Development of an Analytical Method of Nereistoxin and Nereistoxin-related Pesticides in Agricultural Products by LC-MS/MS
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A simultaneous analytical method was developed for the quantification and confirmation of nereistoxin and nereistoxin-related pesticides in agricultural products. These pesticides were extracted with a 2% L-cysteine solution in 0.05 N HCI and hydrolyzed using ammonium hydoxide and 3% nickel(II) chloride solution, purified using dispersive solid phase extraction (d-SPE) kit, and then analyzed by LC-MS/MS. To prevent the matrix effect, all analytes were quantified using matrix-matched calibrations, as assessed by the determination coefficient (R2) of the range from 0.9951-1.000. The LOD and LOQ were satisfactory for determining low residual levels of the pesticides in agricultural products. The accuracy and precision of the method were evaluated based on recoveries with five replicates at three fortification levels (LOQ, 10×LOQ and 50×LOQ). The mean recoveries of nereistoxin and nereistoxin-related pesticides in agricultural products were 75.3-108.0% with a coefficient of variation of 0.8-7.0%. All the optimized results were excellent, as assessed by the Ministry of Food and Drug Safety guidelines and the Codex Alimentarius Commission guidelines for pesticide residue analysis. This study provides fundamental data for setting the residue definition and maximum residue limits for nereistoxin and nereistoxin-related pesticides in agricultural products.
Abstract
A simultaneous analytical method was developed for the quantification and confirmation of nereistoxin and nereistoxin-related pesticides in agricultural products. These pesticides were extracted with a 2% L-cysteine solution in 0.05 N HCI and hydrolyzed using ammonium hydoxide and 3% nickel(II) chloride solution, purified using dispersive solid phase extraction (d-SPE) kit, and then analyzed by LC-MS/MS. To prevent the matrix effect, all analytes were quantified using matrix-matched calibrations, as assessed by the determination coefficient (R2) of the range from 0.9951-1.000. The LOD and LOQ were satisfactory for determining low residual levels of the pesticides in agricultural products. The accuracy and precision of the method were evaluated based on recoveries with five replicates at three fortification levels (LOQ, 10×LOQ and 50×LOQ). The mean recoveries of nereistoxin and nereistoxin-related pesticides in agricultural products were 75.3-108.0% with a coefficient of variation of 0.8-7.0%. All the optimized results were excellent, as assessed by the Ministry of Food and Drug Safety guidelines and the Codex Alimentarius Commission guidelines for pesticide residue analysis. This study provides fundamental data for setting the residue definition and maximum residue limits for nereistoxin and nereistoxin-related pesticides in agricultural products.
참고문헌 (17)
- Durán-Lara EF, "Natural organic compounds for application in organic farming", Agriculture, 10(2), pp.41~ (2020)[DOI]
- Mfarrej MFB, "Competitive, sustainable natural pesticides", Acta Ecologica Sinica, 39(2), pp.145~151 (2019)[DOI]
- Zhang J, "Development, optimization, and validation of a method for detection of cartap, thiocyclam, thiosultap-monosodium, and thiosultap-disodium residues in plant foods by GC-ECD", Food Chemistry, 371, pp.131198~ (2022)[DOI]
- Park YJ, "Advanced analytical method of nereistoxin using mixed-mode cationic exchange solid-phase extraction and GC", MS, 2015, pp.252, 143~149
- Yang SH, "Simultaneous determination of nereistoxin insecticides in foods of animal origins by combining pH‑dependent reversible partitioning with hydrophilic interaction chromatography‑mass spectrometry", Scientific Reports, 12, pp.10208~ (2022)[DOI]
- López-Ruiz R, "A laboratory study on dissipation and risk assessment of the proinsecticide thiocyclam and its metabolite nereistoxin in tomato using liquid chromatography high resolution mass spectrometry", Food Chemistry, 344, pp.128720~ (2021)[DOI]
- Gupta VK, "Amelioration of hepatotoxic and neurotoxic effect of cartap by aloe vera in wistar rats", Toxics, 11(5), pp.472~ (2023)[DOI]
- Suganthan N, "Dengue fever complicated with acute liver failure : A case report of expanded dengue syndrome and literature review", SAGE Open Medical Casa Reports, 8, pp.2050313X20913428~ (2020)[DOI]
- Abdusolievich KN, "Dynamics of development of the microvasculature and tissue structures of the large intestine in case of sequential pesticide poisoning", Journal of Survey in Fisheries Sciences, 10(1), pp.352~361 (2023)[DOI]
- Gupta M, "Cartap poisoning : an unusual poisoning in North India", International Journal of Scientific Reports, 1(1), pp.99~101 (2015)[DOI]
- Takahashi F, "Sonochemical preparation of gold nanoparticles for sensitive colorimetric determination of nereistoxin insecticides in environmental samples", Talanta, 188, pp.651~657 (2018)[DOI]
- Liu W, "Highly sensitive and selective colorimetric detection of cartap residue in agricultural products", Talanta, 101, pp.382~387 (2012)[DOI]
- Mitsuji I, "An analytical method of bensultap residues in crops and soils", Journal of Pesticide Science, 11(4), pp.547~555 (1986)[DOI]
- Zhou W, "Matrix effects and application of matrix effect factor", Bioanalysis, 9, pp.1839~1844 (2017)[DOI]
- Nischwitz V, "Optimisation of an HPLC selected reaction monitoring electrospray tandem mass spectrometry method for the detection of 50 arsenic species", Journal of Analytical Atomic Spectrometry, 21, pp.1277~1286 (2006)[DOI]
- Huang Y, "Determination of multi-pesticide residues in green tea with a modified QuEChERS protocol coupled to HPLC-MS", MS, 2019, pp.275, 255~264
- García AJN, "Multi-pesticide residue analysis in nutraceuticals from grape seed extracts by gas chromatography coupled to triple quadrupole mass spectrometry", Food Control, 47, pp.369~380 (2015)[DOI]
