-
Je něco špatně v tomto záznamu ?
Simultaneous determination of ten anticoagulant rodenticides in tissues by column-switching UHPLC-ESI-MS/MS
P. Maršálek, H. Modrá, V. Doubková, V. Večerek,
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články, práce podpořená grantem, validační studie
NLK
ProQuest Central
od 2011-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2003-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 2011-01-01 do Před 1 rokem
- MeSH
- antikoagulancia analýza MeSH
- hmotnostní spektrometrie s elektrosprejovou ionizací metody MeSH
- játra chemie MeSH
- ledviny chemie MeSH
- limita detekce MeSH
- psi MeSH
- rodenticidy analýza MeSH
- Sus scrofa MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- vysokoúčinná kapalinová chromatografie metody MeSH
- zvířata MeSH
- Check Tag
- psi MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- validační studie MeSH
This paper describes the development of a method for the simultaneous determination of ten anticoagulant rodenticides (coumafuryl, warfarin, pindone, coumatetralyl, coumachlor, difenacoum, bromadiolone, brodifacoum, chlorophacinone and flocoumafen) in the liver and kidney based on column-switching liquid chromatography coupled with heated electrospray ionization tandem mass spectrometry. The simple sample preparation includes extraction with methanol. A C18 trapping column was used for online solid-phase extraction before analytical separation with the mobile phase comprising a mixture of 0.1% formic acid in water, methanol and acetonitrile. Chromatographic separation was achieved using a Thermo Hypersil ultra high-performance liquid chromatography (UHPLC) C18 column with the mobile phase consisting of 5 mM ammonium formate buffer (pH = 9) and methanol. The column-switching procedure ensured no matrix effects during electrospray ionization (ESI). Extraction recoveries ranged between 91 and 100% for liver and between 89 and 97% for kidney. The method showed good linearity up to 750 ng g(-1). The limit of detection ranged between 0.001 and 0.022 ng g(-1) for liver and between 0.001 and 0.028 ng g(-1) for kidney. The developed method was successfully used in several animal poisoning cases.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16028302
- 003
- CZ-PrNML
- 005
- 20161006121358.0
- 007
- ta
- 008
- 161005s2015 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00216-015-8954-1 $2 doi
- 024 7_
- $a 10.1007/s00216-015-8954-1 $2 doi
- 035 __
- $a (PubMed)26280206
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Maršálek, Petr $u Department of Veterinary Public Health and Animal Welfare, Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences Brno, 612 42, Brno, Czech Republic. marsalekp@vfu.cz.
- 245 10
- $a Simultaneous determination of ten anticoagulant rodenticides in tissues by column-switching UHPLC-ESI-MS/MS / $c P. Maršálek, H. Modrá, V. Doubková, V. Večerek,
- 520 9_
- $a This paper describes the development of a method for the simultaneous determination of ten anticoagulant rodenticides (coumafuryl, warfarin, pindone, coumatetralyl, coumachlor, difenacoum, bromadiolone, brodifacoum, chlorophacinone and flocoumafen) in the liver and kidney based on column-switching liquid chromatography coupled with heated electrospray ionization tandem mass spectrometry. The simple sample preparation includes extraction with methanol. A C18 trapping column was used for online solid-phase extraction before analytical separation with the mobile phase comprising a mixture of 0.1% formic acid in water, methanol and acetonitrile. Chromatographic separation was achieved using a Thermo Hypersil ultra high-performance liquid chromatography (UHPLC) C18 column with the mobile phase consisting of 5 mM ammonium formate buffer (pH = 9) and methanol. The column-switching procedure ensured no matrix effects during electrospray ionization (ESI). Extraction recoveries ranged between 91 and 100% for liver and between 89 and 97% for kidney. The method showed good linearity up to 750 ng g(-1). The limit of detection ranged between 0.001 and 0.022 ng g(-1) for liver and between 0.001 and 0.028 ng g(-1) for kidney. The developed method was successfully used in several animal poisoning cases.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a antikoagulancia $x analýza $7 D000925
- 650 _2
- $a vysokoúčinná kapalinová chromatografie $x metody $7 D002851
- 650 _2
- $a psi $7 D004285
- 650 _2
- $a ledviny $x chemie $7 D007668
- 650 _2
- $a limita detekce $7 D057230
- 650 _2
- $a játra $x chemie $7 D008099
- 650 _2
- $a rodenticidy $x analýza $7 D012378
- 650 _2
- $a hmotnostní spektrometrie s elektrosprejovou ionizací $x metody $7 D021241
- 650 _2
- $a Sus scrofa $7 D034421
- 650 _2
- $a tandemová hmotnostní spektrometrie $x metody $7 D053719
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 655 _2
- $a validační studie $7 D023361
- 700 1_
- $a Modrá, Helena $u Department of Veterinary Public Health and Animal Welfare, Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences Brno, 612 42, Brno, Czech Republic.
- 700 1_
- $a Doubková, Veronika $u Department of Veterinary Public Health and Animal Welfare, Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences Brno, 612 42, Brno, Czech Republic.
- 700 1_
- $a Večerek, Vladimír $u Department of Veterinary Public Health and Animal Welfare, Faculty of Veterinary Hygiene and Ecology, University of Veterinary and Pharmaceutical Sciences Brno, 612 42, Brno, Czech Republic.
- 773 0_
- $w MED00006638 $t Analytical and bioanalytical chemistry $x 1618-2650 $g Roč. 407, č. 25 (2015), s. 7849-54
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/26280206 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20161005 $b ABA008
- 991 __
- $a 20161006121747 $b ABA008
- 999 __
- $a ok $b bmc $g 1166616 $s 952932
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 407 $c 25 $d 7849-54 $e 20150818 $i 1618-2650 $m Analytical and bioanalytical chemistry $n Anal Bioanal Chem $x MED00006638
- LZP __
- $a Pubmed-20161005