Neu H C, Fu K P
Antimicrob Agents Chemother. 1978 Apr;13(4):657-64. doi: 10.1128/AAC.13.4.657.
The in vitro activity of cefuroxime, a cephalosporin antibiotic, was investigated against 604 isolates and compared with the activity of other beta-lactam compounds. Cefuroxime had activity comparable to that of other cephalosporins, including cefamandole and cefoxitin, against streptococcal and staphylococcal species; most streptococci were inhibited by 0.1 mug or less per ml, and staphylococci were inhibited by 1.6 mug or less per ml. Enterococci were relatively resistant. Cefuroxime inhibited beta-lactamase-producing Neisseria gonorrhoeae and Haemophilus influenzae. Cefuroxime had excellent activity against members of the Enterobacteriaceae; 83% of beta-lactamase-producing Escherichea coli, 100% of Salmonella, 100% of Klebsiella, 90% of Proteus mirabilis, 95% of Citrobacter, 56% of Enterobacter, and 58% of Shigella were inhibited by 12.5 mug/ml. Cefuroxime had activity comparable to that of cefamandole and cefoxitin; it inhibited isolates of E. coli and Klebsiella resistant to cefamandole and inhibited Enterobacter and Citrobacter resistant to cefoxitin. Many isolates of Serratia, some indole-positive strains of Proteus, and Bacteroides fragilis were resistant to cefuroxime. Resistance of cefuroxime to hydrolysis by beta-lactamases played a major role in its activity against both gram-positive and gram-negative organisms.
对头孢呋辛(一种头孢菌素类抗生素)的体外活性进行了研究,以检测其对604株菌株的作用,并与其他β-内酰胺类化合物的活性进行比较。头孢呋辛对链球菌和葡萄球菌的活性与其他头孢菌素(包括头孢孟多和头孢西丁)相当;大多数链球菌每毫升被0.1微克或更低浓度抑制,葡萄球菌每毫升被1.6微克或更低浓度抑制。肠球菌相对耐药。头孢呋辛可抑制产β-内酰胺酶的淋病奈瑟菌和流感嗜血杆菌。头孢呋辛对肠杆菌科细菌具有优异的活性;每毫升12.5微克可抑制83%产β-内酰胺酶的大肠杆菌、100%的沙门氏菌、100% 的克雷伯菌属、90%的奇异变形杆菌、95%的柠檬酸杆菌、56%的肠杆菌属和58%的志贺菌属。头孢呋辛的活性与头孢孟多和头孢西丁相当;它可抑制对头孢孟多耐药的大肠杆菌和克雷伯菌属菌株,以及对头孢西丁耐药的肠杆菌属和柠檬酸杆菌属菌株。许多沙雷氏菌属菌株、一些吲哚阳性变形杆菌菌株和脆弱拟杆菌对头孢呋辛耐药。头孢呋辛对β-内酰胺酶水解的耐药性在其对革兰氏阳性菌和革兰氏阴性菌的活性中起主要作用。