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更昔洛韦凝胶剂的制备及质量控制 被引量:8

The preparation and quality control of ganciclovir gel
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摘要 目的 制备更昔洛韦凝胶剂。方法 以卡波普水凝胶为基质制备更昔洛韦凝胶剂 ,采用紫外分光光度法进行含量测定 ,并进行稳定性和皮肤刺激性试验。结果 更昔洛韦在 2 5 2nm处有最大吸收 ,在 4~ 16 μg ml浓度与吸收度线性关系良好。结论 更昔洛韦凝胶剂性质稳定 ,皮肤刺激性小 ,制备简单 ,易于质量控制 ,适用于医院配制。 Objective To prepare ganciclovir gel.Methods The carbomor hydrogel has been chosen as the basic for ganciclovir gel,and the UV method was employed to determine the content. Tests were carried out to investigate the stability and skin irritability. Results Ganciclovir showed a maximum absorbance at 252nm in solution and exhibited a good linear relationship with absorbance over the range of 4~16μg/ml. Conclusion Ganciclovir gel is stable and low in skin irritation with convenient usage as the advantage,easy to control,which means a reliable and proper preparation for the hospital.
出处 《广东药学》 2002年第4期24-25,共2页 Guangdong Pharmaceutical Journal
关键词 更昔洛韦 凝胶剂 制备 质量控制 ganciclovir gel quality control
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  • 1熊增慧,吴海燕,黄砚青,郭秋月.更昔洛韦在家兔体内药动学研究[J].中国药学杂志,1996,31(12):739-742. 被引量:9
  • 2[3]Sastry SV, Reddylk, Khan MA. Atenolol Gastrointestinal Therapentic System: Optimization of for mulation Variables Using Response Surface Methodology J. Controlled Release 1997,45(2):121.
  • 3[4]Meshali MM, EL Sayed GM, EL said Y et al. Preparation and Evaluation of Theophylline Sustained Release Tablets Drng Dev Ind pharm.1996,22(4) :373.
  • 4陆义诚,中国医院药学杂志,1995年,15卷,7期,333页

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