-
1
-
-
0025310728
-
Prodrugs for the improvement of drug absorption via different routes of administration
-
L. P. Balant, E. Doelker, and P. Buri: Prodrugs for the improvement of drug absorption via different routes of administration. Eur. J. Drug Metab. Pharmacokinet. 15, 143-153 (1990).
-
(1990)
Eur. J. Drug Metab. Pharmacokinet.
, vol.15
, pp. 143-153
-
-
Balant, L.P.1
Doelker, E.2
Buri, P.3
-
2
-
-
0019781021
-
Prodrug design
-
R. E. Notari: Prodrug design. Pharmacol Ther. 14, 25-53 (1981).
-
(1981)
Pharmacol Ther.
, vol.14
, pp. 25-53
-
-
Notari, R.E.1
-
3
-
-
0001935155
-
Physical model approach to design of drugs with improved intestinal absorption
-
(E. B. Roche, ed.), American Pharmaceutical Association Academy of Pharmaceutical Sciences, Washington, D.C.
-
N. F. H. Ho, J. Y. Park, W. Morozowich, and W. I. Higuchi: Physical model approach to design of drugs with improved intestinal absorption. In "Design of Biopharmaceutical Properties through Prodrugs and Analogs" (E. B. Roche, ed.), pp. 201-227. American Pharmaceutical Association Academy of Pharmaceutical Sciences, Washington, D.C., 1977.
-
(1977)
Design of Biopharmaceutical Properties Through Prodrugs and Analogs
, pp. 201-227
-
-
Ho, N.F.H.1
Park, J.Y.2
Morozowich, W.3
Higuchi, W.I.4
-
4
-
-
0018604964
-
Pharmacokinetics of ampicillin and its prodrugs bacampicillin and pivampicillin in man
-
M. Ehrnebo, S. Nilsson, and L. O. Boreus: Pharmacokinetics of ampicillin and its prodrugs bacampicillin and pivampicillin in man. J. Pharmacokinet. Biopharm. 7, 429-451 (1979).
-
(1979)
J. Pharmacokinet. Biopharm.
, vol.7
, pp. 429-451
-
-
Ehrnebo, M.1
Nilsson, S.2
Boreus, L.O.3
-
5
-
-
0020403483
-
Enalapril maleate and a lysine analogue (MK-521): Disposition in man
-
E. H. Ulm, M. Hichens, H. J. Gomez, A. E. Till, E. Hand, T. C. Vassil, J. Biollaz, H. R. Brunner, and J. L. Schelling: Enalapril maleate and a lysine analogue (MK-521): disposition in man. Br. J. Clin. Pharmacol. 14, 357-362 (1982).
-
(1982)
Br. J. Clin. Pharmacol.
, vol.14
, pp. 357-362
-
-
Ulm, E.H.1
Hichens, M.2
Gomez, H.J.3
Till, A.E.4
Hand, E.5
Vassil, T.C.6
Biollaz, J.7
Brunner, H.R.8
Schelling, J.L.9
-
6
-
-
0023948145
-
Disposition of fosinopril sodium in healthy subjects
-
S. M. Singhvi, K. L. Duchin, R. A. Morrison, D. A. Willard, D. W. Everett, and M. Frantz: Disposition of fosinopril sodium in healthy subjects. Br. J. Clin. Pharmacol 25, 9-15 (1988).
-
(1988)
Br. J. Clin. Pharmacol
, vol.25
, pp. 9-15
-
-
Singhvi, S.M.1
Duchin, K.L.2
Morrison, R.A.3
Willard, D.A.4
Everett, D.W.5
Frantz, M.6
-
7
-
-
0029015068
-
A novel series of orally active antiplatelet agents
-
J. A. Zablocki, F. S. Tjoeng, P. R. Bovy, M. Miyano, R. B. Garland, K. Williams, L. Schretzman, M. E. Zupec, J. G. Rico, R. J. Lindmark, M. V. Toth, D. E. McMackins, S. P. Adams, S. G. Panzer-Knodle, N. S. Nicholson, B. B. Taite, A. K. Salyers, L. W. King, J. G. Campion, and L. P. Feigen: A novel series of orally active antiplatelet agents. Bioorgan. Med. Chem. 3, 539-551 (1995).
-
(1995)
Bioorgan. Med. Chem.
, vol.3
, pp. 539-551
-
-
Zablocki, J.A.1
Tjoeng, F.S.2
Bovy, P.R.3
Miyano, M.4
Garland, R.B.5
Williams, K.6
Schretzman, L.7
Zupec, M.E.8
Rico, J.G.9
Lindmark, R.J.10
Toth, M.V.11
McMackins, D.E.12
Adams, S.P.13
Panzer-Knodle, S.G.14
Nicholson, N.S.15
Taite, B.B.16
Salyers, A.K.17
King, L.W.18
Campion, J.G.19
Feigen, L.P.20
more..
-
8
-
-
84951599649
-
Design of prodrugs through consideration of enzyme-substrate specificities
-
(E. B. Roche, ed.), American Pharmaceutical Association Academy of Pharmaceutical Sciences, Washington, D.C.
-
G. L. Amidon, R. S. Pearlman, and G. D. Leesman: Design of prodrugs through consideration of enzyme-substrate specificities. In "Design of Biopharmaceutical Properties through Prodrugs and Analogs" (E. B. Roche, ed.), pp. 281-315. American Pharmaceutical Association Academy of Pharmaceutical Sciences, Washington, D.C., 1977.
-
(1977)
Design of Biopharmaceutical Properties Through Prodrugs and Analogs
, pp. 281-315
-
-
Amidon, G.L.1
Pearlman, R.S.2
Leesman, G.D.3
-
9
-
-
0027472110
-
Prodrugs of peptides. 18. Synthesis and evaluation of various esters of desmopressin (dDAVP)
-
A.M. Kahns, A. Buur, and H. Bundgaard: Prodrugs of peptides. 18. Synthesis and evaluation of various esters of desmopressin (dDAVP). Pharmacol. Res. 10, 68-74 (1993).
-
(1993)
Pharmacol. Res.
, vol.10
, pp. 68-74
-
-
Kahns, A.M.1
Buur, A.2
Bundgaard, H.3
-
10
-
-
0023614883
-
Possible physiological roles of carboxylic ester hydrolases
-
F.-J. Leinweber: Possible physiological roles of carboxylic ester hydrolases. Drug Metab. Rev. 18, 379-439 (1987).
-
(1987)
Drug Metab. Rev.
, vol.18
, pp. 379-439
-
-
Leinweber, F.-J.1
-
11
-
-
0021996062
-
Clinical significance of esterases in man
-
F. M. Williams: Clinical significance of esterases in man. Clin. Pharmacokinet. 10, 392-403 (1985).
-
(1985)
Clin. Pharmacokinet.
, vol.10
, pp. 392-403
-
-
Williams, F.M.1
-
12
-
-
0014736282
-
Intestinal drug absorption and metabolism. I. Comparison of methods and models to study physiological factors of in vitro and in vivo intestinal absorption
-
W. H. Barr and S. Riegelman: Intestinal drug absorption and metabolism. I. Comparison of methods and models to study physiological factors of in vitro and in vivo intestinal absorption. J. Pharm Sci. 59, 154-163 (1970).
-
(1970)
J. Pharm Sci.
, vol.59
, pp. 154-163
-
-
Barr, W.H.1
Riegelman, S.2
-
13
-
-
0028793072
-
(+)-Bufuralol 1′-hydroxylase activity in human and rhesus monkey intestine and liver
-
T. Prueksaritanont, L. M. Dwyer, and A. E. Cribb: (+)-Bufuralol 1′-hydroxylase activity in human and rhesus monkey intestine and liver. Biochem. Pharmacol. 50, 1521-1525 (1995).
-
(1995)
Biochem. Pharmacol.
, vol.50
, pp. 1521-1525
-
-
Prueksaritanont, T.1
Dwyer, L.M.2
Cribb, A.E.3
-
14
-
-
71849104860
-
Protein measurement with the Folin phenol reagent
-
O. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randall: Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193, 265-275 (1951).
-
(1951)
J. Biol. Chem.
, vol.193
, pp. 265-275
-
-
Lowry, O.H.1
Rosebrough, N.J.2
Farr, A.L.3
Randall, R.J.4
-
15
-
-
0018606615
-
Noncompartmental determination of the steady-state volume of distribution
-
L. Z. Benet and R. L. Galeazzi: Noncompartmental determination of the steady-state volume of distribution. J. Pharm. Sci. 68, 1071-1074 (1979).
-
(1979)
J. Pharm. Sci.
, vol.68
, pp. 1071-1074
-
-
Benet, L.Z.1
Galeazzi, R.L.2
-
16
-
-
0026457407
-
Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction
-
M. F. Hebert, J. P. Roberts, T. Prueksaritanont, and L. Z. Benet: Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction. Clin. Pharmacol. Ther. 52, 453-457 (1992).
-
(1992)
Clin. Pharmacol. Ther.
, vol.52
, pp. 453-457
-
-
Hebert, M.F.1
Roberts, J.P.2
Prueksaritanont, T.3
Benet, L.Z.4
-
17
-
-
0017335453
-
Prediction of hepatic extraction from in vitro measurement of intrinsic clearance
-
A. Rane, G. R. Wilkinson, and D. G. Shand: Prediction of hepatic extraction from in vitro measurement of intrinsic clearance. J. Pharmacol. Exp. Ther. 200, 420-424 (1977).
-
(1977)
J. Pharmacol. Exp. Ther.
, vol.200
, pp. 420-424
-
-
Rane, A.1
Wilkinson, G.R.2
Shand, D.G.3
-
18
-
-
0029114038
-
Species differences in the metabolism of a potent HIV-1 reverse transcriptase inhibitor L-738,372: In vivo and in vitro studies in rats, dogs, monkeys, and humans
-
T. Prueksaritanont, S. K. Balani, L. M. Dwyer, J. D. Ellis, L. R. Kauffman, S. L. Varga, S. M. Pitzenberger, and A. D. Theoharides: Species differences in the metabolism of a potent HIV-1 reverse transcriptase inhibitor L-738,372: in vivo and in vitro studies in rats, dogs, monkeys, and humans. Drug Melab. Dispos. 23, 688-695 (1995).
-
(1995)
Drug Melab. Dispos.
, vol.23
, pp. 688-695
-
-
Prueksaritanont, T.1
Balani, S.K.2
Dwyer, L.M.3
Ellis, J.D.4
Kauffman, L.R.5
Varga, S.L.6
Pitzenberger, S.M.7
Theoharides, A.D.8
-
20
-
-
0015342479
-
Relative amounts of hepatic and renal carboxylesterase in mammalian species
-
D. J. Ecobichon: Relative amounts of hepatic and renal carboxylesterase in mammalian species. Res. Commun. Chem. Pathol. Pharmacol. 3, 629-636 (1972).
-
(1972)
Res. Commun. Chem. Pathol. Pharmacol.
, vol.3
, pp. 629-636
-
-
Ecobichon, D.J.1
-
21
-
-
0029998275
-
Comparative studies of drug metabolizing enzymes in dog, monkey and human small intestines and in Caco-2 cells
-
T. Prueksaritanont, L. M. Gorham, J. Hochman, L. Trans, and K. P. Vyas: Comparative studies of drug metabolizing enzymes in dog, monkey and human small intestines and in Caco-2 cells. Drug Metab. Dispos. 24, 634-642 (1996).
-
(1996)
Drug Metab. Dispos.
, vol.24
, pp. 634-642
-
-
Prueksaritanont, T.1
Gorham, L.M.2
Hochman, J.3
Trans, L.4
Vyas, K.P.5
-
22
-
-
0028342648
-
Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance
-
J.B. Houston: Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance. Biochem. Pharmacol. 47, 1469-1479 (1994).
-
(1994)
Biochem. Pharmacol.
, vol.47
, pp. 1469-1479
-
-
Houston, J.B.1
-
23
-
-
0018967595
-
Interspecies variation in liver weight, hepatic blood flow, and antipyrine intrinsic clearance: Extrapolation of data to benzodiazepines and phenytoin
-
H. Boxenbaum: Interspecies variation in liver weight, hepatic blood flow, and antipyrine intrinsic clearance: extrapolation of data to benzodiazepines and phenytoin. J. Pharmacokinet. Biopharmacol. 8, 165-176 (1980).
-
(1980)
J. Pharmacokinet. Biopharmacol.
, vol.8
, pp. 165-176
-
-
Boxenbaum, H.1
-
24
-
-
0025132942
-
Caco-2 cell monolayer as a model for drug transport across the intestinal mucosa
-
A. R. Hilgers, R. A. Conradi, and P. S. Burton: Caco-2 cell monolayer as a model for drug transport across the intestinal mucosa. Pharmacol. Res. 7, 902-910 (1990).
-
(1990)
Pharmacol. Res.
, vol.7
, pp. 902-910
-
-
Hilgers, A.R.1
Conradi, R.A.2
Burton, P.S.3
-
25
-
-
0025804183
-
Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells
-
P. Artursson and J. Karlsson: Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells. Biochem. Biophys. Res. Commun. 175, 880-885 (1991).
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.175
, pp. 880-885
-
-
Artursson, P.1
Karlsson, J.2
-
26
-
-
0025357347
-
Reevaluation of the absorption of carbenoxolone using an in situ rat intestinal technique
-
J. Banchard and L. M. Tang: Reevaluation of the absorption of carbenoxolone using an in situ rat intestinal technique. J. Pharm. Sci. 79, 411-414 (1990).
-
(1990)
J. Pharm. Sci.
, vol.79
, pp. 411-414
-
-
Banchard, J.1
Tang, L.M.2
-
27
-
-
0029865476
-
Effects of structural modifications on the intestinal permeability of angiotensin II receptor antagonists and the correlation of in vitro, in situ, and in vivo absorption
-
M. D. Ribadeneira, B. J. Aungst, C. J. Eyermann, and S.-M. Huang: Effects of structural modifications on the intestinal permeability of angiotensin II receptor antagonists and the correlation of in vitro, in situ, and in vivo absorption. Pharm. Res. 13, 227-233 (1996).
-
(1996)
Pharm. Res.
, vol.13
, pp. 227-233
-
-
Ribadeneira, M.D.1
Aungst, B.J.2
Eyermann, C.J.3
Huang, S.-M.4
-
28
-
-
0021926518
-
The area under the curve of metabolites for drugs and metabolites cleared by the liver and extrahepatic organs
-
P. J. M. Klippert and J. Noordhoek: The area under the curve of metabolites for drugs and metabolites cleared by the liver and extrahepatic organs. Drug Metab. Dispos. 13, 97-101 (1985).
-
(1985)
Drug Metab. Dispos.
, vol.13
, pp. 97-101
-
-
Klippert, P.J.M.1
Noordhoek, J.2
|