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壳聚糖盐酸盐修饰的染料木黄酮负载纳米脂质载体对人晶状体上皮细胞的细胞摄取增强及抗增殖作用

Enhanced cellular uptake and anti-proliferating effect of chitosan hydrochlorides modified genistein loaded NLC on human lens epithelial cells.

作者信息

Zhang Wenji, Liu Jinlu, Zhang Qi, Li Xuedong, Yu Shihui, Yang Xinggang, Kong Jun, Pan Weisan

机构信息

School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.

Department of ophthalmology, Affiliated Fourth Hospital of China Medical University, Shenyang 110005, China.

出版信息

Int J Pharm. 2014 Aug 25;471(1-2):118-26. doi: 10.1016/j.ijpharm.2014.05.030. Epub 2014 May 22.


DOI:10.1016/j.ijpharm.2014.05.030
PMID:24858387
Abstract

This study was attempted to increase the cellular uptake of developed genistein loaded nanostructured lipid carriers (NLC) into human lens epithelial (HLE) cells by chitosan hydrochlorides coatings when applied in post lens capsule (PCO) treatment, and to provide further understanding of the uptake and anti-proliferation mechanisms inside. NLCs were produced using melt-emulsification method and were subsequently coated with chitosan hydrochlorides by adsorption. The uptake of various particle sizes were evaluated and visualized by confocal laser scanning microscopy (CLSM), showing a size-dependent manner. The uptake of NLC was proved to be endocytosed in an energy dependent and clathrin-mediated endocytosis to HLE cells by the decrease in uptake at lower temperature, when pre-saturated by blank NLC and in the presence of NaN3 and sucrose. CH coating improved the uptake percentage of NLC irrespective of the particle size, without influencing the uptake mechanism. Cell apoptosis was tested using PI and Annexin V-FITC/PI staining, followed by flow cytometer analysis. Higher anti-proliferation effect was observed for CH-NLC in inhibiting the growth of HLE cells by causing more apoptosis. Results above indicate that GEN-NLC surface modified by chitosan hydrochlorides could enhance the trans-cellular performance and anti-proliferating effect as PCO therapy.

摘要

本研究旨在通过壳聚糖盐酸盐包被,提高所制备的负载染料木黄酮的纳米结构脂质载体(NLC)在晶状体后囊膜(PCO)治疗中对人晶状体上皮(HLE)细胞的细胞摄取,并进一步了解其摄取和抗增殖机制。采用熔融乳化法制备NLC,随后通过吸附法用壳聚糖盐酸盐进行包被。通过共聚焦激光扫描显微镜(CLSM)评估和观察不同粒径的摄取情况,呈现出粒径依赖性。通过低温下摄取量的降低、用空白NLC预饱和以及在NaN3和蔗糖存在的情况下,证明NLC的摄取是通过能量依赖性和网格蛋白介导的内吞作用进入HLE细胞的。壳聚糖包被提高了NLC的摄取百分比,而与粒径无关,且不影响摄取机制。使用PI和膜联蛋白V-FITC/PI染色检测细胞凋亡,随后进行流式细胞仪分析。观察到壳聚糖- NLC在通过诱导更多凋亡来抑制HLE细胞生长方面具有更高的抗增殖作用。上述结果表明,壳聚糖盐酸盐修饰的染料木黄酮- NLC作为PCO治疗可增强跨细胞性能和抗增殖效果。

相似文献

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Enhanced cellular uptake and anti-proliferating effect of chitosan hydrochlorides modified genistein loaded NLC on human lens epithelial cells.

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[8]
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