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甘氨环素类药物替加环素的研究进展 被引量:11

Advances in the study of tigecycline——a novel glycylcycline
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摘要 由于导致严重感染的多药耐药菌发生率上升,临床迫切需要寻求新型抗菌药物,尤其需要能够有效克服现有耐药机制的全新药物。替加环素为新型抗菌甘氨环素类药物,即米诺环素的衍生物,能够克服与四环素类绝大部分相关的耐药机制。体外试验显示替加环素尽管对铜绿假单胞菌无效,对变形杆菌属的作用较差,但对耐万古霉素肠球菌、耐甲氧西林金黄色葡萄球菌、耐青霉素肺炎链球菌和其他多药耐药革兰阴性菌均具有良好活性。Ⅲ期临床试验已就替加环素治疗由多药耐药菌引起危及生命的感染的作用进行了研究,其抗菌谱新颖广阔,具有良好的临床应用前景。 New antimicrobial agents are urgently needed for clinical use due to the increasing incidence of serious and life-threatening diseases caused by multidrug-resistant bacteria. The need to develop new agents that effectively overcome existing mechanisms of resistance to currently available drugs has become paramount. Tigecycline, the first in a new class of antimicrobials, the glycylcyclines, is an analogue of minocycline with additional properties that negate most mechanisms mediating resistance to the tetracy- clines. In vitro testing, resistance to tigecycline by Pseudomonas aeruginosa and reduced susceptibility among Proteus species do occur, but it has revealed that tigecycline has activity against vancomycin-resistant enterococci, methicillin-resistant Staphylococcus aureus, penicillin-resistant Streptococcus pneumoniae and many species of multidrug-resistant Gram-negative bacteria. Tigecycline is being evaluated in multicentre Phase Ⅲ clinical trials for treatment of many serious and life-threatening infections in which multidrug-resistant bacterial organisms may be found. Tigecycline appears to hold promise as a novel expanded spectrum antibiotic.
作者 任少华
出处 《国外医学(药学分册)》 2007年第2期106-109,114,共5页 Foreign Medical Sciences(Section of Pharmarcy)
关键词 感染 细菌 替加环素 甘氨环素类 infection bacteria tigecycline glycylcyclines
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参考文献14

  • 1Kasbekar N.Tigecycline:a new glycylcycline antimicrobial agent[J].Am J Health-Syst Pharm,2006,63 (13):1235-1243. 被引量:1
  • 2Rubinstein E,Vaughan D.Tigecycline:a novel glycylcycline[J].Drugs,2005,65 (10):1317-1336. 被引量:1
  • 3Bauer G,Berens C,Projan SJ,et al.Comparison of tetracycline and tigecycline binding to ribosomes mapped by dimethylsulphate and drug-directed Fe^2+ cleavage of 16S rRNA[J].J Antimicrob Chemother,2004,53(4):592 -599. 被引量:1
  • 4Pankey GA.Tigecycline[J].J Antimicrob Chemother,2005,56(3):470-480. 被引量:1
  • 5Meagher AK,Ambrose PG,Grasela TH,et al.The pharmacokinetic and pharmacodynamic profile of tigecycline[J].Clin Infect Dis,2005,41 (Suppl 5):S333-S340. 被引量:1
  • 6Hoban DJ,Bouchillon SK,Johnson BM,et al.In vitro activity of tigecycline against 6792 Gram-negative and Gram-positive clinical isolates from the global Tigecycline Evaluation and Surveillance Trial (TEST Program,2004)[J].Diagn Microbiol Infect Dis,2005,52(3):215 -227. 被引量:1
  • 7Pachon-Ibanez ME,Jimenez-Mejias ME,Pichardo C,et al.Activity of tigecycline (GAR-936) against Acinetobacter baumannii strains,including those resistant to imipenem[J].Antimicrob Agents Chemother,2004,48 (11):4479-4481. 被引量:1
  • 8LaPlante KL,Rybak MJ.Clinical glycopeptide-intermediate Staphylococci tested against arbekacin,daptomycin,and tigecycline[J].Diagn Microbiol Infect Dis,2004,50(2):125 -130. 被引量:1
  • 9Garrison MW,Neumiller JJ,Setter SM.Tigecycline:an investigational glycylcycline antimicrobial with activity against resistant Gram-positive organisms[J].Clin Ther,2005,27 (1):12-22. 被引量:1
  • 10Sader HS,Jones RN,Dowzicky MJ,et al.Antimicrobial activity of tigecycline tested against nosocomial bacterial pathogens from patients hospitalized in the intensive care unit[J].Diagn Microbiol Infect Dis,2005,52 (3):203-208. 被引量:1

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