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Kinetic Determination of Drug Particles Concentration via Enzyme-Catalyzed Decomposition of Hydrogen Peroxide

机译:酶催化过氧化氢分解动力学测定药物颗粒浓度

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摘要

The inhibition effect of blood pressure control drug particles, metoprolol (C_(34)H_(56)N2O_(12)), and atenolol (C_(14)H_(22)N2O3), on the enzyme catalyzed decomposition of hydrogen peroxide reaction has been investigated by ultraviolet spectrophotometry. The results obtained when hydrogen peroxide was spectrophotometrically monitored were compared with those previously obtained from electrochemical measurements. As expected, the two series of measurements were shown to be consistent with the reaction sloichiometry. The Lineweaver-Burk linear equation was used to determine the Michaelis-Menten constant (K_M) and the maximum reaction rate (r_(max)). Based on the variation of the Michaelis-Menten constant, respectively, the maximum reaction rate with inhibitor concentration, it was determined the inhibition parameters that characterize the enzyme-inhibitor (EI) and the enzyme-inhibitor-substrate (EIS) complexes. A mixed inhibition mechanism has been established for both drugs. Due to its selectivity and sensitivity, the development of a kinetic method for trace analysis of drugs, based on their inhibition effect on the enzyme-catalyzed reaction rate appears to be promising.
机译:血压控制药物颗粒美托洛尔(C_(34)H_(56)N2O_(12))和阿替洛尔(C_(14)H_(22)N2O3)对酶催化的过氧化氢分解反应具有抑制作用通过紫外分光光度法进行了研究。用分光光度法监测过氧化氢时获得的结果与先前从电化学测量中获得的结果进行了比较。正如预期的那样,这两个系列的测量结果与反应化学计量是一致的。使用Lineweaver-Burk线性方程式确定Michaelis-Menten常数(K_M)和最大反应速率(r_(max))。基于Michaelis-Menten常数的变化,即最大反应速率随抑制剂浓度的变化,确定了表征酶-抑制剂(EI)和酶-抑制剂-底物(EIS)复合物的抑制参数。已经建立了两种药物的混合抑制机制。由于其选择性和敏感性,基于药物对酶催化反应速率的抑制作用,开发一种用于药物痕量分析的动力学方法似乎很有希望。

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