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首页> 外文期刊>Russian Journal of Physical Chemistry >Inclusion complexation of Itraconazole with β-and 2-hydroxypropyl-β-cyclodextrins in aqueous solutions
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Inclusion complexation of Itraconazole with β-and 2-hydroxypropyl-β-cyclodextrins in aqueous solutions

机译:伊曲康唑与β-和2-羟丙基-β-环糊精的包合物

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The inclusion behavior of Itraconazole (Itra) with β-cyclodextrin (β-CD) and 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) was investigated by using phase solubility and molecular mechanics techniques. The effects of pH and temperature on complex stabilit were also explored. The aqueous solubility of Itra was significantly enhanced as CD concentration increased. Itra tends to form 1: 3 complexes with β-and HP-β-CD at pH ≥ 4 and 1: 2 at pH 2. Thermodynamic parameters for Itra/HP-β-CD show that the 1: 1 complex is driven by enthalpy but retarded by entropy changes. In contrast, the formation of 1: 2 and 1: 3 complexes is largely favored by entropy due to higher desolvation induced by total enclosure of Itra with two (or three) favorably interacting CD molecules. The inclusion mode of Itra/β-CD complexes was proved by molecular mechanics technique, which provided a powerful means for understanding inclusion interactions and processes.
机译:利用相溶解度和分子力学技术研究了伊曲康唑(Itra)与β-环糊精(β-CD)和2-羟丙基-β-环糊精(HP-β-CD)的包合行为。还探讨了pH和温度对复杂稳定剂的影响。随着CD浓度的增加,Itra的水溶性显着增强。 Itra倾向于与pH≥4的β-和HP-β-CD形成1:3的复合物,而在pH 2时与1:2形成复合物。但由于熵的变化而受阻。相比之下,由于Itra与两个(或三个)相互作用的CD分子完全包封会导致较高的去溶剂化作用,因此熵极大地促进了1:2和1:3配合物的形成。通过分子力学技术证明了Itra /β-CD复合物的包合方式,为理解包合物的相互作用和过程提供了有力的手段。

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