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Incorporation of high performance liquid chromatography with resonance Rayleigh scattering detection for determination of procaine and lidocaine in human plasma

机译:结合高效液相色谱和共振瑞利散射检测法测定人血浆中的普鲁卡因和利多卡因

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A reliable and novel high performance liquid chromatography (HPLC) incorporating resonance Rayleigh scattering (RRS) detection was developed for the determination of procaine (Pro) and lidocaine (Lid). This method was based on the weak intensity of RRS of procaine and lidocaine, which can be enhanced by the addition of Erythrosin Yellowish (E-Y) in pH 4.4 acidic medium. The RRS signal was detected at λ_(ex) = λ_(em) = 370 nm. The conditions of separation and detection were optimized (pH, proportion of organic phase, flow rate, reaction temperature, concentration of E-Y and the length of reaction tube). The shape of ion-association complexes was observed by scanning electron microscopy. The reasons for RRS enhancement and the nature of the ion-association complexes were discussed by quantum chemistry calculation, scanning electron microscopy and absorption spectroscopy. The calibration curves of procaine and lidocaine were linear in the range from 0.005 to 15.375 μg mL~(-1) and the limit of detection (S//V = 3) was 2.3 ng mL~(-1) for procaine and 15 ng mL~(-1) for lidocaine. The developed method was validated for the assay of procaine and lidocaine in human plasma samples. The recoveries were between 97.8% and 105.9% which is within acceptable limits.
机译:开发了一种可靠的新型高效液相色谱(HPLC),并结合了共振瑞利散射(RRS)检测技术来测定普鲁卡因(Pro)和利多卡因(Lid)。该方法基于普鲁卡因和利多卡因的RRS强度较弱,这可以通过在pH 4.4酸性介质中添加赤藓红微黄(E-Y)来增强。在λ_(ex)=λ_(em)= 370 nm处检测到RRS信号。优化了分离和检测条件(pH,有机相比例,流速,反应温度,E-Y浓度和反应管长度)。通过扫描电子显微镜观察离子缔合配合物的形状。通过量子化学计算,扫描电子显微镜和吸收光谱讨论了RRS增强的原因和离子缔合配合物的性质。普鲁卡因和利多卡因的校准曲线在0.005至15.375μgmL〜(-1)范围内呈线性关系,普鲁卡因和15 ng的检出限(S // V = 3)为2.3 ng mL〜(-1)。利多卡因mL〜(-1)验证了所开发的方法可用于测定人血浆样品中的普鲁卡因和利多卡因。回收率在97.8%至105.9%之间,在可接受的范围内。

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