Nord C E, Lindmark A, Persson I
Department of Microbiology, Huddinge University Hospital, Karolinska Institute, Sweden.
Eur J Clin Microbiol Infect Dis. 1993 Oct;12(10):784-6. doi: 10.1007/BF02098471.
The in vitro activity of DMG-Mino and DMG-DM Dot against 350 anaerobic bacterial strains including anaerobic cocci, Propionibacterium acnes, Clostridium perfringens, Clostridium difficile, Bacteroides fragilis, other Bacteroides species and fusobacteria was determined by the agar dilution method. Their activity was compared with that of minocycline, doxycycline, piperacillin, cefoxitin, imipenem, clindamycin and metronidazole. DMG-Mino and DMG-DM Dot and imipenem were the most active agents tested. DMG-Mino and DMG-DM Dot had in vitro activity superior to that of minocycline and doxycycline.
采用琼脂稀释法测定了DMG-米诺环素和DMG-DM点针对350株厌氧细菌菌株的体外活性,这些菌株包括厌氧球菌、痤疮丙酸杆菌、产气荚膜梭菌、艰难梭菌、脆弱拟杆菌、其他拟杆菌属物种和梭杆菌属。将它们的活性与米诺环素、多西环素、哌拉西林、头孢西丁、亚胺培南、克林霉素和甲硝唑进行了比较。DMG-米诺环素、DMG-DM点和亚胺培南是所测试的活性最强的药物。DMG-米诺环素和DMG-DM点的体外活性优于米诺环素和多西环素。