Application of an UHPLC–MS/MS method to tissue distribution and excretion study of 2-(2-hydroxypropanamido) benzoic acid in rats

2017 ◽  
Vol 1070 ◽  
pp. 54-61 ◽  
Author(s):  
Qili Zhang ◽  
Jiao Guan ◽  
Shasha Li ◽  
Yunli Zhao ◽  
Zhiguo Yu
2020 ◽  
Vol 16 (3) ◽  
pp. 328-334
Author(s):  
Jie Ge ◽  
Jin-Wen Wang ◽  
Qi-Yan Guo ◽  
Ai-Dong Wen

Objective: A validated liquid chromatography-tandem mass spectrometry method (LCMS/ MS) was established to simultaneously determine the concentration of triflusal and its main metabolite 2-hydroxy-4-trifluoromethyl benzoic acid(HTB) in human urine. Methods: The separation was performed on a Dikma C18 column using isocratic elution with acetonitrile-4 mmol/L ammonium acetate aqueous solution containing 0.3 % formic acid water (78: 28, V/V). The method involved extraction with methanol using protein precipitation. The precursor-toproduct ion transitions with multiple reaction monitoring was m/z 247.1→161.1, 204.8→106.7and 136.9→93.0 for triflusal, HTB and salicylic acid(IS), respectively. The method showed good linear relationships over the ranges of 0.08 to 48 μg/mL and0.5 to 50 μg/mL. Results: It was the first time that a urinary excretion study of triflusal capsule as oral. The cumulative urinary recovery showed 8.5% and 2.7% for triflusal and HTB, respectively. Conclusion: This method was successfully used for evaluating the pharmacokinetic properties of triflusal and HTB in urine in Chinese healthy subjects.


Renal Failure ◽  
2015 ◽  
Vol 37 (7) ◽  
pp. 1208-1218 ◽  
Author(s):  
Amit D. Kandhare ◽  
Subhash L. Bodhankar ◽  
V. Mohan ◽  
Prasad A. Thakurdesai

Author(s):  
Yu Mingming ◽  
Wang Yuanhong ◽  
Ma Fugang ◽  
Yu Weijie ◽  
Jiang Tingfu ◽  
...  

Biologia ◽  
2006 ◽  
Vol 61 (6) ◽  
Author(s):  
Ingrid Pauliková ◽  
Anna Hrabovská ◽  
Otto Helia ◽  
Ferdinand Devínsky

AbstractButyrylcholinesterase (BuChE) occurs in a multiple molecular forms whose catalytic activity depends on tissue distribution and species. The hypothesis led us to the study of BuChE catalytic properties focused on the inter-tissue and inter-species level with benzoylcholine and N-alkyl derivates of benzoylcholine (BCHn) as substrates. These compounds are soft disinfectants easily biodegradable to biologically inactive hydrolytic products, substituted choline and benzoic acid. Different sources of BuChE were used: rabbit and rat liver microsomal fraction (membrane-anchored enzyme) and serum (soluble form). Hydrolytic activity of both these BuChE forms was compared to rat recombinant BuChE (rBuChE). Hydrolytic product (benzoic acid) formation was recorded as function of time, and hydrolytic rate was determined. Tissue distribution of BuChE plays an important role in hydrolysis of BCHn. High BuChE activity was observed in a serum of both studied species rat and rabbit and was significantly dependent on a structure of substrates. Activity of soluble serum forms was the same as that for the rBuChE. Significant change of BuChE activity was recorded on the inter-species level in the microsomal fractions. It is because the rabbit microsomal BuChE activity had absolutely different course for all substrates as compared to rat microsomes. Inhibitory studies of BCHn enzymatic hydrolysis of all BuChE forms were performed to determine the level of BuChE participation in BCHn hydrolysis. It can be concluded that short-chain BCHn substrates are exclusively hydrolyzed by BuChE from all studied sources except for the rabbit liver microsomal fraction. Rabbit seems to have different enzymes involved in the hydrolysis of all studied BCHn compounds.


Phytomedicine ◽  
2013 ◽  
Vol 20 (6) ◽  
pp. 558-563 ◽  
Author(s):  
Li Liang ◽  
Xueying Liu ◽  
Qingwei Wang ◽  
Sikun Cheng ◽  
Shengyong Zhang ◽  
...  

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