文献类型: 外文期刊
作者: Fang, Bo;Shan, Tianyu;Chen, Sailing;Pan, Fei;Yang, Xue;Xiao, Ding;Huang, Feihe;Mao, Zhengwei
作者机构:
期刊名称: ACS CENTRAL SCIENCE
ISSN: 2374-7943
年卷期: 2025 年
页码:
收录情况: SCIE(2025版) ; ; EI(2025版)
摘要: To date, the number of reported mesoporous metal-organic frameworks (MOFs) remains limited. Herein, we report a novel mesoporous potassium-based MOF (K-MOF), designated as KMOF-1, whose precise structure was determined by using single-crystal X-ray diffraction. KMOF-1 used 18-crown-6 units as the organic linkers and potassium ions as the metal centers, forming a framework topological structure with interconnected four-membered rings. The specific surface area of the synthesized KMOF-1 was determined by the Brunauer-Emmett-Teller method, which showed a high specific surface area of 1034 m2/g. KMOF-1 was demonstrated to be a promising drug carrier, exhibiting encapsulation capabilities for various drugs and maintaining stability for a defined period under simulated physiological conditions. Using vascular endothelial growth factor (VEGF) aptamers as model drugs, we further confirmed the effective loading of VEGF aptamers in KMOF-1 (KMOF-1@VEGF) and the ability of KMOF-1@VEGF to release VEGF aptamers responsively in acidic environments. Additionally, in vitro studies showed that KMOF-1 protected VEGF aptamers from degradation by nucleases, allowing them to be effectively taken up by cells. This novel K-MOF, with its biocompatible metal centers, mesoporous channels, and demonstrated efficacy as a drug carrier, offers a significant advancement in developing MOF-based drug delivery systems.
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