Sharkawi Marco M Z, Mohamed Norhan R, El-Saadi Mohammed T, Amin Noha H
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Beni-Suef University, Alshaheed Shehata Ahmed Hegazy St., Beni-Suef 62514, Egypt.
Department of Medicinal Chemistry, Faculty of Pharmacy, Beni-Suef University, Beni-Suef 62514, Egypt.
Anal Methods. 2023 Feb 23;15(8):1016-1027. doi: 10.1039/d3ay00081h.
To date no analytical method has been developed for the determination of the BEGEV regimen and no study has investigated the kinetic interaction between the drugs, to give us priorities for further clinical study, so two rapid, accurate, sensitive and ecofriendly chromatographic methods were developed for the simultaneous determination of bendamustine (BEN), gemcitabine (GEM) and vinorelbine (VIB) using sildenafil (SIL) as an internal standard (IS) for the purpose of an pharmacokinetics study in rats. Firstly, the LC-MS/MS method was performed using a mixture of methanol and a 0.1% aqueous solution of formic acid as the mobile phase on a ZORBAX Eclipse Plus C (4.6 mm × 150 mm, 5 μm) column as the stationary phase. BEN, GEM and VIB were ionized by positive ions and detected in the multi-reaction monitoring (MRM) mode using precursor → products of / 358.20 → 228.25 for BEN, / 264.05 → 112.15 for GEM, / 779.55 → 122.20 for VIB and / 475.00 → 58.35 for SIL. Secondly, TLC-densitometry was applied on TLC silica gel plates using methanol : ethyl acetate (8 : 2, v/v) as the developing system when the separated peaks were scanned at 280 nm. FDA guidelines were followed for validation of the proposed methods, which presented acceptable ranges; then they were applied for an study in rats with a quantitative determination of each drug after single or combined administration for an investigation of any suspected drug-drug interaction, and all pharmacokinetic parameters were calculated for therapeutic drug monitoring of those drugs. Green analytical chemistry principles were considered during all the procedural steps to ensure the greenness and the safety of the methods, which were evaluated using four assessment tools, eco-scale assessment, the national environmental method index (NEMI), the green analytical procedure index (GAPI) and the analytical greenness metric approach (AGREE), and the results were satisfactory.
迄今为止,尚未开发出用于测定BEGEV方案的分析方法,也没有研究调查过这些药物之间的动力学相互作用,以便为我们进一步的临床研究提供优先事项。因此,开发了两种快速、准确、灵敏且环保的色谱方法,以西地那非(SIL)作为内标(IS),同时测定大鼠体内的苯达莫司汀(BEN)、吉西他滨(GEM)和长春瑞滨(VIB),用于大鼠的药代动力学研究。首先,采用甲醇和0.1%甲酸水溶液的混合物作为流动相,在ZORBAX Eclipse Plus C(4.6 mm×150 mm,5μm)柱作为固定相上进行LC-MS/MS分析。BEN、GEM和VIB通过正离子电离,并在多反应监测(MRM)模式下进行检测,使用的前体→产物分别为:BEN为/358.20→228.25,GEM为/264.05→112.15,VIB为/779.55→122.20,SIL为/475.00→58.35。其次,在TLC硅胶板上应用薄层色谱扫描法,以甲醇∶乙酸乙酯(8∶2,v/v)作为展开系统,在280 nm处扫描分离的峰。所提出的方法按照FDA指南进行验证,验证结果在可接受范围内;然后将其应用于大鼠研究,在单次或联合给药后对每种药物进行定量测定,以研究任何可疑的药物相互作用,并计算所有药代动力学参数,用于这些药物的治疗药物监测。在所有程序步骤中都考虑了绿色分析化学原则,以确保方法的绿色性和安全性,使用四种评估工具进行评估,即生态规模评估、国家环境方法指数(NEMI)、绿色分析程序指数(GAPI)和分析绿色度度量方法(AGREE),结果令人满意。