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LC determination of dinitrosopiperazine in simulated gastric juice.

机译:液相色谱法测定模拟胃液中的二亚硝基哌嗪。

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摘要

A simple and specific reversed phase HPLC method for the determination of dinitrosopiperazine in simulated gastric juice using UV detection was reported. The chromatographic resolution of the analyte and the internal standard isosorbide dinitrate was performed without extraction from the gastric juice on a reversed phase ODS column. Isocratic elution was carried out with methanol-0.02 M sodium dihydrogen phosphate (60:40 v/v, pH 3.0) at a flow rate of 1.0 ml min(-1) with UV detection at 238 nm. The calibration graph was linear over the concentration range 0.072-2.88 microg ml(-1) of dinitrosopiperazine with minimum detectability (S/N=2) of 0.01 microg ml(-1) (8 x 10(-8) M). Inter-day and intra-day precisions calculated as % RSD were in the range 0.32-0.38% and 0.19-0.25% respectively. Inter-day and intra-day accuracies calculated as % error were in the range 0.18-0.21 and 0.08-0.11% respectively. The proposed method was successfully applied to the study of the possible in-vivo production of DNPZ under the standard nitrosation conditions recommended by WHO.
机译:报道了一种简单且特异性的反相HPLC方法,使用紫外检测器测定模拟胃液中的二硝基哌嗪。无需在反相ODS色谱柱上从胃液中萃取,即可进行分析物和内标硝酸异山梨酯二硝酸盐的色谱分离。用甲醇-0.02 M磷酸二氢钠(60:40 v / v,pH 3.0)以1.0 ml min(-1)的流速进行等度洗脱,并在238 nm处进行UV检测。校准曲线在浓度为0.072-2.88 microg ml(-1)的二亚硝基哌嗪上呈线性,最小可检测性(S / N = 2)为0.01 microg ml(-1)(8 x 10(-8)M)。以%RSD计算的日间和日内精度分别在0.32-0.38%和0.19-0.25%的范围内。以%误差计算的日间和日内精度分别在0.18-0.21和0.08-0.11%的范围内。该方法已成功应用于世界卫生组织推荐的标准亚硝化条件下DNPZ可能体内生产的研究。

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