2,4,5-T was extracted with acetone at below pH 1Γ0 and the extract was concentrated. After adding 100 g litre~1 sodium chloride solution to the residual solution, 2,4,5-T was extracted with ethyl acetate ] hexane (20 ] 80 by volume). The extract was evaporated to dryness and the residue was dissolve
Determination of a new antihypertensive agent (2R,4R)-2-(2-Hydroxyphenyl)-3-(3-mercaptopropionyl)-4-thiazolidinecarboxylic Acid in Blood by High-Performance Liquid Chromatography with Electrochemical Detection
β Scribed by Kazutake Shimada; Makoto Tanaka; Toshio Nambara; Yutaka Imai
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 327 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0022-3549
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β¦ Synopsis
A sensitive method has been developed for the determination of a new antihypertensive agent, (2H,4H)-2-(2-hydroxyphenyl)-3-(3mercaptopropionyl)-4-thiazolidinecarboxylic acid (I), in human blood. Because the drug is unstable in biological fluids, it was immediately derivatized by treating the freshly drawn blood specimens with N-(4-ani-1inophenyl)maleimide. The adduct was separated and determined by high-performance liquid chromatography with electrochemical detection o n a reverse-phase column. The assay method was satisfactory with respect to the sensitivity and precision, providing a quantitation limit of ' 2 ng/ml and coefficient of variation of 3%. Preliminary pharmacokinetic data were obtained by orally administering I to two patients with essential hypertension.
Keyphrases 0 Antihypertensive agents-(')R,4H)-2-(2-hydroxyphen-yI)-:{-( :~-mercaptopropionyl)-4-thiazolidinecar~~xylic acid, determination in human blood, high-performance liquid chromatography with elec-
π SIMILAR VOLUMES
The preparative separation of the enantiomers of the title compound, a versatile chiral building block for the synthesis of unnatural amino acid esters, by high performance liquid chromatography on a chiral stationary phase (CSP), is reported for the first time. The CSP consists of amylose-(3,5-dime