Suppr超能文献

头孢曲松形成的V(IV)O(2+)配合物在血浆和红细胞中的表征及生物转化

Characterization and biotransformation in the plasma and red blood cells of V(IV)O(2+) complexes formed by ceftriaxone.

作者信息

Sanna Daniele, Fabbri Davide, Serra Maria, Buglyó Péter, Bíró Linda, Ugone Valeria, Micera Giovanni, Garribba Eugenio

机构信息

Istituto CNR di Chimica Biomolecolare, Trav. La Crucca 3, I-07040 Sassari, Italy.

Department of Inorganic and Analytical Chemistry, University of Debrecen, P.O. Box 21, H-4010 Debrecen, Hungary.

出版信息

J Inorg Biochem. 2015 Jun;147:71-84. doi: 10.1016/j.jinorgbio.2014.12.021. Epub 2014 Dec 29.

Abstract

The coordination mode and geometry in aqueous solution of oxidovanadium(IV) complexes formed by a third-generation cephalosporin, ceftriaxone (H3cef), were studied by spectroscopic (EPR, electron paramagnetic resonance), pH-potentiometric and computational (DFT, density functional theory) methods. The behavior of the model systems containing 6-hydroxy-2-methyl-3-thioxo-3,4-dihydro-1,2,4-triazine-5(2H)-one (H2hmtdt) and 3-benzylthio-6-hydroxy-2-methyl-1,2,4-triazine-5(2H)-one (Hbhmt) was examined for comparison. The stability of the tautomers of ceftriaxone and 6-hydroxy-2-methyl-3-thioxo-3,4-dihydro-1,2,4-triazine-5(2H)-one in the neutral, mono- and bi-anionic form was calculated by DFT methods, both in the gas phase and in aqueous solution, and the electron density on the oxygen atoms of the hydroxytriazinone ring was related to the pKa of the ligands. The data demonstrate that ceftriaxone coordinates V(IV)O(2+) forming mono- and bis-chelated complexes with (Oket, O(-)) donor set and formation of five-membered chelate rings. The geometry of the bis-chelated complex, cis-VO(Hcef)2(H2O), is cis-octahedral and this species can deprotonate, around physiological pH, to form the corresponding mono-hydroxido cis-VO(Hcef)2(OH). The interaction of cis-VO(Hcef)2(H2O) with apo-transferrin (apo-hTf) was studied and the results suggest that V(IV)O(2+) distributes between (VO)apo-hTf/(VO)2apo-hTf and cis-VO(Hcef)2(H2O), whereas mixed complexes are not formed for charge and steric effects. The interaction of cis-VO(Hcef)2(H2O) with red blood cells shows that ceftriaxone helps V(IV)O(2+) ion to cross the erythrocyte membrane. Inside the cell cis-VO(Hcef)2(H2O) decomposes and the same species formed by inorganic V(IV)O(2+) are observed. The relationship between the biotransformation in the plasma and red blood cells and the potential pharmacological activity of V(IV)O(2+) species of ceftriaxone is finally discussed.

摘要

采用光谱法(电子顺磁共振波谱,EPR)、pH电位滴定法和计算方法(密度泛函理论,DFT)研究了第三代头孢菌素头孢曲松(H3cef)形成的氧化钒(IV)配合物在水溶液中的配位模式和几何结构。为作比较,研究了含有6-羟基-2-甲基-3-硫代-3,4-二氢-1,2,4-三嗪-5(2H)-酮(H2hmtdt)和3-苄硫基-6-羟基-2-甲基-1,2,4-三嗪-5(2H)-酮(Hbhmt)的模型体系的行为。通过DFT方法计算了头孢曲松和6-羟基-2-甲基-3-硫代-3,4-二氢-1,2,4-三嗪-5(2H)-酮中性、单阴离子和双阴离子形式互变异构体在气相和水溶液中的稳定性,并且将羟基三嗪酮环上氧原子的电子密度与配体的pKa相关联。数据表明,头孢曲松与V(IV)O(2+)配位形成具有(Oket,O(-))供体集的单螯合和双螯合配合物,并形成五元螯合环。双螯合配合物顺式-VO(Hcef)2(H2O)的几何结构为顺式八面体,并且该物种在生理pH附近可以去质子化,形成相应的单羟基顺式-VO(Hcef)2(OH)。研究了顺式-VO(Hcef)2(H2O)与脱铁转铁蛋白(脱铁hTf)的相互作用,结果表明V(IV)O(2+)分布在(VO)脱铁hTf/(VO)2脱铁hTf和顺式-VO(Hcef)2(H2O)之间,而由于电荷和空间效应未形成混合配合物。顺式-VO(Hcef)2(H2O)与红细胞的相互作用表明,头孢曲松有助于V(IV)O(2+)离子穿过红细胞膜。在细胞内,顺式-VO(Hcef)2(H2O)分解,并且观察到由无机V(IV)O(2+)形成的相同物种。最后讨论了血浆和红细胞中的生物转化与头孢曲松V(IV)O(2+)物种潜在药理活性之间的关系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验