TY - JOUR
T1 - Determination of 1-nitropyrene in herbs after selective enrichment by a sol-gel-generated immunoaffinity column
AU - Spitzer, Birgit
AU - Cichna-Markl, Margit
AU - Markl, Peter
AU - Sontag, Gerhard
AU - Knopp, D
AU - Niessner, R
N1 - DOI: 10.1016/S0021-9673(99)01311-4
Coden: JCRAE
Affiliations: Institute for Analytical Chemistry, Univ. Vienna, W., Vienna, Austria; Inst. Hydrochemistry Chem. Balneol., Tech. Univ. Munich, M., Munich, Germany
Adressen: Sontag, G.; Institute for Analytical Chemistry; University of Vienna; Waehringerstrasse 38 A-1090 Vienna, Austria; email: [email protected]
Source-File: AnalytChemScopus.csv
Import aus Scopus: 2-s2.0-0034595734
Importdatum: 12.02.2007 12:08:41
22.10.2007: Datenanforderung 1934 (Import Sachbearbeiter)
PY - 2000
Y1 - 2000
N2 - Using the determination of 1-nitropyrene as an example the paper demonstrates the advantages of including a highly selective sol-gel-generated immunoaffinity column in the sequence of clean-up steps necessary to determine haptens in complex matrices. The sol-gel method to immobilise antibodies enlarges the variety of immunoaffinity columns available and leads to mechanically stable columns with constant retention characteristics. The sample preparation scheme proposed combines acetonitrile extraction, size- exclusion and immunoaffinity chromatography. 1-Nitropyrene is then separated by reversed-phase HPLC from interfering compounds and determined after catalytic on-line reduction to the corresponding amine by spectrofluorimetry. Concentrations in the range from 0.1 to 1.4 œg/kg 1-nitropyrene were detected in herbs. (C) 2000 Elsevier Science B.V.
AB - Using the determination of 1-nitropyrene as an example the paper demonstrates the advantages of including a highly selective sol-gel-generated immunoaffinity column in the sequence of clean-up steps necessary to determine haptens in complex matrices. The sol-gel method to immobilise antibodies enlarges the variety of immunoaffinity columns available and leads to mechanically stable columns with constant retention characteristics. The sample preparation scheme proposed combines acetonitrile extraction, size- exclusion and immunoaffinity chromatography. 1-Nitropyrene is then separated by reversed-phase HPLC from interfering compounds and determined after catalytic on-line reduction to the corresponding amine by spectrofluorimetry. Concentrations in the range from 0.1 to 1.4 œg/kg 1-nitropyrene were detected in herbs. (C) 2000 Elsevier Science B.V.
U2 - 10.1016/S0021-9673(99)01311-4
DO - 10.1016/S0021-9673(99)01311-4
M3 - Article
SN - 0021-9673
VL - 880
SP - 113
EP - 120
JO - Journal of Chromatography A
JF - Journal of Chromatography A
IS - 1-2
ER -