Method for evaluating honeysuckle characteristics based on marker flavonoids screened by metabolome
A technology of flavonoids and honeysuckle is applied in the field of labeling flavonoids to evaluate honeysuckle and its processed products, which can solve the problems of limited research throughput, inability to efficiently, systematically and comprehensively characterize, and achieve the effect of broad application prospects and rapid repeatability.
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Embodiment 1
[0037] Embodiment 1 preparation of flavonoid extract
[0038] (1) Collection of honeysuckle flower buds / flowers at different developmental stages
[0039] According to previous reports (Xiaofei Shang et al., 2011, Journal of Ethnopharmacology), the formation of honeysuckle flower buds is divided into six representative periods, namely the juvenile bud stage, the third green stage and the third green stage. stage), the second white stage, the completewhite stage, the silver flowering stage and the gold flowering stage. According to reports by other researchers (Jie Wu et al., 2015, Scientific Reports), the juvenile bud stage can be subdivided into the Milei stage and the early bud stage. The specific morphological characteristics are shown in Table 1.
[0040] Table 1 Morphological characteristics of Lonicera japonica at different stages of flower development
[0041]
[0042]
[0043] Collect and weigh the honeysuckle flower buds / flowers ( figure 1 ) 2-3g, three biol...
Embodiment 2
[0046] Example 2 Detection of Honeysuckle Flavonoids Samples Based on LC-MS / MS
[0047] The instrumentation system for data acquisition includes ultra-high performance liquid chromatography and tandem mass spectrometry.
[0048] Liquid phase conditions mainly include: ① Chromatographic column: Waters ACQUITY UPLC HSS T3 C18 1.8 μm; ② Mobile phase A: ultrapure water (containing 0.04% acetic acid by volume); Mobile phase B: acetonitrile (containing 0.04% acetic acid by volume); ③Elution gradient: 0-11min, 95-5% mobile phase A, 5-95% mobile phase B; 11-12min, 5% mobile phase A, 95% mobile phase B; 12-12.1min, 5-95% Mobile phase A, 95-5% mobile phase B; 12.1-15min, 95% mobile phase A, 5% mobile phase B; ④ flow rate 0.3-0.4mL / min; column temperature 40°C; injection volume 2μL.
[0049] The mass spectrometry conditions mainly include: the temperature of the electrospray ion source is 500°C; the mass spectrometry voltage is 5500 V; the curtain gas is 25 psi; the collision-induced io...
Embodiment 3
[0050] Example 3 Analysis of detection results of honeysuckle flower buds / flowers flavonoids
[0051] (1) Qualitative and quantitative analysis of flavonoid metabolites
[0052] Mass spectrometry data were processed using the software Analyst 1.6.3. Mainly based on the public database of metabolite information, the qualitative analysis of the first-order spectrum and second-order spectrum data detected by mass spectrometry is carried out. Metabolite structure analysis refers to existing public mass spectrometry databases such as MassBank, KNAPSAcK, HMDB, MoTo DB, and METLIN. The characteristic ions of each substance were screened out by the triple quadrupole, the signal intensity (CPS) of the characteristic ions was obtained in the detector, and the mass spectrum file of the sample was opened with MultiaQuant software. After obtaining the metabolite mass spectrometry data of different samples, the peak area integration of all the mass spectrum peaks of the substance is perfo...
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