-
Something wrong with this record ?
Simplified solid-phase extraction procedure combined with liquid chromatography tandem-mass spectrometry for multiresidue assessment of pharmaceutical compounds in environmental liquid samples
C. Afonso-Olivares, T. Čadková, Z. Sosa-Ferrera, JJ. Santana-Rodríguez, L. Nováková,
Language English Country Netherlands
Document type Journal Article
- MeSH
- Water Pollutants, Chemical analysis isolation & purification MeSH
- Chromatography, Liquid MeSH
- Solid Phase Extraction * MeSH
- Pharmaceutical Preparations analysis isolation & purification MeSH
- Limit of Detection MeSH
- Environmental Monitoring methods MeSH
- Wastewater chemistry MeSH
- Fresh Water chemistry MeSH
- Tandem Mass Spectrometry * MeSH
- Publication type
- Journal Article MeSH
To follow the twelve "green analytical chemistry" (GAC) principles, it is necessary to continuously develop analytical extraction and determination methodologies to assess the presence of micropollutants, such as pharmaceuticals, in environmental samples. A reduction in the analysis time and solvent quantity, which is one of the GAC principles, has been achieved through a simplified solid-phase extraction (SPE) procedure combined with high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the determination of twenty-three pharmaceuticals in liquid environmental samples using N-vinylpyrrolidone-divinylbenzene copolymer (OASIS HLB) cartridges. The optimal SPE conditions were studied. In these optimized conditions, 82.6% of the data have a median recovery above 70% for all compounds in each sample. The relative standard deviations (RSDs) were below 14.4% and 22.0% for intra- and inter-day repeatability, respectively. Method detection limits (MDLs) and method quantification limits (MQLs) ranged from 0.011 to 188ngL(-1) and from 0.033 to 628ngL(-1), respectively. The applicability of the method was evaluated in real samples from natural and conventional wastewater treatment plants (WWTPs), and results were obtained in concentration ranges from 0.013 to 91.5μgL(-1) and from 0.004 to 49.1μgL(-1), respectively.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17023329
- 003
- CZ-PrNML
- 005
- 20170720123134.0
- 007
- ta
- 008
- 170720s2017 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.chroma.2017.01.059 $2 doi
- 035 __
- $a (PubMed)28131588
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Afonso-Olivares, C $u Instituto Universitario de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas de Gran Canaria, Spain. $7 gn_A_00002030
- 245 10
- $a Simplified solid-phase extraction procedure combined with liquid chromatography tandem-mass spectrometry for multiresidue assessment of pharmaceutical compounds in environmental liquid samples / $c C. Afonso-Olivares, T. Čadková, Z. Sosa-Ferrera, JJ. Santana-Rodríguez, L. Nováková,
- 520 9_
- $a To follow the twelve "green analytical chemistry" (GAC) principles, it is necessary to continuously develop analytical extraction and determination methodologies to assess the presence of micropollutants, such as pharmaceuticals, in environmental samples. A reduction in the analysis time and solvent quantity, which is one of the GAC principles, has been achieved through a simplified solid-phase extraction (SPE) procedure combined with high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the determination of twenty-three pharmaceuticals in liquid environmental samples using N-vinylpyrrolidone-divinylbenzene copolymer (OASIS HLB) cartridges. The optimal SPE conditions were studied. In these optimized conditions, 82.6% of the data have a median recovery above 70% for all compounds in each sample. The relative standard deviations (RSDs) were below 14.4% and 22.0% for intra- and inter-day repeatability, respectively. Method detection limits (MDLs) and method quantification limits (MQLs) ranged from 0.011 to 188ngL(-1) and from 0.033 to 628ngL(-1), respectively. The applicability of the method was evaluated in real samples from natural and conventional wastewater treatment plants (WWTPs), and results were obtained in concentration ranges from 0.013 to 91.5μgL(-1) and from 0.004 to 49.1μgL(-1), respectively.
- 650 _2
- $a chromatografie kapalinová $7 D002853
- 650 _2
- $a monitorování životního prostředí $x metody $7 D004784
- 650 _2
- $a sladká voda $x chemie $7 D005618
- 650 _2
- $a limita detekce $7 D057230
- 650 _2
- $a léčivé přípravky $x analýza $x izolace a purifikace $7 D004364
- 650 12
- $a extrakce na pevné fázi $7 D052616
- 650 12
- $a tandemová hmotnostní spektrometrie $7 D053719
- 650 _2
- $a odpadní voda $x chemie $7 D062065
- 650 _2
- $a chemické látky znečišťující vodu $x analýza $x izolace a purifikace $7 D014874
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Čadková, T $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, Heyrovského 1203, 500 05 Hradec Králové, Czechia.
- 700 1_
- $a Sosa-Ferrera, Z $u Instituto Universitario de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas de Gran Canaria, Spain.
- 700 1_
- $a Santana-Rodríguez, J J $u Instituto Universitario de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas de Gran Canaria, Spain. Electronic address: josejuan.santana@ulpgc.es.
- 700 1_
- $a Nováková, L $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, Heyrovského 1203, 500 05 Hradec Králové, Czechia.
- 773 0_
- $w MED00004962 $t Journal of chromatography. A $x 1873-3778 $g Roč. 1487, č. - (2017), s. 54-63
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28131588 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20170720 $b ABA008
- 991 __
- $a 20170720123627 $b ABA008
- 999 __
- $a ok $b bmc $g 1239010 $s 984242
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 1487 $c - $d 54-63 $e 20170123 $i 1873-3778 $m Journal of chromatography. A, Including electrophoresis and other separation methods $n J Chromatogr A $x MED00004962
- LZP __
- $a Pubmed-20170720