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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >DSC, X-ray and FTIR studies of a gemfibrozil/dimethyl-beta-cyclodextrin inclusion complex produced by co-grinding
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DSC, X-ray and FTIR studies of a gemfibrozil/dimethyl-beta-cyclodextrin inclusion complex produced by co-grinding

机译:通过共研磨生产的吉霉嘧啶/二甲基β-环糊精包合物的DSC,X射线和FTIR研究

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摘要

The steps of formation of an inclusion complex produced by the co-grinding of gemfibrozil and dimethyl-beta-cyclodextrin were investigated by differential scanning calorimetry (DSC), X-ray powder diffractometry (XRPD) and Fourier transform infrared (FTIR) spectroscopy with curve-fitting analysis. The endothermic peak at 59.25degC reflecting the melting of gemfibrozil progressively disappeared from the DSC curves of the products on increase of the duration of co-grinding. The crystallinity of the samples too gradually decreased, and after 35 min of co-grinding the product was totally amorphous. Up to this co-grinding time, XRPD and FTIR investigations indicated a linear correlation between the cyclodextrin complexation and the co-grinding time. After co-grinding for 30 min, the ratio of complex formation did not increase. These studies demonstrated that co-grinding is a suitable method for the complexation of gemfibrozil with dimethyl-beta-cyclodextrin. XRPD analysis revealed the amorphous state of the gemfibrozil-dimethyl-beta-cyclodextrin product. FTIR spectroscopy with curve-fitting analysis may be useful as a semiquantitative analytical method for discriminating the molecular and amorphous states of gemfibrozil.
机译:通过差示扫描量热法(DSC),X射线粉末衍射术(XRPD)和傅里叶变换红外(FTIR)光谱,研究了通过共磨削吉哌齐和二甲基β-环糊精和二甲基β-环糊精的夹杂基β-环糊精和傅立叶变换红外(FTIR)光谱法形成的掺入络合物的步骤 - 分析。 59.25DEGC的吸热峰反映了Gemfibrozil的熔化,从产品的DSC曲线上逐渐消失,增加了共研磨的持续时间。样品的结晶度过于逐渐降低,并且在共研磨35分钟后,产物完全无定形。达到该共研磨时间,XRPD和FTIR调查表明环糊精络合与共研磨时间之间的线性相关性。共研磨30分钟后,复杂形成的比例没有增加。这些研究表明,共研磨是用二甲基β-环糊精络合吉法育芽孢杆菌的合适方法。 XRPD分析揭示了Gemfibrozil-二甲基β-环糊精产物的无定形状态。具有曲线拟合分析的FTIR光谱可用作鉴别Gemfibrozil的分子和无定形状态的半定量分析方法。

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