Please use this identifier to cite or link to this item: 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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