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Chitosan-based nanoparticles as drug delivery systems: a review on two decades of research

机译:基于壳聚糖的纳米粒子作为药物递送系统:两十年的研究综述

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摘要

Chitosan (CS) is one of the most functional natural biopolymer widely used in the pharmaceutical field due to its biocompatibility and biodegradability. These privileges lead to its application in the synthesis of nanoparticles for the drug during the last two decades. This article gives rise to a general review of the different chitosan nanoparticles (CSNPs) preparation techniques: Ionic gelation, emulsion cross-linking, spray-drying, emulsion-droplet coalescence method, nanoprecipitation, reverse micellar method, desolvation method, modified ionic gelation with radial polymerisation and emulsion solvent diffusion, from the point of view of the methodological and mechanistic aspects involved. The physicochemical behaviour of CSNPs including drug loading, drug release, particles size, zeta potential and stability are briefly discussed. This review also directs to bring an outline of the major applications of CSNPs in drug delivery according to drug and route of administration. Finally, derivatives of CSNPs and CS nano-complexes are also discussed.
机译:壳聚糖(CS)是由于其生物相容性和生物降解性而广泛应用于药物领域中最常用的天然生物聚合体之一。这些特权导致其在过去二十年中合成药物的纳米颗粒的应用。本文引发了对不同壳聚糖纳米粒子(CSNP)制备技术的一般性综述:离子凝胶化,乳液交联,喷雾干燥,喷雾干燥,乳液 - 液滴聚结法,纳米沉淀,反向胶束方法,降解方法,改性离子凝胶化径向聚合和乳液溶剂扩散,从涉及的方法论和机械方面的角度来看。简要讨论了CSNP,包括药物负载,药物释放,颗粒尺寸,Zeta电位和稳定性的CSNP的物理化学行为。该审查还指示根据药物和行政途径推动CSNPS在药物交付中的主要应用概要。最后,还讨论了CSNP和CS纳米复合物的衍生物。

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