Koleva M, Joneidi M, Budewski O
Pharmazie. 1975 Mar;30(3):168-9.
A quantitative method for the determination of vitamins A and E is proposed based on the direct densitometry of thinlayer chromatographic spots. An appropriate solvent system for the chromatographic separation of the vitamins and the conditions under which a linear relationship between the absorbed light and the logarithm of concentration exists (1--10 mug range) are found. The precision of the method is evaluated by a statistical treatment of the results. Satisfactory reproducibility is established-- the variation coefficient for the determination of the two vitamins is about 4--5%. The method is applied for the analysis of oil and aqueous injection solutions, mixtures containing the three vitamins A, E and D2 and some pharmaceutical preparations (Pharmavit¿ and Devitforte¿). The presence of the decomposition products and other substances (other pharmaceuticals, stabilizers, solubilizers etc.) does not affect the determination. The analysis is performed without preliminary treatment of the sample.
提出了一种基于薄层色谱斑点直接光密度法测定维生素A和E的定量方法。找到了用于维生素色谱分离的合适溶剂系统以及存在吸收光与浓度对数呈线性关系的条件(1-10微克范围)。通过对结果的统计处理评估该方法的精密度。建立了令人满意的重现性——两种维生素测定的变异系数约为4-5%。该方法用于分析油剂和水性注射液、含有维生素A、E和D2的混合物以及一些药物制剂(Pharmavit®和Devitforte®)。分解产物和其他物质(其他药物、稳定剂、增溶剂等)的存在不影响测定。分析无需对样品进行预处理。