Method for rapidly detecting ganoderic acid G in ganoderma lucidum spore oil
A technology of Ganoderma lucidum spore oil and detection method, which is applied in the field of rapid detection of Ganoderma lucidum acid G in Ganoderma lucidum spore oil, can solve problems such as low sensitivity, and achieve the effects of low cost, low cost and harm reduction.
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Embodiment 1
[0044] The rapid qualitative analysis of ganoderma acid G in the ganoderma lucidum spore oil of embodiment 1
[0045] Sample: taken from the commercially available Ganoderma lucidum spore oil A.
[0046] a. Weigh 0.4 g of spore oil, add 2 mL of anhydrous methanol for oscillation, and place in an ultrasonic extractor for 10 minutes of sonication.
[0047] b. Shake the extract and filter.
[0048] Qualitative analysis:
[0049] Take 200 μL of filtrate and add 100 μL of concentrated sulfuric acid to shake well, then take 100 μL of the solution as the solution to be tested, add 400 μL of gold nano-enhancer, add 100 μL of acidifier, shake well and test, according to 555cm -1 (±3cm -1 ), 1176cm -1 (±3cm -1 ) to evaluate whether there is a characteristic Raman peak:
[0050] The liquid to be tested is at 555cm -1 (±3cm -1 ), 1176cm -1 (±3cm -1 ) has a characteristic peak (see figure 1 ), it means that the sample contains ganoderma acid G.
Embodiment 2
[0051] The rapid qualitative analysis of ganoderma acid G in the ganoderma lucidum spore oil of embodiment 2
[0052] Sample: taken from the commercially available Ganoderma lucidum spore oil B.
[0053] a. Weigh 0.4 g of spore oil, add 3.2 mL of anhydrous methanol for oscillation, and place in an ultrasonic extractor to sonicate for 10 minutes.
[0054] b. Shake the extract and filter.
[0055] Qualitative analysis:
[0056] Take 200 μL of filtrate and add 200 μL of concentrated sulfuric acid to shake well, then take 100 μL of the solution as the test solution, add 300 μL of gold nano-enhancer, add 50 μL of acidifier, shake well and test, according to 555cm -1 (±3cm -1 ), 1176cm -1 (±3cm -1 ) to evaluate whether there is a characteristic Raman peak:
[0057] The liquid to be tested is at 555cm -1 (±3cm -1 ), 1176cm -1 (±3cm -1 ) there is no characteristic peak, it means that there is no ganoderma acid G in the sample.
Embodiment 3
[0058] The rapid qualitative analysis of ganoderma acid G in the ganoderma lucidum spore oil of embodiment 3
[0059] Sample: taken from the commercially available ganoderma lucidum spore oil C.
[0060] a. Weigh 0.4 g of spore oil, add 4 mL of anhydrous methanol for oscillation, and place in an ultrasonic extractor for 10 minutes of sonication.
[0061] b. Shake the extract and filter.
[0062] Qualitative analysis:
[0063] Take 200 μL of filtrate and add 40 μL of concentrated sulfuric acid to shake well, then take 100 μL of the solution as the solution to be tested, add 200 μL of gold nano-enhancer, add 100 μL of acidifier, shake well and test, according to 555cm -1 (±3cm -1 ), 1176cm -1 (±3cm -1 ) to evaluate whether there is a characteristic Raman peak:
[0064] The liquid to be tested is at 555cm -1 (±3cm -1 ), 1176cm -1 (±3cm -1 ) has a characteristic peak (see figure 1 ), it means that the sample contains ganoderma acid G.
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