-
Je něco špatně v tomto záznamu ?
The effect of membrane thickness on supported liquid membrane extractions in-line coupled to capillary electrophoresis for analyses of complex samples
L. Ryšavá, M. Dvořák, P. Kubáň,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články
- MeSH
- analýza moči přístrojové vybavení metody MeSH
- biochemická analýza krve přístrojové vybavení metody MeSH
- elektroforéza kapilární * MeSH
- lidé MeSH
- membrány umělé * MeSH
- rozpouštědla chemie MeSH
- tělesné tekutiny chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
The effect of membrane thickness on extraction performance was systematically examined in extractions through supported liquid membranes (SLM), which were in-line coupled to capillary electrophoresis (CE). Three porous polypropylene membranes with different thickness (25, 100 and 170 μm) were used as supports for SLM extractions of model basic drugs (nortriptyline, papaverine, haloperidol and loperamide) from complex samples. The analytes were transferred through the SLMs by a pH gradient and were in-line injected, separated and quantified using a commercial CE instrument with ultraviolet (UV) detection. Transfers of the model drugs through SLM decreased with the increased membrane thickness (in the order: 25 > 100 > 170 μm) and highest transfers were achieved for the thinnest membrane. Interferences from complex sample matrices were efficiently eliminated, moreover, impregnation of the 25 μm membrane required significantly reduced volume of organic solvent. Mechanical stability of the impregnated 25 μm membrane was excellent during in-line injections, which necessitated direct contact of CE separation capillary with the SLM. Repeatability of the hyphenated SLM-CE-UV method (using the 25 μm membrane) was lower than 11% (RSD values of peak areas) and calibration curves were strictly linear in 0.5-30 μg/mL concentration range (coefficients of determination ≥ 0.997). Transfers of the basic drugs from donor solutions (standard and undiluted human urine/plasma) through the SLMs ranged from 45 to 231% and limits of detection were between 0.02 and 0.15 μg/mL.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19027732
- 003
- CZ-PrNML
- 005
- 20190823093504.0
- 007
- ta
- 008
- 190813s2019 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.chroma.2019.02.067 $2 doi
- 035 __
- $a (PubMed)30853166
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Ryšavá, Lenka $u Institute of Analytical Chemistry of the Czech Academy of Sciences, Veveří 97, CZ-60200 Brno, Czech Republic; Institute of Food Science and Biotechnology, Faculty of Chemistry, Brno University of Technology, Purkyňova 118, CZ-61200, Brno, Czech Republic.
- 245 14
- $a The effect of membrane thickness on supported liquid membrane extractions in-line coupled to capillary electrophoresis for analyses of complex samples / $c L. Ryšavá, M. Dvořák, P. Kubáň,
- 520 9_
- $a The effect of membrane thickness on extraction performance was systematically examined in extractions through supported liquid membranes (SLM), which were in-line coupled to capillary electrophoresis (CE). Three porous polypropylene membranes with different thickness (25, 100 and 170 μm) were used as supports for SLM extractions of model basic drugs (nortriptyline, papaverine, haloperidol and loperamide) from complex samples. The analytes were transferred through the SLMs by a pH gradient and were in-line injected, separated and quantified using a commercial CE instrument with ultraviolet (UV) detection. Transfers of the model drugs through SLM decreased with the increased membrane thickness (in the order: 25 > 100 > 170 μm) and highest transfers were achieved for the thinnest membrane. Interferences from complex sample matrices were efficiently eliminated, moreover, impregnation of the 25 μm membrane required significantly reduced volume of organic solvent. Mechanical stability of the impregnated 25 μm membrane was excellent during in-line injections, which necessitated direct contact of CE separation capillary with the SLM. Repeatability of the hyphenated SLM-CE-UV method (using the 25 μm membrane) was lower than 11% (RSD values of peak areas) and calibration curves were strictly linear in 0.5-30 μg/mL concentration range (coefficients of determination ≥ 0.997). Transfers of the basic drugs from donor solutions (standard and undiluted human urine/plasma) through the SLMs ranged from 45 to 231% and limits of detection were between 0.02 and 0.15 μg/mL.
- 650 _2
- $a biochemická analýza krve $x přístrojové vybavení $x metody $7 D001774
- 650 _2
- $a tělesné tekutiny $x chemie $7 D001826
- 650 12
- $a elektroforéza kapilární $7 D019075
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a membrány umělé $7 D008567
- 650 _2
- $a rozpouštědla $x chemie $7 D012997
- 650 _2
- $a analýza moči $x přístrojové vybavení $x metody $7 D016482
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Dvořák, Miloš $u Institute of Analytical Chemistry of the Czech Academy of Sciences, Veveří 97, CZ-60200 Brno, Czech Republic.
- 700 1_
- $a Kubáň, Pavel $u Institute of Analytical Chemistry of the Czech Academy of Sciences, Veveří 97, CZ-60200 Brno, Czech Republic. Electronic address: kuban@iach.cz.
- 773 0_
- $w MED00004962 $t Journal of chromatography. A $x 1873-3778 $g Roč. 1596, č. - (2019), s. 226-232
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30853166 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190813 $b ABA008
- 991 __
- $a 20190823093719 $b ABA008
- 999 __
- $a ok $b bmc $g 1432881 $s 1066192
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 1596 $c - $d 226-232 $e 20190228 $i 1873-3778 $m Journal of chromatography. A, Including electrophoresis and other separation methods $n J Chromatogr A $x MED00004962
- LZP __
- $a Pubmed-20190813