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Volumn 53, Issue 10, 2009, Pages 4542-4544

In vitro bactericidal activity of iclaprim in human plasma

Author keywords

[No Author keywords available]

Indexed keywords

FUSIDIC ACID; ICLAPRIM; LINEZOLID; TEICOPLANIN; VANCOMYCIN;

EID: 70349345798     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.00766-09     Document Type: Article
Times cited : (20)

References (12)
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    • Bailey, E. M., M. J. Rybak, and G. W. Kaatz. 1991. Comparative effect of protein binding on the killing activities of teicoplanin and vancomycin. Antimicrob. Agents Chemother. 35:1089-1092.
    • (1991) Antimicrob. Agents Chemother. , vol.35 , pp. 1089-1092
    • Bailey, E.M.1    Rybak, M.J.2    Kaatz, G.W.3
  • 3
    • 70349355418 scopus 로고    scopus 로고
    • Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically, approved standard
    • Clinical and Laboratory Standards Institute. 7th ed. Clinical and Laboratory Standards Institute, Wayne, PA
    • Clinical and Laboratory Standards Institute. 2006. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically, approved standard, 7th ed. CLSI document M7-A7, vol.26, no.2. Clinical and Laboratory Standards Institute, Wayne, PA.
    • (2006) CLSI Document M7-A7 , vol.26 , Issue.2
  • 6
    • 0002515716 scopus 로고
    • Antimicrobial combinations
    • V. Lorian (ed.), Lippincott Williams and Wilkins, Baltimore, MD
    • Eliopoulos, G. M., and R. C. Moellering, Jr. 1991. Antimicrobial combinations, p. 432-492. In V. Lorian (ed.), Antibiotics in laboratory medicine, 3rd ed. Lippincott Williams and Wilkins, Baltimore, MD.
    • (1991) Antibiotics in Laboratory Medicine, 3rd Ed. , pp. 432-492
    • Eliopoulos, G.M.1    Moellering Jr., R.C.2
  • 8
    • 33748089329 scopus 로고    scopus 로고
    • Comparative activity of the new lipoglycopeptide telavancin in the presence and absence of serum against 50 glycopeptide non-susceptible staphylococci and three vancomycin-resistant Staphylococcus aureus
    • Leuthner, K. D., C. M. Cheung, and M. J. Rybak. 2006. Comparative activity of the new lipoglycopeptide telavancin in the presence and absence of serum against 50 glycopeptide non-susceptible staphylococci and three vancomycin-resistant Staphylococcus aureus. J. Antimicrob. Chemother. 58:338-343.
    • (2006) J. Antimicrob. Chemother. , vol.58 , pp. 338-343
    • Leuthner, K.D.1    Cheung, C.M.2    Rybak, M.J.3
  • 9
    • 0003922953 scopus 로고    scopus 로고
    • Methods for determining bactericidal activity of antimicrobial agents, approved guideline
    • National Committee for Clinical Laboratory Standards. National Committee for Clinical Laboratory Standards, Wayne, PA
    • National Committee for Clinical Laboratory Standards. 1999. Methods for determining bactericidal activity of antimicrobial agents, approved guideline, NCCLS document M26-A. National Committee for Clinical Laboratory Standards, Wayne, PA.
    • (1999) NCCLS Document M26-A
  • 10
    • 62549149036 scopus 로고    scopus 로고
    • Increased hydrophobic interactions of iclaprim with Staphylococcus aureus dihydrofolate reductase are responsible for the increase in affinity and antibacterial activity
    • Oefner, C., M. Bandera, A. Haldimann, H. Laue, H. Schulz, S. Mukhija, S. Parisi, L. Weiss, S. Lociuro, and G. E. Dale. 2009. Increased hydrophobic interactions of iclaprim with Staphylococcus aureus dihydrofolate reductase are responsible for the increase in affinity and antibacterial activity. J. Antimicrob. Chemother. 63:687-698.
    • (2009) J. Antimicrob. Chemother. , vol.63 , pp. 687-698
    • Oefner, C.1    Bandera, M.2    Haldimann, A.3    Laue, H.4    Schulz, H.5    Mukhija, S.6    Parisi, S.7    Weiss, L.8    Lociuro, S.9    Dale, G.E.10
  • 11
    • 38849190721 scopus 로고    scopus 로고
    • Iclaprim, a diaminopyrimidine dihydrofolate reductase inhibitor for the potential treatment of antibiotic-resistant staphylococcal infections
    • Peppard, W. J., and C. D. Schuenke. 2008. Iclaprim, a diaminopyrimidine dihydrofolate reductase inhibitor for the potential treatment of antibiotic-resistant staphylococcal infections. Curr. Opin. Investig. Drugs 9:210-225.
    • (2008) Curr. Opin. Investig. Drugs , vol.9 , pp. 210-225
    • Peppard, W.J.1    Schuenke, C.D.2
  • 12
    • 0031893770 scopus 로고    scopus 로고
    • Comparative in vitro activities and postantibiotic effects of the oxazolidinone compounds eperezolid (PNU-100592) and linezolid (PNU- 100766) versus vancomycin against Staphylococcus aureus, coagulase-negative staphylococci, Enterococcus faecalis, and Enterococcus faecium
    • Rybak, M. J., D. M. Cappelletty, T. Moldovan, J. R. Aeschlimann, and G. W. Kaatz. 1998. Comparative in vitro activities and postantibiotic effects of the oxazolidinone compounds eperezolid (PNU-100592) and linezolid (PNU- 100766) versus vancomycin against Staphylococcus aureus, coagulase-negative staphylococci, Enterococcus faecalis, and Enterococcus faecium. Antimicrob. Agents Chemother. 42:721-724.
    • (1998) Antimicrob. Agents Chemother. , vol.42 , pp. 721-724
    • Rybak, M.J.1    Cappelletty, D.M.2    Moldovan, T.3    Aeschlimann, J.R.4    Kaatz, G.W.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.