Detection method of extract of seed of Mucuna macrocarpa Wall
A detection method and extract technology, applied in the detection field of quinoa bean extract, can solve problems such as harsh analysis conditions, difficult separation, lack of content analysis methods, etc.
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Embodiment 1
[0018] The preparation of embodiment 1 need testing solution
[0019] 3-Carboxyl-tetrahydroisoquinoline components 1-3 and LD have poor solubility in conventional solvents such as water and ethanol, and are easily oxidized. The content gap between LD and other components is large, so the preparation method of the original medicinal material for testing more critical. The present invention selects acid solution ultrasonic extraction for use, by extracting acid concentration (0.02-0.2mol L -1 [H + ]), the amount of extraction solvent (10, 20, 30 times), the extraction time (30, 60, 90min) were investigated and optimized, and finally the optimal preparation method of the original medicinal material for the test was established, and the corresponding quinoa bean extract for the test The preparation method of product solution.
[0020] Maodou MD-1 (20091101, white seed coat, Baise, Guangxi) and Maodou MD-2 (20111212, black seed coat, Nanning, Guangxi) are the dried seeds of Mucu...
Embodiment 2
[0023] The HPLC detection of embodiment 2 need testing product
[0024] Components 1-3 are characteristic components in quinoa bean, which can be used as quality control indicators of quinoa bean extract. Such components are similar in structure to LD and have strong polarity. They are hardly retained on conventional C18 columns, and the resolution is not good. After further research, the present invention, through comparison of various chromatographic columns, finally selects hydrophilic C18 chromatographic column and methanol solution (0-5%; more preferably 0-3%) as mobile equal degree elution, combined with modification Agent (0.5-1.5% acetic acid, 5-10mmol·L -1 Ammonium acetate, adjust pH2-4) and elution flow rate (0.5, 0.8, 1.0mL·min -1 ) optimization, the following chromatographic conditions were finally selected, components 1-3 and LD all obtained ideal baseline separation, thereby establishing a simultaneous quantitative analysis method for such components in the qui...
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