Stability study of common vasoactive drugs diluted in five types of solutions.

IF 4.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2025-09-19 eCollection Date: 2025-01-01 DOI:10.3389/fphar.2025.1670183
Han Yang, Bingbing Xiang, Deiying Gong, Guoyan Zhao, Wensheng Zhang
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引用次数: 0

Abstract

Background: Vasoactive drugs are widely used during the perioperative period. Different vasoactive drugs have specific recommended solutions for dilution as stated in their instructions, but non-recommended solutions are sometimes used in clinical practice. The impact of using non-recommended solutions on drug stability remains unclear. This study investigated the stability of various commonly used vasoactive drugs diluted with five commonly used solutions-0.9% sodium chloride injection, sodium lactate Ringer's injection, glucose sodium chloride injection, 5% glucose injection, and 10% glucose injection-under room temperature (24 °C ± 1 °C) without light protection.

Methods: Each drug was diluted to clinically common concentrations using the five solutions mentioned above. Five samples of 100 µL each were prepared for each drug. The samples were stored at room temperature without light protection and observed at 0, 2, 4, 6, and 8 h for changes in appearance and pH. High-performance liquid chromatography (HPLC) was used to measure the drug content at each time point. The drug content at 0 h was set as 100%, and the content at other time points was calculated relative to this baseline.

Results: Within 8 h, all solutions remained clear and transparent. Except for amiodarone hydrochloride, nicardipine hydrochloride, propafenone hydrochloride, and diltiazem hydrochloride, which showed significant pH changes after dilution, the pH changes of the other solutions were less than 0.1. Except for isoproterenol hydrochloride, the content of the other tested drugs showed no significant differences within 8 h.

Conclusion: When diluted with the five commonly used solutions and stored at room temperature without light protection for 8 h, the tested drugs maintained stable properties.

常用血管活性药物在五种溶液中稀释的稳定性研究。
背景:血管活性药物广泛应用于围手术期。不同的血管活性药物在其说明书中有特定的推荐稀释溶液,但在临床实践中有时使用非推荐的稀释溶液。使用非推荐溶液对药物稳定性的影响尚不清楚。本研究采用0.9%氯化钠注射液、乳酸钠林格氏注射液、葡萄糖氯化钠注射液、5%葡萄糖注射液、10%葡萄糖注射液5种常用溶液稀释多种常用血管活性药物,在室温(24℃±1℃)下无遮光条件下的稳定性。方法:采用上述5种溶液将每种药物稀释至临床常用浓度。每种药物制备5个样品,每个100µL。将样品置于室温下无遮光保存,分别于0、2、4、6、8 h观察样品外观和ph值的变化。采用高效液相色谱法测定各时间点药物含量。取0 h时的药物含量为100%,其他时间点相对于该基线计算含量。结果:在8 h内,所有溶液保持清澈透明。除盐酸胺碘酮、盐酸尼卡地平、盐酸普罗帕酮、盐酸地尔硫卓稀释后pH变化显著外,其余溶液pH变化均小于0.1。除盐酸异丙肾上腺素外,其余被试药物在8 h内含量无显著差异。结论:5种常用溶液稀释后,室温下无光照保存8 h,被试药物性能稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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