EEC models used to describe the electrochemical processes most studied by
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",isbn:"978-1-80356-273-5",printIsbn:"978-1-80356-272-8",pdfIsbn:"978-1-80356-274-2",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!1,isSalesforceBook:!1,isNomenclature:!1,hash:"e1d9662c334dd78ab35bfb57c3bf106e",bookSignature:"Dr. Fabio Arturo Iannotti",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/11675.jpg",keywords:"Skeletal Muscle Diseases, Rare Skeletal Muscle Diseases, Basic Research, Molecular Mechanisms of Disease, Translational Research, Diagnostic Technologies, Functional Tests, Disease Models, Innovative Therapies, Drug Repositioning, Drug Discovery, Emerging Technologies",numberOfDownloads:24,numberOfWosCitations:0,numberOfCrossrefCitations:0,numberOfDimensionsCitations:0,numberOfTotalCitations:0,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"February 11th 2022",dateEndSecondStepPublish:"April 19th 2022",dateEndThirdStepPublish:"June 18th 2022",dateEndFourthStepPublish:"September 6th 2022",dateEndFifthStepPublish:"November 5th 2022",dateConfirmationOfParticipation:null,remainingDaysToSecondStep:"2 months",secondStepPassed:!0,areRegistrationsClosed:!0,currentStepOfPublishingProcess:4,editedByType:null,kuFlag:!1,biosketch:"Dr. Fabio Arturo Iannotti received his Bachelor's Degree in Biotechnology Science at the University of Naples “Federico II” in 2006 with the highest degree. In 2010, he graduated with a Ph.D. in Neuroscience at the University of Naples “Federico II”. He published many papers on his areas of research in international peer-reviewed journals and for his pioneering studies has received awards from both national and international scientific societies.",coeditorOneBiosketch:null,coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"281317",title:"Dr.",name:"Fabio",middleName:"Arturo",surname:"Iannotti",slug:"fabio-iannotti",fullName:"Fabio Iannotti",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRdOdQAK/Profile_Picture_1644820016099",biography:"Currently researcher at the CNR-ICB Institute of Biomolecular Chemistry of Pozzuoli, Napoli (Italy), Fabio Arturo Iannotti has as major focus of his research activity the role of the endocannabinoid system and TRP in epilepsy and muscle development. Dr. Fabio Arturo Iannotti received his Bachelor Degree in Biotecnology Science (Medical curricula) at University of Naples \\'Federico II\\' in 2006 (with 110/110 cum laude). In 2010, Dr. Iannotti graduated with a PhD in Neuroscience at University of Naples \\'Federico II\\'. The focus of his thesis was on the role of voltage-gated potassium channels Kv7 during the neuronal excitoxicity as well as skeletal muscle cell differentiation. During the three years of the PhD program, Dr. Iannotti has been introduced to the field of ion channels, particularly voltage-gated ion channels; he has been instrumental in setting up RT-PCR and quantitative RT-PCR techniques in our lab, focusing onto research themes which would allow to combine both molecular and functional approaches in the study of ion channels during muscle cell differentiation. He has become familiar with most molecular biology (cloning, mutagenesis, PCR and RT-PCR, Southern and Northern blotting, gene silencing via RNAi, …) as well as with protein biochemistry techniques (protein extraction, immunoprecipitation, Western blotting, in-vitro translation, …) and morphological methods (confocal and conventional immunofluorescence). He is also familiar with imaging tools for intracellular ion concentration analysis, and has more recently gained considerable experience with electrophysiological techniques (specifically, patch-clamp). During this time (2009-2010), he also researched at the University of California-Davis assessing changes to the phosphorylation state of potassium channels in in vivo models of epilepsy. In 2011, he started his postdoc at the Institute of Biomolecular Chemistry (ICB)/ National Council of Research (CNR) and during this period he also visited the University of Reading (2012-2013), researching the potential involvement of TRP channels in epilepsy and muscle development. Since 2014, he was promoted to the position of research fellow at ICB. To date, Dr. Iannotti has published many papers on these areas of research in international peer reviewed journals, and has received awards from both national and international scientific societies for his work. He is member of international scientific societies and referee for international peer reviewed journal with high impact factor.",institutionString:"Institute of Biomolecular Chemistry (ICB)",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"1",totalChapterViews:"0",totalEditedBooks:"0",institution:null}],coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"16",title:"Medicine",slug:"medicine"}],chapters:[{id:"81290",title:"Musculoskeletal Abnormalities Caused by Cystic Fibrosis",slug:"musculoskeletal-abnormalities-caused-by-cystic-fibrosis",totalDownloads:24,totalCrossrefCites:0,authors:[null]}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},personalPublishingAssistant:{id:"278926",firstName:"Ivana",lastName:"Barac",middleName:null,title:"Ms.",imageUrl:"https://mts.intechopen.com/storage/users/278926/images/8058_n.jpg",email:"ivana.b@intechopen.com",biography:"As an Author Service Manager my responsibilities include monitoring and facilitating all publishing activities for authors and editors. From chapter submission and review, to approval and revision, copyediting and design, until final publication, I work closely with authors and editors to ensure a simple and easy publishing process. I maintain constant and effective communication with authors, editors and reviewers, which allows for a level of personal support that enables contributors to fully commit and concentrate on the chapters they are writing, editing, or reviewing. I assist authors in the preparation of their full chapter submissions and track important deadlines and ensure they are met. I help to coordinate internal processes such as linguistic review, and monitor the technical aspects of the process. As an ASM I am also involved in the acquisition of editors. Whether that be identifying an exceptional author and proposing an editorship collaboration, or contacting researchers who would like the opportunity to work with IntechOpen, I establish and help manage author and editor acquisition and contact."}},relatedBooks:[{type:"book",id:"6550",title:"Cohort Studies in Health Sciences",subtitle:null,isOpenForSubmission:!1,hash:"01df5aba4fff1a84b37a2fdafa809660",slug:"cohort-studies-in-health-sciences",bookSignature:"R. Mauricio Barría",coverURL:"https://cdn.intechopen.com/books/images_new/6550.jpg",editedByType:"Edited by",editors:[{id:"88861",title:"Dr.",name:"R. Mauricio",surname:"Barría",slug:"r.-mauricio-barria",fullName:"R. 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The construction industry is an example in where steel is essential, which requires durable and strong structures for the build of bridges, tunnels, towers, buildings, airports, roads, plants and railways. Many of these constructions are usually outdoors, exposed to the atmosphere conditions, additionally, the surrounding environment where these steels are placed for their service is often highly polluted, that it often degrades the steel structure at a considerable corrosion rate. Some of those steels are also design to be used in the; mining industry, pipeline transport of fluids, shipbuilding, agriculture equipment and heavy machinery, among others. During their usage, steels are also severely damaged by one type of corrosion mechanism [1, 2, 3, 4]. According to Zaki Ahmad [5] the concept of corrosion must be defined taking into account the environment in which the metal-materials are place to serve for long periods of exposure time, thus, all the environments are considered corrosive to some degree of damage as follows; i) air humidity, ii) fresh, distilled, salt and marine water, iii) natural urban, marine and industrial atmospheres, iv) steam and gases, v) ammonia and hydrogen sulfide, vi) sulfur dioxide and oxides of nitrogen, vii) fuel gases, acids, alkalis and soils.
Therefore, the concept of corrosion in steels is then define as a natural electrochemical process that destroys the integrity of the metal structure in the presence of any environment containing moisture and oxygen. This process involves two electrode reactions that can occur in a spontaneously way at the interface between the metal and the aqueous environment according to the thermodynamic’s Law; One, is the reaction of metal-base with chemical species from the environment (
Physical and chemical model that represents the concrete failure by corrosion on the steel reinforcement [
In other conditions, a thin oxide film can grow on metal-base to provide the protection against corrosion attack, that steels require in order to be useful when they are exposed to severe atmospheric conditions during their usage. This passive film is so thin that it is invisible to the naked eye; however, this film can be self-repaired immediately, when it is suddenly scratched or intentionally removed. An example of this outstanding property is the existence of several types of stainless steels that usually contains a significant proportion of chromium (12 to 25 wt.% Cr) with nickel and molybdenum to prevent the formation of ferrous hydroxide
For conventional steels produced by casting process, the most useful steel products are those that contain small amounts of alloying elements such as plain carbon steels (Mn, Si, S, P), alloyed steels (Cu, Ni, Cr or Al) and tool or machinery steels (W, Mo, Co, B and V). This alloying provides mechanical strength, ductility, machinability, and a substantial corrosion resistance. Although, these steels do not have the same ability of corrosion protection as the stainless steel does; the oxide film formed on the surface has only a few micrometers thick with microporous or growth defects, so it is possible to inferred that this oxide layer does not protect the metal from corrosion attack, this means a temporally low passivity is considered. However, in aggressive aqueous solutions the porous oxide layer can dissolve or break-down at least some areas of the film, therefore, leading to the Fe-base to a further localized attack. In industrial applications, the surface properties of the steel have a significant impact on their service life and performance. Among the several surface treatments to provide protection through a thick hard layer, diffusion techniques are using such as powder pack, gaseous atmosphere, plasma, ion beam and salt baths, that depends on the diffusion time and atmosphere concentration, these being a high effective treatment and less expensive. Additionally, carburizing, nitriding or boriding, are also well-known as thermochemical surface treatments [11, 12, 13, 14, 15].
Acid solutions are frequently used in many applications concerning industrial processes and are considered as the most corrosive media for steels. Acids like HCl, H2SO4, HNO3, H3PO4, H2CrO3, and some alkalis such NH3 are frequently used for surface cleaning, removal of rust deposits, pickling processes, chemical attack, metal surface treatments, and wastewater systems. Other relevant uses are metal-processing equipment, chemical processing, pipelines, food processing, chemical and petrochemical plants. Therefore, printed research works report several cases of using organic molecules compounds (imidazole, 2mercapto-benzimidazole, pyridine, thidiazole, pyrrolidine, triazole, among others) that have provided a significant corrosion inhibition property for steels during their exposure to acid media [16, 17, 18, 19, 20, 21, 22, 23, 24]. These molecules must contain in their structure functional electronegative groups, π electrons, heteroatoms or heteroatoms of nitrogen, sulfur and oxygen with aromatic and heterocyclic rings. These reports generally indicate that the molecules are dissolved in an ethanol-water solution and then added in small concentrations (ppm) to the acid media, in all the cases, a barrier layer of organic molecules is formed onto the metal surface by an adsorption mechanism, thus giving corrosion protection on steels under-service at aggressive conditions [16, 18, 20, 24].
According to Florian B. Mansfeld (1988) in his research
The practical estimation of
Cases of
Steels measured in their received condition.
Kinetic oxidation reaction at different aqueous solutions.
Steel corroded at non-stationary condition.
Corrosion monitor in concrete reinforced materials.
Inhibition using organic molecules.
Inhibition in natural liquids extracted from plants.
Hard-coatings as protection.
Corrosion monitor in steels used as food containers or beverages.
Since the middle of the 18th century, the Impedance Spectroscopy (IS) technique has been established as a popular theoretical approach to study the electrical properties of conducting materials and their interfaces. However, in the last quarter-century, IS becomes a practical tool that is successfully applied in electrochemistry as an analytical method widely used in many disciplines such as materials science, corrosion technology, semiconductors, conducting polymers, ceramics, coatings, energy storage, and solid-state. Electrochemical Impedance Spectroscopy (EIS) is considered as a new technique with astounding advantages [36, 37, 38].
The concept of impedance in electronic devices is generally treated as a purely complex phenomenological amount and is considered as one of the most important physical characteristics that concerns the resistance that the medium opposes to the propagation of sound (acoustic impedance,
Another quality of
Schematic simulation of the electrochemical interface metal/electrolyte (electrical double layer) and its representative equivalent electrical circuit
Electrochemical impedance spectroscopy (EIS) is the analytical method widely used to study the electrochemical systems by applying a small
where
Sinusoidal waveform response in linear system showing phase-shift angle that is used to describe the electrochemical reactions at the interfaces [
where
in order to preserve the linear behavior in electrochemical systems, a small amplitude of
taking into account the electrical parameters of
then, impedance (
Vector representation of impedance as complex number;
considering the relationship between the potential and current amplitude, it results the total of the impedance as a complex number, as it follows;
however, the use of the current as a perturbation signal is also designed for certain electrochemical applications. Once the experimental data are collected, a series of potential-time and current-time are obtained, which correspond to the impedance at each frequency studied. The representation of the
Experimentally speaking, when an
Representation of a corrosion cell and its equivalent electrical circuit (
As mention above,
EEC models used to describe the electrochemical processes most studied by
Impedance and phase shift angle response for the passive
A single
On the other hand, when two passive components are combined in a
Impedance data simulation of a simplest EEC model; a)
Two-time constants could be expected in Figure 7a (circuit #2 is the combination of parallel
Impedance data simulation of
Where
Other types of impedance spectra commonly observed in the printed research works, are similar to that reproduced with the simulation using circuit #5 or #6. Circuit #5 is the similar arrangement of circuit #3, in which the ideal capacitor
Impedance data simulation of
In real cases the shape of Nyquist plot does not always show a perfect semicircle as it is observed for pure capacitor, it is necessary to replace capacitor (
In Figure 9 is shown the configuration of
The validation of the parameters obtained through an analogous
Causality. The response of the system is due only to the perturbation applied and does not contain significant components from spurious sources.
Linearity. The perturbation and response of the system are linearly related
Stability. The system must be stable in the sense that it returns to its original state after the perturbation is removed.
The impedance must be finite-valued at
It has been shown that when a corroding system obeys the just mentioned four criteria the impedance data will converse correctly. However, the inverse is not always true. It is still possible to have a correct
One of the principal applications of
Typical impedance spectra showing the effects of the amplitude signal in; a)
The results show that when an alternate electrical pulse
AC amplitude signal dependence on capacitance value for an ideal
The same behavior is observed for stainless steel SS316 plate immersed in HCl 1 M (Figure 10b), the metal interface exposed to the acid solution allows the electron transfer rate at the equilibrium potential (Ecorr) after applying lower amplitudes of the stimulus signal (between 1 to 20 mV), the impedance diagrams for this conditions do not show changes caused by the current flows into the system. In this sense the metal interface working similar as the ideal capacitor allowing ions loading charging such as Cl− and OH− with capacitances ranging between 40 to 80 μF/cm2, which is indicated by a well-defined one time constant due to the presence of a protective oxide layer (passive condition) and can be easily represented by the
Figure 12 shows the typical impedance behavior of a steel with specification of AISI 8620 (0.20 wt.%C, 0.90 wt.%Mn, 0.35 wt.%Si, 0.60 wt.%Cr, 0.70 wt.%Ni, 0.25 wt.%Mo) in its received condition after exposed to different aqueous solutions such as distilled water, NaCl 0.5 M, HCl 1 M, H2SO4 1 M. The supplied voltage signal has an amplitude of 10 mV that fluctuating around the corrosion potential (−654 mV) in the frequency range of 1 MHz to 1 mHz, the response obtained is represented in Bode diagrams in which the impedance module and the phase angle serve as functions of the Log frequency, these diagrams indicate the sensitivity of the
Bode plots of impedance response of corroding 8620 plate at different aqueous solutions; distilled water, NaCl at 0.5 N, HCl at 1 M and H2SO4 at 1 M.
On the other hand, when the pH of the aqueous solution decreases to an acidified stage by the presence of ions such as Na+, Cl−, OH−, SO4−, H+, the shape of the impedance diagrams has been change, for example, for NaCl solution, a slightly acidified substance breaks-out almost the integrity of the natural oxide layer that covers the metal matrix and the response related to ion charge transfer to the metal interface is observed at lower frequencies. In addition to, an increase in current is also observed of about 34.479 μA/cm2 and a |
EIS parameters of simulated data to equivalent electrical circuit (
Comparison of experimental and fitted EIS data for 8620 steel after exposure to distilled water.
Same behavior was observed for impedance-monitored corrosion tests for a 316 stainless steel plate (18.24 wt.%Cr, 8.07 wt.%Ni, 1.76 wt.%Mn, 0.5 wt.%Si, 0.27 wt.%Mo as principal alloying elements) after exposure to different aqueous solutions such as distilled water, 0.5 N NaCl, 0.5 N KCL, 1 M HCl or 0.5 M H2SO4, Table 4 shows the dissolution reaction. The impedance spectra that is shown in Figure 14 indicates one of the advantages of the
Electrolyte | Concentration | Cdl (μF/cm2) | Reaction |
---|---|---|---|
Distilled water | Pure-1lt | 5.45 | — |
Sodium chloride, NaCl | 29.2 gr/lt (0.5 N) | 93.62 | |
Potassium chloride, KCl | 37.27 gr/lt (0.5 N) | 165.3 | |
Hydrochloric acid, HCl | 15.56 ml/lt (1 M) | 302.4 | |
Sulfuric acid, H2SO4 | 27.11 ml/lt (1 M) | 313 |
Capacitance of electrical double layer for the stainless steel SS316 during its exposure to different electrolytes.
Impedance response of corroding stainless steel (SS316) during exposure to (1) distilled water, (2) NaCl 0.5 N, (3) KCl 0.5 N, (4) HCl 1 M, and (5) H2SO4 1 M.
Other application of the
Experimental impedance diagrams of corroding pipeline steel (API-5 L-X70) during exposure to HCl 1 M at different electrode rotation speed (0 to 1500 rpm). a) Bode plots representation and b) Nyquist complex plane.
At the steady-state conditions, without rotation, the impedance response is related to electrons flow from the aqueous media to the metal interface allowing the formation of an interfacial layer over the metal surface, called an electrical double layer or a thin oxide film, which is indicated by the distortion of the semicircle presenting two time constants not very well-defined, besides in the diagram of bode two changes of slopes are shown for the impedance module. When applying rotation from 20 to 200 rpm an increase in the magnitude of the Zreal and Zimag is observed due to the reaction kinetics at which the interfacial layer is forming at instantaneous rate and is controlled by electron charge and mass transfer mechanism. However, at turbulent conditions (>500 rpm) it does not allow the ions adsorption at the metal interface to maintain the presence of the double electrochemical layer or oxide film allowing only transients of electron transfer as a function of time, which promote the interfacial degradation of the steel. Therefore, the impedance diagrams show that under equilibrium conditions there is a corrosion rate controlled by the presence of a natural oxide on the steel surface, but this increased by the hydrodynamic conditions at turbulent flow, which is what is seen in real cases of application. But at moderate rotation speed the mass transport toward to the metal surface is carried out, giving opportunity to adsorption of molecules that come from the aqueous solution, which is consistent with the review literature [59].
EIS spectra for the particular system of concrete with reinforcing steel exposed to different days of a CO2(g) environment, carbonation process [
The
Particularly, the Mexican’s oil-industry still uses tubular steel pipes for the specific purpose of transporting hydrocarbons or natural gas. Most of the lines are buried, so the national network extends over quite large distances, crossing varied terrains conditions some with rivers, others with salt-laden marshes, or polluted industrial or urban zones alike; the ambient temperatures and load pressure for the buried-pipelines network vary widely, to put it simply vulnerable to corrosion attack. Steel pipes are corroded as a result of iron oxidation during its exposure of longer service periods. Therefore, corrosion problems are directly related to ever-present economical and production losses, as well as environment affectations, though human losses also happen. Providing effective inhibiting substances that are added to processing fluids may reduce internal corrosion problems; there are a wide variety of organic substances known to act as corrosion inhibitors. Figure 16 have demonstrated that small inhibitor quantities of organic molecules (2-Mercaptobenzimidazole,
Furthermore, Natural liquid-extracts like
EIS spectra in bode plots obtained from the pipeline steel API-5 L-X52 samples immersed in H2SO4 1 M as a function of the different concentration of natural molecules.
Other attractive uses of the
In this study, in particular a powder-pack boriding was used on AISI-SAE 1045 steel and SS316 stainless steel as surface thermochemical treatment to improve hardness and wear resistance to the steel samples, due to its low cost of hard coating processing. Boriding can also enhance the corrosion resistance of ferrous materials as shown in Figure 19. The results indicate that a single boride layer of Fe2B is formed on the 1045 steel surface, its morphology consisting a deep saw-tooth derived from the existence of diffusion paths (porosity and micro-cracks) in the surface of the steel matrix, in which the boron atoms are interstitial inserted to the surface forming a stable phase. For the borided stainless steel SS304 at the same conditions forms two-well defined layers on the surface, the columnar phase that was growth on the 1045 steel is less intense for SS304, this is due to the high concentration of chromium and nickel on the substrate surface, so the diffusion of boron stops by reacting immediately to form interstitial compounds of CrB, Cr2B or Ni3B in combination with FeB and Fe2B. EIS for the borided 1045 steel were recorded over 72 days of exposure to HCl 1 M solution, which the hard coating degrades slowly due to the defects on the coating structure that allow Cl− ions infiltrate, this is denote by changing the
Steel-can containers are manufactured from thin metal plates and are commonly used for the distribution or storage of food or beverages. Most conventional steel beverage cans have bent to form a tube and then welding both sides leaving a firm seam, then joining the bottom end to the tube, finally, the steel can is filling-out with the content. However, it is necessary to mention that the steels cans have an internal polymer coating or have been treated by electroplating to coated internally with a thin layer of tin in order to prevent any oxidizing or electrochemical corrosion during the steel exposure to the liquid product that it contains, which could be carbonated soft drinks, alcoholic drinks, fruit juices, teas, herbal teas, energy drinks and others [64, 65]. Despite of this internal coating having the good quality, it may fracture during storage or dissolve in small amounts in the liquid product, which depends on certain factors such as temperature, stowage load and handling of the products during their storage, as well as the chemical composition of the liquid and steel. Due to this, efforts have been managed to replace tin-based coatings by chemical compounds derived from epoxy resins or polymers. Nevertheless, the set-up of the factors mention above may situate the metal container (e.g. steel cans) at a potential risk to develop internal corrosion.
On the other hand, the sale of beverages storage in steel cans are committed to their handling in warehouse, in this way, there is a predisposition of the people who buy drink-cans, they think if cans are struck or bent the coating has been damaged and could be associated that the liquid product is contaminated with Fe+ ions. The impedance diagrams of Figure 20 show that the
Phase angle EIS response obtained for metal beverage containers at different surface condition after immersed in NaCl 0.5 M as a function on AC amplitude signal. a) Uniform polymer coating, b) scratch defect on coating, c) polished surface no-coating.
In this case experimental corrosion tests on laboratory conditions were performed in a metal container used for the distribution of orange juice in Mexico. This can is made of steel with internally coated by a higher density polymer. Three particular cases are studied as denoted in the scheme of Figure 20;
This review study is related to the basic aspects of EIS to understand the corrosion mechanism of industrial steels that serve at different corrosive conditions, which has a great interest on giving an educational orientation and practical teaching guide of how to use the outstanding Electrochemical Impedance Spectroscopy (EIS) technique in metal corrosion technology. Therefore, this review considers a wide variety of practical electrochemical impedance cases based on the fundamental and qualities aspects of EIS theory and its experimental interpretation. This book chapter also serves as a support for postgraduate students to have a criterion in deciding through their own experiences when using the electrochemical impedance technique. The practical cases discussed here are part of the research experienced of Dr. Héctor Herrera Hernández (DR.3H) and his students & research group. It is worth to mention that EIS has been extended to various disciplines of science and technology, thus demonstrating great efficiency in evaluating the performance and integrity of metallic materials as can be seen in detail in the practical examples presented in this review work. So, EIS is not only applied to stationary conditions, but also more complex variables can be monitored such as: flow parameters, variable that undoubtedly represents the real conditions and could be an interesting challenge for analyzing and interpreting these phenomena by means of EIS data. The fitting EIS data using a mathematical model such as an equivalent electrical circuit is a critical process in the analysis and validation of EIS data for the acquisition of the system’s electrical parameters that can be related to the corrosion rate of the material under study and also gives information of its capacity of electrons charge. Finally, EIS seeks to obtain information on the system and its evolution with time by applying a sinusoidal voltage as a function of frequency range, in order to determine the properties and feasibility of materials that serve under severe service conditions, such as industrial steels as is this case of the reviewed book chapter.
The authors dedicate this chapter to the memory of Professor Florian B. Mansfeld, USC.
The authors would like to acknowledge and express their gratitude to CONACyT for the SNI distinction as research membership and the monthly stipend received. Héctor Herrera Hernández (DR.3H) also would like to thanks to CIDETEQ and Secretaria de Investigación y Estudios Avanzados SIyEA/UAEM for their financial support through research project (4602/2018E). This project was conducted in the (Laboratory of Electrochemical and Corrosion of Industrial Materials at UAEM). Finally, DR.3H dedicates this work in memory to Professor
Phospholipids are major constituent of cellular membrane hence they have excellent biocompability. They are amphiphilic molecules which usually built by glycerol backbone with two different polarity groups attached to it. On the one hand is the hydrophilic group renowned as the head group which then becomes the basis of species classification of phospholipids, such as phosphatidylcholine (PC), phosphatidyletanolamine (PE), and phosphatidylserine (PS). On the other hand is the hydrophobic fatty acyl chains distinguished as the tails. The variation of the length and the saturation, the bonding position of fatty acyl chains to glycerol backbone as well as the head group type become a crucial part of their application, for instance in drug delivery systems.
The development of phospholipids based drug delivery systems have been proven prominent by the emergence of many phospholipid-related drug formulation. Among of them are doxorubicin in stealth liposomes for cancer treatment, which has been on the market since 1995 [1, 2]; Verteporfin in cationic liposomes for molecular degeneration [3] and vincristine in conventional liposome for Non-Hodgkin lymphoma [2]. They have been used in clinic, and achieve good results. Many more phospholipids based liposomal preparation have been developed to find better therapeutic results [4, 5, 6]. Furthermore various sources, synthetic and natural, have been explored [2, 7].
The isolation of phospholipids from natural sources cost lower than synthesizing them hence the preference is the isolation of natural phospholipids. For natural origin, the more pure they are, the greater the value is [8]. Phospholipids from natural origin can be refined into diverse levels, comprising food and pharmaceutical grade [2, 9]. In term of natural phospholipids, different source enhance the species variety of phospholipids [7]. Egg yolk and soybean phospholipids mainly consist of phosphatidylcholine species but they have differences in the tail portions which influence their physical, chemical properties and their applications. Other natural phospholipids that currently are being explored extensively are sunflower [10, 11, 12], candlenut [13], jack bean [14], sesame [13, 15, 16, 17] and coconut [13, 15, 16, 18, 19, 20, 21, 22].
Coconut is one of the native plantations in tropical countries and produces mainly copra and coconut oil. Exploration of coconut by-products such as coconut phospholipids needs to be done to increase the added value of these coconut plantations. Previous studies have found that dried coconut contain phospholipids from cephaline species with their fatty acyl chains are dodecanoic and octanoic acyl chains [15]. Purification with eluent chloroform: methanol (9:1) follows by identification using thin layer chromatography (TLC) also detects the presence of phosphatidylcholine (PC), phosphatidyletanolamine (PE), and phosphatidylserine (PS) species in coconut phospholipids (CocoPLs) [20, 21].
In the matter of its application, coconut liposomes (CocoPLs liposomes) have been used in the encapsulation of hydrophilic agent namely carboxyfluoresence and vitamin C and resulted in that CocoPLs liposomes has high efficiency of encapsulation [16, 19, 22]. The addition of cholesterol improves the encapsulation efficiency and low storage temperature reduces CocoPLs liposomes leakage. The results advocated the CocoPLs potency as drug delivery material. Moreover since we have established that CocoPLs consist of many phospholipid species therefore it would be valuable to study the component of the species and their capability as drug delivery system. In this study we explore the isolation and purification of coconut phospholipid species specifically coconut phosphatidylethanolamine (CocoPEs) and utilization of their liposomes (CocoPEs liposomes) for vitamin C encapsulation with various cholesterol concentrations. To our knowledge this is the first study of such.
Materials used in this study were ripe coconut meat purchased from local market, TLC silica gel 60 F254 plate, silica gel powder 60 G for thin layer chromatography, various solvents and regents for analytical grade.
Isolation technique was carried out based on the previous method used [20, 21]. Briefly coconut meat powder was macerated in a chloroform: methanol (2:1, v/v) mixture. The filtrate obtained was washed using 0.9% NaCl. The lipid was evaporated until thick coconut lipid extract were obtained. The extract was then subjected to solvent partition using n-hexane and ethanol 87%. The lower phase was evaporated to yield brownish yellow extract of CocoPLs.
About 5 g of CocoPLs was mixed with 5 g of silica gel in a small amount of chloroform: methanol (9:1, v/v) solution to form a silica slurry. The slurry was then stirred until the mixture was dried and formed fine powder of CocoPLs-SG.
A total of 80 mg of silica gel was poured into a chromatography column and compressed by vacuum. The column was rinsed using chloroform:methanol (9:1, v/v) eluent and vacuumed until all the eluent was eluted. The CocoPLs-SG powder was poured onto the column. Then the column was subjected to compression. Elution was performed using 10 ml of chloroform:methanol (9:1, v/v) solution. Fraction eluted from the column was collected into clean vials. The fraction was analyzed using TLC plate. The spot on the TLC plate was identified with 10% H2SO4 and ninhydrin. Elution was repeated every 10 ml of the eluent until the TLC plate did not show any spot when subjected to identification. The CocoPLs fractions contained ethanolamine species were gathered into an evaporating flask and evaporated at 40°C to obtain dark brownish gel of CocoPEs.
Both CocoPLs and CocoPEs obtained were characterized using FT-IR (Prestige 21 Shimadzu), GC-MS (Shimadzu QP2010S), and LCMSMS (Waters Xevo TQD) and DSC (Shimadzu DSC-60A). The FTIR was employed to probe the phospholipids functional groups. The GC-MS was used to determine the phospholipids fatty acyl chains. The LC-MS/MS was for identifying the chemical component of CocoPEs and the DSC analysis was carried out to explore the CocoPEs phase behavior.
In this research, vitamin C (VC) was used as a model for hydrophilic drug to be encapsulated in coconut liposome [13, 16, 17, 22]. Stock solution of 500 ppm CocoPEs with cholesterol concentration (0%, 10%, 20%, 30%, 40% w/w) were made. A total of 2 mL of each stock solution was diluted with chloroform to 10 mL and poured into a test tube. The liquid solution was evaporated using N2 gas flow to form a thin layer. After that hydration process was carried out. Around 10 mL of phosphate buffer solution was added to the thin film. The mixture was subjected to freeze-thawing process until the thin film was dispersed completely. The dispersions contained empty coconut liposome and was used as control. Other set of dispersions were prepared by adding 8 ppm (
where
A brownish yellow gel of CocoPLs was obtained from dried coconut meat (
CocoPLs.
In the separation process using vacuum column chromatography, CocoPLs was eluted continuously using chloroform:methanol (9:1, v/v). Each fraction of 10 mL eluent was collected and subjected to identification. As much as 520 fractions were obtained to elute CocoPEs from the CocoPLs samples completely. Identification by TLC using 10% H2SO4 and ninhydrin spotting agent [23] resulted in that CocoPEs were present in the 105th to the 520th fraction.
The fraction contained CocoPEs were then combined and evaporated to remove the eluent that resulted in dark brown CocoPEs gel (
CocoPEs.
The functional groups identification of CocoPLs and CocoPEs was conducted by FTIR spectra analysis. The FTIR spectra of both CocoPLs and CocoPEs were displayed on Figure 3. To analyze further the spectra were scrutinized using a deconvolution program [21, 24], at wavenumbers 3500–2800 cm−1 and 1800–700 cm−1 as presented in Figure 4.
CocoPLs and CocoPEs absorption spectra.
Deconvolution results: (a) CocoPLs at wavenumbers 1800–700 cm−1; (b) CocoPLs at wavenumbers 3500–2800 cm−1; (c) CocoPEs at wavenumbers 1800–700 cm−1; (d) CocoPEs at wavenumbers 3500–2800 cm−1.
The absorption data obtained from both FTIR spectra and deconvolution analysis were compared (see Table 1) to the specific infrared absorption area for phospholipids proposed by Stuart [25] and Hudiyanti et al. [20, 21]. The presence of a typical spectrum of phospholipids was clearly revealed. Significant differences between CocoPLs and CocoPEs spectra was disclosed by the typical absorption of choline and ethanolamine groups on both spectra of CocoPLs and CocoPEs. The choline group absorptions; (CH3)3N+ asymmetric bending and (CH3)3N+ asymmetry stretching; were not present on the CocoPEs spectra. The typical absorption that indicate the presence of ethanolamine species by N-H vibration absorptions was displayed on CocoPLs and CocoPEs spectra. This evident indicated that CocoPLs contained choline and ethanolamine species while CocoPEs did not contain choline species. From The FTIR spectra point of view this data disclosed that the CocoPEs separation from CocoPLs was successful.
No. | Absorption type | References [15, 20, 21, 25] (cm−1) | CocoPLs (cm−1) | CocoPEs (cm−1) | CocoPLs Deconvolution (cm−1) | CocoPEs Deconvolution (cm−1) |
---|---|---|---|---|---|---|
1. | ||||||
2. | =C-H stretching | 3010 | — | — | 3001 | 3002 |
3. | CH3 asymmetric stretching | 2956 | — | — | 2958 | 2956 |
4. | CH2 asymmetric stretching | 2920 | 2924 | 2924 | 2923 | 2919 |
5. | CH3 symmetric stretching | 2870 | — | — | 2885 | 2890 |
6. | CH2 symmetric stretching | 2850 | 2854 | 2854 | 2850 | 2848 |
7. | C=O stretching, sn-1 chain trans-conformation | 1730 | 1735 | 1735 | 1738 | 1739 |
8. | ||||||
9. | CH2 scissoring | 1473, 1472, 1468, 1463 | — | — | — | — |
10. | CH3 asymmetric bending | 1460 | 1458 | 1458 | 1461 | 1464 |
11. | (CH3)3N+ symmetric bending | 1405 | — | — | — | — |
12. | CH3 symmetric bending | 1378 | 1373 | 1373 | 1376 | 1378 |
13. | CH3 rocking ribbon progression | 1400–1200 | — | — | 1333 | 1266 |
14. | PO2−asymmetric stretching | 1228 | 1226 | 1242 | 1225 | 1222 |
15. | CO-O-C asymmetric stretching | 1170 | 1165 | — | 1150 | 1165 |
16. | PO2− symmetric stretching | 1085 | — | 1080 | 1106 | 1107 |
17. | CO-O-C symmetric stretching | 1070 | 1072 | — | 1071 | 1070 |
18. | C-O-P stretching | 1047 | — | — | 1020 | 1003 |
19. | ||||||
20. | P-O asymmetric stretching | 820 | 817 | — | 813 | 819 |
21. | CH2 rocking | 730, 720, 718 | 717 | 725 | 714 | 713 |
Typical Absorption of CocoPLs and CocoPEs functional groups.
Bold entries represented the typical absorption of choline and ethanolamine groups on both spectra of CocoPLs and CocoPEs.
The fatty acyl chains content of CocoPLs and CocoPEs was analyzed by GC-MS. The CocoPLs chromatogram was presented on Figure 5. A total of nine peaks was recognized. Seven peaks were with abundance above 1%. The chromatogram suggested that there were at least 9 types of fatty acyl chains present on the CocoPLs. The MS reading revealed the identity of these fatty acyl chains. Three fatty acyl chains worth mentioning with the abundance more than 10%, i.e., lauric acid, palmitic acid and oleic acid which were indicated by peak number 3 (abundance of 11.31%); peak number 5 (15.26%); and peak number 7 (55.18%). The result was in agreement with previous research [15, 20, 21]. The seven fatty acyl chains recognized in CocoPLs was displayed on Table 2.
CocoPLs chromatogram.
Peak number | tR (min) | Fatty acyl chains | Area (%) |
---|---|---|---|
3. | 29.164 | Lauric acid, C12:0 (dodecanoic acid) | 11.31 |
4. | 34.037 | Myristic acid, C14:0 (tetradecanoic acid) | 5.71 |
5. | 38.497 | Palmitic acid, C16:0 (hexadecanoic acid) | 15.26 |
6. | 41.872 | Linoleic acid, C18:2 (9(Z),12(Z)-octadecadienoic acid) | 6.00 |
7. | 42.117 | Oleic acid, C18:1 (9(Z)-octadecenoic acid) | 55.18 |
8. | 42.482 | Stearic acid, C18:0 (octadecanoic acid) | 3.97 |
9. | 52.794 | Lignoceric acid, C24:0 (tetracosanoic acid) | 1.49 |
The fatty acyl chains of CocoPLs.
The chromatogram of CocoPEs was disclosed on Figure 6. The resulting chromatogram exposed the presence of five peaks with abundance above 1% which suggested the presence of five types of fatty acyl chains in the CocoPEs. Three of them had great abundance i.e. capric, linoleic and oleic acids as indicated by peak number 2, 3 and 4 and with abundance of 17.09%, 43.17% and 31.88% respectively. The MS reading of fatty acyl chains content in the CocoPEs was tabulated on Table 3.
CocoPEs chromatogram.
Peak number | tR (min) | Fatty acyl chains | Area (%) |
---|---|---|---|
2. | 38.566 | Capric acid, C10:0 (decanoic acid) | 17.09 |
3. | 42.041 | Linoleic acid, C18:2 (9(Z),12(Z)-octadecadienoic acid) | 43.17 |
4. | 42.198 | Oleic acid, C18:1 (9(Z)-octadecenoic acid) | 31.88 |
5. | 42.555 | Stearic acid, C18: 0 (octadecanoic acid) | 5.93 |
8. | 46.186 | Arachidic acid, C20:0 (eicosanoic acid) | 1.04 |
The Fatty acyl chains of CocoPEs.
Tables 2 and 3 revealed differences to some extent in fatty acyl chains composition between CocoPLs and CocoPEs. CocoPLs had more variation in fatty acyl chains type compared to CocoPEs. This fact plausible considering that CocoPEs was obtained from the separation of CocoPLs. The separation was mainly based on the common head group namely ethanolamine that reflected on the polarity of the separated CocoPEs molecules hence the choice of the separation eluent. More over fatty acyl chains profile were closely related to the position of phospholipid species in the bio-membrane bilayer [26, 27, 28]. Phosphatidylethanolamine (PE) species generally would be positioned in the inner leaflet of bilayer due to their molecular geometry, i.e. cylinder [2]. The PE species molecular shape was supported by more abundance composition of unsaturated fatty acyl chains in the CocoPEs extract, Table 3.
Based on the fatty acyl chains of the CocoPEs we conducted parent ion screening using LCMSMS. The CocoPEs parent ion spectrogram was presented on Figure 7. The spectrogram gave us a representation of the molecular species composing CocoPEs extract. At least 11 molecular species of CocoPEs were found. The CocoPEs molecular species was tabulated on Table 4. The molecular species was predicted based on the head group and combination of two fatty acyl chains for the nonpolar part of CocoPEs species. These similar species would govern the CocoPEs phase behavior and other properties as well.
CocoPEs spectrogram.
No. | m/z (M-H) | Molecular weight | CocoPEs molecular species | |
---|---|---|---|---|
Head group | Fatty acyl chains | |||
1. | 554 | 555 | Ethanolamine | Capric acid Capric acid |
2. | 662 | 663 | Ethanolamine | Capric acid Linoleic acid |
3. | 664 | 665 | Ethanolamine | Capric acid Oleic acid |
4. | 666 | 667 | Ethanolamine | Capric acid Stearic acid |
5. | 694 | 695 | Ethanolamine | Capric acid Arachidic acid |
6. | 770 | 771 | Ethanolamine | Linoleic acid Linoleic acid |
7. | 774 | 775 | Ethanolamine | Oleic acid Oleic acid |
8. | 776 | 777 | Ethanolamine | Oleic acid Stearic acid |
9. | 802 | 803 | Ethanolamine | Linoleic acid Arachidic acid |
10. | 806 | 807 | Ethanolamine | Stearic acid Arachidic acid |
11. | 834 | 835 | Ethanolamine | Arachidic acid Arachidic acid |
CocoPEs molecular species prediction.
Every phospholipid species has unique phase behavior that related to their molecular structure and phase behavior. The phase behavior of CocoPLs and CocoPEs were investigated by thermal analysis using DSC. The thermogram for CocoPLs, Figure 8, exhibited a small peak at 28.85°C and larger peak at 83.95°C. These peaks indicated that CocoPLs underwent phase changes as temperature changes. A pre-transition process from planar-shaped gel (Lb′) to the rippling phase (Pb′) was at a temperature of 28.85°C (Tp), then proceed with the main transition from gel (Lb′) to the liquid crystal phase (La) at a temperature of 83.95°C (Tm) [29, 30, 31]. Tp and Tm were the pre-transition and melting temperature correspondingly.
Thermal analysis of CocoPLs.
Different phase behavior of CocoPEs was exhibited in Figure 9. The thermogram for CocoPEs was more complex than CocoPLs indicated that CocoPEs had more complex phase transition than CocoPLs. CocoPEs displayed pre-transition process from planar-shaped gel (Lb′) to a rippling phase (Pb′) at a temperature of 25.29°C (Tp), followed by a major transition from gel (Lb′) to liquid crystal phase (La) at a temperature of 32.62°C (Tm), and then a transition from the liquid crystal phase (La) to hexagonal phase (H) at a temperature of 65.53°C (Th) [32]. The hexagonal phase formation was consistent to cylindrical molecular shape attributed to CocoPEs. The CocoPEs gradual change of phase was estimated because of the similar molecular species composing CocoPEs.
Thermal analysis of CocoPEs.
The phase behavior of CocoPEs dan CocoPLs above indicated that they were both had complex self-assembly structures which would be beneficial for future applications [2].
Phospholipids has long been known as drug delivery substance due to their liposome forming ability. Liposome was a spherical aggregation structure with bilayer phospholipid as its shell surrounding aqueous core. This unique structure was especially a perfect vehicle for delivering hydrophilic and hydrophobic drugs with storage and controlled release purposes. In this paper as a preliminary study for further application of coconut phospholipid as drug delivery material we used vitamin C as a hydrophilic drug model to be encapsulated in coconut liposomes. Vitamin C was a hydrophilic drug and would be encapsulated inside the aqueous core of liposome. The study lead to that encapsulation efficiency of vitamin C in CocoPEs were higher than CocoPLs i.e. 94.44% and 92.40% respectively, Figure 10.
Encapsulation efficiency of CocoPLs and CocoPEs liposomes with cholesterol composition variation.
In relation to their application as drug delivery, liposomes were usually made from phospholipid and a small amount of cholesterol. Cholesterol was added to the liposome membrane to control liposome rigidity and penetrability [33]. Therefore to explore the effect of cholesterol on the encapsulation efficiency of coconut liposomes we also prepared coconut liposomes with several different concentration of cholesterol namely 10%, 20%, 30% and 40%. The encapsulation efficiency of the liposomes were presented on Figure 10. The results suggested that addition of cholesterol up to 40% in the liposome’s membrane reduced the encapsulation efficiency of CocoPEs and CocoPLs liposomes. Furthermore CocoPEs liposomes demonstrated slighter reduction than CocoPLs liposomes. The encapsulation efficiency of CocoPEs diminished gradually as the cholesterol concentration increased while for CocoPLs liposomes the decline was arbitrary. Addition up to 30% of cholesterol only reduced the CocoPEs encapsulation efficiency to around 80% while CocoPLs was as low as 52%. Cholesterol effect on the encapsulation efficiency of CocoPEs liposomes more consistent than CocoPLs. We suspected it was due to the molecular composition of the phospholipid in the membrane. The molecular composition was represented by the composition of functional group and fatty acyl chains in the CocoPEs and CocoPLs, Tables 1–3. In the liposome membrane cholesterol interacted with CocoPEs and CocoPLs through their functional groups and fatty acyl chains. Cholesterol with small hydrophilic head group i.e., –OH and big and rigid hydrophobic steroid ring would interact better with small head group phospholipid species like CocoPEs than CocoPLs which had big spherical choline group and possibly other head groups as well. The composition of fatty acyl with double bonds also suspected would give more room for cholesterol hydrophobic moiety. The fatty acyl chains would assume “kink” structure at the double bond position [34, 35] and allocate more space hence more comfortable for cholesterol to integrate. With smaller number of fatty acyl chains type and higher concentration of double bond made cholesterol effect became more systematic in the CocoPEs liposome membrane. The data gave an insight about the application of CocoPEs as encapsulation material. CocoPEs was a good candidate for encapsulation hydrophilic material.
A total of (
DH and KA would like to express their gratitude of financial support by DIPA Selain APBN FSM UNDIP Riset Madya, 2018.
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His studies in robotics lead him not only to a PhD degree but also inspired him to co-found and build the International Journal of Advanced Robotic Systems - world's first Open Access journal in the field of robotics.",institutionString:null,institution:{name:"TU Wien",country:{name:"Austria"}}},{id:"441",title:"Ph.D.",name:"Jaekyu",middleName:null,surname:"Park",slug:"jaekyu-park",fullName:"Jaekyu Park",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/441/images/1881_n.jpg",biography:null,institutionString:null,institution:{name:"LG Corporation (South Korea)",country:{name:"Korea, South"}}},{id:"465",title:"Dr",name:"Christian",middleName:null,surname:"Martens",slug:"christian-martens",fullName:"Christian Martens",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:null},{id:"479",title:"Dr.",name:"Valentina",middleName:null,surname:"Colla",slug:"valentina-colla",fullName:"Valentina Colla",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/479/images/358_n.jpg",biography:null,institutionString:null,institution:{name:"Sant'Anna School of Advanced Studies",country:{name:"Italy"}}},{id:"494",title:"PhD",name:"Loris",middleName:null,surname:"Nanni",slug:"loris-nanni",fullName:"Loris Nanni",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/494/images/system/494.jpg",biography:"Loris Nanni received his Master Degree cum laude on June-2002 from the University of Bologna, and the April 26th 2006 he received his Ph.D. in Computer Engineering at DEIS, University of Bologna. On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. His research interests include pattern recognition, bioinformatics, and biometric systems (fingerprint classification and recognition, signature verification, face recognition).",institutionString:null,institution:null},{id:"496",title:"Dr.",name:"Carlos",middleName:null,surname:"Leon",slug:"carlos-leon",fullName:"Carlos Leon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Seville",country:{name:"Spain"}}},{id:"512",title:"Dr.",name:"Dayang",middleName:null,surname:"Jawawi",slug:"dayang-jawawi",fullName:"Dayang Jawawi",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Technology Malaysia",country:{name:"Malaysia"}}},{id:"528",title:"Dr.",name:"Kresimir",middleName:null,surname:"Delac",slug:"kresimir-delac",fullName:"Kresimir Delac",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/528/images/system/528.jpg",biography:"K. 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Liposuction is a procedure to improve the body contour and not a surgery to reduce weight, although recently people who have failed in their plans to lose weight look at liposuction as a means to contour their body figure. Tumescent liposuction of large volumes requires a meticulous selection of each patient; their preoperative evaluation and perioperative management are essential to obtain the expected results. The various techniques of general anesthesia are the most recommended and should be monitored in the usual way, as well as monitoring the total doses of infiltrated local anesthetics to avoid systemic toxicity. The management of intravenous fluids is controversial, but the current trend is the restricted use of hydrosaline solutions. The most feared complications are deep vein thrombosis, pulmonary thromboembolism, fat embolism, lung edema, hypothermia, infections and even death. 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Skin substitutes offer a solution to the problem of insufficient autologous skin graft availability in major burn wound closure. A growing body of evidence supports the role of skin substitutes in both acute major burns and secondary burn scar resurfacing. Classification of skin substitutes has become increasingly complex given the large variety of synthetic and biologic dermal matrices now available as the result of ongoing advances in regenerative medicine techniques. Classification systems are required to assist clinicians with selection and comparison of outcomes across a wide diversity of skin substitutes. Professor John Greenwood, invented, designed and developed one such dermal substitute, \\'Biodegradable Temporising Matrix\\', which is approved for use across the globe for reconstruction of major burns and complex wounds. This chapter provides a review of available classification systems for skin substitutes with a summary of the latest evidence in relation to their role and impact on burn wound outcomes. Future developments toward the elusive ‘ideal’ skin substitute may be possible through ongoing research efforts focused on clinical translation of modern skin tissue engineering techniques for burn wound reconstruction.",book:{id:"11723",title:"Wound Healing - Recent Advances and Future Opportunities",coverURL:"https://cdn.intechopen.com/books/images_new/11723.jpg"},signatures:"Elizabeth Concannon, Lindsay Damkat-Thomas, Patrick Coghlan and John E. 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State-of-the-art renewal has highlighted the involvement of mesenchymal stem/stromal cell (MSC)-based cytotherapy for various allergic disease management including atopic dermatitis, pediatric asthma, allergic rhinitis, and urticaria, which largely attributes to the unique immunomodulatory properties and mode of action via autocrine and paracrine, direct- or trans-differentiation. 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Alcoholic liver disease (ALD) is the most frequent cause of severe chronic liver disease in Europe and worldwide. ALD can progress from alcoholic fatty liver to alcoholic steatohepatitis and alcoholic liver cirrhosis, the grade of fibrosis being the key prognostic factor for the severity of the diseases. This chapter will present the place of liver elastography in the noninvasive assessment of ALD. 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',book:{id:"11287",title:"Chronic Kidney Disease - Beyond the Basics",coverURL:"https://cdn.intechopen.com/books/images_new/11287.jpg"},signatures:"Maha Najeeb Haddad"},{id:"82410",title:"Clinical Application of Repetitive Peripheral Magnetic Stimulation in Rehabilitation",slug:"clinical-application-of-repetitive-peripheral-magnetic-stimulation-in-rehabilitation",totalDownloads:2,totalDimensionsCites:0,doi:"10.5772/intechopen.105787",abstract:"Repetitive peripheral magnetic stimulation (rPMS) is a noninvasive method involving the repetitive magnetic stimulation of peripheral nerves and muscles. Recently, its potential as a new neuromodulation technique for sensory motor disorders has been recognized. Its advantages include less pain than with electrical stimulation and that neuromuscular stimulation can be performed over clothing. These advantages make it a practical and straightforward adjunct tool widely used in clinical practice. In particular, the combination of rPMS and general rehabilitation reportedly promotes functional improvement in stroke patients with difficult involuntary contractions. This chapter reviews rPMS and its potential clinical applications in rehabilitation.",book:{id:"11832",title:"Neurorehabilitation and Physical Therapy",coverURL:"https://cdn.intechopen.com/books/images_new/11832.jpg"},signatures:"Ryu Ushio, Kousuke Tamura, Shoya Fujikawa, Chihiro Ohsumi, Shun Sawai, Ryosuke Yamamoto and Hideki Nakano"},{id:"82411",title:"Potential Applications of Motor Imagery for Improving Standing Posture Balance in Rehabilitation",slug:"potential-applications-of-motor-imagery-for-improving-standing-posture-balance-in-rehabilitation",totalDownloads:1,totalDimensionsCites:0,doi:"10.5772/intechopen.105779",abstract:"Improving standing posture balance is an essential role of rehabilitation to prevent falls in the elderly and stroke victims. Recently, motor imagery has been reported to be an effective method to improve standing posture balance. Motor imagery is a simulation of a movement in the brain without actual movement. Motor imagery is believed to have a common neural basis with actual movement and is effective in reconstructing motor functions. Recently, it has also been shown that motor imagery can be enhanced through use in combination with neuromodulation techniques. 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