Physical compatibility of ibuprofen and selected parenteral drugs during simulated y-site administration

IF 0.4 4区 医学 Q4 PHARMACOLOGY & PHARMACY Acta poloniae pharmaceutica Pub Date : 2023-06-29 DOI:10.32383/appdr/167804
K. Dettlaff, K. Dominiak, Marta Klimaszewska, A. Gostyńska
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Abstract

Intravenous ibuprofen (IBF) is indicated for short-term acute moderate pain and fever management. Limited data concerning the compatibility of intravenous IBF and other parenteral medications makes it inconvenient to use in polypharmacy-required patients. The simultaneous administration of two incompatible drugs is a health- or even life-threatening medical error. This study was performed to evaluate the physical compatibility of two intravenous IBF doses (600 mg/100 mL, 400 mg/100 mL) during Y-site administration with common parenteral medications. Eight infusion fluids, seven ready-to-use solutions for infusion, and thirty concentrates or powders for solutions for infusion were examined. All these drugs, if relevant, were reconstituted and diluted following the manufacturer's instructions to achieve concentrations found most commonly in clinical practice. Samples were prepared by mixing IBFs and selected drug product solutions at the 1:1 volume ratio. All samples underwent visual inspection and determination of pH and turbidity before combining with IBF and in time points (0, 30, 60, and 120 minutes) after simulated Y-site administration with IBF. In the case of propofol, which is an emulsion for infusion, lipid droplet size, zeta potential, and polydispersity index were also determined. The incompatibilities were observed for IBF combinations with amiodarone, ciprofloxacin, clemastine, gentamicin, vinpocetine, and calcium chloride.
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模拟y位点给药过程中布洛芬与选定的肠外药物的物理相容性
静脉注射布洛芬(IBF)适用于短期急性中度疼痛和发烧治疗。关于静脉注射IBF和其他胃肠外药物的兼容性的有限数据使得在需要多药治疗的患者中使用不方便。同时服用两种不相容的药物是一种健康甚至危及生命的医疗错误。本研究旨在评估Y位给药期间两种静脉注射IBF剂量(600 mg/100 mL、400 mg/100 mL)与普通胃肠外药物的物理兼容性。检查了8种输液、7种用于输液的即用溶液和30种用于输液溶液的浓缩物或粉末。所有这些药物,如果相关的话,按照制造商的说明进行重组和稀释,以达到临床实践中最常见的浓度。通过将IBF和选定的药物产品溶液以1:1的体积比混合来制备样品。所有样品在与IBF联合用药前以及在模拟Y位点IBF给药后的时间点(0、30、60和120分钟)进行目视检查并测定pH和浊度。在丙泊酚(一种用于输注的乳液)的情况下,还测定了脂滴大小、ζ电位和多分散指数。观察到IBF与胺碘酮、环丙沙星、氯马汀、庆大霉素、长春西汀和氯化钙的组合存在不相容性。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
74
审稿时长
6-12 weeks
期刊介绍: The international journal of the Polish Pharmaceutical Society is published in 6 issues a year. The journal offers Open Access publication of original research papers, short communications and reviews written in English, in all areas of pharmaceutical sciences. The following areas of pharmaceutical sciences are covered: Analysis, Biopharmacy, Drug Biochemistry, Drug Synthesis, Natural Drugs, Pharmaceutical Technology, Pharmacology and General. A bimonthly appearing in English since 1994, which continues “Acta Poloniae Pharmaceutica”, whose first issue appeared in December 1937. The war halted the activity of the journal’s creators. Issuance of “Acta Poloniae Pharmaceutica” was resumed in 1947. From 1947 the journal appeared irregularly, initially as a quarterly, then a bimonthly. In the years 1963 – 1973 alongside the Polish version appeared the English edition of the journal. Starting from 1974 only works in English are published in the journal. Since 1995 the journal has been appearing very regularly in two-month intervals (six books a year). The journal publishes original works from all fields of pharmacy, summaries of postdoctoral dissertations and laboratory notes.
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