-
1
-
-
0031786518
-
Linear correlation of the fraction of oral dose absorbed of 64 drugs between humans and rats
-
Chiou, W. L.; Barve, A. Linear correlation of the fraction of oral dose absorbed of 64 drugs between humans and rats. Pharm. Res. 1998, 15, 1792-1795.
-
(1998)
Pharm. Res
, vol.15
, pp. 1792-1795
-
-
Chiou, W.L.1
Barve, A.2
-
2
-
-
0034017007
-
Evaluation of using dogs as an animal model to study the fraction of oral dose absorbed of 43 drugs in humans
-
Chiou, W. L.; Jeomg, H. Y.; Chung, S. M.; Wu, T. C. Evaluation of using dogs as an animal model to study the fraction of oral dose absorbed of 43 drugs in humans. Pharm. Res. 2000, 17, 135-140.
-
(2000)
Pharm. Res
, vol.17
, pp. 135-140
-
-
Chiou, W.L.1
Jeomg, H.Y.2
Chung, S.M.3
Wu, T.C.4
-
3
-
-
0036296060
-
Comparison of oral absorption and bioavailability of drugs between monkey and human
-
Chiou, W. L.; Buehler, P. W. Comparison of oral absorption and bioavailability of drugs between monkey and human. Pharm. Res. 2002, 19, 868-874.
-
(2002)
Pharm. Res
, vol.19
, pp. 868-874
-
-
Chiou, W.L.1
Buehler, P.W.2
-
4
-
-
0022623781
-
Comparison of gastrointestinal pH in dogs and humans: Implications on the use of the beagle dog as a model for oral absorption in humans
-
Lui, C. Y.; Amidon, G. L.; Berardi, R. R.; Fleisher, D.; Youngberg, C.; Dressman, J. B. Comparison of gastrointestinal pH in dogs and humans: implications on the use of the beagle dog as a model for oral absorption in humans. J. Pharm. Sci. 1986, 75, 271-274.
-
(1986)
J. Pharm. Sci
, vol.75
, pp. 271-274
-
-
Lui, C.Y.1
Amidon, G.L.2
Berardi, R.R.3
Fleisher, D.4
Youngberg, C.5
Dressman, J.B.6
-
5
-
-
0025667024
-
Gastric acidity-dependent bioavailability of commercial sustained release preparations of indomethacin, evaluated by gastric acidity-controlled beagle dogs
-
Yamada, I.; Goda, T.; Kawata, M.; Shiotoki, T.; Ogawa, K. Gastric acidity-dependent bioavailability of commercial sustained release preparations of indomethacin, evaluated by gastric acidity-controlled beagle dogs. Chem. Pharm. Bull. 1990, 38, 3112-3115.
-
(1990)
Chem. Pharm. Bull
, vol.38
, pp. 3112-3115
-
-
Yamada, I.1
Goda, T.2
Kawata, M.3
Shiotoki, T.4
Ogawa, K.5
-
6
-
-
0031737097
-
Different absorption profiles of deramciclane in man and in dog
-
Kanarva, H.; Klebovich, I.; Drabant, S.; Urtti, A.; Nevalainen, T. Different absorption profiles of deramciclane in man and in dog. J. Pharm. Pharmacol. 1998, 50, 1087-1093.
-
(1998)
J. Pharm. Pharmacol
, vol.50
, pp. 1087-1093
-
-
Kanarva, H.1
Klebovich, I.2
Drabant, S.3
Urtti, A.4
Nevalainen, T.5
-
7
-
-
0025064788
-
Gastrointestinal absorption of chlorothiazide: Evaluation of a method using salicylazosulfapyridine and acetaminophen as the marker compounds of the gastrointestinal transit time in beagle dog
-
Mizuta, H.; Kawazoe, Y.; Ogawa, K. Gastrointestinal absorption of chlorothiazide: Evaluation of a method using salicylazosulfapyridine and acetaminophen as the marker compounds of the gastrointestinal transit time in beagle dog. Chem. Pharm. Bull. 1990, 38, 2810-2813.
-
(1990)
Chem. Pharm. Bull
, vol.38
, pp. 2810-2813
-
-
Mizuta, H.1
Kawazoe, Y.2
Ogawa, K.3
-
8
-
-
0022966980
-
Comparison of canine and human gastrointestinal physiology
-
Dressman, J. B. Comparison of canine and human gastrointestinal physiology. Pharm. Res. 1986, 3, 123-131.
-
(1986)
Pharm. Res
, vol.3
, pp. 123-131
-
-
Dressman, J.B.1
-
9
-
-
0031965728
-
Effects of codeine on the agitating force and gastrointestinal transit time in dogs, for use in drug absorption studies
-
Katori, N.; Aoyagi, N.; Kojoma, S. Effects of codeine on the agitating force and gastrointestinal transit time in dogs, for use in drug absorption studies. Biol. Pharm. Bull. 1998, 21, 418-420.
-
(1998)
Biol. Pharm. Bull
, vol.21
, pp. 418-420
-
-
Katori, N.1
Aoyagi, N.2
Kojoma, S.3
-
10
-
-
0037847616
-
Gastrointestinal transit of liquids in unfed cynomolgus monkeys
-
Kondo, H.; Takahashi, Y.; Watanabe, T.; Yokohama, S.; Watanabe, J. Gastrointestinal transit of liquids in unfed cynomolgus monkeys. Biopharm. Drug Dispos. 2003, 24, 131-140.
-
(2003)
Biopharm. Drug Dispos
, vol.24
, pp. 131-140
-
-
Kondo, H.1
Takahashi, Y.2
Watanabe, T.3
Yokohama, S.4
Watanabe, J.5
-
11
-
-
1542436531
-
Suitability of the cynomolgus monkey as an animal model for drug absorption studies of oral dosage forms from viewpoint of gastrointestinal physiology
-
Ikegami, K.; Tagawa, K.; Narisawa, S.; Osawa, T. Suitability of the cynomolgus monkey as an animal model for drug absorption studies of oral dosage forms from viewpoint of gastrointestinal physiology. Biol. Pharm. Bull. 2003, 26, 1442-1447.
-
(2003)
Biol. Pharm. Bull
, vol.26
, pp. 1442-1447
-
-
Ikegami, K.1
Tagawa, K.2
Narisawa, S.3
Osawa, T.4
-
12
-
-
2442680354
-
A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. I. Clearance
-
Ward, K. W.; Smith, B. R. A comprehensive quantitative and qualitative evaluation of extrapolation of intravenous pharmacokinetic parameters from rat, dog, and monkey to humans. I. Clearance. Drug Metab. Dispos. 2004, 32, 603-611.
-
(2004)
Drug Metab. Dispos
, vol.32
, pp. 603-611
-
-
Ward, K.W.1
Smith, B.R.2
-
13
-
-
33646818650
-
Marked species difference in the bioavailability of midazolam in cynomolgus monkeys and humans
-
Sakuda, S.; Akabane, T.; Teramura, T. Marked species difference in the bioavailability of midazolam in cynomolgus monkeys and humans. Xenobiotica 2006, 36, 331-340.
-
(2006)
Xenobiotica
, vol.36
, pp. 331-340
-
-
Sakuda, S.1
Akabane, T.2
Teramura, T.3
-
14
-
-
34547209778
-
Asymmetric intestinal first-pass metabolism causes minimal oral bioavailability of midazolam in cynomolgus monkey
-
Nishimura, T.; Amano, N.; Kubo, Y.; Ono, M.; Kato, Y.; Fujita, H.; Kimura, Y.; Tsuji, A. Asymmetric intestinal first-pass metabolism causes minimal oral bioavailability of midazolam in cynomolgus monkey. Drug Metab. Dispos. 2007, 35, 1275-1284.
-
(2007)
Drug Metab. Dispos
, vol.35
, pp. 1275-1284
-
-
Nishimura, T.1
Amano, N.2
Kubo, Y.3
Ono, M.4
Kato, Y.5
Fujita, H.6
Kimura, Y.7
Tsuji, A.8
-
15
-
-
0029998275
-
Comparative studies of drug-metabolizing enzymes in dog, monkey, and human small intestines, and in caco-2 cells
-
Prueksaritanont, T.; Gorham, M. L.; Hochman, H. J.; Tran, O. L.; Vyas, K. Comparative studies of drug-metabolizing enzymes in dog, monkey, and human small intestines, and in caco-2 cells. Drug Metab. Dispos. 1996, 24, 634-642.
-
(1996)
Drug Metab. Dispos
, vol.24
, pp. 634-642
-
-
Prueksaritanont, T.1
Gorham, M.L.2
Hochman, H.J.3
Tran, O.L.4
Vyas, K.5
-
16
-
-
25644458477
-
Glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4- oxazoleacetic acid (TA-1801A) in humans: Species differences in liver and intestinal microsomes
-
Kaji, H.; Kume, T. Glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4- oxazoleacetic acid (TA-1801A) in humans: species differences in liver and intestinal microsomes. Drug Metab. Pharmacokinet. 2005, 20, 206-211.
-
(2005)
Drug Metab. Pharmacokinet
, vol.20
, pp. 206-211
-
-
Kaji, H.1
Kume, T.2
-
17
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon, G. L.; Lennernäs, H.; Shah, V. P.; Crison, J. R. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 1995, 12, 413-420.
-
(1995)
Pharm. Res
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernäs, H.2
Shah, V.P.3
Crison, J.R.4
-
18
-
-
0029855969
-
Comparison between permeability coefficients in rat and human jejunum
-
Fagerholm, U.; Johansson, M.; Lennernäs, H. Comparison between permeability coefficients in rat and human jejunum. Pharm. Res. 1996, 13, 1336-1342.
-
(1996)
Pharm. Res
, vol.13
, pp. 1336-1342
-
-
Fagerholm, U.1
Johansson, M.2
Lennernäs, H.3
-
19
-
-
0030905160
-
Jejunal permeability: A comparison between the ussing chamber technique and the single-pass perfusion in humans
-
Lennernäs, H.; Nylander, S.; Ungell, A. L. Jejunal permeability: A comparison between the ussing chamber technique and the single-pass perfusion in humans. Pharm. Res. 1997, 14, 667-671.
-
(1997)
Pharm. Res
, vol.14
, pp. 667-671
-
-
Lennernäs, H.1
Nylander, S.2
Ungell, A.L.3
-
20
-
-
4644327060
-
A possibility to predict the absorbability of poorly water-soluble drugs in human based on rat intestinal permeability assessed by an in vitro chamber method
-
Watanabe, E.; Takahashi, M.; Hayashi, M. A possibility to predict the absorbability of poorly water-soluble drugs in human based on rat intestinal permeability assessed by an in vitro chamber method. Eur. J. Pharm. Biopharm. 2004, 58, 659-665.
-
(2004)
Eur. J. Pharm. Biopharm
, vol.58
, pp. 659-665
-
-
Watanabe, E.1
Takahashi, M.2
Hayashi, M.3
-
22
-
-
0027275566
-
Physiological parameters in laboratory animals and humans
-
Davies, B.; Morris, T. Physiological parameters in laboratory animals and humans. Pharm. Res. 1993, 10 (7), 1093-1095.
-
(1993)
Pharm. Res
, vol.10
, Issue.7
, pp. 1093-1095
-
-
Davies, B.1
Morris, T.2
-
23
-
-
0003495105
-
-
10th ed, Japanese ed, Hirokawa Publishing Co, Tokyo
-
Goodman, L. S.; Hardman, J. G.; Limbird, L. E. Goodman & Gilman's the Pharmacological Basis of Therapeutics; 10th ed., Japanese ed.; Hirokawa Publishing Co.: Tokyo, 2003.
-
(2003)
Goodman & Gilman's the Pharmacological Basis of Therapeutics
-
-
Goodman, L.S.1
Hardman, J.G.2
Limbird, L.E.3
-
24
-
-
33644854071
-
Tissue-specific mRNA expression profiles of human ATP-binding cassette and solute carrier transporter superfamilies
-
Nishimura, M.; Naito, S. Tissue-specific mRNA expression profiles of human ATP-binding cassette and solute carrier transporter superfamilies. Drug Metab. Pharmacokinet. 2005, 20, 452-477.
-
(2005)
Drug Metab. Pharmacokinet
, vol.20
, pp. 452-477
-
-
Nishimura, M.1
Naito, S.2
-
25
-
-
0028944202
-
Evaluation of gastrointestinal transit controlled- beagle dog as a suitable animal model for bioavailability testing of sustained-release acetaminophen dosage form
-
Yamada, K.; Furuya, A.; Akimoto, M.; Maki, T.; Suwa, T.; Ogata, H. Evaluation of gastrointestinal transit controlled- beagle dog as a suitable animal model for bioavailability testing of sustained-release acetaminophen dosage form. Int. J. Pharm. 1995, 119, 1-10.
-
(1995)
Int. J. Pharm
, vol.119
, pp. 1-10
-
-
Yamada, K.1
Furuya, A.2
Akimoto, M.3
Maki, T.4
Suwa, T.5
Ogata, H.6
-
26
-
-
0023715382
-
Estimating human oral fraction dose absorbed: A correlation using rat intestinal membrane permeability for passive and carrier-mediated compounds
-
Amidon, G. L.; Sinko, P. J.; Fleisher, D. Estimating human oral fraction dose absorbed: A correlation using rat intestinal membrane permeability for passive and carrier-mediated compounds. Pharm. Res. 1988, 5, 651-654.
-
(1988)
Pharm. Res
, vol.5
, pp. 651-654
-
-
Amidon, G.L.1
Sinko, P.J.2
Fleisher, D.3
-
27
-
-
0025804183
-
Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells
-
Artursson, P.; Karlsson, J. Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells. Biochem. Biophys. Res. Commun. 1991, 175, 880-885.
-
(1991)
Biochem. Biophys. Res. Commun
, vol.175
, pp. 880-885
-
-
Artursson, P.1
Karlsson, J.2
-
28
-
-
0034031969
-
Optimized conditions for prediction of intestinal drug permeability using Caco-2 cells
-
Yamashita, S.; Furubayashi, T.; Kataoka, M.; Sakane, T.; Sezaki, H.; Tokuda, H. Optimized conditions for prediction of intestinal drug permeability using Caco-2 cells. Eur. J. Pharm. Sci. 2000, 10, 195-204.
-
(2000)
Eur. J. Pharm. Sci
, vol.10
, pp. 195-204
-
-
Yamashita, S.1
Furubayashi, T.2
Kataoka, M.3
Sakane, T.4
Sezaki, H.5
Tokuda, H.6
-
29
-
-
0033014877
-
Net secretion of furosemide is subject to indomethacin inhibition, as observed in Caco-2 monolayers and excised rat jejunum
-
Flanagan, S. D.; Benet, L. Z. Net secretion of furosemide is subject to indomethacin inhibition, as observed in Caco-2 monolayers and excised rat jejunum. Pharm. Res. 1999, 16, 221-224.
-
(1999)
Pharm. Res
, vol.16
, pp. 221-224
-
-
Flanagan, S.D.1
Benet, L.Z.2
-
30
-
-
0036166635
-
Comparion of furosemide and vinblastine secretion from cell line overexpressing multidrug resintance protein (P-glycoprotein) and multidrug resintance-associated protein (MRP1 and MRP2)
-
Flanagan, S. D.; Cummins, C. L.; Susanto, M.; Liu, X.; Takahashi, L. H.; Benet, L. Z. Comparion of furosemide and vinblastine secretion from cell line overexpressing multidrug resintance protein (P-glycoprotein) and multidrug resintance-associated protein (MRP1 and MRP2). Pharmacology 2002, 64, 126-134.
-
(2002)
Pharmacology
, vol.64
, pp. 126-134
-
-
Flanagan, S.D.1
Cummins, C.L.2
Susanto, M.3
Liu, X.4
Takahashi, L.H.5
Benet, L.Z.6
-
31
-
-
0037260573
-
Impact of MRP2 on the biliary excretion and intestinal absorption of furosemide, probenicid, and methotrexate using eisai hyperbilirubinemic rats
-
Chen, C.; Scott, D.; Hanson, E.; Franco, J.; Berryman, E.; Volberg, M.; Liu, X. Impact of MRP2 on the biliary excretion and intestinal absorption of furosemide, probenicid, and methotrexate using eisai hyperbilirubinemic rats. Pharm. Res. 2003, 20, 31-37.
-
(2003)
Pharm. Res
, vol.20
, pp. 31-37
-
-
Chen, C.1
Scott, D.2
Hanson, E.3
Franco, J.4
Berryman, E.5
Volberg, M.6
Liu, X.7
-
32
-
-
0021917028
-
Quantitative account of propranolol metabolism in urine of normal man
-
Walle, T.; Walle, U. K.; Olanoff, L. S. Quantitative account of propranolol metabolism in urine of normal man. Drug Metab. Dispos. 1985, 13, 204-209.
-
(1985)
Drug Metab. Dispos
, vol.13
, pp. 204-209
-
-
Walle, T.1
Walle, U.K.2
Olanoff, L.S.3
-
33
-
-
0028020099
-
Cytochrome P450 isozymes involved in propranolol metabolism in human liver microsomes. The role of CYP2D6 as ring-hydroxylase and CYP1A2 as N-desisopropylase
-
Masubuchi, Y.; Hosokawa, S.; Horie, T.; Suzuki, T.; Ohmori, S.; Kitada, M.; Narimatsu, S. Cytochrome P450 isozymes involved in propranolol metabolism in human liver microsomes. The role of CYP2D6 as ring-hydroxylase and CYP1A2 as N-desisopropylase. Drug Metab. Dispos. 1994, 22, 909-915.
-
(1994)
Drug Metab. Dispos
, vol.22
, pp. 909-915
-
-
Masubuchi, Y.1
Hosokawa, S.2
Horie, T.3
Suzuki, T.4
Ohmori, S.5
Kitada, M.6
Narimatsu, S.7
-
35
-
-
33747814457
-
Prominent but reverse stereoselectivity in propranolol glucuronidation by UDP-glucuronosyltransferases 1A9 and 1A10
-
Sten, T.; Qvisen, S.; Uutela, P.; Luukkanen, L.; Kostiainen, R.; Finel, M. Prominent but reverse stereoselectivity in propranolol glucuronidation by UDP-glucuronosyltransferases 1A9 and 1A10. Drug Metab. Dispos. 2006, 34, 1488-1494.
-
(2006)
Drug Metab. Dispos
, vol.34
, pp. 1488-1494
-
-
Sten, T.1
Qvisen, S.2
Uutela, P.3
Luukkanen, L.4
Kostiainen, R.5
Finel, M.6
-
36
-
-
0014286598
-
Thiry-Vella dog as a biological model for drug absorption from the intestinal mucosa
-
Sample, R. G.; Rossi, G. V.; Packman, E. W. Thiry-Vella dog as a biological model for drug absorption from the intestinal mucosa. J. Pharm. Sci. 1968, 57, 759-798.
-
(1968)
J. Pharm. Sci
, vol.57
, pp. 759-798
-
-
Sample, R.G.1
Rossi, G.V.2
Packman, E.W.3
-
37
-
-
0027254888
-
Pharmacokinetics of naproxen, its metabolite O-desmethylnaproxen, and their acyl glucuronides in humans
-
Vree, T. B.; van den Biggelaar-Martea, M.; Verwey-van Wissen, C. P.; Vree, J. B.; Guelen, P. Pharmacokinetics of naproxen, its metabolite O-desmethylnaproxen, and their acyl glucuronides in humans. Biopharm. Drug Dispos. 1993, 14, 491-502.
-
(1993)
Biopharm. Drug Dispos
, vol.14
, pp. 491-502
-
-
Vree, T.B.1
van den Biggelaar-Martea, M.2
Verwey-van Wissen, C.P.3
Vree, J.B.4
Guelen, P.5
-
38
-
-
0041664961
-
Regional transport and metabolism of ropivacaine and its CYP3A4 metabolite PPX in human intestine
-
Berggren, S.; Lennernäs, P.; Ekelund, M.; Westom, B.; Hoogstraate, J.; Lennernäs, H. Regional transport and metabolism of ropivacaine and its CYP3A4 metabolite PPX in human intestine. J. Pharm. Pharmacol. 2003, 55, 963-972.
-
(2003)
J. Pharm. Pharmacol
, vol.55
, pp. 963-972
-
-
Berggren, S.1
Lennernäs, P.2
Ekelund, M.3
Westom, B.4
Hoogstraate, J.5
Lennernäs, H.6
-
39
-
-
0035675648
-
The impact of P-glycoprotein efflux on enterocyte residence time and enterocyte-based metabolism of verapamil
-
Johnson, B. M.; Charman, W. N.; Porter, C. J. The impact of P-glycoprotein efflux on enterocyte residence time and enterocyte-based metabolism of verapamil. J. Pharm. Pharmacol. 2001, 53, 1611-1619.
-
(2001)
J. Pharm. Pharmacol
, vol.53
, pp. 1611-1619
-
-
Johnson, B.M.1
Charman, W.N.2
Porter, C.J.3
-
40
-
-
0023488459
-
Glucuronidation in vitro and in vivo. Comparison of intestinal and hepatic conjugation of morphine, naloxone, and buprenorphine
-
Mistry, M.; Houston, J. B. Glucuronidation in vitro and in vivo. Comparison of intestinal and hepatic conjugation of morphine, naloxone, and buprenorphine. Drug Metab. Dispos. 1987, 15, 710-717.
-
(1987)
Drug Metab. Dispos
, vol.15
, pp. 710-717
-
-
Mistry, M.1
Houston, J.B.2
-
41
-
-
0035209568
-
The role of hepatic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism
-
Fisher, M. B.; Paine, M. F.; Strelevitz, T. J.; Wrighton, S. A. The role of hepatic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism. Drug Metab. Rev. 2001, 33, 273-297.
-
(2001)
Drug Metab. Rev
, vol.33
, pp. 273-297
-
-
Fisher, M.B.1
Paine, M.F.2
Strelevitz, T.J.3
Wrighton, S.A.4
-
42
-
-
34250329999
-
Intestinal UGTs as potential modifiers of pharmacokinetics and biological responses to drugs and xenobiotics
-
Ritter, J. K. Intestinal UGTs as potential modifiers of pharmacokinetics and biological responses to drugs and xenobiotics. Expert Opin. Drug Metab. Toxcol. 2007, 3, 93-107.
-
(2007)
Expert Opin. Drug Metab. Toxcol
, vol.3
, pp. 93-107
-
-
Ritter, J.K.1
|