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Flow injection tyrosinase biosensor for direct determination of acetaminophen in human urine
A. Frangu, K. Pravcová, P. Šilarová, T. Arbneshi, M. Sýs,
Jazyk angličtina Země Německo
Typ dokumentu hodnotící studie, časopisecké články
Grantová podpora
project No. SGS-2018-001
Institutional Student Grand, University of Pardubice
CEEPUS CIII CZ 0212 10 1617 network for mobility
CEEPUS CIII: Education of Modern Analytical and Bioanalytical Methods
NLK
ProQuest Central
od 2013-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2003-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 2013-01-01 do Před 1 rokem
- MeSH
- Agaricus enzymologie MeSH
- analýza moči přístrojové vybavení metody MeSH
- biosenzitivní techniky přístrojové vybavení metody MeSH
- design vybavení MeSH
- lidé MeSH
- limita detekce MeSH
- neopioidní analgetika moč MeSH
- paracetamol moč MeSH
- průtoková injekční analýza přístrojové vybavení metody MeSH
- tyrosinasa chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
An amperometric biosensor compatible with a flow injection analysis (FIA) for highly selective determination of acetaminophen (APAP) in a sample of human urine was developed. This biosensor is also suitable for use in the routine pharmaceutical practice. To prove this statement, two different commercially available pharmaceutical formulations were analyzed. This nano-(bio)electroanalytical device was made from a commercially available screen-printed carbon electrode covered by a thin layer of non-functionalized graphene (NFG) as amperometric transducer. A biorecognition layer was prepared from mushroom (Agaricus bisporus) tyrosinase (EC 1.14.18.1) cross-linked using glutaraldehyde, where resulting aggregates were covered by Nafion®, a known ion exchange membrane. Owing to the use of tyrosinase and presence of NFG, the developed analytical instrument is able to measure even at potentials of 0 V. Linear ranges differ according to choice of detection potential, namely up to 130 μmol L-1 at 0 V, up to 90 μmol L-1 at -0.1 V, and up to 70 μmol L-1 at -0.15 V. The first mentioned linear range is described by the equation Ip [μA] = 0.236 - 0.1984c [μmol L-1] and correlation coefficient r = 0.9987; this equation was used to quantify the content of APAP in each sample. The limit of detection of APAP was estimated to be 1.1 μmol L-1. A recovery of 96.8% (c = 25 μmol L-1, n = 5 measurements) was calculated. The obtained results show that FIA is a very selective method for APAP determination, being comparable to the chosen reference method of reversed-phase high-performance liquid chromatography.
Citace poskytuje Crossref.org
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- $a Frangu, Arbër $u Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Prishtina, Str. Mother Teresa, 10 000, Prishtina, Republic of Kosovo. Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, 532 10, Pardubice, Czech Republic.
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- $a An amperometric biosensor compatible with a flow injection analysis (FIA) for highly selective determination of acetaminophen (APAP) in a sample of human urine was developed. This biosensor is also suitable for use in the routine pharmaceutical practice. To prove this statement, two different commercially available pharmaceutical formulations were analyzed. This nano-(bio)electroanalytical device was made from a commercially available screen-printed carbon electrode covered by a thin layer of non-functionalized graphene (NFG) as amperometric transducer. A biorecognition layer was prepared from mushroom (Agaricus bisporus) tyrosinase (EC 1.14.18.1) cross-linked using glutaraldehyde, where resulting aggregates were covered by Nafion®, a known ion exchange membrane. Owing to the use of tyrosinase and presence of NFG, the developed analytical instrument is able to measure even at potentials of 0 V. Linear ranges differ according to choice of detection potential, namely up to 130 μmol L-1 at 0 V, up to 90 μmol L-1 at -0.1 V, and up to 70 μmol L-1 at -0.15 V. The first mentioned linear range is described by the equation Ip [μA] = 0.236 - 0.1984c [μmol L-1] and correlation coefficient r = 0.9987; this equation was used to quantify the content of APAP in each sample. The limit of detection of APAP was estimated to be 1.1 μmol L-1. A recovery of 96.8% (c = 25 μmol L-1, n = 5 measurements) was calculated. The obtained results show that FIA is a very selective method for APAP determination, being comparable to the chosen reference method of reversed-phase high-performance liquid chromatography.
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