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新型糖肽类抗生素奥利万星 被引量:3

A new glycopeptide antimicrobial-oritavancin
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摘要 奥利万星(oritavancin,LY333328)是一种半合成的新型的糖肽类抗生素,作用机制与万古霉素和替考拉宁相同,即抑制G+菌细胞壁的生物合成。具有独特的药动学性质。其抗菌谱包括金葡球菌、耐甲氧西林金葡球菌(MRSA);表皮葡萄球菌及凝固酶阴性葡萄球菌(CoNS),包括耐甲氧西林及一些耐替考拉宁菌;肠球菌,包括耐万古霉素替考拉宁(vanA)屎肠球菌和粪肠球菌;链球菌,包括化脓性链球菌和肺炎链球菌,包括耐青霉素肺炎链球菌;G+厌氧菌,包括消化链球菌属、短小棒状杆菌和艰难梭状芽胞杆菌。在治疗皮肤和软组织感染上已取得了良好的效果。现对其作用机制、抗菌活性、药动学及临床研究做一综述。 Oritavancin, a semisynthetic glycopeptide, mechanism of action is same as vancomycin-inhibiting biosynthesis of Gram-positive bacteria cell wall. The antibacterial spectrum of oritavancin covers staphylococcus aureus, including methicillin-resistant strains; staphylococcus epidermidis and other coagulase-negative staphylococci, including methicillin-resistant and some teicoplanin-resistant strains; enterococci, including vancomycin-resistant, teicoplanin-resistant isolates of enterococcus faecium and enterococcus faecalis; streptococci, including streptococcus pyogenes and streptococcus pneumoniae, including penicillin-resistant isolates;Gram-positive anaerobic bacteria. It has a long-term half-life and has been dosed once-daily in clinical trials. Oritavancin has been shown to be effective for the treatment of patients with complicated skin and skin structure infections.
机构地区 卫生部北京医院
出处 《中国新药杂志》 CAS CSCD 北大核心 2007年第14期1141-1144,共4页 Chinese Journal of New Drugs
关键词 奥利万星 糖肽类抗生素 抗菌活性 药动学 临床研究 oritavancin glycopeptide antimicrobial antibacterial activity pharmacokinetics clinical study
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参考文献26

  • 1RARENTI F, BERETTA G, BERTI M, et al. Teichomycins new antibiotics from Actinoplanes leichomyceticus nov sp I, description of the producer strain, fermentation studies and biological propert [ J]. J Antibiot, 1978,31 (4) :276 - 283.
  • 2罗清平,沈亚领,迟莉丽,魏东芝.一种新糖肽抗生素LY333328的抗菌活性与作用机制[J].国外医药(抗生素分册),2004,25(5):221-225. 被引量:1
  • 3BEAUREGARD DA,WILLIAMS DH, GWYNN MN, et al. Dimerization and membrane anchom in the extracellular targeting of vancomycin group antibiotics[ J]. A ntimlcrob Agents Chemother , 1995,39(3 ) :781 -785.
  • 4LE TOURNEAU DL,HOBBS JN,ALLEN NE. Molecular interactions of Ly264826 and its p-chlorobenzyl derivative [ C ]// LY191145, with dipeptidyl and didepsipeptidyl ligands, abstr.F250, In program and abstracts of the 35th inter Science conference on antimicrobial agents and chemotherapy American society for microbiology, Woshington, 1995 : 156.
  • 5NICAS TI, MULLEN DL, FLOKOWITSCH JE. Semisynthetic glycopeptide antibiotics derived from L Y264826 active against vancomycin-resistant enterococci [ J ]. Antimicrob Agents Chemother, 1996,40 ( 9 ) : 2194 - 2199.
  • 6COYLE EA, RYBAK MJ. Activity of oritavancin ( L Y333328), an investigational glycopeptide, compared to that of vancomycin against muhidrug-resistant Streptococcus pneumoniae in an in vitro pharmacodynamic model[ J ]. A ntimicrob Agent Chemother ,2001, 45 (3) :706 - 709.
  • 7FEKETY E, IN FL, MANDELL J E, et al. Principles and practice of infectious diseases[M]. New York: 4thed Churchill Livingston, 1995:346.
  • 8JONES RN, BARRETr MS, ERWIN ME. In vitro activity and spectrum of LY333328, a novel glycopeptide derivative[ J]. Antimicrob Agents Chemother, 1997,41 (2) :488 - 493.
  • 9FRAISE AP, ANDREWS J, WISE R. Activity of a new glycopeptide antibiotic ( LY333328 ) against enterococci and other resistant gram-positive organisms [ J]. J Antimicrob Chemother, 1997,40(3 ) :423 -425.
  • 10PATEL R, ROUSE MS, PIPER KE, et al. In vitro activity of LY333328 against vancomycin-resistant enterococci, methicillinresistant Staphylococcus aureus, and penicillin-resistant Streptococcus pneumoniae [ J]. Diagn Microbiol Infect Dis, 1998,30 (2) :89 -92.

二级参考文献22

  • 1Al-Nawas B, Swantes J, Shah PM. In vitro activity of LY333328, a new glycopeptide, against extracellular and intracellular vancomycin-risistant enterococci[J]. Infction ,2000,28(4) :214
  • 2Barrett JF. Oritavancin[J]. Curr Opin Investig Drugs ,2001,2(8): 1039
  • 3Nicas TI,Mullen DL,Flokowitsch JE,et al.Semisynthetic glycopeptide antibiotics derived from LY264826 active against vancomycin - resistant enterococci [J]. Antimicrkb Agents Chemother,1996,40(9):2194
  • 4Garcla-Garrote F, Cercenado E, Alcala L. In vitro activity of the new glycopeptide LY333328 against multiply resistant gram- Posistive clinical isolates [J]. Antimicrob Agents Chemother, 1998,42 (9): 2452
  • 5Azzan SM, Agnes l, Vallois JM. Activity and diffusion of LY333328 in experimental endocarditis due to vancomycinresistant Enterococcus faecalis [J]. Antimicrob. Agents Chemother, 1999,43 (1): 115
  • 6Zelenitsky SA, Karlowsky JA,Nicas TN. Time - kill curves for a semisynthetic glycopeptide,LY333328,against vancomycin-susceptible and vancomycin - resistant Enterococcus faecium strain [J]. Antimicrob Agents Chemother,1997,41(6):1407
  • 7Le Tourneau DL, Hobbs JN, Allen NE. Molecular interactions of Ly264826 and its p - chlorobenzyl derivative[R]. Woshng ton: LY191145, with dipeptidyl and didepsipeptidyl ligands, abstr. F250, In program and abstracts of the 35th inter Science conference on
  • 8Coyle EA, Rybak MJ. Activity of oritavancin (LY333328),an investigational glycopeptide, compared to that of vancomycin against multidrug-resistant Streptococcus pneumoniae in an in vitro pharmacodynamic model [J]. Antimicrob Agents Chemother ,2001,45(3) :
  • 9Rarenti F, Beretta G, Berti M, et al. Teichomycins new antibiotics from Actinoplanes leichomyceticus nov sp I, description of the producer strain, fermentation studies and biological propert [J]. J Antibiot, 1978,31: 276
  • 10Steele-Moore L,Maclntosh A ,Furdess K.In vivo activity of an investigational glycopeptide antibiotic LY333328[R].woshington: In Abstracts of the 96th General Meeting of the American Society for Microbiology, 1996:143

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