Quality detection method of Dendrobium catenatum Lindley
A quality detection method, the technology of Dendrobium officinale, applied in the direction of biochemical equipment and methods, microbiological determination/inspection, measuring devices, etc., can solve the problems that cannot fully reflect the overall curative effect, achieve pertinence of explanation and strong applicability, and solve The Curse of Dimensionality, Efficient Discrimination and Quality Control Effects
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Embodiment 1
[0051] The generation sequencing of embodiment 1 dendrobium officinale
[0052] First-generation sequencing primer sequences:
[0053] ITS-26SE: 5'GAATTCCCCGGTTCGCTCGCCGTTAC 3';
[0054] ITS-17SE: 5' ACGAATTCATGGTCCGGTGAAGTGTTCG 3'.
[0055] 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.
[0056] Through the first-generation sequencing, the species of Dendrobium to be tested was identified as Dendrobium officinale.
Embodiment 2
[0057] The extraction method of embodiment 2 Dendrobium officinale
[0058] Take the dry sample of Dendrobium officinale, 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 Erlenmeyer flask, add 50mL of 75% Methanol (V water: V methanol = 25:75), after ultrasonication for 30 minutes at room temperature, it was taken out, filtered, the filtrate was concentrated to dryness by rotary evaporation, dissolved in 75% methanol solvent (V water: V methanol = 25:75), and finally transferred to Dilute to volume in a 10ml volumetric flask, shake well, and filter with a 0.45 μm microporous membrane to obtain a sample solution of Dendrobium officinale.
Embodiment 3
[0059] The chromatographic detection method of the Dendrobium officinale extract of embodiment 3
[0060] ①Preparation of reference solution
[0061] 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.
[0062] 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.
[0063] ②Extraction and processing method of samples for determination of small molecule components in Dendrobium officinale:
[0064] Take 1.00g of the powder of this product (passed through a No. 3 sieve), accurately weigh it, put it in a 100ml volum...
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