| Autor: |
Jain B; Institute of Forensic Science & Criminology, Panjab University, Chandigarh 160014, India., Jain R; Central Forensic Science Laboratory, Forensic Toxicology Division, Plot #2, Sector 36-A, Dakshin Marg, Chandigarh 160036, India., Kabir A; Department of Chemistry and Biochemistry, Florida International University, Miami, FL 33199, USA., Sharma S; Institute of Forensic Science & Criminology, Panjab University, Chandigarh 160014, India. |
| Jazyk: |
angličtina |
| Zdroj: |
Molecules (Basel, Switzerland) [Molecules] 2022 Oct 24; Vol. 27 (21). Date of Electronic Publication: 2022 Oct 24. |
| DOI: |
10.3390/molecules27217188 |
| Abstrakt: |
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. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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