Dipartimento di Scienze Farmaceutiche, Università degli Studi di Modena e Reggio Emilia, Via Campi 183, 41125 Modena, Italy.
J Chromatogr A. 2010 Dec 24;1217(52):8136-45. doi: 10.1016/j.chroma.2010.10.044. Epub 2010 Oct 28.
In this study, configurational and chemical stability of (R,R),(S,S),(R,S),(S,R)-3,6-dimethyl-2,3,5,6-tetrahydro[1,2,4]thiadiazino[6,5,4-hi]indole 1,1-dioxide (1) were investigated by dynamic and stopped-flow HPLC methods. Single epimeric mixtures (R,R),(R,S)-1 and (S,S),(S,R)-1 were obtained combining synthetic and chromatographic strategies. Separation of (R,R)-1 and (R,S)-1 was achieved by chiral chromatography and absolute configuration of eluted epimers has been assigned basing on molecular modelling calculations. Epimerization and hydrolysis of (R,R),(R,S)-1 have been studied by classical off-column, dynamic HPLC and stopped-flow HPLC methods. The influence of different parameters, such as temperature, pH and dielectric constant was evaluated. The data obtained indicate that (R,R),(R,S)-1 undergoes to a rapid epimerization in aqueous solvent and hydrolysis in acidic conditions. Moreover, epimerization and hydrolysis were investigated in presence of an artificial membrane and in physiological buffers (pH 2.2 and 7.0 at 37.5°C) to simulate in vivo conditions.
在这项研究中,通过动态和停流 HPLC 方法研究了(R,R)、(S,S)、(R,S)、(S,R)-3,6-二甲基-2,3,5,6-四氢[1,2,4]噻二嗪并[6,5,4-hi]吲哚 1,1-二氧化物(1)的构象和化学稳定性。通过合成和色谱策略相结合,获得了单一非对映混合物(R,R)、(R,S)-1 和(S,S)、(S,R)-1。通过手性色谱分离(R,R)-1 和(R,S)-1,并基于分子建模计算确定了洗脱非对映异构体的绝对构型。通过经典的柱外、动态 HPLC 和停流 HPLC 方法研究了(R,R)、(R,S)-1 的外消旋化和水解。评估了不同参数(如温度、pH 值和介电常数)的影响。所得数据表明,(R,R)、(R,S)-1 在水溶剂中迅速发生外消旋化,并在酸性条件下水解。此外,还在人工膜和生理缓冲液(37.5°C 时 pH 值为 2.2 和 7.0)中研究了外消旋化和水解,以模拟体内条件。