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ROS‐Responsive Camptothecin Prodrug Nanoparticles for On‐Demand Drug Release and Combination of Chemotherapy and Photodynamic Therapy
Author(s) -
Chu Bingyang,
Qu Ying,
He Xinlong,
Hao Ying,
Yang Chengli,
Yang Yun,
Hu Danrong,
Wang Fangfang,
Qian Zhiyong
Publication year - 2020
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202005918
Subject(s) - prodrug , camptothecin , in vivo , photodynamic therapy , drug delivery , photosensitizer , nanomedicine , materials science , conjugate , pharmacology , cancer research , biophysics , nanotechnology , chemistry , nanoparticle , biochemistry , medicine , biology , photochemistry , organic chemistry , mathematical analysis , microbiology and biotechnology , mathematics
Minimizing drug leakage in systemic circulation, synchronizing the in vivo fate of multiple drugs, and precisely controlling tumor locoregional drug release, remain challenging for nanomedicine‐based cancer therapy. Here, a reactive oxygen species (ROS)‐responsive camptothecin (CPT) prodrug delivery system (MPEG‐(TK‐CPT)‐PPa) is developed, in which CPT and photosensitizer pyropheophorbide‐a (PPa) are concurrently conjugated to the same poly(ethylene glycol) methyl ether (MPEG) via ROS‐responsive thioketal (TK) and lipid linkage. The synthesized MPEG‐(TK‐CPT)‐PPa conjugate self‐assembles to form nanoparticles (NPs) (43.6 ± 0.8 nm) in solution. The covalently conjugated prodrug prevents drug leakage during systemic circulation and synchronizes the in vivo distribution of the two drugs. The generated fluorescence signal of PPa helps precisely track and locate the NPs at tumor sites. Under the guidance of imaging, a near‐infrared laser locally irradiates tumor tissue upon reaching the strongest fluorescence. The ROS generated by PPa not only cleaves the TK linkage and then triggers locoregional, controllable and on‐demand CPT release, but also exhibits cytotoxic effects on tumor cells. Thus, CPT‐mediated chemotherapy and PPa‐induced photodynamic therapy lead to the combined and enhanced suppression of tumor growth. Accordingly, such laser‐triggered, localized, controllable, and on‐demand drug release systems may provide an alternative option for CPT formulations.