Determination of the plant growth regulator chlormequat in food by liquid chromatography-electrospray ionisation tandem mass spectrometry

Citation
J. Hau et al., Determination of the plant growth regulator chlormequat in food by liquid chromatography-electrospray ionisation tandem mass spectrometry, J CHROMAT A, 878(1), 2000, pp. 77-86
Citations number
17
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
Volume
878
Issue
1
Year of publication
2000
Pages
77 - 86
Database
ISI
SICI code
Abstract
A confirmatory method for the determination of trace levels of chlormequat in a variety of different food matrices was developed. It entails a single clean-up step over a solid-phase cation exchange resin and subsequent liqui d chromatography-electrospray ionisation tandem mass spectrometry using a s table isotopically labelled internal standard. Mass spectral acquisition wa s done in selected reaction monitoring mode, selecting the transitions from both the Cl-35 and the Cl-37 isotope of chlormequat. Recoveries after extr action and clean-up, determined with radio-labelled chlormequat and average d over the spiking range (16-65 mu g kg(-1)) in four different commodities, were within 88-96%, with a coefficient of variation better than 8%. The me thod can be applied to pears, pear juice concentrates, fruit purees, and ce real products, with typical limits of detection for chlormequat estimated a t 2-5 mu g kg(-1). A survey of different food commodities revealed that chl ormequat was detectable - albeit at very low levels - in many of the food s amples analysed, with the highest concentration recorded in pears purchased in Switzerland and of South African origin (5.5 mg kg(-1)). Measurements w ere also conducted on two LC-MS instruments and demonstrate the versatility and robustness of the method and its applicability to instruments of diffe rent ion source design. (C) 2000 Elsevier Science B.V. All rights reserved.