Quality detection method of Dendrobium denneanum Kerr
A quality inspection method and technology of Dendrobium candidum, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve problems such as the inability to fully reflect the overall curative effect, achieve strong interpretation pertinence and applicability, effectively identify and control quality, and achieve The effect of correlation analysis
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Embodiment 1
[0052] Example 1 Generation sequencing of Dendrobium sheath
[0053] First-generation sequencing primer sequences:
[0054] ITS-26SE: 5'GAATTCCCCGGTTCGCTCGCCGTTAC 3';
[0055] ITS-17SE: 5' ACGAATTCATGGTCCGGTGAAGTGTTCG 3'.
[0056] The amplification and sequencing parameters are: denaturation at 98°C for 2 minutes and then PCR cycle, the PCR cycle parameters are 98°C for 20s; 52°C for 30s; 68°C for 1min, 38 cycles, 68°C for 7min, set 4°C after the amplification, and perform Generation Molecular Sequencing.
[0057] Through the first generation sequencing, the species of Dendrobium to be tested was identified as Dendrobium sheathing.
Embodiment 2
[0058] The extraction method of embodiment 2 dendrobium sheath
[0059] Take the dried sample of Dendrobium sheathing, pulverize it with a pulverizer, pass through a pharmacopoeia sieve (aperture 0.335mm), accurately weigh 1.000g of Dendrobium powder (the weighing error cannot exceed 0.2%), place it in a 100ml conical flask, add 50mL 75 % methanol (V water: V methanol = 25:75), take it out after ultrasonication for 30 minutes at room temperature, filter, and concentrate the filtrate to dryness by rotary evaporation, dissolve it with 75% methanol solvent (V water: V methanol = 25:75), and finally transfer Dilute it to a 10ml volumetric flask, shake well, and filter with a 0.45 μm microporous membrane to obtain a sample solution of Dendrobium sheathing.
Embodiment 3
[0060] Example 3 Chromatographic detection method of Dendrobium sheath extract
[0061] ①Preparation of reference solution
[0062] Accurately weigh 4.10 mg of Schaftoside and 4.08 mg of naringenin, place them in 10 ml volumetric flasks, add 75% (V / V) methanol to dissolve and dilute, shake well, and use them as stock solutions. Refrigerate at 4°C for later use.
[0063] Then accurately draw a certain amount of reference substance stock solution and dilute with 75% methanol to accurately prepare a mixed reference substance solution of schaffertoside and naringenin. Through different dilution ratios, 7 concentration points of the prepared components were diluted. into a high performance liquid chromatograph.
[0064] ②Extraction and processing method of samples for determination of small molecule components of Dendrobium sheathing:
[0065] Take 1.00g of the powder of this product (passed through a No. 3 sieve), accurately weigh it, put it in a 100ml volumetric flask, add 50...
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