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超高效液相色谱法同时测定多种维生素矿物质胶囊中10种脂溶性维生素

Simultaneous Determination of 10 Fat-Soluble Vitamins by Ultra-Performance Liquid Chromatography in Multivitamins With Minerals Capsules.

作者信息

Jeelani Salika, Kassymbek Zarema

机构信息

Analytical Development Laboratory, United States Pharmacopeial Convention (USP), Rockville, Maryland, USA.

出版信息

J Sep Sci. 2025 May;48(5):e70167. doi: 10.1002/jssc.70167.

Abstract

A novel and accurate ultra-high performance liquid chromatography (UHPLC) method combined with UV detector was developed for the simultaneous determination of 10 fat-soluble vitamins (retinyl acetate, retinyl palmitate, beta carotene, alpha tocopherol, alpha tocopheryl acetate, alpha tocopheryl acid succinate, ergocalciferol, cholecalciferol, phytonadione, and menaquinone-7) in multivitamin with mineral capsules. The chromatographic separation was achieved on a Waters XBridge Sheild C18 (100 × 2.1 mm, 1.7 µm) column. The mobile phase comprised of 0.1% formic acid (v/v) in water and 0.1% formic acid in acetonitrile (v/v) delivered in a gradient mode. An enhanced and simple sample preparation procedure involving enzyme digestion of the gel coating of the capsules and ultra-sonication was developed compared to the complex and time-consuming saponification methods. The method was validated to fulfill International Conference on Harmonization (ICH) requirements and included specificity, linearity, accuracy, precision, and robustness. The linearity of the method was excellent (R > 0.999), the RSD for the precision was < 5% and the recovery of the vitamins was in the range of 99.2%-101.9%, demonstrating that the method is suitable for analysis of fate-soluble vitamins in multivitamin capsules. The developed method could be incorporated into the USP-NF Multivitamin with minerals capsules monograph.

摘要

建立了一种新颖且准确的超高效液相色谱(UHPLC)法,结合紫外检测器,用于同时测定多维元素矿物质胶囊中10种脂溶性维生素(醋酸视黄酯、棕榈酸视黄酯、β-胡萝卜素、α-生育酚、醋酸α-生育酚、琥珀酸α-生育酚、麦角钙化醇、胆钙化醇、叶绿醌和甲萘醌-7)。色谱分离在Waters XBridge Sheild C18(100×2.1 mm,1.7 µm)柱上进行。流动相由0.1%甲酸(v/v)的水溶液和0.1%甲酸(v/v)的乙腈溶液组成,采用梯度洗脱模式。与复杂且耗时的皂化法相比,开发了一种改进且简单的样品制备程序,包括对胶囊的凝胶包衣进行酶消化和超声处理。该方法经过验证,符合国际协调会议(ICH)的要求,包括特异性、线性、准确性、精密度和稳健性。该方法线性良好(R>0.999),精密度的相对标准偏差(RSD)<5%,维生素的回收率在99.2%-101.9%范围内,表明该方法适用于分析多维元素胶囊中的脂溶性维生素。所开发的方法可纳入美国药典 - 国家处方集(USP-NF)多维元素矿物质胶囊专论中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b307/12096806/4f6dd13ad6b4/JSSC-48-e70167-g001.jpg

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