Using of HPLC coupled with coulometric detector for the determination of biotin in pharmaceuticals
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作者:
Zerzanova, A.
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Charles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech RepublicCharles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
Zerzanova, A.
[1
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Zizkovsky, V.
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Charles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech RepublicCharles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
Zizkovsky, V.
[1
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Kucera, R.
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Charles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech RepublicCharles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
Kucera, R.
[1
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Klimes, J.
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Charles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech RepublicCharles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
Klimes, J.
[1
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Jesensky, I.
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Charles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech RepublicCharles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
Jesensky, I.
[1
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Dohnal, J.
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Zentiva AS, Prague 10237 10, Czech RepublicCharles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
Dohnal, J.
[2
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Barron, D.
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Univ Barcelona, Dept Analyt Chem, E-08028 Barcelona, SpainCharles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
Barron, D.
[3
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机构:
[1] Charles Univ Prague, Fac Pharm, Dept Pharmaceut Chem & Drug Control, Hradec Kralove 50005, Czech Republic
The method for the determination of biotin by high performance liquid chromatography (HPLC) coupled with coulometric detector is presented here. Chromatographic and detection conditions were tested. A LiChrospher 60RP-select B column (250 mm x 4 mm; 5 mu m) and the mobile phase containing 0.24 mol/L aqueous solution of acetic acid and acetonitrile in the ratio 85:15 (v/v) were found as the most suitable. The flow rate was 1 mL/min and the injected volume of the sample was 20 mu L. The hydrodynamic voltammograrn of biotin was measured and according to obtained data the detection parameters were set - channel I 600 mV, channel II 900 mV, sensitivity 1 mu A. The developed method has been validated. The calibration curve is linear in the range 15-3600 ng/mL, correlation coefficient is 0.9998, limits of detection and quantification are 5 and 15 ng/mL, respectively. Recovery of the spiked samples was 98.67% with R.S.D. 0.255% on average. The developed method has been successfully applied for determination of biotin in pharmaceutical preparations. (c) 2007 Elsevier B.V. All rights reserved.
机构:
Charles Univ Prague, Fac Sci, Dept Analyt Chem, UNESCO Lab Environm Electrochem, Albertov 6, CZ-12843 Prague 2, Czech RepublicCharles Univ Prague, Fac Sci, Dept Analyt Chem, UNESCO Lab Environm Electrochem, Albertov 6, CZ-12843 Prague 2, Czech Republic
Dejmkova, Hana
Daniel, Marjorie de Araujo
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Univ Fed Rio Grande do Sul, Ave Paulo Gama,110 Farroupilha, BR-90040060 Porto Alegre, RS, BrazilCharles Univ Prague, Fac Sci, Dept Analyt Chem, UNESCO Lab Environm Electrochem, Albertov 6, CZ-12843 Prague 2, Czech Republic
Daniel, Marjorie de Araujo
PROCEEDINGS OF THE INTERNATIONAL CONFERENCE MODERN ELECTROCHEMICAL METHODS XXXVIII,
2018,
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