Lab Pharm Biopharm, Department of Biotechnology, Yuanpei University, Hsin Chu, Taiwan, ROC.
J Pharm Biomed Anal. 2010 Nov 2;53(3):799-803. doi: 10.1016/j.jpba.2010.06.010. Epub 2010 Jun 19.
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.
采用傅里叶变换红外光谱(FTIR)光谱和曲线拟合分析以及差示扫描量热法(DSC)定量研究了洛拉他定(LOR)和羟丙基-β-环糊精(HP-β-CD)以 1:1 或 1:2 的摩尔比共研磨形成包合物的形成步骤。还检查了 LOR 和 HP-β-CD 混合物的相溶解度研究和共蒸发固体产物。结果表明,LOR 的水溶解度随 HP-β-CD 浓度的增加呈线性增加,其中相溶解度图被分类为 A(L)型。较高的表观稳定常数(2.22×10(4)M(-1))表明 LOR 与 HP-β-CD 之间形成的包合物非常稳定。对于 LOR 的熔点的吸热峰在 134.6°C 逐渐从 LOR/HP-β-CD 共研磨混合物的 DSC 曲线中消失,随着共蒸发固体产物的消失而消失。由于共研磨过程或蒸发后 LOR 与 HP-β-CD 之间形成了包合物,因此 LOR/HP-β-CD 共研磨混合物或共蒸发固体产物中此吸热峰的消失。此外,随着共研磨时间的增加,在包合物中观察到与 LOR 相关的 1676cm(-1)处的 IR 峰从 1703cm(-1)(CO 伸缩)向下移动,并且在 1235cm(-1)处的 IR 峰从 1227cm(-1)(C-O 伸缩)向上移动,但 HP-β-CD 的 O-H 伸缩的 1646cm(-1)峰移至 1640cm(-1)。15 分钟共研磨混合物的 IR 光谱与共蒸发固体产物的 IR 光谱相同,强烈表明研磨过程可以导致 LOR 和 HP-β-CD 之间形成包合物。通过曲线拟合分析,在 LOR/HP-β-CD 共研磨混合物和共蒸发固体产物的 1740-1600cm(-1) 区域的 FTIR 光谱中,肯定获得了三个组件(1700、1676 和 1640cm(-1))及其组成。检测到的 1700cm(-1)的组分是由于包合物中未包含的 LOR。这表明,FTIR 光谱与曲线拟合分析相结合可能有助于鉴别包合物中的组分和组成。