纳米载体
纳米颗粒
化学
纳米技术
前药
金属有机骨架
药品
聚合物
生物相容性材料
水介质
水溶液
材料科学
化学工程
有机化学
生物医学工程
药理学
吸附
工程类
医学
生物化学
作者
Violeta Rodriguez-Ruiz,Andrei Maksimenko,Resmi Anand,Sandra Monti,Valentina Agostoni,Patrick Couvreur,Maria Lampropoulou,Konstantina Yannakopoulou,Ruxandra Gref
标识
DOI:10.3109/1061186x.2015.1073294
摘要
Metal-organic frameworks (MOFs) are coordination polymers of interest for biomedical applications. Of particular importance, nanoparticles made of iron(III) trimesate (MIL-100, MIL standing for Material Institut Lavoisier) (nanoMOFs) can be conveniently synthesised under mild and green conditions. They were shown to be biodegradable, biocompatible and efficient to encapsulate a variety of active molecules. We have addressed here the challenges to encapsulate a highly hydrophilic anticancer prodrug, phosphated gemcitabin (Gem-MP) known for its instability and inability to bypass cell membranes. MIL-100 nanoMOFs acted as efficient "nanosponges", soaking Gem-MP from its aqueous solution with almost perfect efficiency (>98%). Maximal loadings reached ∼30 wt% reflecting the strong interaction between the drug and the iron trimesate matrices. Neither degradation nor loss of crystalline structure was observed after the loading process. Storage of the loaded nanoMOFs in water did not result in drug release over three days. However, Gem-MP was released in media containing phosphates, as a consequence to particle degradation. Drug-loaded nanoMOFs were effective against pancreatic PANC-1 cells, in contrast to free drug and empty nanoMOFs. However, an efflux phenomenon could contribute to reduce the efficacy of the nanocarriers. Size optimization and surface modification of the nanoMOFs are expected to further improve these findings.
科研通智能强力驱动
Strongly Powered by AbleSci AI