摘要
目的考察不同生产厂家的头孢哌酮钠的质量,为临床提供使用依据。方法应用紫外分光光度计,pH值测定仪,分别测定头孢哌酮钠在常温条件下配置后4h内含量、pH值的变化情况。结果与结论在常温条件下,以生理盐水作溶媒,六厂家的头孢哌酮钠质量无明显差别。但拥有专利的原研厂家的药品质量较稳定。
OBJECTIVE To evaluate the puality of factories, use the basis for clinical offering. METHODS Injection Cefoperazone Natrin produced by 6 different The contents and pH were measured by UV luminosity and pH determine. RESULTS and CONCLUSION The products from six factories were all proved qualified within 4 hours at usual temperature, maked the solvent with physiology brine and having no the obvious difference. The drug produced by the factory holding the patent right are more stable.
出处
《海峡药学》
2006年第3期26-27,共2页
Strait Pharmaceutical Journal
关键词
头孢哌酮钠
质量
评价
Cefoperazone natrin
Quality
Evaluation