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
相关论文
共 50 条
  • [31] A hydrogen-bonded tetramer in (2RS,4SR)-7-bromo-2-(2-methylphenyl)-2,3,4,5-tetrahydro-1H-naphtho[1,2-b]azepin-4-ol and a three-dimensional hydrogen-bonded framework in (2RS,4SR)-2-(3-methylthiophen-2-yl)-2,3,4,5-tetrahydro-1H-naphtho[1,2-b]azepin-4-ol
    Yepes, Andres F.
    Palma, Alirio
    Cobo, Justo
    Glidewell, Christopher
    ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 2013, 69 : 448 - +
  • [32] 标记15N-(2RS,3RS)-1-(4-氯苯基)-4,4-二甲基-2-(1H-1,2,4-三唑-1-基)戊-3-醇的合成
    陈馥衡
    李增民
    范浚深
    曹丽微
    农药, 1987, (06) : 3 - 5
  • [33] 标记15N-(2RS,3RS)-1-(4-氯苯基)-4,4-二甲基-2-(1H-1,2,4-三唑-1-基)-戊-3-醇的新合成方法
    范浚深
    将建中
    陈馥衡
    北京农业大学学报, 1989, (04) : 430+449 - 430
  • [34] Structural analysis of (S)-1-((1H-benzo[d][1,2,3]triazol-1-yl)oxy)-3-(4-(2-methoxyphenyl)piperazin-1-yl)propan-2-ol and binding mechanism with α1A-adrenoceptor: TDDFT calculations, X-ray crystallography and molecular docking
    Xu, Wei
    Shao, Binhao
    Xu, Xingjie
    Jiang, Renwang
    Yuan, Mu
    JOURNAL OF MOLECULAR STRUCTURE, 2016, 1106 : 485 - 490
  • [35] The crystal structure of t-butyl 7-[3-(4-fluorophenyl)-1-(propan-2-yl)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoate, C28H34FNO4
    Vergiro, Tchuente Fofeu Alex
    Xie, Tai-Yang
    Zou, Jing
    Xu, Xin-Xin
    Xu, Rou-Han
    Jiang, Cheng-Jun
    ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES, 2024, 239 (03): : 367 - 369
  • [36] Discovery of (2R)-N-[3-[2-[(3-Methoxy-1-methyl-pyrazol-4-yl)amino]pyrimidin-4-yl]-1H-indol-7-yl]-2-(4-methylpiperazin-1-yl)propenamide (AZD4205) as a Potent and Selective Janus Kinase 1 Inhibitor
    Su, Qibin
    Banks, Erica
    Bebernitz, Geraldine
    Bell, Kirsten
    Borenstein, Cassandra F.
    Chen, Huawei
    Chuaqui, Claudio E.
    Deng, Nanhua
    Ferguson, Andrew D.
    Kawatkar, Sameer
    Grimster, Neil P.
    Ruston, Linette
    Lyne, Paul D.
    Read, Jon A.
    Peng, Xianyou
    Pei, Xiaohui
    Fawell, Stephen
    Tang, Zhanlei
    Throner, Scott
    Vasbinder, Melissa M.
    Wang, Haoyu
    Winter-Holt, Jon
    Woessner, Richard
    Wu, Allan
    Yang, Wenzhan
    Zinda, Michael
    Kettle, Jason G.
    JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (09) : 4517 - 4527
  • [37] Determination of 5-n-Butyl-4-{4-[2-(1H-tetrazole-5-yl)-1H-pyrrol-1-yl]phenylmethyl}-2,4-dihydro-2-(2,6-dichloridephenyl)-3H-1,2,4-triazol-3-one, a New Angiotensin Type 1 Receptor Antagonist in Rat Plasma by LC-ESI-MS: Application to Pharmacokinetic Studies
    Bei Yan
    Guang-ji Wang
    Jian-guo Sun
    Fen-zhi Sun
    Xiao-yu Li
    Xiao-ming Wu
    Jin-yi Xu
    Yuan-ting Zheng
    Hua Lv
    Chromatographia, 2007, 66 : 55 - 61
  • [38] Determination of 5-n-Butyl-4-{4-[2-(1H-tetrazole-5-yl)1H-pyrrol-1-yl]phenylmethyl}-2,4-dihydro-2-(2,6-dichloridephenyl)-3H-1,2,4-triazol-3-one,a new Angiotensin type 1 receptor antagonist in rat plasma by LC-ESI-MS: Application to pharmacokinetic studies
    Yan, Bei
    Wang, Guang-ji
    Sun, Jian-Guo
    Sun, Fen-zhi
    Li, Xiao-Yu
    Wu, Xiao-ming
    Xu, Jin-yi
    Zheng, Yuan-ting
    Lv, Hua
    CHROMATOGRAPHIA, 2007, 66 (1-2) : 55 - 61
  • [39] Simultaneous LC-MS-MS Determination of HM30181A, [2-(2-{4-[2-(6,7-Dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-phenyl}-2H-tetrazol-5-yl)-4,5-dimethoxyphenyl]amide, as a new P-Glycoprotein Inhibitor and Its Two Metabolites, M1 and M2, in Human Plasma: Application to a Pharmacokinetic Study
    Choi, Young Hee
    Oh, Seul
    Yoon, Seo-Hyun
    Kim, Tae-Eun
    Gu, Namyi
    Kim, Eun Young
    Kim, Han Kyong
    Yu, Kyung-Sang
    Jang, In-Jin
    Shin, Sang-Goo
    Cho, Joo-Youn
    CHROMATOGRAPHIA, 2011, 73 (3-4) : 273 - 280
  • [40] Simultaneous LC–MS–MS Determination of HM30181A, [2-(2-{4-[2-(6,7-Dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-phenyl}-2H-tetrazol-5-yl)-4,5-dimethoxyphenyl]amide, as a new P-Glycoprotein Inhibitor and Its Two Metabolites, M1 and M2, in Human Plasma: Application to a Pharmacokinetic Study
    Young Hee Choi
    Seul Oh
    Seo-Hyun Yoon
    Tae-Eun Kim
    Namyi Gu
    Eun Young Kim
    Han Kyong Kim
    Kyung-Sang Yu
    In-Jin Jang
    Sang-Goo Shin
    Joo-Youn Cho
    Chromatographia, 2011, 73 : 273 - 280