-
1
-
-
0032883045
-
Effects of food on clinical pharmacokinetics
-
Singh B.N. Effects of food on clinical pharmacokinetics. Clin. Pharmacokinet. 37 (1999) 213-255
-
(1999)
Clin. Pharmacokinet.
, vol.37
, pp. 213-255
-
-
Singh, B.N.1
-
2
-
-
0242288522
-
Dietary effects on drug metabolism and transport
-
Harris R.Z., Jang G.R., and Tsunoda S. Dietary effects on drug metabolism and transport. Clin. Pharmacokinet. 42 (2003) 1071-1088
-
(2003)
Clin. Pharmacokinet.
, vol.42
, pp. 1071-1088
-
-
Harris, R.Z.1
Jang, G.R.2
Tsunoda, S.3
-
4
-
-
33845467297
-
Predicting pharmacokinetic food effects using biorelevant solubility media and physiologically based modeling
-
Jones H.M., Parrott N., Ohlenbusch G., and Lavé T. Predicting pharmacokinetic food effects using biorelevant solubility media and physiologically based modeling. Clin. Pharmacokinet. 45 (2006) 1213-1226
-
(2006)
Clin. Pharmacokinet.
, vol.45
, pp. 1213-1226
-
-
Jones, H.M.1
Parrott, N.2
Ohlenbusch, G.3
Lavé, T.4
-
5
-
-
33847632169
-
Development and validation of a preclinical food effect model
-
Lentz K.A., Quitko M., Morgan D.G., Grace J.E., Gleason C., and Marathe P.H. Development and validation of a preclinical food effect model. J. Pharm. Sci. 96 (2007) 459-472
-
(2007)
J. Pharm. Sci.
, vol.96
, pp. 459-472
-
-
Lentz, K.A.1
Quitko, M.2
Morgan, D.G.3
Grace, J.E.4
Gleason, C.5
Marathe, P.H.6
-
6
-
-
33747759752
-
Biorelevant dissolution media as a predictive tool for glyburide a class II drug
-
Wei H., and Löbenberg R. Biorelevant dissolution media as a predictive tool for glyburide a class II drug. Eur. J. Pharm. Sci. 29 (2006) 45-52
-
(2006)
Eur. J. Pharm. Sci.
, vol.29
, pp. 45-52
-
-
Wei, H.1
Löbenberg, R.2
-
7
-
-
33748936522
-
Effect of food intake on the oral absorption of poorly water-soluble drugs: in vitro assessment of drug dissolution and permeation assay system
-
Kataoka M., Masaoka Y., Sakuma S., and Yamashita S. Effect of food intake on the oral absorption of poorly water-soluble drugs: in vitro assessment of drug dissolution and permeation assay system. J. Pharm. Sci. 95 (2006) 2051-2061
-
(2006)
J. Pharm. Sci.
, vol.95
, pp. 2051-2061
-
-
Kataoka, M.1
Masaoka, Y.2
Sakuma, S.3
Yamashita, S.4
-
8
-
-
0028948839
-
A theoretical basis for a biopharmaceutics drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon G.L., Lennernas H., Shah V.P., and Crison J.R. A theoretical basis for a biopharmaceutics drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 12 (1995) 413-420
-
(1995)
Pharm. Res.
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
10
-
-
17644380257
-
Predicting drug disposition via application of BCS: transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system
-
Wu C.-Y., and Benet L.Z. Predicting drug disposition via application of BCS: transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm. Res. 22 (2005) 11-23
-
(2005)
Pharm. Res.
, vol.22
, pp. 11-23
-
-
Wu, C.-Y.1
Benet, L.Z.2
-
11
-
-
0030797273
-
Human jejunal effective permeability and its correlation with preclinical drug absorption models
-
Lennernas H. Human jejunal effective permeability and its correlation with preclinical drug absorption models. J. Pharm. Pharmacol. 49 (1997) 627-638
-
(1997)
J. Pharm. Pharmacol.
, vol.49
, pp. 627-638
-
-
Lennernas, H.1
-
12
-
-
0032217095
-
The fundamental variables of the biopharmaceutics classification system (BCS): a commentary
-
van de Waterbeemd H. The fundamental variables of the biopharmaceutics classification system (BCS): a commentary. Eur. J. Pharm. Sci. 7 (1998) 1-3
-
(1998)
Eur. J. Pharm. Sci.
, vol.7
, pp. 1-3
-
-
van de Waterbeemd, H.1
-
13
-
-
0033407634
-
The biopharmaceutics classification system (BCS): class III drugs-better candidates for BA/BE waiver?
-
Blume H.H., and Schug B.S. The biopharmaceutics classification system (BCS): class III drugs-better candidates for BA/BE waiver?. Eur. J. Pharm. Sci. 9 (1999) 117-121
-
(1999)
Eur. J. Pharm. Sci.
, vol.9
, pp. 117-121
-
-
Blume, H.H.1
Schug, B.S.2
-
14
-
-
0032927254
-
Drug, meal and formulation interactions influencing drug absorption after oral administration, clinical implications
-
Fleisher D., Li C., Zhou Y., Pao L.H., and Karim A. Drug, meal and formulation interactions influencing drug absorption after oral administration, clinical implications. Clin. Pharmacokinet. 36 (1999) 233-254
-
(1999)
Clin. Pharmacokinet.
, vol.36
, pp. 233-254
-
-
Fleisher, D.1
Li, C.2
Zhou, Y.3
Pao, L.H.4
Karim, A.5
-
15
-
-
0343527392
-
Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards
-
Löbenberg R., and Amidon G.L. Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. Eur. J. Pharm. Biopharm. 50 (2000) 3-12
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 3-12
-
-
Löbenberg, R.1
Amidon, G.L.2
-
16
-
-
0035468033
-
Physicochemical profiling (solubility, permeability and charge state)
-
Avdeef A. Physicochemical profiling (solubility, permeability and charge state). Curr. Top. Med. Chem. 1 (2001) 277-351
-
(2001)
Curr. Top. Med. Chem.
, vol.1
, pp. 277-351
-
-
Avdeef, A.1
-
17
-
-
0035157333
-
Effect of common excipients on Caco-2 transport of low-permeability drugs
-
Rege B.D., Yu L.X., Hussain A.S., and Polli J.E. Effect of common excipients on Caco-2 transport of low-permeability drugs. J. Pharm. Sci. 90 (2001) 1776-1786
-
(2001)
J. Pharm. Sci.
, vol.90
, pp. 1776-1786
-
-
Rege, B.D.1
Yu, L.X.2
Hussain, A.S.3
Polli, J.E.4
-
18
-
-
0035048583
-
Compound mixtures in Caco-2 cell permeability screens as a means to increase screening capacity
-
Tannergren C., Langguth P., and Hoffmann K.J. Compound mixtures in Caco-2 cell permeability screens as a means to increase screening capacity. Pharmazie 56 (2001) 337-342
-
(2001)
Pharmazie
, vol.56
, pp. 337-342
-
-
Tannergren, C.1
Langguth, P.2
Hoffmann, K.J.3
-
19
-
-
0036240009
-
Report on the International Workshop on the Biopharmaceutics Classification System (BCS): scientific and regulatory aspects in practice
-
Kanfer I. Report on the International Workshop on the Biopharmaceutics Classification System (BCS): scientific and regulatory aspects in practice. J. Pharm. Pharm. Sci. 5 (2002) 1-4
-
(2002)
J. Pharm. Pharm. Sci.
, vol.5
, pp. 1-4
-
-
Kanfer, I.1
-
20
-
-
0036118602
-
The effect of amiloride on the in vivo effective permeability of amoxicillin in human jejunum: experience from a regional perfusion technique
-
Lennernas H., Knutson L., Knutson T., Hussain A., Lesko L., Salmonson T., and Amidon G.L. The effect of amiloride on the in vivo effective permeability of amoxicillin in human jejunum: experience from a regional perfusion technique. Eur. J. Pharm. Sci. 15 (2002) 271-277
-
(2002)
Eur. J. Pharm. Sci.
, vol.15
, pp. 271-277
-
-
Lennernas, H.1
Knutson, L.2
Knutson, T.3
Hussain, A.4
Lesko, L.5
Salmonson, T.6
Amidon, G.L.7
-
21
-
-
0036000312
-
A mechanistic approach to understanding the factors affecting drug absorption: a review of fundamentals
-
Martinez M.N., and Amidon G.L. A mechanistic approach to understanding the factors affecting drug absorption: a review of fundamentals. J. Clin. Pharmacol. 42 (2002) 620-643
-
(2002)
J. Clin. Pharmacol.
, vol.42
, pp. 620-643
-
-
Martinez, M.N.1
Amidon, G.L.2
-
22
-
-
0036224723
-
Optimized conditions for MDCK permeability and turbidimetric solubility studies using compounds representative of BCS classes I-IV
-
Taub M.E., Kristensen L., and Frokjaer S. Optimized conditions for MDCK permeability and turbidimetric solubility studies using compounds representative of BCS classes I-IV. Eur. J. Pharm. Sci. 15 (2002) 331-340
-
(2002)
Eur. J. Pharm. Sci.
, vol.15
, pp. 331-340
-
-
Taub, M.E.1
Kristensen, L.2
Frokjaer, S.3
-
23
-
-
0035997323
-
Biopharmaceutics classification system: the scientific basis for biowaiver extensions
-
Yu L.X., Amidon G.L., Polli J.E., Zhao H., Mehta M.U., Conner D.P., Shah V.P., Lesko L.J., Chen M.L., Lee V.H., and Hussain A.S. Biopharmaceutics classification system: the scientific basis for biowaiver extensions. Pharm. Res. 19 (2002) 921-925
-
(2002)
Pharm. Res.
, vol.19
, pp. 921-925
-
-
Yu, L.X.1
Amidon, G.L.2
Polli, J.E.3
Zhao, H.4
Mehta, M.U.5
Conner, D.P.6
Shah, V.P.7
Lesko, L.J.8
Chen, M.L.9
Lee, V.H.10
Hussain, A.S.11
-
24
-
-
0037434541
-
Absorption classification of oral drugs based on molecular surface properties
-
Bergström C.A., Strafford M., Lazorova L., Avdeef A., Luthman K., and Artursson P. Absorption classification of oral drugs based on molecular surface properties. J. Med. Chem. 46 (2003) 558-570
-
(2003)
J. Med. Chem.
, vol.46
, pp. 558-570
-
-
Bergström, C.A.1
Strafford, M.2
Lazorova, L.3
Avdeef, A.4
Luthman, K.5
Artursson, P.6
-
25
-
-
0344687432
-
The effect of ketoconazole on the in vivo intestinal permeability of fexofenadine using a regional perfusion technique
-
Tannergren C., Knutson T., Knutson L., and Lennernas H. The effect of ketoconazole on the in vivo intestinal permeability of fexofenadine using a regional perfusion technique. Br. J. Clin. Pharmacol. 55 (2003) 182-190
-
(2003)
Br. J. Clin. Pharmacol.
, vol.55
, pp. 182-190
-
-
Tannergren, C.1
Knutson, T.2
Knutson, L.3
Lennernas, H.4
-
26
-
-
3843097202
-
Classification of orally administered drugs on the World Health Organization Model of Essential Medicines according to the biopharmaceutics classification system
-
Lindenberg M., Kopp S., and Dressman J.B. Classification of orally administered drugs on the World Health Organization Model of Essential Medicines according to the biopharmaceutics classification system. Eur. J. Pharm. Biopharm. 58 (2004) 265-278
-
(2004)
Eur. J. Pharm. Biopharm.
, vol.58
, pp. 265-278
-
-
Lindenberg, M.1
Kopp, S.2
Dressman, J.B.3
-
27
-
-
0037204544
-
Prediction of drug solubility from structure
-
Jorgensen W.L., and Duffy E.M. Prediction of drug solubility from structure. Adv. Drug Deliv. Rev. 54 (2002) 355-366
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 355-366
-
-
Jorgensen, W.L.1
Duffy, E.M.2
-
28
-
-
15244339914
-
In silico predictions of drug solubility and permeability: two rate-limiting barriers to oral drug absorption
-
Bergström C.A. In silico predictions of drug solubility and permeability: two rate-limiting barriers to oral drug absorption. Basic Clin. Pharmacol. Toxicol. 96 (2005) 156-161
-
(2005)
Basic Clin. Pharmacol. Toxicol.
, vol.96
, pp. 156-161
-
-
Bergström, C.A.1
-
29
-
-
33747116165
-
Computational models to predict aqueous drug solubility, permeability and intestinal absorption
-
Bergström C.A. Computational models to predict aqueous drug solubility, permeability and intestinal absorption. Expert Opin. Drug Metab. Toxicol. 1 (2005) 613-627
-
(2005)
Expert Opin. Drug Metab. Toxicol.
, vol.1
, pp. 613-627
-
-
Bergström, C.A.1
-
30
-
-
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., and Fleisher D. Estimating human oral fraction dose absorbed: a correlation using rat intestinal membrane permeability for passive and carrier-mediated compounds. Pharm. Res. 5 (1988) 651-654
-
(1988)
Pharm. Res.
, vol.5
, pp. 651-654
-
-
Amidon, G.L.1
Sinko, P.J.2
Fleisher, D.3
-
31
-
-
1442302325
-
Intestinal drug transporters: in vivo function and clinical importance
-
Kunta J.R., and Sinko P.J. Intestinal drug transporters: in vivo function and clinical importance. Curr. Drug Met. 5 (2004) 109-124
-
(2004)
Curr. Drug Met.
, vol.5
, pp. 109-124
-
-
Kunta, J.R.1
Sinko, P.J.2
-
32
-
-
34447337731
-
Prediction of human pharmacokinetics - gastrointestinal absorption
-
Fagerholm U. Prediction of human pharmacokinetics - gastrointestinal absorption. J. Pharm. Pharmacol. 59 (2007) 905-916
-
(2007)
J. Pharm. Pharmacol.
, vol.59
, pp. 905-916
-
-
Fagerholm, U.1
-
33
-
-
0029738490
-
First-pass metabolism of midazolam by the human intestine
-
Paine M.F., Shen D.D., Kunze K.L., Perkins J.D., Marsh C.L., McVicar J.P., Barr D.M., Gillies B.S., and Thummel K.E. First-pass metabolism of midazolam by the human intestine. Clin. Pharmacol. Ther. 60 (1996) 14-24
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 14-24
-
-
Paine, M.F.1
Shen, D.D.2
Kunze, K.L.3
Perkins, J.D.4
Marsh, C.L.5
McVicar, J.P.6
Barr, D.M.7
Gillies, B.S.8
Thummel, K.E.9
-
34
-
-
0035078138
-
Anatomical and physiological parameters affecting gastrointestinal absorption in humans and rats
-
DeSesso J.M., and Jacobson C.F. Anatomical and physiological parameters affecting gastrointestinal absorption in humans and rats. Food Chem. Toxicol. 39 (2001) 209-228
-
(2001)
Food Chem. Toxicol.
, vol.39
, pp. 209-228
-
-
DeSesso, J.M.1
Jacobson, C.F.2
-
35
-
-
33644847684
-
Transporters as a determinant of drug clearance and tissue distribution
-
Shitara Y., Horie T., and Sugiyama Y. Transporters as a determinant of drug clearance and tissue distribution. Eur. J. Pharm. Sci. 27 (2006) 425-446
-
(2006)
Eur. J. Pharm. Sci.
, vol.27
, pp. 425-446
-
-
Shitara, Y.1
Horie, T.2
Sugiyama, Y.3
-
36
-
-
33644684769
-
Transporters and drug discovery: why, when, and how
-
Kim R.B. Transporters and drug discovery: why, when, and how. Mol. Pharm. 3 (2005) 26-32
-
(2005)
Mol. Pharm.
, vol.3
, pp. 26-32
-
-
Kim, R.B.1
-
37
-
-
33747090656
-
Variability in mRNA expression of ABC- and SLC-transporters in human intestinal cells: comparison between human segments and Caco-2 cells
-
Seithel A., Karlsson J., Hilgendorf C., Björquist A., and Ungell A.L. Variability in mRNA expression of ABC- and SLC-transporters in human intestinal cells: comparison between human segments and Caco-2 cells. Eur. J. Pharm. Sci. 28 (2006) 291-299
-
(2006)
Eur. J. Pharm. Sci.
, vol.28
, pp. 291-299
-
-
Seithel, A.1
Karlsson, J.2
Hilgendorf, C.3
Björquist, A.4
Ungell, A.L.5
-
38
-
-
33750181267
-
Regional levels of drug transporters along the human intestinal tract: co-expression of ABC and SLC transporters and comparison with Caco-2 cells
-
Englund G., Rorsman F., Rönnblom A., Karlbom U., Lazorova L., Gråsjö J., Kindmark A., and Artursson P. Regional levels of drug transporters along the human intestinal tract: co-expression of ABC and SLC transporters and comparison with Caco-2 cells. Eur. J. Pharm. Sci. 29 (2006) 269-277
-
(2006)
Eur. J. Pharm. Sci.
, vol.29
, pp. 269-277
-
-
Englund, G.1
Rorsman, F.2
Rönnblom, A.3
Karlbom, U.4
Lazorova, L.5
Gråsjö, J.6
Kindmark, A.7
Artursson, P.8
-
39
-
-
32244434196
-
Characterization of the human upper gastrointestinal contents under conditions simulating bioavailability/bioequivalence studies
-
Kalantzi L., Goumas K., Kalioras V., Abrahamsson B., Dressman J.B., and Reppas C. Characterization of the human upper gastrointestinal contents under conditions simulating bioavailability/bioequivalence studies. Pharm. Res. 23 (2006) 165-176
-
(2006)
Pharm. Res.
, vol.23
, pp. 165-176
-
-
Kalantzi, L.1
Goumas, K.2
Kalioras, V.3
Abrahamsson, B.4
Dressman, J.B.5
Reppas, C.6
-
40
-
-
34548082187
-
Parallel monitoring of plasma and intraluminal drug concentrations in man after oral administration of fosamprenavir in the fasted and fed state
-
Brouwers J., Tack J., Lammert F., and Augustijns P. Parallel monitoring of plasma and intraluminal drug concentrations in man after oral administration of fosamprenavir in the fasted and fed state. Pharm. Res. 24 (2007) 1862-1869
-
(2007)
Pharm. Res.
, vol.24
, pp. 1862-1869
-
-
Brouwers, J.1
Tack, J.2
Lammert, F.3
Augustijns, P.4
-
41
-
-
0029825085
-
Effects of food on drug absorption
-
Welling P.G. Effects of food on drug absorption. Annu. Rev. Nutr. 16 (1996) 383-415
-
(1996)
Annu. Rev. Nutr.
, vol.16
, pp. 383-415
-
-
Welling, P.G.1
-
42
-
-
0031750861
-
Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs
-
Galia E., Nicolaides E., Hörter D., Löbenberg R., Reppas C., and Dressman J.B. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm. Res. 15 (1998) 698-705
-
(1998)
Pharm. Res.
, vol.15
, pp. 698-705
-
-
Galia, E.1
Nicolaides, E.2
Hörter, D.3
Löbenberg, R.4
Reppas, C.5
Dressman, J.B.6
-
43
-
-
0033805179
-
In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs
-
Dressman J.B., and Reppas C. In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs. Eur. J. Pharm. Sci. 11 (2000) S73-S80
-
(2000)
Eur. J. Pharm. Sci.
, vol.11
-
-
Dressman, J.B.1
Reppas, C.2
-
44
-
-
0021921239
-
Absorption of minocycline hydrochloride and tetracycline hydrochloride, effect of food, milk, and iron
-
Leyden J.J. Absorption of minocycline hydrochloride and tetracycline hydrochloride, effect of food, milk, and iron. J. Am. Acad. Dermatol. 12 (1985) 308-312
-
(1985)
J. Am. Acad. Dermatol.
, vol.12
, pp. 308-312
-
-
Leyden, J.J.1
-
45
-
-
0032909820
-
Meal composition effects on the oral bioavailability of indinavir in HIV-infected patients
-
Carver P.L., Fleisher D., Zhou S.Y., Kaul D., Kazanjian P., and Li C. Meal composition effects on the oral bioavailability of indinavir in HIV-infected patients. Pharm. Res. 16 (1999) 718-724
-
(1999)
Pharm. Res.
, vol.16
, pp. 718-724
-
-
Carver, P.L.1
Fleisher, D.2
Zhou, S.Y.3
Kaul, D.4
Kazanjian, P.5
Li, C.6
-
46
-
-
0022447519
-
Concomitant food intake can increase the bioavailability of propranolol by transient inhibition of its presystemic primary conjugation
-
Liedholm H., and Melander A. Concomitant food intake can increase the bioavailability of propranolol by transient inhibition of its presystemic primary conjugation. Clin. Pharmacol. Ther. 40 (1986) 29-36
-
(1986)
Clin. Pharmacol. Ther.
, vol.40
, pp. 29-36
-
-
Liedholm, H.1
Melander, A.2
-
47
-
-
34548178015
-
The value meal: how to save $1,700 per month or more on lapatinib
-
Ratain M.J., and Cohen E.E. The value meal: how to save $1,700 per month or more on lapatinib. J. Clin. Oncol. 25 (2007) 3397-3398
-
(2007)
J. Clin. Oncol.
, vol.25
, pp. 3397-3398
-
-
Ratain, M.J.1
Cohen, E.E.2
-
48
-
-
0036073540
-
Food-drug interactions
-
Schmidt L.E., and Dalhoff K. Food-drug interactions. Drugs. 62 (2002) 1481-1502
-
(2002)
Drugs.
, vol.62
, pp. 1481-1502
-
-
Schmidt, L.E.1
Dalhoff, K.2
-
49
-
-
0027946920
-
Design of drugs through a consideration of drug metabolism and pharmacokinetics
-
Smith D.A. Design of drugs through a consideration of drug metabolism and pharmacokinetics. Eur. J. Drug Metab. Pharmacokinet. 3 (1994) 193-199
-
(1994)
Eur. J. Drug Metab. Pharmacokinet.
, vol.3
, pp. 193-199
-
-
Smith, D.A.1
-
50
-
-
25144450046
-
Apical/basolateral surface expression of drug transporters and its role in vectorial drug transport
-
Ito K., Suzuki H., Horie T., and Sugiyama Y. Apical/basolateral surface expression of drug transporters and its role in vectorial drug transport. Pharm. Res. 22 (2005) 1559-1577
-
(2005)
Pharm. Res.
, vol.22
, pp. 1559-1577
-
-
Ito, K.1
Suzuki, H.2
Horie, T.3
Sugiyama, Y.4
-
51
-
-
0032518290
-
The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors
-
Kim R.B., Fromm M.F., Wandel C., Leake B., Wood A.J., Roden D.M., and Wilkinson G.R. The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors. J. Clin. Invest. 101 (1998) 289-294
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 289-294
-
-
Kim, R.B.1
Fromm, M.F.2
Wandel, C.3
Leake, B.4
Wood, A.J.5
Roden, D.M.6
Wilkinson, G.R.7
-
52
-
-
0034763005
-
Rational use of in vitro P-glycoprotein assays in drug discovery
-
Polli J.W., Wring S.A., Humphreys J.E., Huang L., Morgan J.B., Webster L.O., and Serabjit-Singh C.S. Rational use of in vitro P-glycoprotein assays in drug discovery. J. Pharmacol. Exp. Ther. 299 (2001) 620-628
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.299
, pp. 620-628
-
-
Polli, J.W.1
Wring, S.A.2
Humphreys, J.E.3
Huang, L.4
Morgan, J.B.5
Webster, L.O.6
Serabjit-Singh, C.S.7
-
53
-
-
0036224723
-
Optimized conditions for MDCK permeability and turbidimetric solubility studies using compounds representative of BCS classes I-IV
-
Taub M.E., Kristensen L., and Frokjaer S. Optimized conditions for MDCK permeability and turbidimetric solubility studies using compounds representative of BCS classes I-IV. Eur. J. Pharm. Sci. 15 (2002) 331-340
-
(2002)
Eur. J. Pharm. Sci.
, vol.15
, pp. 331-340
-
-
Taub, M.E.1
Kristensen, L.2
Frokjaer, S.3
-
54
-
-
0029927801
-
Transport properties are not altered across Caco-2 cells with heightened TEER despite underlying physiological and ultrastructural changes
-
Lu S., Gough A.W., Bobrowski W.F., and Stewart B.H. Transport properties are not altered across Caco-2 cells with heightened TEER despite underlying physiological and ultrastructural changes. J. Pharm. Sci. 85 (1996) 270-273
-
(1996)
J. Pharm. Sci.
, vol.85
, pp. 270-273
-
-
Lu, S.1
Gough, A.W.2
Bobrowski, W.F.3
Stewart, B.H.4
-
55
-
-
0030990079
-
In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in man-fact or myth
-
Yee S. In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in man-fact or myth. Pharm. Res. 14 (1997) 763-766
-
(1997)
Pharm. Res.
, vol.14
, pp. 763-766
-
-
Yee, S.1
-
56
-
-
0036632950
-
Studies on intestinal absorption of sulpiride (1): carrier-mediated uptake of sulpiride in the human intestinal cell line Caco-2
-
Watanabe K., Sawano T., Terada K., Endo T., Sakata M., and Sato J. Studies on intestinal absorption of sulpiride (1): carrier-mediated uptake of sulpiride in the human intestinal cell line Caco-2. Biol. Pharm. Bull. 25 (2002) 885-890
-
(2002)
Biol. Pharm. Bull.
, vol.25
, pp. 885-890
-
-
Watanabe, K.1
Sawano, T.2
Terada, K.3
Endo, T.4
Sakata, M.5
Sato, J.6
-
57
-
-
0036781112
-
Studies on intestinal absorption of sulpiride (2): transepithelial transport of sulpiride across the human intestinal cell line Caco-2
-
Watanabe K., Sawano T., Endo T., Sakata M., and Sato J. Studies on intestinal absorption of sulpiride (2): transepithelial transport of sulpiride across the human intestinal cell line Caco-2. Biol. Pharm. Bull. 25 (2002) 1345-1350
-
(2002)
Biol. Pharm. Bull.
, vol.25
, pp. 1345-1350
-
-
Watanabe, K.1
Sawano, T.2
Endo, T.3
Sakata, M.4
Sato, J.5
-
58
-
-
0036805724
-
Comparison of human duodenum and Caco-2 gene expression profiles for 12,000 gene sequences tags and correlation with permeability of 26 drugs
-
Sun D., Lennernas H., Welage L.S., Barnett J.L., Landowski C.P., Foster D., Fleisher D., Lee K.D., and Amidon G.L. Comparison of human duodenum and Caco-2 gene expression profiles for 12,000 gene sequences tags and correlation with permeability of 26 drugs. Pharm. Res. 19 (2002) 1400-1416
-
(2002)
Pharm. Res.
, vol.19
, pp. 1400-1416
-
-
Sun, D.1
Lennernas, H.2
Welage, L.S.3
Barnett, J.L.4
Landowski, C.P.5
Foster, D.6
Fleisher, D.7
Lee, K.D.8
Amidon, G.L.9
-
59
-
-
33745370633
-
Intestinal absorptive transport of the hydrophilic cation ranitidine: a kinetic modeling approach to elucidate the role of uptake and efflux transporters and paracellular vs. transcellular transport in Caco-2 cells
-
Bourdet D.L., Pollack G.M., and Thakker D.R. Intestinal absorptive transport of the hydrophilic cation ranitidine: a kinetic modeling approach to elucidate the role of uptake and efflux transporters and paracellular vs. transcellular transport in Caco-2 cells. Pharm. Res. 23 (2006) 1178-1187
-
(2006)
Pharm. Res.
, vol.23
, pp. 1178-1187
-
-
Bourdet, D.L.1
Pollack, G.M.2
Thakker, D.R.3
-
60
-
-
34547169521
-
Expression of thirty-six drug transporter genes in human intestine, liver, kidney, and organotypic cell lines
-
Hilgendorf C., Ahlin G., Seithel A., Artursson P., Ungell A.L., and Karlsson J. Expression of thirty-six drug transporter genes in human intestine, liver, kidney, and organotypic cell lines. Drug Metab. Dispos. 35 (2007) 1333-1340
-
(2007)
Drug Metab. Dispos.
, vol.35
, pp. 1333-1340
-
-
Hilgendorf, C.1
Ahlin, G.2
Seithel, A.3
Artursson, P.4
Ungell, A.L.5
Karlsson, J.6
-
61
-
-
23844510921
-
Development of stably transfected monolayer overexpressing the human apical sodium-dependent bile acid transporter (hASBT)
-
Balakrishnan A., Sussman D.J., and Polli J.E. Development of stably transfected monolayer overexpressing the human apical sodium-dependent bile acid transporter (hASBT). Pharm. Res. 22 (2005) 1269-1280
-
(2005)
Pharm. Res.
, vol.22
, pp. 1269-1280
-
-
Balakrishnan, A.1
Sussman, D.J.2
Polli, J.E.3
-
62
-
-
33745769730
-
Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug target
-
Balakrishnan A., and Polli J.E. Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug target. Mol. Pharm. 3 (2006) 223-230
-
(2006)
Mol. Pharm.
, vol.3
, pp. 223-230
-
-
Balakrishnan, A.1
Polli, J.E.2
-
63
-
-
34248202064
-
Peptide transporter substrate identification during permeability screening in drug discovery: comparison of transfected MDCK-hPepT1 cells to Caco-2 cells
-
Balimane P.V., Chong S., Patel K., Quan Y., Timoszyk J., Han Y.H., Wang B., Vig B., and Faria T.N. Peptide transporter substrate identification during permeability screening in drug discovery: comparison of transfected MDCK-hPepT1 cells to Caco-2 cells. Arch. Pharm. Res. 30 (2007) 507-518
-
(2007)
Arch. Pharm. Res.
, vol.30
, pp. 507-518
-
-
Balimane, P.V.1
Chong, S.2
Patel, K.3
Quan, Y.4
Timoszyk, J.5
Han, Y.H.6
Wang, B.7
Vig, B.8
Faria, T.N.9
-
64
-
-
15344340313
-
Citrus juices inhibit the function of human organic anion-transporting polypeptide OATP-B
-
Satoh H., Yamashita F., Tsujimoto M., Murakami H., Koyabu N., Ohtani H., and Sawada Y. Citrus juices inhibit the function of human organic anion-transporting polypeptide OATP-B. Drug Metab. Dispos. 33 (2005) 518-523
-
(2005)
Drug Metab. Dispos.
, vol.33
, pp. 518-523
-
-
Satoh, H.1
Yamashita, F.2
Tsujimoto, M.3
Murakami, H.4
Koyabu, N.5
Ohtani, H.6
Sawada, Y.7
-
65
-
-
22944446686
-
Identification of the hepatic efflux transporters of organic anions using double-transfected Madin-Darby canine kidney II cells expressing human organic anion-transporting polypeptide 1B1 (OATP1B1)/multidrug resistance-associated protein 2, OATP1B1/multidrug resistance 1, and OATP1B1/breast cancer resistance protein
-
Matsushima S., Maeda K., Kondo C., Hirano M., Sasaki M., Suzuki H., and Sugiyama Y. Identification of the hepatic efflux transporters of organic anions using double-transfected Madin-Darby canine kidney II cells expressing human organic anion-transporting polypeptide 1B1 (OATP1B1)/multidrug resistance-associated protein 2, OATP1B1/multidrug resistance 1, and OATP1B1/breast cancer resistance protein. J. Pharmacol. Exp. Ther. 314 (2005) 1059-1067
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.314
, pp. 1059-1067
-
-
Matsushima, S.1
Maeda, K.2
Kondo, C.3
Hirano, M.4
Sasaki, M.5
Suzuki, H.6
Sugiyama, Y.7
-
66
-
-
0037155204
-
Transcellular transport of organic anions across a double-transfected Madin-Darby canine kidney II cell monolayer expressing both human organic anion-transporting polypeptide (OATP2/SLC21A6) and multidrug resistance-associated protein 2 (MRP2/ABCC2)
-
Sasaki M., Suzuki H., Ito K., Abe T., and Sugiyama Y. Transcellular transport of organic anions across a double-transfected Madin-Darby canine kidney II cell monolayer expressing both human organic anion-transporting polypeptide (OATP2/SLC21A6) and multidrug resistance-associated protein 2 (MRP2/ABCC2). J. Biol. Chem. 277 (2002) 6497-6503
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 6497-6503
-
-
Sasaki, M.1
Suzuki, H.2
Ito, K.3
Abe, T.4
Sugiyama, Y.5
-
67
-
-
18044372268
-
Vectorial transport of the peptide CCK-8 by double-transfected MDCKII cells stably expressing the organic anion transporter OATP1B3 (OATP8) and the export pump ABCC2
-
Letschert K., Komatsu M., Hummel-Eisenbeiss J., and Keppler D. Vectorial transport of the peptide CCK-8 by double-transfected MDCKII cells stably expressing the organic anion transporter OATP1B3 (OATP8) and the export pump ABCC2. J. Pharmacol. Exp. Ther. 313 (2005) 549-556
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.313
, pp. 549-556
-
-
Letschert, K.1
Komatsu, M.2
Hummel-Eisenbeiss, J.3
Keppler, D.4
-
68
-
-
33747838057
-
Inhibition of bile acid transport across Na+/taurocholate cotransporting polypeptide (SLC10A1) and bile salt export pump (ABCB 11)-coexpressing LLC-PK1 cells by cholestasis-inducing drugs
-
Mita S., Suzuki H., Akita H., Hayashi H., Onuki R., Hofmann A.F., and Sugiyama Y. Inhibition of bile acid transport across Na+/taurocholate cotransporting polypeptide (SLC10A1) and bile salt export pump (ABCB 11)-coexpressing LLC-PK1 cells by cholestasis-inducing drugs. Drug Metab. Dispos. 34 (2006) 1575-1581
-
(2006)
Drug Metab. Dispos.
, vol.34
, pp. 1575-1581
-
-
Mita, S.1
Suzuki, H.2
Akita, H.3
Hayashi, H.4
Onuki, R.5
Hofmann, A.F.6
Sugiyama, Y.7
-
69
-
-
0242585000
-
Midazolam exhibits characteristics of a highly permeable P-glycoprotein substrate
-
Tolle-Sander S., Rautio J., Wring S., Polli J.W., and Polli J.E. Midazolam exhibits characteristics of a highly permeable P-glycoprotein substrate. Pharm. Res. 20 (2003) 757-764
-
(2003)
Pharm. Res.
, vol.20
, pp. 757-764
-
-
Tolle-Sander, S.1
Rautio, J.2
Wring, S.3
Polli, J.W.4
Polli, J.E.5
-
70
-
-
0036175307
-
Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4
-
Cummins C.L., Jacobsen W., and Benet L.Z. Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4. J. Pharmacol. Exp. Ther. 300 (2002) 1036-1045
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.300
, pp. 1036-1045
-
-
Cummins, C.L.1
Jacobsen, W.2
Benet, L.Z.3
-
71
-
-
0037382316
-
In vivo modulation of intestinal CYP3A metabolism by P-glycoprotein: studies using the rat single-pass intestinal perfusion model
-
Cummins C.L., Salphati L., Reid M.J., and Benet L.Z. In vivo modulation of intestinal CYP3A metabolism by P-glycoprotein: studies using the rat single-pass intestinal perfusion model. J. Pharmacol. Exp. Ther. 305 (2003) 306-314
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.305
, pp. 306-314
-
-
Cummins, C.L.1
Salphati, L.2
Reid, M.J.3
Benet, L.Z.4
-
72
-
-
0345866819
-
CYP3A4-transfected Caco-2 cells as a tool for understanding biochemical absorption barriers: studies with sirolimus and midazolam
-
Cummins C.L., Jacobsen W., Christians U., and Benet L.Z. CYP3A4-transfected Caco-2 cells as a tool for understanding biochemical absorption barriers: studies with sirolimus and midazolam. J. Pharmacol. Exp. Ther. 308 (2004) 143-155
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.308
, pp. 143-155
-
-
Cummins, C.L.1
Jacobsen, W.2
Christians, U.3
Benet, L.Z.4
-
73
-
-
27144482673
-
Glucuronidation and the transport of the glucuronide metabolites in LLC-PK1 cells
-
Chang J.H., and Benet L.Z. Glucuronidation and the transport of the glucuronide metabolites in LLC-PK1 cells. Mol. Pharm. 2 (2005) 428-434
-
(2005)
Mol. Pharm.
, vol.2
, pp. 428-434
-
-
Chang, J.H.1
Benet, L.Z.2
-
74
-
-
33846571368
-
Effect of OATP1B transporter inhibition on the pharmacokinetics of atorvastatin in healthy volunteers
-
Lau Y.Y., Huang Y., Frassetto L., and Benet L.Z. Effect of OATP1B transporter inhibition on the pharmacokinetics of atorvastatin in healthy volunteers. Clin. Pharmacol. Ther. 81 (2007) 194-204
-
(2007)
Clin. Pharmacol. Ther.
, vol.81
, pp. 194-204
-
-
Lau, Y.Y.1
Huang, Y.2
Frassetto, L.3
Benet, L.Z.4
-
75
-
-
0025337223
-
Effect of food on the pharmacokinetics of cyclosporine in healthy subjects following oral and intravenous administration
-
Gupta S.K., and Benet L.Z. Effect of food on the pharmacokinetics of cyclosporine in healthy subjects following oral and intravenous administration. J. Clin. Pharmacol. 30 (1990) 643-653
-
(1990)
J. Clin. Pharmacol.
, vol.30
, pp. 643-653
-
-
Gupta, S.K.1
Benet, L.Z.2
-
77
-
-
2342557118
-
Media to simulate the postprandial stomach I. Matching the physiochemical characteristics of standard breakfasts
-
Klein S., Butler J., Hempenstall J.M., Reppas C., and Dressman J.B. Media to simulate the postprandial stomach I. Matching the physiochemical characteristics of standard breakfasts. J. Pharm. Pharmacol. 56 (2004) 605-610
-
(2004)
J. Pharm. Pharmacol.
, vol.56
, pp. 605-610
-
-
Klein, S.1
Butler, J.2
Hempenstall, J.M.3
Reppas, C.4
Dressman, J.B.5
-
78
-
-
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., and 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. 75 (1986) 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
-
79
-
-
0030614844
-
Physiochemical and physiological mechanisms for the effects of food on drug absorption: the role of lipids and pH
-
Charman W.N., Porter C.J.H., Mithani S., and Dressman J.B. Physiochemical and physiological mechanisms for the effects of food on drug absorption: the role of lipids and pH. J. Pharm. Sci. 86 (1997) 269-282
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 269-282
-
-
Charman, W.N.1
Porter, C.J.H.2
Mithani, S.3
Dressman, J.B.4
-
80
-
-
0001297576
-
Intestinal lipid absorption
-
Johnson R. (Ed), Raven Press, New York
-
Tso P. Intestinal lipid absorption. In: Johnson R. (Ed). Physiology of the Gastrointestinal Tract (1994), Raven Press, New York 1867-1907
-
(1994)
Physiology of the Gastrointestinal Tract
, pp. 1867-1907
-
-
Tso, P.1
-
81
-
-
7044234508
-
Inhibitory effect of a bitter melon extract on the P-glycoprotein activity in intestinal Caco-2 cells
-
Konishi T., Satsu H., Hatsugai Y., Aizawa K., Inakuma T., Nagata S., Sakuda S.H., Nagasawa H., and Shimizu M. Inhibitory effect of a bitter melon extract on the P-glycoprotein activity in intestinal Caco-2 cells. Br. J. Pharmacol. 143 (2004) 379-387
-
(2004)
Br. J. Pharmacol.
, vol.143
, pp. 379-387
-
-
Konishi, T.1
Satsu, H.2
Hatsugai, Y.3
Aizawa, K.4
Inakuma, T.5
Nagata, S.6
Sakuda, S.H.7
Nagasawa, H.8
Shimizu, M.9
-
82
-
-
21544438456
-
A bitter melon extract inhibits the P-glycoprotein activity in intestinal Caco-2 cells: monoglyceride as an active compound
-
Konishi T., Satsu H., Hatsugai Y., Aizawa K., Inakuma T., Nagata S., Sakuda S.H., Nagasawa H., and Shimizu M. A bitter melon extract inhibits the P-glycoprotein activity in intestinal Caco-2 cells: monoglyceride as an active compound. Biofactors 22 (2004) 71-74
-
(2004)
Biofactors
, vol.22
, pp. 71-74
-
-
Konishi, T.1
Satsu, H.2
Hatsugai, Y.3
Aizawa, K.4
Inakuma, T.5
Nagata, S.6
Sakuda, S.H.7
Nagasawa, H.8
Shimizu, M.9
-
83
-
-
0037203703
-
Simulated intestinal fluid as transport medium in the Caco-2 cell culture model
-
Ingels F., Deferme S., Destexhe E., Oth M., Van den Mooter G., and Augustijns P. Simulated intestinal fluid as transport medium in the Caco-2 cell culture model. Int. J. Pharm. 232 (2002) 183-192
-
(2002)
Int. J. Pharm.
, vol.232
, pp. 183-192
-
-
Ingels, F.1
Deferme, S.2
Destexhe, E.3
Oth, M.4
Van den Mooter, G.5
Augustijns, P.6
-
84
-
-
33745769730
-
Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug target
-
Balakrishnan A., and Polli J.E. Apical sodium dependent bile acid transporter (ASBT, SLC10A2): a potential prodrug target. Mol. Pharm. 3 (2006) 223-230
-
(2006)
Mol. Pharm.
, vol.3
, pp. 223-230
-
-
Balakrishnan, A.1
Polli, J.E.2
-
85
-
-
2442719906
-
Unmasking the dynamic interplay between efflux transporters and metabolic enzymes
-
Benet L.Z., Cummins C.L., and Wu C.Y. Unmasking the dynamic interplay between efflux transporters and metabolic enzymes. Int. J. Pharm. 277 (2004) 3-9
-
(2004)
Int. J. Pharm.
, vol.277
, pp. 3-9
-
-
Benet, L.Z.1
Cummins, C.L.2
Wu, C.Y.3
-
86
-
-
0142106303
-
Transporter-enzyme interactions: implications for predicting drug-drug interactions from in vitro data
-
Benet L.Z., Cummins C.L., and Wu C.Y. Transporter-enzyme interactions: implications for predicting drug-drug interactions from in vitro data. Curr. Drug Metab. 4 (2003) 393-398
-
(2003)
Curr. Drug Metab.
, vol.4
, pp. 393-398
-
-
Benet, L.Z.1
Cummins, C.L.2
Wu, C.Y.3
-
87
-
-
0036159433
-
Fruit juices inhibit organic anion transporting polypeptide-mediated drug uptake to decrease the oral availability of fexofenadine
-
Dresser G.K., Bailey D.G., Leake B.F., Schwarz U.I., Dawson P.A., Freeman D.J., and Kim R.B. Fruit juices inhibit organic anion transporting polypeptide-mediated drug uptake to decrease the oral availability of fexofenadine. Clin. Pharmacol. Ther. 71 (2002) 11-20
-
(2002)
Clin. Pharmacol. Ther.
, vol.71
, pp. 11-20
-
-
Dresser, G.K.1
Bailey, D.G.2
Leake, B.F.3
Schwarz, U.I.4
Dawson, P.A.5
Freeman, D.J.6
Kim, R.B.7
-
88
-
-
0029870373
-
Effect of food on the relative bioavailability of oral ganciclovir
-
Lavelle J., Follansbee S., Trapnell C.B., Buhles W.C., Griffy K.G., Jung D., Dorr A., and Connor J. Effect of food on the relative bioavailability of oral ganciclovir. J. Clin. Pharmacol. 36 (1996) 238-241
-
(1996)
J. Clin. Pharmacol.
, vol.36
, pp. 238-241
-
-
Lavelle, J.1
Follansbee, S.2
Trapnell, C.B.3
Buhles, W.C.4
Griffy, K.G.5
Jung, D.6
Dorr, A.7
Connor, J.8
-
89
-
-
27644444751
-
A quantitative approach to probe the dependence and correlation of food-effect with aqueous solubility, dose/solubility ratio, and partition coefficient (Log P) for orally active drugs administered as immediate-release formulations
-
Singh B.N. A quantitative approach to probe the dependence and correlation of food-effect with aqueous solubility, dose/solubility ratio, and partition coefficient (Log P) for orally active drugs administered as immediate-release formulations. Drug Dev. Res. 65 (2005) 55-75
-
(2005)
Drug Dev. Res.
, vol.65
, pp. 55-75
-
-
Singh, B.N.1
-
90
-
-
34249037098
-
Predicting effect of food on extent of drug absorption based on physicochemical properties
-
Gu C.H., Li H., Levons J., Lentz K., Gandhi R.B., Raghavan K., and Smith R.L. Predicting effect of food on extent of drug absorption based on physicochemical properties. Pharm. Res. 24 (2007) 1118-1130
-
(2007)
Pharm. Res.
, vol.24
, pp. 1118-1130
-
-
Gu, C.H.1
Li, H.2
Levons, J.3
Lentz, K.4
Gandhi, R.B.5
Raghavan, K.6
Smith, R.L.7
-
91
-
-
0034461768
-
Drug-like properties and the causes of poor solubility and poor permeability
-
Lipinski C.A. Drug-like properties and the causes of poor solubility and poor permeability. J. Pharmacol. Toxicol. Methods. 44 (2000) 235-249
-
(2000)
J. Pharmacol. Toxicol. Methods.
, vol.44
, pp. 235-249
-
-
Lipinski, C.A.1
-
92
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski C.A., Lombardo F., Dominy B.W., and Feeney P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug. Deliv. Rev. 46 (2001) 3-26
-
(2001)
Adv. Drug. Deliv. Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
93
-
-
34547651036
-
Current perspectives in dissolution testing of conventional and novel dosage forms
-
Azarmi S., Roa W., and Löbenberg R. Current perspectives in dissolution testing of conventional and novel dosage forms. Int. J. Pharm. 28 (2007) 12-21
-
(2007)
Int. J. Pharm.
, vol.28
, pp. 12-21
-
-
Azarmi, S.1
Roa, W.2
Löbenberg, R.3
-
94
-
-
0036181818
-
In vitro simulation of food effect on dissolution of deramciclane film-coated tablets and correlation with in vivo data in healthy volunteers
-
Al-Behaisi S., Antal I., Morovján G., Szúnyog J., Drabant S., Marton S., and Klebovich I. In vitro simulation of food effect on dissolution of deramciclane film-coated tablets and correlation with in vivo data in healthy volunteers. Eur. J. Pharm. Sci. 15 (2002) 157-162
-
(2002)
Eur. J. Pharm. Sci.
, vol.15
, pp. 157-162
-
-
Al-Behaisi, S.1
Antal, I.2
Morovján, G.3
Szúnyog, J.4
Drabant, S.5
Marton, S.6
Klebovich, I.7
-
95
-
-
0024801189
-
Ethanol enhances the hemodynamic effects of felodipine
-
Bailey D.G., Spence J.D., Edgar B., Bayliff C.D., and Arnold J.M. Ethanol enhances the hemodynamic effects of felodipine. Clin. Invest. Med. 12 (1989) 357-362
-
(1989)
Clin. Invest. Med.
, vol.12
, pp. 357-362
-
-
Bailey, D.G.1
Spence, J.D.2
Edgar, B.3
Bayliff, C.D.4
Arnold, J.M.5
-
96
-
-
0242469224
-
The effects of fruit juices on drug disposition: a new model for drug interactions
-
Dresser G.K., and Bailey D.G. The effects of fruit juices on drug disposition: a new model for drug interactions. Eur. J. Clin. Invest. 33 (2003) 10-16
-
(2003)
Eur. J. Clin. Invest.
, vol.33
, pp. 10-16
-
-
Dresser, G.K.1
Bailey, D.G.2
-
97
-
-
13944275994
-
Effect of grapefruit juice volume on the reduction of fexofenadine bioavailability: possible role of organic anion transporting polypeptides
-
Dresser G.K., Kim R.B., and Bailey D.G. Effect of grapefruit juice volume on the reduction of fexofenadine bioavailability: possible role of organic anion transporting polypeptides. Clin. Pharmacol. Ther. 77 (2005) 170-177
-
(2005)
Clin. Pharmacol. Ther.
, vol.77
, pp. 170-177
-
-
Dresser, G.K.1
Kim, R.B.2
Bailey, D.G.3
-
98
-
-
4344594700
-
Transport characteristics of fexofenadine in the Caco-2 cell model
-
Petri N., Tannergren C., Rungstad D., and Lennernas H. Transport characteristics of fexofenadine in the Caco-2 cell model. Pharm. Res. 21 (2004) 1398-1404
-
(2004)
Pharm. Res.
, vol.21
, pp. 1398-1404
-
-
Petri, N.1
Tannergren, C.2
Rungstad, D.3
Lennernas, H.4
-
99
-
-
14344265920
-
Effect of fruit juices on the oral bioavailability of fexofenadine in rats
-
Kamath A.V., Yao M., Zhang Y., and Chong S. Effect of fruit juices on the oral bioavailability of fexofenadine in rats. J. Pharm. Sci. 94 (2005) 233-239
-
(2005)
J. Pharm. Sci.
, vol.94
, pp. 233-239
-
-
Kamath, A.V.1
Yao, M.2
Zhang, Y.3
Chong, S.4
-
100
-
-
0042349753
-
Effects of grapefruit juice on intestinal P-glycoprotein evaluation using digoxin in humans
-
Parker R.B., Yates C.R., Soberman J.E., and Laizure S.C. Effects of grapefruit juice on intestinal P-glycoprotein evaluation using digoxin in humans. Pharmacotherapy 23 (2003) 979-987
-
(2003)
Pharmacotherapy
, vol.23
, pp. 979-987
-
-
Parker, R.B.1
Yates, C.R.2
Soberman, J.E.3
Laizure, S.C.4
-
101
-
-
16344378672
-
Grapefruit juice ingestion significantly reduces talinolol bioavailability
-
Schwarz U.I., Seemann D., Oertel R., Miehlke S., Kuhlish E., Fromm M.F., Kim R.B., Bailey D.G., and Kirch W. Grapefruit juice ingestion significantly reduces talinolol bioavailability. Clin. Pharmacol. Ther. 77 (2005) 291-301
-
(2005)
Clin. Pharmacol. Ther.
, vol.77
, pp. 291-301
-
-
Schwarz, U.I.1
Seemann, D.2
Oertel, R.3
Miehlke, S.4
Kuhlish, E.5
Fromm, M.F.6
Kim, R.B.7
Bailey, D.G.8
Kirch, W.9
-
102
-
-
0037103569
-
Modulation of P-glycoprotein expression and function by curcumin in multidrug-resistant human KB cells
-
Anuchapreeda S., Leechanachai P., Smith M.M., Ambudkar S.V., and Limtrakul P. Modulation of P-glycoprotein expression and function by curcumin in multidrug-resistant human KB cells. Biochem. Pharmacol. 64 (2002) 573-582
-
(2002)
Biochem. Pharmacol.
, vol.64
, pp. 573-582
-
-
Anuchapreeda, S.1
Leechanachai, P.2
Smith, M.M.3
Ambudkar, S.V.4
Limtrakul, P.5
-
103
-
-
0037371275
-
Effects of the flavonoids biochanin A, morin, phloretin, and silymarin on P-glycoprotein-mediated transport
-
Zhang S., and Morris M.E. Effects of the flavonoids biochanin A, morin, phloretin, and silymarin on P-glycoprotein-mediated transport. J. Pharmacol. Exp. Ther. 304 (2003) 1258-1267
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.304
, pp. 1258-1267
-
-
Zhang, S.1
Morris, M.E.2
-
104
-
-
4344602767
-
Inhibition of P-glycoprotein function by tea catechins in KB-C2 cells
-
Kitagawa S., Nabekura T., and Kamiyama S. Inhibition of P-glycoprotein function by tea catechins in KB-C2 cells. J. Pharm. Pharmacol. 56 (2004) 1001-1005
-
(2004)
J. Pharm. Pharmacol.
, vol.56
, pp. 1001-1005
-
-
Kitagawa, S.1
Nabekura, T.2
Kamiyama, S.3
-
105
-
-
21244503047
-
Inhibition of P-glycoprotein transport function and reversion of MDR1 multidrug resistance by cnidiadin
-
Barthomeuf C., Grassi J., Demeule M., Fournier C., Boivin D., and Béliveau R. Inhibition of P-glycoprotein transport function and reversion of MDR1 multidrug resistance by cnidiadin. Cancer Chemother. Pharmacol. 56 (2005) 173-181
-
(2005)
Cancer Chemother. Pharmacol.
, vol.56
, pp. 173-181
-
-
Barthomeuf, C.1
Grassi, J.2
Demeule, M.3
Fournier, C.4
Boivin, D.5
Béliveau, R.6
-
106
-
-
24944493255
-
Effects of alkyl gallates on P-glycoprotein function
-
Kitagawa S., Nabekura T., Kamiyama S., Takahashi T., Nakamura Y., Kashiwada Y., and Ikeshiro Y. Effects of alkyl gallates on P-glycoprotein function. Biochem. Pharmacol. 70 (2005) 1262-1266
-
(2005)
Biochem. Pharmacol.
, vol.70
, pp. 1262-1266
-
-
Kitagawa, S.1
Nabekura, T.2
Kamiyama, S.3
Takahashi, T.4
Nakamura, Y.5
Kashiwada, Y.6
Ikeshiro, Y.7
-
107
-
-
33645100643
-
Effects of herbal extracts on the function of human organic anion-transporting polypeptide OATP-B
-
Fuchikami H., Satoh H., Tsujimoto M., Ohdo S., Ohtani H., and Sawada Y. Effects of herbal extracts on the function of human organic anion-transporting polypeptide OATP-B. Drug Metab. Dispos. 34 (2006) 577-582
-
(2006)
Drug Metab. Dispos.
, vol.34
, pp. 577-582
-
-
Fuchikami, H.1
Satoh, H.2
Tsujimoto, M.3
Ohdo, S.4
Ohtani, H.5
Sawada, Y.6
-
108
-
-
0036805387
-
Effect of organic isothiocyanates on the P-glycoprotein- and MRP1-mediated transport of daunomycin and vinblastine
-
Tseng E., Kamath A., and Morris M.E. Effect of organic isothiocyanates on the P-glycoprotein- and MRP1-mediated transport of daunomycin and vinblastine. Pharm. Res. (2002) 1509-1515
-
(2002)
Pharm. Res.
, pp. 1509-1515
-
-
Tseng, E.1
Kamath, A.2
Morris, M.E.3
-
109
-
-
25444524567
-
Modulatory effects of plant phenols on human multidrug resistance proteins 1, 4, and 5 (ABCC1, 4 and 5)
-
Wu C.-P., Calcagno A.M., Hladky S.B., Ambudkar S.V., and Barrand M.A. Modulatory effects of plant phenols on human multidrug resistance proteins 1, 4, and 5 (ABCC1, 4 and 5). FEBS J. 272 (2005) 4725-4740
-
(2005)
FEBS J.
, vol.272
, pp. 4725-4740
-
-
Wu, C.-P.1
Calcagno, A.M.2
Hladky, S.B.3
Ambudkar, S.V.4
Barrand, M.A.5
-
110
-
-
0035991638
-
The influence of lipids on stereoselective pharmacokinetics of halofantrine: important implications in food-effect studies involving drugs that bind to lipoproteins
-
Brocks D.R., and Wasan K.M. The influence of lipids on stereoselective pharmacokinetics of halofantrine: important implications in food-effect studies involving drugs that bind to lipoproteins. J. Pharm. Sci. 91 (2002) 1817-1826
-
(2002)
J. Pharm. Sci.
, vol.91
, pp. 1817-1826
-
-
Brocks, D.R.1
Wasan, K.M.2
-
111
-
-
0031852495
-
Association of halofantrine with postprandially derived plasma lipoproteins decreases its clearance relative to administration in the fasted state
-
Humberstone A.J., Porter C.J., Edwards G.A., and Charman W.N. Association of halofantrine with postprandially derived plasma lipoproteins decreases its clearance relative to administration in the fasted state. J. Pharm. Sci. 87 (1998) 936-942
-
(1998)
J. Pharm. Sci.
, vol.87
, pp. 936-942
-
-
Humberstone, A.J.1
Porter, C.J.2
Edwards, G.A.3
Charman, W.N.4
-
112
-
-
33646433407
-
A clinical single-pass perfusion investigation of the dynamic in vivo secretory response to a dietary meal in human proximal small intestine
-
Persson E.M., Nilsson R.G., Hansson G.I., Löfgren L.J., Libäck F., Knutson L., Abrahamsson B., and Lennernäs H. A clinical single-pass perfusion investigation of the dynamic in vivo secretory response to a dietary meal in human proximal small intestine. Pharm. Res. 23 (2006) 742-751
-
(2006)
Pharm. Res.
, vol.23
, pp. 742-751
-
-
Persson, E.M.1
Nilsson, R.G.2
Hansson, G.I.3
Löfgren, L.J.4
Libäck, F.5
Knutson, L.6
Abrahamsson, B.7
Lennernäs, H.8
-
113
-
-
0342617694
-
Lipid-based vehicles for the oral delivery of poorly water soluble drugs
-
Humberstone A.J., and Charman W.N. Lipid-based vehicles for the oral delivery of poorly water soluble drugs. Adv. Drug Deliv. Rev. 25 (1997) 103-128
-
(1997)
Adv. Drug Deliv. Rev.
, vol.25
, pp. 103-128
-
-
Humberstone, A.J.1
Charman, W.N.2
-
114
-
-
33847100504
-
The effect of a high-fat meal on the pharmacodynamics of a model lipophilic compound that binds extensively to triglyceride-rich lipoproteins
-
Gershkovich P., Shtainer D., and Hoffman A. The effect of a high-fat meal on the pharmacodynamics of a model lipophilic compound that binds extensively to triglyceride-rich lipoproteins. Int. J. Pharm. 333 (2007) 1-4
-
(2007)
Int. J. Pharm.
, vol.333
, pp. 1-4
-
-
Gershkovich, P.1
Shtainer, D.2
Hoffman, A.3
-
115
-
-
34547115712
-
Effect of a high-fat meal on absorption and disposition of lipophilic compounds: the importance of degree of association with triglyceride-rich lipoproteins
-
Gershkovich P., and Hoffman A. Effect of a high-fat meal on absorption and disposition of lipophilic compounds: the importance of degree of association with triglyceride-rich lipoproteins. Eur. J. Pharm. Sci. 32 (2007) 24-32
-
(2007)
Eur. J. Pharm. Sci.
, vol.32
, pp. 24-32
-
-
Gershkovich, P.1
Hoffman, A.2
-
116
-
-
33847394968
-
Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs
-
Porter C.J., Trevaskis N.L., and Charman W.N. Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs. Nat. Rev. Drug Discov. 6 (2007) 231-248
-
(2007)
Nat. Rev. Drug Discov.
, vol.6
, pp. 231-248
-
-
Porter, C.J.1
Trevaskis, N.L.2
Charman, W.N.3
-
117
-
-
0028079609
-
Influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine in a crossover comparison with the market formulation
-
Mueller E.A., Kovarik J.M., van Bree J.B., Grevel J., Lücker P.W., and Kutz K. Influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine in a crossover comparison with the market formulation. Pharm. Res. 11 (1994) 151-155
-
(1994)
Pharm. Res.
, vol.11
, pp. 151-155
-
-
Mueller, E.A.1
Kovarik, J.M.2
van Bree, J.B.3
Grevel, J.4
Lücker, P.W.5
Kutz, K.6
-
118
-
-
0027962341
-
Minor influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine
-
Mueller E.A., Kovarik J.M., and Kutz K. Minor influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine. Transplant. Proc. 26 (1994) 2957-2958
-
(1994)
Transplant. Proc.
, vol.26
, pp. 2957-2958
-
-
Mueller, E.A.1
Kovarik, J.M.2
Kutz, K.3
-
119
-
-
1242291941
-
Drug solubilization behavior during in vitro digestion of suspension formulations of poorly water-soluble drugs in triglyceride lipids
-
Kaukonen A.M., Boyd B.J., Charman W.N., and Porter C.J. Drug solubilization behavior during in vitro digestion of suspension formulations of poorly water-soluble drugs in triglyceride lipids. Pharm. Res. 21 (2004) 254-260
-
(2004)
Pharm. Res.
, vol.21
, pp. 254-260
-
-
Kaukonen, A.M.1
Boyd, B.J.2
Charman, W.N.3
Porter, C.J.4
-
121
-
-
0842289328
-
Probing drug solubilization patterns in the gastrointestinal tract after administration of lipid-based delivery systems: a phase diagram approach
-
Kossena G.A., Charman W.N., Boyd B.J., Dunstan D.E., and Porter C.J. Probing drug solubilization patterns in the gastrointestinal tract after administration of lipid-based delivery systems: a phase diagram approach. J. Pharm. Sci. 93 (2004) 332-348
-
(2004)
J. Pharm. Sci.
, vol.93
, pp. 332-348
-
-
Kossena, G.A.1
Charman, W.N.2
Boyd, B.J.3
Dunstan, D.E.4
Porter, C.J.5
-
122
-
-
16444375502
-
Influence of the intermediate digestion phases of common formulation lipids on the absorption of a poorly water-soluble drug
-
Kossena G.A., Charman W.N., Boyd B.J., and Porter C.J. Influence of the intermediate digestion phases of common formulation lipids on the absorption of a poorly water-soluble drug. J. Pharm. Sci. 94 (2005) 481-492
-
(2005)
J. Pharm. Sci.
, vol.94
, pp. 481-492
-
-
Kossena, G.A.1
Charman, W.N.2
Boyd, B.J.3
Porter, C.J.4
-
123
-
-
0141680636
-
Effect of lipid excipients on in vitro pancreatic lipase activity
-
Subramanian R., and Wasan K.M. Effect of lipid excipients on in vitro pancreatic lipase activity. Drug Dev. Ind. Pharm. 29 (2003) 885-890
-
(2003)
Drug Dev. Ind. Pharm.
, vol.29
, pp. 885-890
-
-
Subramanian, R.1
Wasan, K.M.2
-
124
-
-
4744367567
-
Potential mechanisms by which Peceol increases the gastrointestinal absorption of amphotericin B
-
Risovic V., Sachs-Barrable K., Boyd M., and Wasan K.M. Potential mechanisms by which Peceol increases the gastrointestinal absorption of amphotericin B. Drug. Dev. Ind. Pharm. 30 (2004) 767-774
-
(2004)
Drug. Dev. Ind. Pharm.
, vol.30
, pp. 767-774
-
-
Risovic, V.1
Sachs-Barrable, K.2
Boyd, M.3
Wasan, K.M.4
-
125
-
-
39149138551
-
Potential mechanisms by which lipid excipients increase the oral gastrointestinal absorption of drugs: a case study using amphotericin B
-
Wasan K.M., Sachs-Barrable K., and Lee S.D. Potential mechanisms by which lipid excipients increase the oral gastrointestinal absorption of drugs: a case study using amphotericin B. Bull. Tech. Gattefossé (2006) 31-42
-
(2006)
Bull. Tech. Gattefossé
, pp. 31-42
-
-
Wasan, K.M.1
Sachs-Barrable, K.2
Lee, S.D.3
-
126
-
-
0043212075
-
Biological, pharmaceutical, and analytical considerations with respect to the transport media used in the absorption screening system, Caco-2
-
Ingels F.M., and Augustijns P.F. Biological, pharmaceutical, and analytical considerations with respect to the transport media used in the absorption screening system, Caco-2. J. Pharm. Sci. 92 (2003) 1545-1558
-
(2003)
J. Pharm. Sci.
, vol.92
, pp. 1545-1558
-
-
Ingels, F.M.1
Augustijns, P.F.2
|