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Volumn 16, Issue 6, 1999, Pages 930-938

Venous irritation, pharmacokinetics, and tissue distribution of tirilazad in rats following intravenous administration of a novel supersaturated submicron lipid emulsion

Author keywords

Pharmacokinetics; Submicron lipid emulsion; Supersaturation; Tirilazad; Tissue distribution; Venous irritation

Indexed keywords

LIPID EMULSION; TIRILAZAD;

EID: 0032982451     PISSN: 07248741     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1018846607804     Document Type: Article
Times cited : (23)

References (21)
  • 2
    • 0024518123 scopus 로고
    • The 21-aminosteroids: Potent inhibitors of lipid peroxidation for the treatment of central nervous system trauma and ischemia
    • 2. J. M. Braughler, E. D. Hall, E. J. Jacobsen, J. M. McCall, and E. D. Means. The 21-aminosteroids: Potent inhibitors of lipid peroxidation for the treatment of central nervous system trauma and ischemia. Drugs Future 14:143-152 (1989).
    • (1989) Drugs Future , vol.14 , pp. 143-152
    • Braughler, J.M.1    Hall, E.D.2    Jacobsen, E.J.3    McCall, J.M.4    Means, E.D.5
  • 3
    • 0027419603 scopus 로고
    • Evaluation of the pharmacokinetics and tolerability of tirilazad mesylate, a 21-aminosteroid free radical scavenger: I. Single-dose administration
    • 3. J. C. Fleishaker, G. R. Peters, and K. S. Cathcart. Evaluation of the pharmacokinetics and tolerability of tirilazad mesylate, a 21-aminosteroid free radical scavenger: I. Single-dose administration. J. Clin. Pharmacol. 33:175-181 (1993).
    • (1993) J. Clin. Pharmacol. , vol.33 , pp. 175-181
    • Fleishaker, J.C.1    Peters, G.R.2    Cathcart, K.S.3
  • 4
    • 0027418840 scopus 로고
    • Evaluation of the pharmacokinetics and tolerability of tirilazad mesylate, a 21-aminosteroid free radical scavenger: I. Multiple-dose administration
    • 4. J. C. Fleishaker, G. R. Peters, K. S. Cathcart, and R. C. Steenwyk. Evaluation of the pharmacokinetics and tolerability of tirilazad mesylate, a 21-aminosteroid free radical scavenger: I. Multiple-dose administration. J. Clin. Pharmacol. 33:182-190 (1993).
    • (1993) J. Clin. Pharmacol. , vol.33 , pp. 182-190
    • Fleishaker, J.C.1    Peters, G.R.2    Cathcart, K.S.3    Steenwyk, R.C.4
  • 6
    • 0017663470 scopus 로고
    • Parenteral use of diazepam in an emulsion formulation. A clinical study
    • 6. A. M. Thorn-Alquist. Parenteral use of diazepam in an emulsion formulation. A clinical study. Acta Anaesth. Scand. 21:400-404 (1977).
    • (1977) Acta Anaesth. Scand. , vol.21 , pp. 400-404
    • Thorn-Alquist, A.M.1
  • 7
    • 0026718939 scopus 로고
    • Dissolving methohexital in a lipid emulsion reduces pain associated with intravenous injection
    • 7. P. Westrin, C. Jonmarker, and O. Werner. Dissolving methohexital in a lipid emulsion reduces pain associated with intravenous injection. Anaesthesiology 76:930-934 (1992).
    • (1992) Anaesthesiology , vol.76 , pp. 930-934
    • Westrin, P.1    Jonmarker, C.2    Werner, O.3
  • 8
    • 0028335617 scopus 로고
    • Less-painful emulsion formulations for intravenous administration of clarithromycin
    • 8. M. W. Lovell, H. W. Johnson, H.-W. Hui, J. B. Cannon, P. K. Gupta, and C. C. Hsu. Less-painful emulsion formulations for intravenous administration of clarithromycin. Int. J. Pharm. 109:45-57 (1994).
    • (1994) Int. J. Pharm. , vol.109 , pp. 45-57
    • Lovell, M.W.1    Johnson, H.W.2    Hui, H.-W.3    Cannon, J.B.4    Gupta, P.K.5    Hsu, C.C.6
  • 9
    • 0024397420 scopus 로고
    • A new formulation of etomidate in lipid emulsion. Bioavailability and venous irritation
    • 9. H. Stuttmann, A. Doenicke, J. Kugler, and M. Laub. A new formulation of etomidate in lipid emulsion. Bioavailability and venous irritation. Anaesthesist. 38:421-423 (1989).
    • (1989) Anaesthesist. , vol.38 , pp. 421-423
    • Stuttmann, H.1    Doenicke, A.2    Kugler, J.3    Laub, M.4
  • 10
    • 0021241617 scopus 로고
    • Pharmacology of an emulsion formulation of ICI 35868
    • 10. J. B. Glen and S. C. Hunter. Pharmacology of an emulsion formulation of ICI 35868. Br. J. Anaesth. 56:617-625 (1984).
    • (1984) Br. J. Anaesth. , vol.56 , pp. 617-625
    • Glen, J.B.1    Hunter, S.C.2
  • 11
    • 0013572347 scopus 로고    scopus 로고
    • A novel stable supersaturated submicron lipid emulsion of tirilazad
    • In press.
    • 11. Y. Wang and A. L. Cory. A novel stable supersaturated submicron lipid emulsion of tirilazad. Pharma. Dev. Tech. In press.
    • Pharma. Dev. Tech.
    • Wang, Y.1    Cory, A.L.2
  • 12
    • 0013571992 scopus 로고    scopus 로고
    • RSTRIP-Exponential stripping and parameter estimation, v 5.0, Micromath Scientific Software, Salt Lake City, UT.
    • 12. RSTRIP-Exponential stripping and parameter estimation, v 5.0, Micromath Scientific Software, Salt Lake City, UT.
  • 14
    • 0013621674 scopus 로고    scopus 로고
    • SAS Institute, Inc. Cary, N. C.
    • 14. SAS Institute, Inc. Cary, N. C.
  • 16
    • 0031972957 scopus 로고    scopus 로고
    • Formulation-dependent pharmacokinetics and pharmacodynamics of propofol in rats
    • 16. D. Sandeep and W. F. Ebling. Formulation-dependent pharmacokinetics and pharmacodynamics of propofol in rats. J. Pharm. Pharmacol. 50:37-42 (1998).
    • (1998) J. Pharm. Pharmacol. , vol.50 , pp. 37-42
    • Sandeep, D.1    Ebling, W.F.2
  • 17
    • 0029993739 scopus 로고    scopus 로고
    • Pharmacokinetics of highly lipophilic antitumor agent palmitoyl rhizoxin incorporated in lipid emulsions in rats
    • 17. A. Kurihara, Y. Shibayama, A. Mizota, A. Yasuno, M. Ikeda, and M. Hisaoka. Pharmacokinetics of highly lipophilic antitumor agent palmitoyl rhizoxin incorporated in lipid emulsions in rats. Biol. Pharm. Bull. 19:252-258 (1996).
    • (1996) Biol. Pharm. Bull. , vol.19 , pp. 252-258
    • Kurihara, A.1    Shibayama, Y.2    Mizota, A.3    Yasuno, A.4    Ikeda, M.5    Hisaoka, M.6
  • 18
    • 0027322235 scopus 로고
    • Blood clearance and tissue distribution of various formulations of α-tocopherol injection after intravenous administration
    • 18. Y. Kato, K. Watanabe, M. Nakakura, and T. Hosokawa. Blood clearance and tissue distribution of various formulations of α-tocopherol injection after intravenous administration. Chem. Pharm. Bull. 41:599-604 (1993).
    • (1993) Chem. Pharm. Bull. , vol.41 , pp. 599-604
    • Kato, Y.1    Watanabe, K.2    Nakakura, M.3    Hosokawa, T.4
  • 19
    • 0025774893 scopus 로고
    • Plasma compability of injectables: Comparison of intravenous U-74006, a 21-aminosteroid antioxidant, with Dilantin brand of parenteral phenytoin
    • 19. J. W. Cox, G. P. Sage, M. A. Wynalda, R. G. Ulrich, P. G. Larson, and C. C. Su. Plasma compability of injectables: Comparison of intravenous U-74006, a 21-aminosteroid antioxidant, with Dilantin brand of parenteral phenytoin. J. Pharm. Sci. 80(4):371-375 (1991).
    • (1991) J. Pharm. Sci. , vol.80 , Issue.4 , pp. 371-375
    • Cox, J.W.1    Sage, G.P.2    Wynalda, M.A.3    Ulrich, R.G.4    Larson, P.G.5    Su, C.C.6
  • 20
    • 0020406528 scopus 로고
    • The targeting of drugs parenterally by use of microspheres
    • 20. L. Illum. The targeting of drugs parenterally by use of microspheres. J. Parenteral Sci. Technol. 36(6):242-248(1982).
    • (1982) J. Parenteral Sci. Technol. , vol.36 , Issue.6 , pp. 242-248
    • Illum, L.1
  • 21
    • 0024321034 scopus 로고
    • Pharmacokinetics and excretion of the 21-aminosteroid antioxidant U-74006F in rat and perfused rat liver
    • 21. J. W. Cox, P. G. Larson, M. A. Wynalda, V. K. Sood, M. T. Verburg, and R. N. Pullen. Pharmacokinetics and excretion of the 21-aminosteroid antioxidant U-74006F in rat and perfused rat liver. Drug Metab. Dispos. 17:373-379 (1989).
    • (1989) Drug Metab. Dispos. , vol.17 , pp. 373-379
    • Cox, J.W.1    Larson, P.G.2    Wynalda, M.A.3    Sood, V.K.4    Verburg, M.T.5    Pullen, R.N.6


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