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Greener analysis of eleven basic drugs in blood and urine using carbowax 20M based biofluid sampler (BFS) device.
Jain, Bharti; Jain, Rajeev; Kabir, Abuzar; Ali, Nemat; Rashid Khan, Mohammad; Sharma, Shweta.
Affiliation
  • Jain B; Central Forensic Science Laboratory, Directorate of Forensic Science Services, Ministry of Home Affairs, Govt. of India, Dakshin Marg, Sector - 36A, Chandigarh 160036, India; Institute of Forensic Science & Criminology, Panjab University, Chandigarh 160014, India.
  • Jain R; Central Forensic Science Laboratory, Directorate of Forensic Science Services, Ministry of Home Affairs, Govt. of India, Dakshin Marg, Sector - 36A, Chandigarh 160036, India. Electronic address: rajeev.jain-as@gov.in.
  • Kabir A; Global Forensic and Justice Center, Department of Chemistry and Biochemistry, Florida International University, Miami, FL, USA.
  • Ali N; Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
  • Rashid Khan M; Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
  • Sharma S; Institute of Forensic Science & Criminology, Panjab University, Chandigarh 160014, India. Electronic address: 25shweta@pu.ac.in.
Article in En | MEDLINE | ID: mdl-39353248
ABSTRACT
For the first time, a novel biofluid sampler (BFS) and sample preparation device is applied for the analysis of 11 basic drugs (i.e., pheniramine, chlorpheniramine, fluoxetine, tramadol, amitriptyline, ketamine, diazepam, chlordiazepoxide, clozapine, chlorpromazine, dothiepin) in biological matrices (i.e., blood and urine). BFS utilizes advanced, highly effective sorbents derived from sol-gel sorbent coating technology onto cellulose fabric substrate, improving sample collection and retention. BFS has the capability to retain a biological sample from 10 to 1000 µL without requiring any dilution or pre-treatment of the sample. The biological samples were pipetted onto the BFS device and dried at room temperature. Subsequently, adsorbed analytes were back-extracted into 1000 µL of methanol without requiring any imposed external diffusion process and then analyzed by gas chromatography-mass spectrometry (GC-MS). A one-factor-at-a-time (OFAT) screening procedure was used to extensively screen and optimize several parameters, including sample volume, elution time, solvent volume, and solvent type. Under the optimal conditions of the study, the method was found to be linear within the range 0.1-10 µg mL-1 for both blood and urine. Quantification limits were established for blood samples within the range of 0.072-0.095 µg mL-1 and for urine samples within the range of 0.050-0.069 µg mL-1. The precisions within and between days were less than 7% and 10%, respectively. The target analytes showed good recoveries utilizing the recommended protocol, with ranges of 45.1%-103.4%. Furthermore, the methodology has been effectively implemented in forensic toxicology case work. Moreover, the green characteristics and applicability of the suggested methodology was evaluated using softwares i.e., AGREE and BAGI.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Document type: Article Affiliation country: India Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Document type: Article Affiliation country: India Country of publication: Netherlands