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      Evaluation of Hemagglutination Activity of Chitosan Nanoparticles Using Human Erythrocytes

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          Abstract

          Chitosan is a polysaccharide composed of randomly distributed chains of β-(1-4) D-glucosamine and N-acetyl-D-glucosamine. This compound is obtained by partial or total deacetylation of chitin in acidic solution. The chitosan-based hemostatic agents have been gaining much attention in the management of bleeding. The aim of this study was to evaluate in vitro hemagglutination activity of chitosan nanoparticles using human erythrocytes. The preparation of nanoparticles was achieved by ionotropic gelification technique followed by neutralization with NaOH 1 mol/L −1. The hemagglutination activity was performed on a solution of 2% erythrocytes (pH 7.4 on PBS) collected from five healthy volunteers. The hemolysis determination was made by spectrophotometric analysis. Chitosan nanoparticle solutions without NaOH addition changed the reddish colour of the wells into brown, suggesting an oxidative reaction of hemoglobin and possible cell lysis. All neutralized solutions of chitosan nanoparticles presented positive haemagglutination, without any change in reaction color. Chitosan nanoparticles presented hemolytic activity ranging from 186.20 to 223.12%, while neutralized solutions ranged from 2.56 to 72.54%, comparing to distilled water. Results highlight the need for development of new routes of synthesis of chitosan nanoparticles within human physiologic pH.

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          Most cited references35

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          Biodegradation, biodistribution and toxicity of chitosan.

          Chitosan is a natural polysaccharide that has attracted significant scientific interest during the last two decades. It is a potentially biologically compatible material that is chemically versatile (-NH2 groups and various M(w)). These two basic properties have been used by drug delivery and tissue engineering scientists to create a plethora of formulations and scaffolds that show promise in healthcare. Despite the high number of published studies, chitosan is not approved by the FDA for any product in drug delivery, and as a consequence very few biotech companies are using this material. This review will aim to provide information on these biological properties that affect chitosan's safe use in drug delivery. The term "Chitosan" represents a large group of structurally different chemical entities that may show different biodistribution, biodegradation and toxicological profiles. Here we aim to review research in this area and critically discuss chitosan's potential to be used as a generally regarded as safe (GRAS) material. 2009 Elsevier B.V. All rights reserved.
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            Formation mechanism of monodisperse, low molecular weight chitosan nanoparticles by ionic gelation technique.

            Chitosan nanoparticles have been extensively studied for drug and gene delivery. In this paper, monodisperse, low molecular weight (LMW) chitosan nanoparticles were prepared by a novel method based on ionic gelation using sodium tripolyphosphate (TPP) as cross-linking agent. The objective of this study was to solve the problem of preparation of chitosan/TPP nanoparticles with high degree of monodispersity and stability, and investigate the effect of various parameters on the formation of LMW chitosan/TPP nanoparticles. It was found that the particle size distribution of the nanoparticles could be significantly narrowed by a combination of decreasing the concentration of acetic acid and reducing the ambient temperature during cross-linking process. The optimized nanoparticles exhibited a mean hydrodynamic diameter of 138 nm with a polydispersity index (PDI) of 0.026 and a zeta potential of +35 mV, the nanoparticles had good storage stability at room temperature up to at least 20 days.
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              Development of a chitosan-based wound dressing with improved hemostatic and antimicrobial properties.

              Hemorrhage remains a leading cause of early death after trauma, and infectious complications in combat wounds continue to challenge caregivers. Although chitosan dressings have been developed to address these problems, they are not always effective in controlling bleeding or killing bacteria. We aimed to refine the chitosan dressing by incorporating a procoagulant (polyphosphate) and an antimicrobial (silver). Chitosan containing different amounts and types of polyphosphate polymers was fabricated, and their hemostatic efficacies evaluated in vitro. The optimal chitosan-polyphosphate formulation (ChiPP) accelerated blood clotting (p = 0.011), increased platelet adhesion (p=0.002), generated thrombin faster (p = 0.002), and absorbed more blood than chitosan (p 99.99% kill of Staphylococcus aureus consistently. The silver dressing also significantly reduced mortality from 90% to 14.3% in a P. aeruginosa wound infection model in mice. Although the dressing exerted severe cytotoxicity against cultured fibroblasts, wound healing was not inhibited. This study demonstrated for the first time, the application of polyphosphate as a hemostatic adjuvant, and developed a new chitosan-based composite with potent hemostatic and antimicrobial properties.
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                Author and article information

                Journal
                Biomed Res Int
                Biomed Res Int
                BMRI
                BioMed Research International
                Hindawi Publishing Corporation
                2314-6133
                2314-6141
                2015
                11 February 2015
                : 2015
                : 247965
                Affiliations
                17 Grupo de Estudos e Pesquisas em Imunologia Humana (GEPIH), Escola Tecnica de Saúde da UFPB, Universidade Federal da Paraíba, 58051-900 João Pessoa, PB, Brazil
                2Departamento de Fisiologia e Patologia, Centro de Ciencias da Saúde, Universidade Federal da Paraíba, 58051-900 João Pessoa, PB, Brazil
                3Centro de Pesquisas Aggeu Magalhães (CPqAM/FIOCRUZ) e Laboratório de Imunopatologia Keio Asami (LIKA), Universidade Federal de Pernambuco, 50670-901 Recife, PE, Brazil
                4Departamento de Engenharia de Materiais, Centro de Tecnologia, Universidade Federal da Paraíba, 58051-900 João Pessoa, PB, Brazil
                5Núcleo de Biomateriais, NEPBIO, Centro de Ciências da Saúde, Universidade Federal da Paraíba, 58051-900 João Pessoa, PB, Brazil
                6Departamento de Engenharia, Universidade Federal de Lavras, 37200-000 Lavras, MG, Brazil
                7Departamento de Odontologia Clínica e Social, Centro de Ciencias da Saúde, Universidade Federal da Paraíba, 58051-900 João Pessoa, PB, Brazil
                Author notes
                *Lúcio Roberto Castellano: luciocastellano@ 123456gmail.com

                Academic Editor: Jianshu Li

                Article
                10.1155/2015/247965
                4339715
                25759815
                401c113d-1d7d-4f37-ba92-f5ebe2bcd16c
                Copyright © 2015 Jefferson Muniz de Lima et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 October 2014
                : 20 January 2015
                : 21 January 2015
                Categories
                Research Article

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