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氨基甲酸酯连接的双效抗菌剂Ro 24 - 4383的体外和体内活性

In vitro and in vivo activity of carbamate-linked dual-action antibacterial Ro 24-4383.

作者信息

Beskid G, Albrecht H A, Fallat V, Keith D D, Lipschitz E R, McGarry C M, McGarry D H, Rossman P, Siebelist J

机构信息

Department of Chemotherapy, Hoffmann-La Roche, Nutley, N.J.

出版信息

Chemotherapy. 1991;37(5):310-7. doi: 10.1159/000238873.

Abstract

Ro 24-4383 contains desacetylcefotaxime linked by a carbamate bond at the 3' position to ciprofloxacin. Ro 24-4383 was active against 99% of the 363 gram-positive and gram-negative aerobes tested in vitro, while the comparative agents cefotaxime and ciprofloxacin were active against 77 and 97%, respectively. The activities (ED50: mg/kg s.c.) of Ro 24-4383, cefotaxime and ciprofloxacin in systemic murine infections were: Escherichia coli 257, 1.4, less than 0.5, less than 0.2; Klebsiella pneumoniae A, 11, 30, 0.7; Enterobacter cloacae 5699, 3.2, 35, less than 0.2; Citrobacter freundii BS16, 3, 41, less than 0.5; Serratia marcescens SM, 35, greater than 100, 1.6; Pseudomonas aeruginosa 5712, 67, 100, 10; P. aeruginosa 8780, 33, 193, 3; Staphylococcus aureus Smith (oxacillin-susceptible), 12, 3.7, 1; S. aureus 753 (oxacillin-resistant), 28, greater than 100, 2; Streptococcus pneumoniae 6301, 10, 15, greater than 50, and S. pyogenes 4, 3.3, 1.6, 54. Ro 24-4383, although inactive against the S.-pneumoniae-induced pneumonia following one administration of the agent, was highly active (ED50 = 1.5) when three treatments were given following infection. Ro 24-4383 was active against the K.-pneumoniae-induced pneumonia (ED50 = 37), as well as the meningitis induced by S. pneumoniae (ED50 = 158) or K. pneumoniae (ED50 = 100). The protective effect of Ro 24-4383 was demonstrated when administered 8 h before infection with E. coli (ED50 = 37) and 4 h before infection with S. pyogenes (ED50 = 199).

摘要

Ro 24 - 4383含有去乙酰头孢噻肟,它在3'位通过氨基甲酸酯键与环丙沙星相连。Ro 24 - 4383对体外测试的363株革兰氏阳性和革兰氏阴性需氧菌中的99%有活性,而对照药物头孢噻肟和环丙沙星的活性分别为77%和97%。Ro 24 - 4383、头孢噻肟和环丙沙星在全身性小鼠感染中的活性(ED50:mg/kg皮下注射)分别为:大肠杆菌257,257、1.4、小于0.5、小于0.2;肺炎克雷伯菌A,11、30、0.7;阴沟肠杆菌5699,3.2、35、小于0.2;弗氏柠檬酸杆菌BS16,3、41、小于0.5;粘质沙雷氏菌SM,35、大于100、1.6;铜绿假单胞菌5712,67、100、10;铜绿假单胞菌8780,33、193、3;金黄色葡萄球菌史密斯株(对苯唑西林敏感),12、3.7、1;金黄色葡萄球菌753(对苯唑西林耐药),28、大于100、2;肺炎链球菌6301,10、15、大于50,以及化脓性链球菌4、3.3、1.6、54。Ro 24 - 4383虽然在单次给药后对肺炎链球菌引起的肺炎无活性,但在感染后给予三次治疗时活性很高(ED50 = 1.5)。Ro 24 - 4383对肺炎克雷伯菌引起的肺炎(ED50 = 37)以及肺炎链球菌(ED50 = 158)或肺炎克雷伯菌(ED50 = 100)引起的脑膜炎有活性。当在感染大肠杆菌前8小时(ED50 = 37)和感染化脓性链球菌前4小时(ED50 = 199)给药时,Ro 24 - 4383的保护作用得到了证明。

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