Determination of Cyanide in Blood by High Performance Liquid Chromatography with Fluorescence Detection

S. Chinaka, N. Takayama
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引用次数: 3

Abstract

Simultaneous determination of inorganic ions including cyanide by photometric ion chromatography was useful for a cyanide analysis in drinks, but not applicable to that in blood, because of its poor resolution for cyanide and chloride. In this report, to determine cyanide in blood, we adopted a selective and sensitive method for cyanide based on a fluorometric reaction with 2,3-naphthalenedialdehyde (NDA) and taurine to afford 1-cyanobenz[f]isoindole derivative. Cyanide was extracted from blood by adding water and methanol to whole blood, and then derivatized with NDA and taurine. The cyanide derivative was analyzed on a reversed-phase high performance liquid chromatograph system with fluorescence detector.   In the analysis of standard solutions, the reagent blank showed a minor peak of cyanide corresponding to ca. 0.04 ng/ml. Thus the lower detection limit for cyanide standard solution was 0.1 ng/ml as 2.5-fold concentration of the reagent blank peak. The peak seemed to be due to trace cyanide in reagents, however, it was so minor peak that it didn't interfere with cyanide determination in blood. The calibration curve for cyanide standard solution was linear in the range 0.1-200 ng/ml. In the blood analysis, the method enabled us to determine cyanide from healthy persons level (ca. 10 ng/ml) to fatal level (ca. 3000 ng/ml) employing the same treatment.
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高效液相色谱-荧光检测法测定血液中氰化物
光度离子色谱法同时测定含氰化物的无机离子可用于饮料中的氰化物分析,但由于其对氰化物和氯化物的分辨率较差,因此不适用于血液中的氰化物分析。在本报告中,为了测定血液中的氰化物,我们采用了一种基于2,3-萘二醛(NDA)和牛磺酸的荧光反应得到1-氰苯[f]异吲哚衍生物的选择性灵敏的氰化物测定方法。将水和甲醇加入全血中提取血液中的氰化物,然后与NDA和牛磺酸衍生。在带荧光检测器的反相高效液相色谱仪上对氰化物衍生物进行了分析。在标准溶液分析中,试剂空白中氰化物出现一个小峰,约为0.04 ng/ml。因此,氰化物标准溶液的检测下限为0.1 ng/ml,为试剂空白峰浓度的2.5倍。这个峰值似乎是由于试剂中痕量氰化物引起的,但这个峰值非常小,不会影响血液中氰化物的测定。在0.1 ~ 200 ng/ml范围内,氰化物标准溶液的校准曲线呈线性关系。在血液分析中,采用相同的处理方法,该方法使我们能够确定从健康人水平(约10纳克/毫升)到致命水平(约3000纳克/毫升)的氰化物。
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