-
1
-
-
33750579770
-
Drug discovery in jeopardy
-
P. Cuatrecasas. Drug discovery in jeopardy. J. Clin. Invest. 116(11):2837-2842 (2006).
-
(2006)
J. Clin. Invest.
, vol.116
, Issue.11
, pp. 2837-2842
-
-
Cuatrecasas, P.1
-
2
-
-
4344645978
-
Can the pharmaceutical industry reduce attrition rates?
-
I. Kola, and J. Landis. Can the pharmaceutical industry reduce attrition rates? Nature Reviews Drug Discov. 3(8):711-715 (2004).
-
(2004)
Nature Reviews Drug Discov.
, vol.3
, Issue.8
, pp. 711-715
-
-
Kola, I.1
Landis, J.2
-
3
-
-
20444465945
-
The impact of early ADME profiling on drug discovery and development strategy
-
J. Wang, and L. Urban. The impact of early ADME profiling on drug discovery and development strategy. Drug Discov. 4:73-86 (2004).
-
(2004)
Drug Discov.
, vol.4
, pp. 73-86
-
-
Wang, J.1
Urban, L.2
-
4
-
-
0037364162
-
ADMET in silico modeling: Towards prediction paradise?
-
H. Van de Waterbeemd, and E. Gifford. ADMET in silico modeling: Towards prediction paradise? Nat. Rev. 2(3):192-204 (2003).
-
(2003)
Nat. Rev.
, vol.2
, Issue.3
, pp. 192-204
-
-
Van de Waterbeemd, H.1
Gifford, E.2
-
5
-
-
3042781869
-
In silico ADME prediction: Data, models, facts, myths
-
F. Lombardo, E. Gifford, and M. Y. Shalaeva. In silico ADME prediction: Data, models, facts, myths. Minirev Med. Chem. 3(8):861-875 (2003).
-
(2003)
Minirev Med. Chem.
, vol.3
, Issue.8
, pp. 861-875
-
-
Lombardo, F.1
Gifford, E.2
Shalaeva, M.Y.3
-
6
-
-
0031024171
-
Experimental and computational approaches to Estimate solubiliy and permeability in drug discovery and development settings
-
C. A. Lipinski, F. Lombardo B. W. Dominy et al. Experimental and computational approaches to Estimate solubiliy and permeability in drug discovery and development settings. Adv. Drug. Deliv. Rev. 23(1-3):3-25 (1997).
-
(1997)
Adv. Drug. Deliv. Rev.
, vol.23
, Issue.1-3
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
-
7
-
-
0033840471
-
Predicting human oral bioavailability of a compound: Development of a novel quantitative structure-bioavailability relationship
-
C. W. Andrews, L. Bennett, and L. X. Yu. Predicting human oral bioavailability of a compound: Development of a novel quantitative structure-bioavailability relationship. Pharm. Res. 17(6):639-44 (2000).
-
(2000)
Pharm. Res.
, vol.17
, Issue.6
, pp. 639-644
-
-
Andrews, C.W.1
Bennett, L.2
Yu, L.X.3
-
8
-
-
0034729673
-
QSAR model for drug human oral bioavailability
-
F. Yoshida, and J. G. Topliss. QSAR model for drug human oral bioavailability. J. Med. Chem. 43(13):2575-2585 (2000).
-
(2000)
J. Med. Chem.
, vol.43
, Issue.13
, pp. 2575-2585
-
-
Yoshida, F.1
Topliss, J.G.2
-
9
-
-
0037030653
-
Molecular properties that influence the oral bioavailability of drug candidates
-
D. F. Veber, S. R. Johnson, H. Y. Cheng, B. R. Smith, K. W. Ward, and K. D. Kopple. Molecular properties that influence the oral bioavailability of drug candidates. J. Med. Chem. 45:2615-2623 (2002).
-
(2002)
J. Med. Chem.
, vol.45
, pp. 2615-2623
-
-
Veber, D.F.1
Johnson, S.R.2
Cheng, H.Y.3
Smith, B.R.4
Ward, K.W.5
Kopple, K.D.6
-
10
-
-
6344252814
-
Diaz HGA topological sub-structural approach for predicting human intestinal absorption of drugs
-
M. A. C. Perez, M. B. Sanz, L. R. Torres, R. G. Avalos, and M. P. Gonzalez. Diaz HGA topological sub-structural approach for predicting human intestinal absorption of drugs. Eur. J. Med. Chem. 39(11):905-916 (2004).
-
(2004)
Eur. J. Med. Chem.
, vol.39
, Issue.11
, pp. 905-916
-
-
Perez, M.A.C.1
Sanz, M.B.2
Torres, L.R.3
Avalos, R.G.4
Gonzalez, M.P.5
-
11
-
-
26644468131
-
Prediction of gastro-intestinal absorption using multivariate adaptive regression splines
-
E. Deconinck, Q. S. Xu, R. Put, D. Coomans, D. L. Massart, and Y. Vander Heyden. Prediction of gastro-intestinal absorption using multivariate adaptive regression splines. J. Pharm. Biomed Anal. 39(5):1021-1030 (2005).
-
(2005)
J. Pharm. Biomed Anal.
, vol.39
, Issue.5
, pp. 1021-1030
-
-
Deconinck, E.1
Xu, Q.S.2
Put, R.3
Coomans, D.4
Massart, D.L.5
Vander Heyden, Y.6
-
12
-
-
33845419542
-
Evaluation of chromatographic descriptors for the prediction of gastro-intestinal absorption of drugs
-
E. Deconinck, H. Ates, N. Callebaut, E. Van Gyseghem, and Y. Vander Heyden. Evaluation of chromatographic descriptors for the prediction of gastro-intestinal absorption of drugs. J. Chromatogr., A. 1138(1-2):190-202 (2007).
-
(2007)
J. Chromatogr. A
, vol.1138
, Issue.1-2
, pp. 190-202
-
-
Deconinck, E.1
Ates, H.2
Callebaut, N.3
Van Gyseghem, E.4
Vander Heyden, Y.5
-
13
-
-
33846855555
-
ADME evaluation in drug discovery. 7. Prediction of oral absorption by correlation and classification
-
T. Hou, J. Wang, W. Zhang, and X. Xu. ADME evaluation in drug discovery. 7. Prediction of oral absorption by correlation and classification. J. Chem. Inf. Model. 47(1):208-218 (2007).
-
(2007)
J. Chem. Inf. Model
, vol.47
, Issue.1
, pp. 208-218
-
-
Hou, T.1
Wang, J.2
Zhang, W.3
Xu, X.4
-
14
-
-
37249042636
-
ADME evaluation in drug discovery. 8. The prediction of human intestinal absorption by a support vector machine
-
T. Hou, J. Wang, and Y. Li. ADME evaluation in drug discovery. 8. The prediction of human intestinal absorption by a support vector machine. J. Chem. Inf. Model. 47(6):2408-2415 (2007).
-
(2007)
J. Chem. Inf. Model
, vol.47
, Issue.6
, pp. 2408-2415
-
-
Hou, T.1
Wang, J.2
Li, Y.3
-
15
-
-
34247245174
-
ADME evaluation in drug discovery. Can oral bioavailability in humans be effectively predicted by simple molecular property-based rules?
-
T. Hou, J. Wang, W. Zhang, and X. Xu. ADME evaluation in drug discovery. Can oral bioavailability in humans be effectively predicted by simple molecular property-based rules? J. Chem. Inf. Model. 47(2):460-463 (2007).
-
(2007)
J. Chem. Inf. Model
, vol.47
, Issue.2
, pp. 460-463
-
-
Hou, T.1
Wang, J.2
Zhang, W.3
Xu, X.4
-
16
-
-
0022070123
-
Absorption potential: Estimation of the fraction absorbed for orally administered compounds
-
J. Dressman, G. Amidon, and D. Fleisher. Absorption potential: Estimation of the fraction absorbed for orally administered compounds. J. Pharm. Sci. 74(5):588-589 (1985).
-
(1985)
J. Pharm. Sci.
, vol.74
, Issue.5
, pp. 588-589
-
-
Dressman, J.1
Amidon, G.2
Fleisher, D.3
-
17
-
-
0030444550
-
Guidance in the setting of drug particle size specifications to minimize variability in absorption
-
K. Johnson, and A. Swindell. Guidance in the setting of drug particle size specifications to minimize variability in absorption. Pharm. Res. 13(12):1795-1798 (1996).
-
(1996)
Pharm. Res.
, vol.13
, Issue.12
, pp. 1795-1798
-
-
Johnson, K.1
Swindell, A.2
-
18
-
-
0032531309
-
Compartmental transit and dispersion model analysis of small intestinal transit flow in humans
-
L. Yu, J. Crison, and G. Amidon. Compartmental transit and dispersion model analysis of small intestinal transit flow in humans. Int. J. Pharm. 171(2):157-163 (1996).
-
(1996)
Int. J. Pharm.
, vol.171
, Issue.2
, pp. 157-163
-
-
Yu, L.1
Crison, J.2
Amidon, G.3
-
19
-
-
0032531309
-
Characterisation of small intestinal transit time distribution in humans
-
L. Yu, and G. Amidon. Characterisation of small intestinal transit time distribution in humans. Int. J. Pharm. 171(2):157-163 (1998).
-
(1998)
Int J Pharm.
, vol.171
, Issue.2
, pp. 157-163
-
-
Yu, L.1
Amidon, G.2
-
20
-
-
0031982148
-
Saturable small intestinal drug absorption in humans: Modeling and interpretation of cefatrizine data
-
L. Yu, and G. Amidon. Saturable small intestinal drug absorption in humans: Modeling and interpretation of cefatrizine data. Eur. J. Pharm. Biopharm. 45(2):199-203 (1998).
-
(1998)
Eur. J. Pharm. Biopharm.
, vol.45
, Issue.2
, pp. 199-203
-
-
Yu, L.1
Amidon, G.2
-
21
-
-
0035478779
-
Predicting the impact of physiological and biochemical processes on oral drug bioavailability
-
B. Agoram, W. Woltosz, and M. Bolger. Predicting the impact of physiological and biochemical processes on oral drug bioavailability. Adv. Drug Deliv. Rev. 50(S1):S41-67 (2001).
-
(2001)
Adv. Drug Deliv. Rev.
, vol.50
, Issue.S1
-
-
Agoram, B.1
Woltosz, W.2
Bolger, M.3
-
22
-
-
0011975740
-
Theoretical model studies of intestinal drug absorption V. Non-steady-state fluid flow and absorption
-
P. Ni, N. Ho, J. Fox, H. Leuenberger, and W. Higuchi. Theoretical model studies of intestinal drug absorption V. Non-steady-state fluid flow and absorption. Int. J. Pharm. 5(1):33-47 (1980).
-
(1980)
Int. J. Pharm.
, vol.5
, Issue.1
, pp. 33-47
-
-
Ni, P.1
Ho, N.2
Fox, J.3
Leuenberger, H.4
Higuchi, W.5
-
23
-
-
0002698633
-
Advancing quantitative and mechanistic approaches in interfacing gastrointestinal drug absorption studies in animals and humans
-
In W. Crouthamel and A. Sarapu (eds.) American Pharmaceutical Association, Washington
-
N. Ho, J. Park, P. Ni, and W. Higuchi. Advancing quantitative and mechanistic approaches in interfacing gastrointestinal drug absorption studies in animals and humans. In W. Crouthamel and A. Sarapu (eds.), Animal Models for Oral Drug Delivery. In Situ and In Vivo Approaches, American Pharmaceutical Association, Washington, 1983, pp. 27-106.
-
(1983)
Animal Models for Oral Drug Delivery. In Situ and In Vivo Approaches
, pp. 27-106
-
-
Ho, N.1
Park, J.2
Ni, P.3
Higuchi, W.4
-
24
-
-
0344084044
-
A physiological model for simulating gastrointestinal flow and drug absorption in rats
-
S. Willmann, W. Schmitt, J. Keldenich, and J. Dressman. A physiological model for simulating gastrointestinal flow and drug absorption in rats. Pharm. Res. 20(11):1766-1771 (2003).
-
(2003)
Pharm. Res.
, vol.20
, Issue.11
, pp. 1766-1771
-
-
Willmann, S.1
Schmitt, W.2
Keldenich, J.3
Dressman, J.4
-
25
-
-
3242778534
-
A physiological model for the estimation of the fraction dose absorbed in humans
-
S. Willmann, W. Schmitt, J. Keldenich, J. Lippert, and J. Dressman. A physiological model for the estimation of the fraction dose absorbed in humans. J. Med. Chem. 47(16):4022-4031 (2004).
-
(2004)
J. Med. Chem.
, vol.47
, Issue.16
, pp. 4022-4031
-
-
Willmann, S.1
Schmitt, W.2
Keldenich, J.3
Lippert, J.4
Dressman, J.5
-
26
-
-
34250004062
-
Development and validation of a physiology-based model for the prediction of oral absorption in monkeys
-
S. Willmann, A. N. Ediginton, and J. Dressman. Development and validation of a physiology-based model for the prediction of oral absorption in monkeys. Pharm. Res. 24(7):1275-1282 (2007).
-
(2007)
Pharm. Res.
, vol.24
, Issue.7
, pp. 1275-1282
-
-
Willmann, S.1
Ediginton, A.N.2
Dressman, J.3
-
27
-
-
0031026707
-
Simulation models to predict oral drug absorption from in vitro data
-
G. M. Grass. Simulation models to predict oral drug absorption from in vitro data. Adv. Drug Deliv. Rev. 23:199-219 (1997).
-
(1997)
Adv. Drug Deliv. Rev.
, vol.23
, pp. 199-219
-
-
Grass, G.M.1
-
28
-
-
0033999569
-
Development of predictive pharmacokinetic simulation models for drug discovery
-
D. A. Norris, G. D. Leesman, P. J. Sinko, and G. M. Grass. Development of predictive pharmacokinetic simulation models for drug discovery. J. Controlled Release. 65:55-62 (2000).
-
(2000)
J. Controlled Release
, vol.65
, pp. 55-62
-
-
Norris, D.A.1
Leesman, G.D.2
Sinko, P.J.3
Grass, G.M.4
-
29
-
-
0036803219
-
Prediction of intestinal absorption: Comparative assessment of GastroPlusä and IDEAä
-
N. Parrott, and Th. Lavé. Prediction of intestinal absorption: comparative assessment of GastroPlusä and IDEAä. Euro. J. Pharm. Sci. 17:51-61 (2002).
-
(2002)
Euro. J. Pharm. Sci.
, vol.17
, pp. 51-61
-
-
Parrott, N.1
Lavé, Th.2
-
30
-
-
0032939195
-
Heterogenous tube model for the study of small intestinal transit flow
-
A. Kalampokis, P. Argyrakis, and P. Macheras. Heterogenous tube model for the study of small intestinal transit flow. Pharm. Res. 16(1):87-91 (1999).
-
(1999)
Pharm. Res.
, vol.16
, Issue.1
, pp. 87-91
-
-
Kalampokis, A.1
Argyrakis, P.2
Macheras, P.3
-
31
-
-
0032750117
-
A heterogenous tube model of intestinal drug absorption based on probabilistic concepts
-
A. Kalampokis, P. Argyrakis, and P. Macheras. A heterogenous tube model of intestinal drug absorption based on probabilistic concepts. Pharm. Res. 16(11):1764-1769 (1999).
-
(1999)
Pharm. Res.
, vol.16
, Issue.11
, pp. 1764-1769
-
-
Kalampokis, A.1
Argyrakis, P.2
Macheras, P.3
-
32
-
-
15244344542
-
Application of full physiological models for pharmaceutical drug candidate selection and extrapolation of pharmacokinetics to man
-
N. Parrott, H. Jones, N. Paquereau, and T. Lavé. Application of full physiological models for pharmaceutical drug candidate selection and extrapolation of pharmacokinetics to man. Basic & Clin. Pharmacol. Toxicol. 96:193-199 (2005).
-
(2005)
Basic & Clin. Pharmacol. Toxicol
, vol.96
, pp. 193-199
-
-
Parrott, N.1
Jones, H.2
Paquereau, N.3
Lavé, T.4
-
33
-
-
28444451169
-
A strategy for preclinical formulation development using GastroPlusä as pharmacokinetic simulation tool and a statistical screening design applied to a dog study
-
M. Kuentz, S. Nick, N. Parrott, and D. Roethlisberger. A strategy for preclinical formulation development using GastroPlusä as pharmacokinetic simulation tool and a statistical screening design applied to a dog study. Eur. J. Pharm. Sci. 27(1):91-99 (2006).
-
(2006)
Eur. J. Pharm. Sci.
, vol.27
, Issue.1
, pp. 91-99
-
-
Kuentz, M.1
Nick, S.2
Parrott, N.3
Roethlisberger, D.4
-
34
-
-
0028948839
-
A theoretical basis for a biopharmaceutical drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
G. Amidon, H. Lennernas, V. Shah, and J. Crison. A theoretical basis for a biopharmaceutical drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 12(3):413-420 (1995).
-
(1995)
Pharm. Res.
, vol.12
, Issue.3
, pp. 413-420
-
-
Amidon, G.1
Lennernas, H.2
Shah, V.3
Crison, J.4
-
35
-
-
0031750861
-
Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs
-
E. Galia, E. Nicolaides, D. Hörter, R. Löbenberg, Ch. Reppas, and J. Dressman. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm. Res. 15(5):698-705 (1998).
-
(1998)
Pharm. Res.
, vol.15
, Issue.5
, pp. 698-705
-
-
Galia, E.1
Nicolaides, E.2
Hörter, D.3
Löbenberg, R.4
Reppas, Ch.5
Dressman, J.6
-
36
-
-
1842576537
-
Dissolution media simulation the intralumenal composition of the small intestinal intestine: Physiological issues and practical aspects
-
M. Vertzoni, N. Fotaki, E. Kostewicz, E. Stippler, Ch. Leuner, E. Nicolaides, J. Dressman, and Ch. Reppas. Dissolution media simulation the intralumenal composition of the small intestinal intestine: physiological issues and practical aspects. J. Pharm. Pharmacol. 56:453-562 (2004).
-
(2004)
J. Pharm. Pharmacol.
, vol.56
, pp. 453-562
-
-
Vertzoni, M.1
Fotaki, N.2
Kostewicz, E.3
Stippler, E.4
Leuner, Ch.5
Nicolaides, E.6
Dressman, J.7
Reppas, Ch.8
-
37
-
-
1942434691
-
Development of clinical dosage forms for a poorly water soluble drug I: Application of polyethylene glycol-polysorbate 80 solid dispersion carrier system
-
R. M. Dannenfelser, H. He, Y. Joshi, S. Bateman, and A. Serajuddin. Development of clinical dosage forms for a poorly water soluble drug I: application of polyethylene glycol-polysorbate 80 solid dispersion carrier system. J. of Pharm. Sci. 93(5):1165-1175 (2004).
-
(2004)
J. of Pharm. Sci.
, vol.93
, Issue.5
, pp. 1165-1175
-
-
Dannenfelser, R.M.1
He, H.2
Joshi, Y.3
Bateman, S.4
Serajuddin, A.5
-
38
-
-
33746893861
-
In silico Modeling of non-linear drug absorption for the P-gp substrate talinolol and of consequences for the resulting pharmacodynamic effect
-
M. Tubic, D. Wagner, H. Spahn-Langguth, M. Bolger, and P. Langguth. In silico Modeling of non-linear drug absorption for the P-gp substrate talinolol and of consequences for the resulting pharmacodynamic effect. Pharm. Res. 23(8):1712-1720 (2006).
-
(2006)
Pharm. Res.
, vol.23
, Issue.8
, pp. 1712-1720
-
-
Tubic, M.1
Wagner, D.2
Spahn-Langguth, H.3
Bolger, M.4
Langguth, P.5
-
39
-
-
33747759752
-
Biorelevant dissolution media as a predictive tool for glyburide a class II drug
-
H. Wei, and R. Löbenberg. Biorelevant dissolution media as a predictive tool for glyburide a class II drug. Euro. J. Pharm. Sci. 29:45-52 (2006).
-
(2006)
Euro. J. Pharm. Sci.
, vol.29
, pp. 45-52
-
-
Wei, H.1
Löbenberg, R.2
-
40
-
-
36549043514
-
A critical evaluation of fasted state simulating gastric fluid (FaSSGF) that contains sodium lauryl sulfate and proposal of a modified recipe
-
A. Aburub, D. S. Risley, and D. Mishra. A critical evaluation of fasted state simulating gastric fluid (FaSSGF) that contains sodium lauryl sulfate and proposal of a modified recipe. Int. J. Pharm. 347:16-22 (2008).
-
(2008)
Int. J. Pharm.
, vol.347
, pp. 16-22
-
-
Aburub, A.1
Risley, D.S.2
Mishra, D.3
-
41
-
-
0031913402
-
Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms
-
J. Dressman, G. Amidon, C. Reppas, and V. Shah. Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms. Pharm. Res. 15:11-22 (1998).
-
(1998)
Pharm. Res.
, vol.15
, pp. 11-22
-
-
Dressman, J.1
Amidon, G.2
Reppas, C.3
Shah, V.4
-
42
-
-
0004117882
-
-
Marcel Dekker, New York
-
G. A. Lewis, D. Mathieu, and R. Phan-Tan-Luu. Pharmaceutical Experimental Design. Marcel Dekker, New York, 1999, pp 27-184.
-
(1999)
Pharmaceutical Experimental Design
, pp. 27-184
-
-
Lewis, G.A.1
Mathieu, D.2
Phan-Tan-Luu, R.3
-
43
-
-
0142031028
-
Design of experiment (DoE) methods maximize information from a minimal number of animals in special cases of preclinical bioavailability testing
-
M. Kuentz, D. Röthlisberger, and W. Richter. Design of experiment (DoE) methods maximize information from a minimal number of animals in special cases of preclinical bioavailability testing. Pharm. Dev. Technol. 8(4):453-458 (2003).
-
(2003)
Pharm. Dev. Technol.
, vol.8
, Issue.4
, pp. 453-458
-
-
Kuentz, M.1
Röthlisberger, D.2
Richter, W.3
-
44
-
-
57149090187
-
Mefenamic Acid
-
In 2nd edn. Churchill Livingston, Edinburg, London
-
C. Dollery. Mefenamic Acid. In Therapeutic Drugs. 2nd edn. Churchill Livingston, Edinburg, London, 1998, pp M21-M24.
-
(1998)
Therapeutic Drugs
-
-
Dollery, C.1
-
45
-
-
0033941118
-
Influence of the particle size of mefenamic acid on dissolution and bioavailability of tablets (article in German)
-
D. Hummel, and St. Buchmann. Influence of the particle size of mefenamic acid on dissolution and bioavailability of tablets (article in German). Pharm. Ind. 62(6):452-456 (2000).
-
(2000)
Pharm. Ind.
, vol.62
, Issue.6
, pp. 452-456
-
-
Hummel, D.1
Buchmann, St.2
|