• 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

相似文献

1
Evaluation of the in vitro bactericidal action of ciprofloxacin on cells of Escherichia coli in the logarithmic and stationary phases of growth.环丙沙星对处于对数生长期和稳定期的大肠杆菌细胞的体外杀菌作用评估。
Antimicrob Agents Chemother. 1985 Oct;28(4):524-7. doi: 10.1128/AAC.28.4.524.
2
Influence of pH and human urine on the antibacterial activity of ciprofloxacin, norfloxacin and ofloxacin.pH值和人尿对环丙沙星、诺氟沙星和氧氟沙星抗菌活性的影响。
Drugs Exp Clin Res. 1985;11(5):335-8.
3
Assessment of the in vitro and in vivo activity of ciprofloxacin measured against current standards of therapy.根据当前治疗标准评估环丙沙星的体外和体内活性。
Drugs Exp Clin Res. 1985;11(5):343-50.
4
Postantibiotic effect of ciprofloxacin compared with that of five other quinolones.环丙沙星与其他五种喹诺酮类药物的抗生素后效应比较。
Chemotherapy. 1991;37(6):420-5. doi: 10.1159/000238889.
5
Urinary bactericidal activity and pharmacokinetics of enoxacin versus norfloxacin and ciprofloxacin in healthy volunteers after a single oral dose.单次口服给药后,依诺沙星与诺氟沙星和环丙沙星在健康志愿者体内的尿杀菌活性及药代动力学比较
Int J Antimicrob Agents. 1998 Apr;10(1):31-8. doi: 10.1016/s0924-8579(98)00014-4.
6
Isolation and characterization of an Escherichia coli strain exhibiting partial tolerance to quinolones.一株对喹诺酮类药物表现出部分耐受性的大肠杆菌菌株的分离与鉴定
Antimicrob Agents Chemother. 1989 May;33(5):705-9. doi: 10.1128/AAC.33.5.705.
7
In vitro evaluation of A-56619 (difloxacin) and A-56620: new aryl-fluoroquinolones.A-56619(二氟沙星)和A-56620:新型芳基氟喹诺酮类药物的体外评价
Antimicrob Agents Chemother. 1986 Feb;29(2):193-200. doi: 10.1128/AAC.29.2.193.
8
Antagonism between bactericidal activities of 4-quinolones and coumarins gives insight into 4-quinolone killing mechanisms.4-喹诺酮类与香豆素类杀菌活性之间的拮抗作用为深入了解4-喹诺酮类的杀菌机制提供了线索。
Microbios. 1994;77(311):121-31.
9
Mutant prevention concentration of nalidixic acid, ciprofloxacin, clinafloxacin, levofloxacin, norfloxacin, ofloxacin, sparfloxacin or trovafloxacin for Escherichia coli under different growth conditions.不同生长条件下大肠杆菌对萘啶酸、环丙沙星、克林沙星、左氧氟沙星、诺氟沙星、氧氟沙星、司帕沙星或曲伐沙星的突变预防浓度。
J Antimicrob Chemother. 2004 Feb;53(2):252-7. doi: 10.1093/jac/dkh036. Epub 2003 Dec 19.
10
Antimicrobial activity of ciprofloxacin against Pseudomonas aeruginosa, Escherichia coli, and Staphylococcus aureus determined by the killing curve method: antibiotic comparisons and synergistic interactions.采用杀菌曲线法测定环丙沙星对铜绿假单胞菌、大肠杆菌和金黄色葡萄球菌的抗菌活性:抗生素比较及协同相互作用
Antimicrob Agents Chemother. 1985 Aug;28(2):331-42. doi: 10.1128/AAC.28.2.331.

引用本文的文献

1
Environmental conditions define the energetics of bacterial dormancy and its antibiotic susceptibility.环境条件决定了细菌休眠的能量状态及其对抗生素的敏感性。
Biophys J. 2023 Aug 22;122(16):3207-3218. doi: 10.1016/j.bpj.2023.06.023. Epub 2023 Jul 4.
2
Antibiotic combinations reduce Staphylococcus aureus clearance.抗生素联合治疗会降低金黄色葡萄球菌清除率。
Nature. 2022 Oct;610(7932):540-546. doi: 10.1038/s41586-022-05260-5. Epub 2022 Oct 5.
3
Exogenous metabolite feeding on altering antibiotic susceptibility in Gram-negative bacteria through metabolic modulation: a review.外源性代谢物通过代谢调节改变革兰氏阴性菌对抗生素敏感性的研究进展:综述。
Metabolomics. 2022 Jul 4;18(7):47. doi: 10.1007/s11306-022-01903-w.
4
Soft Materials that Intercept, Respond to, and Sequester Bacterial Siderophores.拦截、响应并螯合细菌铁载体的软材料。
Chem Mater. 2021 Jul 13;33(13):5401-5412. doi: 10.1021/acs.chemmater.1c01530. Epub 2021 Jul 1.
5
Comparative Activity of Ceftriaxone, Ciprofloxacin, and Gentamicin as a Function of Bacterial Growth Rate Probed by Escherichia coli Chromosome Replication in the Mouse Peritonitis Model.以大肠杆菌染色体复制为指标研究头孢曲松、环丙沙星和庆大霉素在小鼠腹膜炎模型中的细菌生长率相关比较活性。
Antimicrob Agents Chemother. 2019 Jan 29;63(2). doi: 10.1128/AAC.02133-18. Print 2019 Feb.
6
Influence of Different Peritoneal Dialysis Fluids on the In Vitro Activity of Cefepime, Ciprofloxacin, Ertapenem, Meropenem and Tobramycin Against Escherichia Coli.不同腹膜透析液对头孢吡肟、环丙沙星、厄他培南、美罗培南和妥布霉素体外抗大肠杆菌活性的影响
Perit Dial Int. 2016;36(6):662-668. doi: 10.3747/pdi.2015.00161. Epub 2016 Sep 28.
7
Disruption of Membrane by Colistin Kills Uropathogenic Escherichia coli Persisters and Enhances Killing of Other Antibiotics.黏菌素破坏细胞膜可杀死尿路致病性大肠杆菌持留菌并增强其他抗生素的杀菌效果。
Antimicrob Agents Chemother. 2016 Oct 21;60(11):6867-6871. doi: 10.1128/AAC.01481-16. Print 2016 Nov.
8
Nanocrystalline hydroxyapatite and zinc-doped hydroxyapatite as carrier material for controlled delivery of ciprofloxacin.纳米晶羟基磷灰石和锌掺杂羟基磷灰石作为环丙沙星控释载体材料
3 Biotech. 2011 Oct;1(3):173-186. doi: 10.1007/s13205-011-0021-9. Epub 2011 Aug 24.
9
Bactericidal activity of ACH-702 against nondividing and biofilm Staphylococci.ACH-702 对非分裂和生物膜葡萄球菌的杀菌活性。
Antimicrob Agents Chemother. 2012 Jul;56(7):3812-8. doi: 10.1128/AAC.00092-12. Epub 2012 Apr 30.
10
Ecotoxicological effects of ciprofloxacin on freshwater species: data integration and derivation of toxicity thresholds for risk assessment.环丙沙星对淡水物种的生态毒理学效应:数据整合与毒性阈值推导及其用于风险评估
Ecotoxicology. 2012 May;21(4):1167-76. doi: 10.1007/s10646-012-0871-x. Epub 2012 Feb 29.

本文引用的文献

1
The in vitro and in vivo activity of ciprofloxacin.环丙沙星的体外和体内活性。
Eur J Clin Microbiol. 1984 Aug;3(4):339-43. doi: 10.1007/BF01977490.
2
Antibacterial activities of ciprofloxacin, norfloxacin, oxolinic acid, cinoxacin, and nalidixic acid.环丙沙星、诺氟沙星、恶喹酸、西诺沙星和萘啶酸的抗菌活性。
Antimicrob Agents Chemother. 1984 May;25(5):633-7. doi: 10.1128/AAC.25.5.633.
3
In-vitro studies with ciprofloxacin, a new 4-quinolone compound.使用新型4-喹诺酮化合物环丙沙星进行的体外研究。
J Antimicrob Chemother. 1984 Apr;13(4):333-46. doi: 10.1093/jac/13.4.333.
4
Ciprofloxacin, a quinolone carboxylic acid compound active against aerobic and anaerobic bacteria.环丙沙星,一种对需氧菌和厌氧菌均有活性的喹诺酮羧酸化合物。
Antimicrob Agents Chemother. 1984 Mar;25(3):319-26. doi: 10.1128/AAC.25.3.319.
5
In vitro activity of ciprofloxacin (Bay o 9867).环丙沙星(拜耳o 9867)的体外活性。
Antimicrob Agents Chemother. 1983 Oct;24(4):568-74. doi: 10.1128/AAC.24.4.568.
6
In vitro activity of ciprofloxacin, norfloxacin and nalidixic acid.环丙沙星、诺氟沙星和萘啶酸的体外活性。
Eur J Clin Microbiol. 1983 Apr;2(2):111-5. doi: 10.1007/BF02001575.
7
In vitro activity of Bay 09867, a new quinoline derivative, compared with those of other antimicrobial agents.新型喹啉衍生物Bay 09867与其他抗菌药物的体外活性比较。
Antimicrob Agents Chemother. 1983 Apr;23(4):559-64. doi: 10.1128/AAC.23.4.559.
8
Investigations into the mechanism of action of the antibacterial agent norfloxacin.对抗菌剂诺氟沙星作用机制的研究。
J Antimicrob Chemother. 1984 May;13 Suppl B:9-23. doi: 10.1093/jac/13.suppl_b.9.
9
Escherichia coli K-12 mutants resistant to nalidixic acid: genetic mapping and dominance studies.耐萘啶酸的大肠杆菌K-12突变体:基因定位与显性研究。
J Bacteriol. 1969 Jul;99(1):238-41. doi: 10.1128/jb.99.1.238-241.1969.

环丙沙星对处于对数生长期和稳定期的大肠杆菌细胞的体外杀菌作用评估。

Evaluation of the in vitro bactericidal action of ciprofloxacin on cells of Escherichia coli in the logarithmic and stationary phases of growth.

作者信息

Zeiler H J

出版信息

Antimicrob Agents Chemother. 1985 Oct;28(4):524-7. doi: 10.1128/AAC.28.4.524.

DOI:10.1128/AAC.28.4.524
PMID:2934022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC180297/
Abstract

Cells of Escherichia coli Neumann and E. coli KL16 were suspended in phosphate-buffered saline pH 7.4 and allowed to reach stationary growth conditions. Ciprofloxacin was added at different concentrations, and time-kill curves were constructed. It could be demonstrated that the number of viable cells was reduced quickly by several logs for E. coli Neumann, whereas a weak and slow killing effect was observed with E. coli KL16. When ciprofloxacin or norfloxacin was added to logarithmically growing cultures of E. coli Neumann or E. coli KL16, no principal differences in the killing rate for the two strains could be observed. Ciprofloxacin, however, was more bactericidal than norfloxacin. It was also demonstrated that the bactericidal action of ciprofloxacin on cells in the stationary growth phase was better at pH 7.4 than at pH 8.6. This dependence is different from that observed in MIC studies, in which the MIC were lower at pH 8.0 than at pH 7.2. It was also found that the bactericidal action of ciprofloxacin or norfloxacin on cells of E. coli Neumann in the stationary phase of growth could not be reduced by the addition of chloramphenicol, whereas under conditions of logarithmic growth the rapid killing effect of ciprofloxacin was reduced in the presence of chloramphenicol.

摘要

将大肠杆菌Neumann菌株和大肠杆菌KL16菌株的细胞悬浮于pH 7.4的磷酸盐缓冲盐水中,使其达到稳定生长条件。加入不同浓度的环丙沙星,并绘制时间-杀菌曲线。结果表明,对于大肠杆菌Neumann菌株,活菌数量迅速减少了几个对数级,而对于大肠杆菌KL16菌株,观察到的杀菌作用较弱且缓慢。当将环丙沙星或诺氟沙星添加到对数生长期的大肠杆菌Neumann菌株或大肠杆菌KL16菌株培养物中时,未观察到两种菌株在杀菌速率上的主要差异。然而,环丙沙星比诺氟沙星的杀菌作用更强。还证明了环丙沙星对处于稳定生长期的细胞的杀菌作用在pH 7.4时比在pH 8.6时更好。这种依赖性与在最低抑菌浓度(MIC)研究中观察到的不同,在MIC研究中,pH 8.0时的MIC低于pH 7.2时的MIC。还发现,添加氯霉素不能降低环丙沙星或诺氟沙星对处于生长稳定期的大肠杆菌Neumann菌株细胞的杀菌作用,而在对数生长条件下,氯霉素存在时环丙沙星的快速杀菌作用会降低。