Bansal M B, Dhawan V K, Thadepalli H
Chemotherapy. 1982;28(3):200-3. doi: 10.1159/000238076.
The antimicrobial efficacy of BU-2313B, a new antibiotic, was evaluated in comparison with clindamycin, chloramphenicol and cefoxitin against 265 clinical anaerobic isolates. BU-2313B inhibited 88% of 66 isolates of Bacteroides fragilis tested at 2 micrograms/ml, whereas clindamycin, chloramphenicol and cefoxitin inhibited 98, 97 and 92% of them at 2, 8 and 16 micrograms/ml, respectively. BU-2313B was severalfold more effective than chloramphenicol and cefoxitin, but it was eight times less effective than clindamycin.
将新型抗生素BU - 2313B与克林霉素、氯霉素和头孢西丁进行比较,评估了其对265株临床厌氧分离株的抗菌效果。在2微克/毫升的浓度下,BU - 2313B对测试的66株脆弱拟杆菌分离株中的88%有抑制作用,而克林霉素、氯霉素和头孢西丁在2、8和16微克/毫升的浓度下分别对其中98%、97%和92%有抑制作用。BU - 2313B的效力比氯霉素和头孢西丁高几倍,但比克林霉素低八倍。