Preparation method and active part of pharmaceutical composition for preventing and treating acute coronary syndrome
A technology of active parts and compositions, applied in the field of a group of active parts obtained in the preparation method and preparation process, can solve the problems of troublesome decoction, difficulty in clinical drug development and new drug development, and large dosage
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experiment example 1
[0034] EXPERIMENTAL EXAMPLE 1 EXTRACTION PROCESS OPTIMIZATION
[0035] 1. Test method
[0036] (1) Extraction method: take by weighing about 10.8g of the four flavors of raw materials, and its weight ratio is honeysuckle: Scrophulariaceae: Angelica: licorice = 3: 3: 2: 1, and carry out according to the factors and levels selected in the orthogonal test table extract.
[0037] (2) Selection of extraction conditions: According to the existence characteristics of compounds in traditional Chinese medicine, water and ethanol are selected as extraction solvents, and the four factors of ethanol concentration, dosage, extraction time, and extraction times are investigated, and each factor is limited to three levels. See Table 1 for details.
[0038] Table 1 Factor level table
[0039] Level
A ethanol concentration (%)
BExtraction time (h)
D extraction times
1
0
2
1∶6
2
2
55
3
...
experiment example 2
[0050] Inhibitory effect of the extract of Experimental Example 2 on the binding of NF-κB response elements
[0051] 1. Experimental steps
[0052] (1) Experimental materials: NF-κB-RE cells (pGL4.32[luc2P / NF-kappaB-RE]293A, Institute of Materia Medica, Chinese Academy of Medical Sciences), MEM-α medium (Gibco), fetal bovine serum (Gibco) , 96-well culture plate (Costar, 3599), Bright-Glo Luciferase luciferase detection reagent (Promaga), water-jacketed CO2 cell incubator (Sanyo, Japan), Safire2 high-speed multi-channel continuous wavelength microplate reader (TECAN, Austria ), EnSpire TM 2300 Multilabel Reader (PerkinElmer Corporation).
[0053] (2) Test samples:
[0054] Eight extracts obtained by the method described in Example 1 were provided by Beijing University of Traditional Chinese Medicine.
[0055] (3) Experimental steps:
[0056] Digest and count the logarithmically grown NF-κB-RE cells in the culture flask, and use 100ul system, 5×10 3 / well density inocula...
experiment example 3
[0067] The agonistic effect of experimental example three extracts on peroxisome proliferator receptor (PPARγ)
[0068] 1 material
[0069] 1.1 Reagents:
[0070] African green ape kidney cells (CV-1), PPRE plasmid, PPAR plasmid, RXRα plasmid, MEM-α medium (Gibco), fetal bovine serum (Gibco), Bright-Glo Luciferase luciferase detection reagent (Promega) , rosiglitazone.
[0071] 1.2 Instruments:
[0072] Water Jacketed CO 2 Cell incubator (Sanyo, Japan), EnSpireTM 2300MultilabelReader (PerkinElmer).
[0073] 2 methods
[0074] 2.1 Extraction of the test product
[0075] 8 extracts obtained by the method described in Example 1 are numbered 1 # -8 # , provided by Beijing University of Traditional Chinese Medicine.
[0076] 2.2 Cell Culture
[0077] African green ape kidney cells (CV-1) were cultured in DMEM medium supplemented with 10% FBS and 1% antibiotics (penicillin / streptomycin) in a 5% CO2 incubator at 37°C.
[0078] 2.3 Transfection and luciferase gene expressio...
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