Kirk E M, Fell A F
Pharmaceutical Chemistry, School of Pharmacy, University of Bradford, U.K.
Clin Chem. 1989 Jul;35(7):1288-92.
A sensitive method for the determination of vitamin K1(20) in serum microsamples (50 microL) has been developed, utilizing solid-phase extraction with C8 Bond-Elut columns and reversed-phase narrow-bore high-performance liquid chromatography [2.1 mm (i.d.), column] with a nonaqueous eluent. Recovery from serum (49 ng/mL) was 76% (n = 2). Peak homogeneity was assessed by photodiode array detection with absorbance ratio, spectral normalization, and transformation to the first- and second-derivative chromatograms. Calibration data at 248 nm over two ranges (20-200 ng/mL, 200-4000 ng/mL) varied linearly with concentration and were suitable for studies of vitamin K1 supplementation. By comparison with conventional columns, sensitivity was increased twofold.
已开发出一种用于测定血清微量样本(50微升)中维生素K1(20)的灵敏方法,该方法利用C8 Bond-Elut柱进行固相萃取,并采用反相窄内径高效液相色谱法[2.1毫米(内径)柱],使用非水流动相。从血清(49纳克/毫升)中的回收率为76%(n = 2)。通过光电二极管阵列检测,利用吸光度比、光谱归一化以及转换为一阶和二阶导数色谱图来评估峰纯度。在248纳米处,两个浓度范围(20 - 200纳克/毫升,200 - 4000纳克/毫升)的校准数据与浓度呈线性关系,适用于维生素K1补充研究。与传统色谱柱相比,灵敏度提高了两倍。