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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of phosphorus using capillary electrophoresis and micro-high-performance liquid chromatography hyphenated with inductively coupled plasma mass spectrometry for the quantification of nucleotides
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Determination of phosphorus using capillary electrophoresis and micro-high-performance liquid chromatography hyphenated with inductively coupled plasma mass spectrometry for the quantification of nucleotides

机译:使用毛细管电泳和电感耦合等离子体质谱联用的微型高效液相色谱法测定磷,用于定量核苷酸

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We performed the quantification of phosphorus in deoxynucleotides using capillary electrophoresis (CE) and micro-HPLC (mu HPLC) hyphenated with inductively coupled plasma mass spectrometry (ICP-MS) DNA and its component units have conventionally been determined by photometry, however, more selective and sensitive methods are needed for small biological samples CE and mu HPLC offer the advantages of good separation and small consumption of samples. and ICP-MS is a highly sensitive technique for the determination of a chemical element Therefore, we have developed an interface device for combining CE and mu HPLC with ICP-MS for quantifying nucleotides based on phosphorus content. The interface utilizes 4.5 mu L/min for nebulizing and effective introduction of the sample into ICP The samples of nucleotides and free phosphoric acid were well separated in the CE-ICP-MS measurement, and the calibration Curves (1-100 mu g/mL of the nucleotides showed a linear(R-2 > 0.999)increase in intensity Similarly, the samples of nucleotides were baseline separated using mu HPLC-ICP-MS, and the calibration cut were linear (R-2 > 0 998). The detection limits of these species and phosphorus in nucleotides using CE-ICP-MS and mu HPLC-ICP-MS were 0.77-6.5 ng/mL and 4.0-6.5 ng/mL, respectively These values were about one or two orders lower than those in a previous report. The sample volumes of these experiments were calculated to be about 10 nL and 50 nL per analysis. Therefore, these analytical methods have the potential to be useful for the determination of biological samples, Such as DNA and RNA molecules.
机译:我们使用毛细管电泳(CE)和通过电感耦合等离子体质谱(ICP-MS)联用的微型HPLC(μHPLC)对脱氧核苷酸中的磷进行了定量分析,其组成单元通常通过光度法测定,但是选择性更高小型生物样品需要灵敏的方法CE和mu HPLC具有良好的分离性和样品消耗量少的优点。 ICP-MS是测定化学元素的高度灵敏技术。因此,我们开发了一种接口装置,可将CE和mu HPLC与ICP-MS结合使用,以根据磷含量定量核苷酸。该界面利用4.5μL / min的雾化效率并将样品有效地引入ICP中。在CE-ICP-MS测量中,核苷酸和游离磷酸的样品已得到很好的分离,并且校准曲线(1-100μg / mL核苷酸的强度呈线性增加(R-2> 0.999)。类似地,使用mu HPLC-ICP-MS对核苷酸样品进行基线分离,校正标度为线性(R-2> 0 998)。使用CE-ICP-MS和mu HPLC-ICP-MS对这些种类和磷的核苷酸限制分别为0.77-6.5 ng / mL和4.0-6.5 ng / mL,这些值比标准样品中的低约1或2个数量级。这些实验的样本量每次分析分别约为10 nL和50 nL,因此,这些分析方法有可能用于测定生物样本,例如DNA和RNA分子。

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