Regulatory limit of selected heavy metals.
\\n\\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\\n\\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\\n"}]',published:!0,mainMedia:{caption:"Highly Cited",originalUrl:"/media/original/117"}},components:[{type:"htmlEditorComponent",content:'IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\nThroughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\nReleased this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\n'}],latestNews:[{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"},{slug:"intechopen-identified-as-one-of-the-most-significant-contributor-to-oa-book-growth-in-doab-20210809",title:"IntechOpen Identified as One of the Most Significant Contributors to OA Book Growth in DOAB"}]},book:{item:{type:"book",id:"965",leadTitle:null,fullTitle:"Novel Strategies in Ischemic Heart Disease",title:"Novel Strategies in Ischemic Heart Disease",subtitle:null,reviewType:"peer-reviewed",abstract:'The first edition of this book will provide a comprehensive overview of ischemic heart disease, including epidemiology, risk factors, pathogenesis, clinical presentation, diagnostic tests, differential diagnosis, treatment, complications and prognosis. 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They are substances with high electrical conductivity which voluntarily lose their electrons to form cations. Metals are found all over the earth including the atmosphere, earth crust, water bodies, and can also accumulate in biological organisms including plants and animals. Among the 35 natural existing metals, 23 possess high specific density above 5 g/cm3 with atomic weight greater than 40.04 and are generally termed heavy metals [1, 2]. Theses metals generally termed heavy metals include: antimony, tellurium, bismuth, tin, thallium, gold, arsenic, cerium, gallium, cadmium, chromium, cobalt, copper, iron, lead, mercury, manganese, nickel, platinum, silver, uranium, vanadium, and zinc [1, 2]. This category of metals termed heavy metals have not only been known for their high density but most importantly for their adverse effects to the ecosystem and living organisms [3]. Some of these heavy metals such as cobalt, chromium, copper, magnesium, iron, molybdenum, manganese, selenium, nickel and zinc are essential nutrients that are required for various physiological and biochemical functions in the body and may result to deficiency diseases or syndromes if not in adequate amounts [4] but in large doses they may cause acute or chronic toxicities.
These heavy metals are distributed in the environment through several natural processes such as volcanic eruptions, spring waters, erosion, and bacterial activity, and through anthropogenic activities which include fossil fuel combustion, industrial processes, agricultural activities as well as feeding [5]. These heavy metals do bioaccumulate in living organisms and the human body through various processes causing adverse effects. In the human body, these heavy metals are transported and compartmentalized into body cells and tissues binding to proteins, nucleic acids destroying these macromolecules and disrupting their cellular functions. As such, heavy metal toxicity can have several consequences in the human body. It can affect the central nervous function leading to mental disorder, damage the blood constituents and may damage the lungs, liver, kidneys and other vital organs promoting several disease conditions [6]. Also, long term accumulation of heavy metals in the body may result in slowing the progression of physical, muscular and neurological degenerative processes that mimic certain diseases such as Parkinson’s disease and Alzheimer’s disease [6]. More so, repeated long-term contact with some heavy metals or their compounds may even damage nucleic acids, cause mutation, mimic hormones thereby disrupting the endocrine and reproductive system and eventually lead to cancer [7].
This chapter will highlight on the various sources of heavy metals and the processes that promote their exposure and bioaccumulation in the human body. More focus will be laid on the various mechanisms that lead to heavy metal toxicity with emphasis on macromolecule and cellular damages, carcinogenesis, neurotoxicity and the molecular basis for their noxious effects. The various toxic effects along with the signs and symptoms of some heavy metals in the human body will be discussed.
Heavy metals are naturally present in our environment. They are present in the atmosphere, lithosphere, hydrosphere and biosphere [8]. Although these heavy metals are present in the ecosystem, their exposure to humans is through various anthropogenic activities of man. In the earth crust, these heavy metals are present in ores which are recovered during mining activities as minerals. In most ores heavy metals such as arsenic, iron, lead, zinc, gold, nickel, silver and cobalt exist as sulfides while others such as manganese, aluminum, selenium gold, and antimony exist as oxides. Certain heavy metals such as copper, iron and cobalt can exist both as sulfide and oxide ores. Some sulfides may contain two or more heavy metals together such as chalcopyrite, (CuFeS2) which contains both copper and iron. During these mining activities, heavy metals are released from the ore and scattered in open in the environment; left in the soil, transported by air and water to other areas. Furthermore, when these heavy metals are used in the industries for various industrial purposes, some of these elements are released into the air during combustion or into the soil or water bodies as effluents. More so, the industrial products such as paints, cosmetics, pesticides, and herbicides also serve as sources of heavy metals. Heavy metals may be transported through erosion, run-off or acid rain to different locations on soils and water bodies. As reviewed from [9], the sources of specific heavy metals are described below.
Arsenic is the 20th most abundant element on earth and the 33rd on the periodic table. The inorganic forms such as arsenite and arsenate compounds are lethal to humans and other organisms in the environment. Humans get in contact with arsenic through several means which include industrial sources such as smelting and microelectronic industries. Drinking water may be contaminated with arsenic which is present in wood preservatives, herbicides, pesticides, fungicides and paints [10].
Lead is a slightly bluish, bright silvery metal in a dry atmosphere. The main sources of lead exposure include drinking water, food, cigarette, industrial processes and domestic sources. The industrial sources of lead include gasoline, house paint, plumbing pipes, lead bullets, storage batteries, pewter pitchers, toys and faucets [11]. Lead is released into the atmosphere from industrial processes as well as from vehicle exhausts. Therefore, it may get into the soil and flow into water bodies which can be taken up by plants and hence human exposure of lead may also be through food or drinking water [12].
The metallic mercury is a shiny silver-white, odorless liquid metal which becomes colorless and odorless gas upon heating. Mercury is used in producing dental amalgams, thermometers and some batteries. Also, it can be found in some chemical, electrical-equipment, automotive, metal-processing, and building industries. Mercury can exist in a gaseous form thus it can be inhaled. Other forms of mercury contamination in humans may be through anthropogenic activities such as municipal wastewater discharges, agriculture, incineration, mining, and discharges of industrial wastewater [13].
This metal is mostly used in industries for the production of paints, pigments alloys, coatings, batteries as well as plastics. Majority of cadmium, about three-fourths is used as electrode component in producing alkaline batteries. Cadmium is emitted through industrial processes and from cadmium smelters into sewage sludge, fertilizers, and groundwater which can remain in soils and sediments for several decades and taken up by plants. Therefore, significant human exposure to cadmium can be by the ingestion of contaminated foodstuffs especially cereals, grains, fruits and leafy vegetables as well as contaminated beverages [14, 15]. Also, humans may get exposed to cadmium by inhalation through incineration of municipal waste.
Chromium is a metal that is present in petroleum and coal, chromium steel, pigment oxidants, fertilizers, catalyst, oil well drilling and metal plating tanneries. Chromium is extensively used in industries such as wood preservation, electroplating, metallurgy, production of paints and pigments, chemical production, tanning, and pulp and paper production. These industries play a major role in chromium pollution with an adverse effect on biological and ecological species [16]. Following the anthropogenic activities by humans, disposal of sewage and use of fertilizers may lead to the release of chromium into the environment [16]. Therefore, these industrial and agricultural practices increase the environmental contamination of chromium. Environmental pollution by chromium has been mostly by the hexavalent chromium in recent years [17].
This is a heavy metal which is used in industries to produce copper pipes, cables, wires, copper cookware, etc. It is also used to make copper intrauterine devices and birth control pills. Copper in the form of copper sulfate is added to drinking water and swimming pools [18]. Due to man’s anthropogenic and industrial activities, it can accumulate in the soil and up taken by plants. As such, copper is present in some nuts, avocado, wheat germ and bran etc.
This metal is added to gasoline as methylcyclopentadienyl manganese tricarbonyl (MMT) and thus, gasoline fumes contain a very toxic form of manganese [19].
It is used in the production of batteries, nickel-plated jewelry, machine parts, nickel plating on metallic objects, manufacture of steel, cigarette smoking, wire, electrical parts, etc. Also, it can be found in food stuff such as imitation whip cream, unrefined grains and cereals, commercial peanut butter, hydrogenated vegetable oils, as well as contaminated alcoholic beverages [19]. The various sources of heavy metals are summarized in Figure 1.
Pathway of heavy metals sources and exposure to humans.
Humans may directly get in contact with heavy metals by consuming contaminated food stuffs, sea animals, and drinking of water, through inhalation of polluted air as dust fumes, or through occupational exposure at workplace [20]. The contamination chain of heavy metals almost usually follows this cyclic order: from industry, to the atmosphere, soil, water and foods then human [8]. These heavy metals can be taken up through several routes. Some heavy metals such as lead, cadmium, manganese, arsenic can enter the body through the gastrointestinal route; that is, through the mouth when eating food, fruits, vegetables or drinking water or other beverages. Others can enter the body by inhalation while others such as lead can be absorbed through the skin.
Most heavy metals are distributed in the body through blood to tissues [21]. Lead is carried by red blood cells to the liver and kidney and subsequently redistributed to the teeth, bone and hair mostly as phosphate salt [20]. Cadmium initially binds to blood cells and albumin, and subsequently binds to metallothionein in kidney and liver tissue. Following its distribution from blood to the lungs, manganese vapor diffuses across the lung membrane to the Central nervous system (CNS). Organic salts of manganese which are lipid soluble are distributed in the intestine for fecal elimination while inorganic manganese salts which are water soluble are distributed in plasma and kidney for renal elimination. Arsenic is distributed in blood and accumulates in heart, lung, liver, kidney, muscle and neural tissues and also in the skin, nails and hair. The regulatory limit for some selected heavy metals is shown in Table 1.
Heavy metals | EPA limits in drinking water (ppm) | OSHA limit in workplace air (mg) | FDA limit in bottled water/food (ppm) |
---|---|---|---|
Arsenic | 0.01 | 10 | – |
Barium | 2.0 | 0.5 | – |
Cadmium | 0.005 | 5 | 0.005 |
Chromium | 0.1 | 1 | 1 |
Lead | 0.015 | 0.15 | – |
Mercury | 0.002 | 0.1 | 1 |
Selenium | 0.05 | 0.2 | – |
Silver | 0.0001 | 0.01 | – |
Zinc | 5 | 5 | – |
Regulatory limit of selected heavy metals.
ppm, parts per million; mg, milligram; EPA, Environmental Protection Agency; OSHA, Occupational Safety and Health Administration; FDA, Food and Drug Administration.
Certain heavy metals are known to generate free radicals which may lead to oxidative stress and cause other cellular damages (see [22] for review). The mechanism of free radical generation is specific to the type of heavy metal.
Iron is a useful heavy metal in the human body as it is a constituent of certain biological molecules like the hemoglobin and involved in various physiological activities. However, in its free state, iron is one of the heavy metals generally known to generate hydroxyl radical (OH•) as shown below by the Fenton reaction.
Net reaction (Haber-Weiss reaction):
In addition to the above reactions, the following reactions below can also occur:
Hydroxyl radical (OH•) is the most common free radical generated by the oxidation of iron. OH• is capable of reacting with biological molecules such as proteins, lipids and DNA damaging them. When OH• reacts with guanine, a nitrogenous base of nucleic acids, it leads to the generation of 8-oxo-7,8-dihydro-20-deoxyguanosine (8-oxo-dG) and 2,6-diamino-5-formamido-4-hydroxypyrimidine (FAPy-G), in which the former is a good marker for oxidative damage [23].
It is well documented that metal-induced generation of oxygen reactive species can attack polyunsaturated fatty acid such as phospholipids. The first of such observation was first presented by Bucher et al. [24] who showed that iron-generated OH• can oxidize lipid membranes through a process known as lipid peroxidation. Following his experimental observations, he proposed the following mechanism:
Steps of lipid peroxidation:
At the initiation stage, the radical (R•)/OH• attacks the lipid membrane to form a radial lipid. This radical lipid further propagates the formation of peroxyl lipid radical by reacting with dioxygen molecule or with a lipid. This reaction further promotes damage of the lipid molecule. At the termination stage, two radical lipid molecules and/or with a peroxyl lipid radical reacts to form a stable lipid molecule. The major aldehyde product of lipid peroxidation is malondialdehyde and it serves as a marker for lipid peroxidation.
Generally, proteins are not easily damaged by H2O2 and other simple oxidants unless transition metals are present. Thus, protein damaged are usually metal-catalyzed and involves oxidative scission, bityrosine cross links, loss of histidine residues, the introduction of carbonyl groups, and the formation of protein-centered alkyl (R•), alkoxyl (RO•) and alkylperoxyl (ROO•) radicals [25].
Copper ions have been identified to participate in the formation of reactive oxygen species (ROS) as cupric (Cu2+) and cuprous (Cu1+) which can participate in oxidation and reduction reactions. The Cu2+ in the presence of biological reductants such as glutathione (GSH) or ascorbic acid can be reduced to Cu+ which is capable of catalyzing the decomposition of H2O2 to form OH•
The OH• radical formed is capable of reacting with several biomolecules. Experimental studies confirmed that copper is also capable of inducing DNA strand breaks and oxidation of bases
Chromium (Cr), particularly Cr4+ has been shown in
Cobalt (Co), particularly Co2+ has been shown to generate superoxide (•O2−) from the decomposition of H2O2 [30].
Vanadium is a heavy metal that occurs in various oxidative states and has been shown to generate free radical. In the plasma, vanadium (V) is rapidly reduced to vanadium (IV) by NADPH and ascorbic acid antioxidants which bind to plasma proteins for transportation [31].
More so under physiological conditions at approximately pH of 7, V(IV) can generate OH• from the decomposition of H2O2 according to the Fenton reaction.
Arsenic has also been shown to generate free radicals such as superoxide (O2•–), singlet oxygen (1O2), nitric oxide (NO•), hydrogen peroxide (H2O2), the peroxyl radical (ROO•) [32], dimethylarsinic peroxyl radicals ((CH3)2AsOO•) and also the dimethylarsinic radical ((CH3)2As•) [33] in some studies though the mechanism for the generation of all these reactive species remains unclear.
Some heavy metals are known to have carcinogenic effect. Several signaling proteins or cellular regulatory proteins that participate in apoptosis, cell cycle regulation, DNA repair, DNA methylation, cell growth and differentiation are targets of heavy metals [34]. Thus, heavy metals may induce carcinogenic effect by targeting a number of these proteins. More so, the carcinogenic effects of certain heavy metals have been related to the activation of redox-sensitive transcription factors such as AP-1, NF-κB and p53 through the recycling of electrons by antioxidant network. These transcription factors control the expression of protective genes that induce apoptosis, arrest the proliferation of damaged cells, repair damaged DNA and power the immune system [22]. Metal signalization of transcription factor AP-1 and NF-κB has been observed in the mitogen-activated protein (MAP) kinase pathways where the nuclear transcription factor NF-κB, is involved in controlling inflammatory responses while AP-1 is involved in cell growth and differentiation [22]. The p53 protein is an important protein in cell division as it guards a cell-cycle checkpoint and control cell division [35]. Inactivation of p53 allows uncontrolled cell division and thus p53 gene disruption has been associated with most human cancers. Also, AP-1 and NF-κB family of transcription factors are involved in both cell proliferation and apoptosis, and also regulate p53. Heavy metals generated free radicals inside the cell selectively activates these transcription factors and thus, may suggest that cell proliferation or cell death may be related to the exposure to carcinogenic metals. There exist various mechanisms of heavy metal-induced carcinogenesis.
Arsenic-induced carcinogenic mechanisms include epigenetic alterations, damage to the dynamic DNA maintenance system and generation of ROS [36, 37]. Alterations of histones, DNA methylation, and miRNA are the key epigenetic changes induced by arsenic which have shown to possess potentials to cause malignant growth [37]. In vitro studies have shown arsenic to alter the expression of p53 protein which also led to decreased expression of p21, one downstream target [38]. Arsenic compounds have been shown in an
The mechanism of lead-induced carcinogenic process is postulated to induce DNA damage, disrupt DNA repair system and cellular tumor regulatory genes through the generation of ROS [42]. Studies have supported with evidence that ROS generation by lead is key in altering chromosomal structure and sequence [42]. Lead can disrupt transcription processes by replacing zinc in certain regulatory proteins [42].
Little is known on the potential of mercury to act as a mutagen or carcinogen. However, the proposed mechanism of mercury-induced cancer is through the generation of free radicals inducing oxidative stress thereby damaging biomolecules. Mercury has been shown to induce malignant growth through the generation of free radicals as well as disruption of DNA molecular structure, the repair and maintenance system [43].
Nickel has an extensive range of carcinogenic mechanisms which include regulation of transcription factors, controlled expression of certain genes and generation of free radicals. Nickel has been shown to be implicated in regulating the expression of specific long non-coding RNAs, certain mRNAs and microRNAs. Nickel can promote methylation of promoter and induce the down regulation of maternally expressed gene 3 (MEG3) thereby upregulating hypoxia-inducible factor-1α, two proteins which are known to be implicated in carcinogenesis [44]. It has also been demonstrated that nickel can generate free radicals, which contributes to carcinogenic processes [45].
Cadmium has been implicated in promoting apoptosis, oxidative stress, DNA methylation and DNA damage.
The main cause of cancer due to iron intoxication is through the generation of free radicals. A school of thought produced a mechanism for iron-induced cancer whereby bile acids (deoxycholic acid), iron(II) complexes, vitamins K and oxygen interact to generate free radicals which induced oncogenic effect in the colon.
Some heavy metals such as lead and manganese may affect the brain and cause neurological toxicity as reviewed from [46].
Lead toxicity is targeted towards the memory and learning processes of the brain and can be mediated through three processes. Lead can impair learning and memory in the brain by inhibiting the N-methyl-d-aspartate receptor (NMDAR) and can block neurotransmission by inhibit neurotransmitter release, block the neuronal voltage-gated calcium (Ca2+) channels (VGCCs) and reduce the expression of brain-derived neurotrophic factor (BDNF).
The NMDAR is known to enhance learning and memory mediated by the hippocampus [47] as this has been confirmed in animal studies in which animals exposed to lead during its developmental process exhibit similar learning deficits comparable to those with the absence or impaired NMDARs [48, 49]. In the hippocampus, NMDAR is a neural receptor which consists of two or more subunits; an obligatory NR1 subunit and one or more subunits from the NR2 particularly NR2A, NR2B and NR3 families. Lead has been shown to be a potent, non-competitive antagonist of the NMDAR [50, 51, 52, 53], preferentially with high affinity at a regulatory site on the NR2A subunit [54]. This has been further supported in electrophysiological studies in which recombinant receptors for the subunits have shown NR2A-NMDARs to be more potently inhibited by lead than NR2B-NMDARs [55]. More so, lead has been shown to decrease the content of NR2A in the hippocampus and also alter the expression of NR1 spliced variants [56, 57] suggesting lead exposure disrupts the normal ontogeny of NMDAR.
Lead can decrease neurotransmission as long term exposure of rats to low levels of lead has shown reduction in the release of Ca2+-dependent glutamate and γ-aminobutyric acid (GABA) in the hippocampus [58, 59]. This indicates dysfunction of presynaptic neuron signalization in the hippocampus as a result of lead exposure [60]. More so, lead exposure also impairs two postsynaptic currents; inhibitory post synaptic currents (IPSCs) and excitatory post synaptic currents (EPSCs) which are dependent on the release of presynaptic neurotransmitter such as glutamate and GABA. Thus, lead exposure leads to reductions in IPSCs and EPSCs indicating a deficit in glutamatergic and GABAergic neurotransmission systems. Also, lead has been shown to reduce the expression of key presynaptic proteins such as synaptobrevin (Syb) and synaptophysin (Syn) involved in vesicular neurotransmitter release [59, 60]. Lead can disrupt neurotransmission by inhibiting the neuronal voltage-gated calcium (Ca2+) channels (VGCCs) [61]. Thus, inhibition of presynaptic VGCCs may reduce the influx of Ca2+ which is required for fast release of vesicular neurotransmitter thus interfering with neurotransmission. It is now suggested that inhibition of either NMDARs or VGCCs by lead would result in a significant decrease of Ca2+ influx into the cell. Reduction of Ca2+ entry into the cell will prevent neurotransmitter release and thus impair signalization leading to neurological disease states [62, 63]. Lead can also reduce the expression of brain-derived neurotrophic factor (BDNF), a trans-synaptic signaling molecule that is released from both axons and dendrites which is involved in synaptic development and neurotransmitter release [64]. BDNF activity is also dependent on Ca2+ and thus has been implicated in the development of neurological diseases.
Manganese is known to accumulate in the mitochondria of neurons, astrocytes and oligodendrocytes cells and disrupts ATP synthesis [65] by inhibiting the F1/F0 ATP synthase [65] or complex 1 (NADH dehydrogenase) of the mitochondrial respiration chain [66]. More so, it has recently been shown that manganese inhibits ATP synthesis at two sites in the brain mitochondria which are either the glutamate/aspartate exchanger or the complex II (succinate dehydrogenase) depending on the mitochondrial energy source [67]. The disruption of ATP synthesis by manganese leads to decreased intracellular ATP levels and generation of free radicals thereby increasing oxidative stress [68] which may contribute to manganese cellular toxicity [69]. Furthermore, manganese can oxidize dopamine (DA) to react with quinone species thereby disrupting the dopaminergic system (for review, see [70]). This has been shown in animal studies were manganese exposure has led to specific deficits in the dopaminergic system [71]. The DA reactive species are taken up by the dopamine transporter (DAT1) thus causing dopaminergic neurotoxicity [72].
When heavy metals are ingested through food or water into the body, they are acidified by the acid medium of the stomach. In this acidic medium, they are oxidized to their various oxidative states (Zn2+, Cd2+, Pb2+, As2+, As3+, Ag+, Hg2+, etc.) which can readily bind to biological molecules such as proteins and enzymes to form stable and strong bonds. The most common functional group that heavy metals bind is the thio groups (SH group of cysteine and SCH3 group of methionine). Cadmium has been shown to inhibit human thiol transferases such as thioredoxin reductase, glutathione reductase, thioredoxin
Reactions of Heavy metals with sulphydryl groups of proteins or enzymes (A) = Intramolecular bonding; (B) = Intermolecular bonding; P = Protein; E = Enzyme; M = Metal.
In the above reaction, the oxidized heavy metal replaces the hydrogen of the SH group and the methyl of the SCH3 group thereby inhibiting the function of the protein or activity of the enzyme. For example, methylmercury (MeHg) strongly inhibits the activity of l-glutamine d-fructose-6-phosphate amidotransferase in yeast [75].
Heavy metal-bound proteins may be a substrate for certain enzymes. In such situations, the heavy metal-bound protein fits into an enzyme in a highly specific pattern to form an enzyme-substrate complex and thus cannot accommodate any other substrate until it is freed. As such, the product of the substrate is not formed as the enzyme is blocked and therefore, the heavy metal remains embedded in the tissue leading to dysfunctions, abnormalities and damages in the body. Inhibition of thiol transferases lead to increased oxidative stress and cell damage. For example, toxic arsenic present in fungicides, herbicides and insecticides can attack –SH groups in enzymes to inhibit their catalytic activities as shown in Figure 3.
Reaction of arsenic with the thio group of enzymes.
Also, heavy metal toxicity may be induced by the replacement of a metallo-enzyme by another metal ion of similar size. Cadmium displaces zinc and calcium ions from zinc finger proteins and metalloproteins [76, 77]. For instance, cadmium can replace zinc in certain dehydrogenating enzymes, leading to cadmium toxicity. Such replacement can convert the enzyme structurally to an inactive form and completely alter its activity. These heavy metals in their ionic species such as Pb2+, Cd2+, Ag+ Hg2+ and As3+ form very stable biotoxic compounds with proteins and enzymes and are difficult to be dissociated.
Heavy metals may also inhibit protein folding. This was first observed when heavy metals such as cadmium, lead, mercury and arsenite were shown to effectively interfere with the refolding of chemically denatured proteins [78]. It was also observed that when protein misfolded in the presence of heavy metals, the misfolded protein could not be rescued in the presence of reduced glutathione or EDTA chelator. The order of heavy metal in terms of their efficacy in folding inhibition is mercury > cadmium > lead and correlates with the relative stability of their monodentate complexes with imidazole, thiol and carboxylate groups in proteins [79].
Heavy metal may cause proteins to aggregate as arsenite-induced protein aggregation was observed and shown to be concentration-dependent. Also, the aggregates contained a wide variety of proteins enriched in functions related to metabolism, protein folding, protein synthesis and stabilization [79].
Mechanisms of heavy metal intoxication in humans.
Heavy metal toxicity can have several health effects in the body. Heavy metals can damage and alter the functioning of organs such as the brain, kidney, lungs, liver, and blood. Heavy metal toxicity can either be acute or chronic effects. Long-term exposure of the body to heavy metal can progressively lead to muscular, physical and neurological degenerative processes that are similar to diseases such as Parkinson’s disease, multiple sclerosis, muscular dystrophy and Alzheimer’s disease. Also, chronic long-term exposure of some heavy metals may cause cancer [7]. The various health effects of some heavy metals will be highlighted below.
Arsenic exposure can lead to either acute or chronic toxicity. Acute arsenic poisoning can lead to the destruction of blood vessels, gastrointestinal tissue and can affect the heart and brain. Chronic arsenic toxicity which is termed arsenicosis usually focus on skin manifestations such as pigmentation and keratosis [81]. Lower level exposure to arsenic can cause nausea and vomiting, reduced production of erythrocytes and leukocytes and damage blood vessels, cause abnormal heart beat and pricking sensation in hands and legs. Long-term exposure can lead to the formation of skin lesions, pulmonary disease, neurological problems, peripheral vascular disease, diabetes mellitus, hypertension and cardiovascular disease [82]. Chronic arsenicosis may results to irreversible changes in the vital organs and possibly lead to death. Also, chronic arsenic exposure can promote the development of a number of cancers which include skin cancer, cancers of the bladder, lung, liver (angiosarcoma), and possibly the colon and kidney cancers [82]. Recently in the United States, the tolerable amount of arsenic in drinking water is 50 μg/liter but there is much concern of lowering this standard dose of population exposures to arsenic as the present dose is believed to increase the risk for cancer. Most environmental scientists studying this problem are of the view that the current tolerable limit of arsenic in drinking water or food be reduced.
Toxicity due to lead exposure is called lead poisoning. Lead poisoning is mostly related to the gastrointestinal tract and central nervous system in children and adults [83]. Lead poisoning can be either acute or chronic. Acute exposure of lead can cause headache, loss of appetite, abdominal pain, fatigue, sleeplessness, hallucinations, vertigo, renal dysfunction, hypertension and arthritis while chronic exposure can result in birth defects, mental retardation, autism, psychosis, allergies, paralysis, weight loss, dyslexia, hyperactivity, muscular weakness, kidney damage, brain damage, coma and may even cause death [81]. Although lead poisoning is preventable, it still remains a dangerous disease as it can affect most of the organs of the body. Exposure to elevated levels of lead can cause the plasma membrane of the blood brain barrier to move into the interstitial spaces leading to edema [84]. Also, lead exposure can disrupt the intracellular second messenger systems and alter the functioning of the central nervous system. Developing fetuses and children are most vulnerable to neurotoxic effects due to lead exposure. A number of prospective epidemiologic studies in children less than 5 years of age have shown that low-level of lead exposure (5–25 μg/dL in blood) resulted to the impairment of intellectual development which was manifested by the lost of intelligence quotient points [85]. As such, the Centers for Disease Control (CDC) in the United States has reduced the tolerable amount of lead in children’s blood from 25 to 10 μg/dL and recommended universal screening of blood lead for all children.
Mercury is an element that can easily combine with other elements to form inorganic and organic mercury. Exposure to elevated levels of metallic, inorganic and organic mercury can damage the kidney, brain and developing fetus [86] while methyl mercury is highly carcinogenic. Organic mercury is lipophilic in nature and thus can easily penetrate cell membranes. Mercury and its compound affects the nervous system and thus increased exposure of mercury can alter brain functions and lead to tremors, shyness, irritability, memory problems and changes in hearing or vision. Short-term exposure to metallic mercury vapors at higher levels can lead to vomiting, nausea, skin rashes, diarrhea, lung damage, high blood pressure, etc. while short-term exposure to organic mercury poisoning can lead to depression, tremors, headache, fatigue, memory problems, hair loss, etc. Since these symptoms are also common in other illness or disease conditions, diagnosis of mercury poisoning may be difficult in such cases [81]. Chronic levels of mercury exposure can lead to erethism, a disease condition characterized by excitability, tremor of the hands, memory loss, timidity, and insomnia. Also, occupational exposure to mercury as observed by researchers has been associated with measurable declines in performance on neurobehavioral tests of motor speed, visual scanning, visuomotor coordination, verbal and visual memory. Dimethylmercury is a very toxic compound that can penetrate the skin through latex gloves and its exposure at very low dose can cause the degeneration of the central nervous system and death. Mercury exposure to pregnant women can affect the fetus and offspring may suffer from mental retardation, cerebellar symptoms, retention of primitive reflexes, malformation and other abnormalities [87]. This has been confirmed in recent studies in which pregnant women exposed to mercury through dietary intake of whale meat and fish showed reduce motor neuron function, loss of memory, impaired speech and neural transmission in their offspring.
Cadmium and its compounds have several health effects in humans. The health effects of cadmium exposure are exacerbated due to the inability of the human body to excrete cadmium. In fact, cadmium is re-absorbed by the kidney thereby limiting its excretion. Short-term exposure to inhalation of cadmium can cause severe damages to the lungs and respiratory irritation while its ingestion in higher dose can cause stomach irritation resulting to vomiting and diarrhea. Long-term exposure to cadmium leads to its deposition in bones and lungs. As such, cadmium exposure can cause bone and lung damage [88]. Cadmium can cause bone mineralization as studies on animals and humans have revealed osteoporosis (skeletal damage) due to cadmium. It has been observed that “Itai-itai” disease, an epidemic of bone fractures in Japan is due to cadmium contamination [89]. Increased cadmium toxicity in this population was found to be associated with increased risk of bone fractures in women, as well as decreased bone density and height loss in males and females. Cadmium is highly toxic to the kidney and it accumulates in the proximal tubular cells in higher concentrations. Thus, cadmium exposure can cause renal dysfunction and kidney disease. Also, cadmium exposure can cause disturbances in calcium metabolism, formation of renal stones and hypercalciuria. Cadmium is also classified as group 1 carcinogens for humans by the International Agency for Research on Cancer. Tobacco is the main source of cadmium uptake in smokers and thus, smokers are more susceptible to cadmium intoxication than non-smokers [90]. Also, cadmium can cause testicular degeneration and a potential risk factor for prostate cancer.
Chromium, in its hexavalent form, is the most toxic species of chromium though some other species such as Chromium (III) compounds are much less toxic and cause little or no health problems. Chromium (VI) has the tendency to be corrosive and also to cause allergic reactions to the body. Therefore, breathing high levels of chromium (VI) can cause irritation to the lining of the nose and nose ulcers. It can also cause anemia, irritations and ulcers in the small intestine and stomach, damage sperm and male reproductive system. The allergic reactions due to chromium include severe redness and swelling of the skin. Exposure of extremely high doses of chromium (VI) compounds to humans can result in severe cardiovascular, respiratory, hematological, gastrointestinal, renal, hepatic, and neurological effects and possibly death [91]. Exposure to chromium compounds can result in the formation of ulcers such as nasal septum ulcer which are very common in chromate workers. Exposure to higher amounts of chromium compounds in humans can lead to the inhibition of erythrocyte glutathione reductase, which in turn lowers the capacity to reduce methemoglobin to hemoglobin.
Iron salts such as iron sulfate, iron sulfate heptahydrate and iron sulfate monohydrate are of low acute toxicity when exposure is through dermal, oral and inhalation routes. However, other forms of iron are of serious health problems. Iron toxicity occurs in four stages. The first stage which commences 6 h after iron overdose is marked by gastrointestinal effects such as vomiting, diarrhea and gastro-intestinal bleeding. The progression to the second stage occurs 6–24 h after an overdose and it is considered as a latent period of apparent medical recovery. The third stage commences between 12 and 96 h after the onset of clinical symptoms and is characterized by hypotension, shocks, lethargy, hepatic necrosis, tachycardia, metabolic acidosis and may sometimes lead to death [93]. The fourth and final stage usually occurs within 2–6 weeks of iron overdose. This stage is marked by the development of strictures and formation of gastrointestinal ulcerations. Meat is rich in iron and thus meat eating countries are at risk of cancer as excess iron uptake increases the risk of cancer. Asbestos contains about 30% of iron and thus workers who are highly exposed to asbestos are at high risk of asbestosis, a condition which is known to cause lung cancer. Iron is known to generate free radicals which are suggested to be responsible for asbestos related cancer. Iron-induced free radicals can initiate cancer by the oxidation of DNA leading to DNA damage [94].
Although manganese is an essential metal for the body, it recently became a metal of global concern when methylcyclopentadienyl manganese tricarbonyl (MMT), which was known to be toxic was introduced as a gasoline additive. MMT has been claimed to be an occupational manganese hazard and linked with the development of Parkinson’s disease-like syndrome of tremour, gait disorder, postural instability, and cognitive disorder [95]. Exposure to elevated levels of manganese can result in neurotoxicity. Manganism is a neurological disease due to manganese characterized by rigidity, action tremour, a mask-like expression, gait disturbances, bradykinesia, micrographia, memory and cognitive dysfunction, and mood disorder [96]. The symptoms of manganism are very similar to that of Parkinson disease. However, the main differences between manganism and Parkinson disease is the insensitivity of manganism to levodopa (l-DOPA) administration and also the differences in the symptoms and progression of the disease [97].
The exposure of heavy metals to humans involve various diverse forms through food and water consumption, inhalation of polluted air, skin contact and most important by occupational exposure at workplace. Though some heavy metals such as iron and manganese are essential for certain biochemical and physiological activities in the body, elevated level in the body can have delirious health effects. Most of the other heavy metals are generally toxic to the body at very low level. The main mechanism of heavy metal toxicity include the generation of free radicals to cause oxidative stress, damage of biological molecules such as enzymes, proteins, lipids, and nucleic acids, damage of DNA which is key to carcinogenesis as well as neurotoxicity. Some of the heavy metal toxicity could be acute while others could be chronic after long-term exposure which may lead to the damage of several organs in the body such as the brain, lungs, liver, and kidney causing diseases in the body.
Benzimidazole is bicyclic heterocyclic aromatic compound in which benzene ring fused to 4 and 5 position of imidazole ring, it contain two nitrogen atoms at 1 and 3 position exhibit both acidic and basic nature called amphotericin nature and exists in two equivalent tautomeric forms, when the hydrogen present at first position nitrogen atom possess acidic nature, when the hydrogen present at third position nitrogen atom possess basic nature (Figures 1) [1]. Benzimidazole is a very important important pharmacophore among all the heterocyclic compounds due to its important pharmacological activities like anti-Alzheimer [2], antibacterial [3], anti cancer [4], anti-diabetic [5], antifungal [6], anti HIV [7], anti leishmanial [8], anti inflammatory [9], analgesic [9], anti malarial [10], anti microbial [11] and anti tubercular [12] activity, there are many benzimidazole derivatives are using to treat many diseases, few presently marketing drugs contain benzimidazole moiety are the bezitramide using as an analgesic, ridinilazole sing as antibacterial, the candesartan, mibefradil using as antihypertensive drugs, mebendazole, albendazole, thiabendazole, and flubendazole usng as antihelminthics, astemizole, bilastine using as antihistamines, pantoprazole, lansoprazole, esomeprazole, ilaprazole using as proton pump inhibitors, bendamustine, selumetinib, galeterone, pracinostat using as antitumor agents and enviradine, samatasvir, and maribavir using as antiviral agents (Figures 2) [13, 14, 15, 16, 17].
Chemistry of benzimidazole [
Structures of marketing drugs containing benzimidazole moiety [
In the year of 2019 Tahlan et al., reported the synthesis and anti cancer activity of the new benzimidazole derivatives, among all the derivatives the compound
Structures of effective anticancer compounds.
In 2015 few authors worked on synthesis of benzimidazole and evaluated the nti-cancer activit, the Gao et al., reported the compound
In 2014 Yoon et al., evaluated the anti cancer activity of synthesized novel benzimidazole derivatives, the compounds
Structures of effective anticancer compounds.
In 2013 Sharma et al., reported the anti cancer activity of synthesized the benzimidazole quinazoline hybrids, the compound
In the year of 2020 Srivastava et al., reported the synthesis and anti HIV activity of the new benzimidazole derivatives, among all the derivatives the compound
Structures of effective anti-HIV compounds.
M. Tonelli et al., reported the antileishmanial activity of newly synthesized benzimidazole derivatives, among all the derivatives compound
Structures of effective anti-leishmanial compounds.
In the year of 2019 S. Manivannan et al., reported the synthesis anti tubercular activity of benzimidazole derivatives, among all the derivatives compound
Structures of effective anti-tubercular compounds.
Structures of effective anti-tubercular compounds.
In the year of 2014 many authors reported the anti tubercular activity of synthesized the new benzimidazole derivatives, Gong et al., reported the compound
In the year of 2013 also many authors evaluated the anti tubercular activity of newly synthesized benzimidazole derivatives, Nandha et al., reported the compound
Structures of effective anti-tubercular compounds.
In 2012 Patel et al., reported the anti tubercular activity of synthesized the benzimidazolyl-1,3,4-oxadiazol-2ylthio-
Structures of effective anti-tubercular compounds.
In 2011 few authors reported the anti tubercular activity of synthesized benzimidaoles, Saleshier et al., reported the compounds
The benimidazole plays in important role in the field of medicinal chemistry, many of the marketing drugs contain benzimidazole moiety are using to illness. In recent medicinal chemistry research the benzimidazole derivatives are in continuous development with many pharmacological activities such as anti-cancer, anti-HIV, anti-leishmanial, anti-tubercular, anti-malarial, anti-inflammatory, anti-diabetic, and so on, to meet pharmacological requirement. The present literature may helpful to researcher, medicinal chemist, pharmacologist to design, to synthesize, to develop pharmacologically active benzimidazole derivatives with low toxicity in future.
All the authors are thankful to managements of respective colleges for providing facilities to carry out the work.
The authors declare no conflict of interest.
Mahender Thatikayala contributed the chemistry, anti cancer, anti leishmanial and anti tubercular activity of benzimidazoles. Anil Kumar Garige, Hemalatha Gadegoni contributed the chemistry and anti HIV activity of benzimidazoles.
No funding applicable.
IntechOpen implements a robust policy to minimize and deal with instances of fraud or misconduct. As part of our general commitment to transparency and openness, and in order to maintain high scientific standards, we have a well-defined editorial policy regarding Retractions and Corrections.
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\\n\\n3. CORRECTIONS
\\n\\nA Correction will be issued by the Academic Editor when:
\\n\\n3.1. ERRATUM
\\n\\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
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\\n\\n4. FINAL REMARKS
\\n\\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\\n\\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\\n\\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
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\\n\\nPolicy last updated: 2017-09-11
\\n"}]'},components:[{type:"htmlEditorComponent",content:'IntechOpen’s Retraction and Correction Policy has been developed in accordance with the Committee on Publication Ethics (COPE) publication guidelines relating to scientific misconduct and research ethics:
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\n\nA Retraction of a Chapter will be issued by the Academic Editor, either following an Author’s request to do so or when there is a 3rd party report of scientific misconduct. Upon receipt of a report by a 3rd party, the Academic Editor will investigate any allegations of scientific misconduct, working in cooperation with the Author(s) and their institution(s).
\n\nA formal Retraction will be issued when there is clear and conclusive evidence of any of the following:
\n\nPublishing of a Retraction Notice will adhere to the following guidelines:
\n\n1.2. REMOVALS AND CANCELLATIONS
\n\n2. STATEMENTS OF CONCERN
\n\nA Statement of Concern detailing alleged misconduct will be issued by the Academic Editor or publisher following a 3rd party report of scientific misconduct when:
\n\nIntechOpen believes that the number of occasions on which a Statement of Concern is issued will be very few in number. In all cases when such a decision has been taken by the Academic Editor the decision will be reviewed by another editor to whom the author can make representations.
\n\n3. CORRECTIONS
\n\nA Correction will be issued by the Academic Editor when:
\n\n3.1. ERRATUM
\n\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
\n\nA published Erratum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n3.2. CORRIGENDUM
\n\nA Corrigendum will be issued by the Academic Editor when it is determined that a mistake in a Chapter is a result of an Author’s miscalculation or oversight. A published Corrigendum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n4. FINAL REMARKS
\n\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\n\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\n\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
\n\nAny suggestions or comments on this Policy are welcome and may be sent to permissions@intechopen.com.
\n\nPolicy last updated: 2017-09-11
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The particle reveals interesting properties at the dimension below 100 nm, mostly from two physical effects. The two physical effects are the quantization of electronic states apparent leading to very sensitive size-dependent effects such as optical and magnetic properties and the high surface-to-volume ratio modifies the thermal, mechanical, and chemical properties of materials. The nanoparticles’ unique physical and chemical properties render them most appropriate for a number of specialist applications.",book:{id:"9109",slug:"engineered-nanomaterials-health-and-safety",title:"Engineered Nanomaterials",fullTitle:"Engineered Nanomaterials - Health and Safety"},signatures:"Takalani Cele",authors:[{id:"305934",title:"Dr.",name:"Takalani",middleName:null,surname:"Cele",slug:"takalani-cele",fullName:"Takalani Cele"}]},{id:"62151",title:"Proton Exchange Membrane Water Electrolysis as a Promising Technology for Hydrogen Production and Energy Storage",slug:"proton-exchange-membrane-water-electrolysis-as-a-promising-technology-for-hydrogen-production-and-en",totalDownloads:3255,totalCrossrefCites:3,totalDimensionsCites:13,abstract:"Proton exchange membrane (PEM) electrolysis is industrially important as a green source of high-purity hydrogen, for chemical applications as well as energy storage. Energy capture as hydrogen via water electrolysis has been gaining tremendous interest in Europe and other parts of the world because of the higher renewable penetration on their energy grid. Hydrogen is an appealing storage medium for excess renewable energy because once stored, it can be used in a variety of applications including power generation in periods of increased demand, supplementation of the natural gas grid for increased efficiency, vehicle fueling, or use as a high-value chemical feedstock for green generation of fertilizer and other chemicals. Today, most of the cost and energy use in PEM electrolyzer manufacturing is contributed by the cell stack manufacturing processes. Current state-of-the-art electrolysis technology involves two options: liquid electrolyte and ion exchange membranes. Membrane-based systems overcome many of the disadvantages of alkaline liquid systems, because the carrier fluid is deionized water, and the membrane-based cell design enables differential pressure operation.",book:{id:"7325",slug:"nanostructures-in-energy-generation-transmission-and-storage",title:"Nanostructures in Energy Generation, Transmission and Storage",fullTitle:"Nanostructures in Energy Generation, Transmission and Storage"},signatures:"Radenka Maric and Haoran Yu",authors:null},{id:"72636",title:"Nanocomposite Materials",slug:"nanocomposite-materials",totalDownloads:2139,totalCrossrefCites:5,totalDimensionsCites:10,abstract:"Nanocomposites are the heterogeneous/hybrid materials that are produced by the mixtures of polymers with inorganic solids (clays to oxides) at the nanometric scale. Their structures are found to be more complicated than that of microcomposites. They are highly influenced by the structure, composition, interfacial interactions, and components of individual property. Most popularly, nanocomposites are prepared by the process within in situ growth and polymerization of biopolymer and inorganic matrix. With the rapid estimated demand of these striking potentially advanced materials, make them very much useful in various industries ranging from small scale to large to very large manufacturing units. With a great deal to mankind with environmental friendly, these offer advanced technologies in addition to the enhanced business opportunities to several industrial sectors like automobile, construction, electronics and electrical, food packaging, and technology transfer.",book:{id:"10072",slug:"nanotechnology-and-the-environment",title:"Nanotechnology and the Environment",fullTitle:"Nanotechnology and the Environment"},signatures:"Mousumi Sen",authors:[{id:"310218",title:"Dr.",name:"Mousumi",middleName:null,surname:"Sen",slug:"mousumi-sen",fullName:"Mousumi Sen"}]},{id:"64843",title:"Polymer Nanocomposites with Different Types of Nanofiller",slug:"polymer-nanocomposites-with-different-types-of-nanofiller",totalDownloads:4028,totalCrossrefCites:19,totalDimensionsCites:52,abstract:"The development of polymer nanocomposites has been an area of high scientific and industrial interest in the recent years, due to several improvements achieved in these materials, as a result of the combination of a polymeric matrix and, usually, an inorganic nanomaterial. The improved performance of those materials can include mechanical strength, toughness and stiffness, electrical and thermal conductivity, superior flame retardancy and higher barrier to moisture and gases. Nanocomposites can also show unique design possibilities, which offer excellent advantages in creating functional materials with desired properties for specific applications. The possibility of using natural resources and the fact of being environmentally friendly have also offered new opportunities for applications. This chapter aims to review the main topics and recent progresses related to polymer nanocomposites, such as techniques of characterization, methods of production, structures, compatibilization and applications. First, the most important concepts about nanocomposites will be presented. Additionally, an approach on the different types of filler that can be used as reinforcement in polymeric matrices will be made. After that, sections about methods of production and structures of nanocomposites will be detailed. Finally, some properties and potential applications that have been achieved in polymer nanocomposites will be highlighted.",book:{id:"6854",slug:"nanocomposites-recent-evolutions",title:"Nanocomposites",fullTitle:"Nanocomposites - Recent Evolutions"},signatures:"Amanda Dantas de Oliveira and Cesar Augusto Gonçalves Beatrice",authors:[{id:"249768",title:"Ph.D.",name:"Amanda",middleName:null,surname:"Oliveira",slug:"amanda-oliveira",fullName:"Amanda Oliveira"},{id:"254512",title:"Ph.D.",name:"Cesar",middleName:"Augusto Gonçalves",surname:"Beatrice",slug:"cesar-beatrice",fullName:"Cesar Beatrice"}]},{id:"38951",title:"Carbon Nanotube Transparent Electrode",slug:"carbon-nanotube-transparent-electrode",totalDownloads:3985,totalCrossrefCites:3,totalDimensionsCites:5,abstract:null,book:{id:"3077",slug:"syntheses-and-applications-of-carbon-nanotubes-and-their-composites",title:"Syntheses and Applications of Carbon Nanotubes and Their Composites",fullTitle:"Syntheses and Applications of Carbon Nanotubes and Their Composites"},signatures:"Jing Sun and Ranran Wang",authors:[{id:"153508",title:"Prof.",name:"Jing",middleName:null,surname:"Sun",slug:"jing-sun",fullName:"Jing Sun"},{id:"153596",title:"Ms.",name:"Ranran",middleName:null,surname:"Wang",slug:"ranran-wang",fullName:"Ranran Wang"}]}],onlineFirstChaptersFilter:{topicId:"17",limit:6,offset:0},onlineFirstChaptersCollection:[{id:"81463",title:"Perovskite-Based Nanomaterials and Nanocomposites for Photocatalytic Decontamination of Water",slug:"perovskite-based-nanomaterials-and-nanocomposites-for-photocatalytic-decontamination-of-water",totalDownloads:15,totalDimensionsCites:0,doi:"10.5772/intechopen.102824",abstract:"The exploration of functional nanomaterials with superior catalytic activity for practical photocatalytic water decontamination is of significant importance. Perovskite-based nanomaterials, which demonstrate excellent photophysical and catalytic properties, are widely investigated as a class of adaptable materials for the photocatalytic degradation of environmental pollutants. This chapter introduces the recent progresses in using perovskite-based nanocomposites with particular emphasis on the applications for effective photocatalytic degradation of organic pollutants in wastewater. It starts by presenting the general principles and mechanisms governing photocatalytic degradation of organic pollutants in water by perovskite, along with the design criteria for perovskite-based nanocomposites. It then explains various strategies used to prepare perovskite-based nanocomposites with the aim of enhancing their photocatalytic activity. By the end of the chapter, the remaining challenges and perspectives for developing efficient perovskite-based photocatalysts with potential large-scale application are highlighted.",book:{id:"10825",title:"Nanocomposite Materials",coverURL:"https://cdn.intechopen.com/books/images_new/10825.jpg"},signatures:"Yousef Faraj and Ruzhen Xie"},{id:"81438",title:"Research Progress of Ionic Thermoelectric Materials for Energy Harvesting",slug:"research-progress-of-ionic-thermoelectric-materials-for-energy-harvesting",totalDownloads:17,totalDimensionsCites:0,doi:"10.5772/intechopen.101771",abstract:"Thermoelectric material is a kind of functional material that can mutually convert heat energy and electric energy. It can convert low-grade heat energy (less than 130°C) into electric energy. Compared with traditional electronic thermoelectric materials, ionic thermoelectric materials have higher performance. The Seebeck coefficient can generate 2–3 orders of magnitude higher ionic thermoelectric potential than electronic thermoelectric materials, so it has good application prospects in small thermoelectric generators and solar power generation. According to the thermoelectric conversion mechanism, ionic thermoelectric materials can be divided into ionic thermoelectric materials based on the Soret effect and thermocouple effect. They are widely used in pyrogen batteries and ionic thermoelectric capacitors. The latest two types of ionic thermoelectric materials are in this article. The research progress is explained, and the problems and challenges of ionic thermoelectric materials and the future development direction are also put forward.",book:{id:"10037",title:"Thermoelectricity - Recent Advances, New Perspectives and Applications",coverURL:"https://cdn.intechopen.com/books/images_new/10037.jpg"},signatures:"Jianwei Zhang, Ying Xiao, Bowei Lei, Gengyuan Liang and Wenshu Zhao"},{id:"81267",title:"Modern State of the Conventional DFT Method Studies and the Limits Following from the Quantum State of the System and Its Total Spin",slug:"modern-state-of-the-conventional-dft-method-studies-and-the-limits-following-from-the-quantum-state-",totalDownloads:11,totalDimensionsCites:0,doi:"10.5772/intechopen.102670",abstract:"At present, the density functional theory (DFT) approach became the most widely used method for study molecules and solids. In the atmosphere of such great popularity, it is particularly important to know the limits of the applicability of DFT methods. In this chapter, I will discuss the modern state of DFT studies basing on the last publications and will consider in detail two cases when the conventional DFT approaches, in which used only electron density and its modifications by gradients, cannot be applied. First, the case related to the total spin S of the state. As I rigorously proved for an arbitrary N-electron state by group theoretical methods, the electron density does not depend on the total spin S of the state. From this follows that the Kohn-Sham equations have the same form for states with different S. The critical survey of elaborated DFT procedures, in which the spin is taken into account, shows that they modified only exchange functionals, and the correlation functionals do not correspond to the spin of the state. The point is that the conception of spin in principle cannot be defined in the framework of the electron density formalism, and this is the main reason of the problems arising in the study by DFT approaches the magnetic properties of the transition metals. The possible way of resolving spin problems can be found in the two-particle reduced density matrix formulation of DFT. In the end, it will be considered the case of the degenerated states, in which, as follows from the adiabatic approximation, the electron density may not be defined, since electronic and nuclear motions cannot be separated, since, the vibronic interaction mixed them.",book:{id:"11001",title:"Density Functional Theory - Recent Advances, New Perspectives and Applications",coverURL:"https://cdn.intechopen.com/books/images_new/11001.jpg"},signatures:"Ilya G. Kaplan"},{id:"80666",title:"Improved Nanocomposite Materials and Their Applications",slug:"improved-nanocomposite-materials-and-their-applications",totalDownloads:20,totalDimensionsCites:0,doi:"10.5772/intechopen.102538",abstract:"Nanotechnologies and nanocomposite materials have gained the attention of scientific community in recent years. Nanocomposite material consists of several phases where at least one, two, or three dimensions are in the nanometer range. Nanocomposites with advanced carbon nanostructures i.e., carbon nanotube (CNTs) and graphene, attachments have been regarded as promising prospects. CNTs and graphene-based improved nanocomposites are usually categorized into various classes based on different types of discontinues phases. The nanocomposites reinforced with carbon nanomaterials i.e., CNTs and graphene have been explored extensively for use as engineering materials in several demanding applications because of their excellent properties. The present book chapter has been prepared in three main sections. In the first portion, nanocomposites and carbon nanofillers i.e., CNTS and graphene have been presented. In the second part, different types of CNTs and graphene-based improved nanocomposites have been described with reported literature. In the third section, focus is on the applications of improved nanocomposites such as energy storage, antimicrobial activity, gene delivery, catalyzed organic reactions, radar adsorbing materials, actuators, wind turbine blades, pollutant removal, aerospace industry, and conductive plastics.",book:{id:"10825",title:"Nanocomposite Materials",coverURL:"https://cdn.intechopen.com/books/images_new/10825.jpg"},signatures:"Tahira Mahmood, Abid Ullah and Rahmat Ali"},{id:"80239",title:"Graphene Related Materials and Composites: Strategies and Their Photocatalytic Applications in Environmental Remediation",slug:"graphene-related-materials-and-composites-strategies-and-their-photocatalytic-applications-in-enviro",totalDownloads:41,totalDimensionsCites:0,doi:"10.5772/intechopen.102404",abstract:"Photochemical reactions hold great promise in solving energy and environment related problems and likely contribute towards development of sustainable society. Despite of recent advancements, the inherent catalytic efficiency of conventional photocatalyst has been severely limited by myriad complexity associated with (i) ineffective light absorption in visible region, (ii) unproductive recombination’s of e−/h+ pair in excited state, and (iii) low chemical stability. Contemporary researches on photocatalysts that can be viable for commercial applications has yet to be realized. Graphene has attracted an immense research interests to enhancing the photocatalysts efficiency endowing from their unique optical and electronic properties and salient features such as surface area, mechanical strength and photochemical stability. In this book chapter, we discussed graphene related material (GRMs) to produce hybrid architectures or nanocomposites that can be used as efficient photocatalysts for the degradation of organic pollutants (dyes, pharmaceutical wastes, pesticides etc.) in wastewater. Lastly, we summarize the key insights in photocatalytic electron transfer mechanism, challenges and future perspective which help understand the rationale of GRMs in this field.",book:{id:"10825",title:"Nanocomposite Materials",coverURL:"https://cdn.intechopen.com/books/images_new/10825.jpg"},signatures:"Santosh S. Patil, Lakshmana Reddy Nagappagari, Ganesh Kamble, Diksha E. Shinde and Kiyoung Lee"},{id:"80751",title:"Ferromagnetism in Mn and Fe Doped LuN: A Potential Candidate for Spintronic Application",slug:"ferromagnetism-in-mn-and-fe-doped-lun-a-potential-candidate-for-spintronic-application",totalDownloads:42,totalDimensionsCites:0,doi:"10.5772/intechopen.99774",abstract:"Diluted magnetic semiconductor (DMS) materials have gained a lot of attention in the last decade due to their possible use in spintronics. In this chapter, the effect of transition metal (TM) i.e., Mn and Fe doping on the structural, electronic, magnetic as well as optical properties of pure and doped LuN has been presented from the first principles density functional theory (DFT) calculation with the Perdew-Burke-Ernzerhof-generalized gradient approximation (PBE-GGA) and Tran Blaha modified Becke-Johnson potential (TB-mBJ) as correlation potentials. The predicted Curie temperature is expected to be greater than room temperature in order to better understand the ferromagnetic phase stability, which has also been confirmed through the formation and cohesive energies. The calculated lattice constants for perfect LuN (rock-salt structure) are in good agreement with the experimental values. Interestingly, doping of Mn and Fe on pure LuN displays indirect band gap to a direct band gap with half metallic and metallic character. The detailed analyses combined with density of state calculations support the assignment that the Half-magnetism and magnetism are closely related to the impurity band at the origin of the hybridization of transition states in the Mn-doped LuN. Absorption spectra are blue shifted upon increase in dopant contents and absorption peaks are more pronounced in UV region. The refractive index and dielectric constant show increase in comparison to the pure LuN. According to the Penn’s model, the predicted band gaps and static actual dielectric constants vary. 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His research interest focuses on computational chemistry and molecular modeling of diverse systems of pharmacological, food, and alternative energy interests by resorting to DFT and Conceptual DFT. He has authored a coauthored more than 255 peer-reviewed papers, 32 book chapters, and 2 edited books. He has delivered speeches at many international and domestic conferences. He serves as a reviewer for more than eighty international journals, books, and research proposals as well as an editor for special issues of renowned scientific journals.",institutionString:"Centro de Investigación en Materiales Avanzados",institution:{name:"Centro de Investigación en Materiales Avanzados",country:{name:"Mexico"}}},{id:"76477",title:"Prof.",name:"Mirza",middleName:null,surname:"Hasanuzzaman",slug:"mirza-hasanuzzaman",fullName:"Mirza Hasanuzzaman",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/76477/images/system/76477.png",biography:"Dr. Mirza Hasanuzzaman is a Professor of Agronomy at Sher-e-Bangla Agricultural University, Bangladesh. He received his Ph.D. in Plant Stress Physiology and Antioxidant Metabolism from Ehime University, Japan, with a scholarship from the Japanese Government (MEXT). Later, he completed his postdoctoral research at the Center of Molecular Biosciences, University of the Ryukyus, Japan, as a recipient of the Japan Society for the Promotion of Science (JSPS) postdoctoral fellowship. He was also the recipient of the Australian Government Endeavour Research Fellowship for postdoctoral research as an adjunct senior researcher at the University of Tasmania, Australia. Dr. Hasanuzzaman’s current work is focused on the physiological and molecular mechanisms of environmental stress tolerance. Dr. Hasanuzzaman has published more than 150 articles in peer-reviewed journals. He has edited ten books and written more than forty book chapters on important aspects of plant physiology, plant stress tolerance, and crop production. According to Scopus, Dr. Hasanuzzaman’s publications have received more than 10,500 citations with an h-index of 53. He has been named a Highly Cited Researcher by Clarivate. He is an editor and reviewer for more than fifty peer-reviewed international journals and was a recipient of the “Publons Peer Review Award” in 2017, 2018, and 2019. He has been honored by different authorities for his outstanding performance in various fields like research and education, and he has received the World Academy of Science Young Scientist Award (2014) and the University Grants Commission (UGC) Award 2018. He is a fellow of the Bangladesh Academy of Sciences (BAS) and the Royal Society of Biology.",institutionString:"Sher-e-Bangla Agricultural University",institution:{name:"Sher-e-Bangla Agricultural University",country:{name:"Bangladesh"}}},{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",slug:"kusal-das",fullName:"Kusal Das",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSBDeQAO/Profile_Picture_1623411145568",biography:"Kusal K. Das is a Distinguished Chair Professor of Physiology, Shri B. M. Patil Medical College and Director, Centre for Advanced Medical Research (CAMR), BLDE (Deemed to be University), Vijayapur, Karnataka, India. Dr. Das did his M.S. and Ph.D. in Human Physiology from the University of Calcutta, Kolkata. His area of research is focused on understanding of molecular mechanisms of heavy metal activated low oxygen sensing pathways in vascular pathophysiology. He has invented a new method of estimation of serum vitamin E. His expertise in critical experimental protocols on vascular functions in experimental animals was well documented by his quality of publications. He was a Visiting Professor of Medicine at University of Leeds, United Kingdom (2014-2016) and Tulane University, New Orleans, USA (2017). For his immense contribution in medical research Ministry of Science and Technology, Government of India conferred him 'G.P. Chatterjee Memorial Research Prize-2019” and he is also the recipient of 'Dr.Raja Ramanna State Scientist Award 2015” by Government of Karnataka. He is a Fellow of the Royal Society of Biology (FRSB), London and Honorary Fellow of Karnataka Science and Technology Academy, Department of Science and Technology, Government of Karnataka.",institutionString:"BLDE (Deemed to be University), India",institution:null},{id:"243660",title:"Dr.",name:"Mallanagouda Shivanagouda",middleName:null,surname:"Biradar",slug:"mallanagouda-shivanagouda-biradar",fullName:"Mallanagouda Shivanagouda Biradar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/243660/images/system/243660.jpeg",biography:"M. S. Biradar is Vice Chancellor and Professor of Medicine of\nBLDE (Deemed to be University), Vijayapura, Karnataka, India.\nHe obtained his MD with a gold medal in General Medicine and\nhas devoted himself to medical teaching, research, and administrations. He has also immensely contributed to medical research\non vascular medicine, which is reflected by his numerous publications including books and book chapters. Professor Biradar was\nalso Visiting Professor at Tulane University School of Medicine, New Orleans, USA.",institutionString:"BLDE (Deemed to be University)",institution:{name:"BLDE University",country:{name:"India"}}},{id:"289796",title:"Dr.",name:"Swastika",middleName:null,surname:"Das",slug:"swastika-das",fullName:"Swastika Das",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/289796/images/system/289796.jpeg",biography:"Swastika N. Das is Professor of Chemistry at the V. P. Dr. P. G.\nHalakatti College of Engineering and Technology, BLDE (Deemed\nto be University), Vijayapura, Karnataka, India. She obtained an\nMSc, MPhil, and PhD in Chemistry from Sambalpur University,\nOdisha, India. Her areas of research interest are medicinal chemistry, chemical kinetics, and free radical chemistry. She is a member\nof the investigators who invented a new modified method of estimation of serum vitamin E. She has authored numerous publications including book\nchapters and is a mentor of doctoral curriculum at her university.",institutionString:"BLDEA’s V.P.Dr.P.G.Halakatti College of Engineering & Technology",institution:{name:"BLDE University",country:{name:"India"}}},{id:"248459",title:"Dr.",name:"Akikazu",middleName:null,surname:"Takada",slug:"akikazu-takada",fullName:"Akikazu Takada",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/248459/images/system/248459.png",biography:"Akikazu Takada was born in Japan, 1935. After graduation from\nKeio University School of Medicine and finishing his post-graduate studies, he worked at Roswell Park Memorial Institute NY,\nUSA. He then took a professorship at Hamamatsu University\nSchool of Medicine. In thrombosis studies, he found the SK\npotentiator that enhances plasminogen activation by streptokinase. He is very much interested in simultaneous measurements\nof fatty acids, amino acids, and tryptophan degradation products. By using fatty\nacid analyses, he indicated that plasma levels of trans-fatty acids of old men were\nfar higher in the US than Japanese men. . He also showed that eicosapentaenoic acid\n(EPA) and docosahexaenoic acid (DHA) levels are higher, and arachidonic acid\nlevels are lower in Japanese than US people. By using simultaneous LC/MS analyses\nof plasma levels of tryptophan metabolites, he recently found that plasma levels of\nserotonin, kynurenine, or 5-HIAA were higher in patients of mono- and bipolar\ndepression, which are significantly different from observations reported before. In\nview of recent reports that plasma tryptophan metabolites are mainly produced by\nmicrobiota. He is now working on the relationships between microbiota and depression or autism.",institutionString:"Hamamatsu University School of Medicine",institution:{name:"Hamamatsu University School of Medicine",country:{name:"Japan"}}},{id:"137240",title:"Prof.",name:"Mohammed",middleName:null,surname:"Khalid",slug:"mohammed-khalid",fullName:"Mohammed Khalid",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/137240/images/system/137240.png",biography:"Mohammed Khalid received his B.S. degree in chemistry in 2000 and Ph.D. degree in physical chemistry in 2007 from the University of Khartoum, Sudan. He moved to School of Chemistry, Faculty of Science, University of Sydney, Australia in 2009 and joined Dr. Ron Clarke as a postdoctoral fellow where he worked on the interaction of ATP with the phosphoenzyme of the Na+/K+-ATPase and dual mechanisms of allosteric acceleration of the Na+/K+-ATPase by ATP; then he went back to Department of Chemistry, University of Khartoum as an assistant professor, and in 2014 he was promoted as an associate professor. In 2011, he joined the staff of Department of Chemistry at Taif University, Saudi Arabia, where he is currently an assistant professor. His research interests include the following: P-Type ATPase enzyme kinetics and mechanisms, kinetics and mechanisms of redox reactions, autocatalytic reactions, computational enzyme kinetics, allosteric acceleration of P-type ATPases by ATP, exploring of allosteric sites of ATPases, and interaction of ATP with ATPases located in cell membranes.",institutionString:"Taif University",institution:{name:"Taif University",country:{name:"Saudi Arabia"}}},{id:"63810",title:"Prof.",name:"Jorge",middleName:null,surname:"Morales-Montor",slug:"jorge-morales-montor",fullName:"Jorge Morales-Montor",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/63810/images/system/63810.png",biography:"Dr. Jorge Morales-Montor was recognized with the Lola and Igo Flisser PUIS Award for best graduate thesis at the national level in the field of parasitology. He received a fellowship from the Fogarty Foundation to perform postdoctoral research stay at the University of Georgia. He has 153 journal articles to his credit. He has also edited several books and published more than fifty-five book chapters. He is a member of the Mexican Academy of Sciences, Latin American Academy of Sciences, and the National Academy of Medicine. He has received more than thirty-five awards and has supervised numerous bachelor’s, master’s, and Ph.D. students. Dr. Morales-Montor is the past president of the Mexican Society of Parasitology.",institutionString:"National Autonomous University of Mexico",institution:{name:"National Autonomous University of Mexico",country:{name:"Mexico"}}},{id:"217215",title:"Dr.",name:"Palash",middleName:null,surname:"Mandal",slug:"palash-mandal",fullName:"Palash Mandal",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/217215/images/system/217215.jpeg",biography:null,institutionString:"Charusat University",institution:null},{id:"49739",title:"Dr.",name:"Leszek",middleName:null,surname:"Szablewski",slug:"leszek-szablewski",fullName:"Leszek Szablewski",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/49739/images/system/49739.jpg",biography:"Leszek Szablewski is a professor of medical sciences. He received his M.S. in the Faculty of Biology from the University of Warsaw and his PhD degree from the Institute of Experimental Biology Polish Academy of Sciences. He habilitated in the Medical University of Warsaw, and he obtained his degree of Professor from the President of Poland. Professor Szablewski is the Head of Chair and Department of General Biology and Parasitology, Medical University of Warsaw. Professor Szablewski has published over 80 peer-reviewed papers in journals such as Journal of Alzheimer’s Disease, Biochim. Biophys. Acta Reviews of Cancer, Biol. Chem., J. Biomed. Sci., and Diabetes/Metabol. Res. Rev, Endocrine. He is the author of two books and four book chapters. He has edited four books, written 15 scripts for students, is the ad hoc reviewer of over 30 peer-reviewed journals, and editorial member of peer-reviewed journals. Prof. Szablewski’s research focuses on cell physiology, genetics, and pathophysiology. He works on the damage caused by lack of glucose homeostasis and changes in the expression and/or function of glucose transporters due to various diseases. He has given lectures, seminars, and exercises for students at the Medical University.",institutionString:"Medical University of Warsaw",institution:{name:"Medical University of Warsaw",country:{name:"Poland"}}},{id:"173123",title:"Dr.",name:"Maitham",middleName:null,surname:"Khajah",slug:"maitham-khajah",fullName:"Maitham Khajah",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/173123/images/system/173123.jpeg",biography:"Dr. Maitham A. Khajah received his degree in Pharmacy from Faculty of Pharmacy, Kuwait University, in 2003 and obtained his PhD degree in December 2009 from the University of Calgary, Canada (Gastrointestinal Science and Immunology). Since January 2010 he has been assistant professor in Kuwait University, Faculty of Pharmacy, Department of Pharmacology and Therapeutics. His research interest are molecular targets for the treatment of inflammatory bowel disease (IBD) and the mechanisms responsible for immune cell chemotaxis. He cosupervised many students for the MSc Molecular Biology Program, College of Graduate Studies, Kuwait University. Ever since joining Kuwait University in 2010, he got various grants as PI and Co-I. He was awarded the Best Young Researcher Award by Kuwait University, Research Sector, for the Year 2013–2014. He was a member in the organizing committee for three conferences organized by Kuwait University, Faculty of Pharmacy, as cochair and a member in the scientific committee (the 3rd, 4th, and 5th Kuwait International Pharmacy Conference).",institutionString:"Kuwait University",institution:{name:"Kuwait University",country:{name:"Kuwait"}}},{id:"195136",title:"Dr.",name:"Aya",middleName:null,surname:"Adel",slug:"aya-adel",fullName:"Aya Adel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/195136/images/system/195136.jpg",biography:"Dr. Adel works as an Assistant Lecturer in the unit of Phoniatrics, Department of Otolaryngology, Ain Shams University in Cairo, Egypt. Dr. Adel is especially interested in joint attention and its impairment in autism spectrum disorder",institutionString:"Ain Shams University",institution:{name:"Ain Shams University",country:{name:"Egypt"}}},{id:"94911",title:"Dr.",name:"Boulenouar",middleName:null,surname:"Mesraoua",slug:"boulenouar-mesraoua",fullName:"Boulenouar Mesraoua",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94911/images/system/94911.png",biography:"Dr Boulenouar Mesraoua is the Associate Professor of Clinical Neurology at Weill Cornell Medical College-Qatar and a Consultant Neurologist at Hamad Medical Corporation at the Neuroscience Department; He graduated as a Medical Doctor from the University of Oran, Algeria; he then moved to Belgium, the City of Liege, for a Residency in Internal Medicine and Neurology at Liege University; after getting the Belgian Board of Neurology (with high marks), he went to the National Hospital for Nervous Diseases, Queen Square, London, United Kingdom for a fellowship in Clinical Neurophysiology, under Pr Willison ; Dr Mesraoua had also further training in Epilepsy and Continuous EEG Monitoring for two years (from 2001-2003) in the Neurophysiology department of Zurich University, Switzerland, under late Pr Hans Gregor Wieser ,an internationally known epileptologist expert. \n\nDr B. Mesraoua is the Director of the Neurology Fellowship Program at the Neurology Section and an active member of the newly created Comprehensive Epilepsy Program at Hamad General Hospital, Doha, Qatar; he is also Assistant Director of the Residency Program at the Qatar Medical School. \nDr B. Mesraoua's main interests are Epilepsy, Multiple Sclerosis, and Clinical Neurology; He is the Chairman and the Organizer of the well known Qatar Epilepsy Symposium, he is running yearly for the past 14 years and which is considered a landmark in the Gulf region; He has also started last year , together with other epileptologists from Qatar, the region and elsewhere, a yearly International Epilepsy School Course, which was attended by many neurologists from the Area.\n\nInternationally, Dr Mesraoua is an active and elected member of the Commission on Eastern Mediterranean Region (EMR ) , a regional branch of the International League Against Epilepsy (ILAE), where he represents the Middle East and North Africa(MENA ) and where he holds the position of chief of the Epilepsy Epidemiology Section; Dr Mesraoua is a member of the American Academy of Neurology, the Europeen Academy of Neurology and the American Epilepsy Society.\n\nDr Mesraoua's main objectives are to encourage frequent gathering of the epileptologists/neurologists from the MENA region and the rest of the world, promote Epilepsy Teaching in the MENA Region, and encourage multicenter studies involving neurologists and epileptologists in the MENA region, particularly epilepsy epidemiological studies. \n\nDr. Mesraoua is the recipient of two research Grants, as the Lead Principal Investigator (750.000 USD and 250.000 USD) from the Qatar National Research Fund (QNRF) and the Hamad Hospital Internal Research Grant (IRGC), on the following topics : “Continuous EEG Monitoring in the ICU “ and on “Alpha-lactoalbumin , proof of concept in the treatment of epilepsy” .Dr Mesraoua is a reviewer for the journal \"seizures\" (Europeen Epilepsy Journal ) as well as dove journals ; Dr Mesraoua is the author and co-author of many peer reviewed publications and four book chapters in the field of Epilepsy and Clinical Neurology",institutionString:"Weill Cornell Medical College in Qatar",institution:{name:"Weill Cornell Medical College in Qatar",country:{name:"Qatar"}}},{id:"282429",title:"Prof.",name:"Covanis",middleName:null,surname:"Athanasios",slug:"covanis-athanasios",fullName:"Covanis Athanasios",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/282429/images/system/282429.jpg",biography:null,institutionString:"Neurology-Neurophysiology Department of the Children Hospital Agia Sophia",institution:null},{id:"190980",title:"Prof.",name:"Marwa",middleName:null,surname:"Mahmoud Saleh",slug:"marwa-mahmoud-saleh",fullName:"Marwa Mahmoud Saleh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/190980/images/system/190980.jpg",biography:"Professor Marwa Mahmoud Saleh is a doctor of medicine and currently works in the unit of Phoniatrics, Department of Otolaryngology, Ain Shams University in Cairo, Egypt. She got her doctoral degree in 1991 and her doctoral thesis was accomplished in the University of Iowa, United States. Her publications covered a multitude of topics as videokymography, cochlear implants, stuttering, and dysphagia. She has lectured Egyptian phonology for many years. Her recent research interest is joint attention in autism.",institutionString:"Ain Shams University",institution:{name:"Ain Shams University",country:{name:"Egypt"}}},{id:"259190",title:"Dr.",name:"Syed Ali Raza",middleName:null,surname:"Naqvi",slug:"syed-ali-raza-naqvi",fullName:"Syed Ali Raza Naqvi",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259190/images/system/259190.png",biography:"Dr. Naqvi is a radioanalytical chemist and is working as an associate professor of analytical chemistry in the Department of Chemistry, Government College University, Faisalabad, Pakistan. Advance separation techniques, nuclear analytical techniques and radiopharmaceutical analysis are the main courses that he is teaching to graduate and post-graduate students. In the research area, he is focusing on the development of organic- and biomolecule-based radiopharmaceuticals for diagnosis and therapy of infectious and cancerous diseases. Under the supervision of Dr. Naqvi, three students have completed their Ph.D. degrees and 41 students have completed their MS degrees. He has completed three research projects and is currently working on 2 projects entitled “Radiolabeling of fluoroquinolone derivatives for the diagnosis of deep-seated bacterial infections” and “Radiolabeled minigastrin peptides for diagnosis and therapy of NETs”. He has published about 100 research articles in international reputed journals and 7 book chapters. Pakistan Institute of Nuclear Science & Technology (PINSTECH) Islamabad, Punjab Institute of Nuclear Medicine (PINM), Faisalabad and Institute of Nuclear Medicine and Radiology (INOR) Abbottabad are the main collaborating institutes.",institutionString:"Government College University",institution:{name:"Government College University, Faisalabad",country:{name:"Pakistan"}}},{id:"58390",title:"Dr.",name:"Gyula",middleName:null,surname:"Mozsik",slug:"gyula-mozsik",fullName:"Gyula Mozsik",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/58390/images/system/58390.png",biography:"Gyula Mózsik MD, Ph.D., ScD (med), is an emeritus professor of Medicine at the First Department of Medicine, Univesity of Pécs, Hungary. He was head of this department from 1993 to 2003. His specializations are medicine, gastroenterology, clinical pharmacology, clinical nutrition, and dietetics. His research fields are biochemical pharmacological examinations in the human gastrointestinal (GI) mucosa, mechanisms of retinoids, drugs, capsaicin-sensitive afferent nerves, and innovative pharmacological, pharmaceutical, and nutritional (dietary) research in humans. He has published about 360 peer-reviewed papers, 197 book chapters, 692 abstracts, 19 monographs, and has edited 37 books. He has given about 1120 regular and review lectures. He has organized thirty-eight national and international congresses and symposia. He is the founder of the International Conference on Ulcer Research (ICUR); International Union of Pharmacology, Gastrointestinal Section (IUPHAR-GI); Brain-Gut Society symposiums, and gastrointestinal cytoprotective symposiums. He received the Andre Robert Award from IUPHAR-GI in 2014. Fifteen of his students have been appointed as full professors in Egypt, Cuba, and Hungary.",institutionString:"University of Pécs",institution:{name:"University of Pecs",country:{name:"Hungary"}}},{id:"277367",title:"M.Sc.",name:"Daniel",middleName:"Martin",surname:"Márquez López",slug:"daniel-marquez-lopez",fullName:"Daniel Márquez López",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/277367/images/7909_n.jpg",biography:"Msc Daniel Martin Márquez López has a bachelor degree in Industrial Chemical Engineering, a Master of science degree in the same área and he is a PhD candidate for the Instituto Politécnico Nacional. His Works are realted to the Green chemistry field, biolubricants, biodiesel, transesterification reactions for biodiesel production and the manipulation of oils for therapeutic purposes.",institutionString:null,institution:{name:"Instituto Politécnico Nacional",country:{name:"Mexico"}}},{id:"196544",title:"Prof.",name:"Angel",middleName:null,surname:"Catala",slug:"angel-catala",fullName:"Angel Catala",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/196544/images/system/196544.jpg",biography:"Angel Catalá studied chemistry at Universidad Nacional de La Plata, Argentina, where he received a Ph.D. in Chemistry (Biological Branch) in 1965. From 1964 to 1974, he worked as an Assistant in Biochemistry at the School of Medicine at the same university. From 1974 to 1976, he was a fellow of the National Institutes of Health (NIH) at the University of Connecticut, Health Center, USA. From 1985 to 2004, he served as a Full Professor of Biochemistry at the Universidad Nacional de La Plata. He is a member of the National Research Council (CONICET), Argentina, and the Argentine Society for Biochemistry and Molecular Biology (SAIB). His laboratory has been interested for many years in the lipid peroxidation of biological membranes from various tissues and different species. Dr. Catalá has directed twelve doctoral theses, published more than 100 papers in peer-reviewed journals, several chapters in books, and edited twelve books. He received awards at the 40th International Conference Biochemistry of Lipids 1999 in Dijon, France. He is the winner of the Bimbo Pan-American Nutrition, Food Science and Technology Award 2006 and 2012, South America, Human Nutrition, Professional Category. In 2006, he won the Bernardo Houssay award in pharmacology, in recognition of his meritorious works of research. Dr. Catalá belongs to the editorial board of several journals including Journal of Lipids; International Review of Biophysical Chemistry; Frontiers in Membrane Physiology and Biophysics; World Journal of Experimental Medicine and Biochemistry Research International; World Journal of Biological Chemistry, Diabetes, and the Pancreas; International Journal of Chronic Diseases & Therapy; and International Journal of Nutrition. He is the co-editor of The Open Biology Journal and associate editor for Oxidative Medicine and Cellular Longevity.",institutionString:"Universidad Nacional de La Plata",institution:{name:"National University of La Plata",country:{name:"Argentina"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",slug:"francisco-javier-martin-romero",fullName:"Francisco Javier Martin-Romero",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",biography:"Francisco Javier Martín-Romero (Javier) is a Professor of Biochemistry and Molecular Biology at the University of Extremadura, Spain. He is also a group leader at the Biomarkers Institute of Molecular Pathology. Javier received his Ph.D. in 1998 in Biochemistry and Biophysics. At the National Cancer Institute (National Institute of Health, Bethesda, MD) he worked as a research associate on the molecular biology of selenium and its role in health and disease. After postdoctoral collaborations with Carlos Gutierrez-Merino (University of Extremadura, Spain) and Dario Alessi (University of Dundee, UK), he established his own laboratory in 2008. The interest of Javier's lab is the study of cell signaling with a special focus on Ca2+ signaling, and how Ca2+ transport modulates the cytoskeleton, migration, differentiation, cell death, etc. He is especially interested in the study of Ca2+ channels, and the role of STIM1 in the initiation of pathological events.",institutionString:null,institution:{name:"University of Extremadura",country:{name:"Spain"}}},{id:"217323",title:"Prof.",name:"Guang-Jer",middleName:null,surname:"Wu",slug:"guang-jer-wu",fullName:"Guang-Jer Wu",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/217323/images/8027_n.jpg",biography:null,institutionString:null,institution:null},{id:"148546",title:"Dr.",name:"Norma Francenia",middleName:null,surname:"Santos-Sánchez",slug:"norma-francenia-santos-sanchez",fullName:"Norma Francenia Santos-Sánchez",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/148546/images/4640_n.jpg",biography:null,institutionString:null,institution:null},{id:"272889",title:"Dr.",name:"Narendra",middleName:null,surname:"Maddu",slug:"narendra-maddu",fullName:"Narendra Maddu",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/272889/images/10758_n.jpg",biography:null,institutionString:null,institution:null},{id:"242491",title:"Prof.",name:"Angelica",middleName:null,surname:"Rueda",slug:"angelica-rueda",fullName:"Angelica Rueda",position:"Investigador Cinvestav 3B",profilePictureURL:"https://mts.intechopen.com/storage/users/242491/images/6765_n.jpg",biography:null,institutionString:null,institution:null},{id:"88631",title:"Dr.",name:"Ivan",middleName:null,surname:"Petyaev",slug:"ivan-petyaev",fullName:"Ivan Petyaev",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Lycotec (United Kingdom)",country:{name:"United Kingdom"}}},{id:"423869",title:"Ms.",name:"Smita",middleName:null,surname:"Rai",slug:"smita-rai",fullName:"Smita Rai",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Integral University",country:{name:"India"}}},{id:"424024",title:"Prof.",name:"Swati",middleName:null,surname:"Sharma",slug:"swati-sharma",fullName:"Swati Sharma",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Integral University",country:{name:"India"}}},{id:"439112",title:"MSc.",name:"Touseef",middleName:null,surname:"Fatima",slug:"touseef-fatima",fullName:"Touseef Fatima",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Integral University",country:{name:"India"}}},{id:"424836",title:"Dr.",name:"Orsolya",middleName:null,surname:"Borsai",slug:"orsolya-borsai",fullName:"Orsolya Borsai",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca",country:{name:"Romania"}}},{id:"422262",title:"Ph.D.",name:"Paola Andrea",middleName:null,surname:"Palmeros-Suárez",slug:"paola-andrea-palmeros-suarez",fullName:"Paola Andrea Palmeros-Suárez",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Guadalajara",country:{name:"Mexico"}}}]}},subseries:{item:{id:"15",type:"subseries",title:"Chemical Biology",keywords:"Phenolic Compounds, Essential Oils, Modification of Biomolecules, Glycobiology, Combinatorial Chemistry, Therapeutic peptides, Enzyme Inhibitors",scope:"Chemical biology spans the fields of chemistry and biology involving the application of biological and chemical molecules and techniques. In recent years, the application of chemistry to biological molecules has gained significant interest in medicinal and pharmacological studies. This topic will be devoted to understanding the interplay between biomolecules and chemical compounds, their structure and function, and their potential applications in related fields. Being a part of the biochemistry discipline, the ideas and concepts that have emerged from Chemical Biology have affected other related areas. 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Fungal infectious illness prevalence and prognosis are determined by the exposure between fungi and host, host immunological state, fungal virulence, and early and accurate diagnosis and treatment. \r\nPatients with both congenital and acquired immunodeficiency are more likely to be infected with opportunistic mycosis. Fungal infectious disease outbreaks are common during the post- disaster rebuilding era, which is characterised by high population density, migration, and poor health and medical conditions.\r\nSystemic or local fungal infection is mainly associated with the fungi directly inhaled or inoculated in the environment during the disaster. The most common fungal infection pathways are human to human (anthropophilic), animal to human (zoophilic), and environment to human (soilophile). Diseases are common as a result of widespread exposure to pathogenic fungus dispersed into the environment. \r\nFungi that are both common and emerging are intertwined. In Southeast Asia, for example, Talaromyces marneffei is an important pathogenic thermally dimorphic fungus that causes systemic mycosis. Widespread fungal infections with complicated and variable clinical manifestations, such as Candida auris infection resistant to several antifungal medicines, Covid-19 associated with Trichoderma, and terbinafine resistant dermatophytosis in India, are among the most serious disorders. \r\nInappropriate local or systemic use of glucocorticoids, as well as their immunosuppressive effects, may lead to changes in fungal infection spectrum and clinical characteristics. Hematogenous candidiasis is a worrisome issue that affects people all over the world, particularly ICU patients. CARD9 deficiency and fungal infection have been major issues in recent years. Invasive aspergillosis is associated with a significant death rate. Special attention should be given to endemic fungal infections, identification of important clinical fungal infections advanced in yeasts, filamentous fungal infections, skin mycobiome and fungal genomes, and immunity to fungal infections.\r\nIn addition, endemic fungal diseases or uncommon fungal infections caused by Mucor irregularis, dermatophytosis, Malassezia, cryptococcosis, chromoblastomycosis, coccidiosis, blastomycosis, histoplasmosis, sporotrichosis, and other fungi, should be monitored. \r\nThis topic includes the research progress on the etiology and pathogenesis of fungal infections, new methods of isolation and identification, rapid detection, drug sensitivity testing, new antifungal drugs, schemes and case series reports. It will provide significant opportunities and support for scientists, clinical doctors, mycologists, antifungal drug researchers, public health practitioners, and epidemiologists from all over the world to share new research, ideas and solutions to promote the development and progress of medical mycology.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/4.jpg",keywords:"Emerging Fungal Pathogens, Invasive Infections, Epidemiology, Cell Membrane, Fungal Virulence, Diagnosis, Treatment"},{id:"5",title:"Parasitic Infectious Diseases",scope:"Parasitic diseases have evolved alongside their human hosts. In many cases, these diseases have adapted so well that they have developed efficient resilience methods in the human host and can live in the host for years. Others, particularly some blood parasites, can cause very acute diseases and are responsible for millions of deaths yearly. Many parasitic diseases are classified as neglected tropical diseases because they have received minimal funding over recent years and, in many cases, are under-reported despite the critical role they play in morbidity and mortality among human and animal hosts. The current topic, Parasitic Infectious Diseases, in the Infectious Diseases Series aims to publish studies on the systematics, epidemiology, molecular biology, genomics, pathogenesis, genetics, and clinical significance of parasitic diseases from blood borne to intestinal parasites as well as zoonotic parasites. We hope to cover all aspects of parasitic diseases to provide current and relevant research data on these very important diseases. In the current atmosphere of the Coronavirus pandemic, communities around the world, particularly those in different underdeveloped areas, are faced with the growing challenges of the high burden of parasitic diseases. At the same time, they are faced with the Covid-19 pandemic leading to what some authors have called potential syndemics that might worsen the outcome of such infections. Therefore, it is important to conduct studies that examine parasitic infections in the context of the coronavirus pandemic for the benefit of all communities to help foster more informed decisions for the betterment of human and animal health.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/5.jpg",keywords:"Blood Borne Parasites, Intestinal Parasites, Protozoa, Helminths, Arthropods, Water Born Parasites, Epidemiology, Molecular Biology, Systematics, Genomics, Proteomics, Ecology"},{id:"6",title:"Viral Infectious Diseases",scope:"The Viral Infectious Diseases Book Series aims to provide a comprehensive overview of recent research trends and discoveries in various viral infectious diseases emerging around the globe. The emergence of any viral disease is hard to anticipate, which often contributes to death. A viral disease can be defined as an infectious disease that has recently appeared within a population or exists in nature with the rapid expansion of incident or geographic range. This series will focus on various crucial factors related to emerging viral infectious diseases, including epidemiology, pathogenesis, host immune response, clinical manifestations, diagnosis, treatment, and clinical recommendations for managing viral infectious diseases, highlighting the recent issues with future directions for effective therapeutic strategies.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/6.jpg",keywords:"Novel Viruses, Virus Transmission, Virus Evolution, Molecular Virology, Control and Prevention, Virus-host Interaction"}],annualVolumeBook:{},thematicCollection:[],selectedSeries:null,selectedSubseries:null},seriesLanding:{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:"May 15th, 2022",hasOnlineFirst:!0,numberOfOpenTopics:4,numberOfPublishedChapters:286,numberOfPublishedBooks:27,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"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"}}},subseries:[{id:"14",title:"Cell and Molecular Biology",keywords:"Omics (Transcriptomics; Proteomics; Metabolomics), Molecular Biology, Cell Biology, Signal Transduction and Regulation, Cell Growth and Differentiation, Apoptosis, Necroptosis, Ferroptosis, Autophagy, Cell Cycle, Macromolecules and Complexes, Gene Expression",scope:"The Cell and Molecular Biology topic within the IntechOpen Biochemistry Series aims to rapidly publish contributions on all aspects of cell and molecular biology, including aspects related to biochemical and genetic research (not only in humans but all living beings). We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics include, but are not limited to: Advanced techniques of cellular and molecular biology (Molecular methodologies, imaging techniques, and bioinformatics); Biological activities at the molecular level; Biological processes of cell functions, cell division, senescence, maintenance, and cell death; Biomolecules interactions; Cancer; Cell biology; Chemical biology; Computational biology; Cytochemistry; Developmental biology; Disease mechanisms and therapeutics; DNA, and RNA metabolism; Gene functions, genetics, and genomics; Genetics; Immunology; Medical microbiology; Molecular biology; Molecular genetics; Molecular processes of cell and organelle dynamics; Neuroscience; Protein biosynthesis, degradation, and functions; Regulation of molecular interactions in a cell; Signalling networks and system biology; Structural biology; Virology and microbiology.",annualVolume:11410,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"79367",title:"Dr.",name:"Ana Isabel",middleName:null,surname:"Flores",fullName:"Ana Isabel Flores",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRpIOQA0/Profile_Picture_1632418099564",institutionString:null,institution:{name:"Hospital Universitario 12 De Octubre",institutionURL:null,country:{name:"Spain"}}},{id:"328234",title:"Ph.D.",name:"Christian",middleName:null,surname:"Palavecino",fullName:"Christian Palavecino",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000030DhEhQAK/Profile_Picture_1628835318625",institutionString:null,institution:{name:"Central University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",fullName:"Francisco Javier Martin-Romero",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",institutionString:null,institution:{name:"University of Extremadura",institutionURL:null,country:{name:"Spain"}}}]},{id:"15",title:"Chemical Biology",keywords:"Phenolic Compounds, Essential Oils, Modification of Biomolecules, Glycobiology, Combinatorial Chemistry, Therapeutic peptides, Enzyme Inhibitors",scope:"Chemical biology spans the fields of chemistry and biology involving the application of biological and chemical molecules and techniques. In recent years, the application of chemistry to biological molecules has gained significant interest in medicinal and pharmacological studies. This topic will be devoted to understanding the interplay between biomolecules and chemical compounds, their structure and function, and their potential applications in related fields. Being a part of the biochemistry discipline, the ideas and concepts that have emerged from Chemical Biology have affected other related areas. This topic will closely deal with all emerging trends in this discipline.",annualVolume:11411,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null,editorialBoard:[{id:"241413",title:"Dr.",name:"Azhar",middleName:null,surname:"Rasul",fullName:"Azhar Rasul",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRT1oQAG/Profile_Picture_1635251978933",institutionString:null,institution:{name:"Government College University, Faisalabad",institutionURL:null,country:{name:"Pakistan"}}},{id:"178316",title:"Ph.D.",name:"Sergey",middleName:null,surname:"Sedykh",fullName:"Sergey Sedykh",profilePictureURL:"https://mts.intechopen.com/storage/users/178316/images/system/178316.jfif",institutionString:null,institution:{name:"Novosibirsk State University",institutionURL:null,country:{name:"Russia"}}}]},{id:"17",title:"Metabolism",keywords:"Biomolecules Metabolism, Energy Metabolism, Metabolic Pathways, Key Metabolic Enzymes, Metabolic Adaptation",scope:"Metabolism is frequently defined in biochemistry textbooks as the overall process that allows living systems to acquire and use the free energy they need for their vital functions or the chemical processes that occur within a living organism to maintain life. Behind these definitions are hidden all the aspects of normal and pathological functioning of all processes that the topic ‘Metabolism’ will cover within the Biochemistry Series. Thus all studies on metabolism will be considered for publication.",annualVolume:11413,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"243049",title:"Dr.",name:"Anca",middleName:null,surname:"Pantea Stoian",fullName:"Anca Pantea Stoian",profilePictureURL:"https://mts.intechopen.com/storage/users/243049/images/system/243049.jpg",institutionString:null,institution:{name:"Carol Davila University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"203824",title:"Dr.",name:"Attilio",middleName:null,surname:"Rigotti",fullName:"Attilio Rigotti",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institutionString:null,institution:{name:"Pontifical Catholic University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"300470",title:"Dr.",name:"Yanfei (Jacob)",middleName:null,surname:"Qi",fullName:"Yanfei (Jacob) Qi",profilePictureURL:"https://mts.intechopen.com/storage/users/300470/images/system/300470.jpg",institutionString:null,institution:{name:"Centenary Institute of Cancer Medicine and Cell Biology",institutionURL:null,country:{name:"Australia"}}}]},{id:"18",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",annualVolume:11414,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",fullName:"Shymaa Enany",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRqB9QAK/Profile_Picture_1626163237970",institutionString:null,institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"profile.detail",path:"/profiles/427930",hash:"",query:{},params:{id:"427930"},fullPath:"/profiles/427930",meta:{},from:{name:null,path:"/",hash:"",query:{},params:{},fullPath:"/",meta:{}}}},function(){var e;(e=document.currentScript||document.scripts[document.scripts.length-1]).parentNode.removeChild(e)}()