纳米颗粒
羧酸盐
介孔材料
生物相容性材料
金属有机骨架
纳米技术
多孔介质
多孔性
体外
化学工程
化学
材料科学
有机化学
生物化学
催化作用
吸附
生物医学工程
工程类
医学
作者
Xin Ma,Zhihao Yu,Farid Nouar,Iurii Dovgaliuk,G. Patriarche,Nicolas Sadovnik,Marco Daturi,Jean‐Marc Grenèche,Mathilde Lepoitevin,Christian Serre
标识
DOI:10.1021/acs.chemmater.3c01495
摘要
Nanoparticles of biocompatible iron carboxylate metal–organic frameworks (MOFs) or nanoMOFs are of great interest for biomedicine, in particular, for controlled drug release. However, little is known about the impact of their synthesis protocols on their defect content and the possible consequences in terms of physicochemical features and cytotoxicity. Here, we report for the first time how the defect content of the benchmark mesoporous iron trimesate MIL-100(Fe) (MIL stands for Materials of Institut Lavoisier) nanoparticles, with similar sizes but obtained from three different green synthesis routes, has a significant impact not only on their intrinsic porosity, stability in body fluids, drug loading capacity, and release but also shows a critical difference of in vitro toxicity and inflammatory response depending on the type of cell lines.
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