首页> 外文期刊>Biotechnology Journal: Healthcare,Nutrition,Technology >Facile preparation of well-defined near-monodisperse chitosan/sodium alginate polyelectrolyte complex nanoparticles (CS/SAL NPs) via ionotropic gelification: A suitable technique for drug delivery systems
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Facile preparation of well-defined near-monodisperse chitosan/sodium alginate polyelectrolyte complex nanoparticles (CS/SAL NPs) via ionotropic gelification: A suitable technique for drug delivery systems

机译:通过离子化凝胶轻松制备明确定义的近单分散的壳聚糖/海藻酸钠聚电解质复合物纳米颗粒(CS / SAL NPs):药物输送系统的合适技术

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摘要

Polymeric nanoparticles have emerged as a promising approach for drug delivery systems. We prepared chitosan (CS)/sodium alginate (SAL) polyelectrolyte complex nanoparticles (CS/SAL NPs) via a simple and mild ionic gelation method by adding a CS solution to a SAL solution, and investigated the effects of molecular weight of the added CS, and the SAL:CS mass ratio on the formation of the polyelectrolyte complex nanoparticles. The well-defined CS/SAL NPs with near-monodisperse particle size of about 160 nm exhibited a pH stable structure, and pH responsive properties with a negatively or positively charged surface. The so-called "electrostatic sponge" structure of the polyelectrolyte complex nanoparticles enhanced their drug-loading capacity towards the differently charged model drug molecules, and favored controlled release. We also found that the drug-loading capacity was influenced by the nature of the drugs and the drug-loading media, while drug release was affected by the solubility of the drugs in the drug-releasing media. The biocompatibility and biodegradability of the polyelectrolytes in the polyelectrolyte complex nanoparticles were maintained by ionic interactions. These results indicate that CS/SAL NPs can represent a useful technique for pH-responsive drug delivery systems.
机译:聚合物纳米颗粒已经成为药物递送系统的一种有前途的方法。我们通过在SAL溶液中添加CS溶液,通过简单温和的离子凝胶法制备了壳聚糖(CS)/藻酸钠(SAL)聚电解质复合纳米颗粒(CS / SAL NPs),并研究了添加的CS的分子量的影响,以及SAL:CS质量比对聚电解质复合物纳米颗粒形成的影响。定义明确的CS / SAL NP具有接近160nm的近单分散粒径,具有pH稳定的结构,并且具有带负电或正电的表面的pH响应特性。聚电解质复合物纳米颗粒的所谓“静电海绵”结构增强了它们对不同电荷的模型药物分子的载药能力,并有利于控制释放。我们还发现载药量受药物和载药介质的性质影响,而药物释放则受药物在释药介质中的溶解度影响。聚电解质络合物纳米颗粒中的聚电解质的生物相容性和生物降解性通过离子相互作用来维持。这些结果表明CS / SAL NPs可以代表pH响应药物传递系统的有用技术。

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