Spectrofluorimetric determination of artemisinin with pyronine B as the substrate for horseradish peroxidase  

作　　者：CHEN Lihua LIU Liuzhan SHEN Hanxi 

机构地区：[1]College of Chemistry, Jishou University, Jishou 416000, China [2]College of Chemistry, Nankai University, Tianjin 300071, China

出　　处：《Chinese Science Bulletin》2005年第17期1834-1838,共5页

基　　金：This work Was supported by the National Natural Science Foundation of China(Grant No.20075012);the Scientific Research Foundation of Hunan Educational Committee(Grant No.02C313).

摘　　要：Enzyme-catalytic fluorescence determination of artemisinin (qinghaosu, QHS) was developed using pyronine B (PB) as substrate of horseradish peroxidase (HRP). The interaction between HRP and QHS was an enzyme-substrate model. The catalytic characteristic of HRP in the oxidation reaction, in which the fluorescence of PB was decreased in the presence of QHS, was studied. The steady-state catalytic rate depended upon enzyme and substrate concentrations, and the Michaelis-Menten parameters Km, Vmax and Kcat were 8.4×10?5 mol · L?1, 7.4×10?6 mol · L?1 s?1 and 50.23 s?1. The catalytic activity of enzyme was inhibited in the presence of deactivated agents and at high temperature, respectively. Under optimum conditions, linear relationship between fluo-rescence intensity change (F0?F) of pyronine B and concen-tration of QHS was in the range of 1.41×10?7―1.27×10?6 mol · L?1. The detection limit (3σ) was determined to be 2.7×10?8 mol · L?1. The proposed method was applied to the concentration determination of QHS in the media of plasma or urine samples.Enzyme-catalytic fluorescence determination of artemisinin （qinghaosu, QHS） was developed using pyronine B （PB） as substrate of horseradish peroxidase （HRP）. The interaction between HRP and QHS was an enzyme-substrate model. The catalytic characteristic of HRP in the oxidation reaction, in which the fluorescence of PB was decreased in the presence of QHS, was studied. The steady-state catalytic rate depended upon enzyme and substrate concentrations, and the Michaelis-Menten parameters Km, Vmax and Kcat were 8.4×10^-5mol·L^-1, 7.4×10^-6mol·L^-1s^-1 and 50.23s^-1. The catalytic activity of enzyme was inhibited in the presence of deactivated agents and at high temperature, respectively. Under optimum conditions, linear relationship between fluorescence intensity change （F0-F） of pyronine B and concen- tration of QHS was in the range of 1.41×10^-7-1.27×10^-6mol·L^-1. The detection limit （3σ） was determined to be 2.7×10^-8mol·L^-1. The proposed method was applied to the concentration determination of QHS in the media of plasma or urine samples.

关 键 词：光谱荧光计 派若宁B 山葵 过氧化酶 荧光亮度 

分 类 号：O644[理学—物理化学]