Quadrupole ion storage tandem mass spectrometry and high-resolution mass spectrometry: complementary application in the measurement of 2,3,7,8-chlorine substituted dibenzo-p-dioxins and dibenzofurans in US foods

Citation
Dg. Hayward et al., Quadrupole ion storage tandem mass spectrometry and high-resolution mass spectrometry: complementary application in the measurement of 2,3,7,8-chlorine substituted dibenzo-p-dioxins and dibenzofurans in US foods, CHEMOSPHERE, 43(4-7), 2001, pp. 407-415
Citations number
17
Categorie Soggetti
Environment/Ecology
Journal title
CHEMOSPHERE
ISSN journal
00456535 → ACNP
Volume
43
Issue
4-7
Year of publication
2001
Pages
407 - 415
Database
ISI
SICI code
0045-6535(200105/06)43:4-7<407:QISTMS>2.0.ZU;2-H
Abstract
The US Food and Drug Administration has simultaneously utilized both high-r esolution mass spectrometry (HRMS) and quadrupole ion storage tandem mass s pectrometry (QISTMS) in the measurement of polychlorinated dibenzo-p-dioxin s/dibenzofurans (PCDD/Fs) in 147 food samples collected in 1998 and 1999 in the US. In 1998, 20 egg samples, six scallop, 10 blue crab, eight American lobster, 10 pollack: 15 striped bass, five rockfish, 10 crawfish, seven aq ua-cultured and 13 wild-caught salmon, along with 19 cream and 18 mozzarell a cheese samples were measured for PCDD/Fs. QISTMS provided limits of detec tion (LODs) close to those produced using HRMS for many congeners in 56 sam ples analyzed by both techniques in 1998 and three salmon and three striped bass collected in 1999. The I-TEQs of the mean levels for measured congene rs in 40 samples of fish and shellfish and 16 cheese and eggs from 1998 ana lyzed by HRMS and QISTMS were 0.99 and 1.1 ng/kg wet weight, respectively. The I-TEQ for mean congener levels in the 40 fish and shellfish measured by HRMS was 1.4 ng/kg wet weight. A higher sample throughput with greater dat a quality at a lower cost is achievable by using both QISTMS and HRMS. (C) 2001 Elsevier Science Ltd. All rights reserved.