\r\n\tHydroxyapatite (HA) is an important member of the calcium phosphate chemical family. It has been used in several medical applications for the past decades, due to its chemical similarity to the mineral phase of bone and high biocompatibility. Several studies demonstrated that bone mineral presents several ion substitutions, so in order to prepare a synthetic material with an even closer composition to bone mineral, HA has been prepared with the incorporation of several ions like, silicon or fluoride. These ions induced not only structural changes on HA lattice, but also on its biocompatibility. \r\n\tSignificant advances in nanotechnologies resulted in the preparation of HA in different forms, with a wider range of applications, from support to drug and gene delivery. \r\n\tThis book aims to collect the most relevant information regarding HA properties, modifications and its application in the biomedical field.
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1. Introduction
Pesticides are substances that exist in our daily lives. Their most widespread use is in agriculture, where they are used to protect crops from pests caused by plants and animals. They are also used to prevent diseases caused by ectoparasites in farm animals and pets. These substances are used in gardening and brought into our homes to protect us from mosquitoes and other insects. Pesticides come into intimate touch with all forms of life through drinking water and eating food. However, the use of these substances is so widespread and poorly controlled that environmental contamination is inevitable.
Pesticide exposure occurs in a variety of ways. Not all living organisms are exposed to the same periods or the same dose, or not even to a single type of pesticide or to the same mixtures. The above may have yet unknown, synergistic, or potentiating effects on organisms.
Insecticides are a class of pesticides used to kill or control insects. It is not only used in agriculture, but also in ornamental gardens, homes, and veterinary medicine. Although the hazardous effects on the environment and the health of living beings are not yet fully understood, they have become one of the primary solutions for crop protection in agriculture. Regardless of the fact that pesticides come in a wide variety of families, the major goal of this chapter is to highlight the effects of imidacloprid (neonicotinoid), chlorpyrifos (organophosphate), and carbaryl (carbamate), insecticides widely used in agriculture, despite recent findings of their neurotoxic effects on several animal species.
2. Worldwide use of insecticides
After herbicides, insecticides are the most extensively used pesticides in agriculture [1]. The principal insecticide consumers by continent were America (44.9%), Asia (29%), Europe (16%), Africa (6.4), and Oceania (3.7%), with the United States being the country with the highest insecticide consumption worldwide (Figure 1) [2]. Recently collected data, dating from 1998 to 2014, indicates that chlorpyrifos was the third most used organophosphate pesticide in the United States, only for corn cultivation, with a total of 1,122kg/ha. In the same country, the most widely used carbamate was carbaryl with a total of 1,024 kg/ha; while imidacloprid was the most used neonicotinoid, with 0.057 kg/ha. During the same time period, chlorpyrifos, carbaryl, and imidacloprid were among the top 10 most widely used insecticides in the United States [3]. Currently, these same pesticides are used in agriculture and are included among the principal insecticides for each insecticide family aforementioned [4, 5, 6].
Figure 1.
Highest to lowest insecticide use by continent.
Furthermore, organophosphate insecticides account for roughly half of all insecticides used worldwide, and chlorpyrifos is one of the most widely used. This insecticide is approved for use on more than 50 food crops in both developed and developing countries [7]. About 50 chemicals belong to the carbamate family, which are utilized as fungicides, herbicides, and nematicides in addition to having insecticidal properties. Carbaryl was the first carbamate to be commercialized, and it is now more widely used than all other carbamates combined [8]. Neonicotinoids, on the other hand, appear to be the most widely employed insecticides worldwide, according to the literature. In fact, imidacloprid is the world’s second most widely used pesticide, after only the controversial herbicide glyphosate [9, 10]. Neonicotinoids have largely replaced carbamates and organophosphates because they are considered less toxic to humans and insects, and they appear to be less resistant to neonicotinoids compared to other conventional insecticide classes [11].
3. Of the molecule, its structure, and mechanism of action
3.1 Chlorpyrifos
Organophosphates are compounds of organic nature that contain phosphorus. Chlorpyrifos (O, O-diethyl-O-3,5,6-trichloropyridin-2-yl phosphorothioate) is an organic thiophosphate of the chloropyridine class [12]. The latter is one of the most widely used organophosphate insecticides in agriculture, primarily used on corn, soy, fruit trees, walnut trees, brussels sprouts, blueberries, broccoli, and cauliflower, among others. This pesticide is also used on golf courses, on ornamental plants, for treating wood, and in homes to combat mosquitoes, cockroaches, and ants [13]. Chlorpyrifos act by irreversibly inhibiting the acetylcholinesterase enzyme activity, which causes acetylcholine accumulation in the synaptic cleft, causing overstimulation of postsynaptic receptors and the consequent signs of intoxication [14].
3.2 Imidacloprid
Imidacloprid [1-[(6-chloropyridin-3-yl) methyl] imidazolidin-2-ylidene] nitramide is a neonicotinoid of the chloropyridinyl class [15], which like the insecticides of the same family, acts as an agonist of nicotinic cholinergic receptors (nAChRs) of insects and mammals [16, 17]. IImidacloprid is used in agriculture for corn, cotton, soybean, potato, wheat, and some vegetable seeds, as well as for soil treatment and foliar application on crops like orange, potato, and cotton. It is also utilized in the treatment of decorative plants and residential areas, industrial vegetation and forestry management [18]. Additionally, it is used as veterinary medicine in presentations such as pipettes or collars for direct application on dogs and cats to prevent infestations by internal and external parasites [19].
3.3 Carbaryl
Carbaryl (1-naphthyl methylcarbamate) is a carbamate-based pesticide. It’s a carbamate ester made up of 1-naphthol and methylcarbamic acid. On plants, this pesticide is insecticidal, acaricidal, and even growth retardant when used in plants. It is currently used to treat corn, soybean, cotton, nuts, fruit, and vegetable crops in agriculture [20]. It is mostly used on apple, nut, and soybean crops in the United States. However, it is found in more than 40 crops around the world, including asparagus, squash, and potatoes. Its non-agricultural uses include ornamental plants, lawns, grass, roads, and buildings [21]. Carbaryl acts by inhibiting acetylcholinesterase. Nevertheless, unlike organophosphates, carbamates do it reversibly [22].
4. Persistence in soil and water
When pesticides are manually or aerially sprayed on seeds, soil, or even directly on plants, they can last for days, months, or even years. They might also filter through the soil into surface and deep waterways, polluting food and water sources for living beings by coming into contact with animal and plant life. Table 1 illustrates the soil-water partition coefficients (Koc) and octanol–water partition coefficients (Kow), which are used to characterize the mobility and bioaccumulation properties of pesticides, respectively. While these coefficients are not the only indicators used to determine pesticide behavior in the environment and in organisms, they do serve as referents for pesticide toxicity.
Table 1.
Crucial physicochemical characteristics for insecticides are chlorpyrifos, carbaryl, and imidacloprid.
The Koc is a coefficient that is used to determine the pesticide concentration “attached” to soil particles as well as the phase present in the solution, i.e., dissolved in the same soil’s water. As a result, the lower the temperature, the higher the Koc of the pesticide in solution, and the greater the likelihood of it leaching into groundwater. The Kow is a coefficient that is used to calculate pesticide concentrations in octanol and water. Pesticides having a high Kow, which are more soluble in octanol and less soluble in water, have been found to accumulate in organisms [23]. Chlorpyrifos accumulates greater in organisms than carbaryl and imidacloprid, as shown in Table 1. It does, however, have a lesser tendency to leak into the soil as compared to them. In this sense, imidacloprid would pose a greater risk as a groundwater pollutant.
To estimate a substance’s environmental fate in diverse environments, scientists must first determine its degradation half-life, or DT50, which is the time it takes for 50% of a chemical to degrade or disappear from water or soil [7]. For the purposes of this review, the three pesticides DT50 examined will be provided below, depending on their average persistence in soil and water,
Chlorpyrifos can have a long persistence even in arctic regions, where its presence has been assessed in samples of ice, snow, a microcosm of water, sediments, air, and flora. The persistence of this pesticide (due to its high resistance to hydrolysis) has been reported to be greater in aquatic habitats than in soil. However, the LD50 in soil, has a wide range of values as reported in the literature, ranging from a few days to four years. It is also suggested to be more stable in low-pH soils, dark settings, and cold environments [7]. Chlorpyrifos DT50 has been found to last from 1 to 120days in the field and up to 180 days in the soil in the absence of light. It is worth noting that in organic soils, the half-life is longer than in mineral soils. A DT50 of 150 to 200 days has been documented in anaerobic pond sediments, while 106 + 54 days has been reported in experimental circumstances of wetland and anaerobic sediments. Chlorpyrifos has a DT50 of 18.7 days in freshwater and 49.4 days in seawater at 10°C, which decreases with increasing temperature [24].
In the case of carbaryl, its DT50 in the soil ranges from 17 to 28 days. It is considered to have low persistence, where it is degraded mainly by the action of light and bacteria. In sandy soil conditions, its half-life is 7 to 14 days, while in clay soil it ranges from 14 to 28 days, hydrolyzing itself rapidly in alkaline soils. The DT50 in water is highly variable, increased in acidic conditions; for example, in acidic water with a pH of 5, degradation is slow and can persist for up to 1500 days [23]. The DT50 of carbaryl in soil has recently been reported to be 16 days, while it can reach 12 and 5.8 days in water and sediments, respectively [25].
Neonicotinoids have a high DT50, which means they can last a long time in the soil, with values in the range from 6.7 to 1230 days, while imidacloprid has the highest DT50, with a value of 35.9 to 1230 days. Though it should be noted that the degradation of neonicotinoids and other pesticides in soil is dependent on pH, temperature, humidity, chemical concentration, and even the presence of microorganisms [26]. As evidence, imidacloprid has been found to remain for 42 to 129 days in vegetated soils and more than 180 days in soils free of vegetation [27]. The data on this insecticide’s water persistence is varied, with half-lives ranging from 1 to 3 hours, 48 hours, and even 31 to 43 days [28].
5. Neurotoxic effects in different animal species
The lethal dose 50 or LD50, is a measure that in toxicology is used to estimate the dose of a test substance that produces 50% of death in a certain animal species. It is used as a reference to determine how toxic it is to humans [29]. The LC50 or lethal concentration 50, corresponds to the concentration of a chemical substance in the air or in the water that causes half of the exposed animals to die [30]. According to the WHO toxicological classification for pesticides (Table 2) [31], both imidacloprid and carbaryl are in class II, which includes those pesticides with moderate toxic effects, while chlorpyrifos is located in class 1b since its LD50 is below 200 mg. Therefore, it is considered highly dangerous. In Table 3, the LD50 or LC50 for chlorpyrifos, carbaryl, and imidacloprid in different animal species are illustrated.
Class
LD50 for rat (mg / kg body weigth)
Oral
Dermal
Ia
Extremely dangerous
<5
<50
Ib
Highly dangerous
5–50
5–200
II
Moderately dangerous
50–2000
200–2000
III
Slightly dangerous
>2000
>2000
U
Acute hazard unlikely
5000 or more
Table 2.
Toxicological classification for pesticides with moderate toxic effects.
Insecticide
Class
Nerve target
LD50 or LC50 in different species
Toxicological classification (WHO)
Rat
Honey bee
Fish
Bird
Acute oral LD50 (mg/kg)
Acute contact LD50 (mg/bee)
Acute exposure LC50 (mg/L)
Acute oral LD50 (mg/kg)
Chlorpyrifos
Organophosphate
AChE
182
0.072
108
27.36
Ia
Carbaryl
Carbamate
AChE
230
0.84
3470
1870.5
II
Imidacloprid
Neonicotinoid
nAChR
439.8
0.061
229,100
35.36
II
Table 3.
Effect of LD50 or LC50: chlorpyrifos, carbaryl, and imidacloprid in different animal species.
6. Neurotoxic effects of chlorpyrifos, carbaryl, and imidacloprid
Although insecticides are substances designed to kill some kinds of insects that cause pests, for decades it has been documented that they can also kill insects that should not be the target of their toxic effects and that overall, are essential for life on planet Earth. The most documented case is the decrease in pollinator populations and its possible association with insecticides utilization. In recent reviews, information supporting that insecticides can interfere with localization capacity, alteration of foraging and motor behavior, olfactory learning, and flight ability has been gathered. Additionally, they negatively impact the immune system and increase the death rate, among other toxic effects in bees [32, 33, 34, 35], bumblebees [36, 37, 38], butterflies and moths [39, 40, 41, 42], ants [43, 44], earthworms [39, 45] and various aquatic invertebrates [46, 47, 48]. They have also been associated with neuronal and colony performance alterations in bumblebees [32]. Insecticides such as dichlorvos, imidacloprid, and malathion, among others, can harm butterfly populations, resulting in decreased survival and changes in feeding and oviposition patterns [49].
Therefore, the effects on non-target insects have received special attention. According to studies on these species, an environmental emergency has been declared due to the decline in their populations. It is worth noting that insecticides have effects not confined to insects, which exacerbates the existing problem because all living beings are exposed to varying degrees of insecticides, making humans vulnerable to their toxic effects. Following, there is a brief overview of the effects identified in the last five years for each of the insecticides that have been the subject of this chapter, grouped into three different types of effects: behavioral, neurochemical, and cellular (Tables 4–6). However, for more detailed information, consider the present bibliography.
Behavioral effects
Chlorpyrifos
Carbaryl
Imidacloprid
Insects
Alters caste differentiation in Plebeia droryana bees [50]. Alters the formation and recovery of olfactory memories in bees [51]. It alters the locomotor activity of the cockroach Nauphoeta cinerea [52]. Alteration of olfactory learning and memory retention in Apis mellifera and Apis cerana bees [53]. Impaired locomotor performance manifested with altered swimming activity in Diamesa zernyi larvae [54].
It causes alterations in the percentage of copulations in adults of Rhynchophorus palmarum (Coleoptera: Curculionidae) [55]. No more recent studies for the review period in the literature.
Paralysis, tremors, prostration, and death in Scaptotrigona postica Latreille bees [56]. Decreased food consumption, digging, and foraging behavior in the red ant Solenopsis Invicta [57]. Alterations in sexual behavior and search for hosts in parasitic wasps Nasonia vitripennis [58]. It affects the queen selection behavior of the stingless bee Plebeia droryana [59]. Reduced visual movement and deterioration in-flight behavior in the migratory locust Locusta [60]. Disruption of copulation in adults of Rhynchophorus palmarum (Coleoptera: Curculionidae) [55].
Aquatic organisms
Alterations in the straightening of the gastropod Gibbula umbilicalis [61]. Irregular hatching patterns in shrimp Artemia salina [62]. Alteration of swimming activity, such as hypoactivity and spasms in the Physalaemus gracilis tadpole [63] Alterations in the swimming pattern in the catfish Heteropneustes fossilis [64].
General hypoactivity, decrease in escape swim, and feeding behavior in tadpoles of the terrestrial Anaxyrus toad [65]. Decrease in hatching speed of shrimp Artemia salina [62]. Delay in the ocular peduncle retraction speed in the blue crab Callinectes sapidus [66]. Hypoactivity, alterations in exploratory, social and feeding behavior in zebrafish exposed during embryonic life [67]. Decreased shell closing time and increased mucus secretion from the gills in the Unio pictorum mussel [68]. Decreased startle behavior and habituation in zebrafish larvae [69].
It decreases exploratory behavior, swimming activity and increases the sensorimotor response to startling stimuli in zebrafish [70]. It alters the swimming behavior and avoidance behavior of the predators of the tadpole Limnodynastes tasmaniensisy [71]. Decreased response to predators in the Lithobates sylvaticus frog [72]. Alterations in swimming and feeding behavior in the Farfantepenaeus aztecus shrimp [73]. Locomotor alterations and decreased aggressive behavior in the Procambarus clarkiies crab [74]. Hypoactivity in the zebrafish Danio rerio [75]. Lethargy is followed by hyperactivity and spasms in the tadpole Leptodactylus latrans [76].
Birds
Salivation, tearing, panting, frequent defecation, tremors, and seizures in broilers [77]. Alteration in migratory orientation in the white-crowned sparrow Zonotrichia leucophrys [78].
Difficulty walking, weak legs, dizziness, frequent defecation, less food consumption, decrease in aggressive behavior [79].
Alteration in migratory orientation in the white-crowned sparrow Zonotrichia leucophrys [78]. Hypoactivity, decreased flight behavior, spasms, drooping wings, ataxia, prostration in the pigeon Zenaida auriculata [80]. Decrease in food consumption and delay in migration in the white-crowned sparrow Zonotrichia leucophrys [81]. Muscle tremors, ataxia, and depression in domestic chickens Gallus gallus domesticus [82].
Non-human vertebrates
Anxiety affects exposure in fetal life in male Wistar rats [83]. Alterations in social behavior and recognition memory in C57Bl6 / J mice [84]. Decreased locomotor activity and muscle strength in Sprague–Dawley rats [85] Alteration of the reference memory; Anxious behavior in male Wistar rats [86]. Catalytic behavior decreased motor coordination and gait disturbances in Swiss mice [87]. Piloerection, tremors, seizures, hypoactivity, among other neurological signs after administration in mice [88]. Impairment of social behavior and sensorimotor reflexes in PON 1/1 mice [89].
Memory and learning deficits. As well as habituation behavior alterations in NMRI mice [90]. Hypoactivity in Norwegian gray rats [91]. Hypersalivation, miotic pupils, lethargy, coma in bats Eidolon helvum [92].
Hypoactivity increased grooming behavior and behaviors associated with anxiety and depression in male Sprague–Dawley rats [93]. Decreased exploratory behavior, a deficit in sensorimotor functions, and depression in male Sprague–Dawley rats [94]. It alters the vocal, auditory, orientation, and memory systems in bats Hipposideros armiger terasensis [95].
Humans
Arm tremors in prenatally exposed children [96]. Alterations in the social and motor function of 3-year-old children are exposed postnatally [97]. Neurobehavioral deficits in exposed Egyptian workers [98].
Semi-conscious state due to acute intoxication [99].
Coma, dyspnea, and sweating in acute poisonings [100]. Drowsiness, confusion, incoherence, lack of orientation, and unconsciousness after acute poisoning [101]. Somnolence, Glasgow Coma Scale with a score of 10/15 and Miotic pupils after acute poisoning [102].
Table 4.
Behavioral effects of chlorpyrifos, carbaryl and imidacloprid on five animal species.
Neurochemical effects
Chlorpyrifos
Carbaryl
Imidacloprid
Insects
Decreased acetylcholinesterase activity and oxidative stress in Nauphoeta cinerea cockroaches’ heads [52]. Lipid peroxidation and protein carbonylation in Diamesa zernyi larvae [54]. Increased levels of acetylcholinesterase in Apis mellifera bees’ heads [103].
Inhibition of carbonic anhydrase in the bee Apis mellifera [104]. Decreased levels of acetylcholinesterase in the head of the bee Apis mellifera [103].
Increased levels of acetylcholinesterase in the heads of the bee Apis mellifera [103]. It decreases the activity of acetylcholinesterase and 8-hydroxy-2-deoxyguanosine, increases the levels of antioxidant enzymes in the brain tissue of the rainbow trout Oncorhynchus mykiss [105].
Aquatics organisms
Cholinesterase inhibition in the protobrain of shrimp Artemia salina [62]. Inhibition of acetylcholinesterase in the gastropod Gibbula umbilicalis [83]. Oxidative stress and acetylcholinesterase inhibition in common carp Cyprinus carpio brain tissue [106]. Decreased acetylcholinesterase activity and oxidative stress in Physalaemus gracilis tadpoles [63]. Cholinesterase inhibition in Chilina gibbosa [107].
Decreased levels of acetylcholine, GABA, choline, tryptophan, and phenylalanine in Danio rerio zebrafish larvae [108]. Cholinesterase inhibition in the protobrain of shrimp Artemia salina [62]. Inhibits acetylcholinesterase activity in the brain of tropical fish Phalloceros harpagos, Pterygoplichthys pardalis, and Astyanax altiparanae [109]. Inhibition of cholinesterase and carboxylesterase in Chilina gibbosa [107].
It increases acetylcholinesterase activity and causes oxidative stress in Gobiocypris rarus fish brain tissue [110]. Inhibition of brachial acetylcholinesterase in Sydney rock oyster [111]. Oxidative stress and acetylcholinesterase inhibition in zebrafish Danio rerio [75]. Inhibition of acetylcholinesterase in the muscle of Astyanax altiparanae fish [112].
Birds
Decreased acetylcholinesterase activity in blood, serum, and plasma of broilers [77]. Inhibition of acetylcholinesterase and butyrylcholinesterase; oxidative stress in the brain of the Coturnix japanica quail [113].
Inhibition of plasma acetylcholinesterase in the vulture Gyps fulvus [114].
It increases the levels of monoamines in the cerebral cortex of the Coturnix coturnix quail [115]. Alteration of acetylcholinesterase and glutathione-S-transferase activity in the muscle and brain of the gray bay-wing bird Agelaioides baduis [116].
Non-human vertebrates
Decreased activity of acetylcholinesterase; down-regulation of genes related to Parkinson’s disease, synaptic transmission, plasticity, and dopaminergic and GABAergic signaling [117]. Acetylcholinesterase increased activity; increased levels of nitric oxide and reactive oxygen species in the amygdala and hippocampus of male Wistar rats [86]. Decreased acetylcholinesterase activity in the brain and cerebellum of Sprague Dawley rats [85]. Decreased dopamine levels and acetylcholinesterase activity in the striatum of Swiss mice [87]. Decreased brain levels of dopamine, serotonin and the activity of monoamine oxidase, acetylcholinesterase, and sodium-potassium ATPase in rats [118].
Acetylcholinesterase inhibition in Norwegian gray rats [91].
Increased acetylcholinesterase activity and calcium levels in the hypothalamus and pituitary of the Wistar rat [119]. Increased levels of epinephrine, norepinephrine, and cortisone in the serum of male Sprague–Dawley rats [93]. Reduction of serotonin, GABA, and dopamine levels, as well as oxidative stress in the brain of male Sprague–Dawley rats [94]. Reduction of GABA and glutathione levels, as well as a decrease in SDH in the albino rat brain [120].
Humans
Humans Decreased intracellular ATP levels and mitochondrial dysfunction in induced pluripotent stem cells [121].
Binding to human melatonin receptors [122]. Inhibition of plasma acetylcholinesterase after acute poisoning [99].
Increases intracellular calcium levels in LUHMES and SH-SY5Y neurons [123].
Table 5.
Neurochemical effects of chlorpyrifos, carbaryl and imidacloprid on five animal species.
Effects on the cellular level
Chlorpyrifos
Carbaryl
Imidacloprid
Insects
No recent studies for the review period in the literature.
No recent studies for the review period in the literature.
Induction of apoptosis by increased levels of caspase-3 and caspase-1 mRNA in the bee Apis mellifera [124]. Apoptosis and autophagy in neurons of the brain of the bee Apis mellifera [124]. Decreased density of synaptic units in the fungal bodies of the bee Apis mellifera [125]. Decreased driving speed in locusta migratoria [60].
Aquatics organisms
Increased expression of BNDF and c-fos in brain tissues of the zebrafish Danio rerio [126]. Degeneration and vacuolization in neurons of the dorsal pars medialis in the catfish Heteropneustes fossilis [64].
No recent studies for the review period in the literature.
Increased expression of BDNF and c-fos in brain tissues of the zebrafish Danio rerio [126].
Birds
Necrosis and degeneration in the brain of broilers [77]. Neurodegeneration, infiltration of mononuclear cells in the brain, and congestion of blood vessels of the meninges of broilers [127]. Neurodegeneration, liquefactive necrosis, vacuolar degeneration, glia cell enlargement, and satellitosis in the broiler brain [128].
No recent studies for the review period in the literature.
Pyknosis, karyolysis, perineuronal edema, reactive astrocytosis, among other histopathological findings in the white Leghorn hen embryos cerebellum [129]. Neurodegeneration, axonal degeneration with demyelination, congestion, perivascular edema, neuronal vacuolization in the Columba livia domestica pigeon [130].
No humans vertebrates
Histological alterations in the brain and cerebellum of Sprague Dawley rats [85]. Lewy body formation and neurodegeneration in the substantia nigra of Swiss albino mice [131]. Gliosis and Purkinje cell degeneration in male Wistar rats [132].
Alterations in normal brain development due to changes in important protein levels during neonatal exposure in NMRI mice [90]. Alterations in the electroencephalogram of the visual and frontal cortex of the male Long Evans rat [133]. Neuroinflammation in the hippocampus of male Wistar rats exposed during pregnancy and lactation [134].
Neurodegeneration and increased GFAP expression in the brain of male Sprague–Dawley rats [94]. Absence of the cellular band of the hippocampal formation in mice [135]. Decreased proteins related to echolocation in different brain regions of the bat Hipposideros armiger terasensis [95]. DNA damage of male Wistar rat brain cells [136].
Humans
Inhibition of voltage-gated calcium channels in human PC12 cells [137]. Inhibition of neurite length, number of neurites, and branch points per neuron in human neural progenitor cells [138]. Apoptotic cell death in human neural stem cells [139]. Alterations in the morphology of different brain regions in exposed children [140].
Associated with meningiomas in people involved in agriculture [141].
Brain edema after acute poisoning [101]. Cell death in neurons of SH-SY5Y human neuroblastoma [142].
Table 6.
Effects on the cellular level of chlorpyrifos, carbaryl and imidacloprid on five animal species.
6.1 Chlorpyrifos
The recent literature regarding chlorpyrifos toxic effects in different species is extensive. However, this chapter has focused on those that are associated with effects on the nervous system. For example, in non-target insects, such as bees, it has been observed that it can have adverse effects on caste differentiation [50], as well as on olfactory learning and memory retention [51, 53]; in cockroaches [52] and mosquito larvae [54] has been associated with locomotor alterations (Table 4) [143]. It has also been documented that chlorpyrifos can cause alterations in acetylcholinesterase activity and induce oxidative stress in different insects [52, 54, 103] and annelids (Table 5). On the other hand, in aquatic organisms such as mollusks, crustaceans, amphibians, and fish, it has been reported that it can cause alterations in locomotor activity [61, 63, 64, 144], inhibit acolinesterase in shrimp [62, 144], copepods [145], common carp [106], tadpoles [63] and snails [61, 107], as well as causing neuronal degeneration in catfish [64]. In toxicity studies carried out in broilers, it has been described that it can cause nervous signs such as salivation, tearing, panting, frequent defecation, tremors, and seizures [77], in sparrows, it can alter the migratory orientation [78] and inhibit acetylcholinesterase activity in broilers [77] and quail (Tables 4 and 5) [113]. Regarding its cellular effects, in repeated studies, chlorpyrifos has been reported to be associated with neurodegeneration in broilers [127, 128]. The neurotoxic effects of chlorpyrifos scale to small mammal species. In fact, in rodents under experimental conditions, it has been seen that it can have anxiogenic effects [83, 86] and cause alterations in the memory of recognition [84] and reference [86] in locomotor activity [85, 87], in social behavior (Table 4) [84, 89].
While, acute poisonings are associated with signs of piloerection, tremors, seizures, and hypoactivity, among other neurological manifestations [88]. Regarding brain neurochemistry in experimental rodents, it has been reported that chlorpyrifos can alter the activity of acetylcholinesterase. It participates in the downregulation of genes related to Parkinson’s disease, causes oxidative stress and decreases dopamine and serotonin levels [86, 87, 117, 118]. Overall, it has also been associated with neurodegeneration in rodents for experimentation [85, 131, 132]. In humans, it has been reported that chlorpyrifos can alter social and motor function in children (Table 5) [96, 97]. As well as having fallout related to neurobehavioral deficits in workers exposed to the insecticide [98]. At the neurochemical level, in an in vitro study with human cells, it was shown that it can decrease intracellular levels of ATP and cause mitochondrial dysfunction [121]. Finally, at the cellular level, it has been reported to cause inhibition of activated calcium channels by voltage [137], alter morphology [138], and induce apoptosis in vitro [139]. In human cells exposed to chlorpyrifos, a recently published study reported that it may be associated with alterations in the morphology of different brain regions in children exposed to the substance (Table 6) [140].
6.2 Carbaryl
Recent studies on the neurotoxic effects associated with carbaryl are scarce. However, it has been reported that in bees, it can inhibit carbonic anhydrase [104] and decrease acetylcholinesterase levels [103], as well as its negative effect on isopod growth and survival (Table 5) [146]. In aquatic organisms, it has been discovered that carbaryl can cause embryonic deformities and growth inhibition in crustaceans [147], affect hatching speed in shrimp [62], locomotives alterations in blue crabs [66], mussels [68], and zebrafish [69]. Besides, in this same species, it has been associated with alterations in exploratory, social, and feeding behavior [67]. Likewise, in tadpoles, it causes hypoactivity, reduction in escape swimming, and feeding behavior (Table 4) [65]. Regarding the effects on brain chemistry, it has been reported that carbaryl may be related to the decrease in the levels of acetylcholine, GABA, choline, tryptophan, and phenylalanine in zebrafish [108]. Additionally, it inhibits acetylcholinesterase in shrimp [62], in some species of tropical fish [109], and also in mollusks (Table 5) [107]. On the other hand, it has been documented that in broilers, acute poisoning can cause walking difficulty, weakness in the legs, dizziness, frequent defecation, less food consumption, and a decrease in aggressive behavior (Table 4) [79]. Overall, acetylcholinesterase inhibition has been reported, particularly in the vulture [114]. Simultaneously, in experimental rodents, it has been associated with deficits in memory and learning. As well as alterations in habitual behavior [90] and hypoactivity [91]. Furthermore, in a supposed carbaryl poisoning in bats, signs such as hypersalivation, miotic pupils, lethargy, and coma were reported [92]. This substance can also inhibit acetylcholinesterase in Norwegian gray rats [91] and in experimental rodents. The above has been related to neurodevelopmental alterations [90], as depicted in the visual and frontal cortex electroencephalogram [133] and hippocampal neuroinflammation [134]. In humans, it has been linked to a semi-conscious state and acetylcholinesterase inhibition after acute poisoning in a 3-year-old child, without further details on other associated neurological signs (Table 4) [99]. Moreover, in an in vitro study, it was observed that carbaryl could bind to human melatonin receptors [122]. Carbaryl was recently associated with meningiomas in people agriculturally involved in an epidemiological investigation [141].
While, acute poisonings are associated with signs of piloerection, tremors, seizures, and hypoactivity, among other neurological manifestations [88]. Regarding brain neurochemistry in experimental rodents, it has been reported that chlorpyrifos can alter the activity of acetylcholinesterase [86, 87, 117, 118]. It participates in the downregulation of genes related to Parkinson’s disease [117], causes oxidative stress [86] and decreases dopamine and serotonin levels [87, 118]. Overall, it has also been associated with neurodegeneration in rodents for experimentation [131, 132]. In humans, it has been reported that chlorpyrifos can alter social and motor function in children [96, 97]. As well as having fallout related to neurobehavioral deficits in workers exposed to the insecticide [98]. At the neurochemical level, in an in vitro study with human cells, it was shown that it can decrease intracellular levels of ATP and cause mitochondrial dysfunction [121]. Finally, at the cellular level, it has been reported to cause inhibition of activated calcium channels by voltage [137], alter morphology [138], and induce apoptosis in vitro [139]. In human cells exposed to chlorpyrifos, a recently published study reported that it may be associated with alterations in the morphology of different brain regions in children exposed to the substance (Table 6) [140].
6.3 Imidacloprid
Despite being considered harmless for most living organisms, neonicotinoid insecticide have been the focus of extensive investigation, as their toxicity has been proven to extend beyond insects [148], to humans. Imidacloprid poisoning in bees has been associated to neurological symptoms such as paralysis and tremors [56], and fire ant exposure has been linked to decreased consumption, foraging, and digging behavior, as well as parasitic wasps with alterations in host-seeking behavior (Table 4) [57, 58]. Reduced visual mobility and degradation in in-flight behavior in lobsters, in addition to influencing queen selection behavior in stingless bees have been other reported consequences of the exposure to this insecticide [59, 60]. Imidacloprid has been linked to a decrease in the density of synaptic units in fungiform bodies [125] and a decrease in driving speed in lobsters [103]. It can also increase acetylcholinesterase levels [103] and induce apoptosis and neuronal autophagy [60, 124]. In edaphic invertebrates, imidacloprid causes diverse effects on the survival, growth, and reproduction of earthworms, springtails, mites, and isopods based on LC50, EC50, and EC20 toxicity tests [149]. In aquatic organisms, a decrease in acetylcholinesterase levels in mollusks has been reported [150], as well as varied effects on exploratory behavior, swimming activity, and sensorimotor response to startling stimuli in zebrafish (Tables 4 and 5) [70].
Moreover, exposure to imidacloprid has been associated with alterations in swimming behavior in tadpoles [71] and shrimp [73], decreased response to predators in frogs [72], and locomotor alterations in crabs [74], zebrafish [75] and tadpoles (Table 4) [76]. At the neurochemical level, it has been proposed that imidacloprid can alter acetylcholinesterase activity and cause oxidative stress in fish [75, 105, 110]. It also inhibits brachial acetylcholinesterase in oysters [111] and in fish muscles (Table 5) [112]. At the cellular level, it has been documented that the above may be associated with increased expression of BNDF and c-fos in the brain tissues of zebrafish (Table 6) [126]. In birds, it has been reported that exposure to imidacloprid can cause hypoactivity, decreased flight behavior, spasms, drooping wings, ataxia, and prostration in pigeons [80]. It has also been stated that it can alter the migratory orientation and delay the time of starting migration in the white-crowned sparrow [151]. In one of the most recently published studies, it was reported that in chickens, it can generate neurological signs such as muscle tremors, ataxia and depression (Table 4) [82]; in quail, it can increase monoamine levels in the cerebral cortex [115] and alter the activity of acetylcholinesterase in the muscles and brain of the gray laurel wing bird (Table 5) [116]. At the cellular level, it has been associated with neurodegeneration in chicken embryos’ cerebellum [129] and pigeons [130]. In experimentation rodents, it has been associated with hypoactivity, increased grooming behavior, and conduct associated with anxiety and depression [93, 94]. While in bats, it may be associated with alterations in the vocal, auditory, orientation, and memory systems (Table 4) [95]. Also, in rodents, it can increase acetylcholinesterase activity [119], adrenaline, norepinephrine, and cortisone levels [93], and reduce serotonin, GABA, dopamine, and glutathione (Table 5) [120, 152]. Regarding the cellular effects, exposure to imidacloprid can also cause neurodegeneration, an increase in the expression of GFAP [152], and DNA damage in neurons [136]. In bats, it has been related to a decrease in proteins related to echolocation in different brain regions [95]. Moreover, in humans, acute imidacloprid poisonings have been associated with neurological signs such as dyspnea, coma, sweating, drowsiness, confusion, incoherence, lack of orientation, and miotic pupils, among others [100, 101, 102]. In an in vitro study with LUHMES and SH-SY5Y cells, an increase in intracellular calcium levels was found [123] (Table 5) On the other hand, after acute poisoning, cerebral edema has been reported as a necropsy finding [101], while in an in vitro study it was revealed that it can cause the death of SH-SY5Y cells [135].
On the other hand, acute poisonings are linked to piloerection, tremors, seizures, and hypoactivity, among other neurological manifestations. Regarding brain neurochemistry in experimental rodents, it has been reported that chlorpyrifos can alter the activity of acetylcholinesterase [86, 87, 117, 118]. It participates in the downregulation of genes related to Parkinson’s disease [117], causes oxidative stress [86] and decreases dopamine and serotonin levels [87, 118]. Overall, it has also been associated with neurodegeneration in rodents for experimentation [85, 132]. In humans, it has been reported that chlorpyrifos can alter social and motor function in children [96, 97]. As well as having fallout related to neurobehavioral deficits in workers exposed to the insecticide [98]. At the neurochemical level, in an in vitro study with human cells, it was shown that it can decrease intracellular levels of ATP and cause mitochondrial dysfunction [121]. Finally, at the cellular level, it has been reported to cause inhibition of activated calcium channels by voltage [137], alter morphology [138], and induce apoptosis in vitro [139]. In human cells exposed to chlorpyrifos, a recently published study reported that it may be associated with alterations in the morphology of different brain regions in children exposed to the substance [140].
7. Conclusions and perspectives
Insecticides are pesticides commonly associated with neurotoxic effects [153] and although the general population is exposed on a daily basis to low doses through water and food [154, 155, 156] the highest risk is presented by agricultural workers, their families and people who live in the areas surrounding the fields, unfortunately, these people are the most exposed and also the least informed about the toxic effects, which leads to bad practices of use, handling and disposal of these substances, which put wildlife and the environment at risk. Since the effects that cause the greatest impact are usually those that directly affect human health, in conclusion some neurotoxic effects associated with the use of insecticides are revealed. In epidemiological studies in humans, organophosphates have been linked to effects such as cholinergic syndrome, polyneuropathy and neuropsychiatric disorders such as cognitive deficits, anxiety, depression, peripheral neuropathy, extrapyramidal symptoms such as dystonia, tremor at rest, bradykinesia, postural instability and rigidity of facial muscles, among others, and have even been associated with neurodegenerative diseases such as Parkinson’s and Alzheimer’s disease [157, 158]; neonicotinoids have been linked to developmental diseases such as autism and anencephaly and in acute poisonings with neurological signs such as memory loss, finger tremors, muscle spasms, coma and dilated pupils [159, 160, 161]; On the other hand, with regard to epidemiological studies on neurotoxicity of carbamates in humans, the literature is limited, however, in the most recently published article, it has been reported that after acute poisoning, these pesticides can cause signs such as coma, drowsiness, seizures, disorientation, tremors and fasciculations, among others [157]. However, although there are epidemiological studies in which the possible relationship between exposure to pesticides and neurological disorders has been determined, to date they remain limited and in fact most of the toxic effects of many pesticides used in the field are unknown. agriculture and therefore it is difficult to determine how we can protect ourselves from them, although there are studies in which the neuroprotective effect of various substances has been experimentally demonstrated, which could counteract the neurotoxic effects of pesticides, for example in the case of pesticides. Organophosphates it has been documented that the flavonoid kaempferol may have protective effects on chlorpyrifos-induced neurotoxicity [162] and that crocin and citric acid may also have the same effect on malathion-induced toxicity [163, 164]; in the case of neonicotinoids, reduced glutathione, curcumin, resveratrol, ascorbic acid, and aqueous ginger extract have been shown to act as neuroprotectors against imidacloprid-induced toxicity [165, 166, 167, 168], as well as curcumin and N-acetylcysteine can protect against acetamiprid-induced neurotoxicity [169, 170]; In the case of carbamates, it has been described that naringenin can combat oxidative stress induced by exposure to carbaryl [171]. Previous studies offer alternatives as possible neuroprotectors, therefore, it is necessary to continue investigating the mechanisms of toxicity and target species of pesticides that exist on the market, before thinking of creating new, more powerful and, of course, more toxic pesticides ; In addition to banning those that pose a high risk to living beings and the environment and making strict policies to control their distribution and sale, since it is clear that it is difficult to live without pesticides, however, it is our duty to use them responsibly.
Acknowledgments
The present work has been possible thanks to Grant from Consejo Nacional de Ciencias y Tecnología (CONACYT) México, registry number 287959.
Conflict of interest
The authors declare no conflict of interest.
\n',keywords:"insecticides, chlorpyrifos, carbaryl, imidacloprid, neurotoxicity",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/79254.pdf",chapterXML:"https://mts.intechopen.com/source/xml/79254.xml",downloadPdfUrl:"/chapter/pdf-download/79254",previewPdfUrl:"/chapter/pdf-preview/79254",totalDownloads:87,totalViews:0,totalCrossrefCites:0,dateSubmitted:"September 3rd 2021",dateReviewed:"September 19th 2021",datePrePublished:"December 2nd 2021",datePublished:"March 30th 2022",dateFinished:"November 7th 2021",readingETA:"0",abstract:"Insecticides are pesticides used to control insects in agriculture, ornamental gardens, homes, and veterinary medicine. Although the toxic effects on the environment and the health of living beings are not fully understood, these pesticides have become the first options for crop protection in agriculture. After herbicides, insecticides are the most extensively used pesticides in agriculture, with large quantities consumed on every continent, primarily in America. Chlorpyrifos, carbaryl, and imidacloprid are among the top ten most used insecticides. Amidst organophosphates, chlorpyrifos has been reported to be used in over fifty food crops. Carbaryl is a carbamate employed as an insecticide, fungicide, herbicide, and nematicide. Similarly, neonicotinoids are the most used insecticide on a global scale. Neonicotinoids include imidacloprid, the second most frequently used pesticide, surpassed only by glyphosate. It is used because it is less toxic to humans. However, insects appear to be less resistant to its compounds. Evidence suggests that these insecticides persist in soils for a long time and have neurotoxic effects in animal species not intended to receive its consequences. Thus, this chapter’s aim is to describe these three pesticides effects and contrast them with the most recent findings regarding their neurotoxic effects in various animal species.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/79254",risUrl:"/chapter/ris/79254",signatures:"Alejandra Mora-Gutiérrez, Carmen Rubio, Ángel Alonso Romero-López and Moisés Rubio-Osornio",book:{id:"10736",type:"book",title:"Neurotoxicity",subtitle:"New Advances",fullTitle:"Neurotoxicity - New Advances",slug:"neurotoxicity-new-advances",publishedDate:"March 30th 2022",bookSignature:"Suna Sabuncuoglu",coverURL:"https://cdn.intechopen.com/books/images_new/10736.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",isbn:"978-1-83968-970-3",printIsbn:"978-1-83968-969-7",pdfIsbn:"978-1-83968-971-0",isAvailableForWebshopOrdering:!0,editors:[{id:"270856",title:"Associate Prof.",name:"Suna",middleName:null,surname:"Sabuncuoglu",slug:"suna-sabuncuoglu",fullName:"Suna Sabuncuoglu"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"419945",title:"Ph.D.",name:"Moisés",middleName:null,surname:"Rubio-Osornio",fullName:"Moisés Rubio-Osornio",slug:"moises-rubio-osornio",email:"ruomon@gmail.com",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"419955",title:"Dr.",name:"Carmen",middleName:null,surname:"Rubio",fullName:"Carmen Rubio",slug:"carmen-rubio",email:"macaru4@yahoo.com.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:{name:"Instituto Nacional de Neurología y Neurocirugía",institutionURL:null,country:{name:"Mexico"}}},{id:"419956",title:"M.Sc.",name:"Alejandra",middleName:null,surname:"Mora-Gutiérrez",fullName:"Alejandra Mora-Gutiérrez",slug:"alejandra-mora-gutierrez",email:"mvzalejandramora@gmail.com",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:{name:"Instituto Nacional de Neurología y Neurocirugía",institutionURL:null,country:{name:"Mexico"}}},{id:"426668",title:"Dr.",name:"Angel",middleName:"Alonso",surname:"Romero-López",fullName:"Angel Romero-López",slug:"angel-romero-lopez",email:"alonso.romerolopez@correo.buap.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:{name:"Benemérita Universidad Autónoma de Puebla",institutionURL:null,country:{name:"Mexico"}}}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Worldwide use of insecticides",level:"1"},{id:"sec_3",title:"3. Of the molecule, its structure, and mechanism of action",level:"1"},{id:"sec_3_2",title:"3.1 Chlorpyrifos",level:"2"},{id:"sec_4_2",title:"3.2 Imidacloprid",level:"2"},{id:"sec_5_2",title:"3.3 Carbaryl",level:"2"},{id:"sec_7",title:"4. Persistence in soil and water",level:"1"},{id:"sec_8",title:"5. Neurotoxic effects in different animal species",level:"1"},{id:"sec_9",title:"6. Neurotoxic effects of chlorpyrifos, carbaryl, and imidacloprid",level:"1"},{id:"sec_9_2",title:"6.1 Chlorpyrifos",level:"2"},{id:"sec_10_2",title:"6.2 Carbaryl",level:"2"},{id:"sec_11_2",title:"6.3 Imidacloprid",level:"2"},{id:"sec_13",title:"7. Conclusions and perspectives",level:"1"},{id:"sec_14",title:"Acknowledgments",level:"1"},{id:"sec_17",title:"Conflict of interest",level:"1"}],chapterReferences:[{id:"B1",body:'Sharma A, Kumar V, Shahzad B. 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Effects of neonicotinoid pesticide exposure on human health: a systematic review. Environmental Health Perspectives. 2017;125(2), 155-162. DOI. https://doi.org/10.1289/EHP515'},{id:"B161",body:'Thompson DA, Lehmler HJ, Kolpin DW, Hladik ML, Vargo JD, Schilling KE, et al. A critical review on the potential impacts of neonicotinoid insecticide use: current knowledge of environmental fate, toxicity, and implications for human health. Environmental Science: Processes & Impacts. 2020;22(6), 1315-1346. DOI. https://doi.org/10.1039/C9EM00586B'},{id:"B162",body:'Hussein RM, Mohamed WR, Omar HA. A neuroprotective role of kaempferol against chlorpyrifos-induced oxidative stress and memory deficits in rats via GSK3β-Nrf2 signaling pathway. Pesticide Biochemistry and Physiology. 2018;152, 29-37. DOI. https://doi.org/10.1016/j.pestbp.2018.08.008'},{id:"B163",body:'Abdel-Salam OM, Youness ER, Mohammed NA, Yassen NN, Khadrawy YA, El-Toukhy SE, et al. 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Evaluation of imidacloprid-induced neurotoxicity in male rats: a protective effect of curcumin. Neurochemistry International. 2014;78, 122-129. DOI. https://doi.org/10.1016/j.neuint.2014.09.004'},{id:"B167",body:'Waseem M, Jain S, Parvez S, Akram M. Ascorbic acid modulates non enzymatic antioxidants in swiss albino mice targeted to imidacloprid: Brain v/s Liver. (2016). https://www.thepharmajournal.com/archives/2016/vol5issue8/PartB/9-10-89-996.pdf.'},{id:"B168",body:'Farag MR, Abou-EL Fotoh MF, EL-Sayed GG, EL-Sayed EW. Modulatory Effect of Ginger Aqueous Extract against Imidacloprid-Induced Neurotoxicity in Rats. Zagazig Veterinary Journal. 2019;47(4), 432-446. DOI. http://doi.org/10.21608/zvjz.2019.14914.1061'},{id:"B169",body:'Dhouib IB, Annabi A, Doghri R, Rejeb I, Dallagi Y, Bdiri Y, et al. Neuroprotective effects of curcumin against acetamiprid-induced neurotoxicity and oxidative stress in the developing male rat cerebellum: biochemical, histological, and behavioral changes. Environmental Science and Pollution Research. 2017;24(35), 27515-27524. DOI. https://doi.org/10.1007/s11356-017-0331-5'},{id:"B170",body:'Khovarnagh N, Seyedalipour B. Antioxidant, histopathological and biochemical outcomes of short-term exposure to acetamiprid in liver and brain of rat: The protective role of N-acetylcysteine and S-methylcysteine. Saudi Pharmaceutical Journal. 2021;29(3), 280-289. DOI. https://doi.org/10.1016/j.jsps.2021.02.004'},{id:"B171",body:'Muthaiah VK, Venkitasamy L, Michael FM, Chandrasekar K, Venkatachalam S. Neuroprotective role of naringenin on carbaryl induced neurotoxicity in mouse neuroblastoma cells. Journal of Pharmacology & Pharmacotherapeutics. 2013;4(3), 192. doi: https://doi.org/10.4103/0976-500X.114599.'}],footnotes:[],contributors:[{corresp:null,contributorFullName:"Alejandra Mora-Gutiérrez",address:null,affiliation:'
Department of Neurochemistry, National Institute of Neurology and Neurosurgery, M.V.S., Mexico
Department of Neurochemistry, National Institute of Neurology and Neurosurgery, M.V.S., Mexico
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Dr. Nawaz did his PhD from University of Sao Paulo, Ribeirao Preto Medical School (Brazil), where he worked on transcriptomic and microRNAs (miRNAs) profiling in the malignant progression of brain tumors (gliomas) with an aim to identify potential therapeutic targets and non-invasive biomarkers. During his PhD, Dr. Nawaz was granted with fellowship from FAPESP (the highest ranked funding body in Brazil), and was also awarded with Science without borders mobility award from Brazilian higher education agency (CAPES) to join the University of Gothenburg for one year PhD exchange, where he worked on mechanisms of packaging therapeutic RNAs into exosomes, which are now used as RNA delivery vehicles. Later, he continued his Postdoc at the University of Gothenburg. He has also served community services, and is the founder of Biochemists Association QUA Islamabad (BAQI), and is junior member of international society for extracellular vesicles (ISEV). 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As a gold Open Access publisher, an Open Access Publishing Fee is payable on acceptance following peer review of the manuscript. In return, we provide high quality publishing services and exclusive benefits for all contributors. IntechOpen is the trusted publishing partner of over 140,000 international scientists and researchers.
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The Open Access Publishing Fee (OAPF) is payable only after your book chapter, monograph or journal article is accepted for publication.
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OAPF Publishing Options
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1,400 GBP Chapter - Edited Volume
\n\t
850 GBP Chapter - Book Series Topic (Annual Volume)
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10,000 GBP Monograph - Long Form
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4,000 GBP Compacts Monograph - Short Form
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During the launching phase journals do not charge an APC, rather they will be funded by IntechOpen.
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*These prices do not include Value-Added Tax (VAT). Residents of European Union countries need to add VAT based on the specific rate in their country of residence. Institutions and companies registered as VAT taxable entities in their own EU member state will not pay VAT as long as provision of the VAT registration number is made during the application process. This is made possible by the EU reverse charge method.
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Services included are:
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An online manuscript tracking system to facilitate your work
\n\t
Personal contact and support throughout the publishing process from your dedicated Author Service Manager
\n\t
Assurance that your manuscript meets the highest publishing standards
\n\t
English language copyediting and proofreading, including the correction of grammatical, spelling, and other common errors
\n\t
XML Typesetting and pagination - web (PDF, HTML) and print files preparation
\n\t
Discoverability - electronic citation and linking via DOI
\n\t
Permanent and unrestricted online access to your work
\n
\n\n
What isn't covered by the Open Access Publishing Fee?
\n\n
If your manuscript:
\n\n
\n\t
Exceeds the number of pages defined by the publishing guidelines, an additional fee per page may be required
\n\t
If a manuscript requires Heavy Editing or Language Polishing, this will incur additional fees.
\n
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Your Author Service Manager will inform you of any items not covered by the OAPF and provide exact information regarding those additional costs before proceeding.
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To explore funding opportunities and learn more about how you can finance your IntechOpen publication, go to our Open Access Funding page. IntechOpen offers expert assistance to all of its Authors. We can support you in approaching funding bodies and institutions in relation to publishing fees by providing information about compliance with the Open Access policies of your funder or institution. We can also assist with communicating the benefits of Open Access in order to support and strengthen your funding request and provide personal guidance through your application process. You can contact us at funders@intechopen.com for further details or assistance.
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Known theories on UF/MF membrane formation from phase inversion (Dr/wet) systems can be prolonged to define the consequences of high or low molecular weight additives. Also, direct material reengineering and surface modification for high-performance anti-fouling of UF/MF membranes are also highlighted. Before the modern final polymeric film, the characterization techniques, particularly molecular weight cut-off, pore size, pore size distribution, and microbiological activity classification, on to the UF/MF membrane surface were presented, respectively. Lab scale to commercial scale UF/MF membrane configuration and market size of UF/MF membranes for pretreatment desalination are described. The significance of UF/MF provided here as an unconventional approach for desalination water pretreatment is in contrast with the current conventionally used technologies. The recent development made in the integration of established desalination processes, such as spiral wound reverse osmosis (SWRO), multi-stage flash (MSF), multi-effect distillation (MED), electrodialysis (ED) desalination, and UF pretreatment, is addressed. Finally, the influence of UF/MF on desalination water pretreatment step on to the energy cost of desalination process system is discussed.",book:{id:"5768",slug:"desalination",title:"Desalination",fullTitle:"Desalination"},signatures:"Iqbal Ahmed, Khaled S. Balkhair, Muhammad H. Albeiruttye and\nAmer Ahmed Jamil Shaiban",authors:[{id:"197244",title:"Associate Prof.",name:"Iqbal",middleName:null,surname:"Ahmed",slug:"iqbal-ahmed",fullName:"Iqbal Ahmed"},{id:"197251",title:"Dr.",name:"Khaled",middleName:null,surname:"S. Balkhair",slug:"khaled-s.-balkhair",fullName:"Khaled S. Balkhair"},{id:"197252",title:"Prof.",name:"Muhammad H",middleName:null,surname:"Albeiruttye",slug:"muhammad-h-albeiruttye",fullName:"Muhammad H Albeiruttye"},{id:"197253",title:"MSc.",name:"Amer",middleName:null,surname:"AhmedJamil Shaiban",slug:"amer-ahmedjamil-shaiban",fullName:"Amer AhmedJamil Shaiban"}]}],mostDownloadedChaptersLast30Days:[{id:"39727",title:"Asymmetric Hydrogenation",slug:"asymmetric-hydrogenation",totalDownloads:12121,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"2874",slug:"hydrogenation",title:"Hydrogenation",fullTitle:"Hydrogenation"},signatures:"Tsuneo Imamoto",authors:[{id:"146245",title:"Prof.",name:"Tsuneo",middleName:null,surname:"Imamoto",slug:"tsuneo-imamoto",fullName:"Tsuneo Imamoto"}]},{id:"55753",title:"Desalination: A Means of Increasing Irrigation Water Sources for Sustainable Crop Production",slug:"desalination-a-means-of-increasing-irrigation-water-sources-for-sustainable-crop-production",totalDownloads:2116,totalCrossrefCites:2,totalDimensionsCites:5,abstract:"Globally, water resources for agricultural production have been on the decline. This is associated with increase in water demand over limited resources and poor quality water that adversely affects crop quality and yield and deteriorates soil properties. Even though soil salinity has been affectingagriculture for thousands of years, significant research has been conducted only in the past 100 years. Desalination, which is the process of reducing the salt content in water to an acceptable level, could be an alternative for improving water quality, thereby increasing water sources and reducing the competition among various users of water. Thus, desalination could lead to improved crop quality, improved crop yield, enhanced all‐year round crop production, and as such become an important tool for effective agricultural water management.",book:{id:"5768",slug:"desalination",title:"Desalination",fullTitle:"Desalination"},signatures:"OrevaOghene Aliku",authors:[{id:"176082",title:"Mr.",name:"OrevaOghene",middleName:null,surname:"Aliku",slug:"orevaoghene-aliku",fullName:"OrevaOghene Aliku"}]},{id:"39734",title:"Transition Metal Sulfide Catalysts for Petroleum Upgrading – Hydrodesulfurization Reactions",slug:"transition-metal-sulfide-catalysts-for-petroleum-upgrading-hydrodesulfurization-reactions",totalDownloads:3811,totalCrossrefCites:3,totalDimensionsCites:8,abstract:null,book:{id:"2874",slug:"hydrogenation",title:"Hydrogenation",fullTitle:"Hydrogenation"},signatures:"A. Infantes-Molina, A. Romero-Pérez, D. Eliche-Quesada, J. Mérida-Robles, A. Jiménez-López and E. Rodríguez- Castellón",authors:[{id:"126325",title:"Dr.",name:"Enrique",middleName:null,surname:"Rodríguez-Castellón",slug:"enrique-rodriguez-castellon",fullName:"Enrique Rodríguez-Castellón"}]},{id:"55122",title:"Low-Cost Multi-Effect Solar Still: Alternative Appropriate Technology for Personal Desalination",slug:"low-cost-multi-effect-solar-still-alternative-appropriate-technology-for-personal-desalination",totalDownloads:1762,totalCrossrefCites:2,totalDimensionsCites:3,abstract:"Multi effect solar still (MES) has a stack of multiple layers for evaporation and condensation. The latent heat dissipated during condensation at the front layers are repeatedly recycled for evaporation at the back layers to increase overall desalination productivity. Despite of high efficiency and long history, MES has not been widely used yet, because of relative high cost. In this chapter, newly designed MES is introduced. Since it has low cost, light weight material and simple structure, it could be easily mass even at less developed country. The cost of production for a 1 m2 unit is expected to be less than 300 USD. Structural features are introduced with experimental result which was outdoor tested with homemade lab prototype with 0.219 m2 effective area. 9kg/m2 per day of fresh water was obtained at sunny day (19.5MJ/m2) in Seoul, Korea, which is close to WHO’s recommended minimal daily water supply for individuals (7.5~15 liters). For more practical implementation, further development on prototype and production process should be made as well as long term outdoor test under actual climate it would be used. Worldwide collaboration would be necessary for speeding up implementation.",book:{id:"5768",slug:"desalination",title:"Desalination",fullTitle:"Desalination"},signatures:"Pak Hunkyun",authors:[{id:"197095",title:"Dr.",name:"Hunkyun",middleName:null,surname:"Pak",slug:"hunkyun-pak",fullName:"Hunkyun Pak"}]},{id:"39725",title:"Asymmetric Hydrogenation and Transfer Hydrogenation of Ketones",slug:"asymmetric-hydrogenation-and-transfer-hydrogenation-of-ketones",totalDownloads:8448,totalCrossrefCites:2,totalDimensionsCites:6,abstract:null,book:{id:"2874",slug:"hydrogenation",title:"Hydrogenation",fullTitle:"Hydrogenation"},signatures:"Bogdan Štefane and Franc Požgan",authors:[{id:"146116",title:"Associate Prof.",name:"Bogdan",middleName:null,surname:"Stefane",slug:"bogdan-stefane",fullName:"Bogdan Stefane"},{id:"147826",title:"Prof.",name:"Franc",middleName:null,surname:"Požgan",slug:"franc-pozgan",fullName:"Franc Požgan"}]}],onlineFirstChaptersFilter:{topicId:"496",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:90,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:107,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:33,numberOfPublishedChapters:330,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:14,numberOfPublishedChapters:145,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:9,numberOfPublishedChapters:139,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:123,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:112,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:21,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:11,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:"2753-6580",doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}}]},series:{item:{id:"11",title:"Biochemistry",doi:"10.5772/intechopen.72877",issn:"2632-0983",scope:"Biochemistry, the study of chemical transformations occurring within living organisms, impacts all areas of life sciences, from molecular crystallography and genetics to ecology, medicine, and population biology. Biochemistry examines macromolecules - proteins, nucleic acids, carbohydrates, and lipids – and their building blocks, structures, functions, and interactions. Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. This Biochemistry Series will address the current research on biomolecules and the emerging trends with great promise.",coverUrl:"https://cdn.intechopen.com/series/covers/11.jpg",latestPublicationDate:"August 2nd, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:33,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"Blumenberg",slug:"miroslav-blumenberg",fullName:"Miroslav Blumenberg",profilePictureURL:"https://mts.intechopen.com/storage/users/31610/images/system/31610.jpg",biography:"Miroslav Blumenberg, Ph.D., was born in Subotica and received his BSc in Belgrade, Yugoslavia. He completed his Ph.D. at MIT in Organic Chemistry; he followed up his Ph.D. with two postdoctoral study periods at Stanford University. Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. He has published more than 100 peer-reviewed research articles and graduated numerous Ph.D. and postdoctoral students.",institutionString:null,institution:{name:"New York University Langone Medical Center",institutionURL:null,country:{name:"United States of America"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"14",title:"Cell and Molecular Biology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",isOpenForSubmission:!0,editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",slug:"rosa-maria-martinez-espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",biography:"Dr. Rosa María Martínez-Espinosa has been a Spanish Full Professor since 2020 (Biochemistry and Molecular Biology) and is currently Vice-President of International Relations and Cooperation development and leader of the research group 'Applied Biochemistry” (University of Alicante, Spain). Other positions she has held at the university include Vice-Dean of Master Programs, Vice-Dean of the Degree in Biology and Vice-Dean for Mobility and Enterprise and Engagement at the Faculty of Science (University of Alicante). She received her Bachelor in Biology in 1998 (University of Alicante) and her PhD in 2003 (Biochemistry, University of Alicante). She undertook post-doctoral research at the University of East Anglia (Norwich, U.K. 2004-2005; 2007-2008).\nHer multidisciplinary research focuses on investigating archaea and their potential applications in biotechnology. She has an H-index of 21. She has authored one patent and has published more than 70 indexed papers and around 60 book chapters.\nShe has contributed to more than 150 national and international meetings during the last 15 years. Her research interests include archaea metabolism, enzymes purification and characterization, gene regulation, carotenoids and bioplastics production, antioxidant\ncompounds, waste water treatments, and brines bioremediation.\nRosa María’s other roles include editorial board member for several journals related\nto biochemistry, reviewer for more than 60 journals (biochemistry, molecular biology, biotechnology, chemistry and microbiology) and president of several organizing committees in international meetings related to the N-cycle or respiratory processes.",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null},{id:"15",title:"Chemical Biology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",isOpenForSubmission:!0,editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",slug:"sukru-beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",biography:"Dr. Şükrü Beydemir obtained a BSc in Chemistry in 1995 from Yüzüncü Yıl University, MSc in Biochemistry in 1998, and PhD in Biochemistry in 2002 from Atatürk University, Turkey. He performed post-doctoral studies at Max-Planck Institute, Germany, and University of Florence, Italy in addition to making several scientific visits abroad. He currently works as a Full Professor of Biochemistry in the Faculty of Pharmacy, Anadolu University, Turkey. Dr. Beydemir has published over a hundred scientific papers spanning protein biochemistry, enzymology and medicinal chemistry, reviews, book chapters and presented several conferences to scientists worldwide. He has received numerous publication awards from various international scientific councils. He serves in the Editorial Board of several international journals. Dr. Beydemir is also Rector of Bilecik Şeyh Edebali University, Turkey.",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",slug:"deniz-ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",biography:"Dr. Deniz Ekinci obtained a BSc in Chemistry in 2004, MSc in Biochemistry in 2006, and PhD in Biochemistry in 2009 from Atatürk University, Turkey. He studied at Stetson University, USA, in 2007-2008 and at the Max Planck Institute of Molecular Cell Biology and Genetics, Germany, in 2009-2010. Dr. Ekinci currently works as a Full Professor of Biochemistry in the Faculty of Agriculture and is the Head of the Enzyme and Microbial Biotechnology Division, Ondokuz Mayıs University, Turkey. He is a member of the Turkish Biochemical Society, American Chemical Society, and German Genetics society. Dr. Ekinci published around ninety scientific papers, reviews and book chapters, and presented several conferences to scientists. He has received numerous publication awards from several scientific councils. Dr. Ekinci serves as the Editor in Chief of four international books and is involved in the Editorial Board of several international journals.",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null},{id:"17",title:"Metabolism",coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",isOpenForSubmission:!0,editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",slug:"yannis-karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",biography:"Yannis Karamanos, born in Greece in 1953, completed his pre-graduate studies at the Université Pierre et Marie Curie, Paris, then his Masters and Doctoral degree at the Université de Lille (1983). He was associate professor at the University of Limoges (1987) before becoming full professor of biochemistry at the Université d’Artois (1996). He worked on the structure-function relationships of glycoconjugates and his main project was the investigations on the biological roles of the de-N-glycosylation enzymes (Endo-N-acetyl-β-D-glucosaminidase and peptide-N4-(N-acetyl-β-glucosaminyl) asparagine amidase). From 2002 he contributes to the understanding of the Blood-brain barrier functioning using proteomics approaches. He has published more than 70 papers. His teaching areas are energy metabolism and regulation, integration and organ specialization and metabolic adaptation.",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null},{id:"18",title:"Proteomics",coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",isOpenForSubmission:!0,editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",slug:"paolo-iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",biography:"Paolo Iadarola graduated with a degree in Chemistry from the University of Pavia (Italy) in July 1972. He then worked as an Assistant Professor at the Faculty of Science of the same University until 1984. In 1985, Prof. Iadarola became Associate Professor at the Department of Biology and Biotechnologies of the University of Pavia and retired in October 2017. Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. He is a Consultant Reviewer for several journals, including the Journal of Chromatography A, Journal of Chromatography B, Plos ONE, Proteomes, International Journal of Molecular Science, Biotech, Electrophoresis, and others. He is also Associate Editor of Biotech.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",slug:"simona-viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",biography:"Simona Viglio is an Associate Professor of Biochemistry at the Department of Molecular Medicine at the University of Pavia. She has been working since 1995 on the determination of proteolytic enzymes involved in the degradation process of connective tissue matrix and on the identification of biological markers of lung diseases. She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. She is an author of about 90 publications (According to Scopus: H-Index: 23; According to WOS: H-Index: 20) on peer-reviewed journals, a member of the “Società Italiana di Biochimica e Biologia Molecolare,“ and a Consultant Reviewer for International Journal of Molecular Science, Journal of Chromatography A, COPD, Plos ONE and Nutritional Neuroscience.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null}]},overviewPageOFChapters:{paginationCount:42,paginationItems:[{id:"82914",title:"Glance on the Critical Role of IL-23 Receptor Gene Variations in Inflammation-Induced Carcinogenesis",doi:"10.5772/intechopen.105049",signatures:"Mohammed El-Gedamy",slug:"glance-on-the-critical-role-of-il-23-receptor-gene-variations-in-inflammation-induced-carcinogenesis",totalDownloads:11,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Chemokines Updates",coverURL:"https://cdn.intechopen.com/books/images_new/11672.jpg",subseries:{id:"18",title:"Proteomics"}}},{id:"82875",title:"Lipidomics as a Tool in the Diagnosis and Clinical Therapy",doi:"10.5772/intechopen.105857",signatures:"María Elizbeth Alvarez Sánchez, Erick Nolasco Ontiveros, Rodrigo Arreola, Adriana Montserrat Espinosa González, Ana María García Bores, Roberto Eduardo López Urrutia, Ignacio Peñalosa Castro, María del Socorro Sánchez Correa and Edgar Antonio Estrella Parra",slug:"lipidomics-as-a-tool-in-the-diagnosis-and-clinical-therapy",totalDownloads:7,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Fatty Acids - Recent Advances",coverURL:"https://cdn.intechopen.com/books/images_new/11669.jpg",subseries:{id:"17",title:"Metabolism"}}},{id:"82440",title:"Lipid Metabolism and Associated Molecular Signaling Events in Autoimmune Disease",doi:"10.5772/intechopen.105746",signatures:"Mohan Vanditha, Sonu Das and Mathew John",slug:"lipid-metabolism-and-associated-molecular-signaling-events-in-autoimmune-disease",totalDownloads:17,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Fatty Acids - Recent Advances",coverURL:"https://cdn.intechopen.com/books/images_new/11669.jpg",subseries:{id:"17",title:"Metabolism"}}},{id:"82483",title:"Oxidative Stress in Cardiovascular Diseases",doi:"10.5772/intechopen.105891",signatures:"Laura Mourino-Alvarez, Tamara Sastre-Oliva, Nerea Corbacho-Alonso and Maria G. 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Main aspects of the topic are: Applying bioinformatics in drug discovery and development; Bioinformatics in clinical diagnostics (genetic variants that act as markers for a condition or a disease); Blockchain and Artificial Intelligence/Machine Learning in personalized medicine; Customize disease-prevention strategies in personalized medicine; Big data analysis in personalized medicine; Translating stratification algorithms into clinical practice of personalized medicine.",annualVolume:11403,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/7.jpg",editor:{id:"351533",title:"Dr.",name:"Slawomir",middleName:null,surname:"Wilczynski",fullName:"Slawomir Wilczynski",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000035U1loQAC/Profile_Picture_1630074514792",institutionString:null,institution:{name:"Medical University of Silesia",institutionURL:null,country:{name:"Poland"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"5886",title:"Dr.",name:"Alexandros",middleName:"T.",surname:"Tzallas",fullName:"Alexandros Tzallas",profilePictureURL:"https://mts.intechopen.com/storage/users/5886/images/system/5886.png",institutionString:"University of Ioannina, Greece & Imperial College London",institution:{name:"University of Ioannina",institutionURL:null,country:{name:"Greece"}}},{id:"257388",title:"Distinguished Prof.",name:"Lulu",middleName:null,surname:"Wang",fullName:"Lulu Wang",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRX6kQAG/Profile_Picture_1630329584194",institutionString:"Shenzhen Technology University",institution:{name:"Shenzhen Technology University",institutionURL:null,country:{name:"China"}}},{id:"225387",title:"Prof.",name:"Reda R.",middleName:"R.",surname:"Gharieb",fullName:"Reda R. Gharieb",profilePictureURL:"https://mts.intechopen.com/storage/users/225387/images/system/225387.jpg",institutionString:"Assiut University",institution:{name:"Assiut University",institutionURL:null,country:{name:"Egypt"}}}]},{id:"8",title:"Bioinspired Technology and Biomechanics",keywords:"Bioinspired Systems, Biomechanics, Assistive Technology, Rehabilitation",scope:'Bioinspired technologies take advantage of understanding the actual biological system to provide solutions to problems in several areas. Recently, bioinspired systems have been successfully employing biomechanics to develop and improve assistive technology and rehabilitation devices. The research topic "Bioinspired Technology and Biomechanics" welcomes studies reporting recent advances in bioinspired technologies that contribute to individuals\' health, inclusion, and rehabilitation. Possible contributions can address (but are not limited to) the following research topics: Bioinspired design and control of exoskeletons, orthoses, and prostheses; Experimental evaluation of the effect of assistive devices (e.g., influence on gait, balance, and neuromuscular system); Bioinspired technologies for rehabilitation, including clinical studies reporting evaluations; Application of neuromuscular and biomechanical models to the development of bioinspired technology.',annualVolume:11404,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/8.jpg",editor:{id:"144937",title:"Prof.",name:"Adriano",middleName:"De Oliveira",surname:"Andrade",fullName:"Adriano Andrade",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRC8QQAW/Profile_Picture_1625219101815",institutionString:null,institution:{name:"Federal University of Uberlândia",institutionURL:null,country:{name:"Brazil"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"49517",title:"Prof.",name:"Hitoshi",middleName:null,surname:"Tsunashima",fullName:"Hitoshi Tsunashima",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYTP4QAO/Profile_Picture_1625819726528",institutionString:null,institution:{name:"Nihon University",institutionURL:null,country:{name:"Japan"}}},{id:"425354",title:"Dr.",name:"Marcus",middleName:"Fraga",surname:"Vieira",fullName:"Marcus Vieira",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003BJSgIQAX/Profile_Picture_1627904687309",institutionString:null,institution:{name:"Universidade Federal de Goiás",institutionURL:null,country:{name:"Brazil"}}},{id:"196746",title:"Dr.",name:"Ramana",middleName:null,surname:"Vinjamuri",fullName:"Ramana Vinjamuri",profilePictureURL:"https://mts.intechopen.com/storage/users/196746/images/system/196746.jpeg",institutionString:"University of Maryland, Baltimore County",institution:{name:"University of Maryland, Baltimore County",institutionURL:null,country:{name:"United States of America"}}}]},{id:"9",title:"Biotechnology - Biosensors, Biomaterials and Tissue Engineering",keywords:"Biotechnology, Biosensors, Biomaterials, Tissue Engineering",scope:"The Biotechnology - Biosensors, Biomaterials and Tissue Engineering topic within the Biomedical Engineering Series aims to rapidly publish contributions on all aspects of biotechnology, biosensors, biomaterial and tissue engineering. We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics can include but are not limited to: Biotechnology such as biotechnological products and process engineering; Biotechnologically relevant enzymes and proteins; Bioenergy and biofuels; Applied genetics and molecular biotechnology; Genomics, transcriptomics, proteomics; Applied microbial and cell physiology; Environmental biotechnology; Methods and protocols. Moreover, topics in biosensor technology, like sensors that incorporate enzymes, antibodies, nucleic acids, whole cells, tissues and organelles, and other biological or biologically inspired components will be considered, and topics exploring transducers, including those based on electrochemical and optical piezoelectric, thermal, magnetic, and micromechanical elements. Chapters exploring biomaterial approaches such as polymer synthesis and characterization, drug and gene vector design, biocompatibility, immunology and toxicology, and self-assembly at the nanoscale, are welcome. Finally, the tissue engineering subcategory will support topics such as the fundamentals of stem cells and progenitor cells and their proliferation, differentiation, bioreactors for three-dimensional culture and studies of phenotypic changes, stem and progenitor cells, both short and long term, ex vivo and in vivo implantation both in preclinical models and also in clinical trials.",annualVolume:11405,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/9.jpg",editor:{id:"126286",title:"Dr.",name:"Luis",middleName:"Jesús",surname:"Villarreal-Gómez",fullName:"Luis Villarreal-Gómez",profilePictureURL:"https://mts.intechopen.com/storage/users/126286/images/system/126286.jpg",institutionString:null,institution:{name:"Autonomous University of Baja California",institutionURL:null,country:{name:"Mexico"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"35539",title:"Dr.",name:"Cecilia",middleName:null,surname:"Cristea",fullName:"Cecilia Cristea",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYQ65QAG/Profile_Picture_1621007741527",institutionString:null,institution:{name:"Iuliu Hațieganu University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"40735",title:"Dr.",name:"Gil",middleName:"Alberto Batista",surname:"Gonçalves",fullName:"Gil Gonçalves",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYRLGQA4/Profile_Picture_1628492612759",institutionString:null,institution:{name:"University of Aveiro",institutionURL:null,country:{name:"Portugal"}}},{id:"211725",title:"Associate Prof.",name:"Johann F.",middleName:null,surname:"Osma",fullName:"Johann F. 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