-
1
-
-
0032927254
-
Drug, meal and formulation interactions influencing drug absorption after oral administration. Clinical implications
-
Fleisher D, Li C, Zhou Y, Pao LH, Karim A. Drug, meal and formulation interactions influencing drug absorption after oral administration. Clinical implications. Clin Pharmacokinet. 1999;36(3):233-54. (Pubitemid 29178760)
-
(1999)
Clinical Pharmacokinetics
, vol.36
, Issue.3
, pp. 233-254
-
-
Fleisher, D.1
Li, C.2
Zhou, Y.3
Pao, L.-H.4
Karim, A.5
-
2
-
-
0242350785
-
Food-effect bioavailability and fed bioequivalence studies
-
US FDA Accessed 02 Jun 2012
-
US FDA. Food-effect bioavailability and fed bioequivalence studies. In: Guidance for industry. http://www.fda.gov/downloads/regulatoryinformation/ guidances/ucm126833.pdf. 2002. Accessed 02 Jun 2012.
-
(2002)
Guidance for Industry
-
-
-
3
-
-
79951997007
-
Utility of physiologically based absorption modeling in implementing quality by design in drug development
-
10.1208/s12248-010-9250-9 21207216 10.1208/s12248-010-9250-9
-
Zhang X, Lionberger RA, Davit BM, Yu LX. Utility of physiologically based absorption modeling in implementing quality by design in drug development. AAPS J. 2011;13(1):59-71. doi: 10.1208/s12248-010-9250-9.
-
(2011)
AAPS J
, vol.13
, Issue.1
, pp. 59-71
-
-
Zhang, X.1
Lionberger, R.A.2
Davit, B.M.3
Yu, L.X.4
-
4
-
-
0021821619
-
Food-induced 'dose-dumping' from a once-a-day theophylline product as a cause of theophylline toxicity
-
Hendeles L, Weinberger M, Milavetz G, Hill 3rd M, Vaughan L. Food-induced "dose-dumping" from a once-a-day theophylline product as a cause of theophylline toxicity. Chest. 1985;87(6):758-65. (Pubitemid 15063777)
-
(1985)
Chest
, vol.87
, Issue.6
, pp. 758-765
-
-
Hendeles, L.1
Weinberger, M.2
Milavetz, G.3
-
5
-
-
0035964221
-
Effect of food on absorption of Dilantin Kapseals and Mylan extended phenytoin sodium capsules
-
Wilder BJ, Leppik I, Hietpas TJ, Cloyd JC, Randinitis EJ, Cook J. Effect of food on absorption of dilantin kapseals and mylan extended phenytoin sodium capsules. Neurology. 2001;57(4):582-9. (Pubitemid 32782983)
-
(2001)
Neurology
, vol.57
, Issue.4
, pp. 582-589
-
-
Wilder, B.J.1
Leppik, I.2
Hietpas, T.J.3
Cloyd, J.C.4
Randinitis, E.J.5
Cook, J.6
-
6
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification - The correlation of in-vitro drug product dissolution and in-vivo bioavailability
-
10.1023/A:1016212804288 1:CAS:528:DyaK2MXksVGqur8%3D
-
Amidon GL, Lennernas H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutic drug classification - the correlation of in-vitro drug product dissolution and in-vivo bioavailability. Pharmaceut Res. 1995;12(3):413-20.
-
(1995)
Pharmaceut Res
, vol.12
, Issue.3
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
7
-
-
17644380257
-
Predicting drug disposition via application of BCS: Transport/absorption/ elimination interplay and development of a biopharmaceutics drug disposition classification system
-
DOI 10.1007/s11095-004-9004-4
-
Wu CY, Benet LZ. Predicting drug disposition via application of BCS: transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm Res. 2005;22(1):11-23. doi: 10.1007/s11095-004-9004-4. (Pubitemid 40558141)
-
(2005)
Pharmaceutical Research
, vol.22
, Issue.1
, pp. 11-23
-
-
Wu, C.-Y.1
Benet, L.Z.2
-
9
-
-
39149115065
-
Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption
-
18199522 10.1016/j.addr.2007.08.043 1:CAS:528:DC%2BD1cXitVOmsr0%3D
-
Custodio JM, Wu C-Y, Benet Leslie Z. Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption. Adv Drug Deliv Rev. 2008;60(6):717-33.
-
(2008)
Adv Drug Deliv Rev
, vol.60
, Issue.6
, pp. 717-733
-
-
Custodio, J.M.1
Wu, C.-Y.2
Benet Leslie, Z.3
-
10
-
-
83555174958
-
BDDCS applied to over 900 drugs
-
10.1208/s12248-011-9290-9 21818695 10.1208/s12248-011-9290-9 1:CAS:528:DC%2BC3MXhsFamsbfE
-
Benet LZ, Broccatelli F, Oprea TI. BDDCS applied to over 900 drugs. AAPS J. 2011;13(4):519-47. doi: 10.1208/s12248-011-9290-9.
-
(2011)
AAPS J
, vol.13
, Issue.4
, pp. 519-547
-
-
Benet, L.Z.1
Broccatelli, F.2
Oprea, T.I.3
-
11
-
-
80053087179
-
Oral formulation strategies to improve solubility of poorly water-soluble drugs
-
10.1517/17425247.2011.606808 21810062 10.1517/17425247.2011.606808 1:CAS:528:DC%2BC3MXht1ajsLnI
-
Singh A, Worku ZA, Van den Mooter G. Oral formulation strategies to improve solubility of poorly water-soluble drugs. Expert Opin Drug Deliv. 2011;8(10):1361-78. doi: 10.1517/17425247.2011.606808.
-
(2011)
Expert Opin Drug Deliv
, vol.8
, Issue.10
, pp. 1361-1378
-
-
Singh, A.1
Worku, Z.A.2
Van Den Mooter, G.3
-
12
-
-
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 CY, Amidon GL, Berardi RR, Fleisher D, Youngberg C, Dressman JB. 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(3):271-4. (Pubitemid 16136927)
-
(1986)
Journal of Pharmaceutical Sciences
, vol.75
, Issue.3
, pp. 271-274
-
-
Lui, C.Y.1
Amidon, G.L.2
Berardi, R.R.3
-
13
-
-
0021815268
-
Effect of size and density on canine gastric emptying of nondigestible solids
-
Meyer JH, Dressman J, Fink A, Amidon G. Effect of size and density on canine gastric-emptying of nondigestible solids. Gastroenterology. 1985;89(4):805-13. (Pubitemid 15015296)
-
(1985)
Gastroenterology
, vol.89
, Issue.4
, pp. 805-813
-
-
Meyer, J.H.1
Dressman, J.2
Fink, A.3
Amidon, G.4
-
14
-
-
0034004361
-
Gastric pH profiles of beagle dogs and their use as an alternative to human testing
-
DOI 10.1016/S0939-6411(99)00070-3, PII S0939641199000703
-
Akimoto M, Nagahata N, Furuya A, Fukushima K, Higuchi S, Suwa T. Gastric pH profiles of beagle dogs and their use as an alternative to human testing. Eur J Pharm Biopharm. 2000;49(2):99-102. (Pubitemid 30126056)
-
(2000)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.49
, Issue.2
, pp. 99-102
-
-
Akimoto, M.1
Nagahata, N.2
Furuya, A.3
Fukushima, K.4
Higuchi, S.5
Suwa, T.6
-
15
-
-
33847632169
-
Development and validation of a preclinical food effect model
-
DOI 10.1002/jps.20767
-
Lentz KA, Quitko M, Morgan DG, Grace JE. Development and validation of a preclinical food effect model. J Pharm Sci. 2007;96(2):459-72. doi: 10.1002/Jps.20767. (Pubitemid 46363575)
-
(2007)
Journal of Pharmaceutical Sciences
, vol.96
, Issue.2
, pp. 459-472
-
-
Lentz, K.A.1
Quitko, M.2
Morgan, D.G.3
Grace Jr., J.E.4
Gleason, C.5
Marathe, P.H.6
-
16
-
-
0003915885
-
-
London: Methuen & Co. Special edition published by Universities Federation for Animal Welfare (UFAW), 1992
-
Russell WMS, Burch RL. The principles of humane experimental technique. London: Methuen & Co. Special edition published by Universities Federation for Animal Welfare (UFAW), 1992; 1959.
-
(1959)
The Principles of Humane Experimental Technique
-
-
Wms, R.1
Burch, R.L.2
-
17
-
-
84863344719
-
PBPK as a tool in regulatory review
-
10.1002/Bdd.1777 22351604 10.1002/bdd.1777 1:CAS:528:DC%2BC38XktFSntbY%3D
-
Huang SM. PBPK as a tool in regulatory review. Biopharm Drug Dispos. 2012;33(2):51-2. doi: 10.1002/Bdd.1777.
-
(2012)
Biopharm Drug Dispos
, vol.33
, Issue.2
, pp. 51-52
-
-
Huang, S.M.1
-
18
-
-
68249162210
-
Prediction of modified release pharmacokinetics and pharmacodynamics from in vitro, immediate release, and intravenous data
-
10.1208/s12248-009-9107-2 19430911 10.1208/s12248-009-9107-2 1:CAS:528:DC%2BD1MXhtVWqs7vM
-
Lukacova V, Woltosz WS, Bolger MB. Prediction of modified release pharmacokinetics and pharmacodynamics from in vitro, immediate release, and intravenous data. AAPS J. 2009;11(2):323-34. doi: 10.1208/s12248-009-9107-2.
-
(2009)
AAPS J
, vol.11
, Issue.2
, pp. 323-334
-
-
Lukacova, V.1
Woltosz, W.S.2
Bolger, M.B.3
-
19
-
-
65549103408
-
Predicting pharmacokinetics of drugs using physiologically based modeling - Application to food effects
-
10.1208/s12248-008-9079-7 19184451 10.1208/s12248-008-9079-7 1:CAS:528:DC%2BD1MXhtVWru7fP
-
Parrott N, Lukacova V, Fraczkiewicz G, Bolger MB. Predicting pharmacokinetics of drugs using physiologically based modeling - application to food effects. AAPS J. 2009;11(1):45-53. doi: 10.1208/s12248-008-9079-7.
-
(2009)
AAPS J
, vol.11
, Issue.1
, pp. 45-53
-
-
Parrott, N.1
Lukacova, V.2
Fraczkiewicz, G.3
Bolger, M.B.4
-
20
-
-
84862776856
-
Predicting drug interaction potential with a physiologically based pharmacokinetic model: A case study of telithromycin, a time-dependent CYP3A inhibitor
-
10.1038/clpt.2011.305 22398966 10.1038/clpt.2011.305 1:CAS:528: DC%2BC38XksVOktbY%3D
-
Vieira MLT, Zhao P, Berglund EG, Reynolds KS, Zhang L, Lesko LJ, et al. Predicting drug interaction potential with a physiologically based pharmacokinetic model: a case study of telithromycin, a time-dependent CYP3A inhibitor. Clin Pharmacol Ther. 2012;91(4):700-8. doi: 10.1038/clpt.2011.305.
-
(2012)
Clin Pharmacol Ther
, vol.91
, Issue.4
, pp. 700-708
-
-
Vieira, M.L.T.1
Zhao, P.2
Berglund, E.G.3
Reynolds, K.S.4
Zhang, L.5
Lesko, L.J.6
-
21
-
-
84858704368
-
Using Simcyp to project human oral pharmacokinetic variability in early drug research to mitigate mechanism-based adverse events
-
10.1002/Bdd.1768 22213407 10.1002/bdd.1768 1:CAS:528: DC%2BC38Xnt1yhsw%3D%3D
-
Shaffer CL, Scialis RJ, Rong HJ, Obach RS. Using Simcyp to project human oral pharmacokinetic variability in early drug research to mitigate mechanism-based adverse events. Biopharm Drug Dispos. 2012;33(2):72-84. doi: 10.1002/Bdd.1768.
-
(2012)
Biopharm Drug Dispos
, vol.33
, Issue.2
, pp. 72-84
-
-
Shaffer, C.L.1
Scialis, R.J.2
Rong, H.J.3
Obach, R.S.4
-
22
-
-
80054989486
-
Precipitation in the small intestine may play a more important role in the in vivo performance of poorly soluble weak bases in the fasted state: Case example nelfinavir
-
10.1016/j.ejpb.2011.04.005 21527341 10.1016/j.ejpb.2011.04.005 1:CAS:528:DC%2BC3MXht1antbrM
-
Shono Y, Jantratid E, Dressman JB. Precipitation in the small intestine may play a more important role in the in vivo performance of poorly soluble weak bases in the fasted state: case example nelfinavir. Eur J Pharm Biopharm. 2011;79(2):349-56. doi: 10.1016/j.ejpb.2011.04.005.
-
(2011)
Eur J Pharm Biopharm
, vol.79
, Issue.2
, pp. 349-356
-
-
Shono, Y.1
Jantratid, E.2
Dressman, J.B.3
-
23
-
-
68349150895
-
Prediction of food effects on the absorption of celecoxib based on biorelevant dissolution testing coupled with physiologically based pharmacokinetic modeling
-
10.1016/j.ejpb.2009.05.009 19465123 10.1016/j.ejpb.2009.05.009 1:CAS:528:DC%2BD1MXpvFygt74%3D
-
Shono Y, Jantratid E, Janssen N, Kesisoglou F, Mao Y, Vertzoni M, et al. Prediction of food effects on the absorption of celecoxib based on biorelevant dissolution testing coupled with physiologically based pharmacokinetic modeling. Eur J Pharm Biopharm. 2009;73(1):107-14. doi: 10.1016/j.ejpb.2009.05.009.
-
(2009)
Eur J Pharm Biopharm
, vol.73
, Issue.1
, pp. 107-114
-
-
Shono, Y.1
Jantratid, E.2
Janssen, N.3
Kesisoglou, F.4
Mao, Y.5
Vertzoni, M.6
-
24
-
-
77955656443
-
Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans
-
10.1016/j.ejpb.2010.05.009 20576487 10.1016/j.ejpb.2010.05.009 1:CAS:528:DC%2BC3cXhtVektL%2FP
-
Shono Y, Jantratid E, Kesisoglou F, Reppas C, Dressman JB. Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans. Eur J Pharm Biopharm. 2010;76(1):95-104. doi: 10.1016/j.ejpb.2010.05.009.
-
(2010)
Eur J Pharm Biopharm
, vol.76
, Issue.1
, pp. 95-104
-
-
Shono, Y.1
Jantratid, E.2
Kesisoglou, F.3
Reppas, C.4
Dressman, J.B.5
-
25
-
-
0034948871
-
Biorelevant dissolution testing to predict the plasma profile of lipophilic drugs after oral administration
-
DOI 10.1023/A:1011071401306
-
Nicolaides E, Symillides M, Dressman JB, Reppas C. Biorelevant dissolution testing to predict the plasma profile of lipophilic drugs after oral administration. Pharm Res. 2001;18(3):380-8. (Pubitemid 32595828)
-
(2001)
Pharmaceutical Research
, vol.18
, Issue.3
, pp. 380-388
-
-
Nicolaides, E.1
Symillides, M.2
Dressman, J.B.3
Reppas, C.4
-
26
-
-
0033805179
-
Vitro-in vivo correlations for lipophilic, poorly water-soluble drugs
-
11033429 10.1016/S0928-0987(00)00181-0 1:CAS:528:DC%2BD3cXntF2gtbY%3D
-
Dressman JB, Reppas C. In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs. Eur J Pharm Sci. 2000;11:S73-80.
-
(2000)
Eur J Pharm Sci
, vol.11
-
-
Dressman, J.B.1
Reppas, C.2
-
27
-
-
0036803219
-
Prediction of intestinal absorption: Comparative assessment of GASTROPLUS™ and IDEA™
-
DOI 10.1016/S0928-0987(02)00132-X, PII S092809870200132X
-
Parrott N, Lave T. Prediction of intestinal absorption: comparative assessment of GASTROPLUS (TM) and IDEA (TM). Eur J Pharm Sci. 2002;17(1-2):51-61. (Pubitemid 35287171)
-
(2002)
European Journal of Pharmaceutical Sciences
, vol.17
, Issue.1-2
, pp. 51-61
-
-
Parrott, N.1
Lave, T.2
-
28
-
-
28444451169
-
A strategy for preclinical formulation development using GastroPlus™ as pharmacokinetic simulation tool and a statistical screening design applied to a dog study
-
DOI 10.1016/j.ejps.2005.08.011, PII S0928098705002575
-
Kuentz M, Nick S, Parrott N, Rothlisberger D. A strategy for preclinical formulation development using GastroPlus (TM) as pharmacokinetic simulation tool and a statistical screening design applied to a dog study. Eur J Pharm Sci. 2006;27(1):91-9. doi: 10.1016/j.ejps.2005.08.011. (Pubitemid 41728259)
-
(2006)
European Journal of Pharmaceutical Sciences
, vol.27
, Issue.1
, pp. 91-99
-
-
Kuentz, M.1
Nick, S.2
Parrott, N.3
Rothlisberger, D.4
-
29
-
-
0032531309
-
Characterization of small intestinal transit time distribution in humans
-
DOI 10.1016/S0378-5173(98)00174-4, PII S0378517398001744
-
Yu LX, Amidon GL. Characterization of small intestinal transit time distribution in humans. Int J Pharm. 1998;171(2):157-63. (Pubitemid 29023108)
-
(1998)
International Journal of Pharmaceutics
, vol.171
, Issue.2
, pp. 157-163
-
-
Yu, L.X.1
Amidon, G.L.2
-
30
-
-
73349092713
-
Practical anticipation of human efficacious doses and pharmacokinetics using in vitro and preclinical in vivo Data
-
10.1208/s12248-009-9136-x 19707878 10.1208/s12248-009-9136-x 1:CAS:528:DC%2BD1MXhsFGmur%2FI
-
Heimbach T, Lakshminarayana SB, Hu WY, He HD. Practical anticipation of human efficacious doses and pharmacokinetics using in vitro and preclinical in vivo Data. AAPS J. 2009;11(3):602-14. doi: 10.1208/s12248-009-9136-x.
-
(2009)
AAPS J
, vol.11
, Issue.3
, pp. 602-614
-
-
Heimbach, T.1
Lakshminarayana, S.B.2
Hu, W.Y.3
He, H.D.4
-
31
-
-
84863786541
-
Novel physiologically based pharmacokinetic modeling of patupilone for human pharmacokinetic predictions
-
10.1007/s00280-012-1863-5 10.1007/s00280-012-1863-5 1:CAS:528: DC%2BC38XnvFOntr0%3D
-
Xia B, Heimbach T, Lin TH, He H, Wang Y, Tan E. Novel physiologically based pharmacokinetic modeling of patupilone for human pharmacokinetic predictions. Canc Chemother Pharmacol. 2012;69(6):1567-82. doi: 10.1007/s00280-012-1863-5.
-
(2012)
Canc Chemother Pharmacol
, vol.69
, Issue.6
, pp. 1567-1582
-
-
Xia, B.1
Heimbach, T.2
Lin, T.H.3
He, H.4
Wang, Y.5
Tan, E.6
-
32
-
-
65549146053
-
Understanding the effect of API properties on bioavailability through absorption modeling
-
10.1208/s12248-008-9061-4 19002590 10.1208/s12248-008-9061-4 1:CAS:528:DC%2BD1MXltVSls74%3D
-
Kesisoglou F, Wu YH. Understanding the effect of API properties on bioavailability through absorption modeling. AAPS J. 2008;10(4):516-25. doi: 10.1208/s12248-008-9061-4.
-
(2008)
AAPS J
, vol.10
, Issue.4
, pp. 516-525
-
-
Kesisoglou, F.1
Wu, Y.H.2
-
33
-
-
33845467297
-
Predicting pharmacokinetic food effects using biorelevant solubility media and physiologically based modelling
-
DOI 10.2165/00003088-200645120-00006
-
Jones HM, Parrott N, Ohlenbusch G, Lave T. Predicting pharmacokinetic food effects using biorelevant solubility media and physiologically based modelling. Clin Pharmacokinet. 2006;45(12):1213-26. (Pubitemid 44904824)
-
(2006)
Clinical Pharmacokinetics
, vol.45
, Issue.12
, pp. 1213-1226
-
-
Jones, H.M.1
Parrott, N.2
Ohlenbusch, G.3
Lave, T.4
-
34
-
-
1042269559
-
Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine
-
DOI 10.1211/0022357022511
-
Kostewicz ES, Wunderlich M, Brauns U, Becker R, Bock T, Dressman JB. Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine. J Pharm Pharmacol. 2004;56(1):43-51. doi: 10.1211/ 0022357022511. (Pubitemid 38195327)
-
(2004)
Journal of Pharmacy and Pharmacology
, vol.56
, Issue.1
, pp. 43-51
-
-
Kostewicz, E.S.1
Wunderlich, M.2
Brauns, U.3
Becker, R.4
Bock, T.5
Dressman, J.B.6
-
35
-
-
34748925493
-
Prediction of human pharmacokinetics using physiologically based modeling: A retrospective analysis of 26 clinically tested drugs
-
DOI 10.1124/dmd.107.015644
-
De Buck SS, Sinha VK, Fenu LA, Nijsen MJ, Mackie CE, Gilissen RAHJ. Prediction of human pharmacokinetics using physiologically based modeling: a retrospective analysis of 26 clinically tested drugs. Drug Metab Dispos. 2007;35(10):1766-80. doi: 10.1124/dmd.107.015644. (Pubitemid 47481568)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.10
, pp. 1766-1780
-
-
De Buck, S.S.1
Sinha, V.K.2
Fenu, L.A.3
Nijsen, M.J.4
Mackie, C.E.5
Gilissen, R.A.H.J.6
-
36
-
-
34047157087
-
The prediction of drug metabolism, tissue distribution, and bioavailability of 50 structurally diverse compounds in rat using mechanism-based absorption, distribution, and metabolism prediction tools
-
DOI 10.1124/dmd.106.014027
-
De Buck SS, Sinha VK, Fenu LA, Gilissen RA, Mackie CE, Nijsen MJ. The prediction of drug metabolism, tissue distribution, and bioavailability of 50 structurally diverse compounds in rat using mechanism-based absorption, distribution, and metabolism prediction tools. Drug Metab Dispos. 2007;35(4):649-59. doi: 10.1124/dmd.106.014027. (Pubitemid 46513269)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.4
, pp. 649-659
-
-
De Buck, S.S.1
Sinha, V.K.2
Fenu, L.A.3
Gilissen, R.A.4
Mackie, C.E.5
Nijsen, M.J.6
-
37
-
-
0036075799
-
Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models of drug disposition
-
DOI 10.1002/jps.10128
-
Poulin P, Theil FP. Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models of drug disposition. J Pharm Sci. 2002;91(5):1358-70. doi: 10.1002/jps.10128. (Pubitemid 34651198)
-
(2002)
Journal of Pharmaceutical Sciences
, vol.91
, Issue.5
, pp. 1358-1370
-
-
Poulin, P.1
Theil, F.-P.2
-
38
-
-
34047170808
-
Regional distribution of solute carrier mRNA expression along the human intestinal tract
-
DOI 10.1124/dmd.106.013342
-
Meier Y, Eloranta JJ, Darimont J, Ismair MG, Hiller C, Fried M, et al. Regional distribution of solute carrier mRNA expression along the human intestinal tract. Drug Metab Dispos. 2007;35(4):590-4. doi: 10.1124/dmd.106. 013342. (Pubitemid 46513261)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.4
, pp. 590-594
-
-
Meier, Y.1
Eloranta, J.J.2
Darimont, J.3
Ismair, M.G.4
Hiller, C.5
Fried, M.6
Kullak-Ublick, G.A.7
Vavricka, S.R.8
-
39
-
-
62649128592
-
The use of drug metabolism for prediction of intestinal permeability
-
10.1021/Mp8001864 10.1021/mp8001864 1:CAS:528:DC%2BD1MXjt1GmtA%3D%3D
-
Chen ML, Yu L. The use of drug metabolism for prediction of intestinal permeability. Mol Pharmaceut. 2009;6(1):74-81. doi: 10.1021/Mp8001864.
-
(2009)
Mol Pharmaceut
, vol.6
, Issue.1
, pp. 74-81
-
-
Chen, M.L.1
Yu, L.2
-
40
-
-
0030003789
-
Estimation of the increase in solubility of drugs as a function of bile salt concentration
-
DOI 10.1023/A:1016062224568
-
Mithani SD, Bakatselou V, TenHoor CN, Dressman JB. Estimation of the increase in solubility of drugs as a function of bile salt concentration. Pharmaceut Res. 1996;13(1):163-7. (Pubitemid 26076314)
-
(1996)
Pharmaceutical Research
, vol.13
, Issue.1
, pp. 163-167
-
-
Mithani, S.D.1
Bakatselou, V.2
TenHoor, C.N.3
Dressman, J.B.4
-
41
-
-
0034947674
-
From MDR to MXR: New understanding of multidrug resistance systems, their properties and clinical significance
-
Litman T, Druley TE, Stein WD, Bates SE. From MDR to MXR: new understanding of multidrug resistance systems, their properties and clinical significance. Cell Mol Life Sci. 2001;58(7):931-59. (Pubitemid 32652819)
-
(2001)
Cellular and Molecular Life Sciences
, vol.58
, Issue.7
, pp. 931-959
-
-
Litman, T.1
Druley, T.E.2
Stein, W.D.3
Bates, S.E.4
-
42
-
-
0030003789
-
Estimation of the increase in solubility of drugs as a function of bile salt concentration
-
DOI 10.1023/A:1016062224568
-
Mithani SD, Bakatselou V, TenHoor CN, Dressman JB. Estimation of the increase in solubility of drugs as a function of bile salt concentration. Pharm Res. 1996;13(1):163-7. (Pubitemid 26076314)
-
(1996)
Pharmaceutical Research
, vol.13
, Issue.1
, pp. 163-167
-
-
Mithani, S.D.1
Bakatselou, V.2
TenHoor, C.N.3
Dressman, J.B.4
-
43
-
-
53849134465
-
Current methods for predicting human food effect
-
10.1208/s12248-008-9025-8 18500565 10.1208/s12248-008-9025-8 1:CAS:528:DC%2BD1cXhtlOgsbvJ
-
Lentz KA. Current methods for predicting human food effect. AAPS J. 2008;10(2):282-8. doi: 10.1208/s12248-008-9025-8.
-
(2008)
AAPS J
, vol.10
, Issue.2
, pp. 282-288
-
-
Lentz, K.A.1
-
44
-
-
85031362524
-
Waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a biopharmaceutics classification system
-
US FDA Accessed 02 Jun 2012
-
US FDA. Waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a biopharmaceutics classification system. In: Guidance for industry. 2000. http://www.fda.gov/ downloads/Drugs/./Guidances/ucm070246.pdf. Accessed 02 Jun 2012.
-
(2000)
Guidance for Industry
-
-
-
45
-
-
0029855969
-
Comparison between permeability coefficients in rat and human jejunum
-
DOI 10.1023/A:1016065715308
-
Fagerholm U, Johansson M, Lennernas H. Comparison between permeability coefficients in rat and human jejunum. Pharm Res. 1996;13(9):1336-42. (Pubitemid 26344978)
-
(1996)
Pharmaceutical Research
, vol.13
, Issue.9
, pp. 1336-1342
-
-
Fagerholm, U.1
Johansson, M.2
Lennernas, H.3
-
46
-
-
0001211542
-
Pharmacokinetics in drug discovery and development: Nonclinical studies
-
G. Welling F.L.S. Tse (eds) 2 Dekker New York
-
Tse FLS. Pharmacokinetics in drug discovery and development: nonclinical studies. In: Welling PG, Tse FLS, editors. Pharmacokinetics: regulatory, industrial, academic perspectives. 2nd ed. New York: Dekker; 1995. p. 300-6.
-
(1995)
Pharmacokinetics: Regulatory, Industrial, Academic Perspectives
, pp. 300-306
-
-
Tse, F.L.S.1
-
47
-
-
80052267476
-
PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 2: Comparative assessment of prediction methods of human volume of distribution
-
doi: 10.1002/jps.22553
-
Jones RD, Jones HM, Rowland M, Gibson CR, Yates JW, Chien JY, et al. PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 2: comparative assessment of prediction methods of human volume of distribution. J Pharm Sci. 2011. doi: 10.1002/jps.22553.
-
(2011)
J Pharm Sci.
-
-
Jones, R.D.1
Jones, H.M.2
Rowland, M.3
Gibson, C.R.4
Yates, J.W.5
Chien, J.Y.6
-
48
-
-
80052268294
-
PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 3: Comparative assessement of prediction methods of human clearance
-
doi: 10.1002/jps.22552
-
Ring BJ, Chien JY, Adkison KK, Jones HM, Rowland M, Jones RD, et al. PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 3: Comparative assessement of prediction methods of human clearance. J Pharm Sci. 2011. doi: 10.1002/jps.22552.
-
(2011)
J Pharm Sci.
-
-
Ring, B.J.1
Chien, J.Y.2
Adkison, K.K.3
Jones, H.M.4
Rowland, M.5
Jones, R.D.6
|