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通过稳定同位素稀释气相色谱-质谱法直接定量测定氰胺。

Direct quantitative determination of cyanamide by stable isotope dilution gas chromatography-mass spectrometry.

作者信息

Hiradate Syuntaro, Kamo Tsunashi, Nakajima Eri, Kato Kenji, Fujii Yoshiharu

机构信息

Department of Biological Safety Science, National Institute for Agro-Environmental Sciences, 3-1-3 Kan-nondai, Tsukuba, Ibaraki 305-8604, Japan.

出版信息

J Chromatogr A. 2005 Dec 9;1098(1-2):138-43. doi: 10.1016/j.chroma.2005.08.035. Epub 2005 Sep 1.

Abstract

Cyanamide is a multifunctional agrochemical used, for example, as a pesticide, herbicide, and fertilizer. Recent research has revealed that cyanamide is a natural product biosynthesized in a leguminous plant, hairy vetch (Vicia villosa). In the present study, gas chromatography-mass spectrometry (GC-MS) equipped with a capillary column for amines was used for direct quantitative determination of cyanamide. Quantitative signals for ((14)N(2))cyanamide, ((15)N(2))cyanamide (internal standard for stable isotope dilution method), and m-(trifluoromethyl)benzonitrile (internal standard for correcting errors in GC-MS analysis) were recorded as peak areas on mass chromatograms at m/z 42 (A(42)), 44 (A(44)), and 171 (A(IS)), respectively. Total cyanamide content, ((14)N(2))cyanamide plus ((15)N(2))cyanamide, was determined as a function of (A(42)+A(44))/A(IS). Contents of ((14)N(2))cyanamide and ((15)N(2))cyanamide were then calculated by multiplying the total cyanamide content by A(42)/(A(42)+A(44)) and A(44)/(A(42)+A(44)), respectively. The limit of detection for the total cyanamide content by the GC-MS analysis was around 1ng. The molar ratio of ((14)N(2))cyanamide to ((15)N(2))cyanamide in the injected sample was equal to the observed A(42)/A(44) value in the range from 0.1 to 5. It was, therefore, possible to use the stable isotope dilution method to quantify the natural cyanamide content in samples; i.e., the natural cyanamide content was derived by subtracting the A(42)/A(44) ratio of the internal standard from the A(42)/A(44) ratio of sample spiked with internal standard, and then multiplying the resulting difference by the amount of added ((15)N(2))cyanamide (SID-GC-MS method). This method successfully gave a reasonable value for the natural cyanamide content in hairy vetch, concurring with the value obtained by a conventional method in which cyanamide was derivatized to a photometrically active compound 4-cyanimido-1,2-naphthoquinone and analyzed with reversed-phase HPLC (CNQ-HPLC method). The determination range of cyanamide in the SID-GC-MS method was almost the same as that in the CNQ-HPLC method; however, the SID-GC-MS method was much simpler than the CNQ-HPLC method.

摘要

氰胺是一种多功能农用化学品,例如用作杀虫剂、除草剂和肥料。最近的研究表明,氰胺是一种在豆科植物毛苕子(Vicia villosa)中生物合成的天然产物。在本研究中,配备胺类毛细管柱的气相色谱 - 质谱联用仪(GC - MS)用于直接定量测定氰胺。((14)N2)氰胺、((15)N2)氰胺(稳定同位素稀释法的内标)和间(三氟甲基)苯甲腈(用于校正GC - MS分析误差的内标)的定量信号分别记录为质量色谱图上m/z 42(A42)、44(A44)和171(AIS)处的峰面积。总氰胺含量,即((14)N2)氰胺加((15)N2)氰胺,根据(A42 + A44)/AIS来测定。然后,通过将总氰胺含量分别乘以A42/(A42 + A44)和A44/(A42 + A44)来计算((14)N2)氰胺和((15)N2)氰胺的含量。GC - MS分析中总氰胺含量的检测限约为1 ng。注入样品中((14)N2)氰胺与((15)N2)氰胺的摩尔比在0.1至5的范围内等于观察到的A42/A44值。因此,可以使用稳定同位素稀释法对样品中的天然氰胺含量进行定量;即,天然氰胺含量是通过从添加内标的样品的A42/A44比值中减去内标的A42/A44比值,然后将所得差值乘以添加((15)N2)氰胺的量来得出(稳定同位素稀释气相色谱 - 质谱法)。该方法成功地给出了毛苕子中天然氰胺含量的合理值,与通过常规方法获得的值一致,在常规方法中,氰胺被衍生化为具有光度活性的化合物4 - 氰胺基 - 1,2 - 萘醌并通过反相高效液相色谱法进行分析(氰胺基萘醌 - 高效液相色谱法)。稳定同位素稀释气相色谱 - 质谱法中氰胺的测定范围与氰胺基萘醌 - 高效液相色谱法几乎相同;然而,稳定同位素稀释气相色谱 - 质谱法比氰胺基萘醌 - 高效液相色谱法简单得多。

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