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使用新型口服头孢菌素头孢克洛进行的体外研究。

In vitro studies with cefaclor, a new oral cephalosporin.

作者信息

Sanders C

出版信息

Antimicrob Agents Chemother. 1977 Oct;12(4):490-7. doi: 10.1128/AAC.12.4.490.

Abstract

In vitro studies were performed to evaluate the activity of cefaclor in comparison with cephalexin against 180 clinical isolates. Broth dilution susceptibility tests showed cefaclor to be 4- to 16-fold more active than cephalexin against Streptococcus pneumoniae, Haemophilus influenzae, and cephalothin-susceptible Enterobacteriaceae. Neither drug was highly active against cephalothin-resistant Enterobacteriaceae or methicillin-resistant Staphylococcus aureus. Cefaclor zones with 30-mug disks were generally larger than cephalexin zones, 4 mm larger than cephalothin zones against Enterobacteriaceae, and 6 mm smaller than cephalothin zones against S. aureus. Quantitative kill curves indicated that killing by both cefaclor and cephalexin was slow and often incomplete over a 24-h period. Cefaclor-induced filamentation of gram-negative bacilli was not as extensive as that produced by cephalexin, and some spherule formation did occur. However, cefaclor was significantly more unstable in solution than cephalexin, with a half-life of less than 6 h at 37 degrees C. Thus, results obtained in tests after prolonged incubation may not provide an accurate measure of cefaclor's activity.

摘要

进行了体外研究,以评估头孢克洛与头孢氨苄相比对180株临床分离菌的活性。肉汤稀释药敏试验表明,头孢克洛对肺炎链球菌、流感嗜血杆菌和对头孢噻吩敏感的肠杆菌科细菌的活性比对头孢氨苄高4至16倍。两种药物对头孢噻吩耐药的肠杆菌科细菌或耐甲氧西林金黄色葡萄球菌均无高活性。含30μg纸片的头孢克洛抑菌圈通常比对头孢氨苄的抑菌圈大,对肠杆菌科细菌的抑菌圈比对头孢噻吩的抑菌圈大4mm,对金黄色葡萄球菌的抑菌圈比对头孢噻吩的抑菌圈小6mm。定量杀菌曲线表明,在24小时内,头孢克洛和头孢氨苄的杀菌作用均缓慢且往往不完全。头孢克洛诱导的革兰氏阴性杆菌丝状化不如头孢氨苄广泛,且确实出现了一些球状体形成。然而,头孢克洛在溶液中的稳定性明显低于头孢氨苄,在37℃下的半衰期不到6小时。因此,长时间孵育后试验获得的结果可能无法准确衡量头孢克洛的活性。

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