Application of green olive extract in preparation of drugs or food or daily necessities for preventing and curing periodontitis
A technology of green olive and extract, which is applied in the field of plant extracts for the prevention and treatment of periodontitis, can solve the problem that no green olive extract inhibits oral anaerobic bacteria, and achieves the reduction of biofilm formation, convenient prevention and significant prevention The effect of action
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[0023] The preparation steps of the green olive extract are as follows: taking green olive branches, leaves or fruits as raw materials, carrying out reflux extraction with water or ethanol aqueous solution, filtering, concentrating the filtrate under reduced pressure to obtain a concentrate, and drying to obtain the green olive extract.
[0024] The preparation parameters of the green olive extracts of Examples 1-14 are shown in Table 1.
[0025] Table 1
[0026]
[0027]
Embodiment 15
[0028] Example 15 Test of green olive extract in vitro inhibition of Porphyromonas gingivalis, Prevotella intermedia and Fusobacterium nucleatum induced by periodontitis
[0029] Porphyromonas gingivalis (Porphyromonas gingivalis) ATCC33277 was purchased from Beijing Beina Chuanglian Biotechnology Research Institute.
[0030] Intermediate Prevotella (Prevotella intermedia) ATCC25611 was purchased from Beijing Beinan Chuanglian Biotechnology Research Institute.
[0031] and Fusobacterium nucleatum (Fusobacterium nucleatum) ATCC10953 were purchased from Beijing Beina Chuanglian Biotechnology Research Institute.
[0032] Test method: Porphyromonas gingivalis ATCC33277, Prevotella intermedia ATCC25611 and Fusobacterium nucleatum ATCC10953 were taken out from the -80°C refrigerator respectively, revived routinely, and inoculated in BHI Agar medium, cultured anaerobically at 37°C (80% N 2 , 10%H 2 , 10% CO 2 ) 48h, pick a single colony and replant it in BHI liquid medium, and cu...
Embodiment 16
[0037] Example 16 Effects of different concentrations of green olive extracts on Porphyromonas gingivalis biofilm formation
[0038] Test method: In this experiment, the plant extract prepared in Example 10 was used to carry out the following tests. The blank control group was Porphyromonas gingivalis ATCC33277 bacterial suspension (200 μL per well). The negative control group was a polyethylene 96-well plate containing absolute ethanol (10 μL per well) containing Porphyromonas gingivalis ATCC33277 suspension (190 μL per well). In the experimental group, 1 / 4MIC, 1 / 2MIC, MIC, 2MIC green olive extracts (10 μL per well) were added to polyethylene 96-well plates containing Porphyromonas gingivalis ATCC33277 suspension (190 μL per well). In triplicate, the same concentration level was repeated 4 times. 37 ℃ anaerobic culture for 48h. Suck out the bacterial suspension in the wells with a micropipette, gently wash the wells 3 times with PBS to remove planktonic bacteria, add fresh...
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