Giorgi Margherita Grotzkyj, Howland Kevin, Martin Colin, Bonner Adrian B
Centre for Health Services Studies, University of Kent, Canterbury, Kent CT2 7NF, UK.
ScientificWorldJournal. 2012;2012:359721. doi: 10.1100/2012/359721. Epub 2012 Mar 12.
An HPLC method was developed and validated for the concurrent detection and quantitation of seven water-soluble vitamins (C, B(1), B(2), B(5), B(6), B(9), B(12)) in biological matrices (plasma and urine). Separation was achieved at 30°C on a reversed-phase C18-A column using combined isocratic and linear gradient elution with a mobile phase consisting of 0.01% TFA aqueous and 100% methanol. Total run time was 35 minutes. Detection was performed with diode array set at 280 nm. Each vitamin was quantitatively determined at its maximum wavelength. Spectral comparison was used for peak identification in real samples (24 plasma and urine samples from abstinent alcohol-dependent males). Interday and intraday precision were <4% and <7%, respectively, for all vitamins. Recovery percentages ranged from 93% to 100%.
建立并验证了一种高效液相色谱法,用于同时检测和定量生物基质(血浆和尿液)中的七种水溶性维生素(维生素C、维生素B1、维生素B2、维生素B5、维生素B6、维生素B9、维生素B12)。在30°C下,使用由0.01%三氟乙酸水溶液和100%甲醇组成的流动相,通过等度洗脱和线性梯度洗脱相结合的方式,在反相C18 - A柱上实现分离。总运行时间为35分钟。使用设置在280 nm的二极管阵列进行检测。每种维生素在其最大波长处进行定量测定。通过光谱比较对实际样品(24份来自戒酒的酒精依赖男性的血浆和尿液样品)中的峰进行鉴定。所有维生素的日间和日内精密度分别<4%和<7%。回收率在93%至100%之间。