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首页> 外文期刊>Journal of separation science. >Rapid characterization and determination of multiple components in Bu-Shen-Yi-Qi-Fang by high-performance liquid chromatography coupled to electrospray ionization and quadrupole time-of-flight mass spectrometry
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Rapid characterization and determination of multiple components in Bu-Shen-Yi-Qi-Fang by high-performance liquid chromatography coupled to electrospray ionization and quadrupole time-of-flight mass spectrometry

机译:高效液相色谱-电喷雾电离和四极杆飞行时间质谱法快速表征和确定补肾益气方中的多种成分

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In this study, a qualitative and quantitative analysis using high-performance liquid chromatography coupled to electrospray ionization and quadrupole time-of-flight mass spectrometry was performed for the quality control of Bu-Shen-Yi-Qi-Fang, a traditional Chinese formula used for asthma. Thirty-four compounds, including flavonoids, isoflavonoids, triterpenoid saponins, and iridoid glycosides were identified or tentatively characterized by comparing their retention times and mass spectra with those of authentic standards or literature data. Sixteen components were considered as the main bioactive constituents of Bu-Shen-Yi-Qi-Fang and they were chosen as the chemical markers in quantitative analysis, including catalpol, leonuride, calycosin-7-O-beta-D-glucoside, hyperoside, acteoside, formononetin-7-O-beta-D-glucoside, epimedin A, calycosin, icariin, epimedin B, epimedin C, formononetin, astragaloside IV, astragaloside II, baohuoside-I, and astragaloside I. The total run time was 20 min. It was found that the calibration curves for all analytes showed good linearity (R-2 > 0.99) within the test ranges. The relative standard deviations for intra-and inter-day precisions were below 3.9 and 11.7%, respectively. The accuracy was evaluated by the recovery test within the range of 89.20-110.71% with the relative standard deviation < 4.8%. The sample was stable for at least 48 h at 4 degrees C. The results showed that the new approach was effective for the quality control of Bu-Shen-Yi-Qi-Fang.
机译:在这项研究中,采用高效液相色谱法结合电喷雾电离和四极杆飞行时间质谱进行了定性和定量分析,以控制传统的中药补肾益气方药的质量。用于哮喘。通过将它们的保留时间和质谱图与真实标准品或文献数据的保留时间和质谱进行比较,鉴定或初步鉴定了34种化合物,包括类黄酮,异类黄酮,三萜类皂苷和铱类糖苷。十六种成分被认为是补肾益气方药的主要生物活性成分,并被选作定量分析中的化学标记,包括梓醇,利尿苷,calycosin-7-O-β-D-葡萄糖苷,多甙,菊苣甙,formononetin-7-O-β-D-葡萄糖苷,表艾替丁A,calycosin,icariin,epimedin B,epimedin C,formononetin,黄芪甲苷IV,黄芪甲苷II,baohuoside-I和黄芪甲苷I。总运行时间为20分钟。 。发现所有分析物的校准曲线在测试范围内均显示出良好的线性(R-2> 0.99)。日内和日间精度的相对标准偏差分别低于3.9和11.7%。通过回收率测试的准确性在89.20-110.71%的范围内,相对标准偏差<4.8%。样品在4摄氏度下稳定至少48小时。结果表明,该新方法对于补肾益气方的质量控制是有效的。

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