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使用新型口服活性广谱头孢菌素头孢曲嗪(SK + F 60771)进行的实验室研究。

Laboratory studies with cefatrizine (SK + F 60771), a new broad-spectrum orally-active cephalosporin.

作者信息

Actor P, Uri J V, Phillips L, Sachs C S, Guarini J R, Zajac I, Berges D A, Dunn G L, Hoover J R, Weisbach J A

出版信息

J Antibiot (Tokyo). 1975 Aug;28(8):594-601. doi: 10.7164/antibiotics.28.594.

Abstract

Cefatrizine (SK&F 60771), a new orally-active semisynthetic cephalosporin antibiotic with broad-spectrum antibacterial activity, was compared with cephalexin and cefazolin for in vitro and in vivo antibacterial activity and pharmacokinetic behavior in laboratory animals. The average MIC values obtained with cefatrizine against gram-positive and gram-negative bacteria were superior to those obtained with cephalexin and somewhat poorer than those of cefazolin. In addition, a large percentage of the enterobacter and enterococcus isolates were found to be susceptible. Cefatrizine had a longer biological half-life and a higher peak serum level than either cefazolin or cephalexin when administered parenterally or orally to mice at 20 mg/kg. It had striking in vivo protective activity in mice infected with Escherichia coli, Klebsiella pneumoniae, Enterobacter cloacae, Hemophilus influenzae, Proteus morganii or Staphylococcus aureus reflecting its superior pharmacokinetic profile in this animal species. A variable pharmacokinetic response between animal species was observed when cefatrizine was administered either orally or parenterally to dogs, squirrel monkeys or rabbits.

摘要

头孢曲嗪(SK&F 60771)是一种新型口服活性半合成头孢菌素抗生素,具有广谱抗菌活性。在实验室动物中,对其体外和体内抗菌活性以及药代动力学行为进行了头孢氨苄和头孢唑林的比较。头孢曲嗪对革兰氏阳性菌和革兰氏阴性菌的平均最低抑菌浓度值优于头孢氨苄,略低于头孢唑林。此外,发现很大比例的肠杆菌和肠球菌分离株敏感。当以20mg/kg的剂量对小鼠进行肠胃外或口服给药时,头孢曲嗪的生物半衰期比头孢唑林或头孢氨苄更长,血清峰值水平更高。在感染大肠杆菌、肺炎克雷伯菌、阴沟肠杆菌、流感嗜血杆菌、摩根变形杆菌或金黄色葡萄球菌的小鼠中,它具有显著的体内保护活性,这反映了其在该动物物种中优越的药代动力学特征。当对狗、松鼠猴或兔子进行肠胃外或口服给药时,观察到不同动物物种之间头孢曲嗪的药代动力学反应存在差异。

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