• Je něco špatně v tomto záznamu ?

Flow-batch analysis of clenbuterol based on analyte extraction on molecularly imprinted polymers coupled to an in-system chromogenic reaction. Application to human urine and milk substitute samples

N. González, M. Grünhut, I. Šrámková, AG. Lista, B. Horstkotte, P. Solich, H. Sklenářová, CC. Acebal,

. 2018 ; 178 (-) : 934-942. [pub] 20171023

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18033562

A fully automated spectrophotometric method based on flow-batch analysis has been developed for the determination of clenbuterol including an on-line solid phase extraction using a molecularly imprinted polymer (MIP) as the sorbent. The molecularly imprinted solid phase extraction (MISPE) procedure allowed analyte extraction from complex matrices at low concentration levels and with high selectivity towards the analyte. The MISPE procedure was performed using a commercial MIP cartridge that was introduced into a guard column holder and integrated in the analyzer system. Optimized parameters included the volume of the sample, the type and volume of the conditioning and washing solutions, and the type and volume of the eluent. Quantification of clenbuterol was carried out by spectrophotometry after in-system post-elution analyte derivatization based on azo-coupling using N- (1-Naphthyl) ethylenediamine as the coupling agent to yield a red-colored compound with maximum absorbance at 500nm. Both the chromogenic reaction and spectrophotometric detection were performed in a lab-made flow-batch mixing chamber that replaced the cuvette holder of the spectrophotometer. The calibration curve was linear in the 0.075-0.500mgL-1 range with a correlation coefficient of 0.998. The precision of the proposed method was evaluated in terms of the relative standard deviation obtaining 1.1% and 3.0% for intra-day precision and inter-day precision, respectively. The detection limit was 0.021mgL-1 and the sample throughput for the entire process was 3.4h-1. The proposed method was applied for the determination of CLB in human urine and milk substitute samples obtaining recoveries values within a range of 94.0-100.0%.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18033562
003      
CZ-PrNML
005      
20181008122219.0
007      
ta
008      
181008s2018 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.talanta.2017.10.040 $2 doi
035    __
$a (PubMed)29136919
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a González, Natalia $u INQUISUR, Departamento de Química, Universidad Nacional del Sur (UNS)-CONICET, Av. Alem 1253, 8000 Bahía Blanca, Argentina.
245    10
$a Flow-batch analysis of clenbuterol based on analyte extraction on molecularly imprinted polymers coupled to an in-system chromogenic reaction. Application to human urine and milk substitute samples / $c N. González, M. Grünhut, I. Šrámková, AG. Lista, B. Horstkotte, P. Solich, H. Sklenářová, CC. Acebal,
520    9_
$a A fully automated spectrophotometric method based on flow-batch analysis has been developed for the determination of clenbuterol including an on-line solid phase extraction using a molecularly imprinted polymer (MIP) as the sorbent. The molecularly imprinted solid phase extraction (MISPE) procedure allowed analyte extraction from complex matrices at low concentration levels and with high selectivity towards the analyte. The MISPE procedure was performed using a commercial MIP cartridge that was introduced into a guard column holder and integrated in the analyzer system. Optimized parameters included the volume of the sample, the type and volume of the conditioning and washing solutions, and the type and volume of the eluent. Quantification of clenbuterol was carried out by spectrophotometry after in-system post-elution analyte derivatization based on azo-coupling using N- (1-Naphthyl) ethylenediamine as the coupling agent to yield a red-colored compound with maximum absorbance at 500nm. Both the chromogenic reaction and spectrophotometric detection were performed in a lab-made flow-batch mixing chamber that replaced the cuvette holder of the spectrophotometer. The calibration curve was linear in the 0.075-0.500mgL-1 range with a correlation coefficient of 0.998. The precision of the proposed method was evaluated in terms of the relative standard deviation obtaining 1.1% and 3.0% for intra-day precision and inter-day precision, respectively. The detection limit was 0.021mgL-1 and the sample throughput for the entire process was 3.4h-1. The proposed method was applied for the determination of CLB in human urine and milk substitute samples obtaining recoveries values within a range of 94.0-100.0%.
650    _2
$a metody pro přípravu analytických vzorků $7 D053000
650    _2
$a klenbuterol $x analýza $x izolace a purifikace $x moč $7 D002976
650    _2
$a barva $7 D003116
650    _2
$a kolorimetrie $7 D003124
650    _2
$a lidé $7 D006801
650    _2
$a limita detekce $7 D057230
650    _2
$a náhražky mléka $x chemie $7 D041941
650    12
$a molekulový imprinting $7 D054802
650    _2
$a polymery $x klasifikace $7 D011108
650    _2
$a rozpouštědla $x chemie $7 D012997
650    _2
$a teplota $7 D013696
650    _2
$a analýza moči $x metody $7 D016482
655    _2
$a časopisecké články $7 D016428
700    1_
$a Grünhut, Marcos $u INQUISUR, Departamento de Química, Universidad Nacional del Sur (UNS)-CONICET, Av. Alem 1253, 8000 Bahía Blanca, Argentina.
700    1_
$a Šrámková, Ivana $u Charles University, Faculty of Pharmacy in Hradec Králové, The Department of Analytical Chemistry, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Lista, Adriana G $u INQUISUR, Departamento de Química, Universidad Nacional del Sur (UNS)-CONICET, Av. Alem 1253, 8000 Bahía Blanca, Argentina.
700    1_
$a Horstkotte, Burkhard $u Charles University, Faculty of Pharmacy in Hradec Králové, The Department of Analytical Chemistry, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Solich, Petr $u Charles University, Faculty of Pharmacy in Hradec Králové, The Department of Analytical Chemistry, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Sklenářová, Hana $u Charles University, Faculty of Pharmacy in Hradec Králové, The Department of Analytical Chemistry, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Acebal, Carolina C $u INQUISUR, Departamento de Química, Universidad Nacional del Sur (UNS)-CONICET, Av. Alem 1253, 8000 Bahía Blanca, Argentina. Electronic address: cacebal@uns.edu.ar.
773    0_
$w MED00004484 $t Talanta $x 1873-3573 $g Roč. 178, č. - (2018), s. 934-942
856    41
$u https://pubmed.ncbi.nlm.nih.gov/29136919 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20181008 $b ABA008
991    __
$a 20181008122706 $b ABA008
999    __
$a ok $b bmc $g 1339501 $s 1030556
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2018 $b 178 $c - $d 934-942 $e 20171023 $i 1873-3573 $m Talanta $n Talanta $x MED00004484
LZP    __
$a Pubmed-20181008

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...