Stable-isotope dilution LC-MS/MS method for quantitative
determination of microcystin conjugates with cysteine and
glutathione in biotic matrices

J 2019

Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices

KOHOUTEK, Jiří, Tereza PROCHÁZKOVÁ, Ondřej ADAMOVSKÝ, Miroslava PALÍKOVÁ, Klára HILSCHEROVÁ et. al.

Základní údaje

Originální název

Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices

Autoři

KOHOUTEK, Jiří (203 Česká republika, domácí), Tereza PROCHÁZKOVÁ (203 Česká republika, domácí), Ondřej ADAMOVSKÝ (203 Česká republika, domácí), Miroslava PALÍKOVÁ (203 Česká republika) a Klára HILSCHEROVÁ (203 Česká republika, garant, domácí)

Vydání

Analytical and Bioanalytical chemistry, HEIDELBERG, SPRINGER HEIDELBERG, 2019, 1618-2642

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10406 Analytical chemistry

Stát vydavatele

Německo

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 3.637

Kód RIV

RIV/00216224:14310/19:00113358

Organizační jednotka

Přírodovědecká fakulta

DOI

http://dx.doi.org/10.1007/s00216-019-01904-0

UT WoS

000475515600024

Klíčová slova anglicky

Microcystin; l-Cysteine; l-Glutathione; LC-MS; MS

Štítky

rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 3. 4. 2020 12:56, Mgr. Marie Šípková, DiS.

Anotace

V originále

Microcystins are cyclic peptide toxins with hepatotoxic and tumor-promoting properties, which are produced in significant quantities (up to tens of mu g/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 5.0ng/g of tissue fresh weight (FW). The calibration was linear within a range of concentrations from 1 to 70ng/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 55ng/g) were found in the tissues of fish after 7weeks 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.

Návaznosti

EF16_013/0001761, projekt VaV

Název: RECETOX RI

LM2015051, projekt VaV

Název: Centrum pro výzkum toxických látek v prostředí (Akronym: RECETOX RI)

Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Výzkumná infrastruktura RECETOX

Citovat

KOHOUTEK, Jiří, Tereza PROCHÁZKOVÁ, Ondřej ADAMOVSKÝ, Miroslava PALÍKOVÁ a Klára HILSCHEROVÁ. Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices. Analytical and Bioanalytical chemistry. HEIDELBERG: SPRINGER HEIDELBERG, 2019, roč. 411, č. 20, s. 5267-5275. ISSN 1618-2642. Dostupné z: https://dx.doi.org/10.1007/s00216-019-01904-0.

@article{1639356,
   author = {Kohoutek, Jiří and Procházková, Tereza and Adamovský, Ondřej and Palíková, Miroslava and Hilscherová, Klára},
   article_location = {HEIDELBERG},
   article_number = {20},
   doi = {http://dx.doi.org/10.1007/s00216-019-01904-0},
   keywords = {Microcystin; l-Cysteine; l-Glutathione; LC-MS; MS},
   language = {eng},
   issn = {1618-2642},
   journal = {Analytical and Bioanalytical chemistry},
   title = {Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices},
   url = {http://dx.doi.org/10.1007/s00216-019-01904-0},
   volume = {411},
   year = {2019}
}

TY  - JOUR
ID  - 1639356
AU  - Kohoutek, Jiří - Procházková, Tereza - Adamovský, Ondřej - Palíková, Miroslava - Hilscherová, Klára
PY  - 2019
TI  - Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices
JF  - Analytical and Bioanalytical chemistry
VL  - 411
IS  - 20
SP  - 5267-5275
EP  - 5267-5275
PB  - SPRINGER HEIDELBERG
SN  - 16182642
KW  - Microcystin
KW  - l-Cysteine
KW  - l-Glutathione
KW  - LC-MS
KW  - MS
UR  - http://dx.doi.org/10.1007/s00216-019-01904-0
L2  - http://dx.doi.org/10.1007/s00216-019-01904-0
N2  - Microcystins are cyclic peptide toxins with hepatotoxic and tumor-promoting properties, which are produced in significant quantities (up to tens of mu g/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 5.0ng/g of tissue fresh weight (FW). The calibration was linear within a range of concentrations from 1 to 70ng/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 55ng/g) were found in the tissues of fish after 7weeks 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.
ER  -

KOHOUTEK, Jiří, Tereza PROCHÁZKOVÁ, Ondřej ADAMOVSKÝ, Miroslava PALÍKOVÁ a Klára HILSCHEROVÁ. Stable-isotope dilution LC-MS/MS method for quantitative determination of microcystin conjugates with cysteine and glutathione in biotic matrices. \textit{Analytical and Bioanalytical chemistry}. HEIDELBERG: SPRINGER HEIDELBERG, 2019, roč.~411, č.~20, s.~5267-5275. ISSN~1618-2642. Dostupné z: https://dx.doi.org/10.1007/s00216-019-01904-0.

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