阿霉素
顺铂
多重耐药
体内
药代动力学
乳腺癌
紫杉醇
药品
内化
抗药性
分布(数学)
癌症
化学
癌症研究
药理学
化疗
医学
药物输送
内科学
生物
数学分析
受体
生物技术
数学
有机化学
微生物学
作者
Ming‐Shien Wen,Qiling Chen,Weiguo Xu,Meng Yu,Yuanyuan Yang,Binhua Zou,Yu Shrike Zhang,Jianxun Ding,Zhiqiang Yu
出处
期刊:Nano Research
[Springer Nature]
日期:2020-11-23
卷期号:14 (3): 846-857
被引量:116
标识
DOI:10.1007/s12274-020-3124-y
摘要
Multidrug-resistance (MDR) featuring complicated and poorly defined mechanisms is a major obstacle to the success of cancer chemotherapy in the clinic. Compound nanoparticles comprising multiple cytostatics with different mechanisms of action are commonly developed to tackle the multifaceted nature of clinical MDR. However, the different pharmacokinetics and release profiles of various drugs result in inconsistent drug internalization and suboptimal drug synergy at the tumor sites. In the present study, a type of self-targeting hyaluronate (HA) nanogels (CDDPHANG/DOX) to reverse drug resistance through the synchronized pharmacokinetics, intratumoral distribution, and intracellular release of topoisomerase II inhibitor doxorubicin (DOX) and DNA-crosslinking agent cisplatin (CDDP) is developed. With prolonged circulation time and enhanced intratumoral accumulation in vivo, CDDPHANG/DOX shows efficient drug delivery into the drug-resistant MCF-7/ADR breast cancer cells and enhanced antitumor activity. Besides, fluorescence imaging of DOX combined with the micro-computed tomography (micro-CT) imaging of CDDP facilitates the visualization of this combination tumor chemotherapy. With visualizable synchronized drug delivery, the self-targeting in situ crosslinked nanoplatform may hold good potential in future clinical therapy of advanced cancers.
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