Application of nicotinamide in preparation of medicine for resisting porphyromonas gingivalis
A technology of porphyromonas and gingival porphyrin, which is applied in the field of biomedicine, can solve the problems of subgingival microbial resistance, tetracycline superinfection and other problems, and achieve good biosafety performance, easy preparation, and good solubility Effect
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Embodiment 1
[0033] Example 1: Culture of strains and formulation of liquid inhibitors
[0034] 1 Preparation for testing strains:
[0035] In this example, the testing strain of the Toxaciopcellosis is obtained from the US Typical Microbial Square Savings Center, the strain number: ATCC BAA-308.
[0036] 2 Component and preparation of medium:
[0037] (1) Cow Hexin Tombsorbent (hereinafter referred to as BHI) Liquid medium Component and formulated method: 37 g of commercially available BHI powder is added to 1000 mL of distilled water, high temperature and high pressure (121.3 ° C, 103.4 kPa) steam sterilization 15 minutes, after cooling;
[0038] (2) Component of 5 μg / ml of Hemin solution and its formulation method: 40g of sodium hydroxide (NaOH) was added to 1000 mL of distilled water, formulated as a NaOH aqueous solution of 1 mol / L, will 50 mg Hemin powder is dissolved in the NaOH aqueous solution of 1 mol / L, and is set to 100 mL, high temperature and high pressure (121.3 ° C, 103.4...
Embodiment 2
[0047] Example 2: Effect of inhibitors on cell Porphyromonas gingivalis growth of bacteria
[0048] Aseptic procedure according to Example 1, the embodiment of Porphyromonas gingivalis Aeromonas bacterial suspension of Example 1 were inoculated in liquid media containing various concentrations of inhibitor to determine the state of growth inhibitors on Porphyromonas gingivalis Aeromonas Impact. Specific methods are as follows: a liquid medium containing various concentrations (8mg / mL, 4mg / mL, 2mg / mL) inhibitor, the culture in Example 1 embodiment to logarithmic phase (OD 600 ≈0.5) of Porphyromonas gingivalis Aeromonas bacterial suspension was diluted to OD 600 ≈0.1, at 37 ℃, strictly anaerobic (10% CO 2 , 10% H 2 , 80% N 2 ) Cultured under conditions for 24 hours, every two hours during reading the OD at a wavelength of 600nm, and the control group (without addition of a liquid medium inhibitor) is determined by comparing the growth of Porphyromonas gingivalis bacterium cell...
Embodiment 3
[0050] Example 3: inhibitor of Porphyromonas gingivalis Aeromonas hemagglutination Function of
[0051] Aseptic procedure according to Example 1, the embodiment of Porphyromonas gingivalis Aeromonas bacterial suspension of Example 1 were inoculated in liquid media containing various concentrations of inhibitor to determine an inhibitor of Porphyromonas gingivalis Aeromonas hemagglutination influence function. Specific methods are as follows: a liquid medium containing various concentrations (8mg / mL, 4mg / mL, 2mg / mL) inhibitor, the culture in Example 1 embodiment to logarithmic phase (OD 600 ≈0.5) of Porphyromonas gingivalis Aeromonas bacterial suspension was diluted to OD 600 ≈0.1, at 37 ℃, strictly anaerobic (10% CO 2 , 10% H 2 , 80% N 2 ) Cultured under conditions for 24 hours. 4 ℃, 5,000 × g rpm for 10 minutes. The precipitate was collected bacteria, table phosphate buffered saline (Phosphate Buffered Saline, referred to as PBS) of claim 1 bacteria resuspended precipitate ...
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