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生物界面的壳聚糖纳米颗粒:对药物递送的影响。

Chitosan Nanoparticles at the Biological Interface: Implications for Drug Delivery.

作者信息

Aibani Noorjahan, Rai Raj, Patel Parth, Cuddihy Grace, Wasan Ellen K

机构信息

College of Pharmacy and Nutrition, University of Saskatchewan, 107 Wiggins Rd, Saskatoon, SK S7N 5E5, Canada.

出版信息

Pharmaceutics. 2021 Oct 14;13(10):1686. doi: 10.3390/pharmaceutics13101686.

Abstract

The unique properties of chitosan make it a useful choice for various nanoparticulate drug delivery applications. Although chitosan is biocompatible and enables cellular uptake, its interactions at cellular and systemic levels need to be studied in more depth. This review focuses on the various physical and chemical properties of chitosan that affect its performance in biological systems. We aim to analyze recent research studying interactions of chitosan nanoparticles (NPs) upon their cellular uptake and their journey through the various compartments of the cell. The positive charge of chitosan enables it to efficiently attach to cells, increasing the probability of cellular uptake. Chitosan NPs are taken up by cells via different pathways and escape endosomal degradation due to the proton sponge effect. Furthermore, we have reviewed the interaction of chitosan NPs upon in vivo administration. Chitosan NPs are immediately surrounded by a serum protein corona in systemic circulation upon intravenous administration, and their biodistribution is mainly to the liver and spleen indicating RES uptake. However, the evasion of RES system as well as the targeting ability and bioavailability of chitosan NPs can be improved by utilizing specific routes of administration and covalent modifications of surface properties. Ongoing clinical trials of chitosan formulations for therapeutic applications are paving the way for the introduction of chitosan into the pharmaceutical market and for their toxicological evaluation. Chitosan provides specific biophysical properties for effective and tunable cellular uptake and systemic delivery for a wide range of applications.

摘要

壳聚糖的独特性质使其成为各种纳米颗粒药物递送应用的理想选择。尽管壳聚糖具有生物相容性并能实现细胞摄取,但其在细胞和全身水平的相互作用仍需更深入地研究。本综述聚焦于影响壳聚糖在生物系统中性能的各种物理和化学性质。我们旨在分析近期有关壳聚糖纳米颗粒(NPs)细胞摄取及其在细胞内各组分间转运过程中相互作用的研究。壳聚糖的正电荷使其能够有效地附着于细胞,增加细胞摄取的概率。壳聚糖纳米颗粒通过不同途径被细胞摄取,并由于质子海绵效应而逃避内体降解。此外,我们还综述了壳聚糖纳米颗粒在体内给药后的相互作用。静脉给药后,壳聚糖纳米颗粒在体循环中立即被血清蛋白冠包围,其生物分布主要在肝脏和脾脏,表明被网状内皮系统摄取。然而,通过利用特定给药途径和对表面性质进行共价修饰,可以提高壳聚糖纳米颗粒对网状内皮系统的逃避能力以及靶向能力和生物利用度。壳聚糖制剂用于治疗应用的正在进行的临床试验为壳聚糖进入医药市场及其毒理学评估铺平了道路。壳聚糖具有特定的生物物理性质,可实现有效且可调节的细胞摄取和全身递送,适用于广泛的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc6/8540112/4aa1fffe0c3a/pharmaceutics-13-01686-g001.jpg

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