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Characterization of Ketoprofen/Methyl-β-Cyclodextrin Complexes Prepared Using Supercritical Carbon Dioxide

机译:使用超临界二氧化碳制备的酮丙烯/甲基-β-环糊精配合物的表征

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摘要

Complexes of methyl-β-cyclodextrin and ketoprofen, a crystalline anti-inflammatory drug with poor water solubility, have been prepared for the first time in the presence of supercritical CO2 at 40°C and 20 MPa. The supercritical treatment allows these pharmaceutical formulations to be prepared without the use of any auxiliary agents or organic solvents. The treated samples were characterized through differential scanning calorimetry, X-ray diffractometry, and the Fourier transform infrared spectroscopy to exclude the presence of crystalline drug and check the formation of the complexes. The increase of the drug dissolution rate was investigated performing in vitro release tests in aqueous solutions. The results showed that the supercritical treatment can be an efficient method to obtain inclusion complexes with enhanced release kinetics. The operating methods of the release tests, that is, the “tablet method” or the “dispersed amount method,” affected both the dissolution rate and its dependence on the drug amount in the samples. On the contrary, the variation of the pH of the dissolution medium did not show any effect on the release rate of the supercritical complexes.
机译:甲基-β-环糊精和酮丙烯的复合物,具有较差的水溶性的结晶抗炎药,首次在40℃和20MPa的超临界CO 2存在下制备。超临界治疗允许这些药物制剂在不使用任何辅助剂或有机溶剂的情况下制备。通过差示扫描量热法,X射线衍射法和傅里叶变换红外光谱表征了处理的样品,以排除结晶药物并检查复合物的形成。研究了药物溶解速率的增加在水溶液中进行了体外释放试验。结果表明,超临界治疗可以是获得具有增强释放动力学的包含复合物的有效方法。释放试验的操作方法,即“片剂法”或“分散量方法”,影响溶出速率及其对样品中药量的依赖性。相反,溶解介质的pH的变化并未显示出对超临界复合物的释放速率的任何影响。

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