Physical Compatibility of Ertapenem and Meropenem in 0.45% Normal Saline and Plasma-Lyte A.

Q4 Medicine
Berah Brown, Jacquelyn Schemmel, Justin P Reinert, Gabriella Baki, Mitchell S Howard, Mariann D Churchwell
{"title":"Physical Compatibility of Ertapenem and Meropenem in 0.45% Normal Saline and Plasma-Lyte A.","authors":"Berah Brown, Jacquelyn Schemmel, Justin P Reinert, Gabriella Baki, Mitchell S Howard, Mariann D Churchwell","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Intravenous medications and fluids must be compatible to ensure patient safety and optimal clinical outcomes. The physical compatibility of ertapenem and meropenem has not been conclusively established in 0.45% sodium chloride and Plasma-Lyte A.</p><p><strong>Methods: </strong>An in vitro analysis of the physical compatibility of ertapenem and meropenem at 10 mg/mL and 20 mg/mL concentrations was conducted in 0.45% sodium chloride and Plasma-Lyte A over 24 hours. Admixtures were prepared in triplicate at hours 0, 1, 5, 8, and 24 and were visually inspected, underwent spectrophotometric testing, and pH analysis.</p><p><strong>Results: </strong>All ertapenem admixtures were found to be physically compatible over 24 hours. Meropenem 10 mg/mL had demonstrable changes in pH and was found to be physically incompatible beyond 8 hours in 0.45% sodium chloride and Plasma-Lyte A. Meropenem 20 mg/mL was found to be physically incompatible beyond 5 hours when mixed in 0.45% sodium chloride.</p><p><strong>Conclusions: </strong>Our results are the first that have demonstrated physical compatibility for ertapenem 10 mg/mL and 20 mg/mL in 0.45% sodium chloride and Plasma-Lyte A. The findings of this meropenem analysis confirm a previous report that evaluated simulated Y-site samples at 1 hour but expanded upon those findings to show physical compatibility at 8 hours and 5 hours for the 10 mg/mL in both fluids and 20 mg/mL in 0.45% sodium chloride concentrations, respectively. Previously published reports of the stability of meropenem indicating a concentration and temperature-dependent are confirmed by this analysis. Chemical stability studies should be undertaken to support these results.</p>","PeriodicalId":14381,"journal":{"name":"International journal of pharmaceutical compounding","volume":"29 5","pages":"430-434"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of pharmaceutical compounding","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Intravenous medications and fluids must be compatible to ensure patient safety and optimal clinical outcomes. The physical compatibility of ertapenem and meropenem has not been conclusively established in 0.45% sodium chloride and Plasma-Lyte A.

Methods: An in vitro analysis of the physical compatibility of ertapenem and meropenem at 10 mg/mL and 20 mg/mL concentrations was conducted in 0.45% sodium chloride and Plasma-Lyte A over 24 hours. Admixtures were prepared in triplicate at hours 0, 1, 5, 8, and 24 and were visually inspected, underwent spectrophotometric testing, and pH analysis.

Results: All ertapenem admixtures were found to be physically compatible over 24 hours. Meropenem 10 mg/mL had demonstrable changes in pH and was found to be physically incompatible beyond 8 hours in 0.45% sodium chloride and Plasma-Lyte A. Meropenem 20 mg/mL was found to be physically incompatible beyond 5 hours when mixed in 0.45% sodium chloride.

Conclusions: Our results are the first that have demonstrated physical compatibility for ertapenem 10 mg/mL and 20 mg/mL in 0.45% sodium chloride and Plasma-Lyte A. The findings of this meropenem analysis confirm a previous report that evaluated simulated Y-site samples at 1 hour but expanded upon those findings to show physical compatibility at 8 hours and 5 hours for the 10 mg/mL in both fluids and 20 mg/mL in 0.45% sodium chloride concentrations, respectively. Previously published reports of the stability of meropenem indicating a concentration and temperature-dependent are confirmed by this analysis. Chemical stability studies should be undertaken to support these results.

厄他培南和美罗培南在0.45%生理盐水和血浆A中的物理相容性。
背景:静脉注射药物和液体必须兼容,以确保患者安全和最佳临床结果。厄他培南与美罗培南在0.45%氯化钠和血浆碱液A中的物理相容性尚未确定。方法:在0.45%氯化钠和血浆碱液A中,以10 mg/mL和20 mg/mL浓度测定厄他培南与美罗培南24h的体外物理相容性。在0、1、5、8和24小时制备一式三份的外加剂,并进行目测、分光光度测试和pH分析。结果:所有厄他培南外加剂在24小时内均具有物理相容性。美罗培南10 mg/mL pH值变化明显,与0.45%氯化钠和血浆碱液a混合8小时后,发现美罗培南20 mg/mL与0.45%氯化钠混合5小时后发现物理不相容。结论:我们的研究结果首次证实了埃他培南10mg /mL和20mg /mL在0.45%氯化钠和血浆-碱液a中的物理相容性。这项美罗培南分析的结果证实了先前的报告,该报告在1小时时评估了模拟y位点样品,但扩展了这些发现,分别显示了10mg /mL液体和20mg /mL 0.45%氯化钠浓度在8小时和5小时时的物理相容性。先前发表的关于美罗培南的稳定性的报告表明其与浓度和温度有关,这一分析证实了这一点。应进行化学稳定性研究以支持这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.40
自引率
0.00%
发文量
62
期刊介绍: The International Journal of Pharmaceutical Compounding (IJPC) is a bi-monthly, scientific and professional journal emphasizing quality pharmaceutical compounding. IJPC is the only publication that covers pharmaceutical compounding topics relevant and necessary to empower pharmacists to meet the needs of today"s patients. No other publication features hands-on, how-to compounding techniques or the information that contemporary pharmacists need to provide individualized care.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书