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Synthesis of nicotinamide-based molecularly imprinted microspheres and in vitro controlled release studies.

机译:基于烟酰胺的分子印迹微球的合成和体外控释研究。

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Nicotinamide (NAM), which is one of the two principal forms, together with nicotinic acid, of vitamin B3, is both a food nutrient and a drug. Controlled NAM release systems are useful to extend the duration of the drug's pharmacological activity and to minimize administration frequency. In this paper, molecularly imprinted polymers (MIPs) have been used as unconventional synthetic polymeric carriers, to prepare drug delivery systems for sustained release of NAM molecules. In the present study, various MIPs micro-spheres have been synthesized by using methacrylic acid as a functional monomer and ethylene glycol dimethacrylate (EGDMA) as a cross-linker. Different stoichiometric ratios of the reagents have been used, in order to evaluate their influence on NAM recognition and release properties. Non-imprinted systems have been also been prepared as controls. MIPs binding capacity has been evaluated; NAM loading and in vitro release studies, in buffer solution (pH 7.2), that mimics blood plasma conditions, have been performed. Polymer P4 has given the best results since it enables it to rebind selectively and to prolong the release of NAM with higher performance than the non-imprinted one.
机译:烟酰胺(NAM)是维生素B3的两种主要形式之一,与烟酸一起,既是食物营养素又是药物。受控的NAM释放系统可用于延长药物药理活性的持续时间,并最大程度地减少给药频率。在本文中,分子印迹聚合物(MIP)已用作非常规合成聚合物载体,以制备用于NAM分子持续释放的药物递送系统。在本研究中,已通过使用甲基丙烯酸作为功能单体和乙二醇二甲基丙烯酸酯(EGDMA)作为交联剂合成了各种MIP微球。为了评估试剂对NAM识别和释放特性的影响,已使用了不同化学计量比的试剂。还准备了非压印系统作为对照。已评估了MIP的结合能力;已在模拟血浆状况的缓冲溶液(pH 7.2)中进行了NAM加载和体外释放研究。聚合物P4具有最佳效果,因为它能够选择性地重新结合并延长NAM的释放,且性能优于未压印的NAM。

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