Targeted analysis with benchtop quadrupole–orbitrap hybrid mass spectrometer: Application to determination of synthetic hormones in animal urine
Creators
- 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.2013.04.017Additional 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.