Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
Talanta. 2018 Aug 15;186:221-228. doi: 10.1016/j.talanta.2018.04.017. Epub 2018 Apr 11.
Carbonyl compounds are widely distributed in organisms, and the commonly used methods for determination of them like UV/fluorescence/mass spectrometry always require derivatization reagents. However, the reported derivatization reagents have significant difference in reactivity, which is very unfavorable for developing highly reactive reagent. In this study, we theoretically investigated the factors affecting the reactivity of hydrazine-based derivatization reagents, and proposed a strategy for filtering highly reactive reagents by quantum chemical calculation. With this strategy, N-propyl-4-hydrazino-1,8-naphthalimide (NPHNA) was filtered out as a fluorescent derivatization reagent. Taking aliphatic aldehydes as representatives, we evaluated the reactivity of NPHNA for carbonyl compounds. The derivatization of NPHNA with aliphatic aldehydes could be finished at room temperature within 60 min or 35 °C within 35 min, which showed higher reactivity than the most popular UV/MS reagent, 2,4-dinitrophenylhydrazine (DNPH). We believe that the strategy we proposed in this work is of great potential to design highly reactive UV/fluorescent/MS labeling reagents for carbonyl compounds and even other analytes.
羰基化合物广泛存在于生物体内,常用于测定它们的方法如紫外/荧光/质谱法,总是需要衍生试剂。然而,已报道的衍生试剂在反应性上有显著差异,这对开发高反应性试剂非常不利。在这项研究中,我们从理论上研究了影响基于肼衍生试剂反应性的因素,并提出了一种通过量子化学计算筛选高反应性试剂的策略。通过该策略,筛选出 N-丙基-4-肼基-1,8-萘二甲酰亚胺(NPHNA)作为荧光衍生试剂。以脂肪醛作为代表,我们评估了 NPHNA 与羰基化合物的反应性。NPHNA 与脂肪醛的衍生反应可以在室温下 60 分钟或 35°C 下 35 分钟内完成,其反应性高于最流行的紫外/质谱试剂 2,4-二硝基苯肼(DNPH)。我们相信,我们在这项工作中提出的策略对于设计用于羰基化合物甚至其他分析物的高反应性紫外/荧光/质谱标记试剂具有很大的潜力。