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叶酸靶向聚合物“绿色”纳米疗法治疗癌症。

Folate targeted polymeric 'green' nanotherapy for cancer.

机构信息

Amrita Center for Nanosciences and Molecular Medicine, Amrita Vishwa Vidyapeetham, Kochi-682 041, Kerala, India.

出版信息

Nanotechnology. 2010 Jul 16;21(28):285107. doi: 10.1088/0957-4484/21/28/285107. Epub 2010 Jun 28.

DOI:10.1088/0957-4484/21/28/285107
PMID:20585151
Abstract

The concept of 'green' chemotherapy by employing targeted nanoparticle mediated delivery to enhance the efficacy of phytomedicines is reported. Poly (lactide-co-glycolide) (PLGA) nanoparticles encapsulating a well known nutraceutical namely, grape seed extract (GSE)-'NanoGSE'-was prepared by a nanoprecipitation technique. The drug-loaded nanoparticles of size approximately 100 nm exhibited high colloidal stability at physiological pH. Molecular receptor targeting of this nanophytomedicine against folate receptor over-expressing cancers was demonstrated in vitro by conjugation with a potential cancer targeting ligand, folic acid (FA). Fluorescence microscopy and flow cytometry data showed highly specific cellular uptake of FA conjugated NanoGSE on folate receptor positive cancer cells. Studies were also conducted to investigate the efficiency of targeted (FA conjugated) versus non-targeted (non-FA conjugated) nanoformulations in causing cancer cell death. The IC(50) values were lowered by a factor of approximately 3 for FA-NanoGSE compared to the free drug, indicating substantially enhanced bioavailability to the tumor cells, sparing the normal ones. Receptor targeting of FA-NanoGSE resulted in a significant increase in apoptotic index, which was also quantified by flow cytometry and fluorescence microscopy. This in vitro study provides a basis for the use of nanoparticle mediated delivery of anticancer nutraceuticals to enhance bioavailability and effectively target cancer by a 'green' approach.

摘要

采用靶向纳米颗粒介导的递送来增强植物药疗效的“绿色”化疗概念得到了报道。通过纳米沉淀技术制备了聚(乳酸-共-乙醇酸)(PLGA)纳米颗粒,包封了一种众所周知的营养保健品,即葡萄籽提取物(GSE)-“NanoGSE”-。载药纳米颗粒的尺寸约为 100nm,在生理 pH 值下表现出高胶体稳定性。通过与潜在的癌症靶向配体叶酸(FA)缀合,证明了这种纳米植物药对叶酸受体过表达癌症的分子受体靶向性。荧光显微镜和流式细胞术数据表明,叶酸受体阳性癌细胞对 FA 缀合的 NanoGSE 的摄取具有高度特异性。还进行了研究,以调查靶向(FA 缀合)与非靶向(非 FA 缀合)纳米制剂在导致癌细胞死亡方面的效率。与游离药物相比,FA-NanoGSE 的 IC 50 值降低了约 3 倍,表明肿瘤细胞的生物利用度大大提高,而正常细胞则得以幸免。FA-NanoGSE 的受体靶向导致凋亡指数显著增加,这也通过流式细胞术和荧光显微镜进行了定量。这项体外研究为通过“绿色”方法利用纳米颗粒介导的抗癌营养保健品递送来提高生物利用度并有效靶向癌症提供了依据。

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