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液相色谱-串联质谱法检测和定量口腔液样本中的美洛昔康和5'-羧基美洛昔康

Liquid Chromatography-Tandem Mass Spectrometry Method for Detection and Quantification of Meloxicam and 5'-Carboxymeloxicam in Oral Fluid Samples.

作者信息

Oliveira Gabriela Moraes, Dionísio Thiago José, Siqueira-Sandrin Viviane Silva, Ferrari Leticia Alves de Lima, Colombini-Ishikiriama Bella Luna, Faria Flávio Augusto Cardoso, Santos Carlos Ferreira, Calvo Adriana Maria

机构信息

Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo (HRAC/USP), Bauru 17012-900, SP, Brazil.

Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Bauru 17012-901, SP, Brazil.

出版信息

Metabolites. 2023 Jun 15;13(6):755. doi: 10.3390/metabo13060755.

Abstract

A sensitive, selective and particularly fast method of liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed and validated for the determination of meloxicam and its main metabolite, 5'-carboxymeloxicam, in oral fluid samples. Meloxicam and its major metabolite were separated using a Shim-Pack XR-ODS 75 L × 2.0 column and C18 pre-column at 40 °C using a mixture of methanol and 10 mM ammonium acetate (80:20, /) with an injection flow rate of 0.3 mL/min. The total time of the analytical run was 5 min. Sixteen volunteers had oral fluid samples collected sequentially before and after taking a meloxicam tablet (15 mg) for up to 96 h. With the concentrations obtained, the pharmacokinetic parameters were determined using the Phoenix WinNonlin software. The parameters evaluated for meloxicam and 5'-carboxymeloxicam in the oral fluid samples showed linearity, accuracy, precision, medium-quality control (MQC-78.12 ng/mL), high-quality control (HQC-156.25 ng/mL), lower limits of quantification (LLOQ-0.6103 ng/mL), low-quality control (LQC-2.44 ng/mL), stability and dilution. Prostaglandin E (PGE) was also detected and quantified in the oral fluid samples, demonstrating the possibility of a pharmacokinetic/pharmacodynamic (PK/PD) study with this methodology. All the parameters evaluated in the validation of the methodology in the oral fluid samples proved to be stable and within the possible variations in each of the described parameters. Through the data presented, the possibility of a PK/PD study was demonstrated, detecting and quantifying meloxicam, its main metabolite and PGE in oral fluid samples using LC-MS/MS.

摘要

开发并验证了一种灵敏、选择性强且特别快速的液相色谱-串联质谱法(LC-MS/MS),用于测定口腔液样本中的美洛昔康及其主要代谢物5'-羧基美洛昔康。美洛昔康及其主要代谢物在40℃下,使用Shim-Pack XR-ODS 75L×2.0色谱柱和C18预柱,以甲醇和10mM醋酸铵(80:20,v/v)的混合物为流动相,进样流速为0.3mL/min进行分离。分析运行总时间为5分钟。16名志愿者在服用美洛昔康片(15mg)之前和之后连续采集口腔液样本,长达96小时。根据获得的浓度,使用Phoenix WinNonlin软件确定药代动力学参数。在口腔液样本中对美洛昔康和5'-羧基美洛昔康评估的参数显示出线性、准确性、精密度、中等质量控制(MQC - 78.12ng/mL)、高质量控制(HQC - 156.25ng/mL)、定量下限(LLOQ - 0.6103ng/mL)、低质量控制(LQC - 2.44ng/mL)、稳定性和稀释性。还在口腔液样本中检测并定量了前列腺素E(PGE),证明了使用该方法进行药代动力学/药效学(PK/PD)研究的可能性。在口腔液样本中对该方法验证时评估的所有参数均证明是稳定的,且在所描述的每个参数的可能变化范围内。通过所呈现的数据,证明了进行PK/PD研究的可能性,即使用LC-MS/MS检测和定量口腔液样本中的美洛昔康、其主要代谢物和PGE。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1739/10302853/137dd2eeab0e/metabolites-13-00755-g001.jpg

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