Harvesting method for improving quality and yield of Dendrobium officinale Kimura et Migo
A harvesting method and technology of Dendrobium candidum, applied in the directions of botanical equipment and methods, harvesters, agricultural machinery and implements, etc., can solve the problem of inconvenient fertilization and water management, poor erection of Dendrobium candidum, lack of overall growth space, etc. To achieve the effect of improving pharmacological and pharmacodynamic activity, enhancing ventilation and light transmittance, and improving antioxidant and anti-inflammatory activities
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Embodiment 1
[0041] Embodiment 1: improve the gathering method of dendrobium officinale quality and output
[0042] 1.1 Experimental grouping:
[0043] The present embodiment is divided into experimental group, control group CK1, control group CK2 three groups altogether, and the harvesting method of each group is as follows:
[0044] (1) Experimental group: adopt the method of the present invention to harvest Dendrobium officinale, specifically comprising the following steps:
[0045] 1) Plant new seedlings from March to June, and the new seedlings are divided into tissue culture seedlings and domesticated seedlings;
[0046] 2) In the second year of planting new seedlings, all the old seedlings of tissue cultured seedlings or domesticated seedlings will be harvested from November to December, leaving only the new seedlings; the indicators of old seedlings harvested during this period conform to the 2020 edition of the Chinese Pharmacopoeia;
[0047] 3) In the third year after the new s...
Embodiment 2
[0086]Example 2 Detection of Antioxidant Activity of the Dendrobium officinale Samples Gained in Example 1
[0087] 2.1 Experimental materials
[0088] Dendrobium officinale (prepared by the harvesting method described in Example 1).
[0089] 2.2 Experimental method
[0090] 2.2.1 Scavenging effect on DPPH free radicals
[0091] Take 2 mL of 0.1 mmol / L DPPH absolute ethanol solution, mix it with 2 mL of the sample to be tested, and react in the dark at room temperature for 30 minutes, and the absorbance at 517 nm is measured as Ai; take 2 mL of the sample to be tested and an equal volume of absolute ethanol Mix and react for 30 min, and measure the absorbance at 517 nm as Aj; then take 2 mL of distilled water and mix it with an equal volume of DPPH solution, perform the same operation as above, measure the absorbance at 517 nm as A0, that is, the removal rate of DPPH by the sample to be tested effect.
[0092] Wherein the calculation formula of the scavenging rate of the s...
Embodiment 3
[0098] Embodiment 3 is aimed at the anti-inflammatory activity detection of the dendrobium candidum sample obtained in embodiment 1
[0099] 3.1 Experimental materials
[0100] Dendrobium officinale (prepared by the harvesting method described in Example 1); RAW264.7 cells (SCSP-5036, purchased from the Cell Bank of the Type Culture Collection Committee of the Chinese Academy of Sciences);
[0101] 3.2 Experimental method
[0102] 3.2.1 LPS-induced RAW264.7 cell inflammation model construction
[0103] Take RAW264.7 cells in good growth state and confluence of 90%, inoculate in cell culture plate at 37 ℃, 5% CO 2 The cells were cultured under conditions, and the cells were divided into blank control group, model group and three drug intervention groups. The specific grouping conditions are shown in Table 5.
[0104] Table 5 Grouping of RAW264.7 cells
[0105]
[0106] 3.2.2 RT-PCR detection of IL-6 and IL-1β mRNA expression
[0107] Refer to the instruction manual of E...
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