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 seven major diterpenoids in Pseudolarix kaempferi by high-performance liquid chromatography DAD method.
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Simultaneous determination of seven major diterpenoids in Pseudolarix kaempferi by high-performance liquid chromatography DAD method.

机译:高效液相色谱DAD法同时测定假山茱seven中的七种主要二萜类化合物。

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摘要

A reversed phase high-performance liquid chromatography method was established for the first time to simultaneously qualify the seven major diterpenoids in Pseudolarix kaempferi, namely pseudolaric acid B O-beta-D-glucopyranoside (1), pseudolaric acid C2 (2), pseudolaric acid C1 (3), deacetylpseudolaric acid A (4), pseudolaric acid A O-beta-D-glucopyranoside (5), pseudolaric acid B (6) and pseudolaric acid A (7). The optimal conditions of separation and detection were achieved on an Inertsil ODS-3 column with gradient elution of methanol and 0.5% aqueous acetic acid (v/v) at the flow rate of 0.6 ml min(-1) within 40 min and detection wavelength set at 262 nm. All calibration curves showed good linear regression (r2>0.9999) within test ranges. This method provided good accuracy with recoveries in the range of 94.3-106.1% and good precision with R.S.D.s of repeatability and intermediate precision less than 0.57% and 4.67%, respectively. The method was successfully applied to qualitative and quantitative determination of 20 P. kaempferi among the 54 samples collected from different areas. The results revealed that the commercial crude drugs were seriously confused and the developed HPLC assay could be used as a suitable qualitative and quantitative determination method for P. kaempferi.
机译:首次建立了反相高效液相色谱法,以同时鉴定假单胞菌中的七个主要二萜类化合物,即假松香酸BO-β-D-吡喃葡萄糖苷(1),假松香酸C2(2),假松香酸C1(3),去乙酰伪藻酸A(4),假烟酸AO-β-D-吡喃葡萄糖苷(5),假烟酸B(6)和假烟酸A(7)。最佳分离和检测条件是在Inertsil ODS-3色谱柱上实现的,在40分钟和检测波长范围内,以0.6 ml min(-1)的流速梯度洗脱甲醇和0.5%乙酸水溶液(v / v)设置在262 nm所有校准曲线在测试范围内均表现出良好的线性回归(r2> 0.9999)。该方法提供了94.3-106.1%的回收率,并且重复精度R.S.D.s分别小于0.57%和4.67%。该方法成功地用于定性和定量测定从不同地区收集的54个样品中的20个山竹假单胞菌。结果表明,市售粗制药物存在严重混淆,所开发的高效液相色谱法可作为一种合适的定性和定量测定方法。

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