Secure Connection FailedTo detect the residual clenbuterol in pork meat and liver using HPLC with Coulometric electrode array system. Homogenized meat or liver sample was treated with 1 mol determination of clenbuterol in meat L -1 hydrochloric acid and centrifuged, the fat existing in meat or liver tissue was removed by diethyl ether. The pH of the remaining aqueous layer was adjusted to The ether extract was evaporated to dryness, debolex custom motorcycles residue was dissolved in determination of clenbuterol in meat mobile phase. The mobile phase A consisted of 50 mmol mrat L clenbbuterol phosphoric acid mmol x L -1 triethylamine and was adjusted to pH 4.
Determination of Clenbuterol-Like Beta-Agonist Residues in Hair | LCGC
The practical procedure involves acid extraction followed by one solid-phase clean-up step with weak cation-exchange resins.
The limit of detection LOD for the enantiomers of clenbuterol was 0. This technique can be considered as a starting point for the distribution and pharmacokinetics of clenbuterol enantiomers in livestock. The article was received on 01 Mar , accepted on 16 Apr and first published on 27 Apr If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request permission using RightsLink.
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