RESUMO
The primary objective of this study was to develop a carboxymethyl cellulose (CMC) and carboxymethyl chitosan (CMCS) hydrogel containing ethylene diamine tetra acetic acid (EDTA) as the materials for wound healing. CMC and CMCS solutions were prepared with a concentration of 4% (w/v). These solutions were made using normal saline serum with a concentration of 0.5% (v/v). Additionally, EDTA with the concentrations of 0.01%, 0.05%, 0.1%, 0.5%, 1%, and 2% (w/v) was included in the prepared polymer solution. The analysis of the hydrogels revealed that they possess porous structures with interconnected pores, with average in size 88.71 ± 5.93 µm. The hydrogels exhibited a swelling capacity of up to 60% of their initial weight within 24 h, as indicated by the weight loss and swelling measurements. The antibacterial experiments showed that the formulated CMC/CMCS/EDTA 0.5% hydrogel inhibited the growth of Staphylococcus aureus and Pseudomonas aeruginosa. Moreover, the produced hydrogels were haemocompatible and biocompatible. At the last stage, the evaluation of wound healing in the animal model demonstrated that the use of the produced hydrogels significantly improved the process of wound healing. Finally, the findings substantiated the effectiveness of the formulated hydrogels as the materials for promoting wound healing and antibacterial agents.
Assuntos
Biofilmes , Carboximetilcelulose Sódica , Quitosana , Quitosana/análogos & derivados , Ácido Edético , Hidrogéis , Pseudomonas aeruginosa , Staphylococcus aureus , Cicatrização , Animais , Quitosana/farmacologia , Ratos , Ácido Edético/farmacologia , Ácido Edético/uso terapêutico , Staphylococcus aureus/efeitos dos fármacos , Pseudomonas aeruginosa/efeitos dos fármacos , Carboximetilcelulose Sódica/farmacologia , Cicatrização/efeitos dos fármacos , Biofilmes/efeitos dos fármacos , Hidrogéis/farmacologia , Modelos Animais de Doenças , Masculino , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Ratos Wistar , Infecções Estafilocócicas/tratamento farmacológico , Infecção dos Ferimentos/tratamento farmacológico , Infecções por Pseudomonas/tratamento farmacológicoRESUMO
OBJECTIVE: Lubrication and free radical scavenging are key features of biomaterials used for viscosupplementation (VS) of joints affected by osteoarthritis (OA). The objective of this study was to describe the non-clinical performance characterization of KiOmedine® CM-Chitosan, a non-animal carboxymethyl chitosan, in order to assess its intended action in VS and to compare it to existing viscosupplements based on crosslinked hyaluronan (HA) formulations. METHOD: The lubrication capacity of the tested viscosupplements (VS) was evaluated in-vitro and ex-vivo. In-vitro, the coefficient of friction (COF) was measured using a novel tribological system. Meanwhile, an ex-vivo biomechanical model in ovine hindlimbs was developed to assess the recovery of join mobility after an intra-articular (IA) injection. Free radical scavenging capacity of HA and KiOmedine® CM-Chitosan formulations was evaluated using the Trolox Equivalent Antioxidant Capacity (TEAC) assay. RESULTS: In the in-vitro tribological model, KiOmedine® CM-Chitosan showed high lubrication capacity with a significant COF reduction than crosslinked HA formulations. In the ex-vivo model, the lubrication effect of KiOmedine® CM-Chitosan following an IA injection in the injured knee was proven again by a COF reduction. The recovery of joint motion was optimal with an IA injection of 3 ml of KiOmedine® CM-Chitosan, which was significantly better than the crosslinked HA formulation at the same volume. In the in-vitro TEAC assay, KiOmedine® CM-Chitosan showed a significantly higher free radical scavenging capacity than HA formulations. CONCLUSION: Overall, the results provide a first insight into the mechanism of action in terms of lubrication and free radical scavenging for the use of KiOmedine® CM-Chitosan as a VS treatment of OA. KiOmedine® CM-Chitosan demonstrated a higher capacity to scavenge free radicals, and it showed a higher recovery of mobility after a knee lesion than crosslinked HA formulations. This difference could be explained by the difference in chemical structure between KiOmedine® CM-Chitosan and HA and their formulations.
Assuntos
Quitosana/análogos & derivados , Sequestradores de Radicais Livres/farmacologia , Viscossuplementos/farmacologia , Animais , Materiais Biocompatíveis/administração & dosagem , Materiais Biocompatíveis/farmacologia , Quitosana/administração & dosagem , Quitosana/farmacologia , Sequestradores de Radicais Livres/administração & dosagem , Injeções Intra-Articulares , Articulação do Joelho/efeitos dos fármacos , Ovinos , Viscossuplementação , Viscossuplementos/administração & dosagemRESUMO
In this study, the inherent safety analysis of large-scale production of chitosan microbeads modified with TiO2 nanoparticles was developed using the Inherent Safety Index (ISI) methodology. This topology was structured based on two main stages: (i) Green-based synthesis of TiO2 nanoparticles based on lemongrass oil extraction and titanium isopropoxide (TTIP) hydrolysis, and (ii) Chitosan gelation and modification with nanoparticles. Stage (i) is divided into two subprocesses for accomplishing TiO2 synthesis, lemongrass oil extraction and TiO2 production. The plant was designed to produce 2033 t/year of chitosan microbeads, taking crude chitosan, lemongrass, and TTIP as the primary raw materials. The process was evaluated through the ISI methodology to identify improvement opportunity areas based on a diagnosis of process risks. This work used industrial-scale process inventory data of the analyzed production process from mass and energy balances and the process operating conditions. The ISI method comprises the Chemical Inherent Safety Index (CSI) and Process Inherent Safety Index (PSI) to assess a whole chemical process from a holistic perspective, and for this process, it reflected a global score of 28. Specifically, CSI and PSI delivered scores of 16 and 12, respectively. The analysis showed that the most significant risks are related to TTIP handling and its physical-chemical properties due to its toxicity and flammability. Insights about this process's safety performance were obtained, indicating higher risks than those from recommended standards.
Assuntos
Segurança Química/métodos , Quitosana/análogos & derivados , Indústria Farmacêutica/métodos , Química Verde/métodos , Nanopartículas Metálicas/química , Microesferas , Gestão da Segurança/métodos , Titânio/química , Quitosana/toxicidade , Nanopartículas Metálicas/toxicidade , Óleos de Plantas/química , Terpenos/química , Titânio/toxicidadeRESUMO
Escherichia coli infection is considered one of the most economically important multi-systemic diseases in poultry farms. Several nanoparticles such as silver, chitosan, and copper oxide are known to be highly toxic to several microbes. However, there are no data concerning their success against in vivo experimental E. coli infection in broilers. Therefore, the present study was designed to investigate the bactericidal effect of low doses of CuO-NPs (5 mg/kg bwt), Ag-NPs (0.5 mg/kg bwt), and Ch-Ag NPs (0.5 mg/kg bwt) against E. coli experimental infection in broilers. One hundred chicks were divided into five groups as follows: (1) control; (2) E. coli (4 × 108 CFU/ml) challenged; (3) E. coli +CuO-NPs; (4) E. coli +Ag-NPs; (5) E. coli +Ch-Ag NPs. The challenged untreated group, not NPs treated groups, recorded the lowest weight gain as well as the highest bacterial count and lesion score in all examined organs. The highest liver content of silver was observed in Ag-NPs treated group compared with the Ch-Ag NPs treated group. Our results concluded that Ch-Ag NPs not only had the best antibacterial effects but also acted as a growth promoter in broilers without leaving any residues in edible organs. We recommend using Ch-Ag NPs in broiler farms instead of antibiotics or probiotics.
Assuntos
Antibacterianos/uso terapêutico , Quitosana/análogos & derivados , Infecções por Escherichia coli/tratamento farmacológico , Nanopartículas Metálicas/uso terapêutico , Doenças das Aves Domésticas/tratamento farmacológico , Animais , Antibacterianos/administração & dosagem , Antibacterianos/química , Galinhas , Cobre/química , Infecções por Escherichia coli/veterinária , Fígado/metabolismo , Nanopartículas Metálicas/administração & dosagem , Nanopartículas Metálicas/química , Prata/químicaRESUMO
In this review, we present the data on the natural occurrence of chitin and its partially or fully deacetylated derivative chitosan, as well as their properties, methods of modification, and potential applications of derivatives with bactericidal, fungicidal, and antioxidant activities. The structure and physicochemical characteristics of the polymers, their functions, and features of chitin microbial synthesis and degradation, including the processes occurring in nature, are described. New data on the hydrolytic microorganisms capable of chitin degradation under extreme conditions are presented. Special attention is focused on the effect of physicochemical characteristics of chitosan, including molecular weight, degree of deacetylation, polydispersity index, and number of amino group derivatives (quaternized, succinyl, etc.) on the antimicrobial and antioxidant properties of modified polymers that can be of particular interest for biotechnology, medicine, and agriculture. Analysis of the available literature data confirms the importance of fundamental research to broaden our knowledge on the occurrence of chitin and chitosan in nature, their role in global biosphere cycles, and prospects of applied research aimed at using chitin, chitosan, and their derivatives in various aspects of human activity.
Assuntos
Antibacterianos/farmacologia , Antifúngicos/farmacologia , Antioxidantes/farmacologia , Quitosana/análogos & derivados , Quitosana/farmacologia , Fungicidas Industriais/farmacologia , Antibacterianos/química , Antibacterianos/metabolismo , Antifúngicos/química , Antifúngicos/metabolismo , Antioxidantes/química , Antioxidantes/metabolismo , Bactérias/metabolismo , Biotecnologia , Quitosana/química , Quitosana/metabolismo , Proteção de Cultivos , Descoberta de Drogas , Fungicidas Industriais/química , Fungicidas Industriais/economia , Fungicidas Industriais/metabolismo , Humanos , Hidrólise , Peso Molecular , PolímerosRESUMO
The composites (LDH-CMC) composed of carboxymethyl chitosan (CMC) and 2D ZnAl layered double hydroxide (LDH) were successfully prepared using the one-step urea method; these composites were characterized by XRD, FT-IR, UV-vis DRS, SEM, BJH/BET, TG-DTG and pHzpc analyses, cyclic voltammetry, and electrochemical impedance spectroscopy. The use of CMC could impact the textural and surface chemical properties of the LDH-CMC composites, where the composites still maintained the 2D layered structure. Incorporating a moderate amount of CMC could increase both the surface area and the permanent charge density of the composites, leading to improved electrochemical performances. The LDH-CMC composite was used as a support matrix for the immobilization of horseradish peroxidase (HRP) on the glass carbon (GC) electrode to construct a biosensor that provides a biocompatible microenvironment for HRP and a pathway for H2O2 diffusion via the high surface area. The HRP biosensor displayed a satisfactory sensitivity and fast response (<3â¯s) toward H2O2 over a wide linear range of 0.02-6.0â¯mmol·L-1 with a low detection limit of 12.4⯵mol·L-1, good anti-interference ability and long-term storage stability. The proposed HRP biosensor was found to be a sensitive, rapid, and disposable sensor with low cost, easy preparation and high selectivity; thus, the proposed biosensor can be used for the real-time detection of trace H2O2 in the biological, clinical and environmental fields.
Assuntos
Técnicas Biossensoriais/métodos , Quitosana/análogos & derivados , Peróxido de Hidrogênio/análise , Hidróxidos/química , Técnicas Biossensoriais/economia , Quitosana/química , Técnicas Eletroquímicas/economia , Técnicas Eletroquímicas/métodos , Peroxidase do Rábano Silvestre/química , Limite de Detecção , Fatores de TempoRESUMO
5-fluorouracil (5-FU) is a specific anti-cancer agent that is generally used to treat gastrointestinal, colorectal, and breast cancer. In this work, chitosan (CS) was extracted from local fish scales using an established method. 5-FU was then converted to 1-acetic acid-5-fluorouracil (FUAC) and reacted with this CS to prepare chitosan-1-acetic acid-5-fluorouracil (CS-FUAC) conjugates as a colon-specific prodrug. All compounds were characterized by Proton nuclear magnetic resonance (¹H-NMR), Fourier-transform infrared (FTIR), and UV-visible spectroscopy. The synthesized compound was subjected to a chemical stability study in phosphate buffer (0.2 M, pH 7.4) and in KCl/HCl buffer (0.2 M, pH 1.2) at different time intervals (0-240 min) and incubation at 37 °C. This revealed a significantly greater stability and a longer half-life for the CS-FUAC than for FUAC. Hemolytic activity results indicated a much lower toxicity for CS-FUAC than for 5-FU and supported consideration of CS-FUAC for further biological screening and application trials. The percentage of FUAC in the conjugates was determined by subjecting the prodrug to treatment in basic media to hydrolyze the amide bond, followed by absorbency measurements at 273 nm. The cytotoxicity studies of the conjugates were also evaluated on human colorectal cancer cell line (HT-29), which showed that the conjugates are more cytotoxic than the free drug. Therefore, CS-FUAC conjugates can be considered to represent potential colon-specific drug delivery agents, with minimal undesirable side effects, for colon cancer therapy.
Assuntos
Antineoplásicos , Quitosana , Neoplasias Colorretais/tratamento farmacológico , Fluoruracila , Pró-Fármacos , Ácido Acético/química , Animais , Antineoplásicos/síntese química , Antineoplásicos/química , Antineoplásicos/farmacologia , Linhagem Celular Tumoral , Quitosana/análogos & derivados , Quitosana/síntese química , Quitosana/química , Quitosana/farmacologia , Neoplasias Colorretais/metabolismo , Neoplasias Colorretais/patologia , Fluoruracila/química , Fluoruracila/farmacologia , Humanos , Pró-Fármacos/síntese química , Pró-Fármacos/química , Pró-Fármacos/farmacologia , CoelhosRESUMO
Chitosan is an abundant and renewable polysaccharide, its derivatives exhibit attractive bioactivities and the wide applications in various biomedical fields. In this paper, two novel cationic chitosan derivatives modified with quaternary phosphonium salts were successfully synthesized via trimethylation, chloride acetylation, and quaternization with tricyclohexylphosphine and triphenylphosphine. The structures and properties of synthesized products in the reactions were characterized by FTIR spectroscopy, ¹H-NMR, 31P-NMR, elemental and thermogravimetric analysis. The antifungal activities of chitosan derivatives against four kinds of phytopathogens, including Phomopsis asparagi, Watermelon fusarium, Colletotrichum lagenarium, and Fusarium oxysporum were tested using the radial growth assay in vitro. The results revealed that the synthesized cationic chitosan derivatives showed significantly improved antifungal efficiency compared to chitosan. It was reasonably suggested that quaternary phosphonium groups enabled the obviously stronger antifungal activity of the synthesized chitosans. Especially, the triphenylphosphonium-functionalized chitosan derivative inhibited the growth of Phomopsis asparagi most effectively, with inhibitory indices of about 80% at 0.5 mg/mL. Moreover, the data demonstrated that the substituted groups with stronger electron-withdrawing ability relatively possessed greater antifungal activity. The results suggest the possibility that cationic chitosan derivatives bearing quaternary phosphonium salts could be effectively employed as novel antifungal biomaterials for application in the field of agriculture.
Assuntos
Antifúngicos/síntese química , Quitosana/análogos & derivados , Quitosana/síntese química , Compostos Organofosforados/síntese química , Compostos de Amônio Quaternário/síntese química , Antifúngicos/farmacologia , Quitosana/farmacologia , Estabilidade de Medicamentos , Fusarium/efeitos dos fármacos , Concentração de Íons de Hidrogênio , Espectroscopia de Ressonância Magnética , Testes de Sensibilidade Microbiana , Compostos Organofosforados/farmacologia , Compostos de Amônio Quaternário/farmacologia , Solubilidade , Espectroscopia de Infravermelho com Transformada de FourierRESUMO
OBJECTIVE: Salivary dysfunction is associated with a range of oral/dental issues, and management of oral symptoms may improve oral function and overall quality of life. The purpose of this pilot study was to evaluate oral symptoms and function in a xerostomic population after use of a proprietary topical for dry mouth, Moisyn (Synedgen Inc., Claremont, CA), which is a polysaccharide-based product. STUDY DESIGN: A pre- and post-test survey was completed by 57 patients with xerostomia. Patients rated their common oral symptoms, based on the Vanderbilt Head and Neck Symptom Survey, before and after 1-week use of Moisyn rinse and spray. Saliva production under resting and chewing stimulation was also assessed. RESULTS: Most patients reported relief from dry mouth symptoms and thick saliva (81.7% and 76.0%, respectively) for more than 30 minutes after product use. Statistically significant reductions were found in 15 of 33 oral symptoms. Symptom improvement ranged from 10.7% to 28.4% for thick saliva, 8.4% to 30.6% for pain, 5.5% to 30.4% for dry mouth, and 12% to 21.3% for taste/diet change. Whole unstimulated/resting saliva improved by 100%, and whole stimulated saliva improved by 23.8%. CONCLUSIONS: These findings suggest that the product has utility in symptom control in patients with xerostomia and may lead to an increase in saliva production.
Assuntos
Quitosana/análogos & derivados , Antissépticos Bucais , Xerostomia/prevenção & controle , Quitosana/farmacologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Resultado do TratamentoRESUMO
Titanium (Ti) has been functionalized with biomolecules for biomedical purposes. However, there is very limited information on the stability of such functionalities. Ti surface functionalized with carboxymethyl chitosan (CMCS) and bone morphogenetic protein 2 (BMP-2) has been reported to inhibit bacterial colonization while at the same time enhances osteoblast functions. In this work, three types of anchoring molecules, (3-aminopropyl) triethoxysilane (Silane), dopamine (DA), and polydopamine (PDA), were used for immobilizing the CMCS on Ti. The CMCS-modified surfaces were subjected to 70% ethanol treatment, autoclaving, and prolonged immersion in phosphate buffered saline (PBS). After the treatment procedures, the ability of the CMCS-modified substrates to inhibit colonization by Staphylococcus epidermidis (S. epidermidis) was assessed to evaluate the stability of the immobilized CMCS. The bacterial adhesion assays showed that the CMCS-DA- and CMCS-PDA-modified Ti remained stable after 70% ethanol treatment, autoclaving, and prolonged immersion in PBS, whereas the CMCS-Silane-modified Ti was less stable after autoclaving and prolonged immersion in PBS. The CMCS-DA- and CMCS-PDA-modified Ti substrates were functionalized with BMP-2 and used to support osteoblast growth. Evaluation of alkaline phosphatase (ALP) activity and calcium deposition from osteoblasts cultured on these substrates, which have been treated with 70% ethanol, or subjected to autoclaving, and prolonged immersion in PBS indicated that the immobilized BMP-2 on these surfaces retained its bioactivity.
Assuntos
Proteína Morfogenética Óssea 2/metabolismo , Quitosana/análogos & derivados , Dopamina/farmacologia , Proteínas Imobilizadas/metabolismo , Indóis/farmacologia , Polímeros/farmacologia , Silanos/farmacologia , Titânio/química , Fosfatase Alcalina/metabolismo , Antibacterianos/farmacologia , Aderência Bacteriana/efeitos dos fármacos , Divisão Celular , Quitosana/farmacologia , Estabilidade de Medicamentos , Osteoblastos/fisiologia , Propilaminas , Staphylococcus epidermidis/crescimento & desenvolvimentoRESUMO
Shiga toxin (Stx)-producing Escherichia coli (STEC) causes diarrhea and colitis in humans that can develop into a life-threatening hemolytic uremic syndrome (HUS). Developing efficient means of controlling STEC diseases, for which no drugs or vaccines are currently available, remains a high priority. We report here the construction and development of chitosan conjugates bearing the Stx ligand trisaccharide globotriose to demonstrate their potential as STEC disease treatment agents. The synthesis was accomplished by grafting a globotriose derivative containing an aldehyde-functionalized aglycone to chitosan amino groups. The obtained globotriose-chitosan conjugate bound with high affinity to Stx and efficiently neutralized its toxicity on Vero cells. Moreover, Stx levels in the gut of infected mice receiving oral doses of the conjugate were greatly diminished, enabling the mice to resist a fatal STEC challenge. The conjugate appears to function as a Stx adsorbent in the gut, preventing toxin entry into the bloodstream and consequent development of HUS. As such, the conjugate could act as a novel agent against STEC disease.
Assuntos
Antibacterianos/química , Quitosana/análogos & derivados , Quitosana/química , Escherichia coli O157/metabolismo , Toxinas Shiga/antagonistas & inibidores , Trissacarídeos/química , Animais , Antibacterianos/síntese química , Antibacterianos/farmacologia , Sequência de Carboidratos , Quitosana/farmacologia , Chlorocebus aethiops , Infecções por Escherichia coli/microbiologia , Infecções por Escherichia coli/prevenção & controle , Feminino , Síndrome Hemolítico-Urêmica/microbiologia , Síndrome Hemolítico-Urêmica/prevenção & controle , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Dados de Sequência Molecular , Toxinas Shiga/metabolismo , Trissacarídeos/farmacologia , Células VeroRESUMO
BACKGROUND: Rosacea is a chronic inflammatory skin disease affecting mostly facial skin. Its origin is multifactorial. Important steps in its treatment are avoidance of any triggering factor and control of skin inflammation. AIM: To assess the benefit of topical applications of a new product (P-3075). PATIENTS/METHODS: A randomized, multicenter, double-blind, placebo-controlled, parallel-group, pilot study was carried out to evaluate the efficacy and tolerability of a cream (P-3075) based on 5% potassium azeloyl diglycinate (PAD, Azeloglicina(®)) and 1% hydroxypropyl chitosan (HPCH). Forty-two patients (rosacea stages I and II) were enrolled and randomized, 28 in the P-3075 group and 14 in the placebo group. They were asked to apply the cream twice daily for 4 weeks. The main assessments were the objective quantification of erythema and skin hydration using the Mexameter(®) and Corneometer(®) devices, respectively. Clinical signs and symptoms were evaluated on a four-point scale. RESULTS: The P-3075 cream applied for 28 days was effective in skin protection by reducing erythema, evaluated both instrumentally and clinically. In addition, the clinical assessments of other symptoms such as flushing, stinging, and burning supported the beneficial effect of the P-3075 cream. CONCLUSIONS: The anti-inflammatory and moisturizing effects of potassium azeloyl diglycinate combined with the protective properties of HPCH allow the new product to be a good candidate for controlling signs and symptoms of rosacea.
Assuntos
Anti-Inflamatórios/uso terapêutico , Quitosana/análogos & derivados , Fármacos Dermatológicos/uso terapêutico , Glicina/análogos & derivados , Rosácea/tratamento farmacológico , Adulto , Anti-Inflamatórios/administração & dosagem , Distribuição de Qui-Quadrado , Quitosana/administração & dosagem , Quitosana/uso terapêutico , Fármacos Dermatológicos/administração & dosagem , Método Duplo-Cego , Eritema/patologia , Feminino , Glicina/administração & dosagem , Glicina/uso terapêutico , Humanos , Masculino , Pessoa de Meia-Idade , Rosácea/patologia , Rosácea/fisiopatologia , Pele/patologia , Pele/fisiopatologia , Adulto JovemRESUMO
One of the ultimate goals of wound healing research is to find effective healing techniques that utilize the regeneration of similar tissues. This involves the modification of various wound dressing biomaterials for proper wound management. The biopolymer chitosan (beta-1,4-D-glucosamine) has natural biocompatibility and biodegradability that render it suitable for wound management. By definition, a biocompatible biomaterial does not have toxic or injurious effects on biological systems. Chemical and physical modifications of chitosan influence its biocompatibility and biodegradability to an uncertain degree. Hence, the modified biomedical-grade of chitosan derivatives should be pre-examined in vitro in order to produce high-quality, biocompatible dressings. In vitro toxicity examinations are more favorable than those performed in vivo, as the results are more reproducible and predictive. In this paper, basic in vitro tools were used to evaluate cellular and molecular responses with regard to the biocompatibility of biomedical-grade chitosan. Three paramount experimental parameters of biocompatibility in vitro namely cytocompatibility, genotoxicity and skin pro-inflammatory cytokine expression, were generally reviewed for biomedical-grade chitosan as wound dressing.
Assuntos
Materiais Biocompatíveis/farmacologia , Quitosana/farmacologia , Cicatrização/efeitos dos fármacos , Animais , Materiais Biocompatíveis/química , Materiais Biocompatíveis/toxicidade , Quitosana/análogos & derivados , Quitosana/toxicidade , Citocinas/metabolismo , Dano ao DNA/efeitos dos fármacos , Humanos , Modelos Biológicos , Pele/citologia , Pele/efeitos dos fármacos , Pele/metabolismoRESUMO
Mercury (Hg) is one of the most toxic heavy metals commonly found in the global environment. Its toxicity is related to the capacity of its compounds to bioconcentrate in organisms and to biomagnify through food chain. A wide range of adsorbents has been used for removing Hg(II) from contaminated water. Chitosan is obtained by alkaline deacetylation of chitin. The adsorption capacity of chitosan depends on the origin of the polysaccharide, and on the experimental conditions in the preparation, that determine the degree of deacetylation. A great number of chitosan derivatives have been obtained by crosslinking with glutaraldehyde or epichlorohydrin among others or by grafting new functional groups on the chitosan backbone with the aim of adsorbing Hg(II). The new functional groups are incorporated to change the pH range for Hg(II) sorption and/or to change the sorption sites in order to increase sorption selectivity. The chemical modification affords a wide range of derivatives with modified properties for specific applications. Hg(II) adsorption on chitosan or chitosan derivatives is now assumed to occur through several single or mixed interactions: chelation or coordination on amino groups in a pendant fashion or in combination with vicinal hydroxyl groups, electrostatic attraction in acidic media or ion exchange with protonated amino groups. This review reports the recent developments in the Hg(II) removal in waste water treatment, using chitosan and its derivatives in order to provide useful information about the different technologies. When possibly the adsorption capacity of chitosan and chitosan derivatives under different experimental conditions is reported to help to compare the efficacy of the Hg(II) removal process. A comparison with the adsorption capacity of other low-cost adsorbents is also tabled.