Literature DB >> 26502727

Residues, dissipation, and risk assessment of spinosad in cowpea under open field conditions.

Zhibo Huan1, Jinhui Luo2, Zhi Xu2, Defang Xie2.   

Abstract

The dissipation and residues of an eco-friendly bio-pesticide, spinosad, in cowpea under field conditions were studied using ultra-performance liquid chromatography with tandem mass spectrometry (UPLC-MSMS) after Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) extraction. The method exhibited good linearity with respect to spinosyn A and spinosyn D in solvent or blank cowpea matrix with correlation coefficients>0.99. Additionally, matrix effects were not significant in the range 0.987-1.014, and the average recoveries at three concentration levels were 75.1-91.1 and 79.4-90.5% for spinosyn A and spinosyn D, respectively. The intra- and inter-day relative standard deviations were 2.5-9.3 and 7.8-9.8% for spinosyn A, respectively, and 4.1-7.9 and 6.6-8.3% for spinosyn D, respectively. The limits of detection (LODs) and limits of quantification (LOQs) were 0.005 and 0.01 mg kg(-1), respectively, for spinosyn A, and 0.002 and 0.005 mg kg(-1), respectively, for spinosyn D. The dissipation of spinosad (sum of spinosyn A and spinosyn D) fitted well to first-order kinetics with half-lives of 0.9-1.5 days. The highest residue (HR) at pre-harvest interval (PHI) of 12 h was 0.321 mg kg(-1). Compared with the maximum residue limit (MRL) set by Codex, a PHI of at least 24 h was recommended. The estimated daily chronic intake of spinosad from cowpea was less than 0.14% of the acceptable daily intake (ADI). Therefore, the risk of consuming cowpea sprayed with spinosad under recommended field conditions was considered acceptable for the Chinese population.

Entities:  

Keywords:  Cowpea; Crop residues; Dissipation; Risk assessment; Spinosad; UPLC-MSMS

Mesh:

Substances:

Year:  2015        PMID: 26502727     DOI: 10.1007/s10661-015-4942-3

Source DB:  PubMed          Journal:  Environ Monit Assess        ISSN: 0167-6369            Impact factor:   2.513


  8 in total

1.  Determination of spinosad and its metabolites in food and environmental matrices. 1. High-performance liquid chromatography with ultraviolet detection.

Authors:  S D West; L T Yeh; L G Turner; D A Schwedler; A D Thomas; D O Duebelbeis
Journal:  J Agric Food Chem       Date:  2000-11       Impact factor: 5.279

Review 2.  Pesticide residues in food--acute dietary exposure.

Authors:  Denis Hamilton; Arpád Ambrus; Roland Dieterle; Allan Felsot; Caroline Harris; Barbara Petersen; Ken Racke; Sue-Sun Wong; Roberto Gonzalez; Keiji Tanaka; Mike Earl; Graham Roberts; Raj Bhula
Journal:  Pest Manag Sci       Date:  2004-04       Impact factor: 4.845

3.  [Determination of spinosyns A and D residues in food by high performance liquid chromatography-tandem mass spectrometry].

Authors:  Jin Zhang; Lizhong Yang; Liyi Lin; Luping Chen; Yu Zhou; Dunming Xu
Journal:  Se Pu       Date:  2011-07

4.  Dissipation and residues of spinosad in eggplant and soil.

Authors:  Ercheng Zhao; Yanjun Xu; Maofeng Dong; Shuren Jiang; Zhiqiang Zhou; Lijun Han
Journal:  Bull Environ Contam Toxicol       Date:  2007-04-17       Impact factor: 2.151

5.  Dissipation kinetics of spinosad on cauliflower (Brassica oleracea var. botrytis. L.) under subtropical conditions of Punjab, India.

Authors:  Kousik Mandal; Gagan Jyot; Balwinder Singh
Journal:  Bull Environ Contam Toxicol       Date:  2009-12       Impact factor: 2.151

6.  Residues, dissipation and safety evaluation of chromafenozide in strawberry under open field conditions.

Authors:  Farag Malhat; Hany M A Badawy; Dalia A Barakat; Ayman N Saber
Journal:  Food Chem       Date:  2013-11-27       Impact factor: 7.514

7.  Environmental fate of spinosad. 1. Dissipation and degradation in aqueous systems.

Authors:  Cheryl B Cleveland; Gary A Bormett; Donald G Saunders; Fred L Powers; Alec S McGibbon; Graham L Reeves; Laura Rutherford; Jesse L Balcer
Journal:  J Agric Food Chem       Date:  2002-05-22       Impact factor: 5.279

8.  Fast and easy multiresidue method employing acetonitrile extraction/partitioning and "dispersive solid-phase extraction" for the determination of pesticide residues in produce.

Authors:  Michelangelo Anastassiades; Steven J Lehotay; Darinka Stajnbaher; Frank J Schenck
Journal:  J AOAC Int       Date:  2003 Mar-Apr       Impact factor: 1.913

  8 in total
  2 in total

1.  Residue distribution and risk assessment of two macrocyclic lactone insecticides in green onion using micro-liquid-liquid extraction (MLLE) technique coupled with liquid chromatography tandem mass spectrometry.

Authors:  Farag Malhat; Osama Abdallah
Journal:  Environ Monit Assess       Date:  2019-08-22       Impact factor: 2.513

2.  Dissipation kinetics of spinosad from tomato under sub-tropical agro-climatic conditions.

Authors:  Totan Adak; Irani Mukherjee
Journal:  Environ Monit Assess       Date:  2016-04-19       Impact factor: 2.513

  2 in total

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