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首页> 外文期刊>International journal of mass spectrometry >Characterization of tenofovir, tenofovir disoproxil fumarate and emtricitabine in aqueous solutions containing sodium ions using ESI-MS, NMR and Ab initio calculations
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Characterization of tenofovir, tenofovir disoproxil fumarate and emtricitabine in aqueous solutions containing sodium ions using ESI-MS, NMR and Ab initio calculations

机译:使用ESI-MS,NMR和Ab initio计算来表征含钠离子的水溶液中的替诺福韦,替诺福韦富马酸替诺福韦和恩曲他滨的特征

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We have discerned some characteristics of protonated and sodiated forms of emtricitabine tenofovir and tenofovir disoproxil fumarate in aqueous solutions using mass spectrometry/mass spectrometry (MS/MS), nuclear magnetic resonance spectroscopy (NMR) and Ab initio calculations. Protonated species exhibited different mass spectral characteristics from sodiated species for the three antiretroviral drugs. Sodiation of the three compounds yields extremely stable conformers which require high excitation energies to detach the sodium cation using MS/MS. In the case of emtricitabine (FTC), collision induced dissociation (CID) of the protonated species with m/z 248 yielded m/z 130 as the major product ion by losing 2-ethyl-1,3-oxathiolane. MS/MS of the sodiated molecular ion [M + Na](+) with m/z 270 would be expected to yield [M + H](+) i.e. m/z 248 by losing the Na+ cation but instead lost 2-ethyl-1,3-oxathiolane and left the Na+ cation well sequestered within the ionic complex. Similar observations were made with tenofovir disoproxil fumarate (TDF) and tenofovir (TFV). Ab initio calculations showed in the case of sodiated TDF and TFV that, the sodium could only be cleaved when a nucleophilic species i.e. PO2 to which it was coordinated to, fragmented requiring activation energy of 1.5 eV. The potential energy barrier to remove the Na+ cation alone was too high to allow the cleavage to proceed. NMR data showed that when TFV or TDF coordinates with Na+ ions at one of the nitrogens at position 1 in the purine moiety of the molecule, it also interacts with oxygens of the phospho group to form an ionic complex and perturbs the chemical environments of several atoms in the periphery. The abundance of sodium cations and their strong interactions with the core structures of Fit, TDF and TFV make sodiated species as the best candidates for their quantitation using MS/MS especially in biological fluids. Evidence for improved sensitivity when sodiated species of some of the antiretroviral (ARV) drugs were used for quantitation exists in the literature. (C) 2016 Elsevier B.V. All rights reserved.
机译:我们已经使用质谱/质谱(MS / MS),核磁共振波谱(NMR)和从头算的方法识别了水溶液中的恩曲他滨替诺福韦和替诺福韦富马酸替诺福韦的质子化形式和盐化形式的一些特征。对于这三种抗逆转录病毒药物,质子化物种表现出与质构化物种不同的质谱特性。三种化合物的糖化产生极其稳定的构象异构体,需要使用高激发能才能使用MS / MS分离钠阳离子。在恩曲他滨(FTC)的情况下,质子化物种与m / z 248的碰撞诱导解离(CID)通过丢失2-乙基-1,3-氧杂硫杂环戊烷产生m / z 130作为主要产物离子。预计通过m / z 270产生的分子离子[M + Na](+)的MS / MS将产生[M + H](+),即m / z 248,这是因为失去了Na +阳离子,但损失了2-乙基-1,3-氧杂硫杂环戊烷和Na +阳离子被隔离在离子配合物中。替诺福韦富马酸替诺福韦(TDF)和替诺福韦(TFV)的观察结果相似。从头算计算表明,在钠化的TDF和TFV的情况下,只有在亲核物质(即与之配合的PO2)碎裂时,才能裂解钠,需要1.5 eV的活化能。仅除去Na +阳离子的势能垒太高而不能进行裂解。 NMR数据显示,当TFV或TDF与分子的嘌呤部分1位上的一个氮原子上的Na +离子配位时,它也与磷酸基团的氧相互作用形成离子配合物,并扰乱了几个原子的化学环境在外围。钠阳离子的丰度及其与Fit,TDF和TFV核心结构的强烈相互作用,使溶解的物种成为使用MS / MS进行定量分析的最佳人选,尤其是在生物流体中。文献中有一些证据表明,使用某些抗逆转录病毒(ARV)药物中的糊状物进行定量时,灵敏度得到了提高。 (C)2016 Elsevier B.V.保留所有权利。

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