替硝唑-聚癸二酸酐控释制剂的制备及释放  被引量:1

Preparation and drug release of the tinidazole-poly(sebacic anhydride) controlled-releasing preparations

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作  者:姚军[1] 马慧丽[1] 王丽军[2] 陈慧[1] 张福林[3] 闫宇卿[3] 

机构地区:[1]河北科技大学化学与制药工程学院,河北石家庄050018 [2](唐山市中医院,河北唐山063000 [3]唐山市第二医院,河北唐山063000

出  处:《中国医院药学杂志》2006年第7期794-796,共3页Chinese Journal of Hospital Pharmacy

基  金:河北省教育厅基金资助项目(编号:2004423)

摘  要:目的:采用HPLC法测定替硝唑-聚癸二酸酐控释制剂的含量,并研究其释药特性。方法:色谱条件为色谱柱:ShimPackVp-ODS柱(250mm×4.6mm,5μm);柱温:室温;流动相:甲醇-水(20:80);流速:1mL·min^-1;检测波长:310nm;进样量:10μL。将替硝唑-聚癸二酸酐控释制剂置于0.1mol·L^-1,pH7.4的磷酸缓冲液(PBS)中,37℃恒温振荡,每24h更换一次缓冲液,测定并计算缓冲液中药物浓度及药物累计释放百分率。结果:替硝唑含量在5.0~100.0mg·L^-1范围内,浓度与吸收度之间线性关系良好(r=0.9999);样品的平均回收率为101.84%,RSD为0.54%(n=4)。释药结果表明,聚癸二酸酐对替硝唑的释放呈一级释放动力学特征,拟合方程:Y=8.0583+34.4558t-3.1925t^2。结论:该方法灵敏,专属,准确,操作简便,可供该制剂的含量测定。OBJECTIVE To develop an HPLC method for the determination of tinidazole-poly (sebacic anhydride) controlled-releasing preparations, and study the drug release characteristic. METHODS Chromatographic conditions included column: Shim-Pack VPODS ( 150 mm×4. 6 mm); column temperature: room temperature; mobilephase: methanol-water(20 : 80) ; flowrate: 1 mL. min^-1 detector: UV 310 nm; injection volume: 10μL. Tinidazole-Poly(sebacic anhydride) controlled-releasing preparations were put in 0. 1 mol·L^-1, pH 7. 4 PBS, vibrating at 37℃. The buffer was changed once in every 24 h, and was determinated and calculated drug concentration and cumulative release percent. RESULTS The calibration curve was linear (r= 0. 999 9) in the range of 5.0 - 100.0 mg·L^-1 for tinidazole, the mean recovery was 101. 84%, with RSD of 0. 539 40% (n = 4). The results of drug release demonstrated that the tinidazole-poly (sebacic anhydride) controlled-releasing preparations followed first order release kinetics, the regression equation was Y= 8, 058 33 + 34. 455 83t- 3. 192 5 t^2. CONCLUSION The method is sensitive, specific, accurate, simple and was suitable for the determination of tinidazole preparations.

关 键 词:替硝唑 聚癸二酸酐 高效液相法 控释 释药特性 

分 类 号:R943[医药卫生—药剂学]

 

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