gomes Heck",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/142388/images/7259_n.jpg",biography:null,institutionString:null,institution:{name:"Universidade Regional do Noroeste do Estado do Rio Grande do Sul",country:{name:"Brazil"}}},{id:"336273",title:"Assistant Prof.",name:"Janja",middleName:null,surname:"Zupan",slug:"janja-zupan",fullName:"Janja Zupan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/336273/images/14853_n.jpeg",biography:"Janja Zupan graduated in 2005 at the Department of Clinical Biochemistry (superviser prof. dr. Janja Marc) in the field of genetics of osteoporosis. Since November 2009 she is working as a Teaching Assistant at the Faculty of Pharmacy, Department of Clinical Biochemistry. In 2011 she completed part of her research and PhD work at Institute of Genetics and Molecular Medicine, University of Edinburgh. She finished her PhD entitled The influence of the proinflammatory cytokines on the RANK/RANKL/OPG in bone tissue of osteoporotic and osteoarthritic patients in 2012. From 2014-2016 she worked at the Institute of Biomedical Sciences, University of Aberdeen as a postdoctoral research fellow on UK Arthritis research project where she gained knowledge in mesenchymal stem cells and regenerative medicine. She returned back to University of Ljubljana, Faculty of Pharmacy in 2016. She is currently leading project entitled Mesenchymal stem cells-the keepers of tissue endogenous regenerative capacity facing up to aging of the musculoskeletal system funded by Slovenian Research Agency.",institutionString:null,institution:{name:"University of Ljubljana",country:{name:"Slovenia"}}},{id:"357453",title:"Dr.",name:"Radheshyam",middleName:null,surname:"Maurya",slug:"radheshyam-maurya",fullName:"Radheshyam Maurya",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/357453/images/16535_n.jpg",biography:null,institutionString:null,institution:{name:"University of Hyderabad",country:{name:"India"}}},{id:"418340",title:"Dr.",name:"Jyotirmoi",middleName:null,surname:"Aich",slug:"jyotirmoi-aich",fullName:"Jyotirmoi Aich",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000038Ugi5QAC/Profile_Picture_2022-04-15T07:48:28.png",biography:"Biotechnologist with 15 years of research including 6 years of teaching experience. Demonstrated record of scientific achievements through consistent publication record (H index = 13, with 874 citations) in high impact journals such as Nature Communications, Oncotarget, Annals of Oncology, PNAS, and AJRCCM, etc. Strong research professional with a post-doctorate from ACTREC where I gained experimental oncology experience in clinical settings and a doctorate from IGIB where I gained expertise in asthma pathophysiology. A well-trained biotechnologist with diverse experience on the bench across different research themes ranging from asthma to cancer and other infectious diseases. An individual with a strong commitment and innovative mindset. Have the ability to work on diverse projects such as regenerative and molecular medicine with an overall mindset of improving healthcare.",institutionString:"DY Patil Deemed to Be University",institution:null},{id:"349288",title:"Prof.",name:"Soumya",middleName:null,surname:"Basu",slug:"soumya-basu",fullName:"Soumya Basu",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000035QxIDQA0/Profile_Picture_2022-04-15T07:47:01.jpg",biography:"Soumya Basu, Ph.D., is currently working as an Associate Professor at Dr. D. Y. Patil Biotechnology and Bioinformatics Institute, Dr. D. Y. Patil Vidyapeeth, Pune, Maharashtra, India. With 16+ years of trans-disciplinary research experience in Drug Design, development, and pre-clinical validation; 20+ research article publications in journals of repute, 9+ years of teaching experience, trained with cross-disciplinary education, Dr. Basu is a life-long learner and always thrives for new challenges.\r\nHer research area is the design and synthesis of small molecule partial agonists of PPAR-γ in lung cancer. She is also using artificial intelligence and deep learning methods to understand the exosomal miRNA’s role in cancer metastasis. Dr. Basu is the recipient of many awards including the Early Career Research Award from the Department of Science and Technology, Govt. of India. She is a reviewer of many journals like Molecular Biology Reports, Frontiers in Oncology, RSC Advances, PLOS ONE, Journal of Biomolecular Structure & Dynamics, Journal of Molecular Graphics and Modelling, etc. She has edited and authored/co-authored 21 journal papers, 3 book chapters, and 15 abstracts. She is a Board of Studies member at her university. She is a life member of 'The Cytometry Society”-in India and 'All India Cell Biology Society”- in India.",institutionString:"Dr. D.Y. Patil Vidyapeeth, Pune",institution:{name:"Dr. D.Y. Patil Vidyapeeth, Pune",country:{name:"India"}}},{id:"354817",title:"Dr.",name:"Anubhab",middleName:null,surname:"Mukherjee",slug:"anubhab-mukherjee",fullName:"Anubhab Mukherjee",position:null,profilePictureURL:"https://intech-files.s3.amazonaws.com/0033Y0000365PbRQAU/ProfilePicture%202022-04-15%2005%3A11%3A18.480",biography:"A former member of Laboratory of Nanomedicine, Brigham and Women’s Hospital, Harvard University, Boston, USA, Dr. Anubhab Mukherjee is an ardent votary of science who strives to make an impact in the lives of those afflicted with cancer and other chronic/acute ailments. He completed his Ph.D. from CSIR-Indian Institute of Chemical Technology, Hyderabad, India, having been skilled with RNAi, liposomal drug delivery, preclinical cell and animal studies. He pursued post-doctoral research at College of Pharmacy, Health Science Center, Texas A & M University and was involved in another postdoctoral research at Department of Translational Neurosciences and Neurotherapeutics, John Wayne Cancer Institute, Santa Monica, California. In 2015, he worked in Harvard-MIT Health Sciences & Technology as a visiting scientist. He has substantial experience in nanotechnology-based formulation development and successfully served various Indian organizations to develop pharmaceuticals and nutraceutical products. He is an inventor in many US patents and an author in many peer-reviewed articles, book chapters and books published in various media of international repute. Dr. Mukherjee is currently serving as Principal Scientist, R&D at Esperer Onco Nutrition (EON) Pvt. Ltd. and heads the Hyderabad R&D center of the organization.",institutionString:"Esperer Onco Nutrition Pvt Ltd.",institution:null},{id:"319365",title:"Assistant Prof.",name:"Manash K.",middleName:null,surname:"Paul",slug:"manash-k.-paul",fullName:"Manash K. Paul",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/319365/images/system/319365.png",biography:"Manash K. Paul is a Principal Investigator and Scientist at the University of California Los Angeles. He has contributed significantly to the fields of stem cell biology, regenerative medicine, and lung cancer. His research focuses on various signaling processes involved in maintaining stem cell homeostasis during the injury-repair process, deciphering lung stem cell niche, pulmonary disease modeling, immuno-oncology, and drug discovery. He is currently investigating the role of extracellular vesicles in premalignant lung cell migration and detecting the metastatic phenotype of lung cancer via machine-learning-based analyses of exosomal signatures. Dr. Paul has published in more than fifty peer-reviewed international journals and is highly cited. He is the recipient of many awards, including the UCLA Vice Chancellor’s award, a senior member of the Institute of Electrical and Electronics Engineers (IEEE), and an editorial board member for several international journals.",institutionString:"University of California Los Angeles",institution:{name:"University of California Los Angeles",country:{name:"United States of America"}}},{id:"311457",title:"Dr.",name:"Júlia",middleName:null,surname:"Scherer Santos",slug:"julia-scherer-santos",fullName:"Júlia Scherer Santos",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/311457/images/system/311457.jpg",biography:"Dr. Júlia Scherer Santos works in the areas of cosmetology, nanotechnology, pharmaceutical technology, beauty, and aesthetics. Dr. Santos also has experience as a professor of graduate courses. Graduated in Pharmacy, specialization in Cosmetology and Cosmeceuticals applied to aesthetics, specialization in Aesthetic and Cosmetic Health, and a doctorate in Pharmaceutical Nanotechnology. Teaching experience in Pharmacy and Aesthetics and Cosmetics courses. She works mainly on the following subjects: nanotechnology, cosmetology, pharmaceutical technology, aesthetics.",institutionString:"Universidade Federal de Juiz de Fora",institution:{name:"Universidade Federal de Juiz de Fora",country:{name:"Brazil"}}},{id:"219081",title:"Dr.",name:"Abdulsamed",middleName:null,surname:"Kükürt",slug:"abdulsamed-kukurt",fullName:"Abdulsamed Kükürt",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/219081/images/system/219081.png",biography:"Dr. Kükürt graduated from Uludağ University in Turkey. He started his academic career as a Research Assistant in the Department of Biochemistry at Kafkas University. In 2019, he completed his Ph.D. program in the Department of Biochemistry at the Institute of Health Sciences. He is currently working at the Department of Biochemistry, Kafkas University. He has 27 published research articles in academic journals, 11 book chapters, and 37 papers. He took part in 10 academic projects. He served as a reviewer for many articles. He still serves as a member of the review board in many academic journals. He is currently working on the protective activity of phenolic compounds in disorders associated with oxidative stress and inflammation.",institutionString:null,institution:{name:"Kafkas University",country:{name:"Turkey"}}},{id:"178366",title:"Dr.",name:"Volkan",middleName:null,surname:"Gelen",slug:"volkan-gelen",fullName:"Volkan Gelen",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/178366/images/system/178366.jpg",biography:"Volkan Gelen is a Physiology specialist who received his veterinary degree from Kafkas University in 2011. Between 2011-2015, he worked as an assistant at Atatürk University, Faculty of Veterinary Medicine, Department of Physiology. In 2016, he joined Kafkas University, Faculty of Veterinary Medicine, Department of Physiology as an assistant professor. Dr. Gelen has been engaged in various academic activities at Kafkas University since 2016. There he completed 5 projects and has 3 ongoing projects. He has 60 articles published in scientific journals and 20 poster presentations in scientific congresses. His research interests include physiology, endocrine system, cancer, diabetes, cardiovascular system diseases, and isolated organ bath system studies.",institutionString:"Kafkas University",institution:{name:"Kafkas University",country:{name:"Turkey"}}},{id:"418963",title:"Dr.",name:"Augustine Ododo",middleName:"Augustine",surname:"Osagie",slug:"augustine-ododo-osagie",fullName:"Augustine Ododo Osagie",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/418963/images/16900_n.jpg",biography:"Born into the family of Osagie, a prince of the Benin Kingdom. I am currently an academic in the Department of Medical Biochemistry, University of Benin. Part of the duties are to teach undergraduate students and conduct academic research.",institutionString:null,institution:{name:"University of Benin",country:{name:"Nigeria"}}},{id:"192992",title:"Prof.",name:"Shagufta",middleName:null,surname:"Perveen",slug:"shagufta-perveen",fullName:"Shagufta Perveen",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/192992/images/system/192992.png",biography:"Prof. Shagufta Perveen is a Distinguish Professor in the Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia. Dr. Perveen has acted as the principal investigator of major research projects funded by the research unit of King Saud University. She has more than ninety original research papers in peer-reviewed journals of international repute to her credit. She is a fellow member of the Royal Society of Chemistry UK and the American Chemical Society of the United States.",institutionString:"King Saud University",institution:{name:"King Saud University",country:{name:"Saudi Arabia"}}},{id:"49848",title:"Dr.",name:"Wen-Long",middleName:null,surname:"Hu",slug:"wen-long-hu",fullName:"Wen-Long Hu",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/49848/images/system/49848.jpg",biography:"Wen-Long Hu is Chief of the Division of Acupuncture, Department of Chinese Medicine at Kaohsiung Chang Gung Memorial Hospital, as well as an adjunct associate professor at Fooyin University and Kaohsiung Medical University. Wen-Long is President of Taiwan Traditional Chinese Medicine Medical Association. He has 28 years of experience in clinical practice in laser acupuncture therapy and 34 years in acupuncture. He is an invited speaker for lectures and workshops in laser acupuncture at many symposiums held by medical associations. He owns the patent for herbal preparation and producing, and for the supercritical fluid-treated needle. Dr. Hu has published three books, 12 book chapters, and more than 30 papers in reputed journals, besides serving as an editorial board member of repute.",institutionString:"Kaohsiung Chang Gung Memorial Hospital",institution:{name:"Kaohsiung Chang Gung Memorial Hospital",country:{name:"Taiwan"}}},{id:"298472",title:"Prof.",name:"Andrey V.",middleName:null,surname:"Grechko",slug:"andrey-v.-grechko",fullName:"Andrey V. Grechko",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/298472/images/system/298472.png",biography:"Andrey Vyacheslavovich Grechko, Ph.D., Professor, is a Corresponding Member of the Russian Academy of Sciences. He graduated from the Semashko Moscow Medical Institute (Semashko National Research Institute of Public Health) with a degree in Medicine (1998), the Clinical Department of Dermatovenerology (2000), and received a second higher education in Psychology (2009). Professor A.V. Grechko held the position of Сhief Physician of the Central Clinical Hospital in Moscow. He worked as a professor at the faculty and was engaged in scientific research at the Medical University. Starting in 2013, he has been the initiator of the creation of the Federal Scientific and Clinical Center for Intensive Care and Rehabilitology, Moscow, Russian Federation, where he also serves as Director since 2015. He has many years of experience in research and teaching in various fields of medicine, is an author/co-author of more than 200 scientific publications, 13 patents, 15 medical books/chapters, including Chapter in Book «Metabolomics», IntechOpen, 2020 «Metabolomic Discovery of Microbiota Dysfunction as the Cause of Pathology».",institutionString:"Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology",institution:null},{id:"199461",title:"Prof.",name:"Natalia V.",middleName:null,surname:"Beloborodova",slug:"natalia-v.-beloborodova",fullName:"Natalia V. Beloborodova",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/199461/images/system/199461.jpg",biography:'Natalia Vladimirovna Beloborodova was educated at the Pirogov Russian National Research Medical University, with a degree in pediatrics in 1980, a Ph.D. in 1987, and a specialization in Clinical Microbiology from First Moscow State Medical University in 2004. She has been a Professor since 1996. Currently, she is the Head of the Laboratory of Metabolism, a division of the Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow, Russian Federation. N.V. Beloborodova has many years of clinical experience in the field of intensive care and surgery. She studies infectious complications and sepsis. She initiated a series of interdisciplinary clinical and experimental studies based on the concept of integrating human metabolism and its microbiota. Her scientific achievements are widely known: she is the recipient of the Marie E. Coates Award \\"Best lecturer-scientist\\" Gustafsson Fund, Karolinska Institutes, Stockholm, Sweden, and the International Sepsis Forum Award, Pasteur Institute, Paris, France (2014), etc. Professor N.V. Beloborodova wrote 210 papers, five books, 10 chapters and has edited four books.',institutionString:"Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology",institution:null},{id:"354260",title:"Ph.D.",name:"Tércio Elyan",middleName:"Azevedo",surname:"Azevedo Martins",slug:"tercio-elyan-azevedo-martins",fullName:"Tércio Elyan Azevedo Martins",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/354260/images/16241_n.jpg",biography:"Graduated in Pharmacy from the Federal University of Ceará with the modality in Industrial Pharmacy, Specialist in Production and Control of Medicines from the University of São Paulo (USP), Master in Pharmaceuticals and Medicines from the University of São Paulo (USP) and Doctor of Science in the program of Pharmaceuticals and Medicines by the University of São Paulo. Professor at Universidade Paulista (UNIP) in the areas of chemistry, cosmetology and trichology. Assistant Coordinator of the Higher Course in Aesthetic and Cosmetic Technology at Universidade Paulista Campus Chácara Santo Antônio. Experience in the Pharmacy area, with emphasis on Pharmacotechnics, Pharmaceutical Technology, Research and Development of Cosmetics, acting mainly on topics such as cosmetology, antioxidant activity, aesthetics, photoprotection, cyclodextrin and thermal analysis.",institutionString:null,institution:{name:"University of Sao Paulo",country:{name:"Brazil"}}},{id:"334285",title:"Ph.D. Student",name:"Sameer",middleName:"Kumar",surname:"Jagirdar",slug:"sameer-jagirdar",fullName:"Sameer Jagirdar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/334285/images/14691_n.jpg",biography:"I\\'m a graduate student at the center for biosystems science and engineering at the Indian Institute of Science, Bangalore, India. I am interested in studying host-pathogen interactions at the biomaterial interface.",institutionString:null,institution:{name:"Indian Institute of Science Bangalore",country:{name:"India"}}},{id:"329248",title:"Dr.",name:"Md. Faheem",middleName:null,surname:"Haider",slug:"md.-faheem-haider",fullName:"Md. Faheem Haider",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/329248/images/system/329248.jpg",biography:"Dr. Md. Faheem Haider completed his BPharm in 2012 at Integral University, Lucknow, India. In 2014, he completed his MPharm with specialization in Pharmaceutics at Babasaheb Bhimrao Ambedkar University, Lucknow, India. He received his Ph.D. degree from Jamia Hamdard University, New Delhi, India, in 2018. He was selected for the GPAT six times and his best All India Rank was 34. Currently, he is an assistant professor at Integral University. Previously he was an assistant professor at IIMT University, Meerut, India. He has experience teaching DPharm, Pharm.D, BPharm, and MPharm students. He has more than five publications in reputed journals to his credit. Dr. Faheem’s research area is the development and characterization of nanoformulation for the delivery of drugs to various organs.",institutionString:"Integral University",institution:{name:"Integral University",country:{name:"India"}}},{id:"329795",title:"Dr.",name:"Mohd Aftab",middleName:"Aftab",surname:"Siddiqui",slug:"mohd-aftab-siddiqui",fullName:"Mohd Aftab Siddiqui",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/329795/images/system/329795.png",biography:"Dr. Mohd Aftab Siddiqui is an assistant professor in the Faculty of Pharmacy, Integral University, Lucknow, India, where he obtained a Ph.D. in Pharmacology in 2020. He also obtained a BPharm and MPharm from the same university in 2013 and 2015, respectively. His area of research is the pharmacological screening of herbal drugs/natural products in liver cancer and cardiac diseases. He is a member of many professional bodies and has guided many MPharm and PharmD research projects. Dr. Siddiqui has many national and international publications and one German patent to his credit.",institutionString:"Integral University",institution:null},{id:"255360",title:"Dr.",name:"Usama",middleName:null,surname:"Ahmad",slug:"usama-ahmad",fullName:"Usama Ahmad",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/255360/images/system/255360.png",biography:"Dr. Usama Ahmad holds a specialization in Pharmaceutics from Amity University, Lucknow, India. He received his Ph.D. from Integral University, Lucknow, India, with his work titled ‘Development and evaluation of silymarin nanoformulation for hepatic carcinoma’. Currently, he is an Assistant Professor of Pharmaceutics, at the Faculty of Pharmacy, Integral University. He has been teaching PharmD, BPharm, and MPharm students and conducting research in the novel drug delivery domain. From 2013 to 2014 he worked on a research project funded by SERB-DST, Government of India. He has a rich publication record with more than twenty-four original journal articles, two edited books, four book chapters, and several scientific articles to his credit. He is a member of the American Association for Cancer Research, the International Association for the Study of Lung Cancer, and the British Society for Nanomedicine. Dr. Ahmad’s research focus is on the development of nanoformulations to facilitate the delivery of drugs.",institutionString:"Integral University",institution:{name:"Integral University",country:{name:"India"}}},{id:"333824",title:"Dr.",name:"Ahmad Farouk",middleName:null,surname:"Musa",slug:"ahmad-farouk-musa",fullName:"Ahmad Farouk Musa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/333824/images/22684_n.jpg",biography:"Dato’ Dr Ahmad Farouk Musa\nMD, MMED (Surgery) (Mal), Fellowship in Cardiothoracic Surgery (Monash Health, Aust), Graduate Certificate in Higher Education (Aust), Academy of Medicine (Mal)\n\n\n\nDato’ Dr Ahmad Farouk Musa obtained his Doctor of Medicine from USM in 1992. He then obtained his Master of Medicine in Surgery from the same university in the year 2000 before subspecialising in Cardiothoracic Surgery at Institut Jantung Negara (IJN), Kuala Lumpur from 2002 until 2005. He then completed his Fellowship in Cardiothoracic Surgery at Monash Health, Melbourne, Australia in 2008. He has served in the Malaysian army as a Medical Officer with the rank of Captain upon completing his Internship before joining USM as a trainee lecturer. He is now serving as an academic and researcher at Monash University Malaysia. He is a life-member of the Malaysian Association of Thoracic & Cardiovascular Surgery (MATCVS) and a committee member of the MATCVS Database. He is also a life-member of the College of Surgeons, Academy of Medicine of Malaysia; a life-member of Malaysian Medical Association (MMA), and a life-member of Islamic Medical Association of Malaysia (IMAM). Recently he was appointed as an Interim Chairperson of Examination & Assessment Subcommittee of the UiTM-IJN Cardiothoracic Surgery Postgraduate Program. As an academic, he has published numerous research papers and book chapters. He has also been appointed to review many scientific manuscripts by established journals such as the British Medical Journal (BMJ). He has presented his research works at numerous local and international conferences such as the European Association for Cardiothoracic Surgery (EACTS) and the European Society of Cardiovascular Surgery (ESCVS), to name a few. He has also won many awards for his research presentations at meetings and conferences like the prestigious International Invention, Innovation & Technology Exhibition (ITEX); Design, Research and Innovation Exhibition, the National Conference on Medical Sciences and the Annual Scientific Meetings of the Malaysian Association for Thoracic and Cardiovascular Surgery. He was awarded the Darjah Setia Pangkuan Negeri (DSPN) by the Governor of Penang in July, 2015.",institutionString:null,institution:{name:"Monash University Malaysia",country:{name:"Malaysia"}}},{id:"30568",title:"Prof.",name:"Madhu",middleName:null,surname:"Khullar",slug:"madhu-khullar",fullName:"Madhu Khullar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/30568/images/system/30568.jpg",biography:"Dr. Madhu Khullar is a Professor of Experimental Medicine and Biotechnology at the Post Graduate Institute of Medical Education and Research, Chandigarh, India. She completed her Post Doctorate in hypertension research at the Henry Ford Hospital, Detroit, USA in 1985. She is an editor and reviewer of several international journals, and a fellow and member of several cardiovascular research societies. Dr. Khullar has a keen research interest in genetics of hypertension, and is currently studying pharmacogenetics of hypertension.",institutionString:"Post Graduate Institute of Medical Education and Research",institution:{name:"Post Graduate Institute of Medical Education and Research",country:{name:"India"}}},{id:"223233",title:"Prof.",name:"Xianquan",middleName:null,surname:"Zhan",slug:"xianquan-zhan",fullName:"Xianquan Zhan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/223233/images/system/223233.png",biography:"Xianquan Zhan received his MD and Ph.D. in Preventive Medicine at West China University of Medical Sciences. He received his post-doctoral training in oncology and cancer proteomics at the Central South University, China, and the University of Tennessee Health Science Center (UTHSC), USA. He worked at UTHSC and the Cleveland Clinic in 2001–2012 and achieved the rank of associate professor at UTHSC. Currently, he is a full professor at Central South University and Shandong First Medical University, and an advisor to MS/PhD students and postdoctoral fellows. He is also a fellow of the Royal Society of Medicine and European Association for Predictive Preventive Personalized Medicine (EPMA), a national representative of EPMA, and a member of the American Society of Clinical Oncology (ASCO) and the American Association for the Advancement of Sciences (AAAS). He is also the editor in chief of International Journal of Chronic Diseases & Therapy, an associate editor of EPMA Journal, Frontiers in Endocrinology, and BMC Medical Genomics, and a guest editor of Mass Spectrometry Reviews, Frontiers in Endocrinology, EPMA Journal, and Oxidative Medicine and Cellular Longevity. He has published more than 148 articles, 28 book chapters, 6 books, and 2 US patents in the field of clinical proteomics and biomarkers.",institutionString:"Shandong First Medical University",institution:{name:"Affiliated Hospital of Shandong Academy of Medical Sciences",country:{name:"China"}}}]}},subseries:{item:{id:"10",type:"subseries",title:"Animal Physiology",keywords:"Physiology, Comparative, Evolution, Biomolecules, Organ, Homeostasis, Anatomy, Pathology, Medical, Cell Division, Cell Signaling, Cell Growth, Cell Metabolism, Endocrine, Neuroscience, Cardiovascular, Development, Aging, Development",scope:"Physiology, the scientific study of functions and mechanisms of living systems, is an essential area of research in its own right, but also in relation to medicine and health sciences. The scope of this topic will range from molecular, biochemical, cellular, and physiological processes in all animal species. Work pertaining to the whole organism, organ systems, individual organs and tissues, cells, and biomolecules will be included. Medical, animal, cell, and comparative physiology and allied fields such as anatomy, histology, and pathology with physiology links will be covered in this topic. Physiology research may be linked to development, aging, environment, regular and pathological processes, adaptation and evolution, exercise, or several other factors affecting, or involved with, animal physiology.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/10.jpg",hasOnlineFirst:!1,hasPublishedBooks:!1,annualVolume:11406,editor:{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. 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