Ultra high performance liquid chromatography with photodiode array detector and quadrupole time-of-flight tandem mass spectrometry coupled with discriminant analysis to evaluate Angelicae pubescentis radix from different regions

被引:20
|
作者
Ge, Ai-Hua [1 ,2 ]
Ma, Wen-Fang [1 ,2 ]
Wang, Chun-Peng [1 ]
Li, Jin [1 ]
He, Jun [1 ,2 ]
Liu, Er-Wei [1 ,2 ]
Adelakum, Tiwalade Adegoke [1 ]
Zhang, Bo-Li [1 ,2 ]
Gao, Xiumei [1 ,2 ]
Chang, Yan-Xu [1 ,2 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Tianjin State Key Lab Modern Chinese Med, Tianjin 300193, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, Tianjin Key Lab Phytochem & Pharmaceut Anal, Tianjin 300193, Peoples R China
基金
中国国家自然科学基金;
关键词
Angelicae pubescentis radix; Coumarins; Daodi medicinal material; Discriminant analysis; Phenolic acids; PHENOLIC-ACIDS; ELECTROSPRAY-IONIZATION; QUANTITATIVE-ANALYSIS; FINGERPRINT ANALYSIS; CHLOROGENIC ACID; ESSENTIAL OIL; TOF-MS; EXTRACT; IDENTIFICATION; FLAVONOIDS;
D O I
10.1002/jssc.201400289
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A rapid and effective method was developed for the qualitative and quantitative analysis of the major chemical constituents in Angelicae pubescentis radix by ultra high performance liquid chromatography with photodiode array detection and quadrupole time-of-flight tandem mass spectrometry. The chromatographic separation was achieved on an ACQUITY UHPLC BEH C-18 column (2.1 x 100 mm, 1.7 mu m). Nine phenolic acids, 30 coumarins, bisabolangelone, and adenosine were identified by quadrupole time-of-flight tandem mass spectrometry. All calibration curves exhibited good linearity (r > 0.9996) within the linear ranges. The relative standard deviation calculated for intraday and interday precision, stability, and accuracy were <5%. The mean recovery ranged from 95.8 to 106%. The overall limits of detection and quantification were 0.025-0.160 and 0.100-0.560 mu g/mL, respectively. Discriminant analysis was investigated as a method for evaluating the quality of the samples with 100% correction in their classification. The results demonstrated that the developed method could successfully be used to differentiate samples from different regions and could be a helpful tool for detection and confirmation of the quality of traditional Chinese medicines.
引用
收藏
页码:2523 / 2534
页数:12
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