Systematic toxicological analysis by high-performance liquid chromatography with diode array detection (HPLC-DAD)

Verfasser / Beitragende:
[Fritz Pragst, Matthias Herzler, Björn-Thoralf Erxleben]
Ort, Verlag, Jahr:
2004
Enthalten in:
Clinical Chemistry and Laboratory Medicine, 42/11(2004-11-01), 1325-1340
Format:
Artikel (online)
ID: 378917455
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024 7 0 |a 10.1515/CCLM.2004.251  |2 doi 
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245 0 0 |a Systematic toxicological analysis by high-performance liquid chromatography with diode array detection (HPLC-DAD)  |h [Elektronische Daten]  |c [Fritz Pragst, Matthias Herzler, Björn-Thoralf Erxleben] 
520 3 |a In recent years, photodiode array detectors (DADs) have been much improved with respect to wavelength accuracy and resolution, sensitivity, linearity and software operation. UV spectra of drugs measured with up-to-date DADs from different manufacturers are in excellent agreement, have the same quality as measured by a conventional UV spectrometer and are highly reproducible. The calculation of similarity parameters by the DAD software includes the entire range of the spectra compared and allows recognition of very small differences. It was shown in a systematic study of more than 2500 toxicologically relevant substances that UV spectra have a very high specificity with respect to substance structure. Therefore, HPLC-DAD in combination with a comprehensive database of UV spectra and retention parameters is one of the most efficient techniques used in systematic toxicological analysis (STA). Furthermore, the method is advantageous for the identification of metabolites, since in many cases they have the same or very similar UV spectra compared with their respective parent substances and their retention times on reversed-phase columns are shifted in a manner typical of the particular biotransformation reaction. Beside these general aspects, practical applications of HPLC-DAD for STA are reviewed with respect to sample preparation and chromatographic conditions. The efficiency of the method is demonstrated for an example of a routine procedure using liquid-liquid extraction with CH2Cl2 and protein precipitation for sample preparation, a system of three isocratic mobile phases with different acetonitrile/phosphate buffer ratios and RP8 columns for chromatography and a database of 2682 UV spectra and relative retention times for substance identification. 
540 |a © Walter de Gruyter 
690 7 |a Medical equipment & techniques  |2 nationallicence 
690 7 |a Medical diagnosis  |2 nationallicence 
690 7 |a Diseases & disorders  |2 nationallicence 
690 7 |a high-performance liquid chromatography  |2 nationallicence 
690 7 |a metabolites of drugs  |2 nationallicence 
690 7 |a photodiode array detector  |2 nationallicence 
690 7 |a systematic toxicological analysis  |2 nationallicence 
690 7 |a UV spectral library  |2 nationallicence 
700 1 |a Pragst  |D Fritz  |u Institute of Legal Medicine, University Hospital Charité, Berlin, Germany  |4 aut 
700 1 |a Herzler  |D Matthias  |u Federal Institute for Risk Assessment (BfR), Berlin, Germany  |4 aut 
700 1 |a Erxleben  |D Björn-Thoralf  |u Shimadzu Europe GmbH, Duisburg, Germany  |4 aut 
773 0 |t Clinical Chemistry and Laboratory Medicine  |d Walter de Gruyter  |g 42/11(2004-11-01), 1325-1340  |x 1434-6621  |q 42:11<1325  |1 2004  |2 42  |o cclm 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Herzler  |D Matthias  |u Federal Institute for Risk Assessment (BfR), Berlin, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Erxleben  |D Björn-Thoralf  |u Shimadzu Europe GmbH, Duisburg, Germany  |4 aut 
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