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一种经DNA工程改造的金属有机框架纳米载体,作为可激活光动力癌细胞消融的通用平台。

A DNA-engineered metal-organic-framework nanocarrier as a general platform for activatable photodynamic cancer cell ablation.

作者信息

Ma Yahui, Chen Renzeng, Chen Xianheng, Sun Yuqi, Wang Yuanbo, Wang Bo

机构信息

Frontiers Science Centre for High Energy Material, Advanced Technology Research Institute (Jinan), Key Laboratory of Cluster Science (Ministry of Education), Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Advanced Research Institute of Multidisciplinary Science, School of Medical Technology, School of Chemistry and Chemical Engineering, Beijing Institute of Technology Beijing 100081 P. R. China

出版信息

Nanoscale Adv. 2022 Nov 29;5(2):361-367. doi: 10.1039/d2na00509c. eCollection 2023 Jan 18.

Abstract

Activatable photodynamic cancer cell ablation constitutes a promising approach to performing highly effective photodynamic therapy (PDT) with mitigated phototoxicity. Regretfully, so far strategies to fabricate activatable PDT agents are only applicable to a limited number of photosensitizers (PSs). Herein, an activatable photodynamic cancer cell ablation platform that can be adopted for versatile PSs is presented. Thereinto, by engineering an iron(iii) carboxylate-based metal-organic framework (MOF), MIL-101(Fe), with DNA grafted after PS loading, both hydrophilic and hydrophobic PSs can undergo negligible unspecific leakage and significant suppression of photosensitization during delivery. Following the reaction between MIL-101 and HO whose level is greatly increased inside the tumor, MIL-101 is selectively degraded to release the loaded PDT agents and recover their photosensitization, controllably killing cancer cells upon HO activation. Such a strategy assisted by a DNA-functionalized MOF significantly expands the varieties of PSs applicable for activatable PDT.

摘要

可激活的光动力癌细胞消融是一种很有前景的方法,可用于进行高效光动力疗法(PDT),同时减轻光毒性。遗憾的是,到目前为止,制造可激活PDT剂的策略仅适用于有限数量的光敏剂(PS)。在此,提出了一种可用于多种PS的可激活光动力癌细胞消融平台。其中,通过构建一种基于羧酸铁(III)的金属有机框架(MOF),即MIL-101(Fe),在负载PS后接枝DNA,亲水性和疏水性PS在递送过程中均可经历可忽略不计的非特异性泄漏以及光致敏的显著抑制。在MIL-101与肿瘤内部水平大幅升高的HO发生反应后,MIL-101被选择性降解,从而释放负载的PDT剂并恢复其光致敏性,在HO激活后可控制地杀死癌细胞。这种由DNA功能化MOF辅助的策略显著扩展了适用于可激活PDT的PS种类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a3/9846515/7e2164c5369d/d2na00509c-f1.jpg

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