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新型口服头孢菌素抗生素BL-S640的体外评价

In vitro evaluation of BL-S640, a new oral cephalosporin antibiotic.

作者信息

Overturf G D, Ressler R L, Marengo P B, Wilkins J

出版信息

Antimicrob Agents Chemother. 1975 Sep;8(3):305-10. doi: 10.1128/AAC.8.3.305.

Abstract

BL-S640, a new oral cephalosporin analogue, was evaluated in vitro against 102 gram-negative and 80 gram-positive bacteria. The antimicrobial spectrum was similar to that of previous cephalosporin analogues. Good antimicrobial activity against strains of Escherichia coli, Klebsiella, staphylococci, and streptococci was demonstrated. Relatively poor activity and/or resistance was noted among most strains of Proteus, Providencia, Pseudomonas, and Serratia. In comparative studies BL-S640 had better activity against strains of Hemophilus influenzae, Staphylococcus aureus, and Enterobacteriaceae than many cephalosporin analogues. Variation of susceptibility results was dependent upon the type of media and inoculum size. Cross-resistance between BL-S640 cephalexin, cephalothin, and cefazolin was demonstrated. Among strains of Klebsiella the more rapid selection of resistance ot other cephalosporins was in contrast to BL-S640. Experience in vitro with BL-S640 has documented its antimicrobial activity,and further studies of pharmacokinetics and therapeutic efficacy are indicated.

摘要

新型口服头孢菌素类似物BL - S640针对102株革兰氏阴性菌和80株革兰氏阳性菌进行了体外评估。其抗菌谱与先前的头孢菌素类似物相似。对大肠杆菌、克雷伯菌、葡萄球菌和链球菌菌株显示出良好的抗菌活性。在变形杆菌、普罗威登斯菌、假单胞菌和沙雷菌的大多数菌株中观察到相对较差的活性和/或耐药性。在比较研究中,BL - S640对流感嗜血杆菌、金黄色葡萄球菌和肠杆菌科菌株的活性比许多头孢菌素类似物更好。药敏结果的差异取决于培养基类型和接种量。证明了BL - S640与头孢氨苄、头孢噻吩和头孢唑林之间存在交叉耐药性。在克雷伯菌菌株中,与BL - S640相比,对其他头孢菌素耐药性的选择更快。对BL - S640的体外实验已证明其抗菌活性,表明需要进一步研究其药代动力学和治疗效果。

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Oral and parenteral cephalosporins: the place of cephalexin in antibacterial therapy.
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