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新型半合成青霉素BRL 36650的体外活性

In vitro activity of BRL 36650, a new semisynthetic penicillin.

作者信息

Hoy J F, Rolston K V, Ho D H, Alvarez M, Thirolf P, Bodey G P

出版信息

Antimicrob Agents Chemother. 1986 Jun;29(6):972-6. doi: 10.1128/AAC.29.6.972.

Abstract

BRL 36650 [sodium 6 beta-(D-2-[(4-ethyl-2, 3-dioxopiperazin-1-yl)carbonylamino]-2-(3,4-dihydroxyphenyl) acetamido)-6 alpha-formamido-penicillinate] is a new semisynthetic penicillin. It was tested in vitro for activity against 884 organisms cultured from blood specimens of cancer patients. BRL 36650 had broad-spectrum activity against the gram-negative bacilli tested but had no gram-positive activity. The MIC against 90% of the Pseudomonas aeruginosa isolates was 3.12 micrograms/ml. The activity of BRL 36650 was superior to that of piperacillin, comparable or slightly inferior to that of aztreonam and ceftazidime, and lower than that of imipenem and amifloxacin. BRL 36650 should prove useful for the management of gram-negative bacillary infections, including those caused by P. aeruginosa.

摘要

BRL 36650[6β-(D-2-[(4-乙基-2,3-二氧代哌嗪-1-基)羰基氨基]-2-(3,4-二羟基苯基)乙酰胺基)-6α-甲酰胺基青霉素酸钠]是一种新型半合成青霉素。对其进行了体外测试,以检测其对从癌症患者血液标本中培养出的884种微生物的活性。BRL 36650对所测试的革兰氏阴性杆菌具有广谱活性,但对革兰氏阳性菌无活性。对90%的铜绿假单胞菌分离株的最低抑菌浓度为3.12微克/毫升。BRL 36650的活性优于哌拉西林,与氨曲南和头孢他啶相当或略低,低于亚胺培南和阿米氟沙星。BRL 36650应被证明对治疗革兰氏阴性杆菌感染有用,包括由铜绿假单胞菌引起的感染。

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