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      Does the Use of Chitosan Contribute to Oxalate Kidney Stone Formation?

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          Abstract

          Chitosan is widely used in the biomedical field due its chemical and pharmacological properties. However, intake of chitosan results in renal tissue accumulation of chitosan and promotes an increase in calcium excretion. On the other hand, the effect of chitosan on the formation of calcium oxalate crystals (CaOx) has not been described. In this work, we evaluated the antioxidant capacity of chitosan and its interference in the formation of CaOx crystals in vitro. Here, the chitosan obtained commercially had its identity confirmed by nuclear magnetic resonance and infrared spectroscopy. In several tests, this chitosan showed low or no antioxidant activity. However, it also showed excellent copper-chelating activity. In vitro, chitosan acted as an inducer mainly of monohydrate CaOx crystal formation, which is more prevalent in patients with urolithiasis. We also observed that chitosan modifies the morphology and size of these crystals, as well as changes the surface charge of the crystals, making them even more positive, which can facilitate the interaction of these crystals with renal cells. Chitosan greatly influences the formation of crystals in vitro, and in vivo analyses should be conducted to assess the risk of using chitosan.

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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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            Aggregation-based crystal growth and microstructure development in natural iron oxyhydroxide biomineralization products.

            Crystals are generally considered to grow by attachment of ions to inorganic surfaces or organic templates. High-resolution transmission electron microscopy of biomineralization products of iron-oxidizing bacteria revealed an alternative coarsening mechanism in which adjacent 2- to 3-nanometer particles aggregate and rotate so their structures adopt parallel orientations in three dimensions. Crystal growth is accomplished by eliminating water molecules at interfaces and forming iron-oxygen bonds. Self-assembly occurs at multiple sites, leading to a coarser, polycrystalline material. Point defects (from surface-adsorbed impurities), dislocations, and slabs of structurally distinct material are created as a consequence of this growth mechanism and can dramatically impact subsequent reactivity.
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              Biological activities of chitosan and chitooligosaccharides

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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Mar Drugs
                Mar Drugs
                marinedrugs
                Marine Drugs
                MDPI
                1660-3397
                29 December 2014
                January 2015
                : 13
                : 1
                : 141-158
                Affiliations
                [1 ]Department of Biochemistry, Biosciences Centre, Federal University of Rio Grande do Norte, Salgado Filho avenue 3000, Natal, RN 59078-970, Brazil; E-Mails: moacirfqn@ 123456gmail.com (M.F.Q.); melo.krt@ 123456gmail.com (K.R.T.M.)
                [2 ]Department of Biochemistry, Biological Sciences Centre, Federal University of Parana, Coronel Francisco H. dos Santos avenue S/N, Curitiba, PR CP 19031, Brazil; E-Mails: popoh_diego@ 123456hotmail.com (D.A.S.); sassaki@ 123456ufpr.br (G.L.S.)
                [3 ]Department of Biochemistry, Molecular Biology, Federal University of São Paulo, Três de Maio street 100, São Paulo, SP 04044-020, Brazil
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: hugo@ 123456cb.ufrn.br ; Tel.: +55-84-3213416.
                Article
                marinedrugs-13-00141
                10.3390/md13010141
                4306929
                25551781
                f7684ffa-cd7d-477a-83ec-693651093503
                © 2014 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 19 June 2014
                : 30 October 2014
                Categories
                Article

                Pharmacology & Pharmaceutical medicine
                urolithiasis,antioxidant activity,calcium oxalate monohydrate crystals,copper chelation

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