메뉴 건너뛰기




Volumn 50, Issue 9, 2006, Pages 2957-2965

Mechanism-based pharmacodynamic models of fluoroquinolone resistance in Staphylococcus aureus

Author keywords

[No Author keywords available]

Indexed keywords

CIPROFLOXACIN; QUINOLINE DERIVED ANTIINFECTIVE AGENT;

EID: 33748677949     PISSN: 00664804     EISSN: None     Source Type: Journal    
DOI: 10.1128/AAC.00736-05     Document Type: Article
Times cited : (32)

References (25)
  • 1
    • 0030009518 scopus 로고    scopus 로고
    • Dosage regimens of antibacterials: Implications of a pharmacokinetic/ pharmacodynamic model
    • Bouvier d'Yvoire, M. J. Y., and P. H. Maire. 1996. Dosage regimens of antibacterials: implications of a pharmacokinetic/pharmacodynamic model. Clin. Drug Investig. 11:229-239.
    • (1996) Clin. Drug Investig. , vol.11 , pp. 229-239
    • Bouvier D'Yvoire, M.J.Y.1    Maire, P.H.2
  • 4
    • 9644287940 scopus 로고    scopus 로고
    • Evolution of ciprofloxacin-resistant Staphylococcus aureus in in vitro pharmacokinetic environments
    • Campion, J. J., P. J. McNamara, and M. E. Evans. 2004. Evolution of ciprofloxacin-resistant Staphylococcus aureus in in vitro pharmacokinetic environments. Antimicrob. Agents Chemother. 48:4733-4744.
    • (2004) Antimicrob. Agents Chemother. , vol.48 , pp. 4733-4744
    • Campion, J.J.1    McNamara, P.J.2    Evans, M.E.3
  • 5
    • 11244349442 scopus 로고    scopus 로고
    • Pharmacodynamic modeling of ciprofloxacin resistance in Staphylococcus aureus
    • Campion, J. J., P. J. McNamara, and M. E. Evans. 2005. Pharmacodynamic modeling of ciprofloxacin resistance in Staphylococcus aureus. Antimicrob. Agents Chemother. 49:209-219.
    • (2005) Antimicrob. Agents Chemother. , vol.49 , pp. 209-219
    • Campion, J.J.1    McNamara, P.J.2    Evans, M.E.3
  • 6
    • 0027769745 scopus 로고
    • Comparison of four basic models of indirect pharmacodynamic responses
    • Dayneka, N. L., V. Garg, and W. J. Jusko. 1993. Comparison of four basic models of indirect pharmacodynamic responses. J. Pharmacokinet. Biopharm. 21:457-478.
    • (1993) J. Pharmacokinet. Biopharm. , vol.21 , pp. 457-478
    • Dayneka, N.L.1    Garg, V.2    Jusko, W.J.3
  • 7
    • 0027087190 scopus 로고
    • Pharmacoimmunodynamics of methylprednisolone: Trafficking of helper T lymphocytes
    • Fisher, L. E., E. A. Ludwig, and W. J. Jusko. 1992. Pharmacoimmunodynamics of methylprednisolone: trafficking of helper T lymphocytes. J. Pharmacokinet. Biopharm. 20:319-331.
    • (1992) J. Pharmacokinet. Biopharm. , vol.20 , pp. 319-331
    • Fisher, L.E.1    Ludwig, E.A.2    Jusko, W.J.3
  • 11
    • 0034896122 scopus 로고    scopus 로고
    • Comparative killing kinetics of the novel des-fluoro(6) quinolone BMS-284756, fluoroquinolones, vancomycin and beta-lactams
    • Gradelski, E., L. Valera, B. Kolek, D. Bonner, and J. Fung-Tomc. 2001. Comparative killing kinetics of the novel des-fluoro(6) quinolone BMS-284756, fluoroquinolones, vancomycin and beta-lactams. Int. J. Antimicrob. Agents 18:43-48.
    • (2001) Int. J. Antimicrob. Agents , vol.18 , pp. 43-48
    • Gradelski, E.1    Valera, L.2    Kolek, B.3    Bonner, D.4    Fung-Tomc, J.5
  • 12
    • 6944234949 scopus 로고    scopus 로고
    • Selection of a moxifloxacin dose that suppresses drug resistance in Mycobacterium tuberculosis, by use of an in vitro pharmacodynamic infection model and mathematical modeling
    • Gumbo, T., A. Louie, M. R. Deziel, L. M. Parsons, M. Salfinger, and G. L. Drusano. 2004. Selection of a moxifloxacin dose that suppresses drug resistance in Mycobacterium tuberculosis, by use of an in vitro pharmacodynamic infection model and mathematical modeling. J. Infect. Dis. 190:1642-1651.
    • (2004) J. Infect. Dis. , vol.190 , pp. 1642-1651
    • Gumbo, T.1    Louie, A.2    Deziel, M.R.3    Parsons, L.M.4    Salfinger, M.5    Drusano, G.L.6
  • 13
    • 0029859964 scopus 로고    scopus 로고
    • DNA strand cleavage is required for replication fork arrest by a frozen topoisomerase-quinolone-DNA ternary complex
    • Hiasa, H., D. O. Yousef, and K. J. Marians. 1996. DNA strand cleavage is required for replication fork arrest by a frozen topoisomerase-quinolone-DNA ternary complex. J. Biol. Chem. 271:26424-26429.
    • (1996) J. Biol. Chem. , vol.271 , pp. 26424-26429
    • Hiasa, H.1    Yousef, D.O.2    Marians, K.J.3
  • 15
    • 0027943266 scopus 로고
    • Physiologic indirect response models characterize diverse types of pharmacodynamic effects
    • Jusko, W. J., and H. C. Ko. 1994. Physiologic indirect response models characterize diverse types of pharmacodynamic effects. Clin. Pharmacol. Ther. 56:406-419.
    • (1994) Clin. Pharmacol. Ther. , vol.56 , pp. 406-419
    • Jusko, W.J.1    Ko, H.C.2
  • 16
    • 0032538454 scopus 로고    scopus 로고
    • The mechanism of inhibition of topoisomerase IV by quinolone antibacterials
    • Khodursky, A. B., and N. R. Cozzarrelli. 1998. The mechanism of inhibition of topoisomerase IV by quinolone antibacterials. J. Biol. Chem. 273:27668-27677.
    • (1998) J. Biol. Chem. , vol.273 , pp. 27668-27677
    • Khodursky, A.B.1    Cozzarrelli, N.R.2
  • 17
    • 0031057479 scopus 로고    scopus 로고
    • The population dynamics of antimicrobial chemotherapy
    • Lipsitch, M., and B. R. Levin. 1997. The population dynamics of antimicrobial chemotherapy. Antimicrob. Agents Chemother. 41:363-373.
    • (1997) Antimicrob. Agents Chemother. , vol.41 , pp. 363-373
    • Lipsitch, M.1    Levin, B.R.2
  • 18
    • 2542482710 scopus 로고    scopus 로고
    • Novel pharmacokinetic-pharmacodynamic model for prediction of outcomes with an extended-release formulation of ciprofloxacin
    • Meagher, A. K., A. Forrest, A. Dalhoff, H. Stass, and J. J. Schentag. 2004. Novel pharmacokinetic-pharmacodynamic model for prediction of outcomes with an extended-release formulation of ciprofloxacin. Antimicrob. Agents Chemother. 48:2061-2068.
    • (2004) Antimicrob. Agents Chemother. , vol.48 , pp. 2061-2068
    • Meagher, A.K.1    Forrest, A.2    Dalhoff, A.3    Stass, H.4    Schentag, J.J.5
  • 19
    • 13244281964 scopus 로고    scopus 로고
    • Pharmacokinetic/pharmacodynamic modeling of antibacterials in vitro and in vivo using bacterial growth and kill kinetics. The minimum inhibitory concentration versus stationary concentration
    • Mouton, J. W., and A. A. Vinks. 2005. Pharmacokinetic/pharmacodynamic modeling of antibacterials in vitro and in vivo using bacterial growth and kill kinetics. The minimum inhibitory concentration versus stationary concentration. Clin. Pharmacokinet. 44:201-210.
    • (2005) Clin. Pharmacokinet. , vol.44 , pp. 201-210
    • Mouton, J.W.1    Vinks, A.A.2
  • 20
    • 0030985564 scopus 로고    scopus 로고
    • Pharmacokinetic-pharmacodynamic modeling of activity of ceftazidime during continuous and intermittent infusion
    • Mouton, J. W., A. A. T. M. M. Vinks, and N. C. Punt. 1997. Pharmacokinetic-pharmacodynamic modeling of activity of ceftazidime during continuous and intermittent infusion. Antimicrob. Agents Chemother. 41:733-738.
    • (1997) Antimicrob. Agents Chemother. , vol.41 , pp. 733-738
    • Mouton, J.W.1    Vinks, A.A.T.M.M.2    Punt, N.C.3
  • 21
    • 0000238336 scopus 로고
    • Method for function minimization
    • Nelder, J. A., and R. Mead. 1965. A simplex method for function minimization. Computing J. 7:308-313.
    • (1965) Computing J. , vol.7 , pp. 308-313
    • Nelder, J.A.1    Mead, R.2
  • 22
    • 0037417066 scopus 로고    scopus 로고
    • Quinolone-DNA interaction: Sequence-dependent binding to single-stranded DNA reflects the interaction within the gyrase-DNA complex
    • Noble, C. G., F. M. Barnard, and A. Maxwell. 2003. Quinolone-DNA interaction: sequence-dependent binding to single-stranded DNA reflects the interaction within the gyrase-DNA complex. Antimicrob. Agents Chemother. 47:854-862.
    • (2003) Antimicrob. Agents Chemother. , vol.47 , pp. 854-862
    • Noble, C.G.1    Barnard, F.M.2    Maxwell, A.3
  • 24
    • 0029564873 scopus 로고
    • Tolrestat pharmacokinetic and pharmacodynamic effects on red blood cell sorbitol levels in normal volunteers and in patients with insulin-dependent diabetes
    • van Griensven, J. M. T., W. J. Jusko, H. H. P. J. Lemkes, R. Kroon, C. J. Verhorst, and S. T. Chiang. 1995. Tolrestat pharmacokinetic and pharmacodynamic effects on red blood cell sorbitol levels in normal volunteers and in patients with insulin-dependent diabetes. Clin. Pharmacol. Ther. 58:631-640.
    • (1995) Clin. Pharmacol. Ther. , vol.58 , pp. 631-640
    • Van Griensven, J.M.T.1    Jusko, W.J.2    Lemkes, H.H.P.J.3    Kroon, R.4    Verhorst, C.J.5    Chiang, S.T.6
  • 25
    • 0028034698 scopus 로고
    • The complex of DNA gyrase and quinolone drugs with DNA forms a barrier to transcription of RNA polymerase
    • Willmott, C. J., S. E. Critchlow, I. C. Eperon, and A. Maxwell. 1994. The complex of DNA gyrase and quinolone drugs with DNA forms a barrier to transcription of RNA polymerase. J. Mol. Biol. 242:351-363.
    • (1994) J. Mol. Biol. , vol.242 , pp. 351-363
    • Willmott, C.J.1    Critchlow, S.E.2    Eperon, I.C.3    Maxwell, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.