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用于递送紫杉醇-维生素E的pH敏感型和叶酸靶向型甲氧基聚乙二醇-聚(组氨酸-异丁烯酸酯)/叶酸-聚乙二醇-维生素E混合胶束及其抗肿瘤活性

pH-sensitive and folic acid-targeted MPEG-PHIS/FA-PEG-VE mixed micelles for the delivery of PTX-VE and their antitumor activity.

作者信息

Di Yan, Li Ting, Zhu Zhihong, Chen Fen, Jia Lianqun, Liu Wenbing, Gai Xiumei, Wang Yingying, Pan Weisan, Yang Xinggang

机构信息

Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University.

Key Laboratory of Ministry of Education for TCM Viscera-State Theory and Applications, Liaoning University of Traditional Chinese Medicine.

出版信息

Int J Nanomedicine. 2017 Aug 16;12:5863-5877. doi: 10.2147/IJN.S141982. eCollection 2017.

Abstract

The aim of this study was to simultaneously introduce pH sensitivity and folic acid (FA) targeting into a micelle system to achieve quick drug release and to enhance its accumulation in tumor cells. Paclitaxel-(+)-α-tocopherol (PTX-VE)-loaded mixed micelles (PHIS/FA/PM) fabricated by poly(ethylene glycol) methyl ether-poly(histidine) (MPEG-PHIS) and folic acid-poly(ethylene glycol)-(+)-α-tocopherol (FA-PEG-VE) were characterized by dynamic light scattering and transmission electron microscopy (TEM). The mixed micelles had a spherical morphology with an average diameter of 137.0±6.70 nm and a zeta potential of -48.7±4.25 mV. The drug encapsulation and loading efficiencies were 91.06%±2.45% and 5.28%±0.30%, respectively. The pH sensitivity was confirmed by changes in particle size, critical micelle concentration, and transmittance as a function of pH. MTT assay showed that PHIS/FA/PM had higher cytotoxicity at pH 6.0 than at pH 7.4, and lower cytotoxicity in the presence of free FA. Confocal laser scanning microscope images demonstrated a time-dependent and FA-inhibited cellular uptake. In vivo imaging confirmed that the mixed micelles targeted accumulation at tumor sites and the tumor inhibition rate was 85.97%. The results proved that the mixed micelle system fabricated by MPEG-PHIS and FA-PEG-VE is a promising approach to improve antitumor efficacy.

摘要

本研究的目的是同时将pH敏感性和叶酸(FA)靶向引入胶束系统,以实现药物快速释放并增强其在肿瘤细胞中的蓄积。通过聚(乙二醇)甲醚-聚(组氨酸)(MPEG-PHIS)和叶酸-聚(乙二醇)-(+)-α-生育酚(FA-PEG-VE)制备的载有紫杉醇-(+)-α-生育酚(PTX-VE)的混合胶束(PHIS/FA/PM),通过动态光散射和透射电子显微镜(TEM)进行表征。混合胶束呈球形,平均直径为137.0±6.70 nm,zeta电位为-48.7±4.25 mV。药物包封率和载药率分别为91.06%±2.45%和5.28%±0.30%。通过粒径、临界胶束浓度和透光率随pH的变化来证实pH敏感性。MTT试验表明,PHIS/FA/PM在pH 6.0时比在pH 7.4时具有更高的细胞毒性,在游离FA存在下细胞毒性较低。共聚焦激光扫描显微镜图像显示了时间依赖性和FA抑制的细胞摄取。体内成像证实混合胶束在肿瘤部位靶向蓄积,肿瘤抑制率为85.97%。结果证明,由MPEG-PHIS和FA-PEG-VE制备的混合胶束系统是提高抗肿瘤疗效的一种有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b91/5566413/76daad15e08f/ijn-12-5863Fig1.jpg

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