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Flow Injection on Line Oxidizing Fluorometry Coupled to Microdialysis Sampling for Studying Phentolamine-Bovine Serum Albumin Interaction

机译:流动注射线氧化荧光法偶联至微透析血清血清白蛋白相互作用的微透析抽样

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Determination of phentolamine-bovine serum albumin (BSA) interaction based on a flow-injection microdialysis sampling fluorescence system (FI-MD-FL) was proposed. The analytical procedure was based on the oxidation of phentolamine by acidic Ce(IV) and monitoring of the fluorescence intensity of the formed Ce(III). The drug of phentolamine and BSA were mixed in different molar ratios in Ringer's solution and incubated in a water bath. The microdialysate samples were on-line merged with acidic Ce(IV) solution by putting a microdialysis probe into the mixed solution and perfused with Ringer's solution at 10 μL min-1. Then the sample was reached the flow cell, excited and monitored at 256/355nm (λex/λem). The dialytic efficiency under the experimental conditions was 38.8±2.2% (n=3). The data obtained was analyzed with Scatchard analysis and Klotz plot. The estimated association constant (K) and the number of the binding site (n) on one molecule of BSA by Scatchard analysis were 1.78×105 L mol-1 and 0.69, respectively. The proposed method has been applied to the study of the binding of phentolamine to bovine serum albumin (BSA) in vitro. The method provided a fast and simple technique for the study of drug-protein interactions.
机译:提出了基于流动注射微透析采样荧光体系(FI-MD-FL)的浮胺胺 - 牛血清白蛋白(BSA)相互作用的测定。分析程序基于苯甲胺氧化通过酸性Ce(IV),并监测形成的Ce(III)的荧光强度。在Ringer溶液中以不同的摩尔比混合芬兰和BSA的药物,并在水浴中温育。通过将微透析探针放入混合溶液中并在10μLmin-1的10μlmin-1中灌注ringer溶液,将微透明酸盐样品与酸性Ce(iv)溶液合并。然后在256 / 355nm(λex/λem)下达到样品,激发和监测样品。在实验条件下的透析效率为38.8±2.2%(n = 3)。通过旋涡分析和klotz图分析所获得的数据。通过Scatchard分析将估计的关联常数(k)和一个分子的BSA分子上的结合位点(N)分别为1.78×105L mol-1和0.69。所提出的方法已被应用于体外浮碱与牛血清白蛋白(BSA)的结合研究。该方法提供了一种快速简便的技术,用于研究药物 - 蛋​​白质相互作用。

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