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DETERMINATION OF OLEANDER GLYCOSIDES IN BIOLOGICAL MATRICES BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY

机译:高效液相色谱法测定生物基质中的主糖苷

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摘要

A high-performance liquid chromatography (HPLC)-fluorescence method was developed for quantitative determination of oleandrin in gastrointestinal contents (stomach, rumen, colon, and cecum contents). Oleandrin was extracted with methylene chloride. The extract was cleaned up on a charcoal solid phase extraction (SPE) column, derivatized with 1-naphthoyl chloride, and quantified by HPLC with a fluorescence detector. The limit of detection was 0.05 ppm. Six replicate fortifications of stomach contents matrix at 0.10 ppm oleandrin gave an average recovery of 85%, with 4.6% CV (relative standard deviation). The diagnostic utility of the method was tested by analyzing samples submitted to the veterinary toxicology laboratory.
机译:开发了一种高效液相色谱(HPLC)荧光方法,用于定量测定胃肠道内容物(胃,瘤胃,结肠和盲肠中的含量)中夹竹桃苷。夹竹桃苷用二氯甲烷萃取。将萃取物在木炭固相萃取(SPE)柱上纯化,用1-萘甲酰氯衍生化,并通过HPLC和荧光检测器进行定量。检出限为0.05ppm。胃内容物基质在0.10 ppm夹竹桃苷的六次重复设防,平均回收率为85%,CV为4.6%(相对标准偏差)。通过分析提交给兽医毒理学实验室的样品,测试了该方法的诊断实用性。

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