On-line solid-phase extraction-HPLC-fluorescence detection for simultaneous determination of puerarin and daidzein in human serum

被引:17
作者
Liu, Ying-Kun [1 ,2 ]
Jia, Xiao-Yan [1 ]
Liu, Xiao [1 ]
Zhang, Zhi-Qi [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Mat Sci, Key Lab Analyt Chem Life Sci Shaanxi Prov, Xian 710062, Peoples R China
[2] Zhejiang Agr & Forestry Univ, Nurturing Stn, State Key Lab Subtrop Silviculture, Linan 311300, Peoples R China
关键词
On-line solid-phase extraction; HPLC-fluorescence detection; Puerarin; Daidzein; Human serum; Response surface methodology; TANDEM MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; MEDICINAL PREPARATIONS; ASSISTED EXTRACTION; PLASMA; RADIX; OPTIMIZATION; COLUMN; URINE; WATER;
D O I
10.1016/j.talanta.2010.06.038
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Response surface methodology (RSM) was applied to the optimization of on-line solid-phase extraction (SPE) parameters, and an automated system of on-line SPE coupled with high-performance liquid chromatography (HPLC) with fluorescence detection was developed for the determination of puerarin and daidzein in human serum. The human serum sample of 50 mu L was injected into a conditioned C18 SPE cartridge, and the matrix was washed out with acetonitrile-KH2PO4-triethylamine buffer (0.01 M, pH 7.4) (3:97, v/v) for 3 min at a flow rate of 0.25 mL/min. Then the target analytes were eluted and transferred to the analytical column. A chromatographic gradient elution was programmed with the mobile phase consisting of acetonitrile and KH2PO4-triethylamine buffer, and the analytes were determined with a fluorescence detector at excitation wavelength of 350 nm and emission wavelength of 472 nm, respectively. The proposed method presented good linear relations (0.85-170 mu g/mL for puerarin and 0.2-40 mu g/mL for daidzein), satisfactory precision (RSD < 8%), and accredited recovery (92.5-107.8%). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1212 / 1217
页数:6
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