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聚乙二醇琥珀酸-α-生育酚酯包载的聚乳酸-羟基乙酸共聚物纳米粒逆转肿瘤多药耐药的体外研究。

Alpha-tocopheryl polyethylene glycol succinate-emulsified poly(lactic-co-glycolic acid) nanoparticles for reversal of multidrug resistance in vitro.

机构信息

Jiangsu Key Laboratory for Supramolecular Medicinal Materials and Applications, College of Life Sciences, Nanjing Normal University, Nanjing 210046, People's Republic of China.

出版信息

Nanotechnology. 2012 Dec 14;23(49):495103. doi: 10.1088/0957-4484/23/49/495103. Epub 2012 Nov 13.

Abstract

Multidrug resistance (MDR) is one of the factors in the failure of anticancer chemotherapy. In order to enhance the anticancer effect of P-glycoprotein (P-gp) substrates, inhibition of the P-gp efflux pump on MDR cells is a good tactic. We designed novel multifunctional drug-loaded alpha-tocopheryl polyethylene glycol succinate (TPGS)/poly(lactic-co-glycolic acid) (PLGA) nanoparticles (TPGS/PLGA/SN-38 NPs; SN-38 is 7-ethyl-10-hydroxy-camptothecin), with TPGS-emulsified PLGA NPs as the carrier and modulator of the P-gp efflux pump and SN-38 as the model drug. TPGS/PLGA/SN-38 NPs were prepared using a modified solvent extraction/evaporation method. Physicochemical characterizations of TPGS/PLGA/SN-38 NPs were in conformity with the principle of nano-drug delivery systems (nDDSs), including a diameter of about 200 nm, excellent spherical particles with a smooth surface, narrow size distribution, appropriate surface charge, and successful drug-loading into the NPs. The cytotoxicity of TPGS/PLGA/SN-38 NPs to MDR cells was increased by 3.56 times compared with that of free SN-38. Based on an intracellular accumulation study relative to the time-dependent uptake and efflux inhibition, we suggest novel mechanisms of MDR reversal of TPGS/PLGA NPs. Firstly, TPGS/PLGA/SN-38 NPs improved the uptake of the loaded drug by clathrin-mediated endocytosis in the form of unbroken NPs. Simultaneously, intracellular NPs escaped the recognition of P-gp by MDR cells. After SN-38 was released from TPGS/PLGA/SN-38 NPs in MDR cells, TPGS or/and PLGA may modulate the efflux microenvironment of the P-gp pump, such as mitochondria and the P-gp domain with an ATP-binding site. Finally, the controlled-release drug entered the nucleus of the MDR cell to induce cytotoxicity. The present study showed that TPGS-emulsified PLGA NPs could be functional carriers in nDDS for anticancer drugs that are also P-gp substrates. More importantly, to enhance the therapeutic effect of P-gp substrates, this work might provide a new insight into the design of pharmacologically inactive excipients that can serve as P-gp modulators instead of drugs that are P-gp inhibitors.

摘要

多药耐药(MDR)是癌症化疗失败的因素之一。为了增强 P-糖蛋白(P-gp)底物的抗癌作用,抑制 MDR 细胞的 P-gp 外排泵是一种很好的策略。我们设计了新型多功能载药 α-生育酚聚乙二醇琥珀酸酯(TPGS)/聚乳酸-羟基乙酸共聚物(PLGA)纳米粒(TPGS/PLGA/SN-38 NPs;SN-38 是 7-乙基-10-羟基喜树碱),以 TPGS 乳化的 PLGA NPs 为载体和 P-gp 外排泵调节剂,以 SN-38 为模型药物。TPGS/PLGA/SN-38 NPs 采用改良的溶剂萃取/蒸发法制备。TPGS/PLGA/SN-38 NPs 的理化性质符合纳米药物传递系统(nDDS)的原理,包括直径约 200nm,表面光滑的优良球形颗粒,粒径分布窄,表面电荷适宜,成功将药物载入 NPs。与游离 SN-38 相比,TPGS/PLGA/SN-38 NPs 对 MDR 细胞的细胞毒性增加了 3.56 倍。基于与时间依赖性摄取和外排抑制相关的细胞内积累研究,我们提出了 TPGS/PLGA NPs 逆转 MDR 的新机制。首先,TPGS/PLGA/SN-38 NPs 以完整 NPs 的形式通过网格蛋白介导的内吞作用提高了载药的摄取。同时,细胞内 NPs 逃避了 MDR 细胞对 P-gp 的识别。SN-38 从 TPGS/PLGA/SN-38 NPs 中释放到 MDR 细胞后,TPGS 或/和 PLGA 可能会调节 P-gp 泵的外排微环境,如线粒体和具有 ATP 结合位点的 P-gp 结构域。最后,控释药物进入 MDR 细胞的核内诱导细胞毒性。本研究表明,TPGS 乳化的 PLGA NPs 可以作为抗癌药物的功能性载体,这些药物也是 P-gp 底物。更重要的是,为了提高 P-gp 底物的治疗效果,这项工作可能为设计可作为 P-gp 调节剂而非 P-gp 抑制剂的药理惰性赋形剂提供新的思路。

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