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Physical and Chemical Compatibility of Injectable Acetaminophen During Simulated Y-Site Administration

机译:模拟Y部位给药期间对乙酰氨基酚的物理和化学相容性

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Purpose: The physical and chemical compatibility of intravenous acetaminophen with commonly administered injectable medications was evaluated.Methods: Simulated Y-site evaluation was accomplished by mixing 2 mL of acetaminophen (10 mg/mL) with 2 mL of an alternative intravenous medication and subsequently storing the mixture in a polypropylene syringe for 4 hours. The aliquot solutions were visually inspected and evaluated for crystal content at 4 hours by infusing 4 mL of the medication mixture through a 0.45-fxm nitrocellulose filter disc. Medication mixtures that were selected for chemical stability testing were analyzed by high-performance liquid chromatography at 0,1, and 4 hours using a Zorbax Eclipse Plus C18, 4.6 x 100 mm, 3.5-|xm column for separation of analytes with subsequent diode-array detection. Medications were considered chemically compatible if the concentrations of all components were >90% of the original concentrations during the 4 hour simulated Y-site compatibility test. Results: U.S. Pharmacopeial Convention (USP) standards for physical particle counts were met for acetaminophen injection (10 mg/mL) when combined with cefoxitin, ceftriaxone, clindamycin, dexamethasone, diphenhydramine, dolasetron, fentanyl, granisetron, hydrocortisone, hydro-morphone, ketorolac, meperidine, methylprednisolone, midazolam, morphine, nalbuphine, ondansetron, piperacillin/tazobactam, ranitidine, and vancomycin. Injectable acetaminophen is incompatible with acyclovir and diazepam and therefore should not be administered concomitantly with either of these products. Further testing confirmed the chemical compatibility of acetaminophen with ceftriaxone, diphenhydramine, granisetron, ketorolac, nalbuphine, ondansetron, piperacillin/ tazobactam, and vancomycin.Conclusion: All medications tested with acetaminophen were physically compatible except for acyclovir and diazepam. All 8 medications tested for chemical compatibility with acetaminophen were stable over the 4 hour simulated Y-site administration study.
机译:目的:评估静脉对乙酰氨基酚与常用注射药物的物理和化学相容性方法:通过将2 mL对乙酰氨基酚(10 mg / mL)与2 mL替代静脉内药物混合并随后储存来完成模拟Y部位评估将混合物在聚丙烯注射器中放置4小时。目视检查等分溶液,并通过0.45-fxm硝化纤维素滤盘注入4mL药物混合物,在4小时时评估晶体含量。使用Zorbax Eclipse Plus C18、4.6 x 100 mm,3.5- | xm色谱柱,在0.1和4小时通过高效液相色谱分析选择用于化学稳定性测试的药物混合物,以分离分析物,随后使用二极管-阵列检测。如果在4小时的模拟Y位点相容性测试中,所有成分的浓度均大于原始浓度的90%,则认为药物具有化学相容性。结果:与头孢西丁,头孢曲松,克林霉素,地塞米松,苯海拉明,多拉西酮,芬太尼,格拉司琼,氢化可的松,氢吗啡酮,酮吗啉联合使用时,对乙酰氨基酚注射液(10 mg / mL)的对乙酰氨基酚注射量符合美国药典公约(USP)标准,哌替西林,甲基强的松龙,咪达唑仑,吗啡,纳布啡,恩丹西酮,哌拉西林/他唑巴坦,雷尼替丁和万古霉素。注射用对乙酰氨基酚与阿昔洛韦和地西epa不相容,因此不应与上述任何一种产品同时使用。进一步的测试证实了对乙酰氨基酚与头孢曲松,苯海拉明,格拉司琼,酮咯酸,纳布啡,恩丹西酮,哌拉西林/他唑巴坦和万古霉素的化学相容性。结论:除阿昔洛韦和地西epa以外,所有对乙酰氨基酚测试的药物均具有物理相容性。在对乙酰氨基酚的化学相容性测试中,所有8种药物在经过4小时的模拟Y站点给药研究中均保持稳定。

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