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酮洛芬与蛋白结合作用的高效液相色谱-迎头分析法研究及其与高效毛细管电泳-迎头分析法的比较
引用本文:周大炜,李发美.酮洛芬与蛋白结合作用的高效液相色谱-迎头分析法研究及其与高效毛细管电泳-迎头分析法的比较[J].色谱,2004,22(6):601-604.
作者姓名:周大炜  李发美
作者单位:1. 天津大学药学院,天津,300072;沈阳药科大学药学院,辽宁,沈阳,110016
2. 沈阳药科大学药学院,辽宁,沈阳,110016
基金项目:国家自然科学基金资助项目(批准号:29975018).
摘    要:采用高效液相色谱-迎头分析法(HPLC-FA),以67 mmol/L (pH 7.4, I=0.17 mol/L) 的等渗磷酸盐缓冲液为流动相,Pinkerton GFF Ⅱ-S5-80内表面反相柱(150 mm×4.6 mm i.d., 5 μm)为固定相,254 nm下检测,研究了酮洛芬与人血清白蛋白(HSA)的结合作用,通过非线性回归参数估算求得酮洛芬与HSA的结合参数。与高效毛细管电泳-迎头分析法(HPCE-FA)相比,HPLC-FA法具有高灵敏度的优势,但进样量较大,分析时间较长。HPLC-F

关 键 词:蛋白结合作用  高效毛细管电泳-迎头分析  高效液相色谱-迎头分析  人血清白蛋白  酮洛芬  
文章编号:1000-8713(2004)06-0601-04
修稿时间:2004年4月7日

Study of Protein Binding in Ketoprofen Using Liquid Chromatography Frontal Analysis in Comparison with Capillary Electrophoresis Frontal Analysis
ZHOU Dawei.Study of Protein Binding in Ketoprofen Using Liquid Chromatography Frontal Analysis in Comparison with Capillary Electrophoresis Frontal Analysis[J].Chinese Journal of Chromatography,2004,22(6):601-604.
Authors:ZHOU Dawei
Institution:College of Pharmaceuticals & Biotechnology, Tianjin University, Tianjin 300072, China. daweil204@yahoo.com
Abstract:A method of high performance liquid chromatography-frontal analysis (HPLC-FA) was developed to study the binding of ketoprofen to human serum albumin (HSA) and it was compared with high performance capillary electrophoresis-frontal analysis (HPCE-FA). The separation was performed using Pinkerton GFF II-S5-80 internal-surface reversed-phase silica column (150 mm x 4.6 mm i.d., 5 microm) at pH 7.4 in a 67 mmol/L isotonic sodium phosphate buffer at 37 degrees C. Other conditions included a flow rate of 0.2 mL/min, UV detection at a wave-length of 254 nm and an injection volume of 950 microL. A trapezoidal peak of the unbound ketoprofen appeared after HSA elution in the chromatogram. The plateau height of the peak was employed to determine the concentration of unbound ketoprofen in the HSA equilibrated sample solution. The HPLC-FA method provides the advantage of high sensitivity and however the disadvantages of large sample size and long analytical time when compared with HPCE-FA. HPLC-FA is applicable to the binding parameter estimation of ketoprofen to both primary and secondary sites, which are 0.37 x 10(6) L/mol and 1.4 for K1 (the association constant) and n (the number for the binding sites per molecule HSA), respectively, and 0.005 x 10(6) L/mol and 7.2 for K2 and n2, respectively. In contrast, HPCE-FA measures parameters for only the secondary binding sites; K2 of 0.018 x 10(6) L/mol and n2 of 2.54 can be estimated. It is found that ketoprofen binds mainly at the primary sites at a lower mole ratio of ketoprofen versus HSA, and the binding at the secondary sites occurs at a higher ratio.
Keywords:high performance capillary electrophoresis-frontal analysis  high performance liquid chromatography-frontal analysis  human serum albumin  protein binding interaction  ketoprofen
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