Abstract
Three gas-liquid chromatographic (G.L.C.) procedures discussed have been designed around the four "esses" of detection tests--speed, sensitivity, simplicity, and specificity. These techniques are admirably applicable to the very low plasma drug levels encountered in blood testing under pre-race conditions. The methods are equally applicable to post-race testing procedures, where both blood and urine samples are tested. Drugs can only rarely be detected by the electron capture detector (E.C.D.) without a prior derivatization step, which conveys to the drug(s) high electron affinity. Because of broad applicability, two derivatizing agents, heptafluorobutyric (HFBA) and pentafluorpropionic (PFPA) anhydrides are employed. The three techniques, allowing broad coverage of various drug classes are: 1) direct derivatization of drugs to form strongly electron capturing amides and esters. 2) reductive fragmentation of drugs with lithium aluminum hydride to form alcohols, with conversion to ester derivatives. 3) oxidative fragmentation of drugs with potassium dichromate to form derivatizable groups, followed by direct derivatization.
Document Type
Article
Publication Date
1976
Digital Object Identifier (DOI)
10.1136/bjsm.10.3.129
Repository Citation
Blake, J. W. and Tobin, Thomas, "The gas-liquid chromatograph and the electron capture detection in equine drug testing." (1976). Maxwell H. Gluck Equine Research Center Faculty Publications. 74.
https://uknowledge.uky.edu/gerc_facpub/74
Notes/Citation Information
Blake, J. W., & Tobin, T. (1976). The gas-liquid chromatograph and the electron capture detection in equine drug testing. British Journal of Sports Medicine, 10(3), 129-132. https://doi.org/10.1136/bjsm.10.3.129