• 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

HR810对419株严格厌氧菌的抗菌活性。

Antimicrobial activity of HR810 against 419 strict anaerobic bacteria.

作者信息

Jones R N, Gerlach E H

出版信息

Antimicrob Agents Chemother. 1985 Mar;27(3):413-5. doi: 10.1128/AAC.27.3.413.

DOI:10.1128/AAC.27.3.413
PMID:3994351
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC176287/
Abstract

HR810 and four other new beta-lactams were tested against 419 recent clinical anaerobic bacterial isolates. HR810 was found to have an antimicrobial spectrum most similar to that of cefotaxime, inhibiting 52.6% of Bacteroides fragilis group strains and 97.2% of all other anaerobic strains at an MIC of less than or equal to 16 micrograms/ml. Cefoxitin was found to have a narrower antimicrobial spectrum against the gram-positive anaerobic bacteria (8.4 to 10.1% less) than HR810 and cefotaxime, respectively.

摘要

对HR810和其他四种新型β-内酰胺类药物针对419株近期临床分离的厌氧细菌进行了测试。结果发现,HR810的抗菌谱与头孢噻肟最为相似,在最低抑菌浓度小于或等于16微克/毫升时,对脆弱拟杆菌群菌株的抑制率为52.6%,对所有其他厌氧菌株的抑制率为97.2%。发现头孢西丁对革兰氏阳性厌氧细菌的抗菌谱比HR810和头孢噻肟分别窄(少8.4%至10.1%)。

相似文献

1
Antimicrobial activity of HR810 against 419 strict anaerobic bacteria.HR810对419株严格厌氧菌的抗菌活性。
Antimicrob Agents Chemother. 1985 Mar;27(3):413-5. doi: 10.1128/AAC.27.3.413.
2
Comparative antimicrobial activity of aminothiazolyl methoxyimino cephalosporins against anaerobic bacteria, including 100 cefoxitin-resistant isolates.氨噻唑基甲氧亚氨基头孢菌素对厌氧菌的比较抗菌活性,包括100株对头孢西丁耐药的分离株。
Diagn Microbiol Infect Dis. 1987 Nov;8(3):157-63. doi: 10.1016/0732-8893(87)90166-0.
3
Susceptibility of intestinal anaerobes to new beta-lactam antibiotics.肠道厌氧菌对新型β-内酰胺类抗生素的敏感性
Chemotherapy. 1984;30(4):237-43. doi: 10.1159/000238274.
4
In vitro activity of flomoxef compared to moxalactam, cefoxitin, cefotaxime, and clindamycin against anaerobes.氟氧头孢与羟羧氧酰胺菌素、头孢西丁、头孢噻肟及克林霉素相比,对厌氧菌的体外活性。
Arzneimittelforschung. 1988 Nov;38(11):1553-6.
5
Susceptibility of anaerobic bacteria to Sch 34343 and other beta-lactam antibiotics.厌氧菌对Sch 34343及其他β-内酰胺类抗生素的敏感性。
J Antimicrob Chemother. 1985 Jun;15 Suppl C:189-91. doi: 10.1093/jac/15.suppl_c.189.
6
In vitro activity of cefbuperazone, a new cephamycin, against anaerobic bacteria.新型头孢霉素头孢哌酮对厌氧菌的体外活性
Antimicrob Agents Chemother. 1985 Apr;27(4):640-2. doi: 10.1128/AAC.27.4.640.
7
In vitro activity of ceftazidime and ceftriaxone.头孢他啶和头孢曲松的体外活性。
Clin Ther. 1983;5(6):603-16.
8
Susceptibility of anaerobic bacteria to antimicrobial agents.厌氧菌对抗菌药物的敏感性。
Pathology. 1988 Jan;20(1):48-52. doi: 10.3109/00313028809085196.
9
A comparison of susceptibility results of the Bacteroides fragilis group and other anaerobes by traditional MIC results and statistical methods.通过传统的最低抑菌浓度(MIC)结果和统计方法对脆弱拟杆菌群及其他厌氧菌的药敏结果进行比较。
J Antimicrob Chemother. 1997 Mar;39(3):319-24. doi: 10.1093/jac/39.3.319.
10
Comparative in vitro beta-lactam activity against aerobic and anaerobic surgical isolates.针对需氧和厌氧手术分离株的体外β-内酰胺活性比较
Diagn Microbiol Infect Dis. 1988 Feb;9(2):105-13. doi: 10.1016/0732-8893(88)90103-4.

引用本文的文献

1
In vitro and in vivo antibacterial activities of E1077, a novel parenteral cephalosporin.新型胃肠外头孢菌素E1077的体外和体内抗菌活性
Antimicrob Agents Chemother. 1993 Jan;37(1):60-6. doi: 10.1128/AAC.37.1.60.
2
The synergistic effect of cefotaxime and desacetylcefotaxime against clinical isolates of anaerobic bacteria.
Drugs. 1988;35 Suppl 2:45-50. doi: 10.2165/00003495-198800352-00011.
3
In vitro antibacterial effects of cephalosporins.头孢菌素的体外抗菌作用。
Drugs. 1987;34 Suppl 2:44-63. doi: 10.2165/00003495-198700342-00006.
4
Antibacterial activities in vitro and in vivo and pharmacokinetics of cefquinome (HR 111V), a new broad-spectrum cephalosporin.新型广谱头孢菌素头孢喹肟(HR 111V)的体外抗菌活性、体内抗菌活性及药代动力学
Antimicrob Agents Chemother. 1991 Jan;35(1):14-9. doi: 10.1128/AAC.35.1.14.

本文引用的文献

1
The activity of nitro-compounds against Bacteroides fragilis is related to their electron affinity.硝基化合物对脆弱拟杆菌的活性与其电子亲和力有关。
J Antimicrob Chemother. 1981 Aug;8(2):91-9. doi: 10.1093/jac/8.2.91.
2
Susceptibility of the Bacteroides fragilis group in the United States in 1981.1981年美国脆弱拟杆菌群的药敏情况。
Antimicrob Agents Chemother. 1983 Apr;23(4):536-40. doi: 10.1128/AAC.23.4.536.
3
Cefoxitin inactivation by Bacteroides fragilis.脆弱拟杆菌对头孢西丁的灭活作用。
Antimicrob Agents Chemother. 1983 Dec;24(6):936-40. doi: 10.1128/AAC.24.6.936.
4
Susceptibility of gram-positive aerobic cocci to the new cephalosporin HR 810.革兰氏阳性需氧球菌对新型头孢菌素HR 810的敏感性
Eur J Clin Microbiol. 1983 Aug;2(4):354-5. doi: 10.1007/BF02019468.
5
In vitro evaluation of HR810, a new wide-spectrum aminothiazolyl alpha-methoxyimino cephalosporin.新型广谱氨噻唑基α-甲氧基氨基头孢菌素HR810的体外评价
Antimicrob Agents Chemother. 1984 Jun;25(6):710-8. doi: 10.1128/AAC.25.6.710.
6
HR 810, a cephalosporin with low affinity for Enterobacter cloacae beta-lactamase.HR 810,一种对阴沟肠杆菌β-内酰胺酶亲和力较低的头孢菌素。
Eur J Clin Microbiol. 1983 Aug;2(4):352-4. doi: 10.1007/BF02019467.
7
Disk diffusion testing, quality control guidelines, and antimicrobial spectrum of HR810, a fourth-generation cephalosporin, in clinical microbiology laboratories.临床微生物实验室中第四代头孢菌素HR810的纸片扩散法检测、质量控制指南及抗菌谱
J Clin Microbiol. 1984 Sep;20(3):409-12. doi: 10.1128/jcm.20.3.409-412.1984.
8
The Antibacterial activity in vitro and beta-lactamase stability of the new cephalosporin HR 810 in comparison with five other cephalosporins and two aminoglycosides.新型头孢菌素HR 810与其他五种头孢菌素及两种氨基糖苷类药物相比的体外抗菌活性及β-内酰胺酶稳定性
Infection. 1983 Sep-Oct;11(5):275-9. doi: 10.1007/BF01641262.
9
HR 810, a new parenteral cephalosporin with a broad antibacterial spectrum.HR 810,一种新型的具有广谱抗菌活性的肠胃外使用的头孢菌素。
Arzneimittelforschung. 1983;33(8):1084-6. doi: 10.1002/chin.198350201.
10
In vitro activity of HR 810, a new broad-spectrum cephalosporin.新型广谱头孢菌素HR 810的体外活性
Eur J Clin Microbiol. 1983 Aug;2(4):345-9. doi: 10.1007/BF02019465.