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鱼类中水溶性B族维生素天然成分的筛选:酶提取、亲水相互作用色谱分离及串联质谱测定

Screening Natural Content of Water-Soluble B Vitamins in Fish: Enzymatic Extraction, HILIC Separation, and Tandem Mass Spectrometric Determination.

作者信息

Chatterjee Niladri Sekhar, Kumar K Ashok, Ajeeshkumar K K, Kumari K R Remya, Vishnu K V, Anandan Rangasamy, Mathew Suseela, Ravishankar C N

机构信息

Central Institute of Fisheries Technology, CIFT Junction, Matsyapuri PO, Willingdon Island, Cochin-682 029, Kerala, India.

出版信息

J AOAC Int. 2017 May 1;100(3):579-585. doi: 10.5740/jaoacint.17-0056. Epub 2017 Mar 16.

Abstract

Despite the potential of LC with tandem MS (MS/MS) in improving sensitivity and selectivity, analytical methods are scarce for the determination of protein-bound and phosphorylated forms of B vitamins in food. This prompted us to develop a method for LC-MS/MS determination of naturally occurring nicotinamide, nicotinic acid, thiamine, pyridoxine, riboflavin, pantothenic acid, biotin, folic acid, and cyanocobalamin in fish. Baseline separation of the vitamins was achieved in a hydrophilic interaction LC condition. An ultrasonication-assisted enzymatic extraction protocol for sample preparation was optimized and validated. The time required for extraction was significantly reduced (to 4 h), while maintaining good extraction efficiency. Acetonitrile content (80%, v/v) in the prepared sample was found to be optimum for excellent peak shape and sensitivity. The dynamic linear range of the vitamins ranged from 2.5 to 500 ng/g, and the regression coefficient values were greater than 0.99. LOQ values ranged from 0.4 to 50 ng/g for the different vitamins. The spike recovery values at 50 and 100 ng/g ranged from 87.5 to 97.5%. The intra- and interday precision values were satisfactory. Accuracy of the developed method was determined by analysis of a Certified Reference Material. The method could also be used for unambiguous determination of the natural content of the target vitamins in fish.

摘要

尽管液相色谱串联质谱法(MS/MS)在提高灵敏度和选择性方面具有潜力,但用于测定食品中蛋白质结合型和磷酸化形式B族维生素的分析方法却很少。这促使我们开发一种液相色谱-质谱联用方法,用于测定鱼类中天然存在的烟酰胺、烟酸、硫胺素、吡哆醇、核黄素、泛酸、生物素、叶酸和钴胺素。在亲水相互作用液相色谱条件下实现了维生素的基线分离。优化并验证了一种超声辅助酶提取样品制备方案。提取所需时间显著缩短(至4小时),同时保持了良好的提取效率。发现制备样品中乙腈含量(80%,v/v)对于获得优异的峰形和灵敏度最为适宜。维生素的动态线性范围为2.5至500 ng/g,回归系数值大于0.99。不同维生素的定量限(LOQ)值范围为0.4至50 ng/g。50和100 ng/g添加水平下的回收率值范围为87.5%至97.5%。日内和日间精密度值令人满意。通过分析有证标准物质确定了所开发方法的准确性。该方法还可用于明确测定鱼类中目标维生素的天然含量。

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