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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:共研磨制备的吉非贝齐/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射线粉末衍射法(XRPD)和傅里叶变换红外光谱(FTIR)光谱研究了吉非贝齐和二甲基-β-环糊精共研磨产生的包合物的形成步骤。拟合分析。随着共研磨时间的增加,反映出吉非贝齐熔融的在59.25℃的吸热峰逐渐从产物的DSC曲线上消失。样品的结晶度也逐渐降低,并且在共研磨35分钟后,产品完全是非晶态的。在此共研磨时间之前,XRPD和FTIR研究表明,环糊精的络合度和共研磨时间之间存在线性关系。共研磨30分钟后,复合物形成的比例没有增加。这些研究表明,共研磨是使吉非贝齐与二甲基-β-环糊精络合的合适方法。 XRPD分析揭示了吉非贝齐-二甲基-β-环糊精产物的非晶态。具有曲线拟合分析的FTIR光谱可用作鉴别吉非贝齐分子和非晶态的半定量分析方法。

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