A method for simultaneous determination of multi-component content in ginkgo biloba extract and its preparation
A technique for Ginkgo biloba leaves and extracts, which is applied in the field of high-performance liquid chromatography for simultaneous determination of multi-component contents in Ginkgo biloba extracts and preparations thereof, can solve the problems of inability to detect flavonoids and phenolic acid components at the same time, and achieves Low-cost, durable, easy-to-achieve results
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[0037] 1. Chromatographic conditions
[0038] Chromatographic column: ACQUITY UPLC BEH C18 (1.7μm, 2.1×150mm);
[0039] Mobile phase B: methanol / acetonitrile (1:1);
[0040] Mobile phase A: ultrapure water (containing 0.1% formic acid);
[0041] Flow rate: 0.3mL / min;
[0042] Column temperature: 35°C;
[0043] Injection volume: 1μL;
[0044]Diode array detector: use 280nm ultraviolet wavelength to detect phenolic acid components, and simultaneously use 360nm ultraviolet wavelength to detect flavonoid glycoside components;
[0045] Analysis time: 35min;
[0046] Gradient elution method:
[0047]
[0048]
[0049] 2. Solution preparation
[0050] (1) Preparation of reference substance stock solution
[0051] Precisely weigh protocatechuic acid, cryptochlorogenic acid, smokylin, rutin, isoquercitrin, quercetin-3-O-glucosyl (1→2) rhamnoside, kaempferol-3-O -Rutinoside, astragalin, cosmoside, narciscin, isorhamnetin-3-O-β-D-glucoside, 3-O-{2-O-[6-O-(p-hydroxy -trans...
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