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高效液相色谱-荧光检测法测定血浆中总同型半胱氨酸
引用本文:廖瑛,梁奕铨,智喜梅,廖志红. 高效液相色谱-荧光检测法测定血浆中总同型半胱氨酸[J]. 色谱, 2000, 18(1): 49-51
作者姓名:廖瑛  梁奕铨  智喜梅  廖志红
作者单位:中山医科大学附属第一医院内分泌研究室,广东,广州,510080
基金项目:广东省科委攻关项目!资助 (962 2 0 5 2 0 1)
摘    要:
 建立了测定血浆中总同型半胱氨酸的柱前衍生、高效液相色谱-荧光检测的分析方法。以Br omobimane作荧光剂,对巯基进行衍生。同型半胱氨酸的最低检测浓度为0.5 μmol/L,线性 浓度范围是2.5~80.0 μmol/L,回收率为94.0%~112.0%,批内、批间相对标准偏差都小于5. 6%。关键词:

关 键 词:高效液相色谱法  荧光检测  同型半胱氨酸
修稿时间:1998-11-23

Determination of Plasma Homocysteine by High Performance Liquid Chromatography with Fluorescence Detection
LIAO Ying,LIANG Yi-quan,ZHI Xi-mei,LIAO Zhi-hong. Determination of Plasma Homocysteine by High Performance Liquid Chromatography with Fluorescence Detection[J]. Chinese journal of chromatography, 2000, 18(1): 49-51
Authors:LIAO Ying  LIANG Yi-quan  ZHI Xi-mei  LIAO Zhi-hong
Affiliation:Research Unit of Endocrinology, First Affiliated Hospital, Sun Yat-sen University of Medical Sciences, Guangzhou 510080, China. liaoying@public.guangzhou.gd.cn
Abstract:
This article report a highly sensitive method specific for the determination of homocysteine in plasma by high performance liquid chromatography with fluorescence detection. Half mL plasma with 100 microL 0.11 mol/L sodium borohydride in 50 mmol/L Tris-HCl (pH 9.0) was kept at 30 degrees C for 30 min, and then 0.5 mL 0.5 mol/L perchloric acid was added. After the mixture was kept at room temperature for 10 min and centrifuged at 15,000 r/min for 10 min, 0.5 mL aliquots of the supernatant solution was pipetted into another vial containing 0.1 mL 3 mmol/L Bromobimane in 1.0 mol/L Na2EDTA (pH 7.0) and 0.7 mL of 90 mmol/L ammonium bicarbonate buffer containing 1.43 mol/L Na2EDTA, pH 8.0. The content was mixed, kept at 37 degrees C for 30 min and centrifuged at 15,000 r/min for 10 min. Then 10 microL aliquots of the supernatant solution was injected into a high performance liquid chromatograph with fluorescence detector. The chromatographic conditions were as follows: an ODS column (4.6 mm i.d. x 150 mm, 5 microns), was eluted with a flow rate of 1.0 mL/min. The fluorescence detector was operated at lambda ex 365 nm and lambda em 475 nm. Mobile phase frompump A was 3% methanol containing 0.25% acetic acid. In gradient elution program the methanol from pump B was as follows: 0-8 min, 5%; 8-15 min, 5%-12%; 15-20 min, 12%; 20-30 min, 12%-20%; 30-32 min, 20%; 32-35 min, 20%-100%; 35-40 min, 100%; 40-43 min, 100%-5%; 43-45 min, 5%. The method proved to be linear in the range of 2.5-80.0 mumol/L with a regression coefficient of 0.9988. The minimum detection limit was 0.5 mumol/L, the recoveries were 94.0%-112.0%, and the RSD values were less than 5.6%.
Keywords:high performance liquid chromatography  fluorescence detection  homocysteine  
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