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卡络磺钠注射液与注射用加替沙星的配伍稳定性考察 被引量:9

Study on the Compatibility of Carbazochrome Sodium Sulfonate Injection and Gatifloxacin for Injection
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摘要 目的:考察卡络磺钠注射液与注射用加替沙星在0.9%氯化钠注射液中的配伍稳定性。方法:采用反相高效液相色谱法-二极管阵列检测器同时测定卡络磺钠注射液与注射用加替沙星在0.9%氯化钠注射液中配伍后,分别在25、37℃放置12h内各时间段的含量,并测定pH值,观察配伍液的外观变化。结果:在25、37℃下、12h内,配伍液外观、pH值及含量均无明显变化。结论:在25、37℃下,卡络磺钠注射液与注射用加替沙星在0.9%氯化钠注射液中在12h内可配伍使用。 OBJECTIVE: To study the compatibility of Carbazochrome sodium sulfonate injection and Gatifloxacin for injection in 0.9% sodium chloride injection. METHODS: Carbazochrome sodium sulfonate injection was combined with gatifloxacin for injection in 0.9% sodium chloride injection. The contents of carbazochrome sodium sulfonate and gatifloxacin in mixture were determined by RP-HPLC-DAD at 25 ℃ or 37 ℃ within 12 h and external appearance and pH were observed. RESULTS: There was no significant change in appearance, pH and the content of carbazochrome sodium sulfonate and gatifloxacin under two temperature conditions within 12 h. CONCLUSION: Carbazochrome sodium sulfonate injection combined with gatifloxacin for injection in 0.9% sodium chloride injection can be used within 12 h at 25 ℃ and 37 ℃.
出处 《中国药房》 CAS CSCD 北大核心 2011年第2期149-151,共3页 China Pharmacy
关键词 反相高效液相色谱法 二极管阵列检测器 卡络磺钠 加替沙星酒己伍 稳定性 RP-HPLC DAD Carbazochrome sodium sulfonate Gatifloxacin Compatibility Stability
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  • 1Christoph KN, Michaela S, Martina K, et al. Concentrations of gatifloxacin in plasma and urine and penetration into prostatic and seminal fluid, ejaculate, and sperm cells after single oral administrations of 400 milligrams to volunteers[J]. Antimicrob Agents Chemother, 2001,45 ( 1 ) : 293.
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  • 4Annette L, Ivonne K, Klaus B, et al. Comparative pharmacokinetics of cipmfloxacin, gatifloxacin, grepafloxaein, levofloxacin,trovafloxacin, and moxifloxacin after single oral administration in healthy volunteers [ J ]. Antimicrob Agents Chemother , 2000, 44(10):2600.
  • 5杜煜,郭惠元.广谱、高效、低毒的新喹诺酮类抗菌药加替沙星[J].国外医药(抗生素分册),2001,22(1):34-39. 被引量:112

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