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Parallel artificial liquid membrane extraction coupled with UPLC-ESI-MS/MS method for high-throughput quantitation of repaglinide in diabetic patients.
Ahmed, Sameh A; Abdallah, Nehad A; Almaghrabi, Mohammed; Alahmadi, Yaser M.
Afiliação
  • Ahmed SA; Pharmacognosy and Pharmaceutical Chemistry Department, College of Pharmacy Taibah University, AlMadinah AlMunawarah, 30001, Saudi Arabia. Electronic address: shassan@taibahu.edu.sa.
  • Abdallah NA; Pharmacognosy and Pharmaceutical Chemistry Department, College of Pharmacy Taibah University, AlMadinah AlMunawarah, 30001, Saudi Arabia.
  • Almaghrabi M; Pharmacognosy and Pharmaceutical Chemistry Department, College of Pharmacy Taibah University, AlMadinah AlMunawarah, 30001, Saudi Arabia.
  • Alahmadi YM; Pharmacy Practice Department, College of Pharmacy, Taibah University, AlMadinah AlMunawarah, 30001, Saudi Arabia.
Talanta ; 269: 125498, 2024 Mar 01.
Article em En | MEDLINE | ID: mdl-38056419
ABSTRACT
A high-throughput therapeutic monitoring method was developed for repaglinide (RPG) in diabetic patients, combining parallel artificial liquid membrane extraction (PALME) with ultraperformance liquid chromatography electrospray ionization tandem mass spectrometry (UPLC-ESI-MS/MS). PALME was performed using a 96-well donor plate comprising a donor solution containing a plasma sample, 50 mM phosphate buffer (pH = 8.0), and cetirizine (CTZ) as internal standard. A polypropylene (PP) porous membrane served as a selective support for the liquid membrane (SLM), preventing nonspecific binding produced by other membranes. The extraction was accomplished across SLM made of PP membrane with dodecyl acetate and 1 % trioctylamine (w/w), and the acceptor solution comprised DMSO and 200 mM formic acid (5050, v/v). The simple workflow for PALME provided analyte enrichment, highly efficient sample cleanup, high throughput analysis, and excellent reproducibility. Method validation met FDA criteria, with a linear plasma calibration range (0.1-100 ng mL-1, r = 0.9995) and a lower limit of quantitation (LLOQ) of 0.1 ng mL-1. Recovery results at 98.9 % affirmed method reliability. The ability to analyze 198 samples per hour, coupled with a reduced amount of solvents, underscores the method's high throughput and eco-friendly profile. The PALME-UPLC-ESI-MS/MS method was successfully applied to therapeutic drug monitoring of RPG in diabetic patients following 2 mg RPG tablet administration, establishing its effectiveness.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Espectrometria de Massas em Tandem Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Espectrometria de Massas em Tandem Idioma: En Ano de publicação: 2024 Tipo de documento: Article