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采用经验证的稳定性指示高效液相色谱法同时测定多种维生素糖浆中的某些水溶性维生素和防腐剂。

Simultaneous determination of some water-soluble vitamins and preservatives in multivitamin syrup by validated stability-indicating high-performance liquid chromatography method.

作者信息

Vidović Stojanka, Stojanović Biljana, Veljković Jelena, Prazić-Arsić Ljiljana, Roglić Goran, Manojlović Dragan

机构信息

Galenika a.d., Batajnicki drum bb, 11070 Belgrade, Serbia.

出版信息

J Chromatogr A. 2008 Aug 22;1202(2):155-62. doi: 10.1016/j.chroma.2008.06.039. Epub 2008 Jul 3.

Abstract

HPLC stability-indicating method has been developed for the simultaneous determination of some water-soluble vitamins (ascorbic acid, thiamine hydrochloride, riboflavin-5'-phosphate sodium, pyridoxine hydrochloride, nicotinamide, D(+)-panthenol) and two preservatives (methylparaben and sodium benzoate) in multivitamin syrup preparation. Water-soluble vitamins, preservatives and their degradants were separated on Zorbax SB-Aq (C(18)) (250 mm x 4.6 mm, 5 microm) column at an ambient temperature. Combined isocratic and gradient elution was performed with a mobile phase consisting of 0.0125 M hexane-1-sulfonic acid sodium salt in 0.1% (m/v) o-phosphoric acid, pH 2.4-2.5 (solvent A) and acetonitrile (solvent B) at the flow-rate 1 ml min(-1). Starting with solvent A an isocratic elution was performed for 15 min, then the composition was changed to 85% of A and 15% of B during the next 20 min and it was constant for 5 min, then the composition was changed to 70% of A and 30% of B during next 15 min and it was constant for 5 min and finally was changed to 100% of A as at the beginning of the elution. Detection was performed with diode array detector at 210, 230 and 254 nm. Multivitamin syrup preparation was subjected to stress testing (forced degradation) in order to demonstrate that degradants from the vitamins, preservatives and/or product excipients do not interfere with the quantification of vitamins and preservatives. Typical validation characteristics: selectivity, accuracy, precision, linearity, range, limit of quantification and limit of detection were evaluated for vitamins and preservatives.

摘要

已开发出一种高效液相色谱稳定性指示方法,用于同时测定多种维生素糖浆制剂中的一些水溶性维生素(抗坏血酸、盐酸硫胺素、核黄素-5'-磷酸钠、盐酸吡哆醇、烟酰胺、D(+)-泛醇)和两种防腐剂(对羟基苯甲酸甲酯和苯甲酸钠)。水溶性维生素、防腐剂及其降解产物在室温下于Zorbax SB-Aq(C(18))(250 mm×4.6 mm,5μm)柱上分离。采用等度洗脱和梯度洗脱相结合的方式,流动相由0.1%(m/v)邻磷酸中含0.0125 M己烷-1-磺酸钠盐、pH 2.4 - 2.5(溶剂A)和乙腈(溶剂B)组成,流速为1 ml min(-1)。起始用溶剂A进行15分钟的等度洗脱,然后在接下来的20分钟内将组成变为85%的A和15%的B并保持5分钟,接着在接下来的15分钟内将组成变为70%的A和30%的B并保持5分钟,最后变为100%的A,如同洗脱开始时一样。使用二极管阵列检测器在210、230和254 nm处进行检测。对多种维生素糖浆制剂进行了强制降解试验,以证明维生素、防腐剂和/或产品辅料的降解产物不会干扰维生素和防腐剂的定量测定。对维生素和防腐剂评估了典型的验证特性:选择性、准确性、精密度、线性、范围、定量限和检测限。

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