Marszałł Marcin Leszek, Lebiedzińska Anna, Czarnowski Wojciech, Szefer Piotr
Department of Toxicology, Medical University of Gdańsk, Al. Gen. J. Hallera 107, Gdańsk 80-416, Poland.
J Chromatogr A. 2005 Nov 11;1094(1-2):91-8. doi: 10.1016/j.chroma.2005.07.091. Epub 2005 Aug 15.
The method for the simultaneous determination of thiamine hydrochloride, pyridoxine hydrochloride and cyanocobalamin by high-performance liquid chromatography (HPLC) with coulometric electrochemical and UV detections is presented. The retention time of vitamins was repeatedly determined by isocratic elution using 0.05 M phosphate buffer-10% methanol and 0.018 M trimethylamine (1 ml min(-1), pH 3.55) as mobile phase with the Supelco LC 18 column 5 microm (25 cm x 4.6 mm). The specificity of the method was demonstrated by the retention characteristics, coulometric electrochemical and UV detection. The limits of detection of thiamine, pyridoxine and cyanocobalamin were: 9.2, 2.7 and 0.08 ng/ml, respectively. The method was characterized also by wide concentration range, high sensitivity and good accuracy (99.6-102.7%). The repeatability of the method was evaluated at different level of concentration of vitamins and the relative standard deviation was below 4.5%. The method was successfully applied for the quantification of Vitamins B1, B6 and B12 in pharmaceutical preparations and dietary supplements.
介绍了一种采用库仑电化学检测和紫外检测的高效液相色谱法(HPLC)同时测定盐酸硫胺素、盐酸吡哆醇和钴胺素的方法。使用0.05M磷酸盐缓冲液-10%甲醇和0.018M三甲胺(1ml min(-1),pH 3.55)作为流动相,在Supelco LC 18 5微米柱(25cm×4.6mm)上通过等度洗脱反复测定维生素的保留时间。通过保留特性、库仑电化学检测和紫外检测证明了该方法的特异性。硫胺素、吡哆醇和钴胺素的检测限分别为:9.2、2.7和0.08ng/ml。该方法还具有浓度范围宽、灵敏度高和准确度好(99.6 - 102.7%)的特点。在不同维生素浓度水平下评估了该方法的重复性,相对标准偏差低于4.5%。该方法成功应用于药物制剂和膳食补充剂中维生素B1、B6和B12的定量分析。