Application of ecological engineering approach for terrestrial and aquatic systems.
\\n\\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\\n\\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\\n"}]',published:!0,mainMedia:{caption:"Highly Cited",originalUrl:"/media/original/117"}},components:[{type:"htmlEditorComponent",content:'IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\nThroughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\nReleased this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"}]},book:{item:{type:"book",id:"516",leadTitle:null,fullTitle:"Advanced Holography - Metrology and Imaging",title:"Advanced Holography",subtitle:"Metrology and Imaging",reviewType:"peer-reviewed",abstract:"Advanced Holography - Metrology and Imaging covers digital holographic microscopy and interferometry, including interferometry in the infra red. Other topics include synthetic imaging, the use of reflective spatial light modulators for writing dynamic holograms and image display using holographic screens. Holography is discussed as a vehicle for artistic expression and the use of software for the acquisition of skills in optics and holography is also presented. Each chapter provides a comprehensive introduction to a specific topic, with a survey of developments to date.",isbn:null,printIsbn:"978-953-307-729-1",pdfIsbn:"978-953-51-4928-6",doi:"10.5772/1027",price:139,priceEur:155,priceUsd:179,slug:"advanced-holography-metrology-and-imaging",numberOfPages:390,isOpenForSubmission:!1,isInWos:1,isInBkci:!1,hash:"bbc41f37a1852fde0085f571ed18c9ca",bookSignature:"Izabela Naydenova",publishedDate:"November 9th 2011",coverURL:"https://cdn.intechopen.com/books/images_new/516.jpg",numberOfDownloads:48608,numberOfWosCitations:32,numberOfCrossrefCitations:9,numberOfCrossrefCitationsByBook:4,numberOfDimensionsCitations:25,numberOfDimensionsCitationsByBook:7,hasAltmetrics:0,numberOfTotalCitations:66,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"October 21st 2010",dateEndSecondStepPublish:"November 18th 2010",dateEndThirdStepPublish:"March 25th 2011",dateEndFourthStepPublish:"April 24th 2011",dateEndFifthStepPublish:"June 23rd 2011",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"32332",title:"Prof.",name:"Izabela",middleName:null,surname:"Naydenova",slug:"izabela-naydenova",fullName:"Izabela Naydenova",profilePictureURL:"https://mts.intechopen.com/storage/users/32332/images/1700_n.png",biography:"Prof. Izabela Naydenova received her MSc in applied optics from the University of Sofia in 1993 and PhD in physics from the Bulgarian Academy of Sciences in 1999. 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Theophanides"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3161",title:"Frontiers in Guided Wave Optics and Optoelectronics",subtitle:null,isOpenForSubmission:!1,hash:"deb44e9c99f82bbce1083abea743146c",slug:"frontiers-in-guided-wave-optics-and-optoelectronics",bookSignature:"Bishnu Pal",coverURL:"https://cdn.intechopen.com/books/images_new/3161.jpg",editedByType:"Edited by",editors:[{id:"4782",title:"Prof.",name:"Bishnu",surname:"Pal",slug:"bishnu-pal",fullName:"Bishnu Pal"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}]},chapter:{item:{type:"chapter",id:"60287",title:"Dendrimers as Drug Nanocarriers: The Future of Gene Therapy and Targeted Therapies in Cancer",doi:"10.5772/intechopen.75774",slug:"dendrimers-as-drug-nanocarriers-the-future-of-gene-therapy-and-targeted-therapies-in-cancer",body:'Cancer is one of the world’s most stressful diseases with no apparent cure in sight for several tumor types and millions of new cases reported every year [1]. Cancer chemotherapy using conventional anticancer agents has been slowed down by several challenges such as severe toxicity, poor membrane permeability, rapid clearance, and narrow therapeutic index. In this regard, a wide range of nanoparticles such as liposomes, polymeric micelles, polymeric nanoparticles, dendrimers, silica nanoparticles, and carbon nanotubes with their structural, physicochemical, and functional diversity can be utilized to enhance drug loading and enable drug internalization in target cancer cells while limiting uptake in normal tissues and cells [2, 3]. The development of smart cancer treatment approaches revolves engineering such unique nanosystems carrying drug and gene payloads that can passively or/and actively target cancer cells [4]. Gene therapy and newer molecular target-based anticancer tactics involve the use of potent but highly labile agents such as monoclonal antibodies, aptamers, siRNA and miRNA that are readily degraded and/or have limited stability
Dendrimers are globular macromolecules sized 1–100 nm with an architecture consisting of three distinct domains: a central core, a hyperbranched mantle, and a corona with peripheral reactive functional groups [10]. The high level of control over the synthesis of dendritic architecture makes dendrimers a nearly perfect (spherical) nanocarrier with predictable properties. Many different kinds of dendrimers, including polyamidoamine (PAMAM), poly(propylene imine) (PPI), poly(glycerol-co-succinic acid), poly-l-lysine (PLL), melamine, triazine, poly(glycerol), poly[2,2-bis(hydroxymethyl)propionic acid], poly(ethylene glycol) (PEG), and carbohydrate-based and citric acid-based ones, have been successfully developed for drug delivery [11–14]. The most widely investigated vectors for medical application are two dendrimers: PAMAM and PPI [15, 16]. Those two amine-terminated dendrimers display stimuli-responsive (pH-dependent) drug release behavior. The tertiary amine groups are deprotonated at high pH (alkaline), causing a collapse of the dendrimer on itself, which is named ‘back folding’ [17]. The utility of dendrimers can be appreciated by their ability to traverse several delivery barriers using two overarching principles, namely active and passive tumor targeting.
Surgery and radiation are the main common treatment in solid tumors as soon as they are recommended to undertake considering the tumor infiltration. These kinds of treatments are considered as local treatments [18]. As it is well recognized, surgery can be disfiguring and radiation can be damaging to local healthy tissues and organs. Chemotherapy is the third option in cancer treatment, which is called adjuvant therapy to surgery and radiotherapy. It is based on cytotoxic effect (cell-killing therapy). The most desirable effect of chemotherapy is to eliminate cancer completely, which is still in most cases the wishful thinking. If such a cure is not possible, the good result is to even stop the growing tumor [19]. Despite some excellent drugs are available, the efficacy of many existing chemotherapeutics is limited by their inability to reach their therapeutic site of action in sufficient amounts to be effective [20]. In most cases, patients are administered with an excess of medications that are distributed throughout the whole body, and thus, it is extremely difficult to avoid distribution into healthy organs and tissues and the depression of the immune system. It always gives the limitation of dosage that can be given and, in turn, prevents these drugs from achieving the potential cures [21]. Current anticancer drugs often have a poor therapeutic index and they cause a lot of side effects [22]. A major concern is when the medications affect non-cancer cells, causing the adverse reduction of red and white blood cells, and affecting the gastrointestinal tract triggering nausea and diarrhea [23]. To reduce, or even better to avoid such side effects, the drug delivery to the tumor is optimized by preparing carriers containing an active agent associated with a molecule capable to accurately target cancer cells such as antibody drug conjugates (ADC) or nanoparticles [24–26].
Dendrimers have been engineered as nanodevices, either in nanocarrier drug approaches or as drugs
Dendrimers have already been used as passive anticancer nanocarriers [38–41]. There are preclinical promising results
Once these molecular machines arrive at the target site inside the living organism, several barriers must be overcome. Nanocarriers are usually internalized by endocytic processes [59], the processes called vesicular internalization. The most widely studied endocytic pathways are clathrin-mediated endocytosis, caveolae-mediated endocytosis, and macropinocytosis, but other cellular pathways have been recently identified, including clathrin- and caveolae-independent endocytosis and phagocytosis [60]. Molecules, which are internalized by the cell membrane, are endocytosed by the early endosomes pathway. They may progress later to late endosomes and lysosomes. If the loading of dendrimer targets the nucleus, thus the nuclear membrane is another barrier that the dendrimer should come across [61].
We should be very careful designing the drug delivery system because unexpectedly our desired nanovector might have its own power. This is what our genetic research has shown—4th generation PPI glycodendrimers with maltotriose molecules directly trigger mechanism of apoptosis in mitochondria of lymphocytes B, particularly those transformed to the leukemic cells. That discovery was successfully patented (US 9,877,85) and applied as a potential drug for lymphoproliferative disorders coming from B cells, such as chronic lymphocytic leukemia (CLL) or B-lymphoma. The power of these glycodendrimers relied on the ability to affect several genetic pathways simultaneously, and as opposed to the commonly used drugs or the new ones already proved by FDA, they affect the cell genome very quickly and efficiently according to the natural death process initiation (Figure 1).
Mechanism of action—PPI-G4-OS-Mal3 dendrimers in B-lymphocyte (the illustration prepared by B. Ziemba).
During the past decades, RNA-based drugs have arisen as good candidates to cure the diseases at the gene and RNA levels. Since 1990, it has been known that nucleic acids can be used to modify protein production in vivo [62]. However, therapeutic RNA delivery has been limited for a long time by many different factors [63]. It is known that naked, single-stranded RNA is easily degraded by nucleases. It can also activate an immune system and is too large to be able to passively cross the cell membrane. Moreover, the negative charge of RNA causes the problem to enter the cell. Therefore, an additional solution should be provided to facilitate cellular entry and escape from endosomes [63, 64]. Typically, cationic polymers (e.g. dendrimers) are used to electrostatically condense the negatively charged RNA into nanoparticles [65]. Very important for effective nucleic acid delivery are modifications made to RNA itself [66], to make it more resistant to degradation and render them unrecognizable by the immune system [67]. RNAs can be modified by means of chemical alterations to the ribose sugar [67, 68], the phosphate linkage, and the individual bases [69–72]. One of such modified RNA is locked nucleic acid (LNA) modification. LNA’s ribose moiety is modified with an extra bridge between the 2′ oxygen and 4′ carbon. The bridge “locks” the ribose in the 3′-
siRNA is not the only RNA drug to be examined for protein knockdown at the clinical stage (NCT01676259) [75, 76]. Antisense oligonucleotides (ASO) were the first RNA drugs successfully reported in clinical trials. They are able to block protein translation through Watson-Crick base pairing with the target mRNA, similar way to siRNA mechanism, and they can also be modified to improve their stability [77–79]. Despite that the ASOs inhibit protein production through the sterically blocking ribosome attachment or eliciting RNase-H activation, they are also able to promote the exon skipping, which may lead to a deletion of faulty sequences within proteins and thus it can make a protein upregulation, that can be used in diseases where certain genes are repressed [80].
An emerging, but less clinically improved, is microRNA (miRNA) platform for protein knockdown. Endogenous miRNAs are non-coding RNAs that are regulatory factors for a variety of cellular pathways and are often downregulated in diseases [81]. Exogenous mRNAs, or miRNA mimics, delivered therapeutically could make a knockdown of several proteins simultaneously, which might be very useful in cancer, where having a single disease-relevant target is rare [82]. The first miRNA mimic therapy to enter clinical trials was MRX-34—a liposomal-encapsulated miRNA mimic from Mirna Therapeutics meant to treat variety of cancers [83]. Despite the big number of carriers, mRNA molecules are significantly larger than (600–10,000 kDa) than the previously discussed siRNAs (~14 kDa) and ASOs (4–10 kDa), which poses an additional challenge for delivery of mRNA therapeutics [84]. Therapeutic applications based on mRNA are currently being explored as vaccinations against cancer, infectious diseases, and gene editing. Cancer mRNA vaccines have experienced accelerated development in cancer immunotherapy. The majority of approaches tested in clinical trials employ adoptive transfer of DCs transfected with mRNA coding for tumor-specific antigens (TSAs) and immunomodulation of T cells with mRNAs expressing chimeric antigen receptors (CARs) or TSAs [85–87].
The most recent and the most sophisticated gene delivery is CRISPR-Cas system that also relies on Watson-Crick base-pairing between a single guide RNA (sgRNA) and a corresponding DNA target site followed by a distinct protospacer-adjacent motif (PAM), which is a 3–5 nucleotide DNA sequence required for binding Cas9 and cleavage of the target sequence. It leads to the double-stranded break (DSB) into a DNA molecule [88]. DSBs can be repaired by cells using non-homologous end joining (NHEJ) and homology-directed repair (HDR). NHEJ results in insertions and deletions causing permanent gene knockout [89]. CRISPR-Cas components based on nanoparticle mRNA delivery are therapeutically attractive due to the temporary ability of mRNA expression. There is also no risk of genomic integration and mRNA cytoplasmic activity, mitigating the need to overcome the nuclear barrier in comparison with pDNA [90]. The major challenges for RNA-based drugs and CRISPR-Cas therapies will be shaping the scope of upcoming clinical trials.
To design the most effective and variety therapies for different kinds of cancer, an effective vector protecting siRNA that is non-toxic and can be targeted at selected cells is necessary [91, 92]. Several classes of dendrimers seem to be good candidates for carriers of oligonucleotides. Cationic carbosilane dendrimers (CBD) characterized by Si─O or Si─C bond and terminated with ammonium or amine groups, form also complexes with siRNAs.
There are many reports presenting promising results in the topic of nucleic acids delivery using complexes called ‘dendriplexes’ [93–95]. Among variety of proposed candidates, PAMAM dendrimers are the most explored dendrimers type, followed by poly(propylene imine) (PPI) dendrimers, poly(l-lysine) (PLL) dendrimers, and some others [96].
PAMAM dendrimers, hydrophilic, biocompatible, and non-immunogenic particles, are build of ethylenediamine core (most commonly) and methyl acrylate and ethylenediamine branches [97, 98]. They have been successfully used as nucleic acid delivery systems in many
The transfection efficiency of PAMAM dendrimers largely depends on their generation, which determines the structure of the PAMAM molecule: higher generations are more compact and spherical than the low ones and provide a surface with a high density of primary amines therefore form more stable dendriplexes with higher efficiency [99, 100]. However, dendrimers with high generations results in higher toxicity due to a large number of terminal cationic groups which can interact with negatively charged cell components, e.g. cell membranes causing their disruption [101, 102]. This disadvantage can be diminishing by surface modification with different targeting or shielding moieties providing with not only low toxicity but also enhance the cell uptake and specific accumulation of nucleic acid molecules inside cells [103–106]. For example, novel targeted nanoparticle system consisting of FLT3 ligand-conjugated PAMAM G7 encapsulating a pivotal tumor suppressor and negative regulator of
A frequent way of using dendriplexes in anticancer therapy is to provide them in conjunction with approved anticancer agents [114–116]. Researchers from Virginia Commonwealth University used nanoplexes of PAMAM dendrimer with polyethylene glycol and lactobionic acid complexed with AEG-1 siRNA against hepatocellular carcinoma (HCC), a fatal cancer with no effective therapy. Applied in the combination with all-trans retinoic acid (ATRA), the complex developed a profound and synergistic inhibition in tumor growth in human HCC xenografts model suggesting, that combinatorial approach might be an effective way to combat resistant types of cancer [117]. Liu et al. used PAPMAM dendrimers as a nanoparticle delivery platform for a MDR1 gene targeting siRNA to reverse multidrug resistance (MDR) in human breast cancer MCF-7/ADR cells. This PAMAM-siMDR1 complex decorated additionally with phospholipid demonstrated high gene silencing efficiency and enhanced cellular uptake of siMDR1 resulting in rising of cellular accumulation of doxorubicin (DOX), inhibition of the tumor cell migration, and due to synergistic work with paclitaxel (PTX), increase of cell apoptosis, and cell phase regulation [118]. More complex system designed in order to achieve effective treatment to MDR breast cancer is PAMAM functionalized graphene oxide (GO-PAMAM) which can load DOX and MMP-9 shRNA plasmid at the same time [119].
It is still a challenging task to deliver the anticancer drugs to brain tumors and overcome the restriction of blood-brain barrier (BBB). He et al. [12] have proposed recently an interesting approach. G4.0 PAMAM dendrimers have been conjugated with two targeted ligands—transferrin and wheat germ agglutinin. Such conjugates were used for crossing the BBB and incorporation drugs to brain tumor cells. That dual-targeting drug carrier system allowed to deliver successfully DOX inside the brain tumor and provided a potential therapy for brain cancer [12].
Dendrimers have been investigated for ophthalmic drug delivery since it offers a number of advantages as a carrier system. They may improve effective delivery of therapeutic agents to intraocular tissues, such as the retina or choroid, using non-invasive delivery methods. Eye cancers are not among the most common but also in this area, scientists have started to look for inspiration in nanoparticles [120]. Kang et al. made a successful single injection of subconjunctival G3.5 PAMAM dendrimer to transgenic murine retinoblastoma with no associated toxicity. The higher dose of nanoparticle even could reach and decrease the tumor burden in the untreated, contralateral eye [121].
Poly(propylene imine) (PPI) dendrimers are constructed from a 1,4-diaminobutane core and propylene imine branches [122]. Positively charged surface of PPI dendrimers provides an interaction with nucleic acids, enabling the dendritic scaffold to be used as a vector for gene transfection [123].
As in the case of the PAMAM dendrimers, the surface of PPI dendrimers can be freely modified to reduce their toxicity and increase their uptake by target cells. A small library of alkanoate-modified PPI G5 dendrimers was developed and tested for their ability to transfect DNA to neuroblastoma Neuro-2a cells. It was shown that a balanced hydrophobic surface modification results in improved transfection, low cytotoxicity, and hemotoxicity [124]. Much larger modifications of PPI dendrimers in order to increase their efficiency as gene carriers have been made by a team of researchers from The State University of New Jersey [123–126]. In 2009, Taratula et al. modified PPI G5-siRNA complex with dithiol-containing cross-linker molecules followed by PEG coating. To direct the complex specifically to the human ovarian and lungs cancer cells, an analog of luteinizing hormone-releasing hormone (LHRH) peptide was conjugated to the end of PEG. The modification and targeting approach confers the complex stability in plasma and intracellular bioavailability, promoted its tumor-specific uptake and accumulation in the cells, and efficient gene silencing. Moreover, in vivo study confirmed high specificity of the proposed targeting delivery approach [125]. A year later, the same team developed a novel way to compact and deliver nucleic acids with lower, third-generation PPI dendrimers by using gold nanoparticles (AuNP) as a “labile catalytic” packaging agents. The AuNP helped dendrimers to compact siRNA but were not included in the final complex. The efficiency of mRNA silencing by this approach was even higher than that with PPI G5 dendrimers [126]. To further improve the efficiency of investigated delivery systems, the authors developed siRNA vectors based on PPI G5 dendrimers and superparamagnetic iron oxide nanoparticles, together with incorporation of PEG coating and LHRH conjugation. This novel multifunctional siRNA delivery system improved selective internalization into cancer cells and increased the efficiency of targeted gene silencing
Poly(l-lysine) (PLL) dendrimers, amino acid-based macromolecules characterized by high biocompatibility and low toxicity, have also been developed as non-viral vectors for gene delivery [136–139]. In example, in 2002 it was reported that dendritic PLL G5 and G6 transfected DNA into several different cell lines with high efficiency and without any cytotoxic effects [139]. The results of more recent studies confirm previous reports. Newly synthesized siRNA carriers containing amphiphilic PLL dendrons exhibited not only the siRNA binding properties but also the ability to inhibit the proliferation of glioblastoma cells while being non-toxic for cell types that share the anatomical space with tumor cells during the course of the disease [140]. Research on the use of PLL dendritic structures as gene carriers in combination with traditional anticancer drugs also yields promising results. PLL G3 dendrimers with a silsesquioxane cubic core were conjugated with a c(RGDfK) peptide through PEG spacer for codelivery of DOX and siRNA to glioblastoma U87 cells. The complex showed high transfection efficiency and gene silencing and was more toxic to U87 cells than free DOX [141].
Although conventional chemotherapy has been the cornerstone in the fight against cancer, is far from being totally satisfactory due to the problems related with their formulation, pharmacokinetics, and the last but not least, severe side effects of such a therapy. Last past decades the huge progress has been made in the understanding of the disease, its molecular background and development of newer targeted therapies. Unfortunately, an effective treatment of several forms of cancer still remains a major challenge. Recent advances in drugs based on dendrimer and gene delivery using dendrimers as a vector has appeared as a great option to overcome the limitations of conventional chemotherapy. Currently, more than 50% of the cancers are not curable and drug nanocarriers might help to decrease this percentage. Nanomedicine represents one of the fastest growing research areas and is regarded as one of the most promising tools for cancer treatment. Several solutions based on nanoparticles have been developed and many are used in clinical cancer care. Liposomes and polymer conjugates were the first nanocarriers to be approved by FDA; however, only five liposomal drugs, two polymer-protein conjugates, and two dendrimers are in the market up to date. Abraxane®, an albumin-bound paclitaxel nanoparticle, has been approved by FDA in 2005 for the treatment of metastatic breast cancer. In 2012 the same drug has been approved for the first-line treatment of advanced non-small lung cancer and in 2013 for the metastatic pancreatic cancer. There was an absence of evidence and guidance, regulatory decisions on nanomedicine therapeutics. The FDA collaborates with the Nanotechnology Characterization Laboratory (NCL) to facilitate the regulatory review and in-depth characterization of nanodrugs in medicine. The European Technology Platform on Nanomedicine (ETPN) set up a European Nano-Characterization Laboratory (EU-NCL) as the part of the Horizon2020 project. The regulatory problems seem to be finally overcome since FDA published the Guidance for Industry (‘Drug Products, Including Biological Products, that Contain Nanomaterials’) in December 2017 (https://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm). Looking into the future, the use of cancer theragnostics, combining anticancer targeted therapy and diagnosis by multifunctional nanoparticles, that combine the therapeutic and imaging agent, might be a revolution in the cancer treatment because they allow to diagnose, visualize, and kill the cancer cells simultaneously and both treatment and diagnostic in the real time. This is a future of medicine, right now it still seems to be a science-fiction movie, but proudly we are coming closer every year to such an amazing progress in diagnostic and treatment thanks to the broad usage of nanoparticles and nanotechnology.
The authors wish to acknowledge the founding support from GeneaMed LTD, Poland and Fulbright Commission support to IFP during the scholarship ‘Fulbright Senior Award 2016-2017’ at the University of California San Diego.
The increase in human activities triggers environmental pollution through the generation and disposal of hazardous wastes in aquatic and terrestrial habitats [1]. Most of these pollutants include inorganic (heavy metals) and organic matter (polyaromatic hydrocarbons (PAH), petroleum hydrocarbons compounds (PHC)) which may cause negative effects on the ecosystem and possibly react with other abiotic factors that attribute to the effect on the structural arrangement of terrestrial and aquatic habitats [2].
In terms of the environment and ecology system, the proper and safe disposal of these hazardous wastes is a key priority for a sustainable ecosystem. This involves the use of various treatment procedures to clean up hazardous waste. For detoxifying heavy metals, radionuclide and organic polluted soils, physicochemical techniques such as filtration, precipitation, electrochemical treatment, soil washing and chelating, oxidation/reduction, ion exchange, reverse osmosis, and stabilization/solidification have been employed. These environmental clean-up procedures have various disadvantages, including inefficiency, the need for a large number of chemical reagents, energy, and high cost, as well as the formation of secondary by-products [3].
Bioremediation is a cost-effective and environmentally tolerable technology that employs a biological process to reduce environmental risks caused by toxic substances and other hazardous pollutants. To treat polluted multiphase systems and sustain the native ecosystem, a combination of bioremediation techniques will be effective. The fundamental premise of bioremediation is to reduce contaminant solubility by adjusting pH, modifying redox processes, and adsorbing toxic substances from polluted sites [3]. Environmental remediation always requires human assistance to achieve effective remediation of contaminants and restoration of ecological balance. However, remediation can be destructive to the ecosystem [4], if the application is not properly addressed to meet the eco-friendly standard required to combat the contemporary issues of pollution [4, 5]. Most small-scale applications of bioremediation approaches using bioremediation agents such as bacteria, fungi, plants, and organic materials have been successful with variation in results, although bioremediation on a large scale has not been widely validated [4]. This chapter aims to propose a cost-effective and eco-friendly bioremediation strategies that could reduce or remove contaminants from the environment and thus stabilizing the ecosystem from heavy metal pollution and oil spills.
There are a lot of different physical, chemical, and biological processes commonly termed bioattenuation, which make pollutants smaller in terms of their size and toxicity as well as how much of them there are. Some examples of these processes are sorption, volatilization, chemical or biological stabilization, and the transformation of contaminants. This entails removing pollutant concentrations from the surrounding through biological methods or perhaps incorporating (oxic and anoxic biodegradation, plant and animal sorption), physical occurrences (changes in weather conditions, dispersion, dilution, diffusion, volatilization, sorption/desorption), and chemical reactions (ion exchange, complexation, abiotic change) [6, 7, 8]. For instance, natural biodegradation and biotransformation are incorporated within the broader notion of common restriction [9, 10]. At the point when the site is contaminated with chemicals, the environment acts in 4 different approaches to facilitate remediation [11]:
Microbes or microorganisms living in soil and groundwater may consume just a small number of chemical or manmade chemicals available as dietary nutrients. When they have completely digested the chemical, they can convert it to water and non-toxic gases.
Chemical compounds can stick to or sorb to the soil, which prevents them from contaminating groundwater or escaping the location.
As contamination travels through soil and groundwater, it can blend in with clean water. This diminishes or weakens the contamination.
Certain chemicals, such as oil and solvents, can disappear, hence, they can transform from liquids to gases within the soil or groundwater. As a result, if these gases reach the earth surface via the air, they may be pulverized by sunlight.
Additionally, if natural attenuation is insufficiently rapid or complete, bioremediation will be accelerated or augmented via biostimulation, bioaugmentation, bioventing, or biopile [11, 12].
This bioremediation approach invigorates the activity of native microbes by adjusting the environmental parameters or the introduction of nutrients [11, 13]. This is carried out with the incentive of natural or normally prevailing parasites or microbial communities [7, 11, 13]. Successive steps involve providing manures, development enhancements and minor elements. Also, by giving other natural prerequisites including pH, temperature and oxygen to enhance their digestion rate and degradation pathway [10, 12]. Similarly, the presence of pollutants even in small quantities can act as a stimulant by spinning for bioremediation proteins. Typically, this type of deterioration is followed by the provision of organic or inorganic nutrients and oxygen to promote the metabolism of native microbes for effective remediation [6]. These nutrients are the fundamental building blocks of life, enabling microorganisms to synthesize vital components such as enzymes, energy, and cell biomass required to degrade the toxin [6, 14]. However, nitrogen, phosphorous and carbon are significantly required to enhance metabolism.
This procedure entails sequentially adding contaminant-degrading microbes (inherent/non-native/genetically modified) to improve the biodegradative efficiency of the native microbial community in the polluted site [8, 11]. Thus, to rapidly grow the natural microbial population and accelerate breakdown at the pollutant’s location. Microorganisms that predominate in polluted sites on a global scale, may surely change significant amounts of harmful substances into non-poisonous structures. This process converts pollutants to by-products like carbon (IV) oxide and water, as well as metabolic intermediates that serve as critical nutrients for cell development [15, 16]. Microorganisms can also be isolated from the remediation environment, cultured autonomously, genetically engineered, and then reintroduced to the site [8, 11]. For persuade, all basic microbes are prevalent in locales where soil and groundwater are polluted with chlorinated ethenes, for example, tetrachloroethylene and trichloroethylene [7, 8, 11]. These are employed to facilitate the effective removal and conversion of these pollutants to non-poisonous ethylene and chloride by in situ microbes [10].
Additionally, genetically modified microbes have been shown to degrade a broad range of environmental contaminants effectively. Since the metabolic pathway can be altered to produce less puzzling and harmless end products [8, 17]. Genetically engineered microorganisms (GEM) have shown viability in bioremediation of soil, groundwater and activated sludge, proving effective degradation abilities of extensive integration of chemical and physical contaminations. GEMs have better enzyme abilities, which makes them better at breaking down a wide spectrum of aromatic hydrocarbons and making the soil more fertile [14, 18]. There are several types of hydrocarbon-degrading microorganisms that include the genera
It is the practice of venting oxygen through the soil to encourage the development of natural or injected microbes and fungus in the soil by supplying oxygen to the soil microbes, which has been termed as bioventing [8, 11, 14]. The use of low air flowrates to supply sufficient oxygen to sustain microbial movement has long been a typical practice in aerobic degradation of substances, and it has been for many years. For example, several scientists have demonstrated that bioremediation of oil-contaminated soil utilizing bioventing may be achieved with reasonable success [19]. Consequently, petroleum residuals and their by-products are biodegraded, and volatile organic compounds, when destroyed, release vapors that slowly permeate through the biologically dynamic soil environment.
Biopile, also known as biocells, bioheaps, biomounds and composts piles are employed to minimize the toxicity of total petroleum hydrocarbon constituents via microbial respiration. Biopiles are an ex-situ bioremediation technology that consists of piling polluted soil onto a compost pile (biopiles) or cells (biocells) or mounds (biomounds) or heaps (bioheap) and stimulating oxic metabolism in the soil via aeration or introduction of minerals or nutrients, bulking agents, and subsequently confining it in a treatment bed with polyethylene material to avoid evaporation, surface runoff, and volatile emissions. Biopiles treatments can transform pollutants into low-toxic by-products through biological processes by utilizing already existing microorganisms to breakdown fuels and oils into carbon dioxide and water.
The biopile technology is made up of commercial roll-off dumpsters or containers that have been turned into fully contained bioremediation units. The biopile units have an impermeable liner to decrease the possibility of leachate movement to the subsurface ecosystem. Excavated soils are combined with soil additives and placed on a treatment area with leachate collecting devices and some type of aeration to maximize and regulate the rate of biodegradation. Air is introduced to the biopile mechanism of piping and pumps, which either power air into the heap under a specific tension or draw air through the heap under a negative tension [8, 20]. Microbial movement, for instance, can boost the adsorption and degradability of petroleum pollutants during funneling and siphoning operations. Biopiles, such as biocells, bioheaps, biomounds, and compost, might alleviate public concern about excavated soil contaminated by vigorously remediable hydrocarbons [8, 13, 19].
Utilizing plants for bioremediation is highly dependent on their ability to break down certain pollutants [21, 22, 23, 24]. Phytoremediation is the process of utilizing plants to degrade, eliminate, or convert contaminants to less hazardous chemicals [25]. Even though plants have been used for soil purification for centuries, scientists have contributed to its advancement and expanded its scope of application throughout the years [7, 11, 13, 14, 17, 18]. This involves the removal of metals, pesticides, solvents, explosives, and raw petroleum, as well as a variety of other pollutants from soils, water (surface and subsurface), and vaporous contaminants [7, 11, 14]. When the plants have accumulated enough toxins, they are harvested and disposed of. Figure 1 shows a graphical presentation of different types of phytoremediation as each mechanism is explained as follows:
Phytostabilization: this entails using plants to minimize soil erosion, so immobilizing contaminants by limiting their movement and accessibility in the soil via the plant roots. Additionally, it prevents metals from moving to the soil or the surface of underground water.
Phytovolatilization: this involves the use of plants to minimize soil erosion, so immobilizing contaminants by limiting their movement and accessibility in the soil via the plant roots. Additionally, it prevents metals from moving to the soil or the surface of underground water.
Phytodegradation: this process includes the degradation or modification of pollutants in the plant tissue by enzymes.
Phytoextraction: this approach involved the extraction of contaminants from the soil and their accumulation in the shoots. Upon that, these plants’ leaves are gathered, burned for energy, and the metals retrieved from the ash are regenerated.
Phytofiltration or rhizofiltration use roots to accumulate and sequester contaminants from polluted water.
Phytostimulation or rhizodegradation: plant roots are employed to digest organic pollutants in the rhizosphere environment and through microbial activity.
Schematic presentation of phytoremediation process (adapted from [
This is when two or more bioremediation methods work together to remove contaminants from the environment. This kind of bioremediation technique can be effectively applied in a multi-contaminated environment. The combinative strategy most likely to be suitable and effective in boosting bioremediation of bauxite residue is a combination of bioaugmentation (incorporation of inocula) [8, 11] and biostimulation (introduction of nutrients to enhance the activity of microorganisms) of the indigenous community in bauxite residue [11, 13].
In this scenario, for instance, biostimulation using organic or inorganic compounds can be applied as the first or basic treatment while bioventing or bioaugmentation using engineered microbes can be applied subsequently as a secondary or tertiary treatment to facilitate the removal or degradation of recalcitrant compounds. Combinations of bioaugmentation and biostimulation have also proven effective, albeit they do not always show significant improvements over bioaugmentation alone. Given the nearly consistent advancement seen with bioaugmentation technology, it is anticipated that bioaugmentation will improve on the outcomes obtained so far with biostimulation for bauxite waste cleanup (provided an appropriate choice of the microbes and adequate trials are prioritized). Based on the simplicity of obtaining and introducing the inoculum, the most suited approach for future research and field trials is combinative bioremediation using biostimulation and bioaugmentation technology.
Several bioremediation mechanisms for reducing or oxidizing contaminants have been discovered over time, such as adsorption, physio-biochemical (biosorption and bioaccumulation) bioleaching, biotransformation, biomineralization, and molecular mechanisms [7, 11].
Environmental pollutants (both organic and inorganic) can be absorbed by microorganisms at specific sites in their cell structure that do not require the dissipation of energy. There are many various kinds of chemicals connected with bacterial cell walls, but their extracellular polymeric substances (EPS) are of particular importance since they have been shown to have significant effects on corrosive base characteristics and metal adsorption [10, 26]. Several studies on the metal binding behavior of EPS have revealed that it has a remarkable capacity to absorb complex metals by a variety of processes that combine ion exchange and micro-precipitation of metals [10, 13]. Bioremediation research and application are still limited in the present scenario due to a lack of understanding of the genetic traits and genome-level properties of the organisms used in metal adsorption, the metabolic route, and the kinetics of metal adsorption [7].
In microscopic organisms, inhibition is advanced through two mechanisms: detoxifying (changing the detrimental metal’s state and rendering it inaccessible) and dynamic efflux (siphoning poisonous heavy metals from cells) [7, 9]. In wastewater or soil, the fundamental redox (oxidation and reduction) reaction occurs between hazardous metals and microorganisms. Additionally, microbes oxidize heavy metals, causing them to lose electrons, which are recognized by active electron acceptors (nitrate, sulphate and ferric oxides) [26]. Additionally, the biosorption process, which consists of a biosorbent’s increased affinity for sorbate (metal ions), is repeated till a balance between the two components is established [18, 26]. For instance,
Bioaccumulation is a term referring to the combination of active and passive techniques of hazardous metal bioremediation. Additionally, bioremediation may entail aerobic or anaerobic microbial activity [10, 12, 13]. Aerobic degradation frequently involves the addition of oxygen atoms to the reactions via monooxygenases, dioxygenases, hydroxylases, oxidative dehalogenases, or chemically active oxygen molecules produced via catalysts including ligninases or peroxidases [10, 11, 12, 13]. Anaerobic contaminant corruptions comprise initial enactment reactions followed by oxidative degradation with the assistance of anaerobic electron acceptors. The act of Immobilization refers to the process of reducing the activation of significant metals in a polluted environment by modifying their physical or synthetic state [7, 12]. Microbes muster metals from polluted sites through leaching, filtering, chelation, methylation and redox transformation of harmful metals [12, 17]. Since significant metals cannot be entirely eliminated, the cycle modifies their oxidation state or organic complex to make them more soluble, less poisonous and precipitated [9, 14].
In bioleaching, naturally occurring microorganisms such as bacteria and fungi solubilize metal sulphides and oxides from ores and secondary wastes. Adsorption, ion exchange, membrane separation, and selective precipitation are some of the processes used to purify solubilized metals. It is a cost-effective and environmentally beneficial technique because it consumes less energy and produces no hazardous gases. It has been applied to leach metals from low-grade ores, and it now provides a substantial global business in the extraction of metals like copper, cobalt, gold, nickel, uranium, zinc, and other elements [27].
This is the procedure for altering the structure of a chemical substance to produce a molecule with higher polarity. Moreover, this metal-microbe interaction process converts hazardous metal and organic chemicals into a less poisonous form. This mechanism has emerged in microorganisms to assist them in adjusting to variations in their surroundings. Bacterial cells have a significant surface-volume ratio, a rapid pace of proliferation, a rapid rate of metabolic activities, and are easy to keep sterile [27]. As a result, they are perfect for biotransformation. Various methods, such as condensing and hydrolyses, forming new carbon bonds, isomerization, inserting functional groups, and oxidation, reduction, and methylation, can be used to attain this objective. Metals may be volatized, reducing their lethal nature, as a result of these interactions.
Biomineralization refers to the mechanisms by which microbes produce minerals, and it can lead to metal extraction from solution, which can be used for decontamination and biorecovery. Dead biota and related products may also serve as a model for mineral deposition, with physicochemical parameters determining whether the process is reversible or not. There are several prevalent microbe-precipitated biominerals with unique chemical features such as high metal sorption capacities and redox catalysis. However, some biominerals can be deposited at nanoscale dimensions, resulting in additional physical, chemical, and biological features that can be used in practical applications [28].
Different components of genetically altered bacteria, such as Deinococcus geothemalis, are active in the removal of heavy metals [9, 14, 18]. Hg2+ reduction has been recorded at high temperatures as a result of the expression of meroperon from
The promising bioremediation technique involves the application of bioturbators. Bioturbation is made up of a series of processes triggered by microbenthic fauna that influences sediment physicochemical characteristics and affects the microbial population which partake in the distribution of nutrients [29]. Bioturbation involves a series of activities such as the reworking of particles, bioirrigation, and other benthic biota related behaviors (i.e. nutrition mode and grazing by animals and organisms) that were responsible for transportation and distribution of porewater and particles along the water-sediments interface [30]. The distribution of dissolved contaminants can be a reworking of sediments by bioturbators through facilitating transportation and biomixing efficiency from overlying water and porewater to deep layers of the sediment [31, 32, 33].
The term “bioturbation” relates to the procedure of completely transforming dangerous hazardous substances into harmless or naturally occurring chemicals. Bioturbation can be done in situ (for example, in field conditions) or ex-situ (for instance, in a microcosm or under controlled conditions). Both scenarios entail the utilization of plants, parasites/fungi, and microorganisms as bioremediators for the biodegradation of toxic pollutants, even though individualized end product may be a different component [34, 35, 36]. Thus, complete breakdown of the contaminants by the bioremediators directly or indirectly may influence the residue structure [34, 37]. Figure 2 presents significant types of contaminant improvement approaches by bioturbators (benthic fauna) in the contaminated environment to facilitate residue treatment.
Schematic representation of bioturbators activities in sediments (i) biodiffusors, (ii) upward conveyors, (iii) downward conveyors, and (iv) regenerators.
Biodiffusors: this is performed through microorganisms’ activities, which often result in the biomixing of uniform and irregular sediments over short separations, resulting in particle interchangeability via molecular diffusion.
Upward conveyors: these are organisms that live vertically head-down in the sediments. They transfer particles from the residue’s deep horizons to its surface. Gravity then returns the particles to the base under the influence of feces pellet agglomeration at the sediment surface.
Downward conveyors: these are head-up feeders that actively pick and consume particles near the surface, as well as discharge in deeper residual layers.
Regenerators: these microorganisms dive into the leftovers and constantly maintain burrows, so transferring dirt from depth to the surface.
The role and effectiveness of bioturbators in bioremediation is dependent on several conditions, such as the chemical type and quantities of contaminants, the physicochemical properties of the environment, and their accessibility to microbes [38]. Bioturbators are responsible for vital changes in the biological and physicochemical aspects of soils and water [38, 39]. Additionally, aerobic bioturbation can increase benthic digestion and supplement components by stimulating oxygen-consuming bacterial networks that are concerned with pollutant mitigation [8, 11]. In other words, bioturbators are well-suited for a dual-purpose mechanism, namely the production of degradative enzymes for specific contaminants and resistance or protection from significant relative dangerous substances such as heavy metals [15, 38, 39]. Controlling and simplifying bioremediation procedures is a difficult process due to a large number of components including the presence of a microbial community with the ability to detoxify pollutants, the contaminants’ accessibility to the microbial community, and abiotic conditions (soil type, temperature, pH, oxygen or other electron acceptors, and substrates) [6, 16, 39].
Bioturbation influences the sediment-water interface’s biological, physical, and chemical properties which accounts for the high rate of mineralization of organic matter in the aquatic environment [40]. This operation changes the sediment column distribution of the contaminants [41]. Bioturbation and biotransport can affect the physicochemical characteristics of sediments and sediment pollutants [42, 43, 44]. Bioturbation controls the organic matter and nutrient digestion enhances pollutant mobility and transformation [45, 46, 47, 48]. The biosorption of organic contaminants into the organic matter during bioremediation reduces its bioavailability for plants (phytoremediation) or degrading organisms (bioaugmentation) [49]. Atrazine removal from sediments is promoted and positively influenced by the adjustment of organic matter and earthworm bioturbation activities, which increases contaminant bioavailability and atrazine sorption rate on their microsites [46, 50]. Previous studies reported positive contributions of earthworm bioturbation to organic pollutant transformation and biodegradation [51, 52] by modifying pore size and metabolism of degrading bacteria groups or accelerating mineralization in bioaugmented soils [50].
Moreover, several studies showed that bioturbation alters the physicochemical characteristics of the water-sediment boundary which promotes the bioavailability of inorganic pollutants to degrading organisms. This is achieved through the modification of sediment particle sizes, pore spaces, moisture content, nutrient content, turbidity, and total organic carbon of the vadose water-sediment [41, 43, 53]. Also, the bioturbation of benthic invertebrates through the mixing of sediments in the underground zone enhanced the electron acceptors (oxygen, nitrate and sulphate) entrance into the vadose zone which triggers geochemical changes that influence metal behavior [54]. The presence of these electron acceptors in the unsaturated zone can activate the RedOx reaction to change the chelating of metals affinities between liquid and solid phases to enhance the quantitative distribution and bioavailability of metal in the sediment [55]. The changes created by the bioturbation-attributed redox potentials, pH, organic content, pore spaces can affect metal sorption capacity and improve metal conversion from one phase to another e.g. Cd, Zn [56, 57, 58].
The activities of bioturbators are affected by some factors which modulate the rate of bioturbation for effective remediation of polluted environments. These factors include the variation in salinity, temperature, density, sediment grain size pH, and concentration.
Variation in salinities in the aquatic environment can influence the metabolism of nutrient and metal releases [59, 60], whether naturally and/or through human-related activities. Remaili et al. [61] noted that hypersalinity has a negative effect on the larger bioturbators which affects the activities of benthic organisms. Gonzalez et al. [62] study found that the salinity levels and tolerance of various bioturbators are distinct. The findings however suggest that ammonia release in the aquatic environment is significantly modified due to the effect of modulating conditions and distinguished by a higher salinity than other nutrients such as phosphorus [62, 63].
Regional variability in temperature is also a crucial factor that regulates the impact of bioturbation in pollutant remediation. In microbial response, metabolism, and degradation of organic matter and metals, temperatures played a fair modulatory function [64]. In the presence of bioturbation activities, the rise in temperatures increases the production of ammonium from the sediment, possibly due to the high level of hydrogenase in microbial species and the increased aerobic conditions in the sediment [64, 65]. Gonzalez et al. [62] reported that an increase in temperature is indirectly proportional to the nutrient dispersion as high temperature decreases nutrient flux (phosphorus) in the sediment but extreme temperatures may be devastating to the microbes. However, an increase in temperature corresponds to the increased rate of metal resuspension and metal solubility as a result of higher bioturbation rates [66, 67].
The bioturbator density influences bioturbation, control bioturbation efficiency for contaminant remediation, which correlates with the increased aerobic microbial activity and emission of pollutants. The increased bioturbation density increased phosphorus release and induced aerobic microbial activity but did not increase the release of ammonia. Animal density is a highly imperative factor, as study reveals that higher densities contribute toward greater degradation and mineralization of organic matter but may also increase nutrients in the overlying water and can, depending on the ecosystem studied, have counterproductive effects on recovery [66]. In response to pollution, the population of certain benthic species such as polychaetes [68] may increase as several systems are deprived of the use of other larger bioturbators.
Another element that influences the high level of organic matter and metals accumulation and the structure and metabolism of microbial communities and their metabolism is the sediment grain size [69, 70]. A recent study also shows a positive association between ammonia, phosphorus release, and aerobic microbial activity for the sediment grain size as Martinez-Garcia et al. [70] noted that the grain size showed less effect at low organic enrichments, but instead, at higher enrichments, coarse sediments contain less organic matter and nutrients while metabolism rate is enhanced. The contaminant bioavailability assessment can be affected by the susceptibility, grain size and behavior of microbes used in bioassays or observed on the ground, and the interaction between various species and microbial populations in highly polluted sediments depauperated by larger invertebrates [1, 71].
The concentration of organic or inorganic contaminants is another factor that regulates the activities of the benthic organisms [72] which tend to either reduce or hinder the activities of the benthic organism at a high concentration, beyond the tolerable limit, which can result in the death of these organisms at extreme condition due to toxicity [5]. Benthic organisms have varying tolerance limits for sediment contaminations and tend to possess special features or activities (such as bioaccumulation or biosorption) to enable them to adapt and function effectively in high pollutant concentrations. For metal remediation, abiotic factor-like pH which works closely with concentration may be a crucial modulating variable that determines the impact of bioturbation in the marine environment which can alter metal speciation and reactivity [66].
Therefore, sediment properties like particle size and concentration as well as contaminant shape (sulphides or organic carbon) can affect the bioavailability of the contaminant. Also, in most environments, temperature and type of organism activity or population density can increase or decrease contaminant exposure or bioavailability for bioremediation [61, 73, 74, 75].
Notwithstanding the benefits (such as environmental friendliness, selectivity, adaptability, self-reproducibility, and the ability to recycle bioproducts) of the bioremediation technique, some setbacks have hindered the successful application of this technology. The delay of the operations and the complexity in managing the procedures are the two most significant disadvantages of this technique of treatment. Since the elimination of significant concentrations of heavy metals is a priority, and that the world has become more aware of the environmental concerns caused by other approaches, microbial procedures offer the most rational and long-term answer for treatment. As previously stated, while a variety of microbial contaminant bioremediation techniques to address contamination have been developed, their extensive use and application on a commercial scale are still restricted by some factors. A further point to mention is that the long-term viability of microbial decontamination is still a subject of significant importance, given the paucity of investigations into its long-term performance. Due to the extremely high accumulation of inorganic contaminants (heavy metals) in heavily inhabited places of the world, updating existing microbial bioremediation technologies to an industrial level by making the procedures quicker, more reusable, and easier to regulate will be a big issue in the future. Furthermore, another limitation of bioremediation is that not all substances are biodegradable while some hydrocarbon components are recalcitrant to microbial breakdown, which restricts the scope of the remediation technique. Even when a material is biodegradable, its downstream operation and breakdown can result in the production of harmful by-products in some situations.
The potential for microorganisms to remediate water and soil pollutants to increase treated water consumption and soil fertility for agricultural output is gaining attention [11, 38]. Recently, research has been conducted to enhance the application of altered organisms delineated specifically to boost their affectability toward hazardous metals [11, 16, 38]. An organism whose genetics have been transformed by the use of synthetic methods, which are driven by an artificial genetic exchange between bacteria, is referred to as a “genetically engineered microorganism [11, 18]. By developing GEM, genetic engineering has enhanced the application and disposal of hazardous wastes in laboratory settings. In addition, the following protocols must be considered during the GEM process: (a) alteration of enzyme selectivity and affinity, (b) pathway development and modulation, (c) bioprocess advancement, surveillance, and control, and (d) bioaffinity bioreporter sensor utilization for chemical detecting, toxicity reduction, and endpoint evaluation [13, 18].
As there are several possibilities for improving degradation performance through genetic engineering approaches, such as genetically controlling the rate kinetics of known metabolic pathways to increase degradation rate, or completely infusing bacterial strains with new metabolic pathways for the degradation of previously recalcitrant compounds [6, 8]. Despite important genes for microorganisms are carried on a single chromosome, defining the specific genes needed for the catabolism of some of these novel substrates may be carried on plasmids [18, 76, 77]. Plasmids were entangled in the catabolism process. As a result, GEM can be successfully used for biodegradation purposes, necessitating immediate research and large-scale deployment. Genetically engineer microbes offer the benefit of developing microbial strains which can tolerate unfriendly upsetting circumstances and can be utilized as a bioremediation tool under different and complicated natural conditions [18, 37, 76, 77]. Additionally, GEM has encouraged the development of “microbial biosensors” capable of precisely quantifying the degree of pollution in a contaminated site.
The current advancement in omics technologies, including genomics, proteomics, transcriptomics, and metabolomics, play a critical role in finding characteristics that optimize remediation solutions [7, 11, 78]. Consequently, phytoremediation was developed, a process for eliminating toxins or their metabolites from plant tissues. This usually shortens the life of the plant and finally volatilizes the toxins into the atmosphere [78]. This disadvantage can be mitigated by managing plants’ metal resistance, accumulation, and breakdown capacity in the presence of various inorganic toxins. To improve metal decomposition in plants, bacterial genes responsible for metal reduction can be integrated into plant tissues. As a result, plant-based bioremediation for a variety of significant metal poisons is cutting-edge due to its eco-friendliness. They are more effective at reducing dangerous substances than Physicochemical approaches, which are less environmentally friendly and potentially detrimental to human health [7, 8].
Notwithstanding, microbial genes can bridle in the transgenic plant for decontamination and collection of inorganic pollutants [7, 11]. The metal-detoxifying chelators, for example, metallothioneins and phytochelatins can give resistance to the plant by upgrading take-up, transport and amassing of different heavy metals [14, 78]. Similarly, transgenic plants with bacterial reductase can augment the volatilization of Hg and Se while absorbing the arsenic in plant shoots [17, 78]. Also, high-biomass-producing plants including poplar, willow and Jatropha can be applied for both phytoremediation and energy generation [7, 14, 26, 78]. Nonetheless, metals can only be removed from soil or water, which is why consuming metal-contaminated plants is advantageous. Thus, metal-accumulating biomasses should be properly preserved or disposed of to avoid posing an environmental hazard [20, 78].
Bioremediation methods include the introduction of growth stimulators (electron acceptors/donors) or nutrients to the rhizosphere to promote microbial growth and bioremediation characteristics of microbes or genetically engineered plants [6, 26, 78]. Multiple small organisms were generated with heavy metals by drainage using synthesized catalysts such as chromate and uranyl reductase in a particular rhizosphere [19, 26, 78]. Although genomics has been studied and applied mostly in microbial genetics and agriculture, such as genetic crops, and now serve as a bioremediation instrument [26, 76]. The application of genomics to bioremediation enables the microorganism to be dissected based on biochemical constraints as well as sub-atomic levels associated with the component [26, 76, 77].
Bioturbation is a very prolific and appealing technology for remediation, cleaning, management, and recovery of environmental contamination caused by microbial activity [11]. Furthermore, phytoremediation is successful at removing both inorganic and organic pollutants from residues or soils [7, 11, 12]. Nonetheless, investigation of resourceful bioremediation approaches for damaged aquatic environments that are based on these two processes to improve wastewater and soil treatment is necessary [10, 17]. Nonetheless, investigation of resourceful bioremediation technologies based on these two processes is important to improve soil and wastewater treatment [11, 17]. In addition, phytoremediation has been generally illustrated as a bioremediation process for heavy metals, such as lead, cadmium, copper, arsenic removal from contaminated soil or water [76, 77]. In essence, aquatic bioturbation combined with phytoremediation is a more effective and alternative method of removing heavy metals by improving cadmium transfers from overlying water to sediment and then into the root system of plants [15, 38].
Additionally, studies have demonstrated that earthworm movement greatly boosted phytoavailability by increasing soil macroporosity and generating cast around plant roots (Figure 3), implying that the physical effect of the earthworm’s bioturbation is a viable mechanism [20, 26]. Interaction between plants and soil-dwelling microorganisms can also enhance phytoremediation known as rhizosphere bioremediation. The study by Leveque et al. [52] to investigate the contribution of earthworm (as bioremediator or bioturbation agent) to phytoremediation showed that earthworms significantly increased the phyto-availability of metal by generating soil macroporosity and developing cast near plant roots in which the main mechanism appears to be the physical impact of earthworm bioturbation. Moore et al. [21], demonstrated the contribution and the effect of bioturbators in the remediation of organic contaminants using the phytoremediation technique. In the study,
Proffered approach to illustrate metal phytoavailability in earthworms’ activities (adapted from [
The use of nanomaterials is extensively gaining attention for components remediation of heavy metals and recovery of valuable via nanotechnology [8, 34]. Conversely, nanobioremediation, which employs nanoparticles to stimulate microbial activity to clear hazardous chemicals from groundwater and soil [14, 17]. Not only can this nanotechnology greatly cut the cost of cleaning contaminated regions, but it also significantly shortens the procedure’s duration. Metal chelating polymers require damaging solvents for mixing and ultrafiltration for division, which can be avoided by inventing metal limiting substances that can be reclaimed by adjusting their pH, temperature, or form, among other parameters [13, 19, 20]. One of the materials is nanoscale modified biopolymers, produced by microorganisms’ intrinsic and protein structure, and whose size can be adjusted at the subatomic level [13]. For instance, polymers and magnetosomes are fabricated proteins for the remediation of infections,
The technique entails using ecological and environmental engineering expertise to create and monitor a sustainable ecosystem or biological system that benefits both humans and the environment. Table 1 and Figure 4 illustrate how to apply ecological engineering in a way that is more beneficial to humanity while maintaining the natural balance. Nevertheless, the majority of these technologies are typically designed with the following objectives in mind: (i) conservation, (ii) ecosystem restoration, (iii) expanding ecological systems to the quantity, quality, and maintainability of their production, and (iv) assembling new ecological systems that would provide routine types of assistance [16, 39, 76, 77, 80].
Ecological-engineering approaches | Terrestrial examples | Aquatic examples |
---|---|---|
Using ecosystems to solve a pollution problem | Phytoremediation | Wastewater wetland |
Imitating or copying ecosystems to reduce or solve a problem | Forest restoration | Replacement wetland |
Recovering an ecosystem after significant disturbance | Mine land restoration | Lake restoration |
Existing ecosystems are modified in an ecologically sound way | Selective timber harvest | Biomanipulation |
Using ecosystems for benefit without destroying the ecological balance | Sustainable agroecosystems | Multi-species aquaculture |
Application of ecological engineering approach for terrestrial and aquatic systems.
Graphical representation of ecological engineering application to balance the ecosystem.
Bioremediation is a cutting-edge and promising approach for treating contaminated soil and water. Microorganisms are also known to generate and use a variety of detoxification methods, including biosorption, bioaccumulation, biotransformation, and biomineralization for the remediation of the contaminated site during the bioremediation process. However, recent bioremediation research, such as bioturbation, which uses live organisms (macrofauna) directly or indirectly with the environment to eliminate toxins, is gaining momentum. The use of organisms to detoxify and recover polluted soil and water has emerged as the most robust, straightforward, and profitable technique. Microorganisms in water and soil have been studied and equipped to eliminate or detoxify harmful compounds discharged into the ecosystem due to anthropogenic processes such as mineral mining, oil and gas production, pesticides, pigments, plastic, organic solvents, fuel, and industrial operations. Nevertheless, a lack of data on microorganisms’ cell reactivity to minor components and heavy metal poisons precludes their successful implementation. As such, the application of molecular genetic technology will enhance the efficiency and address most of the challenges in the large scale application of bioremediation technology.
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Biosensors, Biomaterials and Tissue Engineering",value:9,count:1},{group:"subseries",caption:"Bioinspired Technology and Biomechanics",value:8,count:2},{group:"subseries",caption:"Bioinformatics and Medical Informatics",value:7,count:9}],publicationYearFilters:[{group:"publicationYear",caption:"2021",value:2021,count:4},{group:"publicationYear",caption:"2019",value:2019,count:5},{group:"publicationYear",caption:"2018",value:2018,count:3}],authors:{paginationCount:302,paginationItems:[{id:"198499",title:"Dr.",name:"Daniel",middleName:null,surname:"Glossman-Mitnik",slug:"daniel-glossman-mitnik",fullName:"Daniel Glossman-Mitnik",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/198499/images/system/198499.jpeg",biography:"Dr. Daniel Glossman-Mitnik is currently a Titular Researcher at the Centro de Investigación en Materiales Avanzados (CIMAV), Chihuahua, Mexico, as well as a National Researcher of Level III at the Consejo Nacional de Ciencia y Tecnología, Mexico. His research interest focuses on computational chemistry and molecular modeling of diverse systems of pharmacological, food, and alternative energy interests by resorting to DFT and Conceptual DFT. He has authored a coauthored more than 255 peer-reviewed papers, 32 book chapters, and 2 edited books. He has delivered speeches at many international and domestic conferences. He serves as a reviewer for more than eighty international journals, books, and research proposals as well as an editor for special issues of renowned scientific journals.",institutionString:"Centro de Investigación en Materiales Avanzados",institution:{name:"Centro de Investigación en Materiales Avanzados",country:{name:"Mexico"}}},{id:"76477",title:"Prof.",name:"Mirza",middleName:null,surname:"Hasanuzzaman",slug:"mirza-hasanuzzaman",fullName:"Mirza Hasanuzzaman",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/76477/images/system/76477.png",biography:"Dr. Mirza Hasanuzzaman is a Professor of Agronomy at Sher-e-Bangla Agricultural University, Bangladesh. He received his Ph.D. in Plant Stress Physiology and Antioxidant Metabolism from Ehime University, Japan, with a scholarship from the Japanese Government (MEXT). Later, he completed his postdoctoral research at the Center of Molecular Biosciences, University of the Ryukyus, Japan, as a recipient of the Japan Society for the Promotion of Science (JSPS) postdoctoral fellowship. He was also the recipient of the Australian Government Endeavour Research Fellowship for postdoctoral research as an adjunct senior researcher at the University of Tasmania, Australia. Dr. Hasanuzzaman’s current work is focused on the physiological and molecular mechanisms of environmental stress tolerance. Dr. Hasanuzzaman has published more than 150 articles in peer-reviewed journals. He has edited ten books and written more than forty book chapters on important aspects of plant physiology, plant stress tolerance, and crop production. According to Scopus, Dr. Hasanuzzaman’s publications have received more than 10,500 citations with an h-index of 53. He has been named a Highly Cited Researcher by Clarivate. He is an editor and reviewer for more than fifty peer-reviewed international journals and was a recipient of the “Publons Peer Review Award” in 2017, 2018, and 2019. He has been honored by different authorities for his outstanding performance in various fields like research and education, and he has received the World Academy of Science Young Scientist Award (2014) and the University Grants Commission (UGC) Award 2018. He is a fellow of the Bangladesh Academy of Sciences (BAS) and the Royal Society of Biology.",institutionString:"Sher-e-Bangla Agricultural University",institution:{name:"Sher-e-Bangla Agricultural University",country:{name:"Bangladesh"}}},{id:"187859",title:"Prof.",name:"Kusal",middleName:"K.",surname:"Das",slug:"kusal-das",fullName:"Kusal Das",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSBDeQAO/Profile_Picture_1623411145568",biography:"Kusal K. Das is a Distinguished Chair Professor of Physiology, Shri B. M. Patil Medical College and Director, Centre for Advanced Medical Research (CAMR), BLDE (Deemed to be University), Vijayapur, Karnataka, India. Dr. Das did his M.S. and Ph.D. in Human Physiology from the University of Calcutta, Kolkata. His area of research is focused on understanding of molecular mechanisms of heavy metal activated low oxygen sensing pathways in vascular pathophysiology. He has invented a new method of estimation of serum vitamin E. His expertise in critical experimental protocols on vascular functions in experimental animals was well documented by his quality of publications. He was a Visiting Professor of Medicine at University of Leeds, United Kingdom (2014-2016) and Tulane University, New Orleans, USA (2017). For his immense contribution in medical research Ministry of Science and Technology, Government of India conferred him 'G.P. Chatterjee Memorial Research Prize-2019” and he is also the recipient of 'Dr.Raja Ramanna State Scientist Award 2015” by Government of Karnataka. He is a Fellow of the Royal Society of Biology (FRSB), London and Honorary Fellow of Karnataka Science and Technology Academy, Department of Science and Technology, Government of Karnataka.",institutionString:"BLDE (Deemed to be University), India",institution:null},{id:"243660",title:"Dr.",name:"Mallanagouda Shivanagouda",middleName:null,surname:"Biradar",slug:"mallanagouda-shivanagouda-biradar",fullName:"Mallanagouda Shivanagouda Biradar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/243660/images/system/243660.jpeg",biography:"M. S. Biradar is Vice Chancellor and Professor of Medicine of\nBLDE (Deemed to be University), Vijayapura, Karnataka, India.\nHe obtained his MD with a gold medal in General Medicine and\nhas devoted himself to medical teaching, research, and administrations. He has also immensely contributed to medical research\non vascular medicine, which is reflected by his numerous publications including books and book chapters. Professor Biradar was\nalso Visiting Professor at Tulane University School of Medicine, New Orleans, USA.",institutionString:"BLDE (Deemed to be University)",institution:{name:"BLDE University",country:{name:"India"}}},{id:"289796",title:"Dr.",name:"Swastika",middleName:null,surname:"Das",slug:"swastika-das",fullName:"Swastika Das",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/289796/images/system/289796.jpeg",biography:"Swastika N. Das is Professor of Chemistry at the V. P. Dr. P. G.\nHalakatti College of Engineering and Technology, BLDE (Deemed\nto be University), Vijayapura, Karnataka, India. She obtained an\nMSc, MPhil, and PhD in Chemistry from Sambalpur University,\nOdisha, India. Her areas of research interest are medicinal chemistry, chemical kinetics, and free radical chemistry. She is a member\nof the investigators who invented a new modified method of estimation of serum vitamin E. She has authored numerous publications including book\nchapters and is a mentor of doctoral curriculum at her university.",institutionString:"BLDEA’s V.P.Dr.P.G.Halakatti College of Engineering & Technology",institution:{name:"BLDE University",country:{name:"India"}}},{id:"248459",title:"Dr.",name:"Akikazu",middleName:null,surname:"Takada",slug:"akikazu-takada",fullName:"Akikazu Takada",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/248459/images/system/248459.png",biography:"Akikazu Takada was born in Japan, 1935. After graduation from\nKeio University School of Medicine and finishing his post-graduate studies, he worked at Roswell Park Memorial Institute NY,\nUSA. He then took a professorship at Hamamatsu University\nSchool of Medicine. In thrombosis studies, he found the SK\npotentiator that enhances plasminogen activation by streptokinase. He is very much interested in simultaneous measurements\nof fatty acids, amino acids, and tryptophan degradation products. By using fatty\nacid analyses, he indicated that plasma levels of trans-fatty acids of old men were\nfar higher in the US than Japanese men. . He also showed that eicosapentaenoic acid\n(EPA) and docosahexaenoic acid (DHA) levels are higher, and arachidonic acid\nlevels are lower in Japanese than US people. By using simultaneous LC/MS analyses\nof plasma levels of tryptophan metabolites, he recently found that plasma levels of\nserotonin, kynurenine, or 5-HIAA were higher in patients of mono- and bipolar\ndepression, which are significantly different from observations reported before. In\nview of recent reports that plasma tryptophan metabolites are mainly produced by\nmicrobiota. He is now working on the relationships between microbiota and depression or autism.",institutionString:"Hamamatsu University School of Medicine",institution:{name:"Hamamatsu University School of Medicine",country:{name:"Japan"}}},{id:"137240",title:"Prof.",name:"Mohammed",middleName:null,surname:"Khalid",slug:"mohammed-khalid",fullName:"Mohammed Khalid",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/137240/images/system/137240.png",biography:"Mohammed Khalid received his B.S. degree in chemistry in 2000 and Ph.D. degree in physical chemistry in 2007 from the University of Khartoum, Sudan. He moved to School of Chemistry, Faculty of Science, University of Sydney, Australia in 2009 and joined Dr. Ron Clarke as a postdoctoral fellow where he worked on the interaction of ATP with the phosphoenzyme of the Na+/K+-ATPase and dual mechanisms of allosteric acceleration of the Na+/K+-ATPase by ATP; then he went back to Department of Chemistry, University of Khartoum as an assistant professor, and in 2014 he was promoted as an associate professor. In 2011, he joined the staff of Department of Chemistry at Taif University, Saudi Arabia, where he is currently an assistant professor. His research interests include the following: P-Type ATPase enzyme kinetics and mechanisms, kinetics and mechanisms of redox reactions, autocatalytic reactions, computational enzyme kinetics, allosteric acceleration of P-type ATPases by ATP, exploring of allosteric sites of ATPases, and interaction of ATP with ATPases located in cell membranes.",institutionString:"Taif University",institution:{name:"Taif University",country:{name:"Saudi Arabia"}}},{id:"63810",title:"Prof.",name:"Jorge",middleName:null,surname:"Morales-Montor",slug:"jorge-morales-montor",fullName:"Jorge Morales-Montor",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/63810/images/system/63810.png",biography:"Dr. Jorge Morales-Montor was recognized with the Lola and Igo Flisser PUIS Award for best graduate thesis at the national level in the field of parasitology. He received a fellowship from the Fogarty Foundation to perform postdoctoral research stay at the University of Georgia. He has 153 journal articles to his credit. He has also edited several books and published more than fifty-five book chapters. He is a member of the Mexican Academy of Sciences, Latin American Academy of Sciences, and the National Academy of Medicine. He has received more than thirty-five awards and has supervised numerous bachelor’s, master’s, and Ph.D. students. Dr. Morales-Montor is the past president of the Mexican Society of Parasitology.",institutionString:"National Autonomous University of Mexico",institution:{name:"National Autonomous University of Mexico",country:{name:"Mexico"}}},{id:"217215",title:"Dr.",name:"Palash",middleName:null,surname:"Mandal",slug:"palash-mandal",fullName:"Palash Mandal",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/217215/images/system/217215.jpeg",biography:null,institutionString:"Charusat University",institution:null},{id:"49739",title:"Dr.",name:"Leszek",middleName:null,surname:"Szablewski",slug:"leszek-szablewski",fullName:"Leszek Szablewski",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/49739/images/system/49739.jpg",biography:"Leszek Szablewski is a professor of medical sciences. He received his M.S. in the Faculty of Biology from the University of Warsaw and his PhD degree from the Institute of Experimental Biology Polish Academy of Sciences. He habilitated in the Medical University of Warsaw, and he obtained his degree of Professor from the President of Poland. Professor Szablewski is the Head of Chair and Department of General Biology and Parasitology, Medical University of Warsaw. Professor Szablewski has published over 80 peer-reviewed papers in journals such as Journal of Alzheimer’s Disease, Biochim. Biophys. Acta Reviews of Cancer, Biol. Chem., J. Biomed. Sci., and Diabetes/Metabol. Res. Rev, Endocrine. He is the author of two books and four book chapters. He has edited four books, written 15 scripts for students, is the ad hoc reviewer of over 30 peer-reviewed journals, and editorial member of peer-reviewed journals. Prof. Szablewski’s research focuses on cell physiology, genetics, and pathophysiology. He works on the damage caused by lack of glucose homeostasis and changes in the expression and/or function of glucose transporters due to various diseases. He has given lectures, seminars, and exercises for students at the Medical University.",institutionString:"Medical University of Warsaw",institution:{name:"Medical University of Warsaw",country:{name:"Poland"}}},{id:"173123",title:"Dr.",name:"Maitham",middleName:null,surname:"Khajah",slug:"maitham-khajah",fullName:"Maitham Khajah",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/173123/images/system/173123.jpeg",biography:"Dr. Maitham A. Khajah received his degree in Pharmacy from Faculty of Pharmacy, Kuwait University, in 2003 and obtained his PhD degree in December 2009 from the University of Calgary, Canada (Gastrointestinal Science and Immunology). Since January 2010 he has been assistant professor in Kuwait University, Faculty of Pharmacy, Department of Pharmacology and Therapeutics. His research interest are molecular targets for the treatment of inflammatory bowel disease (IBD) and the mechanisms responsible for immune cell chemotaxis. He cosupervised many students for the MSc Molecular Biology Program, College of Graduate Studies, Kuwait University. Ever since joining Kuwait University in 2010, he got various grants as PI and Co-I. He was awarded the Best Young Researcher Award by Kuwait University, Research Sector, for the Year 2013–2014. He was a member in the organizing committee for three conferences organized by Kuwait University, Faculty of Pharmacy, as cochair and a member in the scientific committee (the 3rd, 4th, and 5th Kuwait International Pharmacy Conference).",institutionString:"Kuwait University",institution:{name:"Kuwait University",country:{name:"Kuwait"}}},{id:"195136",title:"Dr.",name:"Aya",middleName:null,surname:"Adel",slug:"aya-adel",fullName:"Aya Adel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/195136/images/system/195136.jpg",biography:"Dr. Adel works as an Assistant Lecturer in the unit of Phoniatrics, Department of Otolaryngology, Ain Shams University in Cairo, Egypt. Dr. Adel is especially interested in joint attention and its impairment in autism spectrum disorder",institutionString:"Ain Shams University",institution:{name:"Ain Shams University",country:{name:"Egypt"}}},{id:"94911",title:"Dr.",name:"Boulenouar",middleName:null,surname:"Mesraoua",slug:"boulenouar-mesraoua",fullName:"Boulenouar Mesraoua",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94911/images/system/94911.png",biography:"Dr Boulenouar Mesraoua is the Associate Professor of Clinical Neurology at Weill Cornell Medical College-Qatar and a Consultant Neurologist at Hamad Medical Corporation at the Neuroscience Department; He graduated as a Medical Doctor from the University of Oran, Algeria; he then moved to Belgium, the City of Liege, for a Residency in Internal Medicine and Neurology at Liege University; after getting the Belgian Board of Neurology (with high marks), he went to the National Hospital for Nervous Diseases, Queen Square, London, United Kingdom for a fellowship in Clinical Neurophysiology, under Pr Willison ; Dr Mesraoua had also further training in Epilepsy and Continuous EEG Monitoring for two years (from 2001-2003) in the Neurophysiology department of Zurich University, Switzerland, under late Pr Hans Gregor Wieser ,an internationally known epileptologist expert. \n\nDr B. Mesraoua is the Director of the Neurology Fellowship Program at the Neurology Section and an active member of the newly created Comprehensive Epilepsy Program at Hamad General Hospital, Doha, Qatar; he is also Assistant Director of the Residency Program at the Qatar Medical School. \nDr B. Mesraoua's main interests are Epilepsy, Multiple Sclerosis, and Clinical Neurology; He is the Chairman and the Organizer of the well known Qatar Epilepsy Symposium, he is running yearly for the past 14 years and which is considered a landmark in the Gulf region; He has also started last year , together with other epileptologists from Qatar, the region and elsewhere, a yearly International Epilepsy School Course, which was attended by many neurologists from the Area.\n\nInternationally, Dr Mesraoua is an active and elected member of the Commission on Eastern Mediterranean Region (EMR ) , a regional branch of the International League Against Epilepsy (ILAE), where he represents the Middle East and North Africa(MENA ) and where he holds the position of chief of the Epilepsy Epidemiology Section; Dr Mesraoua is a member of the American Academy of Neurology, the Europeen Academy of Neurology and the American Epilepsy Society.\n\nDr Mesraoua's main objectives are to encourage frequent gathering of the epileptologists/neurologists from the MENA region and the rest of the world, promote Epilepsy Teaching in the MENA Region, and encourage multicenter studies involving neurologists and epileptologists in the MENA region, particularly epilepsy epidemiological studies. \n\nDr. Mesraoua is the recipient of two research Grants, as the Lead Principal Investigator (750.000 USD and 250.000 USD) from the Qatar National Research Fund (QNRF) and the Hamad Hospital Internal Research Grant (IRGC), on the following topics : “Continuous EEG Monitoring in the ICU “ and on “Alpha-lactoalbumin , proof of concept in the treatment of epilepsy” .Dr Mesraoua is a reviewer for the journal \"seizures\" (Europeen Epilepsy Journal ) as well as dove journals ; Dr Mesraoua is the author and co-author of many peer reviewed publications and four book chapters in the field of Epilepsy and Clinical Neurology",institutionString:"Weill Cornell Medical College in Qatar",institution:{name:"Weill Cornell Medical College in Qatar",country:{name:"Qatar"}}},{id:"282429",title:"Prof.",name:"Covanis",middleName:null,surname:"Athanasios",slug:"covanis-athanasios",fullName:"Covanis Athanasios",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/282429/images/system/282429.jpg",biography:null,institutionString:"Neurology-Neurophysiology Department of the Children Hospital Agia Sophia",institution:null},{id:"190980",title:"Prof.",name:"Marwa",middleName:null,surname:"Mahmoud Saleh",slug:"marwa-mahmoud-saleh",fullName:"Marwa Mahmoud Saleh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/190980/images/system/190980.jpg",biography:"Professor Marwa Mahmoud Saleh is a doctor of medicine and currently works in the unit of Phoniatrics, Department of Otolaryngology, Ain Shams University in Cairo, Egypt. She got her doctoral degree in 1991 and her doctoral thesis was accomplished in the University of Iowa, United States. Her publications covered a multitude of topics as videokymography, cochlear implants, stuttering, and dysphagia. She has lectured Egyptian phonology for many years. Her recent research interest is joint attention in autism.",institutionString:"Ain Shams University",institution:{name:"Ain Shams University",country:{name:"Egypt"}}},{id:"259190",title:"Dr.",name:"Syed Ali Raza",middleName:null,surname:"Naqvi",slug:"syed-ali-raza-naqvi",fullName:"Syed Ali Raza Naqvi",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259190/images/system/259190.png",biography:"Dr. Naqvi is a radioanalytical chemist and is working as an associate professor of analytical chemistry in the Department of Chemistry, Government College University, Faisalabad, Pakistan. Advance separation techniques, nuclear analytical techniques and radiopharmaceutical analysis are the main courses that he is teaching to graduate and post-graduate students. In the research area, he is focusing on the development of organic- and biomolecule-based radiopharmaceuticals for diagnosis and therapy of infectious and cancerous diseases. Under the supervision of Dr. Naqvi, three students have completed their Ph.D. degrees and 41 students have completed their MS degrees. He has completed three research projects and is currently working on 2 projects entitled “Radiolabeling of fluoroquinolone derivatives for the diagnosis of deep-seated bacterial infections” and “Radiolabeled minigastrin peptides for diagnosis and therapy of NETs”. He has published about 100 research articles in international reputed journals and 7 book chapters. Pakistan Institute of Nuclear Science & Technology (PINSTECH) Islamabad, Punjab Institute of Nuclear Medicine (PINM), Faisalabad and Institute of Nuclear Medicine and Radiology (INOR) Abbottabad are the main collaborating institutes.",institutionString:"Government College University",institution:{name:"Government College University, Faisalabad",country:{name:"Pakistan"}}},{id:"58390",title:"Dr.",name:"Gyula",middleName:null,surname:"Mozsik",slug:"gyula-mozsik",fullName:"Gyula Mozsik",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/58390/images/system/58390.png",biography:"Gyula Mózsik MD, Ph.D., ScD (med), is an emeritus professor of Medicine at the First Department of Medicine, Univesity of Pécs, Hungary. He was head of this department from 1993 to 2003. His specializations are medicine, gastroenterology, clinical pharmacology, clinical nutrition, and dietetics. 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