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高效液相 (HPLC) 荧光法同时测定人血浆中4种硫醇物的浓度
引用本文:杨涛,沈杰.高效液相 (HPLC) 荧光法同时测定人血浆中4种硫醇物的浓度[J].复旦学报(医学版),2014,41(5):679-684.
作者姓名:杨涛  沈杰
作者单位:1复旦大学附属华东医院药剂科 上海 200040; 2上海市老年医学研究所老年临床药理研究室 上海 200040
基金项目:上海市老年医学临床重点实验室建设项目(13dz2260700) The work was supported by Shanghai Key Laboratory of Clinical Geriatric Medicine Project
摘    要: 目的  建立同时测定人血浆中半胱氨酸(cysteine,Cys)、同型半胱氨酸(homocysteine,Hcy)、半胱氨酰甘氨酸(cysteinylglycine,CysGly)和谷胱甘肽(glutathione,GSH)等4种硫醇物的高效液相色谱法(high-performance liquid chromatography,HPLC)。方法  血浆经磷酸盐缓冲液(phosphate buffered saline,PBS)稀释后,用三(2-羧乙基)膦盐酸盐[tris-(2-carboxyethyl)-phosphine hydrochloride,TCEP]还原,用三氯乙酸(trichloroacetic acid,TCA)溶液进行蛋白沉淀,再用7-氟苯呋咱-4-硫酸铵盐(7-fluorobenzofurazan-4-sulfonic acid ammonium salt,SBD-F)进行衍生化反应,荧光检测器检测。色谱条件:色谱柱为Kromasil C18 (250 mm×4.6 mm,5 μm),柱温29 ℃;流动相为甲醇:0.1 mol/L醋酸盐缓冲液(pH=4.5,3.5∶96.5,V/V),流速为0.8 mL/min,等度洗脱。激发波长385 nm,发射波长515 nm。采用外标法定量。结果  Cys、Hcy、CysGly和GSH的线性范围分别为50~800 μmol/L、4~64 μmol/L、10~160 μmol/L和2.5~40 μmol/L。Cys、Hcy、CysGly和GSH的最低检测浓度分别为2.5 μmol/L、1.0 μmol/L、1.0 μmol/L和1.0 μmol/L。各组分日内、日间精密度RSD均<12 %。平均回收率为95.01 %~116.17 %。结论  该方法具有检测时间短、灵敏性高、精密度和准确度好的特点,适用于临床人血浆中硫醇物浓度的常规检测。

关 键 词:高效液相色谱法(HPLC)  同型半胱氨酸(Hcy)  半胱氨酰甘氨酸(CysGly)  半胱氨酸(Cys)  谷胱甘肽(GSH)

Simultaneous determination of four aminothiols in human plasma by high-performance liquid chromatography (HPLC) with fluorimetric detector
YANG Tao,SHEN Jie.Simultaneous determination of four aminothiols in human plasma by high-performance liquid chromatography (HPLC) with fluorimetric detector[J].Fudan University Journal of Medical Sciences,2014,41(5):679-684.
Authors:YANG Tao  SHEN Jie
Institution:1Department of Pharmacy,Huadong Hospital,Fudan University,Shanghai 200040,China;
2Geriatric Clinical Pharmacy Laboratory,Shanghai Institute of Geriatric Medicine,Shanghai 200040,China
Abstract:Objective  To develop a simple high-performance liquid chromatography (HPLC) with fluorimetric dectetor method for simultaneously determining total concentrations of four aminothiols including aminothiols,homocysteine (Hcy),cysteine (Cys),cysteinylglycine (CysGly) and glutathione (GSH) in human plasma.Methods  The human plasma was diluted by phosphate buffered saline (PBS),reduced by tris-(2-carboxyethyl)-hosphine hydrochloride (TCEP),derivated by 7-fluorobenzofurazan-4-sulfonic acid ammonium salt (SBD-F),and detected by fluorimetric detector.The HPLC separation was carried out using a Kromasil C18 (250 mm×4.6 mm,5 μm).The mobile phase was consisted of methanol:0.1 mol/L acetate buffer (pH=4.5,3.5∶96.5,V/V) at a flow rate of 0.8 mL/min,delivered isocratically.The fluorimetric detector was set at excitation and emission wavelengths of 385 nm and 515 nm,respectively.The assay utilizes a quantification method of external standard.Results  The calibration graphs were linear over 50-800 μmol/L,4-64 μmol/L,10-160 μmol/L and 2.5-40 μmol/L for Cys,Hcy,CysGly and GSH,respectively.The lowest limits of quantification for Cys,Hcy,CysGly and GSH were 2.5 μmol/L,1.0 μmol/L,1.0 μmol/L,and 1.0 μmol/L,respectively.The intra-and inter-day precision of RSD was below 12%.The average recovery was ranged from 95.01 % to 116.17 %.Conclusions  The method was proved to be rapid,sensitive,precise,accurate,and suitable for routine clinical determination of aminothiols in human plasma.
Keywords:high performance liquid chromatography (HPLC)  homocysteine (Hcy)  cysteinylglycine (CysGly)  cysteine (Cys)  glutathione (GSH)
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