Song Xia, Wen Yuting, Zhu Jing-Ling, Zhao Feng, Zhang Zhong-Xing, Li Jun
Department of Biomedical Engineering, Faculty of Engineering, Faculty of Engineering, National University of Singapore , 7 Engineering Drive 1, Singapore 117574, Singapore.
Institute of Materials Research and Engineering, A*STAR (Agency for Science, Technology and Research) , 2 Fusionopolis Way, Singapore 138634, Singapore.
Biomacromolecules. 2016 Dec 12;17(12):3957-3963. doi: 10.1021/acs.biomac.6b01344. Epub 2016 Nov 7.
Paclitaxel (PTX), a hydrophobic anticancer drug, is facing several clinical limitations such as low bioavailability and drug resistance. To solve the problems, a well-defined β-cyclodextrin-poly(N-isopropylacrylamide) star polymer was synthesized and used as a nanocarrier to improve the water solubility and aim to thermoresponsive delivery of PTX to cancer cells. The star polymer was able to form supramolecular self-assembled inclusion complex with PTX via host-guest interaction at room temperature, which is below the low critical solution temperature (LCST) of the star polymer, significantly improving the solubilization of PTX. At body temperature (above LCST), the phase transition of poly(N-isopropylacrylamide) segments induced the formation of nanoparticles, which greatly enhanced the cellular uptake of the polymer-drug complex, resulting in efficient thermoresponsive delivery of PTX. In particular, the polymer-drug complex exhibited better antitumor effects than the commercial formulation of PTX in overcoming the multi-drug resistance in AT3B-1 cells.
紫杉醇(PTX)是一种疏水性抗癌药物,面临着生物利用度低和耐药性等多种临床局限性。为了解决这些问题,合成了一种结构明确的β-环糊精-聚(N-异丙基丙烯酰胺)星形聚合物,并将其用作纳米载体以提高水溶性,并旨在将PTX热响应递送至癌细胞。该星形聚合物能够在室温下通过主客体相互作用与PTX形成超分子自组装包合物,该温度低于星形聚合物的低临界溶液温度(LCST),从而显著提高了PTX的溶解度。在体温(高于LCST)下,聚(N-异丙基丙烯酰胺)链段的相变诱导形成纳米颗粒,这大大增强了聚合物-药物复合物的细胞摄取,从而实现了PTX的高效热响应递送。特别是,在克服AT3B-1细胞中的多药耐药性方面,聚合物-药物复合物比PTX的商业制剂表现出更好的抗肿瘤效果。