首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Investigation on the inclusion behavior of Norfloxacin with 2-methyl-β-cyelodextrin
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Investigation on the inclusion behavior of Norfloxacin with 2-methyl-β-cyelodextrin

机译:诺氟沙星与2-甲基-β-环糊精的包合行为研究

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The formation of the complexes of Norfloxacin with 2-methyl-β-cyclodextrin (Me-β-CD) was studied by UV-Vis absorption spectroscopy, fluorescence and nuclear magnetic resonance spectroscopy (NMR). Experimental conditions including Me-β-CD concentration and media acidity were investigated in detail at room temperature. The results suggest that Norfloxacin exists in three molecular forms in aqueous solution at different pH values, namely, the acidic form, the neutral form and the alkaline form). Me-β-CD was more suitable for inclusion of Norfloxacin in the acidic medium. The binding constant (K) of the inclusion complex was determined by fluorescence measurement, and the complexation ratio was determined as 1:1 in the concentration range used in this study. A mechanism was proposed to explain the inclusion process based on the experimental NMR data.
机译:通过紫外-可见吸收光谱,荧光和核磁共振光谱(NMR)研究了诺氟沙星与2-甲基-β-环糊精(Me-β-CD)的配合物的形成。在室温下详细研究了包括Me-β-CD浓度和介质酸度在内的实验条件。结果表明诺氟沙星在水溶液中在不同的pH值下以三种分子形式存在,即酸性形式,中性形式和碱性形式。 Me-β-CD更适合在酸性介质中包含诺氟沙星。通过荧光测量确定包合物的结合常数(K),在本研究使用的浓度范围内,将络合比确定为1:1。提出了一种基于实验NMR数据解释包合过程的机理。

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