Gas chromatographic–mass spectrometric method for the determination of the herbicides paraquat and diquat in plasma and urine samples

• Published in: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Vol. 853; no. 1-2; pp. 260 - 264
• Main Authors: de Almeida, Rafael Menck, Yonamine, Mauricio
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 15.06.2007; Elsevier Science
• Subjects: Analysis; Analytical, structural and metabolic biochemistry; Biological and medical sciences; Diquat; Diquat - blood; Diquat - chemistry; Diquat - urine; Fundamental and applied biological sciences. Psychology; Gas Chromatography-Mass Spectrometry - methods; GC–MS; General pharmacology; Herbicides - blood; Herbicides - chemistry; Herbicides - urine; Humans; Medical sciences; Molecular Structure; Paraquat; Paraquat - blood; Paraquat - chemistry; Paraquat - urine; Pharmacology. Drug treatments; Plasma and urine samples; Reproducibility of Results; SPE; Paraquat; SPE; GC–MS; Diquat; Plasma and urine samples; Urine; Solid phase extraction; Biological fluid; Pesticides; Determination; Herbicide; Blood plasma; GC-MS; Quantitative analysis
• ISSN: 1570-0232; 1873-376X
• DOI: 10.1016/j.jchromb.2007.03.026

In the present work, a method was developed and optimized aiming to determinate the herbicides paraquat (PQ) and diquat (DQ) in human plasma and urine samples. An initial procedure of chemical reduction of the analytes by adding NaBH4 directly in the buffered samples (pH 8.0) was performed. This procedure was necessary to convert the quaternary ammonium substances into more volatile compounds for gas chromatographic analysis. The reduction compounds were extracted with C18 cartridges (solid-phase extraction). Ethyl paraquat (EPQ) was used as internal standard (IS). Gas chromatography–mass spectrometry (GC–MS) was used to identify and quantify the analytes in selected ion monitoring (SIM) mode. The limits of detection were 0.05mg/l for both PQ and DQ. By using the weighted least squares linear regression (1/x12 for plasma and 1/y for urine), the accuracy of the analytical method was improved at the lower end of the calibration curve (from 0.1 to 50mg/l; r>0.98). This method can be readily utilized as an important tool to confirm the suspicion of PQ and/or DQ poisoning and evaluate the extent of the intoxication.