Jiangsu Key Laboratory for Supramolecular Medicinal Materials and Applications, College of Life Sciences, Nanjing Normal University, Nanjing 210046, People's Republic of China.
Nanotechnology. 2012 Dec 14;23(49):495103. doi: 10.1088/0957-4484/23/49/495103. Epub 2012 Nov 13.
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.
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。