Fluorescence Determination of Artemisinin Using Tyrosinase as Catalyst and Pyronine B as Monitor  

Fluorescence Determination of Artemisinin Using Tyrosinase as Catalyst and Pyronine B as Monitor

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作  者:陈莉华 尹红 杨朝霞 张克梅 刘六战 沈含熙 

机构地区:[1]Chemical School, Jishou University, Jishou, Hunan 416000, China [2]Chemical School, Nankai University, Tianjin 300071, China

出  处:《Chinese Journal of Chemistry》2005年第8期1047-1052,共6页中国化学(英文版)

基  金:Project supported by the National Natural Science Foundation of China (No. 20075012) and the Natural Science Foundation of Hunan Educational Committee (No. 02C313).

摘  要:Fluorescence decrease ratio (F0/F) was applied to determination of artemisinin (qinghaosu, QHS) based on the catalytic effect of tyrosinase using tetraethyldiaminoxanthenyl chloride (pyronine B, PB) as monitor. A catalyst used commonly in the decomposition of QHS, tyrosinase, exhibited higher binding activity than hemin, which was expressed as Michaelis-Menten parameters, km, Vmax, and kcat respectively. Interaction of QHS with tyrosinase was inhibited in the presence of deactivating agents at high temperature whereas enhanced by ethanol. Under optimal conditions, a concentration of 1.4×10^-7-8.4×10^-7 mol·L^-1of QHS could be determined on the basis of fluorescence decrease ratio of PB, with a detection limit 3tr of 2.6×10^-9 mol·L^-1. The proposed method was applied to detection of the concentration of QHS in the media of plasma and urine.Fluorescence decrease ratio (F0/F) was applied to determination of artemisinin (qinghaosu, QHS) based on the catalytic effect of tyrosinase using tetraethyldiaminoxanthenyl chloride (pyronine B, PB) as monitor. A catalyst used commonly in the decomposition of QHS, tyrosinase, exhibited higher binding activity than hemin, which was expressed as Michaelis-Menten parameters, km, Vmax, and kcat respectively. Interaction of QHS with tyrosinase was inhibited in the presence of deactivating agents at high temperature whereas enhanced by ethanol. Under optimal conditions, a concentration of 1.4×10^-7-8.4×10^-7 mol·L^-1of QHS could be determined on the basis of fluorescence decrease ratio of PB, with a detection limit 3tr of 2.6×10^-9 mol·L^-1. The proposed method was applied to detection of the concentration of QHS in the media of plasma and urine.

关 键 词:TYROSINASE ARTEMISININ pyronine B fluorescence decrease ratio 

分 类 号:R978.61[医药卫生—药品]

 

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