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Biopartitioning Micellar Chromatography Determination of Nucleosides and Bases in Bailing Capsule

机译:生物分隔胶束色谱法测定百灵胶囊中核苷和碱基的含量

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摘要

In this work, we reported the determination of contents of three nucleosides (uridine, guanosine and adenosine) and two bases (uracil and adenine) in bailing capsule by biopartitioning micellar chromatography. The analytes were carried out on a Sepax-C_(18) (4.6 mm x 250 mm, 5 μm) and mobile phase consisted of 0.02 mol L~(-1) polyoxyethylene (23) lauryl ether (Brij35), 0.02 mol L~(-1) sodium dihydrogen phosphate-disodium hydrogen phosphate (pH = 7.4) and 9.2 g L~(-1) NaCl. The flow rate was 0.6 mL min~(-1), the detection wavelength and column temperature were set up at 260 nm and 37 °C, respectively. Uridine, guanosine, adenosine, uracil and adenine could be completely separated from each other and had good linerarity. The mediod is simple, sensitive,accurate, stable with a better reproducibility. So, it can assess and control the quality of preparations of fermental cordyeps-bailing capsule comprehensively.
机译:在这项工作中,我们报道了通过生物分配胶束色谱法测定保释胶囊中三种核苷(尿苷,鸟苷和腺苷)和两个碱基(尿嘧啶和腺嘌呤)的含量。分析物在Sepax-C_(18)(4.6 mm x 250 mm,5μm)上进行,流动相由0.02 mol L〜(-1)聚氧乙烯(23)月桂基醚(Brij35),0.02 mol L〜 (-1)磷酸二氢钠-磷酸氢二钠(pH = 7.4)和9.2 g L〜(-1)NaCl。流速为0.6 mL min〜(-1),检测波长和色谱柱温度分别设置为260 nm和37°C。尿苷,鸟苷,腺苷,尿嘧啶和腺嘌呤可以完全分离,并且具有良好的线性。方法简单,灵敏,准确,稳定,重现性好。因此,它可以全面地评估和控制发酵虫草诱饵胶囊制剂的质量。

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