Cyclocarya paliurus extract and application thereof
A technology of Cyclocarya paliurus and medicine, applied in the field of Cyclocarya paliurus extract, which can solve the problems of activity and mechanism research.
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Embodiment 1
[0065] 1.1 Treatment of Cyclocarya paliurus medicinal materials: Dry leaves of Cyclocarya paliurus (10Kg), crush and extract with 70% ethanol under reflux at 120°C (100L; 2×2h), concentrate at 60°C to obtain extract, and the concentration time is 2 days. The extract was further dispersed in water, extracted with dichloromethane, ethyl acetate, and n-butanol in sequence, 10 L each time, extracted 3 times, and the extract was concentrated at 60°C for 24 hours to obtain extracts and concentrates of different polar parts. liquid. The dichloromethane part is mainly dammarane-type tetracyclic triterpenoids, which is the No. 1 active part (also known as the dichloromethane active part), marked as QQL-ST, and the n-butanol part is mainly flavonoids The compound, active site number 2 (also known as the n-butanol active site), was annotated as QQL-HT.
[0066] 1.2 Biological activity-oriented screening of active parts of Cyclocarya paliurus: Use models to track and screen the active pa...
Embodiment 2
[0133] 2.1 Immunity-enhancing activity evaluation of dichloromethane active fraction and n-butanol active fraction of Cyclocarya paliurus
[0134] 2.1.1 Experimental Grouping
[0135] 128 experimental animals, weighing 18-22 grams, were randomly divided into 4 groups after one week of adaptive feeding, with 32 mice in each group. Group 1 was tested for organ / body weight, serum hemolysin, and antibody-producing cells; group 2 was tested for delayed hypersensitivity; groups 3-4 were tested for carbon clearance and peritoneal macrophages phagocytosis of chickens Red blood cell experiment. In the experiment, 150 mg / kg QQL-HT, QQL-ST group and a blank control group were set up, with 8 animals in each group. Before the experiment, the test substance was made into a 10mg / mL suspension with distilled water, and the animals in the corresponding dose group were given intragastric administration according to the volume of 0.2mL / 10g BW, and the blank control group was given the same vol...
Embodiment 3
[0192] The application of the dichloromethane active part and the n-butanol active part of Cyclocarya paliurus in the preparation of lipid-lowering medicine.
[0193] 3.2 Evaluation of lipid-lowering activity
[0194] 3.2.1 Establishment and grouping of hyperlipidemia animal models
[0195] After one week of adaptive feeding, the mice were randomly divided into blank control group and model group. The mice in the model group were gavaged with high-fat emulsion (1 mL / kg), and the mice in the blank control group were gavaged with an equal volume of sterile water. Taking the blank control group as a reference, the mice with successful modeling were selected according to the extremely significant difference in TC value (P<0.01) from the blank group, and they were randomly divided into model control group, QQL-ST group and QQL-HT group. During the experiment, the mice in each group had free access to water and food, and the activities and eating conditions of the animals were obs...
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