紫杉醇
多重耐药
细胞毒性
体内
药理学
脂质体
化疗
抗药性
肺癌
癌症
体外
癌症研究
化学
医学
生物
肿瘤科
内科学
生物化学
微生物学
生物技术
作者
Qiying Shen,Yurun Shen,Feiyang Jin,Yong‐Zhong Du,Xiaoying Ying
标识
DOI:10.1080/08982104.2019.1579838
摘要
Multidrug resistance (MDR) is the largest obstacle to the success of chemotherapy. The development of innovative strategies and safe sensitizers is required to overcome MDR. Paclitaxel (PTX) is a widely used chemotherapeutic drug, the application of which has been learn to understand MDR. However, the application and use are severely restricted because of this MDR. Cyclodextrins (CDs) of many carriers, additionally have shown anti-cancer capability in MDR cancer cells. In this study, novel paclitaxel/hydroxypropyl-β-cyclodextrin complex-loaded liposomes (PTXCDL) have been developed in an attempt to overcome MDR in a PTX-resistant human lung adenocarcinoma (A549/T) cell line. The in vitro application of PTXCDL exhibited pH-sensitive PTX release, potent cytotoxicity, and enhanced intracellular accumulation. In comparison to in vivo, PTXCDL also show a stronger inhibition of tumor growth. In comparison, these findings suggest that the PTXCDL provide a novel strategy for effective therapy of resistant cancers by overcoming the drug resistance.
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