Published May 30, 2013 | Version v1
Journal article

Targeted analysis with benchtop quadrupole–orbitrap hybrid mass spectrometer: Application to determination of synthetic hormones in animal urine

  • 1. Departament de Química Analítica, Universitat de Barcelona, Barcelona (Spain)
  • 2. CIBER of Epidemiology and Public Health (CIBERESP), Madrid (Spain)
  • 3. Laboratori Agència Salut Pública de Barcelona, Barcelona (Spain)
  • 4. Mass Spectrometry Laboratory-Organic Pollutants, IDAEA-CSIC, Barcelona (Spain)

Description

Graphical abstract: -- Highlights: •The quadrupole in Q Exactive acts as a powerful filter to reduce ion suppression. •Reducing mass range using quadrupole in targeted modes increases the S/N ratio. •Targeted SIM data dependent scan modes are the most suitable for residue analysis. •A HRMS confirmatory method for synthetic hormones in urine has been developed. •The Q Exactive provides similar sensitivity and enhanced selectivity compared to QqQ. -- Abstract: Sensitive and unequivocal determination of analytes/contaminants in complex matrices is a challenge in the field of food safety control. In this study, various acquisition modes (Full MS/AIF, Full MS + tMS/MS, Full MS/dd MS/MS and tSIM/ddMS/MS) and parameters of a quadrupole–orbitrap hybrid mass spectrometer (Q Exactive) were studied in detail. One of the main conclusions has been that, reducing the scan range for Full MS (using the quadrupole) and targeted modes give higher signal-to-noise (S/N) ratios and thereby better detection limits for analytes in matrix. The use of Q Exactive in a complex case, for the confirmatory analysis of hormones in animal urine is presented. A targeted SIM data dependent MS/MS (tSIM/ddMS/MS) acquisition method for determination of eight synthetic hormones (trenbolone, 17α ethinylestradiol, zeranol, stanozolol, dienestrol, diethylstilbestrol, hexestrol, taleranol) and a naturally occurring hormone (zearalenone) in animal urine were optimized to have sensitive precursors from targeted SIM mode and trigger MS/MS scans over the entire chromatograph peak. The method was validated according to EC/657/2002. CCα (decision limit) for the analytes ranged between 0.11 μg L−1 and 0.69 μg L−1 and CCβ (detection capability) ranged between 0.29 μg L−1 and 0.90 μg L−1

Availability note (English)

Available from http://dx.doi.org/10.1016/j.aca.2013.04.017

Additional details

Identifiers

DOI
10.1016/j.aca.2013.04.017;
PII
S0003-2670(13)00528-X;

Publishing Information

Journal Title
Analytica Chimica Acta
Journal Volume
780
Journal Page Range
p. 65-73
ISSN
0003-2670
CODEN
ACACAM

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45040702
Subject category
S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ANIMALS; CONTROL; DETECTION; FOOD; HORMONES; MASS SPECTROMETERS; SAFETY; SENSITIVITY; URINE
Descriptors DEC
BIOLOGICAL MATERIALS; BIOLOGICAL WASTES; BODY FLUIDS; MATERIALS; MEASURING INSTRUMENTS; SPECTROMETERS; WASTES

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.