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作 者:李雪松[1] 杨龙[1] 钱斌[1] 李小军[1] 晏远智[1] 杨家爱[1]
出 处:《中国药房》2009年第20期1556-1558,共3页China Pharmacy
摘 要:目的:考察头孢哌酮/他唑巴坦钠在含果糖氯化钠注射液和转化糖注射液中的稳定性。方法:采用高效液相色谱(HPLC)法测定头孢哌酮/他唑巴坦钠与含果糖氯化钠注射液和转化糖注射液配伍6h内的含量,并考察其外观、pH值变化。结果:头孢哌酮/他唑巴坦钠与2种注射液配伍后,6h内其含量变化不大,溶液澄清,pH值基本稳定。结论:头孢哌酮/他唑巴坦钠可与含果糖氯化钠注射液和转化糖注射液配伍使用。OBJECTIVE: To study the stability of Cefoperazone Sodium / Tazobactam Sodium in Fructose - contained 0.9% sodium chloride injection or Invertose Injection. METHODS: The contents of Cefoperazone Sodium / Tazobactam Sodium within 6 hours after mixing with Fructose-contained 0.9% sodium chloride injection or Invertose Injection were determined by HPLC, meanwhile the changes in the appearances and the pH values were observed. RESULTS: The contents of Cefoperazone Sodium and Tazobactam Sodium in Fructose-contained 0.9% sodium chloride injection or Invertose Injection were stable within 6 hours, and the mixed solutions were clear and their pH values were stable on the whole. CONCLUSION: Cefoperazone Sodium / Tazobactam Sodium can de mixed with Fructose-contained 0.9% sodium chloride injection or Invertose Injection for clinical use.
关 键 词:头孢哌酮/他唑巴坦钠 果糖注射液 转化糖注射液 配伍 稳定性
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