Nachilobe P, Boison J O, Cassidy R M, Fesser A C
Chemistry Department, University of Saskatchewan, Saskatoon, Canada.
J Chromatogr. 1993 Jul 2;616(2):243-52. doi: 10.1016/0378-4347(93)80392-h.
A high-performance liquid chromatographic (HPLC) method with a detection limit of 5 ng/ml was developed for the analysis of trimethoprim in bovine serum. Trimethoprim and the internal standard, ormetoprim, under alkaline conditions, were first extracted into dichloromethane and then back-extracted into dilute sulphuric acid (0.15 M) and cleaned-up on a C18 cartridge. Trimethoprim was quantified on a C18 column using a triethylammonium acetate-acetonitrile-methanol (16:3:1, v/v/v) mobile phase at a flow-rate of 1.5 ml/min, with ultraviolet detection at 225 nm. This method was used to verify the accuracy of test responses obtained with the Brilliant Black Reduction test, a rapid screening method, for trimethoprim levels in the serum of steers treated with Trivetrin. Confirmation of the presence of trimethoprim in the sample extract was obtained by thermospray HPLC-mass spectrometry.
建立了一种检测限为5 ng/ml的高效液相色谱(HPLC)法,用于分析牛血清中的甲氧苄啶。在碱性条件下,甲氧苄啶和内标奥美普明首先被萃取到二氯甲烷中,然后反萃取到稀硫酸(0.15 M)中,并在C18柱上进行净化。甲氧苄啶在C18柱上进行定量分析,流动相为乙酸三乙铵-乙腈-甲醇(16:3:1,v/v/v),流速为1.5 ml/min,在225 nm处进行紫外检测。该方法用于验证用亮黑还原试验(一种快速筛选方法)获得的试验响应对于用曲菌素治疗的阉牛血清中甲氧苄啶水平的准确性。通过热喷雾HPLC-质谱法确认样品提取物中存在甲氧苄啶。