-
Something wrong with this record ?
Lab-In-Syringe for automated double-stage sample preparation by coupling salting out liquid-liquid extraction with online solid-phase extraction and liquid chromatographic separation for sulfonamide antibiotics from urine
K. Fikarová, B. Horstkotte, D. Machián, H. Sklenářová, P. Solich
Language English Country Netherlands
Document type Journal Article
- MeSH
- Anti-Bacterial Agents * analysis MeSH
- Sodium Chloride * MeSH
- Liquid-Liquid Extraction MeSH
- Solid Phase Extraction MeSH
- Syringes MeSH
- Sulfonamides MeSH
- Chromatography, High Pressure Liquid MeSH
- Publication type
- Journal Article MeSH
A double-stage Lab-In-Syringe automated extraction procedure coupled online to HPLC for the determination of four sulfonamides in urine has been developed. Our method is based on homogeneous liquid-liquid extraction at pH 3 using water-miscible acetonitrile with induction of phase separation by the addition of a saturated solution of kosmotropic salts MgSO4 and NaCl. The procedure allowed extraction of the moderately polar model analytes and the use of a solvent that is compatible with the used separation technique. The automated sample preparation system based on the stirring-assisted Lab-In-Syringe approach was coupled on-line with HPLC-UV for the subsequent separation of the sulfonamide antibiotics. To improve both preconcentration factor and extract cleanup, the analytes were trapped at pH 10 in an anion-exchange resin cartridge integrated into the HPLC injection loop thus achieving a double-stage sample clean-up. Analytes were eluted using an acidic HPLC mobile phase in gradient elution mode. Running the analytes separation and the two-step preparation of the following sample in parallel reduced the total time of analysis to mere 13.5 min. Limits of detection ranged from 5.0 to 7.5 μg/L with linear working ranges of 50-5000 μg/L (r2 > 0.9997) and RSD ≤ 5% (n = 6) at a concentration level of 50 μg/L. Average recovery values were 102.7 ± 7.4% after spiking of urine with sulfonamides at concentrations of 2.5 and 5 mg/L followed by 5 times dilution. To the best of our knowledge, the use of Lab-In-Syringe for the automation of coupled homogeneous liquid-liquid extraction and SPE for preparation of the complex matrices suitable for separation techniques is here presented for the first time.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21019602
- 003
- CZ-PrNML
- 005
- 20210830101204.0
- 007
- ta
- 008
- 210728s2021 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.talanta.2020.121427 $2 doi
- 035 __
- $a (PubMed)33076060
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Fikarová, Kateřina $u Charles University, Faculty of Pharmacy in Hradec Králové, Department of Analytical Chemistry, Akademika Heyrovského 1203, 500 05, Hradec Králové, Czech Republic
- 245 10
- $a Lab-In-Syringe for automated double-stage sample preparation by coupling salting out liquid-liquid extraction with online solid-phase extraction and liquid chromatographic separation for sulfonamide antibiotics from urine / $c K. Fikarová, B. Horstkotte, D. Machián, H. Sklenářová, P. Solich
- 520 9_
- $a A double-stage Lab-In-Syringe automated extraction procedure coupled online to HPLC for the determination of four sulfonamides in urine has been developed. Our method is based on homogeneous liquid-liquid extraction at pH 3 using water-miscible acetonitrile with induction of phase separation by the addition of a saturated solution of kosmotropic salts MgSO4 and NaCl. The procedure allowed extraction of the moderately polar model analytes and the use of a solvent that is compatible with the used separation technique. The automated sample preparation system based on the stirring-assisted Lab-In-Syringe approach was coupled on-line with HPLC-UV for the subsequent separation of the sulfonamide antibiotics. To improve both preconcentration factor and extract cleanup, the analytes were trapped at pH 10 in an anion-exchange resin cartridge integrated into the HPLC injection loop thus achieving a double-stage sample clean-up. Analytes were eluted using an acidic HPLC mobile phase in gradient elution mode. Running the analytes separation and the two-step preparation of the following sample in parallel reduced the total time of analysis to mere 13.5 min. Limits of detection ranged from 5.0 to 7.5 μg/L with linear working ranges of 50-5000 μg/L (r2 > 0.9997) and RSD ≤ 5% (n = 6) at a concentration level of 50 μg/L. Average recovery values were 102.7 ± 7.4% after spiking of urine with sulfonamides at concentrations of 2.5 and 5 mg/L followed by 5 times dilution. To the best of our knowledge, the use of Lab-In-Syringe for the automation of coupled homogeneous liquid-liquid extraction and SPE for preparation of the complex matrices suitable for separation techniques is here presented for the first time.
- 650 12
- $a antibakteriální látky $x analýza $7 D000900
- 650 _2
- $a vysokoúčinná kapalinová chromatografie $7 D002851
- 650 _2
- $a extrakce kapalina-kapalina $7 D059625
- 650 12
- $a chlorid sodný $7 D012965
- 650 _2
- $a extrakce na pevné fázi $7 D052616
- 650 _2
- $a sulfonamidy $7 D013449
- 650 _2
- $a injekční stříkačky $7 D013594
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Horstkotte, Burkhard $u Charles University, Faculty of Pharmacy in Hradec Králové, Department of Analytical Chemistry, Akademika Heyrovského 1203, 500 05, Hradec Králové, Czech Republic. Electronic address: Horstkob@faf.cuni.cz
- 700 1_
- $a Machián, Daniel $u Charles University, Faculty of Pharmacy in Hradec Králové, Department of Analytical Chemistry, Akademika Heyrovského 1203, 500 05, Hradec Králové, Czech Republic
- 700 1_
- $a Sklenářová, Hana $u Charles University, Faculty of Pharmacy in Hradec Králové, Department of Analytical Chemistry, Akademika Heyrovského 1203, 500 05, Hradec Králové, Czech Republic
- 700 1_
- $a Solich, Petr $u Charles University, Faculty of Pharmacy in Hradec Králové, Department of Analytical Chemistry, Akademika Heyrovského 1203, 500 05, Hradec Králové, Czech Republic
- 773 0_
- $w MED00004484 $t Talanta $x 1873-3573 $g Roč. 221, č. - (2021), s. 121427
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33076060 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20210830101204 $b ABA008
- 999 __
- $a ok $b bmc $g 1690431 $s 1140048
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 221 $c - $d 121427 $e 20200723 $i 1873-3573 $m Talanta $n Talanta $x MED00004484
- LZP __
- $a Pubmed-20210728