过氧化氢血浆灭菌破坏盐酸利多卡因注射液的疗效

Dini Aprilia, Ririn Sumiyani, Niniek Tripuspitasari, Ade MWD Pambudi, Christina Avanti
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引用次数: 0

摘要

背景:2%盐酸利多卡因注射液作为麻醉药物,必须保证其无菌性,避免微生物污染。为了保持2%盐酸利多卡因在医院使用前的无菌配制,一些麻醉师选择再消毒。目的:采用超高效液相色谱法(UPLC)研究双氧水灭菌对血浆中利多卡因盐酸水平的影响。方法:将2%盐酸利多卡因样品分为两组,一组用双氧水再灭菌,另一组仅用无菌技术处理。色谱分析采用Waters Corp Acquity UPLC®h级色谱系统和Waters Corp Acquity UPLC®BEH C18色谱柱,流动相为20%乙腈和80%醋酸缓冲液pH 3.4,流速为0.3 mL/min,总持续时间为4.5分钟。结果:经再消毒后,利多卡因盐酸浓度下降1.88%,未再消毒后,利多卡因盐酸浓度下降2.01%。结论:经双氧水血浆灭菌后,利多卡因盐酸浓度明显降低,不符合药典标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrogen Peroxide Plasma Sterilization Sabotages the Efficacy of Lidocaine HCl Injection
Background: Lidocaine injection with 2% HCl as an anesthetic drug must guarantee its sterility to avoid microbial contamination. In efforts to maintain the sterile preparation of Lidocaine HCl 2% before use in hospitals, some anesthesiologists opt for re-sterilization. Objective: This study aimed to evaluate the impact of plasma sterilization using hydrogen peroxide on Lidocaine HCl levels employing a validated Ultra Performance Liquid Chromatography (UPLC) assay. Methods: The 2% Lidocaine HCl samples were separated into two groups, one undergoing re-sterilization with hydrogen peroxide and the other handled only with aseptic techniques. The chromatographic assay was performed using a Waters Corp Acquity UPLC® H-Class system and a Waters Corp Acquity UPLC ® BEH C18 column, with a mobile phase of 20% Acetonitrile and 80% Acetate Buffer pH 3.4, flow rate of 0.3 mL/min, and total duration of 4.5 minutes. Results: The results showed a decrease in Lidocaine HCl levels to 1.88% after re-sterilization and 2.01% without re-sterilization. Conclusion: These findings suggest that re-sterilization with hydrogen peroxide plasma sterilization leads to a significant decrease in Lidocaine HCl levels, causing non-compliance with pharmacopoeia standards.
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