A method for separation and identification of flavonoids in tobacco by liquid chromatography-mass spectrometry
A technology of liquid chromatography and identification method, which is applied in the field of separation and identification of plant extracts, can solve the problems of limited sensitivity of ultraviolet detectors, and achieve the effect of simple and fast sample preparation, high sensitivity, and improved detection efficiency
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Embodiment 1
[0044] ——Isolation and Identification of Isorhamnetin in Tobacco
[0045] (1) Experimental reagents and devices
[0046] Acetonitrile (chromatographic grade), methanol (chromatographic grade), and ethanol (chromatographic grade) were purchased from Merck, Germany. Ultrapure water was produced by a Millipore purification system. Other standard samples were purchased from Sigma-Aldrich, AlfaAesar and Bailingwei. Waters UPLC liquid chromatograph (USA), ABSCIEX5500 triple quadrupole mass spectrometer (USA). SB-50D ultrasonic extractor (Ningbo Xinzhi Biotechnology Co., Ltd.), WatersBEHC18 (15cm×2.1mm×1.7μm) reversed-phase chromatographic column (Waters, USA), MILLI-Q pure water machine (MILLIPORE Company), LD5- 2A centrifuge (Beijing Jingli Centrifuge Co., Ltd.), vortex mixer (Breda, Netherlands), CP2245 analytical balance (sensitivity 0.0001g, Sartorius, Germany).
[0047] (2) Experimental materials
[0048] The mature middle leaves and petals of Yunyan 97, Honghua Dajinyuan,...
Embodiment 2
[0056] ——Isolation and identification of isorhamnetin-3-O-rutinoside from tobacco
[0057] (1) Experimental reagents and devices
[0058] With embodiment 1.
[0059] (2) Experimental materials
[0060] With embodiment 1.
[0061] (3) Experimental method
[0062] With embodiment 1.
[0063] (4) Experimental results
[0064] Since isorhamnetin was found in tobacco samples, it was hypothesized that glycosyl-bound compounds of isorhamnetin also exist in tobacco. The molecular ion of isorhamnetin (315 - ) was used as a characteristic ion to perform a full scan of the parent ion, and it was found that there was an obvious chromatographic peak at the retention time of 4.55min ( Figure 4 ), the detected precursor ion is 623 - . According to 623 - with 315 - There is a neutral loss of 308, and the compound is preliminarily judged to be isorhamnetin-rutinoside. Collection 4.55min at 623 - Ion secondary fragment ion, and submit it to the massbank website (www.massbank.jp) f...
Embodiment 3
[0066] ——Isolation and Identification of Quercetin-3-O-Rutinoside from Tobacco
[0067] (1) Experimental reagents and devices
[0068] With embodiment 1.
[0069] (2) Experimental materials
[0070] With embodiment 1.
[0071] (3) Experimental method
[0072] With embodiment 1.
[0073] (4) Experimental results
[0074] at 151 - When scanning the precursor ion for the characteristic ion, there is an obvious chromatographic peak at the chromatographic retention time of 5.80min, and the detected precursor ion is 301 - . Collection 5.80min at 301 -Ion secondary fragment ion, and submit it to the massbank website (www.massbank.jp) for spectral library comparison, and found that it is very similar to the secondary mass spectrum of quercetin in the spectral library, purchase quercetin The standard substance was compared with the compound to be identified by retention time and secondary mass spectrum, and it was confirmed that it was quercetin. Molecular ion of quercetin 30...
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