• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

β-内酰胺类抗生素对庆大霉素和/或羧苄西林耐药的铜绿假单胞菌菌株的体外活性。

The in vitro activity of beta-lactam antibiotics against gentamicin and/or carbenicillin-resistant Pseudomonas aeruginosa strains.

作者信息

Aisa M L, Omenaca M, Bergua C, Garcia-Moya J B

出版信息

Infection. 1982;10 Suppl 3:S244-8. doi: 10.1007/BF01640682.

DOI:10.1007/BF01640682
PMID:6818157
Abstract

We studied the behaviour of 56 clinical isolates of Pseudomonas aeruginosa strains against the following beta-lactam antibiotics: cefotaxime, cefoperazone, cefsulodin, lamoxactam, Ro 13-9904, azlocillin, mezlocillin and ticarcillin. Twenty-six strains were resistant to gentamicin and 30 to gentamicin and/or carbenicillin. The MICs were measured by the serial dilution test on solid agar. Cefsulodin was the most active cephalosporin against carbenicillin-resistant strains (MIC greater than or equal to 128 mg/l); it inhibited 56.6% of these strains at a concentration of 8 mg/l. Azlocillin was the most active penicillin, inhibiting 79.96% of the same strains at a concentration of 64 mg/l. Cefsulodin was the most active cephalosporin against the gentamicin-resistant group of Pseudomonas aeruginosa strains (MIC greater than or equal to 8 mg/l) which were sensitive to carbenicillin (MIC less than or equal to 64 mg/l). It inhibited 100% of the strains at a concentration of 4 mg/l. All of the penicillins studied inhibited all of the strains in this group. The required concentrations were the following: 16 mg/l for azlocillin, 32 mg/l for mezlocillin and 64 mg/l for ticarcillin.

摘要

我们研究了56株铜绿假单胞菌临床分离株对以下β-内酰胺类抗生素的耐药情况:头孢噻肟、头孢哌酮、头孢磺啶、拉氧头孢、Ro 13-9904、阿洛西林、美洛西林和替卡西林。26株对庆大霉素耐药,30株对庆大霉素和/或羧苄西林耐药。通过固体琼脂上的连续稀释试验测定最低抑菌浓度(MIC)。头孢磺啶是对羧苄西林耐药菌株最有效的头孢菌素(MIC大于或等于128mg/L);在浓度为8mg/L时,它能抑制56.6%的此类菌株。阿洛西林是最有效的青霉素,在浓度为64mg/L时能抑制79.96%的相同菌株。头孢磺啶是对庆大霉素耐药但对羧苄西林敏感(MIC小于或等于64mg/L)的铜绿假单胞菌菌株组最有效的头孢菌素。在浓度为4mg/L时,它能抑制100%的菌株。所有研究的青霉素均能抑制该组中的所有菌株。所需浓度如下:阿洛西林为16mg/L,美洛西林为32mg/L,替卡西林为64mg/L。

相似文献

1
The in vitro activity of beta-lactam antibiotics against gentamicin and/or carbenicillin-resistant Pseudomonas aeruginosa strains.β-内酰胺类抗生素对庆大霉素和/或羧苄西林耐药的铜绿假单胞菌菌株的体外活性。
Infection. 1982;10 Suppl 3:S244-8. doi: 10.1007/BF01640682.
2
[Pseudomonas aeruginosa: acquired in vitro resistance to beta-lactams].铜绿假单胞菌:体外获得性β-内酰胺耐药性
Pathol Biol (Paris). 1983 May;31(5):387-91.
3
In-vitro activity of ciprofloxacin and other beta-lactam antibiotics against gentamicin- and carbenicillin-resistant isolates of Pseudomonas aeruginosa.环丙沙星及其他β-内酰胺类抗生素对庆大霉素和羧苄西林耐药的铜绿假单胞菌分离株的体外活性
J Chemother. 1991 Feb;3(1):3-5. doi: 10.1080/1120009x.1991.11739054.
4
Synergy between cefotaxime, cefsulodin, azlocillin, mezlocillin and aminoglycosides against carbenicillin resistant or sensitive Pseudomonas aeruginosa.头孢噻肟、头孢磺啶、阿洛西林、美洛西林与氨基糖苷类药物联合应用对耐羧苄西林或敏感铜绿假单胞菌的协同作用。
J Antimicrob Chemother. 1980 Jul;6(4):471-7. doi: 10.1093/jac/6.4.471.
5
[Comparison of in vitro bacteriostatic effect of five betalactamins against Pseudomonas aeruginosa (author's transl)].五种β-内酰胺类药物对铜绿假单胞菌体外抑菌作用的比较(作者译)
Pathol Biol (Paris). 1982 Jun;30(6):440-3.
6
[Comparative activity of cefsulodin on Pseudomonas aeruginosa, Acinetobacter and Enterobacteriaceae (author's transl)].头孢磺啶对铜绿假单胞菌、不动杆菌及肠杆菌科细菌的比较活性(作者译)
Pathol Biol (Paris). 1982 Jun;30(6):432-9.
7
Comparison of the in vitro activity of new beta-lactams and aminoglycosides against clinical isolates of Pseudomonas aeruginosa.新型β-内酰胺类药物与氨基糖苷类药物对铜绿假单胞菌临床分离株的体外活性比较。
Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol. 1982 Oct;253(1):110-20.
8
A turbidimetric study of the responses of selected strains of Pseudomonas aeruginosa to eight antipseudomonal beta-lactam antibiotics.对铜绿假单胞菌选定菌株对八种抗假单胞菌β-内酰胺抗生素反应的比浊法研究。
J Infect Dis. 1982 Jan;145(1):110-7. doi: 10.1093/infdis/145.1.110.
9
Effects of inoculum size on the activity of carboxy- and ureido-penicillins and effects of combinations of ureido-penicillins with aminoglycosides against resistant Pseudomonas aeruginosa.接种量对羧基青霉素和脲基青霉素活性的影响以及脲基青霉素与氨基糖苷类药物联合使用对耐药铜绿假单胞菌的影响。
J Antimicrob Chemother. 1986 Jan;17(1):91-5. doi: 10.1093/jac/17.1.91.
10
Comparative antibacterial activities of new beta-lactam antibiotics against Pseudomonas aeruginosa.新型β-内酰胺类抗生素对铜绿假单胞菌的抗菌活性比较
Chemotherapy. 1985;31(4):292-6. doi: 10.1159/000238350.

引用本文的文献

1
Moxalactam (latamoxef). A review of its antibacterial activity, pharmacokinetic properties and therapeutic use.拉氧头孢。对其抗菌活性、药代动力学特性及治疗用途的综述。
Drugs. 1983 Oct;26(4):279-333. doi: 10.2165/00003495-198326040-00001.

本文引用的文献

1
An inocula replicating apparatus for routine testing of bacterial susceptibility to antibiotics.一种用于抗生素细菌敏感性常规检测的接种物复制装置。
Antibiot Chemother (Northfield). 1959 May;9(5):307-11.
2
In vitro antibacterial activity and susceptibility of the cephalosporin Ro 13-9904 to beta-lactamases.头孢菌素Ro 13-9904对β-内酰胺酶的体外抗菌活性及敏感性
Antimicrob Agents Chemother. 1980 Aug;18(2):292-8. doi: 10.1128/AAC.18.2.292.
3
Cefoperazone (T-1551), a new semisynthetic cephalosporin: comparison with cephalothin and gentamicin.
头孢哌酮(T - 1551),一种新型半合成头孢菌素:与头孢噻吩和庆大霉素的比较。
Antimicrob Agents Chemother. 1980 Apr;17(4):743-9. doi: 10.1128/AAC.17.4.743.
4
In vitro activity of HR 756, a new cephalosporin compound.新型头孢菌素化合物HR 756的体外活性
J Antibiot (Tokyo). 1978 Nov;31(11):1170-4. doi: 10.7164/antibiotics.31.1170.
5
Activity of azlocillin and mezlocillin against gram-negative organisms: comparison with other penicillins.阿洛西林和美洛西林对革兰氏阴性菌的活性:与其他青霉素类药物的比较。
Antimicrob Agents Chemother. 1978 Apr;13(4):559-65. doi: 10.1128/AAC.13.4.559.
6
Azlocillin: in vitro studies of a new semisynthetic penicillin.阿洛西林:一种新型半合成青霉素的体外研究
Antimicrob Agents Chemother. 1977 May;11(5):865-70. doi: 10.1128/AAC.11.5.865.