物理吸附
材料科学
吸附
多孔性
化学工程
化学吸附
密度泛函理论
纳米技术
氧化物
多孔介质
一氧化氮
工作(物理)
气相
高分辨率
药物输送
选择性吸附
过程(计算)
作者
Zhe Jia,D. Hu,Yaxuan Su,Hongqing Li,Jinjin Zhang,Heng Ji,Yang Zou,Sen Hong,Ming Liu
标识
DOI:10.1021/acsami.5c18890
摘要
In recent years, gas therapy has demonstrated significant potential in the biomedical field. However, existing gas delivery materials often suffer from a limited loading capacity and potential biotoxicity. Porous organic cages (POCs), an emerging subclass of porous materials, offer distinct advantages for gas adsorption and separation due to their intrinsic porosity, solubility, and structural tunability. Herein, we present the first experimental investigation of POCs for nitric oxide (NO) delivery. The tunable molecular design of POCs enables dual adsorption capabilities mechanisms: physisorption and chemisorption via the incorporation of NO-reactive moieties. Through a combination of experimental characterizations and density functional theory calculations, we demonstrated that NO reacts with amine-functionalized POCs to form NONOates, which enables controlled NO release under physiological conditions. High resolution mass spectroscopy provided direct evidence for the process of the formation of NONOates, facilitated by the well-defined and discrete molecular structure of POCs. This work establishes POCs as a promising platform for NO delivery and highlights their broader potential for biomedical applications beyond gas therapy.
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