Traditional Chinese medicine injection for reversing drug resistance of staphylococcus aureus
A staphylococcus, drug-resistant technology, applied in the direction of antibacterial drugs, pharmaceutical formulations, organic active ingredients, etc., can solve the problems of no drug available for clinical infection treatment, reduced sensitivity of vancomycin, etc., to achieve the elimination of drug-resistant plasmids, The effect of restoring sensitivity and reversing drug resistance
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Embodiment 1
[0065] Embodiment 1, the mensuration of clinical separation MRSA minimum inhibitory concentration value
[0066] Strains to be tested: strain 161017, strain 1611099 and strain ATCC43300.
[0067] 1. Activation and cultivation of bacteria
[0068] Inoculate a single colony of the strain to be tested in MH liquid medium, culture with shaking at 37°C and 280rpm for 18-24h, collect the bacterial liquid, and dilute to OD with MH liquid medium 600nm =0.02, the bacteria solution to be tested was obtained.
[0069] 2. Determination of minimum inhibitory concentration
[0070] 1. Take the diluted Tanreqing injection, use MH liquid medium according to different volume ratios (1 / 2, 1 / 4, 1 / 8, 1 / 16, 1 / 32, 1 / 64, 1 / 128, 1 / 256, 1 / 512, 1 / 1024, Tanreqing injection is 1 part by volume) to dilute to obtain Tanreqing test solution.
[0071] 2. Use MH liquid medium to prepare vancomycin at different concentrations (8 μg / mL, 4 μg / mL, 2 μg / mL, 1 μg / mL, 0.5 μg / mL, 0.25 μg / mL, 0.125 μg / mL, 0.063 μ...
Embodiment 2
[0088] Example 2. Induction of Tanreqing Injection to Clinically Isolated Methicillin-resistant Staphylococcus aureus
[0089] 1. Induction of strain 161017 by Tanreqing injection
[0090] 1. Take 1 part by volume of diluted Tanreqing injection, and dilute it to 8 parts by volume with MH liquid medium to obtain MH liquid medium (medium A) containing Tanreqing. Inoculate strain 161017 in culture medium A, shake culture at 37°C and 280rpm for 16-18h, take 0.1mL of bacterial liquid and spread evenly on MH solid medium, and culture at 37°C until the colony grows, which is recorded as reversal 1 generation .
[0091] Inoculate the strain 161017 in the MH liquid medium, shake and culture at 37°C and 280rpm for 16-18h, take 0.1mL of the bacterial liquid and evenly spread it on the MH solid medium, and culture it statically at 37°C until the colony grows, which is recorded as the first generation of reversal control.
[0092] 2. Inoculate the reversed generation 1 single colony obt...
Embodiment 3
[0122] Embodiment 3, the minimum inhibitory concentration value determination of each generation bacterial strain after induction
[0123] Strains to be tested: strain 161017 (primary generation, reversal 1 generation - reversal 5 generation, reversal 1 generation control - reversal 5 generation control), strain 1611099 (primary generation, reversal 1 generation - reversal 5 generation, reversal 1 generation control - reversal 5 generation control) and strain ATCC43300 (primary generation, reversal 1 generation-reversal 5 generation, reversal 1 generation control-reversal 5 generation control).
[0124] 1. Activation and cultivation of bacteria
[0125] Inoculate a single colony of the strain to be tested in MH liquid medium, culture with shaking at 37°C and 280rpm for 18-24h, collect the bacterial liquid, and dilute to OD with MH liquid medium 600nm =0.02, the bacteria solution to be tested was obtained.
[0126] 2. Determination of minimum inhibitory concentration
[0127...
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