-
1
-
-
0023774987
-
Novel membrane localized inhibitors of iron-dependent lipid peroxidation
-
1. J. M. Braughler, P. S. Burton, R. L. Chase, J. G. Pregenzer, E. J. Jacobsen, F. J. VanDoornik, J. M. Tustin, D. E. Ayer, and G. L. Bundy. Novel membrane localized inhibitors of iron-dependent lipid peroxidation. Biochem. Pharmacol. 37:3853-3860 (1988).
-
(1988)
Biochem. Pharmacol.
, vol.37
, pp. 3853-3860
-
-
Braughler, J.M.1
Burton, P.S.2
Chase, R.L.3
Pregenzer, J.G.4
Jacobsen, E.J.5
VanDoornik, F.J.6
Tustin, J.M.7
Ayer, D.E.8
Bundy, G.L.9
-
2
-
-
0024518123
-
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
-
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
-
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
-
5
-
-
0023613416
-
Lipid emulsions as drug delivery systems
-
5. S. S. Davis, C. Washington, P. West, L. Illum, G. Liversidge, L. Sternson, and R. Kirsh. Lipid emulsions as drug delivery systems. Ann. N. Y. Acad. Sci. 507:75-88 (1987).
-
(1987)
Ann. N. Y. Acad. Sci.
, vol.507
, pp. 75-88
-
-
Davis, S.S.1
Washington, C.2
West, P.3
Illum, L.4
Liversidge, G.5
Sternson, L.6
Kirsh, R.7
-
6
-
-
0017663470
-
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
-
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
-
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
-
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
-
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
-
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
-
-
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
-
-
SAS Institute, Inc. Cary, N. C.
-
14. SAS Institute, Inc. Cary, N. C.
-
-
-
-
16
-
-
0031972957
-
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
-
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
-
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
-
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
-
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
-
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
|