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纳米级锆卟啉金属有机框架材料的结构多样性及其光活性和生物学性能。

Structural diversity of nanoscale zirconium porphyrin MOFs and their photoactivities and biological performances.

作者信息

Zhou Junli, Li Yite, Wang Lei, Xie Zhigang

机构信息

State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, P. R. China.

University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.

出版信息

J Mater Chem B. 2021 Sep 29;9(37):7760-7770. doi: 10.1039/d1tb01311d.

Abstract

Photoactive MOF-based delivery systems are highly attractive for photodynamic therapy (PDT), but the fundamental interplay among structural parameters and photoactivity and biological properties of these MOFs remains unclear. Herein, porphyrinic MOF isomers (TCPP-MOFs), constructing using the same building blocks into distinct topologies, have been selected as ideal models to understand this problem. Both the intramolecular distances and molecular polarization within TCPP-MOFs isomers collectively contribute to the photoactivity of generating reactive oxygen species. Remarkably, the morphology-determined endocytic pathways and cytotoxicity, as well as good biocompatibility have been confirmed for TCPP-MOF isomers without any chemical modification for the first time. Besides the topology-dependent photoactive regulation, this work also provides in-depth insights into the biological effect from the MOF nanoparticles with controllable structural factors, benefiting further applications and clinical transformation.

摘要

基于光活性金属有机框架(MOF)的递送系统对光动力疗法(PDT)极具吸引力,但这些MOF的结构参数、光活性和生物学特性之间的基本相互作用仍不清楚。在此,卟啉基MOF异构体(TCPP-MOFs),即使用相同的构建单元构建成不同的拓扑结构,已被选为理解这一问题的理想模型。TCPP-MOF异构体中的分子内距离和分子极化共同促成了活性氧生成的光活性。值得注意的是,首次证实了未经任何化学修饰的TCPP-MOF异构体的形态决定的内吞途径和细胞毒性以及良好的生物相容性。除了拓扑结构依赖的光活性调节外,这项工作还深入洞察了具有可控结构因素的MOF纳米颗粒的生物学效应,有利于进一步的应用和临床转化。

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