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绿色高效液相色谱法测定人血浆中对乙酰氨基酚和布洛芬:在药代动力学中的应用

Green HPLC method for determination of paracetamol and ibuprofen in human plasma: applications to pharmacokinetics.

作者信息

Helmy Sally A, ElBedaiwy Heba M, Helmy Soha Am, Alamri Rama A, Alhusayni Renad Mh, Almashhadi Ibtihal Ay, Alharbi Aryam Sg, Alharbi Shouq Ad, Ahmed-Anwar Alaa A, Mohamed Mahmoud A

机构信息

Department of Pharmacy Practice, College of Pharmacy, Taibah University, Al Madinah Al Munawarah P.O. Box 42313, Saudi Arabia.

Department of Pharmaceutics, Faculty of Pharmacy, Damanhour University, Damanhour P.O. Box 22516, Egypt.

出版信息

Bioanalysis. 2024 Dec-Dec;16(23-24):1249-1260. doi: 10.1080/17576180.2024.2421704. Epub 2024 Nov 18.

Abstract

Using a straightforward, sensitive and precise liquid chromatographic approach, it is now possible to concurrently measure the amounts of ibuprofen (IBU) and paracetamol (PAR) in human plasma. A µ BondapakTM C18 column (300 mm × 3.9 mm, 15-20 μm) demonstrated acceptable separation when utilizing a mobile phase of 10 mM disodium hydrogen orthophosphate solution and acetonitrile at an 80:20, v/v ratio. The elution was isocratic at room temperature and a flow rate of 1.0 milliliters per minute. The UV detector was set to monitor PAR and IS (tinidazole) for 6.5 min at 254 nm, then IBU for the next 3 min at 220 nm. PAR and IBU showed linearity across the 0.05 to 100 µg/ml concentration range. The precision of the measurements ranged from 98.5% to 105% for PAR and from 95.1% to 102.8% for IBU. The average drug recovery rate was 100% for PAR and 98.9% for IBU. This method was effectively utilized to assess samples from an actual population administered PAR and IBU (325/200 mg) for pharmacokinetic research. The technique employs green and white tools to evaluate their environmental sustainability and efficacy. The suggested strategy was implemented utilizing the Six Sigma method.

摘要

采用一种直接、灵敏且精确的液相色谱方法,现在可以同时测定人血浆中布洛芬(IBU)和对乙酰氨基酚(PAR)的含量。当使用10 mM磷酸氢二钠溶液和乙腈按80:20(v/v)比例的流动相时,µ BondapakTM C18柱(300 mm×3.9 mm,15 - 20 µm)表现出可接受的分离效果。洗脱在室温下以等度方式进行,流速为每分钟1.0毫升。紫外检测器设置为在254 nm处监测PAR和内标物(替硝唑)6.5分钟,然后在220 nm处监测IBU接下来的3分钟。PAR和IBU在0.05至100 µg/ml浓度范围内呈线性。PAR测量的精密度范围为98.5%至105%,IBU为95.1%至102.8%。PAR的平均药物回收率为100%,IBU为98.9%。该方法有效地用于评估实际人群服用PAR和IBU(325/200 mg)进行药代动力学研究的样本。该技术采用绿色和白色工具来评估其环境可持续性和功效。所建议的策略采用六西格玛方法实施。

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