2013•Instrumentation Science & TechnologyRequires access

HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY AND GAS CHROMATOGRAPHY — MASS SPECTROMETRY METHODS FOR THE DETERMINATION OF IMIDACLOPRID, CHLORPYRIFOS, AND BIFENTHRIN RESIDUES IN TEA LEAVES

Nan Gao, Xiaochuan Guo, Kankan Zhang, Deyu Hu

Open publisher page 15 citations

Abstract

□ A sensitive, rapid, and reproducible high-performance liquid chromatography–diode array method and a gas chromatography/mass spectrometry method were developed to determine imidacloprid, chlorpyrifos, and bifenthrin in tea leaves. Solid-phase extraction (SPE) was employed for sample preparation. The extraction solvent used was acetonitrile:toluene (3:1, v/v). Linearity was observed in tea spiked with 0.4–6.0 µ g mL−1 (n = 6) of imidacloprid, 0.8–15.0 µ g mL−1 (n = 6) of chlorpyrifos, and 0.3–6.6 µ g mL−1 (n = 6) for bifenthrin. The correlation coefficients obtained were higher than 0.99 for all pesticides. The limits of detection for imidacloprid, chlorpyrifos, and bifenthrin were 0.06, 0.12, and 0.05 mg kg−1, respectively. The limits of quantification for imidacloprid, chlorpyrifos, and bifenthrin were 0.20, 0.40, and 0.17 mg kg−1, respectively. Recoveries of the analytes were between 80% and 96% with RSDs <10% (intra-day and inter-day). The methods were applied to monitor pesticide residues in tea. The results obtained by both techniques indicated that their feasibility for practical applications.

About this research paper

What this paper is about

□ A sensitive, rapid, and reproducible high-performance liquid chromatography–diode array method and a gas chromatography/mass spectrometry method were developed to determine imidacloprid, chlorpyrifos, and bifenthrin in tea leaves. Solid-phase extraction (SPE) was employed for sample preparation. The extraction solvent used was acetonitrile:toluene (3:1, v/v). Linearity was observed in tea spiked with 0.4–6.0 µ g mL−1 (n = 6) of imidacloprid, 0.8–15.0 µ g mL−1 (n = 6) of chlorpyrifos, and 0.3–6.6 µ g mL−1 (n = 6) for bifenthrin. The correlation coefficients obtained were higher than 0.99 for all pesticides. The limits of detection for imidacloprid, chlorpyrifos, and bifenthrin were 0.06, 0.12, and 0.05 mg kg−1, respectively. The limits of quantification for imidacloprid, chlorpyrifos, and bifenthrin were 0.20, 0.40, and 0.17 mg kg−1, respectively. Recoveries of the analytes were between 80% and 96% with RSDs <10% (intra-day and inter-day). The methods were applied to monitor pesticide residues in tea. The results obtained by both techniques indicated that their feasibility for practical applications.

Why it matters

OpenAlex reports 15 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

□ A sensitive, rapid, and reproducible high-performance liquid chromatography–diode array method and a gas chromatography/mass spectrometry method were developed to determine imidacloprid, chlorpyrifos, and bifenthrin in tea leaves. Solid-phase extraction (SPE) was employed for sample preparation. The extraction solvent used was acetonitrile:toluene (3:1, v/v). Linearity was observed in tea spiked with 0.4–6.0 µ g mL−1 (n = 6) of imidacloprid, 0.8–15.0 µ g mL−1 (n = 6) of chlorpyrifos, and 0.3–6.6 µ g mL−1 (n = 6) for bifenthrin. The correlation coefficients obtained were higher than 0.99 for all pesticides. The limits of detection for imidacloprid, chlorpyrifos, and bifenthrin were 0.06, 0.12, and 0.05 mg kg−1, respectively. The limits of quantification for imidacloprid, chlorpyrifos, and bifenthrin were 0.20, 0.40, and 0.17 mg kg−1, respectively. Recoveries of the analytes were between 80% and 96% with RSDs <10% (intra-day and inter-day). The methods were applied to monitor pesticide residues in tea. The results obtained by both techniques indicated that their feasibility for practical applications.

Key concepts: Bifenthrin, Chromatography, Chemistry, Imidacloprid, Gas chromatography–mass spectrometry, Detection limit, Chlorpyrifos, Mass spectrometry

Related papers

Back to paper searchBrowse research topicsOriginal source
HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY AND GAS CHROMATOGRAPHY — MASS SPECTROMETRY METHODS FOR THE DETERMINATION OF IMIDACLOPRID, CHLORPYRIFOS, AND BIFENTHRIN RESIDUES IN TEA LEAVES — Research Paper | ScholarLens