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Comparison of flower buds and leaves of Tussilago farfara L. by UHPLC-Q Extractive Hybrid Quadrupole Orbitrap MS
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Jing LI1, 2, Juan LI1, 2, Jin-ping JIA3, Jun-jie ZHANG3, Yan YAN1, Xiao-xia GAO1, Xue-mei QIN1, Zhen-yu LI1, *
Acta Pharmaceutica Sinica | 2018, 53(3) : 444 - 452
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Acta Pharmaceutica Sinica | 2018, 53(3): 444-452
ORIGINAL ARTICLES·Pharmaceutical Analysis
Comparison of flower buds and leaves of Tussilago farfara L. by UHPLC-Q Extractive Hybrid Quadrupole Orbitrap MS
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Jing LI1, 2, Juan LI1, 2, Jin-ping JIA3, Jun-jie ZHANG3, Yan YAN1, Xiao-xia GAO1, Xue-mei QIN1, Zhen-yu LI1, *
Affiliations
  • 1. Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China
  • 2. College of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China
  • 3. Scientific Instrument Center, Shanxi University, Taiyuan 030006, China
Published: 2018-03-12 doi: 10.16438/j.0513-4870.2017-0943
Outline
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The flower bud of Tussilago farfara L. has been commonly used in the treatment of cough, bronchitis and asthmatic disorders in the Traditional Chinese Medicine. In Europe, the leaves were also used as herbal drugs with similar pharmacological activities. In order to utilize the leaves, it is important to conduct the chemical comparison between the flower buds and the leaves. In this study, ultra high liquid chromatography (UHPLC) coupled with Q Exactive high resolution mass spectrometry (HR-MS) was used to compare the chemical composition of the flower buds and leaves of T. farfara L. forty three metabolites were identified by the combination of targeted and untargeted approach. The results suggest that the sesquiterpenes, such as tussilagone and 7β-(3'-ethyl-cis-crotonoyloxy)-1α-(2'-methylbutyryloxy)-3(14)-dehydro-Z-notonipetranone were higher in the flower buds. While the phenylpropanoids, such as cholorgenic acid and isochlorogenic acid were higher in the leaves. The flavonoids, such as hyperin and quercetin exhibited no difference between the flower buds and leaves, while the rutin and kaempferol were higher in the flower buds. The leaves and flower buds had similar chemical components, and the phenylpropanoids, which were closely related with the antitussive and expectorant activities, were found at higher concentrations in the leaves. The results presented here laid the basis for the rational utilization of the leaves of T. farfara L.

Tussilago farfara  /  LC-MS  /  chemical comparison
Jing LI, Juan LI, Jin-ping JIA, Jun-jie ZHANG, Yan YAN, Xiao-xia GAO, Xue-mei QIN, Zhen-yu LI. Comparison of flower buds and leaves of Tussilago farfara L. by UHPLC-Q Extractive Hybrid Quadrupole Orbitrap MS[J]. Acta Pharmaceutica Sinica, 2018 , 53 (3) : 444 -452 . DOI: 10.16438/j.0513-4870.2017-0943
Year 2018 volume 53 Issue 3
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Article Info
doi: 10.16438/j.0513-4870.2017-0943
  • Receive Date:2017-09-21
  • Online Date:2026-01-15
  • Published:2018-03-12
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  • Received:2017-09-21
  • Revised:2017-11-21
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Affiliations
    1. Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006, China
    2. College of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China
    3. Scientific Instrument Center, Shanxi University, Taiyuan 030006, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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