• 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
Uptake and intracellular activity of moxifloxacin in human neutrophils and tissue-cultured epithelial cells.莫西沙星在人中性粒细胞和组织培养上皮细胞中的摄取及细胞内活性。
Antimicrob Agents Chemother. 1999 Jan;43(1):12-5. doi: 10.1128/AAC.43.1.12.
2
Uptake and intracellular activity of trovafloxacin in human phagocytes and tissue-cultured epithelial cells.曲伐沙星在人吞噬细胞和组织培养上皮细胞中的摄取及细胞内活性。
Antimicrob Agents Chemother. 1997 Feb;41(2):274-7. doi: 10.1128/AAC.41.2.274.
3
Uptake and intracellular activity of sparfloxacin in human polymorphonuclear leukocytes and tissue culture cells.司帕沙星在人多形核白细胞和组织培养细胞中的摄取及细胞内活性
Antimicrob Agents Chemother. 1992 May;36(5):1053-6. doi: 10.1128/AAC.36.5.1053.
4
Uptake and intracellular activity of ofloxacin isomers in human phagocytic and non-phagocytic cells.氧氟沙星异构体在人吞噬细胞和非吞噬细胞中的摄取及细胞内活性。
Int J Antimicrob Agents. 2000 Aug;15(3):201-5. doi: 10.1016/s0924-8579(00)00161-8.
5
Intracellular activity of ciprofloxacin and moxifloxacin, a new 8-methoxyquinolone, against methicillin-resistant Staphylococcus aureus.环丙沙星与新型8-甲氧基喹诺酮类药物莫西沙星对耐甲氧西林金黄色葡萄球菌的细胞内活性
J Antimicrob Chemother. 1998 Jun;41(6):655-8. doi: 10.1093/jac/41.6.655.
6
Intracellular penetration and activity of BAY Y 3118 in human polymorphonuclear leukocytes.BAY Y 3118在人多形核白细胞中的细胞内渗透及活性
Antimicrob Agents Chemother. 1994 Oct;38(10):2426-9. doi: 10.1128/AAC.38.10.2426.
7
Quantitative analysis of gentamicin, azithromycin, telithromycin, ciprofloxacin, moxifloxacin, and oritavancin (LY333328) activities against intracellular Staphylococcus aureus in mouse J774 macrophages.庆大霉素、阿奇霉素、泰利霉素、环丙沙星、莫西沙星和奥利万星(LY333328)对小鼠J774巨噬细胞内金黄色葡萄球菌活性的定量分析。
Antimicrob Agents Chemother. 2003 Jul;47(7):2283-92. doi: 10.1128/AAC.47.7.2283-2292.2003.
8
Intracellular penetration and activity of gemifloxacin in human polymorphonuclear leukocytes.吉米沙星在人多形核白细胞中的细胞内渗透及活性
Antimicrob Agents Chemother. 2000 Nov;44(11):3193-5. doi: 10.1128/AAC.44.11.3193-3195.2000.
9
Discrepancy between uptake and intracellular activity of moxifloxacin in a Staphylococcus aureus-human THP-1 monocytic cell model.莫西沙星在金黄色葡萄球菌-人THP-1单核细胞模型中的摄取与细胞内活性之间的差异。
Antimicrob Agents Chemother. 2002 Feb;46(2):288-93. doi: 10.1128/AAC.46.2.288-293.2002.
10
Effect of paclitaxel alone or in combination on the intracellular penetration and activity of quinolones in human neutrophils.紫杉醇单独或联合使用对喹诺酮类药物在人中性粒细胞内的渗透及活性的影响。
J Antimicrob Chemother. 1996 Nov;38(5):859-63. doi: 10.1093/jac/38.5.859.

引用本文的文献

1
Macrophage internalization creates a multidrug-tolerant fungal persister reservoir and facilitates the emergence of drug resistance.巨噬细胞内化会产生一个多药耐受真菌持久存贮库,并促进耐药性的出现。
Nat Commun. 2023 Mar 2;14(1):1183. doi: 10.1038/s41467-023-36882-6.
2
Intracellular Penetration and Effects of Antibiotics on Inside Human Neutrophils: A Comprehensive Review.抗生素在人中性粒细胞内的穿透及作用:综述
Antibiotics (Basel). 2019 May 4;8(2):54. doi: 10.3390/antibiotics8020054.
3
A Multilaboratory, Multicountry Study To Determine MIC Quality Control Ranges for Phenotypic Drug Susceptibility Testing of Selected First-Line Antituberculosis Drugs, Second-Line Injectables, Fluoroquinolones, Clofazimine, and Linezolid.一项多实验室、多国研究,以确定选定的一线抗结核药物、二线注射剂、氟喹诺酮类、氯法齐明和利奈唑胺的表型药敏试验的最低抑菌浓度(MIC)质量控制范围。
J Clin Microbiol. 2016 Dec;54(12):2963-2968. doi: 10.1128/JCM.01138-16. Epub 2016 Sep 21.
4
Moxifloxacin: Clinically compatible contrast agent for multiphoton imaging.莫西沙星:用于多光子成像的临床兼容造影剂。
Sci Rep. 2016 Jun 10;6:27142. doi: 10.1038/srep27142.
5
Pharmacokinetics and penetration of moxifloxacin into infected diabetic foot tissue in a large diabetic patient cohort.莫西沙星在大型糖尿病患者队列中感染性糖尿病足组织的药代动力学和渗透。
Eur J Clin Pharmacol. 2011 Feb;67(2):135-42. doi: 10.1007/s00228-010-0903-5. Epub 2010 Sep 25.
6
Moxifloxacin pharmacokinetics/pharmacodynamics and optimal dose and susceptibility breakpoint identification for treatment of disseminated Mycobacterium avium infection.莫西沙星药代动力学/药效学及最佳剂量和药敏折点确定,用于治疗播散性鸟分枝杆菌感染。
Antimicrob Agents Chemother. 2010 Jun;54(6):2534-9. doi: 10.1128/AAC.01761-09. Epub 2010 Apr 12.
7
Defining the role of macrophages in local moxifloxacin tissue concentrations using biopsy data and whole-body physiologically based pharmacokinetic modelling.利用活检数据和基于全身生理的药代动力学模型确定巨噬细胞在局部莫西沙星组织浓度中的作用。
Clin Pharmacokinet. 2009;48(3):181-7. doi: 10.2165/00003088-200948030-00004.
8
Comparative activities of antibiotics against intracellular non-typeable Haemophilus influenzae.抗生素对细胞内不可分型流感嗜血杆菌的比较活性
Wien Klin Wochenschr. 2007;119(9-10):297-302. doi: 10.1007/s00508-007-0784-5.
9
In vivo comparative pharmacokinetics and pharmacodynamics of moxifloxacin and levofloxacin in human neutrophils.莫西沙星和左氧氟沙星在人中性粒细胞中的体内比较药代动力学和药效学。
Clin Drug Investig. 2005;25(10):643-50. doi: 10.2165/00044011-200525100-00003.
10
Intracellular penetration and activity of DX-619 in human polymorphonuclear leukocytes.DX-619在人多形核白细胞中的细胞内渗透及活性
Antimicrob Agents Chemother. 2006 Sep;50(9):3173-4. doi: 10.1128/AAC.00427-06.

本文引用的文献

1
In vitro activity of Bay 12-8039, a new 8-methoxyquinolone.新型8-甲氧基喹诺酮类药物Bay 12-8039的体外活性
Antimicrob Agents Chemother. 1997 Aug;41(8):1818-24. doi: 10.1128/AAC.41.8.1818.
2
Susceptibility of Chlamydia trachomatis to trovafloxacin.
J Antimicrob Chemother. 1997 Jun;39 Suppl B:63-5. doi: 10.1093/jac/39.suppl_2.63.
3
In vitro activity of Bay 12-8039, a new 8-methoxyquinolone, compared to the activities of 11 other oral antimicrobial agents against 390 aerobic and anaerobic bacteria isolated from human and animal bite wound skin and soft tissue infections in humans.新型8-甲氧基喹诺酮类药物Bay 12-8039与其他11种口服抗菌药物对从人类和动物咬伤伤口皮肤及软组织感染中分离出的390株需氧菌和厌氧菌的体外活性比较。
Antimicrob Agents Chemother. 1997 Jul;41(7):1552-7. doi: 10.1128/AAC.41.7.1552.
4
Excellent activity of newer quinolones on Legionella pneumophila in J774 macrophages.
Zentralbl Bakteriol. 1997 Feb;285(3):431-9. doi: 10.1016/s0934-8840(97)80009-6.
5
Uptake and intracellular activity of trovafloxacin in human phagocytes and tissue-cultured epithelial cells.曲伐沙星在人吞噬细胞和组织培养上皮细胞中的摄取及细胞内活性。
Antimicrob Agents Chemother. 1997 Feb;41(2):274-7. doi: 10.1128/AAC.41.2.274.
6
In vitro activity of BAY 12-8039, a new fluoroquinolone.新型氟喹诺酮类药物BAY 12 - 8039的体外活性
Antimicrob Agents Chemother. 1997 Jan;41(1):101-6. doi: 10.1128/AAC.41.1.101.
7
In vitro activity of BAY 12-8039, a new 8-methoxyquinolone.新型8-甲氧基喹诺酮BAY 12-8039的体外活性
Chemotherapy. 1996 Nov-Dec;42(6):410-25. doi: 10.1159/000239474.
8
Inhibitory and bactericidal activities of levofloxacin against Mycobacterium tuberculosis in vitro and in human macrophages.左氧氟沙星对结核分枝杆菌的体外及在人巨噬细胞中的抑制和杀菌活性。
Antimicrob Agents Chemother. 1994 May;38(5):1161-4. doi: 10.1128/AAC.38.5.1161.
9
Intracellular penetration and activity of BAY Y 3118 in human polymorphonuclear leukocytes.BAY Y 3118在人多形核白细胞中的细胞内渗透及活性
Antimicrob Agents Chemother. 1994 Oct;38(10):2426-9. doi: 10.1128/AAC.38.10.2426.
10
Intraleukocytic sequestration as a cause of persistent Staphylococcus aureus peritonitis in continuous ambulatory peritoneal dialysis.白细胞内隐匿作为持续性非卧床腹膜透析患者金黄色葡萄球菌性腹膜炎的一个病因
Am J Med. 1984 Jun;76(6):1035-40. doi: 10.1016/0002-9343(84)90854-4.

莫西沙星在人中性粒细胞和组织培养上皮细胞中的摄取及细胞内活性。

Uptake and intracellular activity of moxifloxacin in human neutrophils and tissue-cultured epithelial cells.

作者信息

Pascual A, García I, Ballesta S, Perea E J

机构信息

Department of Microbiology, School of Medicine, University of Seville, Seville, Spain.

出版信息

Antimicrob Agents Chemother. 1999 Jan;43(1):12-5. doi: 10.1128/AAC.43.1.12.

DOI:10.1128/AAC.43.1.12
PMID:9869557
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC89012/
Abstract

The penetration by moxifloxacin of human neutrophils (polymorphonuclear leukocytes [PMN]) and tissue-cultured epithelial cells (McCoy cells) was evaluated by a fluorometric assay. At extracellular concentrations of 5 mg/liter, the cellular-to-extracellular concentration ratios (C/E) of moxifloxacin in PMN and McCoy cells were 10.9 +/- 1.0 and 8.7 +/- 1.0, respectively (20 min; 37 degrees C). The uptake of moxifloxacin by PMN was rapid, reversible, nonsaturable (at extracellular concentrations ranging from 1 to 50 microg/ml), and not affected by cell viability. The uptake of moxifloxacin was affected by external pH and the environmental temperature. The incubation of PMN in the presence of sodium fluoride, sodium cyanide, and carbonyl cyanide m-chlorophenylhydrazone significantly decreased the C/E of this agent. Neither PMN stimulation nor phagocytosis of opsonized Staphylococcus aureus significantly affected the uptake of moxifloxacin by human PMN. This agent, at concentrations of 0.5, 1, and 5 mg/liter, induced a significant reduction in the survival of intracellular S. aureus in human PMN. In summary, moxifloxacin reaches much higher intracellular concentrations within phagocytic and nonphagocytic cells than extracellular ones, remaining active inside the neutrophils.

摘要

通过荧光测定法评估了莫西沙星在人中性粒细胞(多形核白细胞[PMN])和组织培养上皮细胞(McCoy细胞)中的渗透情况。在细胞外浓度为5毫克/升时,莫西沙星在PMN和McCoy细胞中的细胞内与细胞外浓度比(C/E)分别为10.9±1.0和8.7±1.0(20分钟;37摄氏度)。PMN对莫西沙星的摄取迅速、可逆、不饱和(在细胞外浓度为1至50微克/毫升范围内),且不受细胞活力影响。莫西沙星的摄取受外部pH值和环境温度影响。在存在氟化钠、氰化钠和羰基氰化物间氯苯腙的情况下孵育PMN会显著降低该药物的C/E。无论是PMN刺激还是调理过的金黄色葡萄球菌的吞噬作用均未显著影响人PMN对莫西沙星的摄取。该药物在浓度为0.5、1和5毫克/升时,可显著降低人PMN内细胞内金黄色葡萄球菌的存活率。总之,莫西沙星在吞噬细胞和非吞噬细胞内达到的细胞内浓度比细胞外浓度高得多,在中性粒细胞内仍保持活性。