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Gas Chromatographic Determination of Purines and Pyrimidines from DNA Using Ethyl Chloroformate as Derivatizing Reagent

机译:使用氯甲酸酯作为衍生试剂的DNA从DNA的气相色谱法测定嘌呤和嘧啶

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摘要

An analytical method has been proposed for the separation and determination of guanine, adenine, cytosine, thymine and uracil by gas chromatography (GC) following precolumn derivatization using ethyl chloroformate. The GC separation was achieved from HP-5 (30 m × 0.32 mm id) column with layer thickness 0.25 µm. The linear calibrations were observed within 0.5-50.0 µmol/L for each of the compound and limits of detection were within 0.1-0.17 µmol/L. The derivatization, separation and quantitation was repeatable with intra (n=5) and inter (n=5) variation in terms of peak height/peak area and retention time with relative standard deviation (RSD) within 4.70-6.43%. The method was applied for the analysis of isolated DNA from human blood and plant leaves after acid hydrolysis. The concentration of thymine, adenine, cytosine and guanine in blood samples were observed within 0.602-2.135 µmol/L of each compounds with RSD 2.60-6.00%. The recovery of the nucleobases by standard addition was calculated within 98-108% with RSD 2.5-7.8%.
机译:采用氯甲酸乙酯急性衍生后,已经提出了一种分析方法,用于通过气相色谱(GC)通过气相色谱(GC)分离和测定喹啉,腺嘌呤,胞嘧啶,胸腺嘧啶。通过HP-5(30m×0.32mm ID)塔,层厚度为0.25μm,实现GC分离。对于每种化合物,在0.5-50.0μmol/ L内观察到线性校准,检测限率在0.1-0.17μmol/升之内。衍生化,分离和定量是可重复于interA(n = 5),并且在峰值高度/峰面积和保留时间的帧间(n = 5)变化,并且在4.70-6.43%内具有相对标准偏差(RSD)的保留时间。该方法用于分析酸水解后人血液和植物叶中分离的DNA。在每种化合物的0.602-2.135μmol/ L内观察到血液样品中胸腺嘧啶,腺嘌呤,胞嘧啶和鸟嘌呤的浓度,RSD 2.60-6.00%。通过标准加入回收核碱基的回收率在98-108%以上,RSD 2.5-7.8%计算。

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