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壳聚糖修饰的聚(D,L-丙交酯-共-乙交酯)纳米球用于提高 siRNA 的递送和基因沉默效果。

Chitosan-modified poly(D,L-lactide-co-glycolide) nanospheres for improving siRNA delivery and gene-silencing effects.

机构信息

Laboratory of Pharmaceutical Engineering, Aichi Gakuin University, Nagoya, Japan.

出版信息

Eur J Pharm Biopharm. 2010 Mar;74(3):421-6. doi: 10.1016/j.ejpb.2009.12.007. Epub 2009 Dec 23.

Abstract

Chitosan (CS) surface-modified poly(D,L-lactide-co-glycolide) (PLGA) nanospheres (NS) for a siRNA delivery system were evaluated in vitro. siRNA-loaded PLGA NS were prepared by an emulsion solvent diffusion (ESD) method, and the physicochemical properties of NS were investigated. The level of targeted protein expression and siRNA uptake were examined in A549 cells. CS-modified PLGA NS exhibited much higher encapsulation efficiency than unmodified PLGA NS (plain-PLGA NS). CS-modified PLGA NS showed a positive zeta potential, while plain-PLGA NS were negatively charged. siRNA uptake studies by observation with confocal laser scanning microscopy (CLSM) indicated that siRNA-loaded CS-modified PLGA NS were more effectively taken up by the cells than plain-PLGA NS. The efficiencies of different siRNA preparations were compared at the level of targeted protein expression. The gene-silencing efficiency of CS-modified PLGA NS was higher and more prolonged than those of plain-PLGA NS and naked siRNA. This result correlated with the CLSM studies, which may have been due to higher cellular uptake of CS-modified PLGA NS due to electrostatic interactions. It was concluded that CS-modified PLGA NS containing siRNA could provide an effective siRNA delivery system.

摘要

壳聚糖(CS)修饰的聚(D,L-乳酸-共-乙醇酸)(PLGA)纳米球(NS)用于 siRNA 递药系统的体外评价。通过乳化溶剂扩散(ESD)法制备负载 siRNA 的 PLGA NS,并对 NS 的理化性质进行了研究。在 A549 细胞中检测了靶向蛋白表达和 siRNA 摄取水平。与未修饰的 PLGA NS(普通-PLGA NS)相比,CS 修饰的 PLGA NS 表现出更高的包封效率。CS 修饰的 PLGA NS 具有正 ζ 电位,而普通-PLGA NS 带负电荷。通过共聚焦激光扫描显微镜(CLSM)观察到的 siRNA 摄取研究表明,负载 siRNA 的 CS 修饰的 PLGA NS 比普通-PLGA NS 更有效地被细胞摄取。通过靶向蛋白表达水平比较了不同 siRNA 制剂的效率。CS 修饰的 PLGA NS 的基因沉默效率高于普通-PLGA NS 和裸 siRNA,且持续时间更长。这一结果与 CLSM 研究相关,这可能是由于 CS 修饰的 PLGA NS 通过静电相互作用导致更高的细胞摄取。综上所述,负载 siRNA 的 CS 修饰的 PLGA NS 可作为一种有效的 siRNA 递药系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f6/7127408/a697d66332d6/gr1.jpg

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