-
2
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
Noyes AA, Whitney WR. 1897. The rate of solution of solid substances in their own solutions. J Am Chem Soc 19:930-934.
-
(1897)
J Am Chem Soc
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
3
-
-
33747373878
-
A century of dissolution research: From Noyes and Whitney to the Biopharmaceutics Classification System
-
Dokoumetzidis A, Macheras P. 2006. A century of dissolution research: From Noyes and Whitney to the Biopharmaceutics Classification System. Int J Pharm 321:1-11.
-
(2006)
Int J Pharm
, vol.321
, pp. 1-11
-
-
Dokoumetzidis, A.1
Macheras, P.2
-
4
-
-
84960962793
-
Some physico-chemical factors in drug action
-
Brodie B, Hogben C. 1957. Some physico-chemical factors in drug action. J Pharm Pharmacol 9:345-380.
-
(1957)
J Pharm Pharmacol
, vol.9
, pp. 345-380
-
-
Brodie, B.1
Hogben, C.2
-
5
-
-
0001152155
-
The gastric secretion of drugs: A pH partition hypothesis
-
Shore P, Brodie B, Hogben C. 1957. The gastric secretion of drugs: A pH partition hypothesis. J Pharmacol Exp Ther 119:361-369.
-
(1957)
J Pharmacol Exp Ther
, vol.119
, pp. 361-369
-
-
Shore, P.1
Brodie, B.2
Hogben, C.3
-
8
-
-
0040914512
-
One hundred years of membrane permeability: Does Overton still rule?
-
Al-Awqati Q. 1999. One hundred years of membrane permeability: Does Overton still rule? Nat Cell Biol 1:E201-202.
-
(1999)
Nat Cell Biol
, vol.1
-
-
Al-Awqati, Q.1
-
9
-
-
77649216536
-
International transporter consortium. Membrane transporters in drug development
-
Giacomini KM, Huang SM, Tweedie DJ, Benet LZ, Brouwer KL, Chu X, Dahlin A, Evers R, Fischer V, Hillgren KM, Hoffmaster KA, Ishikawa T, Keppler D, Kim RB, Lee CA, Niemi M, Polli JW, Sugiyama Y, Swaan PW, Ware JA, Wright SH, Yee SW, Zamek-Gliszczynski MJ, Zhang L. 2010. International transporter consortium. Membrane transporters in drug development. Nat Rev Drug Discov 9:215-236.
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 215-236
-
-
Giacomini, K.M.1
Huang, S.M.2
Tweedie, D.J.3
Benet, L.Z.4
Brouwer, K.L.5
Chu, X.6
Dahlin, A.7
Evers, R.8
Fischer, V.9
Hillgren, K.M.10
Hoffmaster, K.A.11
Ishikawa, T.12
Keppler, D.13
Kim, R.B.14
Lee, C.A.15
Niemi, M.16
Polli, J.W.17
Sugiyama, Y.18
Swaan, P.W.19
Ware, J.A.20
Wright, S.H.21
Yee, S.W.22
Zamek-Gliszczynski, M.J.23
Zhang, L.24
more..
-
10
-
-
0001237487
-
The dissolution and diffusion of aspirin in aqueous media
-
Edwards LJ. 1951. The dissolution and diffusion of aspirin in aqueous media. Trans Faraday Soc 47:1191-1210.
-
(1951)
Trans Faraday Soc
, vol.47
, pp. 1191-1210
-
-
Edwards, L.J.1
-
11
-
-
2642628969
-
Physiochemical basis of the buffered acetylsalicylic acid controversy
-
Comment in Levy G, Hayes B. 1960. Physiochemical basis of the buffered acetylsalicylic acid controversy. N Engl J Med 262:1053-1058-The backstory. 2011. AAPS J 13:320-322.]
-
Levy G, Hayes B. 1960. Physiochemical basis of the buffered acetylsalicylic acid controversy. N Engl J Med 262:1053-1058. [Comment in Levy G, Hayes B. 1960. Physiochemical basis of the buffered acetylsalicylic acid controversy. N Engl J Med 262:1053-1058-The backstory. 2011. AAPS J 13:320-322.]
-
(1960)
N Engl J Med
, vol.262
, pp. 1053-1058
-
-
Levy, G.1
Hayes, B.2
-
12
-
-
70449176963
-
Solution rate of theophylline salts and effects from oral administration
-
Nelson E. 1957. Solution rate of theophylline salts and effects from oral administration. J Am Pharm Assoc 46:607-614.
-
(1957)
J Am Pharm Assoc
, vol.46
, pp. 607-614
-
-
Nelson, E.1
-
13
-
-
0004691796
-
Comparison of dissolution and absorption rates of different commercial aspirin tablets
-
Levy G. 1961. Comparison of dissolution and absorption rates of different commercial aspirin tablets. J Pharm Sci 50:388-392.
-
(1961)
J Pharm Sci
, vol.50
, pp. 388-392
-
-
Levy, G.1
-
14
-
-
78651121056
-
Effect of certain tablet formulation factors on dissolution rate of the active ingredient I
-
Levy G. 1963. Effect of certain tablet formulation factors on dissolution rate of the active ingredient I. J Pharm Sci 52:1039-1046.
-
(1963)
J Pharm Sci
, vol.52
, pp. 1039-1046
-
-
Levy, G.1
-
15
-
-
0343580040
-
Effect of certain tablet formulation factors on dissolution rate of the active ingredient II
-
Levy G. 1963. Effect of certain tablet formulation factors on dissolution rate of the active ingredient II. J Pharm Sci 52:1047-1051.
-
(1963)
J Pharm Sci
, vol.52
, pp. 1047-1051
-
-
Levy, G.1
-
16
-
-
0000919395
-
Development of in vitro dissolution tests which correlate quantitatively with dissolution rate-limited drug absorption in man
-
Levy G. 1965. Development of in vitro dissolution tests which correlate quantitatively with dissolution rate-limited drug absorption in man. J Pharm Sci 54:1719-1722.
-
(1965)
J Pharm Sci
, vol.54
, pp. 1719-1722
-
-
Levy, G.1
-
17
-
-
0001668733
-
Bioavailability and bioequivalence requirements
-
Federal Register
-
Federal Register. 1977. Bioavailability and bioequivalence requirements. Federal Register 42:1624-1653.
-
(1977)
Federal Register
, vol.42
, pp. 1624-1653
-
-
-
18
-
-
0006965756
-
Biopharmaceutics: Absorption aspects
-
Wagner JG. 1961. Biopharmaceutics: Absorption aspects. J Pharm Sci 50:359-387.
-
(1961)
J Pharm Sci
, vol.50
, pp. 359-387
-
-
Wagner, J.G.1
-
19
-
-
84881610527
-
-
United States Pharmacopeia (USP) 18. U.S. Pharmacopoeial Convention. Rockville, MD.
-
United States Pharmacopeia (USP) 18. U.S. Pharmacopoeial Convention. Rockville, MD.
-
-
-
-
20
-
-
0022070123
-
Absorption potential: Estimating the fraction absorbed for orally administered compounds
-
Dressman JB, Amidon GL, Fleisher D. 1985. Absorption potential: Estimating the fraction absorbed for orally administered compounds. J Pharm Sci 74:588-589.
-
(1985)
J Pharm Sci
, vol.74
, pp. 588-589
-
-
Dressman, J.B.1
Amidon, G.L.2
Fleisher, D.3
-
21
-
-
0024578889
-
Toward a quantitative approach for the prediction of the fraction of dose absorbed using the absorption potential concept
-
Macheras P, Symillides M. 1989. Toward a quantitative approach for the prediction of the fraction of dose absorbed using the absorption potential concept. Biopharm Drug Dispos 10:43-53.
-
(1989)
Biopharm Drug Dispos
, vol.10
, pp. 43-53
-
-
Macheras, P.1
Symillides, M.2
-
22
-
-
0025821306
-
Predicting fraction dose absorbed in humans using a macroscopic mass balance approach
-
Sinko PJ, Leesman GD, Amidon GL. 1991. Predicting fraction dose absorbed in humans using a macroscopic mass balance approach. Pharm Res 8:979-988.
-
(1991)
Pharm Res
, vol.8
, pp. 979-988
-
-
Sinko, P.J.1
Leesman, G.D.2
Amidon, G.L.3
-
23
-
-
0027473738
-
Estimating the fraction dose absorbed from suspensions of poorly soluble compounds in humans: A mathematical model
-
Oh DM, Curl RL, Amidon GL. 1993. Estimating the fraction dose absorbed from suspensions of poorly soluble compounds in humans: A mathematical model. Pharm Res 10:264-270.
-
(1993)
Pharm Res
, vol.10
, pp. 264-270
-
-
Oh, D.M.1
Curl, R.L.2
Amidon, G.L.3
-
24
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon GL, Lennernäs H, Shah VP, Crison JR. 1995. A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 12:413-420.
-
(1995)
Pharm Res
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernäs, H.2
Shah, V.P.3
Crison, J.R.4
-
25
-
-
84881616642
-
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Guidance for industry waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a Biopharmaceutics Classification System. Rockville, Maryland: FDA.
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). 2000. Guidance for industry waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a Biopharmaceutics Classification System. Rockville, Maryland: FDA.
-
(2000)
-
-
-
26
-
-
1242337282
-
The "high solubility' definition of the current FDA Guidance on Biopharmaceutical Classification System may be too strict for acidic drugs
-
Yazdanian M, Briggs K, Jankovsky C, Hawi A. 2004. The "high solubility' definition of the current FDA Guidance on Biopharmaceutical Classification System may be too strict for acidic drugs. Pharm Res 21:293-299.
-
(2004)
Pharm Res
, vol.21
, pp. 293-299
-
-
Yazdanian, M.1
Briggs, K.2
Jankovsky, C.3
Hawi, A.4
-
27
-
-
15244341878
-
Identification of biowaivers among Class II drugs: Theoretical justification and practical examples
-
Rinaki E, Dokoumetzidis A, Valsami G, Macheras P. 2004. Identification of biowaivers among Class II drugs: Theoretical justification and practical examples. Pharm Res 21:1567-1572.
-
(2004)
Pharm Res
, vol.21
, pp. 1567-1572
-
-
Rinaki, E.1
Dokoumetzidis, A.2
Valsami, G.3
Macheras, P.4
-
28
-
-
17644380257
-
Predicting drug disposition via application of BCS: Transport/absorption/ elimination interplay and development of a biopharmaceutics drug disposition classification system
-
Wu CY, Benet LZ. 2005. Predicting drug disposition via application of BCS: Transport/absorption/ elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm Res 22:11-23.
-
(2005)
Pharm Res
, vol.22
, pp. 11-23
-
-
Wu, C.Y.1
Benet, L.Z.2
-
32
-
-
84867851507
-
Elucidating the role of dose in the biopharmaceutics classification of drugs: The concepts of critical dose, effective in vivo solubility, and dose-dependent BCS
-
Charkoftaki G, Dokoumetzidis A, Valsami G, Macheras P. 2012. Elucidating the role of dose in the biopharmaceutics classification of drugs: The concepts of critical dose, effective in vivo solubility, and dose-dependent BCS. Pharm Res 29:3188-3198.
-
(2012)
Pharm Res
, vol.29
, pp. 3188-3198
-
-
Charkoftaki, G.1
Dokoumetzidis, A.2
Valsami, G.3
Macheras, P.4
-
33
-
-
84870665478
-
The role of BCS (Biopharmaceutics Classification System) and BDDCS (Biopharmaceutics Drug Disposition Classification System) in drug development
-
Benet LZ. 2013. The role of BCS (Biopharmaceutics Classification System) and BDDCS (Biopharmaceutics Drug Disposition Classification System) in drug development. J Pharm Sci 102:34-42.
-
(2013)
J Pharm Sci
, vol.102
, pp. 34-42
-
-
Benet, L.Z.1
-
34
-
-
8344279719
-
-
Eds. Wiley-VCH, Weinheim, Germany.
-
Van de Waterbeemd V, Lennernas H, Artursson P, Eds. 2003. Drug bioavailability. Estimation of solubility, permeability, absorption and bioavailability. Wiley-VCH, Weinheim, Germany.
-
(2003)
Drug bioavailability. Estimation of solubility, permeability, absorption and bioavailability
-
-
Van de, W.V.1
Lennernas, H.2
Artursson, P.3
-
35
-
-
0017130896
-
Method for monitoring hard gelatin capsule disintegration times in humans using external scintigraphy
-
Casey DL, Beihn RM, Digenis GA, Shabhu MB. 1976. Method for monitoring hard gelatin capsule disintegration times in humans using external scintigraphy. J Pharm Sci 65:1412-1413.
-
(1976)
J Pharm Sci
, vol.65
, pp. 1412-1413
-
-
Casey, D.L.1
Beihn, R.M.2
Digenis, G.A.3
Shabhu, M.B.4
-
36
-
-
0017367381
-
Use of 99mTc-labeled triethylenetetramine-polystyrene resin for measuring the gastric emptying rate in humans
-
Digenis GA, Beihn RM, Theodorakis MC, Shambhu MB. 1977. Use of 99mTc-labeled triethylenetetramine-polystyrene resin for measuring the gastric emptying rate in humans. J Pharm Sci 66:442-443.
-
(1977)
J Pharm Sci
, vol.66
, pp. 442-443
-
-
Digenis, G.A.1
Beihn, R.M.2
Theodorakis, M.C.3
Shambhu, M.B.4
-
37
-
-
80052261518
-
In vivo imaging of drug delivery systems in the GI tract
-
Weitschies W, Wilson CG. 2011. In vivo imaging of drug delivery systems in the GI tract. Int J Pharm 417:216-226.
-
(2011)
Int J Pharm
, vol.417
, pp. 216-226
-
-
Weitschies, W.1
Wilson, C.G.2
-
38
-
-
84867860406
-
The influence of gastric emptying kinetics on the drug release from enteric coated pellets in fasted state: An in vitro/in vivo correlation
-
Stefanio M, Locatelli I, Vrečer F, Sever T, Mrhar A, Bogataj M. 2012. The influence of gastric emptying kinetics on the drug release from enteric coated pellets in fasted state: An in vitro/in vivo correlation. Eur J Pharm Biopharm 82:376-382.
-
(2012)
Eur J Pharm Biopharm
, vol.82
, pp. 376-382
-
-
Stefanio, M.1
Locatelli, I.2
Vrečer, F.3
Sever, T.4
Mrhar, A.5
Bogataj, M.6
-
39
-
-
77954309697
-
The transit of dosage forms through the small intestine
-
Yuen KH. 2010. The transit of dosage forms through the small intestine. Int J Pharm 395:9-16.
-
(2010)
Int J Pharm
, vol.395
, pp. 9-16
-
-
Yuen, K.H.1
-
40
-
-
77954316197
-
The transit of dosage forms through the colon
-
Wilson GG. 2010. The transit of dosage forms through the colon. Int J Pharm 395:17-25.
-
(2010)
Int J Pharm
, vol.395
, pp. 17-25
-
-
Wilson, G.G.1
-
41
-
-
27744515754
-
Intestinal fluid volumes and transit of dosage forms as assessed by magnetic resonance imaging
-
Schiller C, Fröhlich CP, Giessmann T, Siegmund W, Mönnikes H, Hosten N, Weitschies W. 2005. Intestinal fluid volumes and transit of dosage forms as assessed by magnetic resonance imaging. Aliment Pharmacol Ther 22:971-979.
-
(2005)
Aliment Pharmacol Ther
, vol.22
, pp. 971-979
-
-
Schiller, C.1
Fröhlich, C.P.2
Giessmann, T.3
Siegmund, W.4
Mönnikes, H.5
Hosten, N.6
Weitschies, W.7
-
42
-
-
52249112060
-
IVIVC of controlled release formulations: Physiological-dynamical reasons for their failure
-
Dokoumetzidis A, Macheras P. 2008. IVIVC of controlled release formulations: Physiological-dynamical reasons for their failure. J Control Release 129:76-80.
-
(2008)
J Control Release
, vol.129
, pp. 76-80
-
-
Dokoumetzidis, A.1
Macheras, P.2
-
43
-
-
0030796952
-
GI drug absorption: Is it time to consider heterogeneity as well as homogeneity
-
Macheras P, Argyrakis P. 1997. GI drug absorption: Is it time to consider heterogeneity as well as homogeneity? Pharm Res 14:842-847.
-
(1997)
Pharm Res
, vol.14
, pp. 842-847
-
-
Macheras, P.1
Argyrakis, P.2
-
44
-
-
33744544180
-
Fractal reaction kinetics
-
Kopelman R. 1988. Fractal reaction kinetics. Science 241:1620-1626.
-
(1988)
Science
, vol.241
, pp. 1620-1626
-
-
Kopelman, R.1
-
46
-
-
0001151974
-
A multicompartmental dynamic computer-controlled model simulating the stomach and small intestine
-
Minekus PM, Havenaar R, Huis in't Veld JH. 1995. A multicompartmental dynamic computer-controlled model simulating the stomach and small intestine. Altern Lab Anim 23:197-209.
-
(1995)
Altern Lab Anim
, vol.23
, pp. 197-209
-
-
Minekus, P.M.1
Havenaar, R.2
Huis in't Veld, J.H.3
-
47
-
-
84881616130
-
-
Simulated biological dissolution and absorption system. Patent US6022733.
-
Tam YK, Anderson KE. 2000. Simulated biological dissolution and absorption system. Patent US6022733.
-
(2000)
-
-
Tam, Y.K.1
Anderson, K.E.2
-
48
-
-
84881609939
-
-
International Publication No. WO 2007/010238.
-
Wickham M, Faulks R. 2007 International Publication No. WO 2007/010238.
-
(2007)
-
-
Wickham, M.1
Faulks, R.2
-
49
-
-
85030493494
-
-
Artificial gut. Patent US6379619.
-
Rozga J, Demetriou A. 2002. Artificial gut. Patent US6379619. pp B1.
-
(2002)
-
-
Rozga, J.1
Demetriou, A.2
-
50
-
-
52949135236
-
Irregular absorption profiles observed from diclofenac extended release tablets can be predicted using a dissolution test apparatus that mimics in vivo physical stresses
-
Garbacz G, Wedemeyer R, Nagel S, Giessmann T, Mönnikes H, Wilson C, Siegmund W, Weitschies W. 2008. Irregular absorption profiles observed from diclofenac extended release tablets can be predicted using a dissolution test apparatus that mimics in vivo physical stresses. Eur J Pharm Biopharm 70:421-428.
-
(2008)
Eur J Pharm Biopharm
, vol.70
, pp. 421-428
-
-
Garbacz, G.1
Wedemeyer, R.2
Nagel, S.3
Giessmann, T.4
Mönnikes, H.5
Wilson, C.6
Siegmund, W.7
Weitschies, W.8
-
51
-
-
85030488488
-
-
Peristaltic movement simulating stirring device for dissolution testing. WO Patent WO/2010/014046.
-
Bogataj M, Cof G, Mrhar A. 2010. Peristaltic movement simulating stirring device for dissolution testing. WO Patent WO/2010/014046.
-
(2010)
-
-
Bogataj, M.1
Cof, G.2
Mrhar, A.3
-
52
-
-
0030818251
-
A population growth model of dissolution
-
Dokoumetzidis A, Macheras P. 1997. A population growth model of dissolution. Pharm Res 14:1122-1126.
-
(1997)
Pharm Res
, vol.14
, pp. 1122-1126
-
-
Dokoumetzidis, A.1
Macheras, P.2
-
54
-
-
0032862166
-
Does the dose-solubility ratio affect the mean dissolution time of drugs?
-
Lánský P, Weiss M. 1999. Does the dose-solubility ratio affect the mean dissolution time of drugs? Pharm Res 16:1470-1476.
-
(1999)
Pharm Res
, vol.16
, pp. 1470-1476
-
-
Lánský, P.1
Weiss, M.2
-
55
-
-
0037335193
-
The mean dissolution time depends on the dose/solubility ratio
-
Rinaki E, Dokoumetzidis A, Macheras P. 2003. The mean dissolution time depends on the dose/solubility ratio. Pharm Res 20:406-408.
-
(2003)
Pharm Res
, vol.20
, pp. 406-408
-
-
Rinaki, E.1
Dokoumetzidis, A.2
Macheras, P.3
-
56
-
-
32544450657
-
Analysis of dissolution data using modified versions of Noyes-Whitney equation and the weibull function
-
Dokoumetzidis A, Papadopoulou V, Macheras P. 2006. Analysis of dissolution data using modified versions of Noyes-Whitney equation and the weibull function. Pharm Res 23:256-261.
-
(2006)
Pharm Res
, vol.23
, pp. 256-261
-
-
Dokoumetzidis, A.1
Papadopoulou, V.2
Macheras, P.3
-
57
-
-
77957268773
-
Random effects in drug dissolution
-
Cupera J, Lansky P. 2010. Random effects in drug dissolution. Eur J Pharm Sci 41:430-439.
-
(2010)
Eur J Pharm Sci
, vol.41
, pp. 430-439
-
-
Cupera, J.1
Lansky, P.2
-
58
-
-
67349234502
-
Fractional kinetics in drug absorption and disposition processes
-
Dokoumetzidis A, Macheras P. 2009. Fractional kinetics in drug absorption and disposition processes. J Pharmacokinet Pharmacodyn 36:165-178.
-
(2009)
J Pharmacokinet Pharmacodyn
, vol.36
, pp. 165-178
-
-
Dokoumetzidis, A.1
Macheras, P.2
-
59
-
-
77955844453
-
Power law IVIVC: An application of fractional kinetics for drug release and absorption
-
Kytariolos J, Dokoumetzidis A, Macheras P. 2010. Power law IVIVC: An application of fractional kinetics for drug release and absorption. Eur J Pharm Sci 41:299-304.
-
(2010)
Eur J Pharm Sci
, vol.41
, pp. 299-304
-
-
Kytariolos, J.1
Dokoumetzidis, A.2
Macheras, P.3
-
60
-
-
79955596530
-
The changing face of the rate concept in biopharmaceutical sciences: From classical to fractal and finally to fractional
-
Dokoumetzidis A, Macheras P. 2011. The changing face of the rate concept in biopharmaceutical sciences: From classical to fractal and finally to fractional. Pharm Res 28:1229-1232.
-
(2011)
Pharm Res
, vol.28
, pp. 1229-1232
-
-
Dokoumetzidis, A.1
Macheras, P.2
-
61
-
-
0024916348
-
Effect of temperature and fat content on the solubility of hydrochlorothiazide and chlorothiazide in milk
-
Macheras P, Koupparis M, Antimisiaris S. 1989. Effect of temperature and fat content on the solubility of hydrochlorothiazide and chlorothiazide in milk. J Pharm Sci 78:933-936.
-
(1989)
J Pharm Sci
, vol.78
, pp. 933-936
-
-
Macheras, P.1
Koupparis, M.2
Antimisiaris, S.3
-
63
-
-
0023038127
-
Drug dissolution studies in milk using the automated flow-injection serial dynamic dialysis technique
-
Macheras P, Koupparis M, Tsaprounis C. 1986. Drug dissolution studies in milk using the automated flow-injection serial dynamic dialysis technique. Int J Pharm 33:125-136.
-
(1986)
Int J Pharm
, vol.33
, pp. 125-136
-
-
Macheras, P.1
Koupparis, M.2
Tsaprounis, C.3
-
64
-
-
0023097483
-
Dissolution of four controlled-release theophylline formulations in milk
-
Macheras P, Koupparis M, Apostolleli E. 1987. Dissolution of four controlled-release theophylline formulations in milk. Int J Pharm 36:73-79.
-
(1987)
Int J Pharm
, vol.36
, pp. 73-79
-
-
Macheras, P.1
Koupparis, M.2
Apostolleli, E.3
-
65
-
-
0024368940
-
An in vitro model for exploring CR theophylline-milk fat interactions
-
Macheras P, Koupparis M, Antimisiaris S. 1989. An in vitro model for exploring CR theophylline-milk fat interactions. Int J Pharm 54:123-130.
-
(1989)
Int J Pharm
, vol.54
, pp. 123-130
-
-
Macheras, P.1
Koupparis, M.2
Antimisiaris, S.3
-
66
-
-
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, Dressman JB. 1998. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm Res 15:698-705.
-
(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
-
67
-
-
84862235954
-
Biorelevant in-vitro performance testing of orally administered dosage forms
-
Reppas C, Vertzoni M. 2012. Biorelevant in-vitro performance testing of orally administered dosage forms. J Pharm Pharmacol 64:919-930.
-
(2012)
J Pharm Pharmacol
, vol.64
, pp. 919-930
-
-
Reppas, C.1
Vertzoni, M.2
-
68
-
-
13844320734
-
Chasing equilibrium: Measuring the intrinsic solubility of weak acids and bases
-
Stuart M, Box K. 2005. Chasing equilibrium: Measuring the intrinsic solubility of weak acids and bases. Anal Chem 77:983-990.
-
(2005)
Anal Chem
, vol.77
, pp. 983-990
-
-
Stuart, M.1
Box, K.2
-
69
-
-
33745053147
-
Equilibrium versus kinetic measurements of aqueous solubility, and the ability of compounds to supersaturate in solution-A validation study
-
Box KJ, Völgyi G, Baka E, Stuart M, Takács-Novák K, Comer JE. 2006. Equilibrium versus kinetic measurements of aqueous solubility, and the ability of compounds to supersaturate in solution-A validation study. J Pharm Sci 95:1298-1307.
-
(2006)
J Pharm Sci
, vol.95
, pp. 1298-1307
-
-
Box, K.J.1
Völgyi, G.2
Baka, E.3
Stuart, M.4
Takács-Novák, K.5
Comer, J.E.6
-
70
-
-
83555174460
-
Precipitation in and supersaturation of contents of the upper small intestine after administration of two weak bases to fasted adults
-
Psachoulias D, Vertzoni M, Goumas K, Kalioras V, Beato S, Butler J, Reppas C. 2011. Precipitation in and supersaturation of contents of the upper small intestine after administration of two weak bases to fasted adults. Pharm Res 28:3145-3158.
-
(2011)
Pharm Res
, vol.28
, pp. 3145-3158
-
-
Psachoulias, D.1
Vertzoni, M.2
Goumas, K.3
Kalioras, V.4
Beato, S.5
Butler, J.6
Reppas, C.7
-
71
-
-
84872082242
-
An in vitro methodology for forecasting luminal concentrations and precipitation of highly permeable lipophilic weak bases in the fasted upper small intestine
-
Psachoulias D, Vertzoni M, Butler J, Busby D, Symillides M, Dressman J, Reppas C. 2012. An in vitro methodology for forecasting luminal concentrations and precipitation of highly permeable lipophilic weak bases in the fasted upper small intestine. Pharm Res 29:3486-3498.
-
(2012)
Pharm Res
, vol.29
, pp. 3486-3498
-
-
Psachoulias, D.1
Vertzoni, M.2
Butler, J.3
Busby, D.4
Symillides, M.5
Dressman, J.6
Reppas, C.7
-
72
-
-
68249128120
-
Supersaturating drug delivery systems: The answer to solubility-limited oral bioavailability?
-
Brouwers J, Brewster ME, Augustijns P. 2009. Supersaturating drug delivery systems: The answer to solubility-limited oral bioavailability? J Pharm Sci 98:2549-2572.
-
(2009)
J Pharm Sci
, vol.98
, pp. 2549-2572
-
-
Brouwers, J.1
Brewster, M.E.2
Augustijns, P.3
-
73
-
-
77957371289
-
Predicting intestinal precipitation-A case example for a basic BCS class II drug
-
Carlert S, Pålsson A, Hanisch G, von Corswant C, Nilsson C, Lindfors L, Lennernäs H, Abrahamsson B. 2010. Predicting intestinal precipitation-A case example for a basic BCS class II drug. Pharm Res 27:2119-2130.
-
(2010)
Pharm Res
, vol.27
, pp. 2119-2130
-
-
Carlert, S.1
Pålsson, A.2
Hanisch, G.3
von Corswant, C.4
Nilsson, C.5
Lindfors, L.6
Lennernäs, H.7
Abrahamsson, B.8
-
74
-
-
84866733801
-
pH-Induced precipitation behavior of weakly basic compounds: Determination of extent and duration of supersaturation using potentiometric titration and correlation to solid state properties
-
Hsieh YL, Ilevbare GA, Van Eerdenbrugh B, Box KJ, Sanchez-Felix MV, Taylor LS. 2012. pH-Induced precipitation behavior of weakly basic compounds: Determination of extent and duration of supersaturation using potentiometric titration and correlation to solid state properties. Pharm Res 29:2738-2753.
-
(2012)
Pharm Res
, vol.29
, pp. 2738-2753
-
-
Hsieh, Y.L.1
Ilevbare, G.A.2
Van Eerdenbrugh, B.3
Box, K.J.4
Sanchez-Felix, M.V.5
Taylor, L.S.6
-
75
-
-
1042269559
-
Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine
-
Kostewicz ES, Wunderlich M, Brauns U, Becker R, Bock T, Dressman JB. 2004. Predicting the precipitation of poorly soluble weak bases upon entry in the small intestine. J Pharm Pharmacol 56:43-51.
-
(2004)
J Pharm Pharmacol
, vol.56
, pp. 43-51
-
-
Kostewicz, E.S.1
Wunderlich, M.2
Brauns, U.3
Becker, R.4
Bock, T.5
Dressman, J.B.6
-
76
-
-
67349204296
-
Postprandial changes in solubilizing capacity of human intestinal fluids for BCS class II drugs
-
Clarysse S, Psachoulias D, Brouwers J, Tack J, Annaert P, Duchateau G, Reppas C, Augustijns P. 2009. Postprandial changes in solubilizing capacity of human intestinal fluids for BCS class II drugs. Pharm Res 26:1456-1466.
-
(2009)
Pharm Res
, vol.26
, pp. 1456-1466
-
-
Clarysse, S.1
Psachoulias, D.2
Brouwers, J.3
Tack, J.4
Annaert, P.5
Duchateau, G.6
Reppas, C.7
Augustijns, P.8
-
77
-
-
0030829862
-
A new approach for direct in vivo dissolution studies of poorly soluble drugs
-
Bonlokke L, Christensen FN, Knutson L, Kristensen HG, Lennernäs H. 1997. A new approach for direct in vivo dissolution studies of poorly soluble drugs. Pharm Res 14:1490-1492.
-
(1997)
Pharm Res
, vol.14
, pp. 1490-1492
-
-
Bonlokke, L.1
Christensen, F.N.2
Knutson, L.3
Kristensen, H.G.4
Lennernäs, H.5
-
78
-
-
41349116109
-
Development of a reaction-limited model of dissolution: Application to official dissolution tests experiments
-
Dokoumetzidis A, Papadopoulou V, Valsami G, Macheras P. 2008. Development of a reaction-limited model of dissolution: Application to official dissolution tests experiments. Int J Pharm 355:114-125.
-
(2008)
Int J Pharm
, vol.355
, pp. 114-125
-
-
Dokoumetzidis, A.1
Papadopoulou, V.2
Valsami, G.3
Macheras, P.4
-
79
-
-
79952237126
-
Supersaturated dissolution data and their interpretation: The TPGS-carbamazepine model case
-
Charkoftaki G, Dokoumetzidis A, Valsami G, Macheras P. 2011. Supersaturated dissolution data and their interpretation: The TPGS-carbamazepine model case. J Pharm Pharmacol 63:352-361.
-
(2011)
J Pharm Pharmacol
, vol.63
, pp. 352-361
-
-
Charkoftaki, G.1
Dokoumetzidis, A.2
Valsami, G.3
Macheras, P.4
-
80
-
-
84874905452
-
From supersaturated drug delivery systems to the rising era of pediatric formulations
-
Charkoftaki G, Valsami G, Macheras P. 2012. From supersaturated drug delivery systems to the rising era of pediatric formulations. Chem Biochem Eng 26:427-434.
-
(2012)
Chem Biochem Eng
, vol.26
, pp. 427-434
-
-
Charkoftaki, G.1
Valsami, G.2
Macheras, P.3
-
82
-
-
67650569218
-
A simulation of oral absorption using classical nucleation theory
-
Sugano K. 2009. A simulation of oral absorption using classical nucleation theory. Int J Pharm 378:142-145.
-
(2009)
Int J Pharm
, vol.378
, pp. 142-145
-
-
Sugano, K.1
-
83
-
-
77957726083
-
Aqueous boundary layers related to oral absorption of a drug: From dissolution of a drug to carrier mediated transport and intestinal wall metabolism
-
Sugano K. 2010. Aqueous boundary layers related to oral absorption of a drug: From dissolution of a drug to carrier mediated transport and intestinal wall metabolism. Mol Pharm 7:1362-1373.
-
(2010)
Mol Pharm
, vol.7
, pp. 1362-1373
-
-
Sugano, K.1
-
85
-
-
80053562546
-
Investigating the effect of solubility and density gradients on local hydrodynamics and drug dissolution in the USP 4 dissolution apparatus
-
D'Arcy DM, Liu B, Corrigan O. 2011. Investigating the effect of solubility and density gradients on local hydrodynamics and drug dissolution in the USP 4 dissolution apparatus. Int J Pharm 419:175-185.
-
(2011)
Int J Pharm
, vol.419
, pp. 175-185
-
-
D'Arcy, D.M.1
Liu, B.2
Corrigan, O.3
-
86
-
-
29244489524
-
Evaluation of hydrodynamics in the basket dissolution apparatus using computational fluid dynamics-dissolution rate implications
-
D'Arcy DM, Corrigan OI, Healy AM. 2006. Evaluation of hydrodynamics in the basket dissolution apparatus using computational fluid dynamics-dissolution rate implications. Eur J Pharm Sci 27:259-267.
-
(2006)
Eur J Pharm Sci
, vol.27
, pp. 259-267
-
-
D'Arcy, D.M.1
Corrigan, O.I.2
Healy, A.M.3
-
87
-
-
67349107479
-
Towards determining appropriate hydrodynamic conditions for in vitro in vivo correlations using computational fluid dynamics
-
D'Arcy DM, Healy AM, Corrigan OI. 2009. Towards determining appropriate hydrodynamic conditions for in vitro in vivo correlations using computational fluid dynamics. Eur J Pharm Sci 37:291-299.
-
(2009)
Eur J Pharm Sci
, vol.37
, pp. 291-299
-
-
D'Arcy, D.M.1
Healy, A.M.2
Corrigan, O.I.3
-
88
-
-
67349266232
-
Mathematical modeling of the fluid dynamics in the flow-through cell
-
Kakhi M. 2009. Mathematical modeling of the fluid dynamics in the flow-through cell. Int J Pharm 376:22-40.
-
(2009)
Int J Pharm
, vol.376
, pp. 22-40
-
-
Kakhi, M.1
-
89
-
-
55749090038
-
Particle diffusional layer thickness in a USP dissolution apparatus II: A combined function of particle size and paddle speed
-
Sheng JJ, Sirois PJ, Dressman JB, Amidon GL. 2008. Particle diffusional layer thickness in a USP dissolution apparatus II: A combined function of particle size and paddle speed. J Pharm Sci 97:4815-4829.
-
(2008)
J Pharm Sci
, vol.97
, pp. 4815-4829
-
-
Sheng, J.J.1
Sirois, P.J.2
Dressman, J.B.3
Amidon, G.L.4
-
90
-
-
84860743411
-
Comparison and analysis of theoretical models for diffusion-controlled dissolution
-
Wang Y, Abrahamsson B, Lindfors L, Brasseur JG. 2012. Comparison and analysis of theoretical models for diffusion-controlled dissolution. Mol Pharm 9:1052-1066.
-
(2012)
Mol Pharm
, vol.9
, pp. 1052-1066
-
-
Wang, Y.1
Abrahamsson, B.2
Lindfors, L.3
Brasseur, J.G.4
-
91
-
-
33747348812
-
Uber die auflosungsgeschwindindigkeit fester Korper
-
Brunner L, Tolloczko S. 1900. Uber die auflosungsgeschwindindigkeit fester Korper. Z Phys Chem 35:283-290.
-
(1900)
Z Phys Chem
, vol.35
, pp. 283-290
-
-
Brunner, L.1
Tolloczko, S.2
-
92
-
-
84887725686
-
Dependence of reaction velocity upon surface and agitation
-
Hixson AW, Crowell JH. 1931. Dependence of reaction velocity upon surface and agitation. Ind Eng Chem 23:923-931.
-
(1931)
Ind Eng Chem
, vol.23
, pp. 923-931
-
-
Hixson, A.W.1
Crowell, J.H.2
-
93
-
-
0034058121
-
On the heterogeneity of drug dissolution and release
-
Macheras P, Dokoumetzidis A. 2000. On the heterogeneity of drug dissolution and release. Pharm Res 17:108-112.
-
(2000)
Pharm Res
, vol.17
, pp. 108-112
-
-
Macheras, P.1
Dokoumetzidis, A.2
-
94
-
-
31144453624
-
On the use of the Weibull function for the discernment of drug release mechanisms
-
Papadopoulou V, Kosmidis K, Vlachou M, Macheras P. 2006. On the use of the Weibull function for the discernment of drug release mechanisms. Int J Pharm 309:44-50.
-
(2006)
Int J Pharm
, vol.309
, pp. 44-50
-
-
Papadopoulou, V.1
Kosmidis, K.2
Vlachou, M.3
Macheras, P.4
-
95
-
-
0000559465
-
Reconstitution of cell membrane structure in vitro and its transformation into an existable system
-
Mueller P, Rudin D, Tien H, Wescott W. 1962. Reconstitution of cell membrane structure in vitro and its transformation into an existable system. Nature 194:979-980.
-
(1962)
Nature
, vol.194
, pp. 979-980
-
-
Mueller, P.1
Rudin, D.2
Tien, H.3
Wescott, W.4
-
96
-
-
1442358760
-
High throughput measurement of permeability
-
van de Waterbeemd H, Lennernas H, Artursson P, Eds. Weinheim, Germany: Willey-VCH
-
Avdeef A. 2005. High throughput measurement of permeability. In Drug bioavailability: Estimation of solubility, permeability and bioavailability; van de Waterbeemd H, Lennernas H, Artursson P, Eds. Weinheim, Germany: Willey-VCH, pp 46-71.
-
(2005)
Drug bioavailability: Estimation of solubility, permeability and bioavailability;
, pp. 46-71
-
-
Avdeef, A.1
-
97
-
-
0021350933
-
Monocarboxylic acid permeation through lipid bilayer membranes
-
Walter A, Gutknecht J. 1984. Monocarboxylic acid permeation through lipid bilayer membranes. J Membr Biol 77:255-264.
-
(1984)
J Membr Biol
, vol.77
, pp. 255-264
-
-
Walter, A.1
Gutknecht, J.2
-
98
-
-
0028149794
-
Substituent contributions to the transport of substituted p-toluic acids across lipid bilayer membranes
-
Xiang TX, Anderson B. 1994. Substituent contributions to the transport of substituted p-toluic acids across lipid bilayer membranes. J Pharm Sci 83:1511-1518.
-
(1994)
J Pharm Sci
, vol.83
, pp. 1511-1518
-
-
Xiang, T.X.1
Anderson, B.2
-
99
-
-
13244285816
-
Cell cultures in drug discovery: An industrial perspective
-
van de Waterbeemd H, Lennernas H, Artursson P, Eds. Weinheim, Germany: Willey-VCH
-
Ungell AL, Karlsson J. 2005. Cell cultures in drug discovery: An industrial perspective. In Drug bioavailability: Estimation of solubility, permeability and bioavailability; van de Waterbeemd H, Lennernas H, Artursson P, Eds. Weinheim, Germany: Willey-VCH, pp 90-131.
-
(2005)
Drug bioavailability: Estimation of solubility, permeability and bioavailability;
, pp. 90-131
-
-
Ungell, A.L.1
Karlsson, J.2
-
100
-
-
0034458680
-
Current methodologies used for evaluation of intestinal permeability and absorption
-
Balimane P, Chong S, Morrison R. 2004. Current methodologies used for evaluation of intestinal permeability and absorption. J Pharmacol Toxicol Methods 44:301-312.
-
(2004)
J Pharmacol Toxicol Methods
, vol.44
, pp. 301-312
-
-
Balimane, P.1
Chong, S.2
Morrison, R.3
-
101
-
-
0002311366
-
High-throughput measurements of solubility profiles
-
Testa B, van de Waterbeemd H, Folkers G, Guy R, Eds. Zurich: Verlag Helvetica Chimica Acta and Weinheim; Wiley-VCH, Weinheim, Germany
-
Avdeef A. 2001. High-throughput measurements of solubility profiles. In Pharmacokinetic optimization in drug research; Testa B, van de Waterbeemd H, Folkers G, Guy R, Eds. Zurich: Verlag Helvetica Chimica Acta and Weinheim; Wiley-VCH, Weinheim, Germany, pp 305-326.
-
(2001)
Pharmacokinetic optimization in drug research;
, pp. 305-326
-
-
Avdeef, A.1
-
102
-
-
0034778663
-
Drug absorption in vitro model: Filter-immobilized artificial membranes. 2. Studies of the permeability properties of lactones in Piper methysticum Forst
-
Avdeef A, Strafford M, Block E, Balogh M, Chambliss W, Khan I. 2001. Drug absorption in vitro model: Filter-immobilized artificial membranes. 2. Studies of the permeability properties of lactones in Piper methysticum Forst. Eur J Pharm Sci 14:271-280.
-
(2001)
Eur J Pharm Sci
, vol.14
, pp. 271-280
-
-
Avdeef, A.1
Strafford, M.2
Block, E.3
Balogh, M.4
Chambliss, W.5
Khan, I.6
-
103
-
-
0035468033
-
Physicochemical profiling (solubility, permeability and charge state)
-
Avdeef A. 2001. Physicochemical profiling (solubility, permeability and charge state). Curr Top Med Chem 1:277-351.
-
(2001)
Curr Top Med Chem
, vol.1
, pp. 277-351
-
-
Avdeef, A.1
-
104
-
-
0032189375
-
Estimation of permeability by diffusion through Caco-2 cell monolayers using the drugś liphophilicity and molecular weight
-
Camenisch G, Alsenz J, van de Waterbeemd H, Folker G. 1998. Estimation of permeability by diffusion through Caco-2 cell monolayers using the drugś liphophilicity and molecular weight. Eur J Pharm Sci 6:313-319.
-
(1998)
Eur J Pharm Sci
, vol.6
, pp. 313-319
-
-
Camenisch, G.1
Alsenz, J.2
van de, W.H.3
Folker, G.4
-
105
-
-
0032696606
-
Effect of molecular charge on intestinal epithelial drug transport: pH-Dependent transport of cationic drugs
-
Palm K, Luthman K, Ros J, Gråsjö J, Artursson P. 1999. Effect of molecular charge on intestinal epithelial drug transport: pH-Dependent transport of cationic drugs. J Pharmacol Exp Ther 291:435-443.
-
(1999)
J Pharmacol Exp Ther
, vol.291
, pp. 435-443
-
-
Palm, K.1
Luthman, K.2
Ros, J.3
Gråsjö, J.4
Artursson, P.5
-
106
-
-
0030964577
-
In vitro absorption studies and their relevance to absorption from the GI tract
-
Ungell AL. 1997. In vitro absorption studies and their relevance to absorption from the GI tract. Drug Dev Ind Pharm 23:879-892.
-
(1997)
Drug Dev Ind Pharm
, vol.23
, pp. 879-892
-
-
Ungell, A.L.1
-
107
-
-
0036294084
-
Molecular factors influencing retention on immobilized artificial membranes (IAM) compared to partitioning in liposomes and n-octanol
-
Taillardat-Bertschinger A, Marca Martinet CA, Carrupt PA, Reist M, Caron G, Fruttero R, Testa B. 2002. Molecular factors influencing retention on immobilized artificial membranes (IAM) compared to partitioning in liposomes and n-octanol. Pharm Res 19:729-737.
-
(2002)
Pharm Res
, vol.19
, pp. 729-737
-
-
Taillardat-Bertschinger, A.1
Marca, M.C.2
Carrupt, P.A.3
Reist, M.4
Caron, G.5
Fruttero, R.6
Testa, B.7
-
108
-
-
0029058745
-
IAM chromatography: An in vitro screen for predicting drug membrane permeability
-
Pidgeon C, Ong S, Liu H, Qiu X, Pidgeon M, Dantzig AH, Munroe J, Hornback WJ, Kasher JS, Glunz L, Szczerba T. 1995. IAM chromatography: An in vitro screen for predicting drug membrane permeability. J Med Chem 38:590-594.
-
(1995)
J Med Chem
, vol.38
, pp. 590-594
-
-
Pidgeon, C.1
Ong, S.2
Liu, H.3
Qiu, X.4
Pidgeon, M.5
Dantzig, A.H.6
Munroe, J.7
Hornback, W.J.8
Kasher, J.S.9
Glunz, L.10
Szczerba, T.11
-
109
-
-
0037188770
-
Immobilized liposome chromatography to study drug-membrane interactions. Correlation with drug absorption in humans
-
Liu XY, Nakamura C, Yang Q, Kamo N, Miyake J. 2002. Immobilized liposome chromatography to study drug-membrane interactions. Correlation with drug absorption in humans. J Chromatogr A 961:113-118.
-
(2002)
J Chromatogr A
, vol.961
, pp. 113-118
-
-
Liu, X.Y.1
Nakamura, C.2
Yang, Q.3
Kamo, N.4
Miyake, J.5
-
110
-
-
19544367831
-
Prediction of drug absorption based on immobilized artificial membrane (IAM) chromatography separation and calculated molecular descriptors
-
Yen TE, Agatonovic-Kustrin S, Evans AM, Nation RL, Ryand J. 2005. Prediction of drug absorption based on immobilized artificial membrane (IAM) chromatography separation and calculated molecular descriptors. J Pharm Biomed Anal 38:472-478.
-
(2005)
J Pharm Biomed Anal
, vol.38
, pp. 472-478
-
-
Yen, T.E.1
Agatonovic-Kustrin, S.2
Evans, A.M.3
Nation, R.L.4
Ryand, J.5
-
111
-
-
0032568397
-
Physicochemical high throughput screening, parallel artificial membrane permeation assay in the description of passive absorption processes
-
Kansy M, Senner F, Gubernator K. 1998. Physicochemical high throughput screening, parallel artificial membrane permeation assay in the description of passive absorption processes. J Med Chem 41:1007-1010.
-
(1998)
J Med Chem
, vol.41
, pp. 1007-1010
-
-
Kansy, M.1
Senner, F.2
Gubernator, K.3
-
112
-
-
60749111590
-
Artificial membrane assays to assess permeability
-
Faller B. 2008. Artificial membrane assays to assess permeability. Current Drug Metabolism 9:886-892.
-
(2008)
Current Drug Metabolism
, vol.9
, pp. 886-892
-
-
Faller, B.1
-
113
-
-
0017412603
-
One hundred and twenty seven cultured human tumor cell lines producing tumors in nude mice
-
Fogh J, Fogh JM, Orfeo T. 1977. One hundred and twenty seven cultured human tumor cell lines producing tumors in nude mice. J Natl Cancer Inst 59:221-226.
-
(1977)
J Natl Cancer Inst
, vol.59
, pp. 221-226
-
-
Fogh, J.1
Fogh, J.M.2
Orfeo, T.3
-
114
-
-
0025311288
-
Epithelial transport of drugs in cell culture. I: A model for studying the passive diffusion of drugs over intestinal absorptive (Caco-2) cells
-
Artursson P. 1990. Epithelial transport of drugs in cell culture. I: A model for studying the passive diffusion of drugs over intestinal absorptive (Caco-2) cells. J Pharm Sci 79:476-482.
-
(1990)
J Pharm Sci
, vol.79
, pp. 476-482
-
-
Artursson, P.1
-
115
-
-
0024593744
-
Characterization of the human colon carcinoma cell line (Caco-2) as a model system for intestinal epithelial permeability
-
Hidalgo IJ, Raub TJ, Borchardt RT. 1989. Characterization of the human colon carcinoma cell line (Caco-2) as a model system for intestinal epithelial permeability. Gastroenterology 96:736-749.
-
(1989)
Gastroenterology
, vol.96
, pp. 736-749
-
-
Hidalgo, I.J.1
Raub, T.J.2
Borchardt, R.T.3
-
116
-
-
0025132942
-
Caco-2 cell monolayers as a model for drug transport across the intestinal mucosa
-
Hilgers AR, Conradi RA, Burton PS. 1990. Caco-2 cell monolayers as a model for drug transport across the intestinal mucosa. Pharm Res 9:902-910.
-
(1990)
Pharm Res
, vol.9
, pp. 902-910
-
-
Hilgers, A.R.1
Conradi, R.A.2
Burton, P.S.3
-
117
-
-
0024505075
-
The Madin-Darby canine kidney (MDCK) epithelial cell monolayers as a model cellular transport barrier
-
Cho MJ, Thompson DP, Cramer CT, Vidmar TJ, Schieszka JF. 1989. The Madin-Darby canine kidney (MDCK) epithelial cell monolayers as a model cellular transport barrier. Pharm Res 6:71-77.
-
(1989)
Pharm Res
, vol.6
, pp. 71-77
-
-
Cho, M.J.1
Thompson, D.P.2
Cramer, C.T.3
Vidmar, T.J.4
Schieszka, J.F.5
-
118
-
-
0030464177
-
Human dipeptide transporter, hPEPT1, stably transfected into Chinese hamster ovary cells
-
Covitz KMY, Amidon GL, Sadée W. 1996. Human dipeptide transporter, hPEPT1, stably transfected into Chinese hamster ovary cells. Pharm Res 13:1631-1634.
-
(1996)
Pharm Res
, vol.13
, pp. 1631-1634
-
-
Covitz, K.M.Y.1
Amidon, G.L.2
Sadée, W.3
-
119
-
-
0021067619
-
Enterocyte-like differentiation and polarization of the human colon carcinoma cell line Caco-2 in culture
-
Pinto M, Robine-Leon S, Appay MD, Kedinger M, Triadou N, Dussaulx E, Lacroix B, Simon-Assmann P, Haffen K, Fogh J, Zweibaum A. 1983. Enterocyte-like differentiation and polarization of the human colon carcinoma cell line Caco-2 in culture. Biol Cell 47:323-330.
-
(1983)
Biol Cell
, vol.47
, pp. 323-330
-
-
Pinto, M.1
Robine-Leon, S.2
Appay, M.D.3
Kedinger, M.4
Triadou, N.5
Dussaulx, E.6
Lacroix, B.7
Simon-Assmann, P.8
Haffen, K.9
Fogh, J.10
Zweibaum, A.11
-
120
-
-
40049083570
-
Caco-2 and emerging alternatives for prediction of intestinal drug transport: A general overview
-
van de Waterbeemd H, Lennernas H, Artursson P, Eds. Weinheim, Germany: Willey-VCH
-
Artursson P, Tavelin S. 2005. Caco-2 and emerging alternatives for prediction of intestinal drug transport: A general overview. In Drug bioavailability: Estimation of solubility, permeability and bioavailability; van de Waterbeemd H, Lennernas H, Artursson P, Eds. Weinheim, Germany: Willey-VCH, pp 72-90.
-
(2005)
Drug bioavailability: Estimation of solubility, permeability and bioavailability;
, pp. 72-90
-
-
Artursson, P.1
Tavelin, S.2
-
121
-
-
0025189818
-
Transport and permeability properties of human Caco-2 cells. An in vitro model for the intestinal epithelial cell barrier
-
Wilson G, Hassan IF, Dix CJ, Williamson I, Mackay M. 1990. Transport and permeability properties of human Caco-2 cells. An in vitro model for the intestinal epithelial cell barrier. J Control Release 11:25-40.
-
(1990)
J Control Release
, vol.11
, pp. 25-40
-
-
Wilson, G.1
Hassan, I.F.2
Dix, C.J.3
Williamson, I.4
Mackay, M.5
-
122
-
-
0027312774
-
Selective paracellular permeability in two models for intestinal absorption: Cultured monolayers of human intestinal epithelial cells and rat intestinal segments
-
Artursson P, Ungell AL, Löfroth JE. 1993. Selective paracellular permeability in two models for intestinal absorption: Cultured monolayers of human intestinal epithelial cells and rat intestinal segments. Pharm Res 10:1123-1129.
-
(1993)
Pharm Res
, vol.10
, pp. 1123-1129
-
-
Artursson, P.1
Ungell, A.L.2
Löfroth, J.E.3
-
123
-
-
0030588714
-
Caco-2 monolayers in experimental and theoretical predictions of drug transport
-
Artursson P, Palm K, Luthman K. 1996. Caco-2 monolayers in experimental and theoretical predictions of drug transport. Adv Drug Deliv Rev 22:67-84.
-
(1996)
Adv Drug Deliv Rev
, vol.22
, pp. 67-84
-
-
Artursson, P.1
Palm, K.2
Luthman, K.3
-
124
-
-
0030588585
-
Carrier-mediated transport and efflux mechanisms in Caco-2 cells
-
Hidalgo I, Li J. 1996. Carrier-mediated transport and efflux mechanisms in Caco-2 cells. Adv Drug Deliv Rev 22:53-66.
-
(1996)
Adv Drug Deliv Rev
, vol.22
, pp. 53-66
-
-
Hidalgo, I.1
Li, J.2
-
125
-
-
0036279841
-
Contribution of saturable active secretion passive trancellular and paracellular diffusion to the overall transport of furosemide across adenocarcinoma (Caco-2) cells
-
Flanagan S, Takahashi L, Liu X, Benet L. 2002. Contribution of saturable active secretion passive trancellular and paracellular diffusion to the overall transport of furosemide across adenocarcinoma (Caco-2) cells. J Pharm Sci 91:1169-1177.
-
(2002)
J Pharm Sci
, vol.91
, pp. 1169-1177
-
-
Flanagan, S.1
Takahashi, L.2
Liu, X.3
Benet, L.4
-
126
-
-
0035152853
-
CYP3A4, CYP3A5, and MDR1 in human small and large intestinal cell lines suitable for drug transport studies
-
Engman H, Lennernas H, Taipalensuu J, Otter C, Leidvik B, Artursson P. 2001. CYP3A4, CYP3A5, and MDR1 in human small and large intestinal cell lines suitable for drug transport studies. J Pharm Sci 90:1736-1751.
-
(2001)
J Pharm Sci
, vol.90
, pp. 1736-1751
-
-
Engman, H.1
Lennernas, H.2
Taipalensuu, J.3
Otter, C.4
Leidvik, B.5
Artursson, P.6
-
127
-
-
0036175307
-
Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4
-
Cummins C, Jacobsen W, Benet L. 2002. Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4. J Pharm Exp Ther 300:1036-1045.
-
(2002)
J Pharm Exp Ther
, vol.300
, pp. 1036-1045
-
-
Cummins, C.1
Jacobsen, W.2
Benet, L.3
-
128
-
-
0032825148
-
Intestinal MDR transport proteins and P-450 enzymes as barriers to oral drug delivery
-
Benet LZ, Izumi T, Zhang Y, Silverman JA, Wacher VJ. 1999. Intestinal MDR transport proteins and P-450 enzymes as barriers to oral drug delivery. J Control Release 62:25-31.
-
(1999)
J Control Release
, vol.62
, pp. 25-31
-
-
Benet, L.Z.1
Izumi, T.2
Zhang, Y.3
Silverman, J.A.4
Wacher, V.J.5
-
129
-
-
0034807802
-
Characterizing the expression of CYP3A4 and efflux transporters (P-gp, MRP, and MRP2) in CYP3A4-transfected Caco-2 cells after induction with sodium butyrate and the phorbol ester 12-O-tetradecanoylphorbol-13-acetate
-
Cummins C, Mangravite L, Benet L. 2001. Characterizing the expression of CYP3A4 and efflux transporters (P-gp, MRP, and MRP2) in CYP3A4-transfected Caco-2 cells after induction with sodium butyrate and the phorbol ester 12-O-tetradecanoylphorbol-13-acetate. Pharm Res 18:1102-1109.
-
(2001)
Pharm Res
, vol.18
, pp. 1102-1109
-
-
Cummins, C.1
Mangravite, L.2
Benet, L.3
-
130
-
-
3242686014
-
Rapid induction of P-glycoprotein expression by high permeability compounds in colonic cells in vitro: A possible source of transporter mediated drug interactions?
-
Collett A, Tanianis-Hughes J, Warhurst G. 2004. Rapid induction of P-glycoprotein expression by high permeability compounds in colonic cells in vitro: A possible source of transporter mediated drug interactions? Biochem Pharmacol 68:783-790.
-
(2004)
Biochem Pharmacol
, vol.68
, pp. 783-790
-
-
Collett, A.1
Tanianis-Hughes, J.2
Warhurst, G.3
-
131
-
-
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, Bjorquist A, Ungell AL. 2006. 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 28:291-299.
-
(2006)
Eur J Pharm Sci
, vol.28
, pp. 291-299
-
-
Seithel, A.1
Karlsson, J.2
Hilgendorf, C.3
Bjorquist, A.4
Ungell, A.L.5
-
132
-
-
34547169521
-
Expression of 36 drug transporter genes in human intestine, liver, kidney, and organotypic cell lines
-
Hilgendorf C, Ahlin G, Seithel A, Artursson P, Ungell AL, Karlsson JE. 2007. Expression of 36 drug transporter genes in human intestine, liver, kidney, and organotypic cell lines. Drug Metab Dispos 35:1333-1340.
-
(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.E.6
-
133
-
-
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, Ronnblom A, Karlbom U, Lazorova L, Grasjo J, Kindmark A, Artursson P. 2006. 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 29:269-277.
-
(2006)
Eur J Pharm Sci
, vol.29
, pp. 269-277
-
-
Englund, G.1
Rorsman, F.2
Ronnblom, A.3
Karlbom, U.4
Lazorova, L.5
Grasjo, J.6
Kindmark, A.7
Artursson, P.8
-
134
-
-
0035821601
-
Experimental and computational screening models for the prediction of intestinal drug absorption
-
Stenberg P, Norinder U, Luthman K, Artursson P. 2001. Experimental and computational screening models for the prediction of intestinal drug absorption. J Med Chem 44:1927-1937.
-
(2001)
J Med Chem
, vol.44
, pp. 1927-1937
-
-
Stenberg, P.1
Norinder, U.2
Luthman, K.3
Artursson, P.4
-
135
-
-
33751003834
-
Presentation of a structurally diverse and commercially available drug data set for correlation and benchmarking studies
-
Sköld C, Winiwarter S, Wernevik J, Bergström F, Engström L, Allen R, Box K, Comer J, Mole J, Hallberg A, Lennernäs H, Lundstedt T, Ungell AL, Karlén A. 2006. Presentation of a structurally diverse and commercially available drug data set for correlation and benchmarking studies. J Med Chem 49:6660-6671.
-
(2006)
J Med Chem
, vol.49
, pp. 6660-6671
-
-
Sköld, C.1
Winiwarter, S.2
Wernevik, J.3
Bergström, F.4
Engström, L.5
Allen, R.6
Box, K.7
Comer, J.8
Mole, J.9
Hallberg, A.10
Lennernäs, H.11
Lundstedt, T.12
Ungell, A.L.13
Karlén, A.14
-
136
-
-
0035514751
-
Three-dimensional quantitative structure-permeability relationship analysis for series of inhibitors of rhinovirus replication
-
Ekins S, Durst GL, Stratford RE, Thorner DA, Lewis R, Loncharich RJ, Wikel JH. 2001. Three-dimensional quantitative structure-permeability relationship analysis for series of inhibitors of rhinovirus replication. J Chem Inf Comput Sci 41:1578-1586.
-
(2001)
J Chem Inf Comput Sci
, vol.41
, pp. 1578-1586
-
-
Ekins, S.1
Durst, G.L.2
Stratford, R.E.3
Thorner, D.A.4
Lewis, R.5
Loncharich, R.J.6
Wikel, J.H.7
-
137
-
-
0035950120
-
Physicochemical determinants of passive membrane permeability: Role of solute hydrogen-bonding potential and volume
-
Goodwin J, Condari R, Ho N, Burton P. 2001. Physicochemical determinants of passive membrane permeability: Role of solute hydrogen-bonding potential and volume. J Med Chem 44:3721-3729.
-
(2001)
J Med Chem
, vol.44
, pp. 3721-3729
-
-
Goodwin, J.1
Condari, R.2
Ho, N.3
Burton, P.4
-
138
-
-
0033636283
-
Mechanisms of transport and structure-permeability relationship of sulfasalazine and its analogs in Caco-2 cell mololayers
-
Liang E, Proudfoot J, Yazdanian M. 2000. Mechanisms of transport and structure-permeability relationship of sulfasalazine and its analogs in Caco-2 cell mololayers. Pharm Res 17:1168-1174.
-
(2000)
Pharm Res
, vol.17
, pp. 1168-1174
-
-
Liang, E.1
Proudfoot, J.2
Yazdanian, M.3
-
139
-
-
0021490671
-
Epithelial properties of human colonic carcinoma cell line Caco-2; electrical parameters
-
Grasset E, Pinto M, Dussaulx E, Zweibaum A. 1984. Epithelial properties of human colonic carcinoma cell line Caco-2; electrical parameters. Am J Physiol 247:C260-C267.
-
(1984)
Am J Physiol
, vol.247
-
-
Grasset, E.1
Pinto, M.2
Dussaulx, E.3
Zweibaum, A.4
-
140
-
-
0032949615
-
MDCK (Madin-Darby canine kidney) cells: A tool for membrane permeability screening
-
Irvine JD, Takahashi L, Lockhart K, Cheong J, Tolan JW, Selick HE, Grove JR. 1999. MDCK (Madin-Darby canine kidney) cells: A tool for membrane permeability screening. J Pharm Sci 88:28-33.
-
(1999)
J Pharm Sci
, vol.88
, pp. 28-33
-
-
Irvine, J.D.1
Takahashi, L.2
Lockhart, K.3
Cheong, J.4
Tolan, J.W.5
Selick, H.E.6
Grove, J.R.7
-
141
-
-
0031824307
-
MDCK cell cultures as an epithelial in vitro model: Cytoskeleton and tight junctions as indicators for the definition of age-related stages by confocal microscopy
-
Rothen-Rutishauser B, Kraemer SD, Braun A, Guenthert M, Wunderli-Allenspach H. 1998. MDCK cell cultures as an epithelial in vitro model: Cytoskeleton and tight junctions as indicators for the definition of age-related stages by confocal microscopy. Pharm Res 15:964-971.
-
(1998)
Pharm Res
, vol.15
, pp. 964-971
-
-
Rothen-Rutishauser, B.1
Kraemer, S.D.2
Braun, A.3
Guenthert, M.4
Wunderli-Allenspach, H.5
-
142
-
-
0036166635
-
Comparison of furosemide and vinblastine secretion from cell lines overexpressing multidrug resistance protein (P-glycoprotein) and multidrug resistance-associated proteins (MRP1 and MRP2)
-
Flanagan SD, Cummins CL, Susanto M, Liu X, Takahashi LH, Benet LZ. 2002. Comparison of furosemide and vinblastine secretion from cell lines overexpressing multidrug resistance protein (P-glycoprotein) and multidrug resistance-associated proteins (MRP1 and MRP2). Pharmacology 64:126-134.
-
(2002)
Pharmacology
, vol.64
, pp. 126-134
-
-
Flanagan, S.D.1
Cummins, C.L.2
Susanto, M.3
Liu, X.4
Takahashi, L.H.5
Benet, L.Z.6
-
143
-
-
0001308329
-
Drug export activity of the human canalicularmultispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA
-
Evers R, Kool L, van Deemter H, Janssen H, Calafat J, Oomen LC, Paulusma CC, Oude Elferink RP, Baas F, Schinkel AH, Borst P. 1998. Drug export activity of the human canalicularmultispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA. J Clin Invest 101:1310-1319.
-
(1998)
J Clin Invest
, vol.101
, pp. 1310-1319
-
-
Evers, R.1
Kool, L.2
van Deemter, H.3
Janssen, H.4
Calafat, J.5
Oomen, L.C.6
Paulusma, C.C.7
Oude, E.R.8
Baas, F.9
Schinkel, A.H.10
Borst, P.11
-
144
-
-
0036298317
-
Are MDCK cells transfected with the human MRP2 gene a good model for human intestinal mucosa?
-
Tang F, Horic K, Borchardt R. 2002. Are MDCK cells transfected with the human MRP2 gene a good model for human intestinal mucosa? Pharm Res 19:773-779.
-
(2002)
Pharm Res
, vol.19
, pp. 773-779
-
-
Tang, F.1
Horic, K.2
Borchardt, R.3
-
145
-
-
0032926354
-
Characterization of the human multidrug resistance protein isoform MRP3 localized to the basolateral hepatocyte membrane
-
König J, Rost D, Cui Y, Keppler D. 1999. Characterization of the human multidrug resistance protein isoform MRP3 localized to the basolateral hepatocyte membrane. Hepatology 29:1156-1163.
-
(1999)
Hepatology
, vol.29
, pp. 1156-1163
-
-
König, J.1
Rost, D.2
Cui, Y.3
Keppler, D.4
-
146
-
-
0035054725
-
The gut as a barrier to drug absorption: Combined role of cytochrome P450 3A and P-glycoprotein
-
Zhang Y, Benet LZ. 2001. The gut as a barrier to drug absorption: Combined role of cytochrome P450 3A and P-glycoprotein. Clin Pharmacokin 40:159-168.
-
(2001)
Clin Pharmacokin
, vol.40
, pp. 159-168
-
-
Zhang, Y.1
Benet, L.Z.2
-
147
-
-
72449178926
-
Membrane permeability in the GI tract: The interplay between microclimate pH and transporters
-
Kristl A. 2009. Membrane permeability in the GI tract: The interplay between microclimate pH and transporters. Chem Biodiver 6:1923-1942.
-
(2009)
Chem Biodiver
, vol.6
, pp. 1923-1942
-
-
Kristl, A.1
-
148
-
-
77949269469
-
Model analysis of the concentration-dependent permeability of P-gp substrates
-
Tachibana T, Kitamura S, Kato M, Mitsui T, Shirasaka Y, Yamashita S, Sugiyama Y. 2010. Model analysis of the concentration-dependent permeability of P-gp substrates. Pharm Res 27:442-446.
-
(2010)
Pharm Res
, vol.27
, pp. 442-446
-
-
Tachibana, T.1
Kitamura, S.2
Kato, M.3
Mitsui, T.4
Shirasaka, Y.5
Yamashita, S.6
Sugiyama, Y.7
-
149
-
-
0022618014
-
Mixing-tank model for predicting dissolution rate control or oral absorption
-
Dressman J, Fleisher D. 1986. Mixing-tank model for predicting dissolution rate control or oral absorption. J Pharm Sci 75:109-116.
-
(1986)
J Pharm Sci
, vol.75
, pp. 109-116
-
-
Dressman, J.1
Fleisher, D.2
-
150
-
-
0029848457
-
Compartmental transit and dispersion model analysis of small intestinal transit flow in humans
-
Yu LX, Crison JR, Amidon GL. 1996. Compartmental transit and dispersion model analysis of small intestinal transit flow in humans. Int J Pharm 10:111-118.
-
(1996)
Int J Pharm
, vol.140
, pp. 111-118
-
-
Yu, L.X.1
Crison, J.R.2
Amidon, G.L.3
-
151
-
-
0031026707
-
Simulation models to predict oral drug absorption from in vitro data
-
Grass GM. 1997. Simulation models to predict oral drug absorption from in vitro data. Adv Drug Deliv Rev 23:199-219.
-
(1997)
Adv Drug Deliv Rev
, vol.23
, pp. 199-219
-
-
Grass, G.M.1
-
152
-
-
0032888376
-
A compartmental absorption and transit model for estimating oral drug absorption
-
Yu LX, Amidon GL. 1999. A compartmental absorption and transit model for estimating oral drug absorption. Int J Pharm 186:119-125.
-
(1999)
Int J Pharm
, vol.186
, pp. 119-125
-
-
Yu, L.X.1
Amidon, G.L.2
-
153
-
-
0035478779
-
Predicting the impact of physiological and biochemical processes on oral drug bioavailability
-
Agoram B, Woltasz WS, Bolger MB. 2001. Predicting the impact of physiological and biochemical processes on oral drug bioavailability. Adv Drug Deliv Rev 50:S41-S67.
-
(2001)
Adv Drug Deliv Rev
, vol.50
-
-
Agoram, B.1
Woltasz, W.S.2
Bolger, M.B.3
-
154
-
-
0011975740
-
Theoretical-model studies of intestinal drug absorption. V. Non-steady-state fluid-flow and absorption
-
Ni PF, Ho NFH, Fox JL, Leuenberger H, Higuchi WI. 1980. Theoretical-model studies of intestinal drug absorption. V. Non-steady-state fluid-flow and absorption. Int J Pharm 5:33-47.
-
(1980)
Int J Pharm
, vol.5
, pp. 33-47
-
-
Ni, P.F.1
Ho, N.F.H.2
Fox, J.L.3
Leuenberger, H.4
Higuchi, W.I.5
-
155
-
-
0344084044
-
A physiologic model for simulating GI flow and drug absorption in rats
-
Willmann S, Schmitt W, Keldenich J, Dressmann JB. 2003. A physiologic model for simulating GI flow and drug absorption in rats. Pharm Res 20:1766-1771.
-
(2003)
Pharm Res
, vol.20
, pp. 1766-1771
-
-
Willmann, S.1
Schmitt, W.2
Keldenich, J.3
Dressmann, J.B.4
-
156
-
-
0032750117
-
A heterogeneous tube model of intestinal drug absorption based on probabilistic concepts
-
Kalampokis A, Argyrakis P, Macheras P. 1999. A heterogeneous tube model of intestinal drug absorption based on probabilistic concepts. Pharm Res 16:1764-1769.
-
(1999)
Pharm Res
, vol.16
, pp. 1764-1769
-
-
Kalampokis, A.1
Argyrakis, P.2
Macheras, P.3
-
157
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski CA, Lombardo F, Dominy BW, Feeney PJ. 1997. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv Drug Deliv Rev 23:4-25.
-
(1997)
Adv Drug Deliv Rev
, vol.23
, pp. 4-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
159
-
-
0037434541
-
Absorption classification of oral drugs based on molecular surface properties
-
Bergström CA, Strafford M, Lazorova L, Avdeef A, Luthman K, Artursson P. 2003. Absorption classification of oral drugs based on molecular surface properties. J Med Chem 46:558-570.
-
(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
-
160
-
-
0038071648
-
Predicting oral absorption and bioavailability
-
Van de Waterbeemd H, Jones B. 2003. Predicting oral absorption and bioavailability. Prog Med Chem 41:1-59.
-
(2003)
Prog Med Chem
, vol.41
, pp. 1-59
-
-
Van de, W.H.1
Jones, B.2
-
161
-
-
0034992583
-
Evaluation of human intestinal absorption data and subsequent derivation of a quantitative structure-activity relationship (QSAR) with the Abraham descriptors
-
Zhao YH, Le J, Abraham MH, Hersey A, Eddershaw PJ, Luscombe CN, Butina D, Beck G, Sherborne B, Cooper I, Platts JA. 2001. Evaluation of human intestinal absorption data and subsequent derivation of a quantitative structure-activity relationship (QSAR) with the Abraham descriptors. J Pharm Sci 90:749-784.
-
(2001)
J Pharm Sci
, vol.90
, pp. 749-784
-
-
Zhao, Y.H.1
Le, J.2
Abraham, M.H.3
Hersey, A.4
Eddershaw, P.J.5
Luscombe, C.N.6
Butina, D.7
Beck, G.8
Sherborne, B.9
Cooper, I.10
Platts, J.A.11
-
162
-
-
0036806339
-
Rate-limited steps of human oral absorption and QSAR studies
-
Zhao YH, Abraham MH, Le J, Hersey A, Luscombe CN, Beck G, Sherborne B, Cooper I. 2002. Rate-limited steps of human oral absorption and QSAR studies. Pharm Res 19:1446-1457.
-
(2002)
Pharm Res
, vol.19
, pp. 1446-1457
-
-
Zhao, Y.H.1
Abraham, M.H.2
Le, J.3
Hersey, A.4
Luscombe, C.N.5
Beck, G.6
Sherborne, B.7
Cooper, I.8
-
163
-
-
1642579654
-
Bioavailability prediction based on molecular structure for a diverse series of drugs
-
Turner JV, Maddalena DJ, Agatonovic-Kustrin S. 2004. Bioavailability prediction based on molecular structure for a diverse series of drugs. Pharm Res 21:68-82.
-
(2004)
Pharm Res
, vol.21
, pp. 68-82
-
-
Turner, J.V.1
Maddalena, D.J.2
Agatonovic-Kustrin, S.3
-
164
-
-
72949083720
-
Bioequivalence: Its history, practice and future
-
Midha KK, McKay G. 2009. Bioequivalence: Its history, practice and future. AAPS J 11:664-670.
-
(2009)
AAPS J
, vol.11
, pp. 664-670
-
-
Midha, K.K.1
McKay, G.2
-
165
-
-
77449083005
-
A history of biopharmaceutics in the Food and Drug Administration
-
Skelly JP. 2010. A history of biopharmaceutics in the Food and Drug Administration. AAPS J 12:44-50.
-
(2010)
AAPS J
, vol.12
, pp. 44-50
-
-
Skelly, J.P.1
-
166
-
-
85030493319
-
-
21 C.F.R. Part 320-Bioavailability and bioequivalence requirements title 21-Food and drugs
-
21 C.F.R. Part 320-Bioavailability and bioequivalence requirements title 21-Food and drugs.
-
-
-
-
167
-
-
84881609592
-
-
Federal Register. Federal Register 34:.
-
Federal Register. 1969. Federal Register 34:2673.
-
(1969)
, pp. 2673
-
-
-
168
-
-
78650437936
-
-
Federal Register.
-
Federal Register. 1970. Federal Register 35:6574.
-
(1970)
Federal Register
, vol.35
, pp. 6574
-
-
-
169
-
-
0003455044
-
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). General Considerations. Rockville, Maryland: FDA
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). 2003. Bioavailability and bioequivalence studies for orally administered drug products. General Considerations. Rockville, Maryland: FDA.
-
(2003)
Bioavailability and bioequivalence studies for orally administered drug products
-
-
-
170
-
-
0028223647
-
Bioequivalence: Performance of several measures of extent of absorption
-
Bois FY, Tozer TN, Hauck WW, Chen ML, Patnaik R, Williams RL. 1994. Bioequivalence: Performance of several measures of extent of absorption. Pharm Res 11:715-722.
-
(1994)
Pharm Res
, vol.11
, pp. 715-722
-
-
Bois, F.Y.1
Tozer, T.N.2
Hauck, W.W.3
Chen, M.L.4
Patnaik, R.5
Williams, R.L.6
-
171
-
-
0028226203
-
Bioequivalence: Performance of several measures of rate of absorption
-
Bois FY, Tozer TN, Hauck WW, Chen ML, Patnaik R, Williams RL. 1994. Bioequivalence: Performance of several measures of rate of absorption. Pharm Res 11:966-974.
-
(1994)
Pharm Res
, vol.11
, pp. 966-974
-
-
Bois, F.Y.1
Tozer, T.N.2
Hauck, W.W.3
Chen, M.L.4
Patnaik, R.5
Williams, R.L.6
-
172
-
-
0034863628
-
Measures of exposure versus measures of rate and extent of absorption
-
Chen ML, Lesko LJ, Williams RL. 2001. Measures of exposure versus measures of rate and extent of absorption. Clin Pharmacokinet 40:565-572.
-
(2001)
Clin Pharmacokinet
, vol.40
, pp. 565-572
-
-
Chen, M.L.1
Lesko, L.J.2
Williams, R.L.3
-
173
-
-
0030455294
-
An improved intercept method for the assessment of absorption rate in bioequivalence studies
-
Macheras P, Symillides M, Reppas C. 1996. An improved intercept method for the assessment of absorption rate in bioequivalence studies. Pharm Res 13:1755-1758.
-
(1996)
Pharm Res
, vol.13
, pp. 1755-1758
-
-
Macheras, P.1
Symillides, M.2
Reppas, C.3
-
174
-
-
0028989927
-
max/AUC is an effective metric in investigations of bioequivalence
-
max/AUC is an effective metric in investigations of bioequivalence. Pharm Res 12:937-942.
-
(1995)
Pharm Res
, vol.12
, pp. 937-942
-
-
Endrenyi, L.1
Tothfalusi, L.2
-
175
-
-
0003922012
-
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Rockville, Maryland: FDA
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). 2001. Statistical approaches to establishing bioequivalence. Rockville, Maryland: FDA.
-
(2001)
Statistical approaches to establishing bioequivalence
-
-
-
177
-
-
0025009945
-
Consensus report from "Bio-International '89': Issues in the evaluation of bioavailability data
-
McGilveray IJ, Midha KK, Skelly JP, Dighe S, Doluisio JT, French IW, Karim A, Burford R. 1990. Consensus report from "Bio-International '89': Issues in the evaluation of bioavailability data. J Pharm Sci 79:945-946.
-
(1990)
J Pharm Sci
, vol.79
, pp. 945-946
-
-
McGilveray, I.J.1
Midha, K.K.2
Skelly, J.P.3
Dighe, S.4
Doluisio, J.T.5
French, I.W.6
Karim, A.7
Burford, R.8
-
178
-
-
0028915498
-
Bio-International 94, Conference on bioavailability, bioequivalence and pharmacokinetic studies
-
Blume HH, McGilveray IJ, Midha KK. 1995. Bio-International 94, Conference on bioavailability, bioequivalence and pharmacokinetic studies. Eur J Pharm Sci 3:113-124.
-
(1995)
Eur J Pharm Sci
, vol.3
, pp. 113-124
-
-
Blume, H.H.1
McGilveray, I.J.2
Midha, K.K.3
-
179
-
-
0027141414
-
Bio-international '92, Conference on bioavailability, bioequivalence and pharmacokinetic studies
-
Blume HH, Midha KK. 1993. Bio-international '92, Conference on bioavailability, bioequivalence and pharmacokinetic studies. J Pharm Sci 11:1186-1189.
-
(1993)
J Pharm Sci
, vol.11
, pp. 1186-1189
-
-
Blume, H.H.1
Midha, K.K.2
-
180
-
-
17444453579
-
Absorption of orally administered highly variable drugs and drug formulations
-
Shah VP, Yacobi A, Barr WH, Benet LZ, Breimer D, Dobrinska MR, Endrenyi L, Fairweather W, Gillespie W, Gonzalez MA, Hooper J, Jackson A, Lesko LJ, Midha KK, Noonan PK, Patnaik R, Williams RL. 1996. Absorption of orally administered highly variable drugs and drug formulations. Pharm Res 13:1590-1594.
-
(1996)
Pharm Res
, vol.13
, pp. 1590-1594
-
-
Shah, V.P.1
Yacobi, A.2
Barr, W.H.3
Benet, L.Z.4
Breimer, D.5
Dobrinska, M.R.6
Endrenyi, L.7
Fairweather, W.8
Gillespie, W.9
Gonzalez, M.A.10
Hooper, J.11
Jackson, A.12
Lesko, L.J.13
Midha, K.K.14
Noonan, P.K.15
Patnaik, R.16
Williams, R.L.17
-
183
-
-
0029567034
-
An approach for widening the bioequivalence acceptance limits in the case of highly variable drugs
-
Boddy AW, Snikeris FC, Kringle RO, Wei GC, Oppermann JA, Midha KK. 1995. An approach for widening the bioequivalence acceptance limits in the case of highly variable drugs. Pharm Res 12:1865-1868.
-
(1995)
Pharm Res
, vol.12
, pp. 1865-1868
-
-
Boddy, A.W.1
Snikeris, F.C.2
Kringle, R.O.3
Wei, G.C.4
Oppermann, J.A.5
Midha, K.K.6
-
184
-
-
0037337782
-
Limits for the scaled average bioequivalence of highly variable drugs and drug products
-
Tothfalusi L, Endrenyi L. 2003. Limits for the scaled average bioequivalence of highly variable drugs and drug products. Pharm Res 20:382-389.
-
(2003)
Pharm Res
, vol.20
, pp. 382-389
-
-
Tothfalusi, L.1
Endrenyi, L.2
-
185
-
-
6344293527
-
Novel scaled average bioequivalence limits based on GMR and variability considerations
-
Karalis V, Symillides M, Macheras P. 2004. Novel scaled average bioequivalence limits based on GMR and variability considerations. Pharm Res 21:1933-1942.
-
(2004)
Pharm Res
, vol.21
, pp. 1933-1942
-
-
Karalis, V.1
Symillides, M.2
Macheras, P.3
-
186
-
-
23244434225
-
Geometric mean ratio dependent scaled bioequivalence limits with leveling-off properties
-
Karalis V, Macheras P, Symillides M. 2005. Geometric mean ratio dependent scaled bioequivalence limits with leveling-off properties. Eur J Pharm Sci 26:54-61.
-
(2005)
Eur J Pharm Sci
, vol.26
, pp. 54-61
-
-
Karalis, V.1
Macheras, P.2
Symillides, M.3
-
187
-
-
33750613025
-
Novel scaled bioequivalence limits with leveling-off properties
-
Kytariolos J, Karalis V, Macheras P, Symillides M. 2006. Novel scaled bioequivalence limits with leveling-off properties. Pharm Res 23:2657-2664.
-
(2006)
Pharm Res
, vol.23
, pp. 2657-2664
-
-
Kytariolos, J.1
Karalis, V.2
Macheras, P.3
Symillides, M.4
-
188
-
-
70349970382
-
Evaluation of bioequivalence for highly variable drugs with scaled average bioequivalence
-
Tothfalusi L, Endrenyi L, Arieta AG. 2009. Evaluation of bioequivalence for highly variable drugs with scaled average bioequivalence. Clin Pharmacokinet 48:725-743.
-
(2009)
Clin Pharmacokinet
, vol.48
, pp. 725-743
-
-
Tothfalusi, L.1
Endrenyi, L.2
Arieta, A.G.3
-
189
-
-
84881610332
-
-
Food and Drug Administration (FDA). Office of Generic Drugs, Draft Guidance for Industry on Bioequivalence Recommendations for Progesterone Capsules.Rockville, Maryland: FDA
-
Food and Drug Administration (FDA). 2011. Office of Generic Drugs, Draft Guidance for Industry on Bioequivalence Recommendations for Progesterone Capsules.Rockville, Maryland: FDA.
-
(2011)
-
-
-
190
-
-
38049184592
-
Bioequivalence approaches for highly variable drugs and drug products
-
Haidar SH, Davit B, Chen ML, Conner D, Lee L, Li QH, Lionberger R, Makhlouf F, Patel D, Schuirmann DJ, Yu LX. 2008. Bioequivalence approaches for highly variable drugs and drug products. Pharm Res 15:237-241.
-
(2008)
Pharm Res
, vol.15
, pp. 237-241
-
-
Haidar, S.H.1
Davit, B.2
Chen, M.L.3
Conner, D.4
Lee, L.5
Li, Q.H.6
Lionberger, R.7
Makhlouf, F.8
Patel, D.9
Schuirmann, D.J.10
Yu, L.X.11
-
191
-
-
57149091543
-
Evaluation of a scaling approach for the bioequivalence of highly variable drugs
-
Haidar SH, Makhlouf F, Schuirmann DJ, Hyslop T, Davit B, Conner D, Yu LX. 2008. Evaluation of a scaling approach for the bioequivalence of highly variable drugs. AAPS J 10:450-454.
-
(2008)
AAPS J
, vol.10
, pp. 450-454
-
-
Haidar, S.H.1
Makhlouf, F.2
Schuirmann, D.J.3
Hyslop, T.4
Davit, B.5
Conner, D.6
Yu, L.X.7
-
194
-
-
84881614963
-
-
AAPS Workshop on Facilitating Oral Product Development and Reducing Regulatory Burden through Novel Approaches to Assess Bioavailability/Bioequivalence. Washington DC
-
Davit B. 2011. Highly variable drugs: Reference-scaled average bioequivalence and sequential design studies. AAPS Workshop on Facilitating Oral Product Development and Reducing Regulatory Burden through Novel Approaches to Assess Bioavailability/Bioequivalence. Washington DC.
-
(2011)
Highly variable drugs: Reference-scaled average bioequivalence and sequential design studies
-
-
Davit, B.1
-
195
-
-
80455143769
-
On the leveling-off properties of the new bioequivalence limits for highly variable drugs of the EMA guideline
-
Karalis V, Symillides M, Macheras P. 2011. On the leveling-off properties of the new bioequivalence limits for highly variable drugs of the EMA guideline. Eur J Pharm Sci 44:497-505.
-
(2011)
Eur J Pharm Sci
, vol.44
, pp. 497-505
-
-
Karalis, V.1
Symillides, M.2
Macheras, P.3
-
196
-
-
84862658878
-
Bioequivalence of highly variable drugs: A comparison of the newly proposed regulatory approaches by FDA and EMA
-
Karalis V, Symillides M, Macheras P. 2012. Bioequivalence of highly variable drugs: A comparison of the newly proposed regulatory approaches by FDA and EMA. Pharm Res 29:1066-1077.
-
(2012)
Pharm Res
, vol.29
, pp. 1066-1077
-
-
Karalis, V.1
Symillides, M.2
Macheras, P.3
-
197
-
-
79959906965
-
The BCS, BDDCS, and regulatory guidances
-
Chen ML, Amidon GL, Benet LZ, Lennernas H, Yu LX. 2011. The BCS, BDDCS, and regulatory guidances. Pharm Res 28:1774-1778.
-
(2011)
Pharm Res
, vol.28
, pp. 1774-1778
-
-
Chen, M.L.1
Amidon, G.L.2
Benet, L.Z.3
Lennernas, H.4
Yu, L.X.5
-
198
-
-
39149115065
-
Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption
-
Custodio J, Wu C, Benet L. 2008. Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption. Adv Drug Deliv Rev 60:717-733.
-
(2008)
Adv Drug Deliv Rev
, vol.60
, pp. 717-733
-
-
Custodio, J.1
Wu, C.2
Benet, L.3
-
199
-
-
77149165406
-
Predicting drug disposition via application of a biopharmaceutics drug disposition classification system
-
Benet L. 2010. Predicting drug disposition via application of a biopharmaceutics drug disposition classification system. Basic Clin Pharmacol Toxicol 106:162-167.
-
(2010)
Basic Clin Pharmacol Toxicol
, vol.106
, pp. 162-167
-
-
Benet, L.1
-
200
-
-
35648978876
-
The use of BDDCS in classifying the permeability of marketed drugs
-
Benet LZ, Amidon GL, Barends DM, Lennernäs H, Polli JE, Shah VP, Stavchansky SA, Yu LX. 2008. The use of BDDCS in classifying the permeability of marketed drugs. Pharm Res 25:483-488.
-
(2008)
Pharm Res
, vol.25
, pp. 483-488
-
-
Benet, L.Z.1
Amidon, G.L.2
Barends, D.M.3
Lennernäs, H.4
Polli, J.E.5
Shah, V.P.6
Stavchansky, S.A.7
Yu, L.X.8
-
201
-
-
84881610863
-
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). Guidance for industry. Extended release oral dosage forms: Development, evaluation, and application of in vitro/in vivo correlations. Rockville, Maryland: FDA
-
Food and Drug Administration (FDA). Center for Drug Evaluation and Research (CDER). 1997. Guidance for industry. Extended release oral dosage forms: Development, evaluation, and application of in vitro/in vivo correlations. Rockville, Maryland: FDA.
-
(1997)
-
-
-
202
-
-
0348107338
-
Quantitative Biopharmaceutics Classification System: The central role of dose/solubility ratio
-
Rinaki E, Valsami G, Macheras P. 2003. Quantitative Biopharmaceutics Classification System: The central role of dose/solubility ratio. Pharm Res 20:1917-1925.
-
(2003)
Pharm Res
, vol.20
, pp. 1917-1925
-
-
Rinaki, E.1
Valsami, G.2
Macheras, P.3
-
204
-
-
47949129181
-
Biopharmaceutics Classification Systems for new molecular entities (BCS-NMEs) and marketed drugs (BCS-MD): Theoretical basis and practical examples
-
Papadopoulou V, Valsami G, Dokoumetzidis A, Macheras P. 2008. Biopharmaceutics Classification Systems for new molecular entities (BCS-NMEs) and marketed drugs (BCS-MD): Theoretical basis and practical examples. Int J Pharm 361:70-77.
-
(2008)
Int J Pharm
, vol.361
, pp. 70-77
-
-
Papadopoulou, V.1
Valsami, G.2
Dokoumetzidis, A.3
Macheras, P.4
-
205
-
-
68349157679
-
Biopharmaceutical classification of drugs using intrinsic dissolution rate (IDR) and rat intestinal permeability
-
Zakeri-Milani P, Barzegar-Jalali M, Azimi M, Valizadeh H. 2009. Biopharmaceutical classification of drugs using intrinsic dissolution rate (IDR) and rat intestinal permeability. Eur J Pharm Biopharm 73:102-106.
-
(2009)
Eur J Pharm Biopharm
, vol.73
, pp. 102-106
-
-
Zakeri-Milani, P.1
Barzegar-Jalali, M.2
Azimi, M.3
Valizadeh, H.4
-
206
-
-
60749105377
-
Using measured pKa, log P and solubility to investigate supersaturation and predict BCS Class
-
Box K, Comer J. 2008. Using measured pKa, log P and solubility to investigate supersaturation and predict BCS Class. Curr Drug Metabol 9:869-878.
-
(2008)
Curr Drug Metabol
, vol.9
, pp. 869-878
-
-
Box, K.1
Comer, J.2
-
207
-
-
35648957629
-
Computational models to assign biopharmaceutics drug disposition classification from molecular structure
-
Khandelwal A, Bahadduri PM, Chang C, Polli JE, Swaan PW, Ekins S. 2007. Computational models to assign biopharmaceutics drug disposition classification from molecular structure. Pharm Res 24:2249-2262.
-
(2007)
Pharm Res
, vol.24
, pp. 2249-2262
-
-
Khandelwal, A.1
Bahadduri, P.M.2
Chang, C.3
Polli, J.E.4
Swaan, P.W.5
Ekins, S.6
-
208
-
-
77955921793
-
The FDA should eliminate the ambiguities in the current BCS biowaiver guidance and make public the drugs for which BCS biowaivers have been granted
-
Benet LZ, Larregieu CA. 2010. The FDA should eliminate the ambiguities in the current BCS biowaiver guidance and make public the drugs for which BCS biowaivers have been granted. Clin Pharmacol Ther 88:405-407.
-
(2010)
Clin Pharmacol Ther
, vol.88
, pp. 405-407
-
-
Benet, L.Z.1
Larregieu, C.A.2
-
209
-
-
84881609642
-
-
European Medicines Agency (EMA).Note for guidance on the clinical requirements for locally applied, locally acting products containing known constituents. CPMP/EWP/239/95 final.
-
European Medicines Agency (EMA). 1995. Note for guidance on the clinical requirements for locally applied, locally acting products containing known constituents. CPMP/EWP/239/95 final.
-
(1995)
-
-
-
210
-
-
84881615513
-
-
Food and Drug Administration (FDA). Draft Guidance on Mesalamine, Suppository/Rectal
-
Food and Drug Administration (FDA). 2007. Draft Guidance on Mesalamine, Suppository/Rectal.
-
(2007)
-
-
-
211
-
-
84881612228
-
-
Food and Drug Administration (FDA). Draft Guidance on Mesalamine, Enema /Rectal. Rockville, Maryland: FDA.
-
Food and Drug Administration (FDA). 2008. Draft Guidance on Mesalamine, Enema /Rectal. Rockville, Maryland: FDA.
-
(2008)
-
-
-
212
-
-
84881611797
-
-
Food and Drug Administration (FDA). Draft Guidance on Mesalamine, Delayed Release Tablet/Oral. Rockville, Maryland: FDA
-
Food and Drug Administration (FDA). 2012. Draft Guidance on Mesalamine, Delayed Release Tablet/Oral. Rockville, Maryland: FDA.
-
(2012)
-
-
-
213
-
-
84881610946
-
-
Food and Drug Administration (FDA). Draft Guidance on Mesalamine, Extended Release Capsule/Oral. Rockville, Maryland: FDA.
-
Food and Drug Administration (FDA). 2012. Draft Guidance on Mesalamine, Extended Release Capsule/Oral. Rockville, Maryland: FDA.
-
(2012)
-
-
-
214
-
-
34548155549
-
Biopharmaceutics classification of selected beta-blockers: Solubility and permeability class membership
-
Yan Y, Faustino PJ, Volpe DA, Lyon RC, Yu LX. 2007. Biopharmaceutics classification of selected beta-blockers: Solubility and permeability class membership. Mol Pharm 4:608-614.
-
(2007)
Mol Pharm
, vol.4
, pp. 608-614
-
-
Yan, Y.1
Faustino, P.J.2
Volpe, D.A.3
Lyon, R.C.4
Yu, L.X.5
-
215
-
-
62649128592
-
The use of drug metabolism for prediction of intestinal permeability
-
Chen ML, Yu L. 2009. The use of drug metabolism for prediction of intestinal permeability. Mol Pharm 6:74-81.
-
(2009)
Mol Pharm
, vol.6
, pp. 74-81
-
-
Chen, M.L.1
Yu, L.2
-
216
-
-
0037436925
-
The power law can describe the 'entire' drug release curve from HPMC-based matrix tablets: A hypothesis
-
Rinaki E, Valsami G, Macheras P. 2003. The power law can describe the 'entire' drug release curve from HPMC-based matrix tablets: A hypothesis. Int J Pharm 255:199-207.
-
(2003)
Int J Pharm
, vol.255
, pp. 199-207
-
-
Rinaki, E.1
Valsami, G.2
Macheras, P.3
-
217
-
-
84881611481
-
-
World Health Organization. Proposal to waive in vivo bioequivalence requirements for WHO model list of essential medicines immediate-release, solid oral dosage forms. WHO Technical Report Series, No. 937.
-
World Health Organization. 2006. Proposal to waive in vivo bioequivalence requirements for WHO model list of essential medicines immediate-release, solid oral dosage forms. WHO Technical Report Series, No. 937.
-
(2006)
-
-
-
218
-
-
84872418710
-
Impact of variability on the choice of biosimilarity limits in assessing follow-on biologics
-
Zhang N, Yang J, Chow SC, Endrenyi L, Chi E. 2013. Impact of variability on the choice of biosimilarity limits in assessing follow-on biologics. Stat Med 32:424-433.
-
(2013)
Stat Med
, vol.32
, pp. 424-433
-
-
Zhang, N.1
Yang, J.2
Chow, S.C.3
Endrenyi, L.4
Chi, E.5
|