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作 者:李健莹 栾晓娇 王凯乾 张迪[1] 于秀[1] 胡美娜[1] 富力 周晓霞[1] 徐缓[1]
机构地区:[1]辽宁师范大学化学化工学院,辽宁大连116029 [2]大连富生天然药物开发有限公司,辽宁大连116600
出 处:《中国药学杂志》2015年第10期872-875,共4页Chinese Pharmaceutical Journal
基 金:国家自然科学基金资助项目(81102394);中国博士后科学基金(2013M530899)
摘 要:目的尝试采用一种新型技术制备人参皂苷Rg3固体分散体,从而提高脂、水难溶药物人参皂苷Rg3的溶解性。方法以醋酸羟丙基甲基纤维素琥珀酸酯为载体制备人参皂苷Rg3固体分散体,利用傅立叶变换近红外光谱、X-射线衍射、差示量热扫描分析及扫描电子显微镜等分析方法表征人参皂苷Rg3固体分散体。利用高效液相色谱法分别测定了人参皂苷Rg3和人参皂苷Rg3固体分散体的平衡溶解度。结果人参皂苷Rg3固体分散体可以增加药物的溶解度,在模拟人十二指肠和空肠p H的条件下人参皂苷Rg3固体分散体的溶解性能显著优于原料药。结论本实验制备人参皂苷Rg3固体分散体的方法操作简单、经济实用,增加人参皂苷Rg3溶解度的效果显著。OBJECTIVE To prepare ginsenoside Rg3( G-Rg3) solid dispersion by atoping a new technology to increase the solubility of G-Rg3. METHODS Hydroxypropyl methylcellulose acetate succinate( HPMCAS) was selected as the carrier to prepare GRg3 solid dispersion. The G-Rg3 solid dispersion was characterized via Fourier transform infrared spectroscopy,X-ray diffractometry,differential scanning calorimetry analysis,and scanning electron microscopy. The equilibrium solubility of G-Rg3 and G-Rg3 solid dispersion were measured by using high-performance liquid chromatography. RESULTS The G-Rg3 solid dispersion was successfully prepared. The solubility of G-Rg3 solid dispersion in the weak acid medium( p H 5. 5 and 6. 4) designed to simulate human duodenum and jejunum was significantly higher than that of G-Rg3. CONCLUSION The preparation method of G-Rg3 solid dispersion is simple,economic,and practical,which can obviously increase the of solubility of G-Rg3.
关 键 词:人参皂苷RG3 固体分散体 醋酸羟丙基甲基纤维素琥珀酸酯 溶解度
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