Busch D F, Kureshi L A, Sutter V L, Finegold S M
Antimicrob Agents Chemother. 1976 Oct;10(4):713-20. doi: 10.1128/AAC.10.4.713.
Anaerobic bacteria recovered from airway-related infections were tested by agar dilution against selected penicillins and cephalosporins available for oral administration. Against 136 isolates, penicillins G and V showed comparable activity, particularly when pharmacological differences were considered. Although many isolates were exquisitely susceptible to the penicillins, only 55% of the Bacteroides species and 72% of all isolates were inhibited at 0.5 mug of penicillin G per ml. Results for penicillin V at 1 mug/ml were similar (59 and 73%). The two cephalosporins were more active at achievable levels, inhibiting 94 to 95% of Bacteroides and 95 to 96% of all isolates at 8 mug/ml. These levels represent approximately 50% of the reported peak serum levels after oral administration of 625 mg of the penicillins and 500 mg of the cephalosporins. Dicloxacillin and nafcillin were tested against 50 isolates. The two were comparably active on a weight basis; dicloxacillin was more active when pharmacological differences were considered, but did not match the other penicillins or the cephalosporins.
从气道相关感染中分离出的厌氧菌,采用琼脂稀释法,针对可供口服的特定青霉素类和头孢菌素类药物进行了测试。对于136株分离菌,青霉素G和V显示出相当的活性,尤其是考虑到药理学差异时。尽管许多分离菌对青霉素极为敏感,但在每毫升含0.5微克青霉素G的情况下,只有55%的拟杆菌属菌种和72%的所有分离菌受到抑制。每毫升含1微克青霉素V时的结果相似(分别为59%和73%)。两种头孢菌素在可达到的浓度水平上活性更高,在每毫升含8微克时,可抑制94%至95%的拟杆菌属菌种和95%至96%的所有分离菌。这些浓度水平约相当于口服625毫克青霉素类药物和500毫克头孢菌素类药物后报告的血清峰值浓度的50%。针对50株分离菌对双氯西林和萘夫西林进行了测试。二者按重量计活性相当;考虑到药理学差异时,双氯西林活性更高,但不及其他青霉素类或头孢菌素类药物。