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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 >Curve-fitting FTIR studies of loratadine/hydroxypropyl-beta-cyclodextrin inclusion complex induced by co-grinding process.
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Curve-fitting FTIR studies of loratadine/hydroxypropyl-beta-cyclodextrin inclusion complex induced by co-grinding process.

机译:共研磨工艺诱导氯雷他定/羟丙基-β-环糊精包合物的曲线拟合FTIR研究。

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摘要

The formation steps of inclusion complex caused by co-grinding loratadine (LOR) and hydroxypropyl-beta-cyclodextrin (HP-beta-CD) with a molar ratio of 1:1 or 1:2 were quantitatively investigated by Fourier transform infrared (FTIR) spectroscopy with curve-fitting analysis and differential scanning calorimetry (DSC). The phase solubility study and the co-evaporated solid products of the mixture of LOR and HP-beta-CD were also examined. The result indicates that the aqueous solubility of LOR was linearly increased with the increase of HP-beta-CD concentrations, in which the phase solubility diagram was classified as A(L) type. The higher apparent stability constant (2.22 x 10(4)M(-1)) reveals that the inclusion complex formed between LOR and HP-beta-CD was quite stable. The endothermic peak at 134.6 degrees C for the melting point of LOR gradually disappeared from DSC curves of LOR/HP-beta-CD coground mixtures by increasing the cogrinding time, as the disappearance of the co-evaporated solid products. The disappearance of this endothermic peak from LOR/HP-beta-CD coground mixture or the co-evaporated solid products was due to the inclusion complex formation between LOR and HP-beta-CD after cogrinding process or evaporation. Moreover, IR peaks at 1676 cm(-1) down-shifted from 1703 cm(-1) (CO stretching) and at 1235 cm(-1) upper-shifted from 1227 cm(-1) (C-O stretching) related to LOR in the inclusion complex were observed with the increase of cogrinding time, but the peak at 1646 cm(-1) due to O-H stretching of HP-beta-CD was shifted to 1640 cm(-1). The IR spectrum of 15 min-coground mixture was the same as the IR spectrum of the co-evaporated solid product, strongly indicating that the grinding process could cause the inclusion complex formation between LOR and HP-beta-CD. Three components (1700, 1676, and 1640 cm(-1)) and their compositions were certainly obtained in the 1740-1600 cm(-1) region of FTIR spectra for the LOR/HP-beta-CD coground mixture and the co-evaporated solid products by curve-fitting analysis. The component of 1700 cm(-1) detected was due to the un-included LOR in the inclusion complex. This implies that FTIR spectroscopy with curve-fitting analysis might be useful for discriminating the components and compositions in the inclusion complex.
机译:通过傅立叶变换红外(FTIR)定量研究了摩尔比为1:1或1:2的氯雷他定(LOR)和羟丙基-β-环糊精(HP-β-CD)共研磨引起的包合物的形成步骤光谱分析和曲线拟合分析和差示扫描量热法(DSC)。还研究了相溶解度研究和LOR和HP-β-CD混合物的共蒸发固体产物。结果表明,LOR的水溶解度随H​​P-β-CD浓度的增加而线性增加,其中相溶解度图被分类为A(L)型。较高的表观稳定性常数(2.22 x 10(4)M(-1))表明,LOR和HP-β-CD之间形成的包合物非常稳定。随着共蒸发固体产物的消失,通过增加共研磨时间,LOR /HP-β-CD共研磨混合物的DSC曲线在134.6摄氏度处的吸热峰逐渐消失。 LOR /HP-β-CD共研磨混合物或共蒸发的固体产物中该吸热峰的消失是由于在共研磨或蒸发后LOR和HP-β-CD之间形成了包合物。此外,IR峰从1703 cm(-1)(CO拉伸)向下偏移的1676 cm(-1)和在1235 cm(-1)(CO拉伸)相关的上方偏移的1235 cm(-1)的IR峰共研磨时间的增加,观察到包合物中的峰,但由于HP-β-CD的OH拉伸,在1646 cm(-1)处的峰移至1640 cm(-1)。共研磨15分钟的混合物的IR光谱与共蒸发的固体产物的IR光谱相同,强烈表明研磨过程可能导致LOR和HP-β-CD之间形成夹杂物。 LOR /HP-β-CD共研磨混合物和共-共混物的三个组分(1700、1676和1640 cm(-1))及其组成肯定是在FTIR光谱的1740-1600 cm(-1)区域中获得的。通过曲线拟合分析分析蒸发的固体产物。检测到1700 cm(-1)的分量是由于包合物中未包含LOR。这意味着带有曲线拟合分析的FTIR光谱对于区分夹杂物中的成分和成分可能有用。

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