A kind of detection method of dendrobium medicinal material
A detection method, the technology of Dendrobium, applied in the direction of measuring device, material separation, analysis of materials, etc., can solve the problems of non-repeatability, one-sided evaluation method, insufficient system, and complete indication of the overall quality of Dendrobium medicinal materials, and achieve good reproducibility , keep the effect intact, and the pre-processing method is simple
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Embodiment 1
[0046] Embodiment 1: Dendrobium candidum detection method
[0047] Instruments and reagents: Instruments: Agilent1200series high performance liquid chromatography (including low-pressure binary gradient pump G1312A, column thermostat G1316A, diode array detector G1315B, Chemstation chemical workstation, American Agilent Technology Co., Ltd.), 100g portable pulverizer (Guangzhou Xulang Machinery Equipment Co., Ltd.) Milli-Q Synthesis ultrapure water purification system (Millipore Company), RQ-250B ultrasonic cleaner (Kunshan Ultrasonic Instrument Co., Ltd.), PB303-N electronic balance (MEETTLER TOLEDO, 0.001g), 0.45μm microporous filter head (Jinteng Company). Reagents: acetonitrile, methanol (chromatographically pure, Fisher Scientific, USA); other reagents are analytically pure; ultrapure water (MilliQ ultrapure water, passed through a 0.45 μm microporous membrane); acetic acid (Beijing Dongfang Fine Chemicals Co., Ltd.).
[0048] The chromatographic conditions for the estab...
Embodiment 2
[0062] Embodiment two: the detection method of Dendrobium chrysoprase
[0063] The difference from Example 1 is:
[0064] Preparation of standard sample solution: take different batches of dry samples of Dendrobium chrysalis, pulverize them with a pulverizer, pass through a pharmacopoeia sieve (aperture 0.335mm), accurately weigh 1.000g of Dendrobium powder, place it in a 100ml Erlenmeyer 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 to a 5ml volumetric flask, shake well, and filter with a 0.45μm microporous membrane to obtain standard sample solutions of different batches.
[0065] Table 3 Similarity evaluation results of 10 batches of Dendrobium drumstick fingerprints
[0066]
[0067] According to the method described ab...
Embodiment 3
[0069] Embodiment three: the detection method of Dendrobium dendrobii
[0070] The difference from Example 1 is:
[0071] Preparation of standard sample solution: take different batches of dry samples of Dendrobium nodii, pulverize them with a pulverizer, pass through a pharmacopoeia sieve (aperture 0.335mm), accurately weigh 1.000g of Dendrobium powder, place it in a 100ml Erlenmeyer 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 to a 5ml volumetric flask, shake well, and filter with a 0.45μm microporous membrane to obtain standard sample solutions of different batches.
[0072] Table 4 Similarity evaluation results of fingerprints of 10 batches of Dendrobium dendrobii
[0073]
[0074] According to the above method, 10 bat...
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