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作 者:武昊昀[1,2] 刘志东[1,2] 李琳[1,2] 李楠[1,2] 郭倩[1,2] 潘卫三[3]
机构地区:[1]天津中医药大学中医药研究院,天津300193 [2]天津中医药大学现代中药发现与制剂技术教育部工程研究中心,天津300193 [3]沈阳药科大学药学院,沈阳110016
出 处:《中国新药杂志》2011年第6期508-513,共6页Chinese Journal of New Drugs
基 金:国家重大新药创制科技重大专项(2009ZX09311-002);国际科技合作计划项目(2007DFC31670);国家科技支撑计划项目(2007BAI47B01)
摘 要:目的:研究pH敏感型黄芩苷眼用原位凝胶剂。方法:采用桨法进行处方的体外释药试验,建立UV法测定体外释药量;应用离体角膜进行体外渗透试验,建立HPLC法测定离体角膜渗透量。结果:凝胶基质黏度随pH值的增大而增大,其拐点在pH 5.8~6.0之间;在一定范围内,亲水凝胶材料用量越大,凝胶基质的缓释作用越好;凝胶体外释放符合Ritger-Peppas方程;离体角膜渗透行为符合零级释放规律。结论:pH敏感型黄芩苷眼用原位凝胶剂达到了缓释释放的目的。Objective:To prepare baicalin pH-triggered ophthalmic in situ gel.Methods:Release behavior of baicalin from pH-triggered in situ gel was explored in a dissolution apparatus with paddle method.The released amount of baicalin from pH-triggered gel was determined by UV;the cornea permeation of gel formulations was determined in rabbit corneas.The permeated amount of baicalin was determined by high performance liquid chromatography.Results:The viscosity of gel increased with increasing pH value.The inflexion of viscosity was from 5.8 to 6.0.The in vitro release behavior of the formulation followed Ritger-Peppas equation.The in vitro permeation behavior followed the zero-order kinetic equation.Conclusion:The release time of baicalin from pH-sensitive ophthalmic in situ gel is longer than eye-drops.
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