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A novel drug carrier based on functional modified nanofiber cellulose and the control release behavior

机译:基于功能改性纳米纤维纤维素的新型药物载体及其控释行为

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This study developed a novel drug carrier based on functional modified bacterial cellulose(BC) which was conjugated with Ibuprofen(IBU) by esterification. BC-Ibuprofen as the macro- molecular prodrugs and drug carrier used to improve the short half-life of the drug, and was able to control release through the hydrolysis of ester bond between the hydroxyl groups of BC with Ibuprofen under different condition. Fourier transform infrared analysis revealed that Ibuprofen had been successfully grafted onto the bacterial cellulose (BC). Thermal and morphological characterization indicated the formation of the BC-Ibuprofen system incompletely reacted maintained the bulk structure of the pristine material such as crystallinity, 3-dimentional network and so on. The drug release behaviours were affected by the ester bond hydrolysis as well as the microstructure characteristics of the modified nanofiber. The release of BC-IBU showed an apparent pH-dependent, fast in alkaline and acid solution but slow relatively in neutral. Such pH-responsiveness, in addition to its morphological characteristics, in this paper suggested a great potential of BC-IBU as a more effective, safe, and stable prodrug candidate.
机译:本研究开发了一种基于功能性修饰细菌纤维素(BC)的新型药物载体,该载体通过酯化与布洛芬(IBU)偶联。 BC-布洛芬作为大分子前药和药物载体,用于改善药物的短半衰期,并能够通过在不同条件下通过BC与布洛芬之间的羟基之间的酯键水解来控制释放。傅里叶变换红外分析表明,布洛芬已成功嫁接到细菌纤维素(BC)上。热学和形态学表征表明不完全反应的BC-布洛芬体系的形成保持了原始材料的整体结构,例如结晶度,3维网络等。酯键水解以及改性纳米纤维的微观结构特征影响药物的释放行为。 BC-IBU的释放表现出明显的pH依赖性,在碱性和酸性溶液中快速释放,而在中性溶液中则相对缓慢。除了其形态特征外,这种pH响应性还表明BC-IBU作为更有效,安全和稳定的前药候选物具有巨大潜力。

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