Liédana Nuria, Lozano Pablo, Galve Alejandro, Téllez Carlos, Coronas Joaquín
Chemical and Environmental Engineering Department and Instituto de Nanociencia de Aragón (INA), Universidad de Zaragoza, 50018 Zaragoza, Spain.
J Mater Chem B. 2014 Mar 7;2(9):1144-1151. doi: 10.1039/c3tb21707h. Epub 2014 Jan 20.
A simple and efficient one-step encapsulation of caffeine was carried out in MOF NH-MIL-88B(Fe) and compared to the traditional three-stage synthesis-activation-encapsulation procedure. Caffeine was added to the synthesis solution of a MOF whose structure was formed around the caffeine itself. The caffeine loading was 35 wt%. The presence of this molecule in the synthesis solution led to swollen CAF@NH-MIL-88B(Fe) when a different framework (NH-MIL-53(Fe)) was obtained without caffeine. For comparison, the ex situ encapsulation of caffeine was also carried out in NH-MIL-88B(Fe), once this material was obtained upon activation of NH-MIL-53(Fe). The release of caffeine and aminoterephthalic acid (the ligand used to obtain MOFs) from different materials was studied both in water and phosphate buffered saline (PBS). Caffeine plays the role of a structure directing agent or template since its presence led to obtaining a different MOF. In addition, caffeine contributed to the liquid phase stability of the MOF, as demonstrated through the release of the ligand from both CAF@NH-MIL-88B(Fe) (slower release) and NH-MIL-88B(Fe) (faster release). Chemical and structural evidence indicated hydrogen bond interactions between caffeine and MOF.
在金属有机框架材料NH-MIL-88B(Fe)中对咖啡因进行了简单高效的一步封装,并与传统的三阶段合成-活化-封装程序进行了比较。将咖啡因添加到金属有机框架材料的合成溶液中,该材料的结构围绕咖啡因自身形成。咖啡因负载量为35 wt%。当在没有咖啡因的情况下获得不同的框架结构(NH-MIL-53(Fe))时,合成溶液中该分子的存在导致CAF@NH-MIL-88B(Fe)膨胀。作为对比,在通过NH-MIL-53(Fe)活化获得这种材料后,也在NH-MIL-88B(Fe)中进行了咖啡因的异位封装。研究了不同材料中咖啡因和氨基对苯二甲酸(用于制备金属有机框架材料的配体)在水和磷酸盐缓冲盐水(PBS)中的释放情况。咖啡因起到了结构导向剂或模板的作用,因为它的存在导致获得了不同的金属有机框架材料。此外,咖啡因有助于提高金属有机框架材料的液相稳定性,这通过CAF@NH-MIL-88B(Fe)(释放较慢)和NH-MIL-88B(Fe)(释放较快)中配体的释放得到了证明。化学和结构证据表明咖啡因与金属有机框架材料之间存在氢键相互作用。