Modified skin tinea fungus test culture medium
A dermatophyte and culture medium technology, applied in the field of fungal color development medium, can solve the problems of different antifungal drugs antibacterial spectrum, need to improve the result judgment standard, antibiotics are not resistant to high temperature, etc., and achieves early and accurate reporting time. The effect of improved efficiency and economical formulation
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Embodiment 1
[0022] 1. Medium preparation:
[0023] Element
[0024] Soy peptone 5g
[0025] Glucose 5g
[0026] Chloramphenicol 0.0625g
[0027] Cycloheximide 0.1g
[0028] 0.1% bromothymol blue 25mL
[0029] Agar 18g
[0030] HCL(1.0N) 4.6-5.0mL
[0031] Add water to 1000mL
[0032] pH5.5±0.1
[0033] Preparation method: Add soybean peptone, glucose and agar to water, heat to dissolve; add bromothymol blue solution while stirring, adjust pH with 1N Hcl; add cycloheximide and chloramphenicol to culture medium at 121°C for 10 Minute autoclave.
[0034] 2. Results report:
[0035] Specimens were inoculated according to the conventional fungal culture method, and the discoloration of the medium and the growth of the strains were regularly observed every day. If the colony diameter was ≤5mm when the discoloration began, there was a 95% possibility of being a dermatophyte, otherwise it was a non-dermatophyte.
Embodiment 2
[0037] 1. Medium preparation:
[0038] Element
[0039] Soy peptone 5g
[0040] Glucose 5g
[0041] Chloramphenicol 0.125g
[0042] Cycloheximide 0.3g
[0043] 0.1% bromothymol blue 50mL
[0044] Agar 19g
[0045] HCL(1.0N) 4.6-5.0mL
[0046] Add water to 1000mL
[0047]pH5.5±0.1
[0048] Preparation method: Add soybean peptone, glucose and agar to water, heat to dissolve; add bromothymol blue solution while stirring, adjust pH with 1N Hcl; add cycloheximide and chloramphenicol to medium; 121°C Autoclave for 10 minutes.
[0049] 2. Results report:
[0050] Specimens were inoculated according to the conventional fungal culture method, and the discoloration of the medium and the growth of the strains were regularly observed every day. If the diameter of the colony was ≤5mm when the discoloration began, there was a 95% possibility of being a dermatophyte, otherwise it was a non-dermatophyte.
Embodiment 3
[0052] 1. Medium preparation:
[0053] Element
[0054] Soy peptone 5g
[0055] Glucose 5g
[0056] Chloramphenicol 0.25g
[0057] Cycloheximide 0.5g
[0058] 0.1% bromothymol blue 100mL
[0059] Agar 20g
[0060] HCL(1.0N) 4.6-5.0mL
[0061] Add water to 1000mL
[0062] pH5.5±0.1
[0063] Preparation method: Add soybean peptone, glucose and agar to water, heat to dissolve; add bromothymol blue solution while stirring, adjust pH with 1N HCL; add cycloheximide and chloramphenicol to medium; 121°C Autoclave for 10 minutes.
[0064] 2. Results report:
[0065] Specimens were inoculated according to the conventional fungal culture method, and the discoloration of the medium and the growth of the strains were regularly observed every day. If the diameter of the colony was ≤5mm when the discoloration began, there was a 95% possibility of being a dermatophyte, otherwise it was a non-dermatophyte.
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