Ponomareva T R, Malakhova V A
Antibiot Khimioter. 1989 Apr;34(4):261-3.
A microbiological procedure for determining dioxidine concentrations in biological fluids with using E. coli AB 2472 rec A 16, a reparation deficient strain as a test organism is described. Cell suspension of the strain 24-hour culture is added to 1.2 per cent agar with Hottinger digest (140 mg per cent of amine nitrogen), 3 g/l of disubstituted sodium phosphate and 0.4 per cent of glucose cooled to 50 degrees C. 10 ml of the medium are added to every Petri dish with metallic cylinders put on the agar. After the medium solidification the cylinders are removed and 0.1 ml of the solution being tested is added to every well. The dishes are incubated for 24 hours under anaerobic conditions. The test system sensitivity is 0.2 microgram/ml of dioxidine. The relationship between the growth inhibition zone and the drug concentration is linear within dioxidine concentrations of 0.2 to 3.2 micrograms/ml.
描述了一种微生物学方法,该方法使用大肠杆菌AB 2472 rec A 16(一种修复缺陷型菌株)作为测试生物体来测定生物流体中的二氧嗪浓度。将该菌株24小时培养物的细胞悬液加入到含有霍廷格消化物(胺氮含量为140mg%)、3g/l磷酸二钠和0.4%葡萄糖且冷却至50℃的1.2%琼脂中。将10ml该培养基加入到每个装有放置在琼脂上的金属圆筒的培养皿中。培养基凝固后,取出圆筒,向每个孔中加入0.1ml待测溶液。将培养皿在厌氧条件下孵育24小时。该测试系统对二氧嗪的灵敏度为0.2微克/毫升。在二氧嗪浓度为0.2至3.2微克/毫升范围内,生长抑制区与药物浓度之间的关系呈线性。