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作 者:王志萍[1] 邓家刚[1] 王勤[1] 李学坚[1] 韦慧鲜[1]
出 处:《中成药》2008年第8期1123-1126,共4页Chinese Traditional Patent Medicine
基 金:广西科学基金项目(桂科基0575084);广西中医学院项目(ZD2005007)
摘 要:目的:优选出提高芒果苷溶解度的最佳分子包合工艺。方法:用比较法筛选羟丙基-β-环糊精(HP-β-CD)对芒果苷分子包合方法及干燥方法,制成的包合物经红外分光光度法、紫外分光光度法、差示热分析、相溶解度图法及溶解度测定。结果:采用搅拌法和冷冻干燥法,HP-β-CD与芒果苷可形成包合物,主、客分子比为1∶1,包合物中芒果苷的溶解度达35.99 mg/mL,比芒果苷原料溶解度0.111 mg/mL增加300多倍。结论:采用搅拌法和冷冻干燥法可制备芒果苷-HP-β-CD包合物,包合工艺稳定,包合后的芒果苷溶解度显著提高。AIM: To study the optimum condition of hydroxypropyl-β-cyclodextrin inclusion for mangiferin in order to improve the solubility of mangiferin. METHODS : By comparing the condition of inclusion of mangiferin in hydroxypropyl-β-cyclodextrin obtained,including its drying method, inclusion compound stood the test of infrared spectrophotometry, UV spectrophotometry, differential scanning calorimetry analysis, phase solubility diagran and solubility determination. RESULTS: The paddling process and freeze drying could put in HP-β-CD inclusion compound use the ratio of host/guest molecules was 1 : 1, the solubility of mangiferin of included complex was 35.99 mg/mL, about 300 times as large as uninclused mangiferin (0.111 mg/mL). CONCLUSION: Hydroxypropyl-β-cyclodextrin inclused mangiferin compound could be prepared by paddling process and freeze drying. Its solubility of the compound improves significantly and it is stable.
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