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基于光响应喜树碱的聚合物前药包覆银纳米颗粒,用于通过纳米材料表面能量转移(NSET)效应追踪药物释放行为。

Photo-responsive camptothecin-based polymeric prodrug coated silver nanoparticles for drug release behaviour tracking via the nanomaterial surface energy transfer (NSET) effect.

作者信息

Li Jiao-Yang, Qiu Liang, Xu Xiao-Fei, Pan Cai-Yuan, Hong Chun-Yan, Zhang Wen-Jian

机构信息

CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, Anhui, China.

出版信息

J Mater Chem B. 2018 Mar 21;6(11):1678-1687. doi: 10.1039/c7tb02998e. Epub 2018 Mar 1.

Abstract

A hybrid drug delivery system was successfully fabricated by attaching a camptothecin (CPT)-based polymeric prodrug onto the surface of silver nanoparticles (AgNPs). PEG was employed as a macro-RAFT agent in RAFT polymerization to synthesize a branched star copolymer, to which CPT is linked through the photo-responsive o-nitrobenzyl linkage. In vitro tests indicate that the fluorescence of CPT in the polymeric prodrug is quenched by AgNPs based on the nanomaterial surface energy transfer (NSET) effect and the fluorescence recovers when the CPT molecules are released from hybrid nanoparticles. Thus, the variation of fluorescence intensity is bound up with the drug release behaviours, which may enable this AgNP-based drug delivery system to trace the intracellular drug release process and observe the distribution of released CPT in cells.

摘要

通过将基于喜树碱(CPT)的聚合物前药连接到银纳米颗粒(AgNP)表面,成功制备了一种混合药物递送系统。在可逆加成-断裂链转移(RAFT)聚合反应中,聚乙二醇(PEG)被用作大分子RAFT试剂,以合成支化星形共聚物,CPT通过光响应性邻硝基苄基连接键与之相连。体外试验表明,基于纳米材料表面能量转移(NSET)效应,聚合物前药中CPT的荧光被AgNP淬灭,而当CPT分子从混合纳米颗粒中释放时,荧光恢复。因此,荧光强度的变化与药物释放行为相关,这可能使这种基于AgNP的药物递送系统能够追踪细胞内药物释放过程,并观察释放的CPT在细胞中的分布。

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