-
Something wrong with this record ?
Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices
J. Kohoutek, T. Procházková, O. Adamovský, M. Palíková, K. Hilscherová,
Language English Country Germany
Document type Journal Article
Grant support
LM2015051
Czech Ministry of Education, Youth and Sports
CZ.02.1.01/0.0/0.0/16_013/0001761
European Structural and Investment Funds
NLK
ProQuest Central
from 2011-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2003-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 2011-01-01 to 1 year ago
- MeSH
- Biomass MeSH
- Chromatography, Liquid methods MeSH
- Cysteine analysis MeSH
- Glutathione analysis MeSH
- Limit of Detection MeSH
- Microcystins analysis chemistry MeSH
- Radioisotope Dilution Technique MeSH
- Reproducibility of Results MeSH
- Cyanobacteria chemistry MeSH
- Tandem Mass Spectrometry methods MeSH
- Publication type
- Journal Article MeSH
Microcystins are cyclic peptide toxins with hepatotoxic and tumor-promoting properties, which are produced in significant quantities (up to tens of μg/L) in freshwater cyanobacterial water blooms. Several studies reported microcystin accumulation in fish with possible food transfer to humans. These compounds are further metabolized to cysteine and glutathione conjugates which can be present in tissues in significant concentrations. In this study, we focused on the development and evaluation of robust and highly sensitive SPE-LC-MS/MS method for the analysis of microcystin conjugates in fish tissue samples. For the first time, we demonstrate the use of isotopically labeled internal standards which are essential for accurate and precise determination of analytes in complex biotic matrices. LLOQs of respective microcystin conjugates (signal-to-noise ratio; S/N > 10, peak-to-peak method) ranged from 3.3 to 5.0 ng/g of tissue fresh weight (FW). The calibration was linear within a range of concentrations from 1 to 70 ng/mL for all analyzed conjugates. The precision and repeatability of the method were very good with recoveries in the range of 88.5-107.6% and relative standard deviations between 8.8 and 13.2% for all analytes. In the follow-up study, fully validated method was used for the determination of microcystin conjugate levels in common carp exposed to microcystin-containing cyanobacterial biomass under controlled conditions. Significant amounts of microcystin conjugates (up to 55 ng/g) were found in the tissues of fish after 7 weeks of exposure. Our method was shown to be robust, sensitive, selective, and suitable for the determination of trace levels of microcystin conjugates in fish tissues.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19034542
- 003
- CZ-PrNML
- 005
- 20191010100640.0
- 007
- ta
- 008
- 191007s2019 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00216-019-01904-0 $2 doi
- 035 __
- $a (PubMed)31129692
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Kohoutek, Jiří $u RECETOX, Faculty of Science, Masaryk University, Kamenice 753/5, 62500, Brno, Czech Republic. jiri.kohoutek@recetox.muni.cz.
- 245 10
- $a Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices / $c J. Kohoutek, T. Procházková, O. Adamovský, M. Palíková, K. Hilscherová,
- 520 9_
- $a Microcystins are cyclic peptide toxins with hepatotoxic and tumor-promoting properties, which are produced in significant quantities (up to tens of μg/L) in freshwater cyanobacterial water blooms. Several studies reported microcystin accumulation in fish with possible food transfer to humans. These compounds are further metabolized to cysteine and glutathione conjugates which can be present in tissues in significant concentrations. In this study, we focused on the development and evaluation of robust and highly sensitive SPE-LC-MS/MS method for the analysis of microcystin conjugates in fish tissue samples. For the first time, we demonstrate the use of isotopically labeled internal standards which are essential for accurate and precise determination of analytes in complex biotic matrices. LLOQs of respective microcystin conjugates (signal-to-noise ratio; S/N > 10, peak-to-peak method) ranged from 3.3 to 5.0 ng/g of tissue fresh weight (FW). The calibration was linear within a range of concentrations from 1 to 70 ng/mL for all analyzed conjugates. The precision and repeatability of the method were very good with recoveries in the range of 88.5-107.6% and relative standard deviations between 8.8 and 13.2% for all analytes. In the follow-up study, fully validated method was used for the determination of microcystin conjugate levels in common carp exposed to microcystin-containing cyanobacterial biomass under controlled conditions. Significant amounts of microcystin conjugates (up to 55 ng/g) were found in the tissues of fish after 7 weeks of exposure. Our method was shown to be robust, sensitive, selective, and suitable for the determination of trace levels of microcystin conjugates in fish tissues.
- 650 _2
- $a biomasa $7 D018533
- 650 _2
- $a chromatografie kapalinová $x metody $7 D002853
- 650 _2
- $a sinice $x chemie $7 D000458
- 650 _2
- $a cystein $x analýza $7 D003545
- 650 _2
- $a glutathion $x analýza $7 D005978
- 650 _2
- $a limita detekce $7 D057230
- 650 _2
- $a mikrocystiny $x analýza $x chemie $7 D052998
- 650 _2
- $a radioisotopová diluční technika $7 D011865
- 650 _2
- $a reprodukovatelnost výsledků $7 D015203
- 650 _2
- $a tandemová hmotnostní spektrometrie $x metody $7 D053719
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Procházková, Tereza $u RECETOX, Faculty of Science, Masaryk University, Kamenice 753/5, 62500, Brno, Czech Republic.
- 700 1_
- $a Adamovský, Ondřej $u RECETOX, Faculty of Science, Masaryk University, Kamenice 753/5, 62500, Brno, Czech Republic.
- 700 1_
- $a Palíková, Miroslava $u Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences, Palackého 1-3, 612 42, Brno, Czech Republic. Department of Zoology, Fisheries, Hydrobiology and Apiculture, Faculty of AgriSciences, Mendel University in Brno, Zemedelska 1, 613 00, Brno, Czech Republic.
- 700 1_
- $a Hilscherová, Klára $u RECETOX, Faculty of Science, Masaryk University, Kamenice 753/5, 62500, Brno, Czech Republic.
- 773 0_
- $w MED00006638 $t Analytical and bioanalytical chemistry $x 1618-2650 $g Roč. 411, č. 20 (2019), s. 5267-5275
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31129692 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20191007 $b ABA008
- 991 __
- $a 20191010101059 $b ABA008
- 999 __
- $a ok $b bmc $g 1451202 $s 1073092
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 411 $c 20 $d 5267-5275 $e 20190525 $i 1618-2650 $m Analytical and bioanalytical chemistry $n Anal Bioanal Chem $x MED00006638
- GRA __
- $a LM2015051 $p Czech Ministry of Education, Youth and Sports
- GRA __
- $a CZ.02.1.01/0.0/0.0/16_013/0001761 $p European Structural and Investment Funds
- LZP __
- $a Pubmed-20191007