Abstract
A high performance liquid chromatographic (HPLC) method was developed for the determination of trenbolone acetate, 17α-trenbolone and 17β-trenbolone in bovine muscle and liver. Bovine muscle sample was extracted with acetonitrile, filtered, and defatted with acetonitrile-saturated n-hexane. The acetonitrile extract after concentration and clean-up with Bond Elut C18 cartridge was ready for HPLC analysis. HPLC conditions were as follows, column: Inertsil ODS-3V, mobile phase: acetonitrile/methanol/H2O (50:10:40, v/v), flow rate: 1 mL/min, and detecting wavelength: UV 340 nm. For bovine muscle, the recoveries were 83.8-98.9% for trenbolone acetate, 17α-trenbolone and 17β-trenbolone spiked at concentrations between 2-4 ppb, and the variation coefficients were 1.2-4.8%. For bovine liver, the recoveries were 82.6-95.7% for the three trenbolones spiked at concentrations between 10-20 ppb, and the variation coefficients were 1.9-6.7%. The detection limits for trenbolone acetate, 17α-trenbolone and 17β-trenbolone were 1, 0.5 and 0.5 ppb in bovine muscle, and 4, 2 and 2 ppb in bovine liver, respectively. After the survey, 30 marketed bovine muscle samples showed no detection of trenbolone acetate and its metabolites.
Recommended Citation
Tsai, C.-F.; Chang, M.-H.; Pan, J.-Q.; and Chou, S.-S.
(2004)
"A method for the determination of trenbolone in bovine muscle and liver,"
Journal of Food and Drug Analysis: Vol. 12
:
Iss.
4
, Article 12.
Available at: https://doi.org/10.38212/2224-6614.2625
