Chinese Journal of Chromatography ›› 2014, Vol. 32 ›› Issue (7): 707-716.DOI: 10.3724/SP.J.1123.2014.03003

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Determination of 21 plant growth regulator residues in fruits by QuEChERS-high performance liquid chromatography-tandem mass spectrometry

HUANG Hehe1,2, ZHANG Jin1, XU Dunming1, ZHOU Yu1, LUO Jia2, LV Meiling3, CHEN Shubin4, WANG Lianzhu1   

  1. 1. Xiamen Entry-Exit Inspection and Quarantine Bureau, Xiamen 361026, China;
    2. Fujian Agriculture and Forestry University, Fuzhou 350002, China;
    3. Agilent Technologies (China) Limited, Beijing 100102, China;
    4. Ningbo Entry-Exit Inspection and Quarantine Bureau, Ningbo 315000, China
  • Received:2014-03-05 Revised:2014-04-17 Online:2014-07-08 Published:2014-06-25

Abstract:

A method for the simultaneous detection of 21 plant growth regulators in fruits by QuEChERS-high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed. The samples were initially extracted with acetonitrile containing 1%(v/v) acetic acid, followed by clean-up using the powder of magnesium sulfate and C18. The resulting samples were separated on a C18 column, and detected under positive and negative multiple reactions monitoring (MRM) mode through polarity switching between time segments. The matrix-matched external standard calibration curves were used for quantitative analysis. The linearities of chlormequat chloride, mepiquat chloride, choline chloride, cyclanilide, forchlorfenuron, thidiazuron, inabenfide, paclobutrazol, uniconazole and triapenthenol were in the concentration range of 0.1-500 μg/L, daminozide and 6-benzylaminopurine in the concentration range of 1.0-500 μg/L, 2,3,5-triiodobenzoic acid, 2,4-D, cloprop, 4-chlorophenoxyacetic acid (4-CPA) and trinexapac-ethyl in the concentration range of 2.0-1000 μg/L, abscisic acid (ABA), gibberellic acid (GA3), 1-naphthaleneacetic acid (NAA) and indol-3-ylacetic acid (IAA) in the concentration range of 10-1000 μg/L, with the correlation coefficients higher than 0.990. The limits of detection and the limits of quantification of the method were 0.020-6.0 μg/kg and 0.10-15.0 μg/kg, respectively. For all the samples, the average spiked recoveries ranged from 73.0% to 111.0%, and the relative standard deviations (RSDs, n=6) were in the range of 3.0%-17.2%. The method is quick, easy, effective, sensitive and accurate, and can meet the requirements for the determination of the 21 plant growth regulator residues in fruits.

Key words: fruits, high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), plant growth regulators, QuEChERS

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