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首页> 外文期刊>Analytical Sciences >Simultaneous Separation and Determination of Eleven Nucleosides and Bases in Beer, Herring Sperm DNA and RNA Soft Capsule by High-Performance Liquid Chromatography
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Simultaneous Separation and Determination of Eleven Nucleosides and Bases in Beer, Herring Sperm DNA and RNA Soft Capsule by High-Performance Liquid Chromatography

机译:高效液相色谱法同时分离测定啤酒,鲱鱼精DNA和RNA软胶囊中的11种核苷和碱基

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A simple and rapid high-performance liquid chromatography method was developed for the determination of eleven nucleosides and bases in beer, herring sperm DNA and RNA soft capsules. The separation was carried out on an Agilent extend-C_(18) column with a simple gradient elution of acetonitrile and water as the mobile phase. Good linear relationships between the peak areas and the concentrations of the analytes were obtained. The detection limits for eleven analytes were in the range of 0.007 – 0.037 mg/L by UV detection at 260 nm. The relative standard deviations (RSDs) of the retention times were in the range of 0.78 – 1.85% for intra-day and 0.87 – 1.94% for inter-day, respectively. The RSDs of the peak areas were in the range of 2.71 – 3.22% for intra-day and 3.03 – 3.39% for inter-day, respectively. This method has been successfully applied to simultaneous determination of eleven nucleosides and bases in beer, herring sperm DNA and RNA soft capsules with the recoveries in the range of 93.7 – 108.3%.
机译:建立了一种简单快速的高效液相色谱方法,用于测定啤酒,鲱鱼精子DNA和RNA软胶囊中的11种核苷和碱基。分离在安捷伦extended-C_(18)色谱柱上进行,以乙腈和水作为流动相的简单梯度洗脱。获得了峰面积与分析物浓度之间的良好线性关系。通过260 nm的紫外检测,对11种分析物的检出限为0.007 – 0.037 mg / L。保留时间的相对标准偏差(RSD)在日内范围为0.78 – 1.85%,在日间范围内为0.87 – 1.94%。高峰地区的日间相对标准偏差分别为2.71 – 3.22%,日间为3.03 – 3.39%。该方法已成功用于啤酒,鲱鱼精子DNA和RNA软胶囊中11种核苷和碱基的同时测定,回收率在93.7 – 108.3%之间。

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