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作 者:谢捷[1] 潘玲燕[1] 朱兴一[1] 王珏[2] 王平[1]
机构地区:[1]浙江工业大学药学院制药工程省部共建教育部重点实验室,浙江杭州310014 [2]国家林业局竹子研究开发中心,浙江杭州310012
出 处:《中成药》2013年第10期2130-2133,共4页Chinese Traditional Patent Medicine
基 金:浙江省国际合作项目(2009C14001);国家自然科学基金(21006097;21176222;21276237);浙江省自然科学基金(Y12B060048)
摘 要:目的将葛根素制成两相及三相分散体系,以提高葛根素的体外溶出速率。方法分别以磷脂和羟丙基-β-环糊精为载体,制备两相固体分散体和包合物,再将磷脂加入到葛根素-羟丙基-β-环糊精中制备三相分散体,分别进行溶解度和体外溶出度实验。对两相固体分散体、包合物和三相分散体进行红外扫描和差示扫描量热分析。结果当葛根素和磷脂的质量比为1∶2时制备的固体分散体葛根素的溶解度为6.54 g/L,包含物中葛根素溶解度为84.03 g/L,三相分散体中葛根素的溶解度为94.41 g/L。体外溶出结果显示15 min时,三相分散体中葛根素的累积溶出百分率达到98.34%。结论磷脂和羟丙基-β-环糊精对葛根素的溶出度具有协同作用。AIM To prepare binary and ternary complexes of puerarin to evaluate their dissolution. METH- ODS Phospholipid (PL) and hydroxypropyl-β-cyclodextrin (HP-β-CD) were used as carrier to prepare binary solid dispersion and binary inclusion complex. Ternary complexes systems were obtained by adding phospholipid to puerarin-HP-β-CD ( 1 : 1 ) systems. All systems were examined for solubility and dissolution properties, and char- acterized by FT-IR and DSC. RESULTS The solubility of puerarin in binary solid dispersion (puerarin : PL of 1 : 2, m/m) was 6.54 g/L, and in binary inclusion complex was 84.03 g/L, while in ternary complexes systems reached 94. 41 g/L. The percent of cumulative dissolution of ternary complexes systems in 15 min was 98.34% . CONCLUSION The synergistic effect between cyclodextrin and phospholipid makes the dissolution and solubility of puerarin increase.
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