Evidence map›Paper›PMID 36364020›Full record

ArticleMolecules (Basel, Switzerland)2022

Rapid Determination of Non-Steroidal Anti-Inflammatory Drugs in Urine Samples after In-Matrix Derivatization and Fabric Phase Sorptive Extraction-Gas Chromatography-Mass Spectrometry Analysis.

Bharti Jain, Rajeev Jain, Abuzar Kabir, Shweta Sharma

Abstract read
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Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Bharti JainInstitute of Forensic Science & Criminology, Panjab University, Chandigarh 160014, India.
Rajeev JainCentral Forensic Science Laboratory, Forensic Toxicology Division, Plot #2, Sector 36-A, Dakshin Marg, Chandigarh 160036, India.ORCID 0000-0001-8146-0946
Abuzar KabirDepartment of Chemistry and Biochemistry, Florida International University, Miami, FL 33199, USA.ORCID 0000-0002-3740-8857
Shweta SharmaInstitute of Forensic Science & Criminology, Panjab University, Chandigarh 160014, India.ORCID 0000-0002-1936-2947

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabric phase sorptive extraction (FPSE) has become a popular sorptive-based microextraction technique for the rapid analysis of a wide variety of analytes in complex matrices. The present study describes a simple and green analytical protocol based on in-matrix methyl chloroformate (MCF) derivatization of non-steroidal anti-inflammatory (NSAID) drugs in urine samples followed by FPSE and gas chromatography-mass spectrometry (GC-MS) analysis. Use of MCF as derivatizing reagent saves substantial amounts of time, reagent and energy, and can be directly performed in aqueous samples without any sample pre-treatment. The derivatized analytes were extracted using sol−gel Carbowax 20M coated FPSE membrane and eluted in 0.5 mL of MeOH for GC-MS analysis. A chemometric design of experiment-based approach was utilized comprising a Placket−Burman design (PBD) and central composite design (CCD) for screening and optimization of significant variables of derivatization and FPSE protocol, respectively. Under optimized conditions, the proposed FPSE-GC-MS method exhibited good linearity in the range of 0.1−10 µg mL−1 with coefficients of determination (R2) in the range of 0.998−0.999. The intra-day and inter-day precisions for the proposed method were lower than <7% and <10%, respectively. The developed method has been successfully applied to the determination of NSAIDs in urine samples of patients under their medication. Finally, the green character of the proposed method was evaluated using ComplexGAPI tool. The proposed method will pave the way for simper analysis of polar drugs by FPSE-GC-MS.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalWater Pollutants, ChemicalFormatesGas Chromatography-Mass SpectrometryHumansWaterAnti-Inflammatory Agents, Non-SteroidalFormatesmethyl chloroformateWaterWater Pollutants, Chemicalderivatizationfabric phase sorptive extractiongas chromatography-mass spectrometrynon-steroidal anti-inflammatory drugsurine analysis

Identifiers

PMID36364020
PMCPMC9657276

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.