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https://hdl.handle.net/11499/8023
Title: | Application of statistical experimental design to the optimisation of microextraction by packed sorbent for the analysis of nonsteroidal anti-inflammatory drugs in human urine by ultra-high pressure liquid chromatography | Authors: | Magiera, S. Gülmez, Şefika Michalik, A. Baranowska, I. |
Keywords: | Microextraction by packed sorbent Nonsteroidal anti-inflammatory drugs Plackett-Burman design Ultra-high pressure liquid chromatography Gradient elution mode Limits of quantification Micro-extraction by packed sorbents Non-steroidal anti-inflammatory drugs Plackett-Burman designs Statistical experimental design Traditional methodologies Ultrahigh pressure Body fluids Chromatography Extraction High pressure liquid chromatography Optimization Sorbents Sorption Drug products acetonitrile acetylsalicylic acid diclofenac ibuprofen ketoprofen naproxen nonsteroid antiinflammatory agent sorbent trifluoroacetic acid aqueous solution article concentration (parameters) controlled study experimental design extraction and extracts human limit of detection limit of quantitation linear system measurement accuracy microextraction by packed sorbent molecular stability Plackett Burman design priority journal process optimization quantitative analysis reliability ultra performance liquid chromatography urinalysis validation study Anti-Inflammatory Agents, Non-Steroidal Chromatography, High Pressure Liquid Chromatography, Reverse-Phase Humans Limit of Detection Solid Phase Microextraction |
Abstract: | A new approach based on microextraction by packed sorbent (MEPS) and a reversed-phase ultra-high pressure liquid chromatography (UHPLC) method was developed and validated for the determination and quantification of nonsteroidal anti-inflammatory drugs (NSAIDs) (acetylsalicylic acid, ketoprofen, diclofenac, naproxen and ibuprofen) in human urine. The important factors that could influence the extraction were previously screened using the Plackett-Burman design approach. The optimal MEPS extraction conditions were obtained using C18 phase as a sorbent, small sample volume (20µL) and a short time period (approximately 5min) for the entire sample preparation step. The analytes were separated on a core-shell column (Poroshell 120 EC-C18; 100mm×3.0mm; 2.7µm) using a binary mobile phase composed of aqueous 0.1% trifluoroacetic acid and acetonitrile in the gradient elution mode (4.5min of analysis time). The analytical method was fully validated based on linearity, limits of detection (LOD), limits of quantification (LOQ), inter- and intra-day precision and accuracy, and extraction yield. Under optimised conditions, excellent linearity (R2>0.9991), limits of detection (1.07-16.2ngmL-1) and precision (0.503-9.15% RSD) were observed for the target drugs. The average absolute recoveries of the analysed compounds extracted from the urine samples were 89.4-107%. The proposed method was also applied to the analysis of NSAIDs in human urine. The new approach offers an attractive alternative for the analysis of selected drugs from urine samples, providing several advantages including fewer sample preparation steps, faster sample throughput and ease of performance compared to traditional methodologies. © 2013 Elsevier B.V. | URI: | https://hdl.handle.net/11499/8023 https://doi.org/10.1016/j.chroma.2013.06.047 |
ISSN: | 0021-9673 |
Appears in Collections: | Fen-Edebiyat Fakültesi Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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