液相色谱法同时分析五种水溶性维生素的稳定性指示方法的建立

Mouloud Yessaad, L. Bernard, D. Bourdeaux, P. Chennell, V. Sautou
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引用次数: 4

摘要

摘要背景:水溶性维生素通常同时包含在药物制剂中作为食物补充剂或肠外营养混合物中。考虑到它们对热、光或pH变化的敏感性,使用经过验证的稳定性指示方法研究它们的稳定性非常重要。因此,我们旨在验证同时定量5种水溶性维生素的液相色谱(LC)稳定性指示方法。方法采用二极管阵列检测器的液相色谱法对4种水溶性B族维生素(烟酰胺、吡哆醇、叶酸、氰钴胺)和抗坏血酸进行分析。在C18固定相上,以溶剂a(含0.2%偏磷酸的水和乙腈98:2)和溶剂B(含100%乙腈)梯度洗脱分离。所有的维生素都在强制降解条件下进行,我们发现得到的降解产物对维生素没有干扰。结果该方法可在30分钟内分离5种水溶性维生素,不受酸/碱溶液、双氧水、温度和光照等因素的干扰。它满足所有的定性和定量验证标准,具有可接受的精度和良好的线性。结论该方法可用于药物制剂中水溶性维生素的稳定性研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Stability Indicating Method for Simultaneous Analysis of Five Water-Soluble Vitamins by Liquid Chromatography
Abstract Background Water-soluble vitamins are often included simultaneously in pharmaceutical formulations as food complements or in parenteral nutrition mixtures. Given their sensitivity to heat, light or pH variations, it is important to study their stability using validated stability indicating methods. We thus aimed to validate a liquid chromatography (LC) stability-indicating method for the simultaneous quantification of 5 water-soluble vitamins. Methods We analyzed four water-soluble B vitamins (nicotinamide, pyridoxine, folic acid, cyanocobalamin) and ascorbic acid using a LC method with diode array detector. They were separated on a C18 stationary phase under gradient elution of solvent A [0.2 % of metaphosphoric acid in water and acetonitrile 98:2] and solvent B (100 % acetonitrile). All vitamins were subjected to forced degradation conditions and we showed that the obtained degradation products didn’t interfere with the vitamins. Results The method allows the separation of the 5 water-soluble vitamins in a 30 minute run without any interference from the breakdown products obtained with acid/alkaline solutions, hydrogen peroxide, temperature and light. It meets all the qualitative and quantitative criteria for validation with an acceptable accuracy and good linearity. Conclusions This stability-indicating method can be used for carrying out stability studies of water-soluble vitamins in pharmaceutical preparations.
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