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淀粉改性海藻酸钠纳米粒用于药物传递应用。

Starch modified alginate nanoparticles for drug delivery application.

机构信息

Research and Post Graduate Department of Chemistry, Bishop Moore College, Maveleikara, Kerala, India.

Research and Post Graduate Department of Chemistry, Bishop Moore College, Maveleikara, Kerala, India.

出版信息

Int J Biol Macromol. 2021 Mar 15;173:277-284. doi: 10.1016/j.ijbiomac.2020.12.227. Epub 2021 Jan 13.

Abstract

Natural polymers have been widely studied as vehicles that have gained much interest in the encapsulation and delivery of drugs and bioactive molecules. In this study, we developed starch-modified alginate nanoparticles using a green facile technique for drug delivery application. The potential of the prepared nanoparticles for controlled drug delivery applications is demonstrated using theophylline and bovine serum albumin as model drugs. The nanoparticles possessed the encapsulation efficiency of 60 to 75%. The results of in vitro drug release studies showed the pH dependent characteristics of the prepared nanoparticles. In vitro cytotoxicity test revealed the biocompatibility of the developed nanoparticles against L929 fibroblast cell lines. The in vitro cellular uptake of nanoparticles was visualized in L929 fibroblast cells using fluorescent microscopy. The preliminary investigation suggests the developed nanoparticle is a promising candidate for drug delivery application.

摘要

天然聚合物作为载体已被广泛研究,因其在药物和生物活性分子的包封和传递方面具有很大的应用兴趣。在本研究中,我们使用绿色简便的技术开发了淀粉改性的海藻酸钠纳米颗粒,用于药物传递应用。使用茶碱和牛血清白蛋白作为模型药物,证明了制备的纳米颗粒在控制药物释放应用中的潜力。纳米颗粒具有 60%至 75%的包封效率。体外药物释放研究结果表明,所制备的纳米颗粒具有 pH 依赖性特征。体外细胞毒性试验表明,所开发的纳米颗粒对 L929 成纤维细胞系具有生物相容性。使用荧光显微镜在 L929 成纤维细胞中可视化观察了纳米颗粒的细胞内摄取。初步研究表明,所开发的纳米颗粒是一种有前途的药物传递应用候选物。

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