Influence of Biological Matrix on Retention Behaviour and Identification Possibilities of Selected Neutral and Acidic Drugs in Thin Layer Chromatography. An Interlaboratory Investigation
- 1 November 1986
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Analytical Toxicology
- Vol. 10 (6) , 245-249
- https://doi.org/10.1093/jat/10.6.245
Abstract
Samples of autopsy blood and liver were spiked individually with aminophenazone, p-aminosalicylic acid, clordiazepoxide, clonazepam, cyclobarbital, furosemide, medazepam, phenacetin, phenazone, and phenobarbital and extracted with diethyl ether at pH 5. The extracts, as well as solutions of pure drugs, were developed in three thin layer chromatographic systems: chloroform:acetone (80:20), ethyl acetate:methanol:ammonia (85:10:5) and chloroform:methanol (90:10). The investigations performed in parallel in two laboratories showed that the intra- and inter-laboratory variability of RF values is larger for drugs extracted from liver. The biological matrix affected both precision and accuracy of results. The number of analysts involved in TLC procedures also affected the intra-laboratory precision.This publication has 5 references indexed in Scilit:
- Impact of Biological Matrix and Isolation Methods on Detectability and Interlaboratory Variations of TLC Rf-Values in Systematic Toxicological AnalysisJournal of Analytical Toxicology, 1984
- Influence of development distance on resolution in thin‐layer chromatographyJournal of High Resolution Chromatography, 1983
- Optimization of Thin Layer Chromatography for Toxicological Screening: Applicability of Shorter Development DistancesJournal of Analytical Toxicology, 1982
- Choice of thin-layer chromatographic systems for the routine screening for acidic drugs during toxicological analysesJournal of Chromatography A, 1978
- Choice of thin-layer chromatographic systems for the routine screening for neutral drugs during toxicological analysesJournal of Chromatography A, 1978