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采用简单绿色的反相高效液相色谱-光电二极管阵列检测法对六种禁忌/联合使用药物进行治疗药物监测;应用于加标人血浆

Therapeutic drug monitoring of six contraindicated/co-administered drugs by simple and green RP-HPLC-PDA; application to spiked human plasma.

作者信息

Hesham Nada, Hegazy Maha A, Wagdy Hebatallah A

机构信息

Pharmaceutical Chemistry Department, Faculty of Pharmacy, The British University in Egypt (BUE), Cairo, 11837, Egypt.

The Health Research Center of Excellence, Drug Research and Development Group, Faculty of Pharmacy, The British University in Egypt, Cairo, 11837, Egypt.

出版信息

BMC Chem. 2024 Apr 5;18(1):66. doi: 10.1186/s13065-024-01161-y.

Abstract

Therapeutic drug monitoring is an important clinical testing of the drugs to monitor their concentrations in plasma in order to guarantee their optimal impact, and to avoid any side effects resulting from drug-drug interactions. A green reversed-phase high-performance liquid chromatographic method using a photodiode array detector (RP-HPLC-PDA) was developed for the simultaneous determination of three carbapenem antibiotics (Imipenem, ertapenem, and meropenem) with the co-formulated drug (cilastatin) and contraindicated drugs (probenecid and warfarin) in spiked human plasma. The separation was achieved at 25 °C using a gradient elution of a mixture of mobile phase A: methanol and mobile phase B: phosphate buffer (pH 3.0). The photodiode array detector was adjusted at 220 nm. Bioanalytical method validation was carried out as per the FDA guidelines, and the method showed good linearity ranges for the six drugs that included their Cmax levels along with low limits of quantification. Based on the results, the method was found to be accurate and precise; with high % recovery and good % RSD, respectively. The method was successfully applied to spiked human plasma, signifying a good potential to be implemented in future TDM studies of these drugs when co-administered together.

摘要

治疗药物监测是一项重要的临床检测,用于监测药物在血浆中的浓度,以确保其最佳疗效,并避免药物相互作用产生的任何副作用。开发了一种使用光电二极管阵列检测器的绿色反相高效液相色谱法(RP-HPLC-PDA),用于同时测定加标人血浆中三种碳青霉烯类抗生素(亚胺培南、厄他培南和美罗培南)以及共同配制的药物(西司他丁)和禁忌药物(丙磺舒和华法林)。在25°C下,使用流动相A(甲醇)和流动相B(pH 3.0的磷酸盐缓冲液)的混合物进行梯度洗脱实现分离。光电二极管阵列检测器设置在220nm。按照FDA指南进行生物分析方法验证,该方法对六种药物显示出良好的线性范围,包括它们的Cmax水平以及低定量限。基于结果,该方法被发现准确且精密;分别具有高回收率和良好的相对标准偏差百分比。该方法成功应用于加标人血浆,表明在这些药物联合给药的未来治疗药物监测研究中具有良好的实施潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32cf/10998319/c0ead71db733/13065_2024_1161_Fig1_HTML.jpg

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