Application of tanshinone IIA to preparing drugs or cosmetics for inhibiting propionibacterium acnes
A technology of Propionibacterium acnes and tanshinone, which is applied in the field of compounds, can solve the problems of surrounding tissue damage, hair follicle wall structure damage, hair follicle integrity damage, etc., and achieve the effect of simple application and easy use
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Embodiment 1
[0037] Example 1 Tanshinone IIA inhibits Propionibacterium acnes
[0038] Experimental strain: Propionibacterium acnes (ATCC6919)
[0039] Medium:
[0040] (1) Liquid medium: tryptone 10g / L, beef extract 10g / L, glucose 5g / L, NaCl 5g / L, yeast extract 3g / L, sodium acetate 3g / L, soluble starch 1g / L, cysteine Dissolve 0.5g / L hydrochloride in distilled water, adjust the pH to 6.8±0.2, and autoclave at 115°C for 20min. (2) Solid medium: add agar 15g / L on the basis of liquid medium.
[0041] Experimental method: Determination of inhibition zone
[0042] Propionibacterium acnes was inoculated in solid medium, and activated under anaerobic conditions at 37°C for 2 days. After activation, the plaque was directly diluted with physiological saline to prepare a bacterial suspension. Take 0.5ml of the activated bacterial suspension in liquid medium, and culture it under anaerobic conditions at 37°C for 2 days, which is the experimental bacterial suspension. The experimental method adop...
Embodiment 2
[0048] Example 2 Tanshinone IIA inhibits Propionibacterium acnes MIC value determination
[0049] Experimental strain: Propionibacterium acnes (ATCC6919)
[0050] Medium: (1) Liquid medium: tryptone 10g / L, beef extract 10g / L, glucose 5g / L, NaCl 5g / L, yeast extract 3g / L, sodium acetate 3g / L, soluble starch 1g / L, semi Cystine hydrochloride 0.5g / L, dissolved in distilled water, adjusted to pH 6.8±0.2, autoclaved at 115°C for 20min. (2) Solid medium: add agar 15g / L on the basis of liquid medium.
[0051] Experimental method: Determination of the minimum inhibitory concentration (MIC value) of traditional Chinese medicine extracts
[0052] Propionibacterium acnes was inoculated in solid medium, and activated under anaerobic conditions at 37°C for 2 days. After activation, the plaque was directly diluted with physiological saline to prepare a bacterial suspension, and the bacterial suspension was diluted with liquid medium. Make the final bacterial concentration l0 5 CFU / mL.
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