阿霉素
姜黄素
多重耐药
谷胱甘肽
纳米载体
药物输送
体内
化学
药理学
PLGA公司
抗药性
药品
体外
细胞毒性
医学
生物化学
化疗
生物
抗生素
内科学
生物技术
有机化学
微生物学
酶
作者
Xuandi Lai,Xinran Geng,Mengqing Li,Mengxiong Tang,Qiong Liu,Mengsu Yang,Lin Shen,Yu Zhu,Shubin Wang
出处
期刊:Nanomedicine
日期:2021-07-01
卷期号:16 (16): 1411-1427
被引量:5
标识
DOI:10.2217/nnm-2021-0100
摘要
Aim: This work aims to develop an injectable nano-drug delivery system to overcome tumor multidrug resistance (MDR). Methods: A drug delivery nanoplatform based on PEGylated PLGA with glutathione (GSH) responsivity was constructed for dual delivery of doxorubicin and curcumin (termed DCNP), and its MDR reversal efficiency was studied in vitro and in vivo. Results: The DCNPs exhibited a rapid drug release profile under high GSH concentration and could enhance the cellular uptake and cytotoxicity of doxorubicin to MDR cancer cells. Moreover, the DCNPs showed better biocompatibility, longer blood circulation and enhanced antitumor efficiency compared with free drugs. Conclusion: The GSH-responsive nanocarrier is believed to be a promising candidate for overcoming tumor MDR.
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