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METHOD FOR DETERMINING THE EFFICIENCY antibacterial drugs for treating inflammatory diseases microbial etiology

机译:确定治疗炎性疾病微生物病因的抗菌药物的方法

摘要

FIELD: biotechnology.;SUBSTANCE: microorganism-causative agent is isolated from the biological material of the patient. The standard suspension of the isolated microorganism-causative and two-fold dilutions of antibacterial preparations with known activity is prepared. Inoculation is carried out. The standard suspension of the isolated causative agent with the volume of 0.1 ml is mixed with 5.0 ml of liquid nutrient medium specific for this pathogen. It is incubated for 24 hours at +37°C. The test 1:100 and control 1:200 dilutions are prepared in the same nutrient medium. Each of the two-fold dilutions of antibacterial preparations in amount of 0.075 ml with an equal amount of the test dilutions is applied in the test cavities of the plate. In the control cavity 0.150 ml of control dilution is applied and incubated for 48 hours at + 37°C. The liquid fraction of the suspension is removed from the cavities. For staining 0.2 ml of 1% solution of crystal violet is added to each cavity. It is exposed at room temperature for 30 min. The contents of the cavities are washed three times with distilled water and 0.2 ml of 99% solution of dimexidum is added to each cavity. It is exposed at room temperature for 15 minutes. The optical density of the medium in the control (ODC) and the test cavities is measured in the optical units (pu) in a microplate reader at the wave-length of 540 nm. When fulfilment of the condition ODC 0.2pu, the greatest two-fold dilution of antibacterial preparation in the test cavity with an optical density less than 0.2 pu is defined as the minimum inhibitory concentration (MIC).;EFFECT: invention enables to improve the accuracy of determination of IPC.;2 ex
机译:领域:生物技术;物质:微生物致病因子是从患者的生物材料中分离出来的。制备具有已知活性的分离的微生物致病菌和两倍稀释度的抗菌制剂的标准混悬液。进行接种。将体积为0.1 ml的分离的病原体的标准悬浮液与5.0 ml对该病原体特有的液体营养培养基混合。将其在+ 37℃下孵育24小时。在相同的营养培养基中制备测试1:100和对照1:200稀释液。将量为0.075 ml的抗菌制剂的两倍稀释液中的每种稀释液与等量的测试稀释液一起施加到平板的测试腔中。在对照腔中,施加0.150ml对照稀释液,并在+ 37℃下孵育48小时。将悬浮液的液体部分从腔中除去。为了染色,将0.2ml 1%的结晶紫溶液添加到每个腔中。将其在室温下暴露30分钟。用蒸馏水将空腔的内容物洗涤三遍,并向每个空腔中加入0.2ml 99%的灭蚁灵溶液。在室温下暴露15分钟。对照(OD C )和测试腔中介质的光密度在酶标仪中以光学单位(pu)在540 nm波长处测量。当满足条件OD C

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