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利巴韦林缓释片的制备及其释放度测定 被引量:3

Preparation of ribavrin sustained release tablets and its drug release
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摘要 目的:制备利巴韦林缓释片,对其释放机制进行考察。方法:建立高效液相色谱(HPLC)体外释放度测定法,以羟丙基甲基纤维素(HPMC)为主要辅料,制备亲水凝胶型骨架片,采用单因素试验筛选辅料种类,通过均匀设计优化出缓释片的处方。结果:所制备的缓释片在8h内呈良好的零级释药特征。结论:以均匀设计优选的利巴韦林缓释片处方合理,体外释放性能良好。 OBJECTIVE To prepare ribavirin sustained release tablets and investigate its release mechanism in vitro. METHODS To establish a HPLC method for determing the content of ribavirin. The water-soluble matrix tablet was preparaed by use of HPMC.The optimal formulation was obtained by uniform design. RESULTS The release profile of the tablets in vitro was fitted well by zeros-order release within 8 hours. CONCLUSION The formulation and the release mechanism in vitro is reasonable.
出处 《中国医院药学杂志》 CAS CSCD 北大核心 2005年第7期628-631,共4页 Chinese Journal of Hospital Pharmacy
关键词 利巴韦林 缓释片 释放度 均匀设计 ribavirin sustained release tablet drug release uniform design
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参考文献7

  • 1董志超,蒋雪涛.羟丙基甲基纤维素在凝胶骨架片的应用[J].国外医药(合成药.生化药.制剂分册),1993,14(1):41-44. 被引量:31
  • 2吕丹,裴元英.羟丙基甲基纤维素-卡波普缓释亲水凝胶骨架片的研制和释药影响因素的考察[J].中国药学杂志,2001,36(9):603-606. 被引量:24
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二级参考文献1

  • 1Cheryl L. Zimmerman. The Effect of Urinary pH Modification on the Disposition of Phenylpropanolamine[J] 1988,Pharmaceutical Research(2):120~122

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