Enantioselective LC/ESI-MS/MS Analysis and Pharmacokinetic and Tissue Distribution Study of (2RS)-1-(7-Methoxy-1H-indol-4-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)-propan-2-ol in Rats

被引:3
|
作者
Walczak, Maria [1 ]
Szymura-Oleksia, Joanna [1 ]
Groszek, Grazyna [2 ]
机构
[1] Jagiellonian Univ, Coll Med, Dept Pharmacokinet & Phys Pharm, PL-30688 Krakow, Poland
[2] Rzeszow Univ Technol, Fac Chem, Dept Ind & Mat Chem, Rzeszow, Poland
关键词
stereoselectivity; derivatization; aminopropan-2-ol; pharmacokinetics; in vivo; PERFORMANCE LIQUID-CHROMATOGRAPHY; STEREOSELECTIVE ANALYSIS; BETA-BLOCKERS; HUMAN PLASMA; PHARMACODYNAMICS; CARVEDILOL; ENANTIOMERS;
D O I
10.1002/chir.22011
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A sensitive and stereospecific liquid chromatography-tandem mass spectrometry method for the quantitative determination of TWo8 enantiomers ((2RS)-1-(7-methoxy-1H-indol-4-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)-propan-2-ol) was developed and validated in rat serum and some tissues. Racemic TWo8 is a new chemical entity, and it has been shown to possess pharmacological activity in vivo. The assay involved the diastereomeric derivatization of racemic TWo8 with 2,3,4,6-tetra-O-acetyl-beta-glucopyranosyl isothiocyanate. The TWo8 diastereoisomers quantification was performed on a triple quadrupole mass spectrometer employing an electrospray ionization technique. The precursor to the product ion transition for TWo8 derivatives and for the internal standard (carbamazepine) was m/z 776.4???387.2 and 237.4???194.4, respectively. The assay was validated with a linear range of 102000?ng/ml of racemic TWo8. The inter-day precisions for (-)-(S)-TWo8 and (+)-(R)-TWo8 were 2.1% to 14.9% and 1.3% to 14.8%, respectively. The inter-day accuracy for (-)-(S)-TWo8 and (+)-(R)-TWo8 was within 86% to 114% and 91% to 114%, respectively. A pilot pharmacokinetic study of this new beta-adrenolytic compound has shown that (-)-(S)-TWo8 is eliminated faster than its antipode. The terminal half-lives of (-)-(S)-TWo8 and (+)-(R)-TWo8 were 3.2 and 3.9?h, respectively. The compound distribution into different organs, evaluated in tissue homogenate samples following TWo8 intravenous administration, showed an enantioselective penetration of TWo8 enantiomers in the liver (p?<?0.03), in the kidney (p?<?0.001), and in the lungs (p?<?0.05). The developed method using liquid chromatography-tandem mass spectrometry method with electrospray ionization could be employed for quantitative determination of compounds with similar structure. Chirality 24:591599, 2012. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:591 / 599
页数:9
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