首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous determination of five marker constituents in traditional Chinese medicinal preparation Le-Mai granule by high performance liquid chromatography.
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Simultaneous determination of five marker constituents in traditional Chinese medicinal preparation Le-Mai granule by high performance liquid chromatography.

机译:高效液相色谱法同时测定中药乐麦颗粒中的五种标志物成分

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摘要

An HPLC method for the simultaneous determination of five marker constituents was established for the quality control of traditional Chinese medicinal preparation Le-Mai granule. The marker constituents were danshensu, protocatechuic acid and protocatechualdehyde from Salviae miltiorrhizae bunge; paeoniflorin from Radix paeoniae rubra and ferulic acid from Rhizoma chuanxiong. Extracted samples were successfully separated on a Diamonsil C(18) column (150mmx4.6mm i.d., 5mum) at 25 degrees C. The mobile phase was a mixture of methanol and 1.0% acetic acid employing gradient elution at a flow rate of 1.0mL/min. Detection was accomplished with a diode-array detector and chromatograms were recorded at 230, 262, 280 and 322nm. The compounds were identified by comparing their retention times and UV spectra in the 200-400nm range with authentic standards. Regression equations revealed good linear relationship (correlation coefficients: 0.9993-0.9999) between the peak areas of the constituents and their concentrations. The average recoveries (n=3) were between 96.2 and 102.5%. The proposed method has been successfully applied to the simultaneous determination of the five marker constituents in three lots of Le-Mai granule.
机译:建立了同时测定五种标志物成分的高效液相色谱法,用于中药乐麦颗粒的质量控制。标记成分为丹参中丹参素,原儿茶酸和原儿茶醛。 pa药中的药苷和川xi的阿魏酸。提取的样品已在25°C的Diamonsil C(18)色谱柱(150mmx4.6mm内径,5mum)上成功分离。流动相是甲醇和1.0%乙酸的混合物,采用梯度洗脱,流速为1.0mL /分钟用二极管阵列检测器完成检测,并在230、262、280和322nm处记录色谱图。通过将其保留时间和200-400nm范围内的UV光谱与真实标准品进行比较来鉴定化合物。回归方程揭示了组分的峰面积与其浓度之间的良好线性关系(相关系数:0.9993-0.9999)。平均回收率(n = 3)在96.2和102.5%之间。该方法已成功应用于三批乐麦颗粒中五种标记物的同时测定。

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