预定位
生物正交化学
光动力疗法
光敏剂
材料科学
膜
单线态氧
生物物理学
组合化学
点击化学
光化学
化学
生物化学
免疫学
生物
有机化学
抗体
氧气
单克隆抗体
放射免疫疗法
作者
Ruili Wei,Yansong Dong,Yalan Tu,Shi‐Wei Luo,Xinrui Pang,Wanli Zhang,Yao Wang,Wenjie Tang,Huikang Yang,Xinhua Wei,Xinqing Jiang,Youyong Yuan,Ruimeng Yang
标识
DOI:10.1021/acsami.1c01259
摘要
Developing novel activatable photosensitizers with excellent plasma membrane targeting ability is urgently needed for smart photodynamic therapy (PDT). Herein, a tumor acidity-activatable photosensitizer combined with a two-step bioorthogonal pretargeting strategy to anchor photosensitizers on the plasma membrane for effective PDT is developed. Briefly, artificial receptors are first anchored on the cell plasma membrane using cell-labeling agents (Az-NPs) via the enhanced permeability and retention effect to achieve the tumor cell labeling. Then, pH-sensitive nanoparticles (S-NPs) modified with dibenzocyclooctyne (DBCO) and chlorin e6 (Ce6) accumulate in tumor tissue and disassemble upon protonation of their tertiary amines in response to the acidic tumor environment, exposing the contained DBCO and Ce6. The selective, highly specific click reactions between DBCO and azide groups enable Ce6 to be anchored on the tumor cell surface. Upon laser irradiation, the cell membrane is severely damaged by the cytotoxic reactive oxygen species, resulting in remarkable cellular apoptosis. Taken together, the membrane-localized PDT by our bioorthogonal pretargeting strategy to anchor activatable photosensitizers on the plasma membrane provides a simple but effective method for enhancing the therapeutic efficacy of photosensitizers in anticancer therapy.
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