Supramolecular nanoparticles constructed by orthogonal assembly of pillar[5]arene-cyclodextrin dimacrocycle for chemo-photodynamic combination therapy  

作　　者：Yongfei Yin Penghao Sun Hongqiang Dong Yi Chen Shigui Chen Lu Wang 

机构地区：[1]The Institute for Advanced Studies,Wuhan University,Wuhan 430072,China

出　　处：《Chinese Chemical Letters》2023年第11期153-158,共6页中国化学快报（英文版）

基　　金：supported by National Natural Science Foundation of China(Nos.21702153 and 21801194);Wuhan Science and Technology Bureau(No.whkxjsj009);the support of the Core Facility of Wuhan University and the Large-scale Instrument and Equipment Sharing Foundation of Wuhan University.

摘　　要：Chemotherapy combined with photodynamic therapy has emerged as a promising strategy for cancer treatment.However,simultaneously delivering chemotherapeutic drugs and photosensitizers and precisely adjusting the ratio of the two components as needed remains a challengeable task.Herein,novel supramolecular nanoparticles(donated as BODIPY-CPT-NPs)for chemo-photodynamic combination cancer therapy are constructed from a glutathione-responsive camptothecin-based prodrug,BODIPY photosensitizer,and dimacrocyclic host molecule through orthogonal host-guest recognitions and co-assembly.With this strategy,the ratio of prodrugs and photosensitizers in nanoparticles can be easily and precisely controlled as needed.Benefiting from the strong host-guest interactions and stable self-assembly,the nanoparticles exhibit excellent stability and photobleaching resistance.Furthermore,camptothecin can be released from nanoparticles for chemotherapy in the presence of reduction agent and single oxygen can be efficiently generated for PDT with light irradiation.The combined effects of the BODIPY-CPT-NPs have been verified in CT26 and HeLa cancer cells.

关 键 词：Supramolecular nanoparticles Host-guest systems Photodynamic therapy Drug delivery PRODRUGS 

分 类 号：R73[医药卫生—肿瘤]