光热治疗
前药
顺铂
热疗
材料科学
体内
多重耐药
组合化学
体外
生物物理学
纳米技术
化学
生物化学
化疗
生物
抗生素
古生物学
生物技术
遗传学
作者
Lingna Wang,Yingjie Yu,Dengshuai Wei,Lingpu Zhang,Xiaoyan Zhang,Guanxin Zhang,Dan Ding,Haihua Xiao,Deqing Zhang
标识
DOI:10.1002/adma.202100599
摘要
Abstract A systematic combination strategy is proposed for overcoming cisplatin resistance using near‐infrared (NIR)‐light‐triggered hyperthermia. A new photothermal polymer DAP‐F is complexed with a reduction‐sensitive amphiphilic polymer P1 to form F‐NPs with photothermal effect. Subsequently, to build the final nanosystem F–Pt‐NPs, F‐NPs are combined with Pt‐NPs, which are obtained by encapsulating a Pt(IV) prodrug with P1 . Mild hyperthermia (43 °C), generated from F–Pt‐NPs induced by an 808 nm NIR laser, have various effects such as: i) enhancing the cellular membrane permeability to promote the uptake of drugs; ii) activating cisplatin by accelerating the glutathione consumption; iii) increasing the Pt‐DNA adducts formation and possibly the formation of a portion of irreparable Pt‐DNA interstrand crosslinks, thereby inhibiting the repair of DNA. In vitro, it is found that even on cisplatin‐resistant A549DDP cells, the IC 50 of F–Pt‐NPs (43 °C) is only 7.0 × 10 −6 m Pt mL −1 . In vivo, on a patient‐derived xenograft model of multidrug resistant lung cancer, the efficacy of the F–Pt‐NPs (43 °C) treatment group shows a tumor inhibition rate of 94%. Taken together, here, an important perspective of resolving cascade drug resistance with the assistance of mild hyperthermia triggered by NIR light is presented, which can be of great significance for clinic translation.
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