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采用固相萃取和带多通道紫外检测的窄孔高效液相色谱法分析血清微量样本中的补充维生素K1(20) 。

Analysis of supplemented vitamin K1(20) in serum microsamples by solid-phase extraction and narrow-bone HPLC with multichannel ultraviolet detection.

作者信息

Kirk E M, Fell A F

机构信息

Pharmaceutical Chemistry, School of Pharmacy, University of Bradford, U.K.

出版信息

Clin Chem. 1989 Jul;35(7):1288-92.

PMID:2758573
Abstract

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.

摘要

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。

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