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采用高效液相色谱法测定多元维生素药物制剂中的八种水溶性和脂溶性维生素。

Determination of eight water- and fat-soluble vitamins in multi-vitamin pharmaceutical formulations by high-performance liquid chromatography.

作者信息

Moreno P, Salvadó V

机构信息

Area de Química Analítica, Departament de Química, Universitat de Girona, Girona, Spain.

出版信息

J Chromatogr A. 2000 Feb 18;870(1-2):207-15. doi: 10.1016/s0021-9673(99)01021-3.

Abstract

In the present work, a reversed-phase high-performance liquid chromatographic procedure has been developed for the determination of water-soluble vitamins (thiamine hydrochloride, pyridoxine hydrochloride, nicotinamide, riboflavin phosphoric ester and cyanocobalamine) and fat-soluble vitamins (retinol palmitate, cholecalciferol, alpha-tocopherol acetate) in multi-vitamin pharmaceutical formulations. The sample treatment proposed consists of a solid-phase extraction with C18 AR cartridges that allow the separation of fat-soluble vitamins, which were retained on the sorbent, from water-soluble vitamins. Afterwards, the water-soluble vitamins were analysed by HPLC on a Nova-Pack C18 (150x3.9 mm, 4 microm) analytical column, using CH3OH-0.05 M CH3COONH4 as mobile phase. The chromatographic analysis of the fat-soluble vitamins was carried out after their sequential elution with methanol and chloroform from C18 sorbent, on the above column. The mobile phase employed was MeOH-CH2CN (95:5, v/v) working at a flow-rate of 2 ml min(-1) in isocratic mode. The solid-phase extraction for these vitamins had been previously optimised. The experimental variables studied were: application volume, elution solvents and cleaning solutions. The UV-Vis detection of vitamins was made at 270 nm for all the water-soluble vitamins (362 nm for B12) and 285 nm for the water-soluble and fat-soluble vitamins present in real samples at different concentration levels. The accuracy of the method was tested obtaining an average recovery ranging between 78 and 116%.

摘要

在本研究中,已开发出一种反相高效液相色谱法,用于测定多种维生素药物制剂中的水溶性维生素(盐酸硫胺素、盐酸吡哆醇、烟酰胺、核黄素磷酸酯和氰钴胺)和脂溶性维生素(视黄醇棕榈酸酯、胆钙化醇、α-生育酚醋酸酯)。所提出的样品处理方法包括使用C18 AR柱进行固相萃取,该方法可将保留在吸附剂上的脂溶性维生素与水溶性维生素分离。之后,水溶性维生素在Nova-Pack C18(150×3.9 mm,4 µm)分析柱上通过高效液相色谱法进行分析,使用甲醇-0.05 M醋酸铵作为流动相。脂溶性维生素在从C18吸附剂上依次用甲醇和氯仿洗脱后,在上述柱上进行色谱分析。所用流动相为甲醇-乙腈(95:5,v/v),以等度模式在2 ml min⁻¹的流速下运行。这些维生素的固相萃取先前已进行了优化。研究的实验变量包括:进样体积、洗脱溶剂和清洗溶液。所有水溶性维生素(B12为362 nm)在270 nm处进行紫外-可见检测,不同浓度水平的实际样品中存在的水溶性和脂溶性维生素在285 nm处进行检测。该方法的准确性经过测试,平均回收率在78%至116%之间。

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