A method for identifying Cordyceps sinensis powder mixed with fermented Cordyceps sinensis powder
A technology of Cordyceps sinensis powder and Cordyceps sinensis, which is applied in the direction of color/spectral characteristic measurement, etc., can solve the problems of market adulteration, difficulty in identifying Cordyceps sinensis fermented Cordyceps sinensis powder, flooding of counterfeit products, etc., to achieve fast and accurate identification, convenient batch identification, The effect of strong economic applicability
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Embodiment 1
[0024] Take a commercially available Cordyceps sinensis capsule sample A, take out the powder, grind and pulverize it, pass through a 100-mesh sieve, then weigh 0.050g of the sample and place it in a 100mL round-bottomed conical flask, add 10mL of 30% ethanol aqueous solution, 40KH Z Frequency ultrasonic extraction for 25min, centrifugation at 5000rpm for 10min to obtain the supernatant. Take out the supernatant and dilute it 4 times, filter it with a 0.45 μm microporous membrane, and scan the ultraviolet spectrum with 12.5 μg / mL adenosine standard as a reference. The scanning conditions are: scanning range 350-220nm, spectral resolution 2nm. The resulting spectrum is shown in figure 1 . It can be seen from the ultraviolet absorption spectrum of the sample that there is no negative absorption value in the 275-250nm band, indicating that the fermented Cordyceps sinensis powder is mixed in the sold Cordyceps sinensis capsules.
Embodiment 2
[0026] Take a commercially available Cordyceps sinensis buccal tablet sample B, grind it and pass through a 100-mesh sieve, then weigh 0.050g of the sample and place it in a 100mL round-bottomed conical flask, add 10mL of 30% ethanol aqueous solution, 40KH Z Frequency ultrasonic extraction for 25min, centrifugation at 5000rpm for 10min to obtain the supernatant. Take out the supernatant and dilute it 4 times, filter it with a 0.45 μm microporous membrane, and scan the ultraviolet spectrum with 12.5 μg / mL adenosine standard as a reference. The scanning conditions are: scanning range 350-220nm, spectral resolution 2nm. The resulting spectrum is shown in figure 2 . It can be seen from the ultraviolet absorption spectrum of the sample that there is a negative absorption value in the 275-250nm band, indicating that more than 10% fermented Cordyceps sinensis powder is not mixed in the sold Cordyceps sinensis buccal tablets.
Embodiment 3
[0028] Take the commercially available Cordyceps capsule sample A, the wild Cordyceps standard product and the fermented Cordyceps powder standard product purchased from China Food and Drug Control Institute and the Cordyceps powder containing 10%, 20%, 40%, 50% fermented Cordyceps powder standard product 7 samples were crushed and passed through a 100-mesh sieve respectively, then weighed 0.050g each, placed in a 100mL round-bottomed Erlenmeyer flask, added 10mL of 30% ethanol aqueous solution, extracted by ultrasonic at 40KHZ frequency for 25min, centrifuged at 5000rpm for 10min to take the supernatant liquid. Take out the supernatant and dilute it 4 times, filter it with a 0.45 μm microporous membrane, take the 12.5 μg / mL adenosine standard solution as a reference, and scan the ultraviolet spectrum of the above 7 samples respectively. The conditions are as follows: Range 350-220nm, spectral resolution 2nm. The ultraviolet scanning spectra obtained by superimposing the wild...
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