-
1
-
-
41649112599
-
Recent advances in high throughput screening for ADME properties
-
Carlson TJ, Fisher MB. 2008. Recent advances in high throughput screening for ADME properties. Comb Chem High Throughput Screen 11:258-264.
-
(2008)
Comb Chem High Throughput Screen
, vol.11
, pp. 258-264
-
-
Carlson, T.J.1
Fisher, M.B.2
-
2
-
-
85047683939
-
Maximising use of in vitro ADMET tools to predict in vivo bioavailability and safety
-
DOI 10.1517/17425225.3.5.641
-
Wang J, Urban L, Bojanic D. 2007. Maximising use of in vitro ADMET tools to predict in vivo bioavailability and safety. Expert Opin Drug Metab Toxicol 3:641-665. (Pubitemid 351320635)
-
(2007)
Expert Opinion on Drug Metabolism and Toxicology
, vol.3
, Issue.5
, pp. 641-665
-
-
Wang, J.1
Urban, L.2
Bojanic, D.3
-
3
-
-
30744469769
-
From in vivo to in vitro/in silico ADME: Progress and challenges
-
Van de Waterbeemd H. 2005. From in vivo to in vitro/in silico ADME: Progress and challenges. Expert Opin Drug Metab Toxicol 1:1-4.
-
(2005)
Expert Opin Drug Metab Toxicol
, vol.1
, pp. 1-4
-
-
Van De Waterbeemd, H.1
-
4
-
-
69249141066
-
Comprehensive assessment of ADMET risks in drug discovery
-
Wang J. 2009. Comprehensive assessment of ADMET risks in drug discovery. Curr Pharm Des 15:2195-2219.
-
(2009)
Curr Pharm des
, vol.15
, pp. 2195-2219
-
-
Wang, J.1
-
5
-
-
0036238280
-
A comparative study of artificial membrane permeability assay for high throughput profiling of drug absorption potential
-
DOI 10.1016/S0223-5234(02)01360-0, PII S0223523402013600
-
Zhu C, Jiang L, Chen TM, Hwang KK. 2002. A comparative study of artificial membrane permeability assay for high throughput profiling of drug absorption potential. Eur J Med Chem 37:399-407. (Pubitemid 34465549)
-
(2002)
European Journal of Medicinal Chemistry
, vol.37
, Issue.5
, pp. 399-407
-
-
Zhu, C.1
Jiang, L.2
Chen, T.-M.3
Hwang, K.-K.4
-
6
-
-
0037173513
-
Prediction of passive intestinal absorption using bio-mimetic artificial membrane permeation assay and the paracellular pathway model
-
DOI 10.1016/S0378-5173(02)00240-5, PII S0378517302002405
-
Sugano K, Takata N, Machida M, Saitoh K, Terada K. 2002. Prediction of passive intestinal absorption using bio-mimetic artificial membrane permeation assay and the paracellular pathway model. Int J Pharm 241:241-251. (Pubitemid 34718026)
-
(2002)
International Journal of Pharmaceutics
, vol.241
, Issue.2
, pp. 241-251
-
-
Sugano, K.1
Takata, N.2
Machida, M.3
Saitoh, K.4
Terada, K.5
-
7
-
-
0025804183
-
Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells
-
Artursson P, Karlsson J. 1991. Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells. Biochem Biophys Res Commun 175:880-885.
-
(1991)
Biochem Biophys Res Commun
, vol.175
, pp. 880-885
-
-
Artursson, P.1
Karlsson, J.2
-
8
-
-
0032949615
-
MDCK (Madin-Darby canine kidney) cells: A tool for membrane permeability screening
-
DOI 10.1021/js9803205
-
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. (Pubitemid 29037364)
-
(1999)
Journal of Pharmaceutical Sciences
, vol.88
, Issue.1
, 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
-
9
-
-
12344274316
-
Exploring the role of different drug transport routes in permeability screening
-
DOI 10.1021/jm049711o
-
Matsson P, Bergstrom CA, Nagahara N, Tavelin S, Norinder U, Artursson P. 2005. Exploring the role of different drug transport routes in permeability screening. J Med Chem 48:604-613. (Pubitemid 40139802)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.2
, pp. 604-613
-
-
Matsson, P.1
Bergstrom, C.A.S.2
Nagahara, N.3
Tavelin, S.4
Norinder, U.5
Artursson, P.6
-
10
-
-
33750181267
-
Regional levels of drug transporters along the human intestinal tract: Co-expression of ABC and SLC transporters and comparison with Caco-2 cells
-
DOI 10.1016/j.ejps.2006.04.010, PII S092809870600114X
-
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. (Pubitemid 44602404)
-
(2006)
European Journal of Pharmaceutical Sciences
, vol.29
, Issue.3-4 SPEC. ISS
, 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
-
11
-
-
2942682950
-
Utility of 96 well Caco-2 cell system for increased throughput of P-gp screening in drug discovery
-
DOI 10.1016/j.ejpb.2004.02.014, PII S0939641104000554
-
Balimane PV, Patel K, Marino A, Chong S. 2004. Utility of 96 well Caco-2 cell system for increased throughput of P-gp screening in drug discovery. Eur J Pharm Biopharm 58:99-105. (Pubitemid 38781010)
-
(2004)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.58
, Issue.1
, pp. 99-105
-
-
Balimane, P.V.1
Patel, K.2
Marino, A.3
Chong, S.4
-
12
-
-
19344367311
-
Validation of the 96 well Caco-2 cell culture model for high throughput permeability assessment of discovery compounds
-
DOI 10.1016/j.ijpharm.2005.03.008, PII S0378517305001869
-
Marino AM, Yarde M, Patel H, Chong S, Balimane PV. 2005. Validation of the 96 well Caco-2 cell culture model for high throughput permeability assessment of discovery compounds. Int J Pharm 297:235-241. (Pubitemid 40720282)
-
(2005)
International Journal of Pharmaceutics
, vol.297
, Issue.1-2
, pp. 235-241
-
-
Marino, A.M.1
Yarde, M.2
Patel, H.3
Chong, S.4
Balimane, P.V.5
-
13
-
-
46849095431
-
Development of an automated 7-day 96-well Caco-2 cell culture model
-
DOI 10.1691/ph.2008.7855
-
Galkin A, Pakkanen J, Vuorela P. 2008. Development of an automated 7-day 96-well Caco-2 cell culture model. Pharmazie 63:464-469. (Pubitemid 351955409)
-
(2008)
Pharmazie
, vol.63
, Issue.6
, pp. 464-469
-
-
Galkin, A.1
Pakkanen, J.2
Vuorela, P.3
-
14
-
-
0034763005
-
Rational use of in vitro P-glycoprotein assays in drug discovery
-
Polli JW, Wring SA, Humphreys JE, Huang L, Morgan JB, Webster LO, Serabjit-Singh CS. 2001. Rational use of in vitro P-glycoprotein assays in drug discovery. J Pharmacol Exp Ther 299:620-628. (Pubitemid 32979675)
-
(2001)
Journal of Pharmacology and Experimental Therapeutics
, vol.299
, Issue.2
, pp. 620-628
-
-
Polli, J.W.1
Wring, S.A.2
Humphreys, J.E.3
Huang, L.4
Morgan, J.B.5
Webster, L.O.6
Serabjit-Singh, C.S.7
-
15
-
-
48749084803
-
A regulatory viewpoint on transporter-based drug interactions
-
Zhang L, Zhang YD, Strong JM, Reynolds KS, Huang SM. 2008. A regulatory viewpoint on transporter-based drug interactions. Xenobiotica 38:709-724.
-
(2008)
Xenobiotica
, vol.38
, pp. 709-724
-
-
Zhang, L.1
Zhang, Y.D.2
Strong, J.M.3
Reynolds, K.S.4
Huang, S.M.5
-
16
-
-
0037122748
-
Graphical model for estimating oral bioavailability of drugs in humans and other species from their Caco-2 permeability and in vitro liver enzyme metabolic stability rates
-
Mandagere AK, Thompson TN, Hwang KK. 2002. Graphical model for estimating oral bioavailability of drugs in humans and other species from their Caco-2 permeability and in vitro liver enzyme metabolic stability rates. J Med Chem 45:304-311.
-
(2002)
J Med Chem
, vol.45
, pp. 304-311
-
-
Mandagere, A.K.1
Thompson, T.N.2
Hwang, K.K.3
-
17
-
-
30744466667
-
Evaluation of an integrated in vitro-in silico PBPK (physiologically based pharmacokinetic) model to provide estimates of human bioavailability
-
DOI 10.1016/j.ijpharm.2005.11.002, PII S0378517305007465
-
Cai H, Stoner C, Reddy A, Freiwald S, Smith D, Winters R, Stankovic C, Surendran N. 2006. Evaluation of an integrated in vitro-in silico PBPK (physiologically based pharmacokinetic) model to provide estimates of human bioavailability. Int J Pharm 308:133-139. (Pubitemid 43097244)
-
(2006)
International Journal of Pharmaceutics
, vol.308
, Issue.1-2
, pp. 133-139
-
-
Cai, H.1
Stoner, C.2
Reddy, A.3
Freiwald, S.4
Smith, D.5
Winters, R.6
Stankovic, C.7
Surendran, N.8
-
18
-
-
34447330544
-
Whole-body physiologically based pharmacokinetic models
-
DOI 10.1517/17425255.3.2.235
-
Nestorov I. 2007. Whole-body physiologically based pharmacokinetic models. Expert Opin Drug Metab Toxicol 3:235-249. (Pubitemid 47321518)
-
(2007)
Expert Opinion on Drug Metabolism and Toxicology
, vol.3
, Issue.2
, pp. 235-249
-
-
Nestorov, I.1
-
19
-
-
15244344542
-
Application of full physiological models for pharmaceutical drug candidate selection and extrapolation of pharmacokinetics to man
-
DOI 10.1111/j.1742-7843.2005.pto960308.x
-
Parrott N, Jones H, Paquereau N, Lave T. 2005. Application of full physiological models for pharmaceutical drug candidate selection and extrapolation of pharmacokinetics to man. Basic Clin Pharmacol Toxicol 96:193-199. (Pubitemid 40387995)
-
(2005)
Basic and Clinical Pharmacology and Toxicology
, vol.96
, Issue.3
, pp. 193-199
-
-
Parrott, N.1
Jones, H.2
Paquereau, N.3
Lave, T.4
-
20
-
-
33646124969
-
A novel strategy for physiologically based predictions of human pharmacokinetics
-
Jones HM, Parrott N, Jorga K, Lave T. 2006. A novel strategy for physiologically based predictions of human pharmacokinetics. Clin Pharmacokinet 45:511-542.
-
(2006)
Clin Pharmacokinet
, vol.45
, pp. 511-542
-
-
Jones, H.M.1
Parrott, N.2
Jorga, K.3
Lave, T.4
-
21
-
-
0035866672
-
High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes
-
DOI 10.1021/jm001020e
-
Wohnsland F, Faller B. 2001. High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes. J Med Chem 44:923-930. (Pubitemid 32861617)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.6
, pp. 923-930
-
-
Wohnsland, F.1
Faller, B.2
-
22
-
-
34447337731
-
Prediction of human pharmacokinetics - Gastrointestinal absorption
-
DOI 10.1211/jpp.59.7.0001
-
Fagerholm U. 2007. Prediction of human pharmacokinetics - Gastrointestinal absorption. J Pharm Pharmacol 59:905-916. (Pubitemid 47051070)
-
(2007)
Journal of Pharmacy and Pharmacology
, vol.59
, Issue.7
, pp. 905-916
-
-
Fagerholm, U.1
-
23
-
-
45949101019
-
Prediction of oral drug absorption in humans - From cultured cell lines and experimental animals
-
DOI 10.1517/17425255.4.5.581
-
Cheng KC, Li C, Uss AS. 2008. Prediction of oral drug absorption in humans - From cultured cell lines and experimental animals. Expert Opin Drug Metab Toxicol 4:581-590. (Pubitemid 351890740)
-
(2008)
Expert Opinion on Drug Metabolism and Toxicology
, vol.4
, Issue.5
, pp. 581-590
-
-
Cheng, K.-C.1
Li, C.2
Uss, A.S.3
-
24
-
-
40549119872
-
The role of permeability in drug ADME/PK, interactions and toxicity - Presentation of a permeability-based classification system (PCS) for prediction of ADME/PK in humans
-
DOI 10.1007/s11095-007-9397-y
-
Fagerholm U. 2008. The role of permeability in drug ADME/PK, interactions and toxicity - Presentation of a permeability-based classification system (PCS) for prediction of ADME/PK in humans. Pharm Res 25:625-638. (Pubitemid 351357725)
-
(2008)
Pharmaceutical Research
, vol.25
, Issue.3
, pp. 625-638
-
-
Fagerholm, U.1
-
25
-
-
0037336533
-
Prediction of the oral absorption of low-permeability drugs using small intestine-like 2/4/A1 cell monolayers
-
DOI 10.1023/A:1022699920043
-
Tavelin S, Taipalensuu J, Soderberg L, Morrison R, Chong S, Artursson P. 2003. Prediction of the oral absorption of low-permeability drugs using small intestine-like 2/4/A1 cell monolayers. Pharm Res 20:397-405. (Pubitemid 36288368)
-
(2003)
Pharmaceutical Research
, vol.20
, Issue.3
, pp. 397-405
-
-
Tavelin, S.1
Taipalensuu, J.2
Soderberg, L.3
Morrison, R.4
Chong, S.5
Artursson, P.6
-
26
-
-
38349174530
-
Effect of P-glycoprotein expression levels on the concentration-dependent permeability of drugs to the cell membrane
-
Shirasaka Y, Sakane T, Yamashita S. 2008. Effect of P-glycoprotein expression levels on the concentration-dependent permeability of drugs to the cell membrane. J Pharm Sci 97:553-565.
-
(2008)
J Pharm Sci
, vol.97
, pp. 553-565
-
-
Shirasaka, Y.1
Sakane, T.2
Yamashita, S.3
-
27
-
-
0030792730
-
Estimation of the relative contribution of the transcellular and paracellular pathway to the transport of passively absorbed drugs in the Caco-2 cell culture model
-
DOI 10.1023/A:1012111008617
-
Pade V, Stavchansky S. 1997. Estimation of the relative contribution of the transcellular and paracellular pathway to the transport of passively absorbed drugs in the Caco-2 cell culture model. Pharm Res 14:1210-1215. (Pubitemid 27432545)
-
(1997)
Pharmaceutical Research
, vol.14
, Issue.9
, pp. 1210-1215
-
-
Pade, V.1
Stavchansky, S.2
-
28
-
-
0028080058
-
Quantitative approaches to delineate paracellular diffusion in cultured epithelial cell monolayers
-
DOI 10.1002/jps.2600831103
-
Adson A, Raub TJ, Burton PS, Barsuhn CL, Hilgers AR, Audus KL, Ho NF. 1994. Quantitative approaches to delineate paracellular diffusion in cultured epithelial cell monolayers. J Pharm Sci 83:1529-1536. (Pubitemid 24348320)
-
(1994)
Journal of Pharmaceutical Sciences
, vol.83
, Issue.11
, pp. 1529-1536
-
-
Adson, A.1
Raub, T.J.2
Burton, P.S.3
Barsuhn, C.L.4
Hilgers, A.R.5
Audus, K.L.6
Ho, N.F.H.7
-
29
-
-
0029102179
-
Passive diffusion of weak organic electrolytes across Caco-2 cell monolayers: Uncoupling the contributions of hydrodynamic, transcellular, and paracellular barriers
-
Adson A, Burton PS, Raub TJ, Barsuhn CL, Audus KL, Ho NF. 1995. Passive diffusion of weak organic electrolytes across Caco-2 cell monolayers: Uncoupling the contributions of hydrodynamic, transcellular, and paracellular barriers. J Pharm Sci 84:1197-1204.
-
(1995)
J Pharm Sci
, vol.84
, pp. 1197-1204
-
-
Adson, A.1
Burton, P.S.2
Raub, T.J.3
Barsuhn, C.L.4
Audus, K.L.5
Ho, N.F.6
-
30
-
-
47949130628
-
Mechanisms underlying saturable intestinal absorption of metformin
-
Proctor WR, Bourdet DL, Thakker DR. Mechanisms underlying saturable intestinal absorption of metformin. Drug Metab Dispos 36:1650-1658.
-
Drug Metab Dispos
, vol.36
, pp. 1650-1658
-
-
Proctor, W.R.1
Bourdet, D.L.2
Thakker, D.R.3
-
31
-
-
0034031969
-
Optimized conditions for prediction of intestinal drug permeability using Caco-2 cells
-
DOI 10.1016/S0928-0987(00)00076-2, PII S0928098700000762
-
Yamashita S, Furubayashi T, Kataoka M, Sakane T, Sezaki H, Tokuda H. 2000. Optimized conditions for prediction of intestinal drug permeability using Caco-2 cells. Eur J Pharm Sci 10:195-204. (Pubitemid 30190095)
-
(2000)
European Journal of Pharmaceutical Sciences
, vol.10
, Issue.3
, pp. 195-204
-
-
Yamashita, S.1
Furubayashi, T.2
Kataoka, M.3
Sakane, T.4
Sezaki, H.5
Tokuda, H.6
-
32
-
-
0043127396
-
Ph-dependent bidirectional transport of weakly basic drugs across Caco-2 monolayers: Implications for drug-drug interactions
-
DOI 10.1023/A:1025032511040
-
Neuhoff S, Ungell AL, Zamora I, Artursson P. 2003. pH-dependent bidirectional transport of weakly basic drugs across Caco-2 monolayers: Implications for drug-drug interactions. Pharm Res 20:1141-1148. (Pubitemid 36951837)
-
(2003)
Pharmaceutical Research
, vol.20
, Issue.8
, pp. 1141-1148
-
-
Neuhoff, S.1
Ungell, A.-L.2
Zamora, I.3
Artursson, P.4
-
33
-
-
47049089769
-
Use of simulated intestinal fluid for Caco-2 permeability assay of lipophilic drugs
-
Fossati L, Dechaume R, Hardillier E, Chevillon D, Prevost C, Bolze S, Maubon N. 2008. Use of simulated intestinal fluid for Caco-2 permeability assay of lipophilic drugs. Int J Pharm 360:148-155.
-
(2008)
Int J Pharm
, vol.360
, pp. 148-155
-
-
Fossati, L.1
Dechaume, R.2
Hardillier, E.3
Chevillon, D.4
Prevost, C.5
Bolze, S.6
Maubon, N.7
-
34
-
-
33750071406
-
Drug adsorption to plastic containers and retention of drugs in cultured cells under in vitro conditions
-
DOI 10.1016/j.ejpb.2006.06.005, PII S093964110600155X
-
Palmgren JJ, Monkkonen J, Korjamo T, Hassinen A, Auriola S. 2006. Drug adsorption to plastic containers and retention of drugs in cultured cells under in vitro conditions. Eur J Pharm Biopharm 64:369-378. (Pubitemid 44585210)
-
(2006)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.64
, Issue.3
, pp. 369-378
-
-
Palmgren, J.J.1
Monkkonen, J.2
Korjamo, T.3
Hassinen, A.4
Auriola, S.5
-
35
-
-
0035800246
-
Permeability of lipophilic compounds in drug discovery using in-vitro human absorption model, Caco-2
-
DOI 10.1016/S0378-5173(01)00698-6, PII S0378517301006986
-
Krishna G, Chen K, Lin C, Nomeir AA. 2001. Permeability of lipophilic compounds in drug discovery using in-vitro human absorption model, Caco-2. Int J Pharm 222:77-89. (Pubitemid 32525789)
-
(2001)
International Journal of Pharmaceutics
, vol.222
, Issue.1
, pp. 77-89
-
-
Krishna, G.1
Chen, K.-J.2
Lin, C.-C.3
Nomeir, A.A.4
-
36
-
-
0030465760
-
Development of Caco-2 cells expressing high levels of cDNA-derived cytochrome P4503A4
-
DOI 10.1023/A:1016428304366
-
Crespi CL, Penman BW, Hu M. 1996. Development of Caco-2 cells expressing high levels of cDNA-derived cytochrome P4503A4. Pharm Res 13:1635-1641. (Pubitemid 26426885)
-
(1996)
Pharmaceutical Research
, vol.13
, Issue.11
, pp. 1635-1641
-
-
Crespi, C.L.1
Penman, B.W.2
Hu, M.3
-
37
-
-
36849049288
-
Development of a high throughput equilibrium solubility assay using miniaturized shake-flask method in early drug discovery
-
DOI 10.1002/jps.20913
-
Zhou L, Yang L, Tilton S, Wang J. 2007. Development of a high throughput equilibrium solubility assay using miniaturized shake-flask method in early drug discovery. J Pharm Sci 96: 3052-3071. (Pubitemid 350221202)
-
(2007)
Journal of Pharmaceutical Sciences
, vol.96
, Issue.11
, pp. 3052-3071
-
-
Zhou, L.1
Yang, L.2
Tilton, S.3
Wang, J.4
-
38
-
-
0033634987
-
The influence of donor and reservoir additives on Caco-2 permeability and secretory transport of HIV protease inhibitors and other lipophilic compounds
-
Aungst BJ, Nguyen NH, Bulgarelli JP, Oates-Lenz K. 2000. The influence of donor and reservoir additives on Caco-2 permeability and secretory transport of HIV protease inhibitors and other lipophilic compounds. Pharm Res 17:1175-1180.
-
(2000)
Pharm Res
, vol.17
, pp. 1175-1180
-
-
Aungst, B.J.1
Nguyen, N.H.2
Bulgarelli, J.P.3
Oates-Lenz, K.4
-
39
-
-
0142074302
-
In vitro system to evaluate oral absorption of poorly water-soluble drugs: Simultaneous analysis on dissolution and permeation of drugs
-
Kataoka M, Masaoka Y, Yamazaki Y, Sakane T, Sezaki H, Yamashita S. 2003. In vitro system to evaluate oral absorption of poorly water-soluble drugs: Simultaneous analysis on dissolution and permeation of drugs. Pharm Res 20:1674-1680.
-
(2003)
Pharm Res
, vol.20
, pp. 1674-1680
-
-
Kataoka, M.1
Masaoka, Y.2
Yamazaki, Y.3
Sakane, T.4
Sezaki, H.5
Yamashita, S.6
-
40
-
-
0036849486
-
Effect of bovine serum albumin on drug permeability estimation across Caco-2 monolayers
-
DOI 10.1016/S0939-6411(02)00089-9, PII S0939641102000899
-
Saha P, Kou JH. 2002. Effect of bovine serum albumin on drug permeability estimation across Caco-2 monolayers. Eur J Pharm Biopharm 54:319-324. (Pubitemid 35341832)
-
(2002)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.54
, Issue.3
, pp. 319-324
-
-
Saha, P.1
Kou, J.H.2
-
41
-
-
32644436135
-
Impact of extracellular protein binding on passive and active drug transport across Caco-2 cells
-
DOI 10.1007/s11095-005-9304-3
-
Neuhoff S, Artursson P, Zamora I, Ungell AL. 2006. Impact of extracellular protein binding on passive and active drug transport across Caco-2 cells. Pharm Res 23:350-359. (Pubitemid 43239592)
-
(2006)
Pharmaceutical Research
, vol.23
, Issue.2
, pp. 350-359
-
-
Neuhoff, S.1
Artursson, P.2
Zamora, I.3
Ungell, A.-L.4
-
42
-
-
44749092580
-
Optimisation of the Caco-2 permeability assay using experimental design methodology
-
Lakeram M, Lockley DJ, Pendlington R, Forbes B. 2008. Optimisation of the Caco-2 permeability assay using experimental design methodology. Pharm Res 25:1544-1551.
-
(2008)
Pharm Res
, vol.25
, pp. 1544-1551
-
-
Lakeram, M.1
Lockley, D.J.2
Pendlington, R.3
Forbes, B.4
-
43
-
-
0036741452
-
Effects of nonionic surfactants on membrane transporters in Caco-2 cell monolayers
-
Rege BD, Kao JP, Polli JE. 2002. Effects of nonionic surfactants on membrane transporters in Caco-2 cell monolayers. Eur J Pharm Sci 16:237-246.
-
(2002)
Eur J Pharm Sci
, vol.16
, pp. 237-246
-
-
Rege, B.D.1
Kao, J.P.2
Polli, J.E.3
-
44
-
-
34250822863
-
Mechanism of inhibition of P-glycoprotein mediated efflux by vitamin e TPGS: Influence on ATPase activity and membrane fluidity
-
DOI 10.1021/mp060121r
-
Collnot EM, Baldes C, Wempe MF, Kappl R, Huttermann J, Hyatt JA, Edgar KJ, Schaefer UF, Lehr CM. 2007. Mechanism of inhibition of P-glycoprotein mediated efflux by vitamin E TPGS: Influence on ATPase activity and membrane fluidity. Mol Pharm 4:465-474. (Pubitemid 46983960)
-
(2007)
Molecular Pharmaceutics
, vol.4
, Issue.3
, pp. 465-474
-
-
Collnot, E.-M.1
Baldes, C.2
Wempe, M.F.3
Kappl, R.4
Huttermann, J.5
Hyatt, J.A.6
Edgar, K.J.7
Schaefer, U.F.8
Lehr, C.-M.9
-
45
-
-
33845731767
-
Enhancement of drug absorption by noncharged detergents through membrane and P-glycoprotein binding
-
DOI 10.1517/17425255.2.5.733
-
Seelig A, Gerebtzoff G. 2006. Enhancement of drug absorption by noncharged detergents through membrane and P-glycoprotein binding. Expert Opin Drug Metab Toxicol 2:733-752. (Pubitemid 46118318)
-
(2006)
Expert Opinion on Drug Metabolism and Toxicology
, vol.2
, Issue.5
, pp. 733-752
-
-
Seelig, A.1
Gerebtzoff, G.2
-
46
-
-
0033427847
-
Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability
-
Yu L, Bridgers A, Polli J, Vickers A, Long S, Roy A, Winnike R, Coffin M. 1999. Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability. Pharm Res 16:1812-1817. (Pubitemid 30040695)
-
(1999)
Pharmaceutical Research
, vol.16
, Issue.12
, pp. 1812-1817
-
-
Yu, L.1
Bridgers, A.2
Polli, J.3
Vickers, A.4
Long, S.5
Roy, A.6
Winnike, R.7
Coffin, M.8
-
47
-
-
0036453655
-
An in vitro examination of the impact of polyethylene glycol 400, Pluronic P85, and vitamin e d-alpha-tocopheryl polyethylene glycol 1000 succinate on P-glycoprotein efflux and enterocyte-based metabolism in excised rat intestine
-
Johnson BM, Charman WN, Porter CJ. 2002. An in vitro examination of the impact of polyethylene glycol 400, Pluronic P85, and vitamin E d-alpha-tocopheryl polyethylene glycol 1000 succinate on P-glycoprotein efflux and enterocyte-based metabolism in excised rat intestine. AAPS PharmSci 4:E40.
-
(2002)
AAPS PharmSci
, vol.4
-
-
Johnson, B.M.1
Charman, W.N.2
Porter, C.J.3
-
48
-
-
33746057821
-
Functional role of P-glycoprotein in limiting peroral drug absorption: Optimizing drug delivery
-
DOI 10.1016/j.cbpa.2006.06.015, PII S1367593106000846, Next-Generation Therapeutics
-
Varma MV, Perumal OP, Panchagnula R. 2006. Functional role of P-glycoprotein in limiting peroral drug absorption: Optimizing drug delivery. Curr Opin Chem Biol 10:367-373. (Pubitemid 44080650)
-
(2006)
Current Opinion in Chemical Biology
, vol.10
, Issue.4
, pp. 367-373
-
-
Varma, M.V.1
Perumal, O.P.2
Panchagnula, R.3
-
49
-
-
34548295855
-
Increased absorption of digoxin from the human jejunum due to inhibition of intestinal transporter-mediated efflux
-
DOI 10.2165/00003088-200746090-00005
-
Igel S, Drescher S, Murdter T, Hofmann U, Heinkele G, Tegude H, Glaeser H, Brenner SS, Somogyi AA, Omari T, Schafer C, Eichelbaum M, Fromm MF. 2007. Increased absorption of digoxin from the human jejunum due to inhibition of intestinal transporter-mediated efflux. Clin Pharmacokinet 46:777-785. (Pubitemid 47347449)
-
(2007)
Clinical Pharmacokinetics
, vol.46
, Issue.9
, pp. 777-785
-
-
Igel, S.1
Drescher, S.2
Murdter, T.3
Hofmann, U.4
Heinkele, G.5
Tegude, H.6
Glaeser, H.7
Brenner, S.S.8
Somogyi, A.A.9
Omari, T.10
Schafer, C.11
Eichelbaum, M.12
Fromm, M.F.13
-
50
-
-
42449083749
-
Differential roles of P-glycoprotein, multidrug resistance-associated protein 2, and CYP3A on saquinavir oral absorption in Sprague-Dawley rats
-
DOI 10.1124/dmd.107.017483
-
Usansky HH, Hu P, Sinko PJ. 2008. Differential roles of P-glycoprotein, multidrug resistance-associated protein 2, and CYP3A on saquinavir oral absorption in Sprague-Dawley rats. Drug Metab Dispos 36:863-869. (Pubitemid 351574883)
-
(2008)
Drug Metabolism and Disposition
, vol.36
, Issue.5
, pp. 863-869
-
-
Usansky, H.H.1
Hu, P.2
Sinko, P.J.3
-
51
-
-
0033730609
-
The role of P-glycoprotein in determining the oral absorption and clearance of the NK2 antagonist, UK-224671
-
Beaumont K, Harper A, Smith DA, Bennett J. 2000. The role of P-glycoprotein in determining the oral absorption and clearance of the NK2 antagonist, UK-224,671. Eur J Pharm Sci 12:41-50.
-
(2000)
Eur J Pharm Sci
, vol.12
, pp. 41-50
-
-
Beaumont, K.1
Harper, A.2
Smith, D.A.3
Bennett, J.4
-
52
-
-
1442302325
-
Intestinal drug transporters: In vivo function and clinical importance
-
Kunta JR, Sinko PJ. 2004. Intestinal drug transporters: In vivo function and clinical importance. Curr Drug Metab 5:109-124.
-
(2004)
Curr Drug Metab
, vol.5
, pp. 109-124
-
-
Kunta, J.R.1
Sinko, P.J.2
-
53
-
-
0037457793
-
Drug-drug interaction mediated by inhibition and induction of P-glycoprotein
-
Lin JH. 2003. Drug-drug interaction mediated by inhibition and induction of P-glycoprotein. Adv Drug Deliv Rev 55:53-81.
-
(2003)
Adv Drug Deliv Rev
, vol.55
, pp. 53-81
-
-
Lin, J.H.1
-
54
-
-
0032885452
-
Role of P-glycoprotein-mediated secretion in absorptive drug permeability: An approach using passive membrane permeability and affinity to P-glycoprotein
-
Doppenschmitt S, Spahn-Langguth H, Regardh CG, Langguth P. 1999. Role of P-glycoprotein-mediated secretion in absorptive drug permeability: An approach using passive membrane permeability and affinity to P-glycoprotein. J Pharm Sci 88:1067-1072.
-
(1999)
J Pharm Sci
, vol.88
, pp. 1067-1072
-
-
Doppenschmitt, S.1
Spahn-Langguth, H.2
Regardh, C.G.3
Langguth, P.4
-
55
-
-
0035987203
-
Evaluation of drug interactions with P-glycoprotein in drug discovery: In vitro assessment of the potential for drug-drug interactions with P-glycoprotein
-
Hochman JH, Yamazaki M, Ohe T, Lin JH. 2002. Evaluation of drug interactions with P-glycoprotein in drug discovery: In vitro assessment of the potential for drug-drug interactions with P-glycoprotein. Curr Drug Metab 3:257-273.
-
(2002)
Curr Drug Metab
, vol.3
, pp. 257-273
-
-
Hochman, J.H.1
Yamazaki, M.2
Ohe, T.3
Lin, J.H.4
-
56
-
-
39749181550
-
Generation of a set of simple interpretable ADMET rules of thumb
-
Gleeson MP. 2008. Generation of a set of simple, interpretable ADMET rules of thumb. J Med Chem 51:817-834.
-
(2008)
J Med Chem
, vol.51
, pp. 817-834
-
-
Gleeson, M.P.1
-
57
-
-
0027312774
-
Selective paracellular permeability in two models of intestinal absorption: Cultured monolayers of human intestinal epithelial cells and rat intestinal segments
-
Artursson P, Ungell AL, Lofroth JE. 1993. Selective paracellular permeability in two models of 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
Lofroth, J.E.3
-
58
-
-
0037335192
-
An improved cell culture model based on 2/ 4/A1 cell monolayers for studies of intestinal drug transport: Characterization of transport routes
-
Tavelin S, Taipalensuu J, Hallbook F, Vellonen KS, Moore V, Artursson P. 2003. An improved cell culture model based on 2/ 4/A1 cell monolayers for studies of intestinal drug transport: Characterization of transport routes. Pharm Res 20:373-381.
-
(2003)
Pharm Res
, vol.20
, pp. 373-381
-
-
Tavelin, S.1
Taipalensuu, J.2
Hallbook, F.3
Vellonen, K.S.4
Moore, V.5
Artursson, P.6
-
59
-
-
10644245087
-
Contribution of the paracellular route to the pH-dependent epithelial permeability to cationic drugs
-
Nagahara N, Tavelin S, Artursson P. 2004. Contribution of the paracellular route to the pH-dependent epithelial permeability to cationic drugs. J Pharm Sci 93:2972-2984.
-
(2004)
J Pharm Sci
, vol.93
, pp. 2972-2984
-
-
Nagahara, N.1
Tavelin, S.2
Artursson, P.3
-
60
-
-
3543003562
-
Correction of permeability with pore radius of tight junctions in Caco-2 monolayers improves the prediction of the dose fraction of hydrophilic drugs absorbed by humans
-
Saitoh R, Sugano K, Takata N, Tachibana T, Higashida A, Nabuchi Y, Aso Y. 2004. Correction of permeability with pore radius of tight junctions in Caco-2 monolayers improves the prediction of the dose fraction of hydrophilic drugs absorbed by humans. Pharm Res 21:749-755.
-
(2004)
Pharm Res
, vol.21
, pp. 749-755
-
-
Saitoh, R.1
Sugano, K.2
Takata, N.3
Tachibana, T.4
Higashida, A.5
Nabuchi, Y.6
Aso, Y.7
-
61
-
-
0028903847
-
Effect of changing intestinal flow rate on a measurement of intestinal permeability
-
Fine KD, Santa Ana CA, Porter JL, Fordtran JS. 1995. Effect of changing intestinal flow rate on a measurement of intestinal permeability. Gastroenterology 108:983-989.
-
(1995)
Gastroenterology
, vol.108
, pp. 983-989
-
-
Fine, K.D.1
Santa Ana, C.A.2
Porter, J.L.3
Fordtran, J.S.4
-
62
-
-
0028934442
-
Characterization of drug transport through tight-junctional pathway in Caco-2 monolayer: Comparison with isolated rat jejunum and colon
-
Tanaka Y, Taki Y, Sakane T, Nadai T, Sezaki H, Yamashita S. 1995. Characterization of drug transport through tight-junctional pathway in Caco-2 monolayer: Comparison with isolated rat jejunum and colon. Pharm Res 12:523-528.
-
(1995)
Pharm Res
, vol.12
, pp. 523-528
-
-
Tanaka, Y.1
Taki, Y.2
Sakane, T.3
Nadai, T.4
Sezaki, H.5
Yamashita, S.6
-
63
-
-
0031786518
-
Linear correlation of the fraction of oral dose absorbed of 64 drugs between humans and rats
-
Chiou WL, Barve A. 1998. Linear correlation of the fraction of oral dose absorbed of 64 drugs between humans and rats. Pharm Res 15:1792-1795.
-
(1998)
Pharm Res
, vol.15
, pp. 1792-1795
-
-
Chiou, W.L.1
Barve, A.2
-
64
-
-
0036846773
-
The use of in vitro metabolic stability for rapid selection of compounds in early discovery based on their expected hepatic extraction ratios
-
Lau YY, Krishna G, Yumibe NP, Grotz DE, Sapidou E, Norton L, Chu I, Chen C, Soares AD, Lin CC. 2002. The use of in vitro metabolic stability for rapid selection of compounds in early discovery based on their expected hepatic extraction ratios. Pharm Res 19:1606-1610.
-
(2002)
Pharm Res
, vol.19
, pp. 1606-1610
-
-
Lau, Y.Y.1
Krishna, G.2
Yumibe, N.P.3
Grotz, D.E.4
Sapidou, E.5
Norton, L.6
Chu, I.7
Chen, C.8
Soares, A.D.9
Lin, C.C.10
-
65
-
-
0025265465
-
Determination of hepatic blood flow in the rat using sequential infusions of indocyanine green or galactose
-
Pollack GM, Brouwer KL, Demby KB, Jones JA. 1990. Determination of hepatic blood flow in the rat using sequential infusions of indocyanine green or galactose. Drug Metab Dispos 18:197-202.
-
(1990)
Drug Metab Dispos
, vol.18
, pp. 197-202
-
-
Pollack, G.M.1
Brouwer, K.L.2
Demby, K.B.3
Jones, J.A.4
-
66
-
-
85031337713
-
-
accessed January to March 2007
-
www.tp-search.jp [accessed January to March 2007].
-
-
-
-
67
-
-
3242888957
-
Calculated molecular properties and multivariate statistical analysis in absorption prediction
-
van de Waterbeemd H, Lennernas H, Artursson P, editors. Weinheim: Wiley-VCH Verlag GmbH & Co
-
Norinder U, Haeberlein M. 2003. Calculated molecular properties and multivariate statistical analysis in absorption prediction. In: van de Waterbeemd H, Lennernas H, Artursson P, editors. Drug bioavailability, methods and principles in medicinal chemistry series. Weinheim: Wiley-VCH Verlag GmbH & Co. pp 358-405.
-
(2003)
Drug Bioavailability, Methods and Principles in Medicinal Chemistry Series
, pp. 358-405
-
-
Norinder, U.1
Haeberlein, M.2
-
68
-
-
33750587653
-
Interaction between miltefosine and amphotericin B: Consequences for their activities towards intestinal epithelial cells and Leishmania donovani promastigotes in vitro
-
Menez C, Buyse M, Besnard M, Farinotti R, Loiseau PM, Barratt G. 2006. Interaction between miltefosine and amphotericin B: Consequences for their activities towards intestinal epithelial cells and Leishmania donovani promastigotes in vitro. Antimicrob Agents Chemother 50:3793-3800.
-
(2006)
Antimicrob Agents Chemother
, vol.50
, pp. 3793-3800
-
-
Menez, C.1
Buyse, M.2
Besnard, M.3
Farinotti, R.4
Loiseau, P.M.5
Barratt, G.6
-
69
-
-
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
-
71
-
-
0035739018
-
A novel approach for prediction of intestinal absorption of drugs in humans based on hydrogen bond descriptors and structural similarity
-
Raevsky OA, Schaper KJ, Artursson P, McFarland JW. 2002. A novel approach for prediction of intestinal absorption of drugs in humans based on hydrogen bond descriptors and structural similarity. Quant Stract-Act Relat 20:402-413.
-
(2002)
Quant Stract-Act Relat
, vol.20
, pp. 402-413
-
-
Raevsky, O.A.1
Schaper, K.J.2
Artursson, P.3
McFarland, J.W.4
-
72
-
-
0029013867
-
Molecular mechanism for the relative binding affinity to the intestinal peptide carrier. Comparison of three ACE-inhibitors: Enalapril, enalaprilat, and lisinopril
-
Swaan PW, Stehouwer MC, Tukker JJ. 1995. Molecular mechanism for the relative binding affinity to the intestinal peptide carrier. Comparison of three ACE-inhibitors: Enalapril, enalaprilat, and lisinopril. Biochim Biophys Acta 1236: 31-38.
-
(1995)
Biochim Biophys Acta
, vol.1236
, pp. 31-38
-
-
Swaan, P.W.1
Stehouwer, M.C.2
Tukker, J.J.3
-
73
-
-
34249064082
-
New methods to evaluate intestinal drug absorption mediated by oligopeptide transporter from in vitro study using Caco-2 cells
-
Yamashita S, Hattori E, Shimada A, Endoh Y, Yamazaki Y, Kataoka M, Sakane T, Sezaki H. 2002. New methods to evaluate intestinal drug absorption mediated by oligopeptide transporter from in vitro study using Caco-2 cells. Drug Metab Pharmacokinet 17:408-415.
-
(2002)
Drug Metab Pharmacokinet
, vol.17
, pp. 408-415
-
-
Yamashita, S.1
Hattori, E.2
Shimada, A.3
Endoh, Y.4
Yamazaki, Y.5
Kataoka, M.6
Sakane, T.7
Sezaki, H.8
-
74
-
-
9644252691
-
Interaction of 31 beta-lactam antibiotics with the H+/peptide symporter PEPT2: Analysis of affinity constants and comparison with PEPT1
-
Luckner P, Brandsch M. 2005. Interaction of 31 beta-lactam antibiotics with the H+/peptide symporter PEPT2: Analysis of affinity constants and comparison with PEPT1. Eur J Pharm Biopharm 59:17-24.
-
(2005)
Eur J Pharm Biopharm
, vol.59
, pp. 17-24
-
-
Luckner, P.1
Brandsch, M.2
-
75
-
-
14644419054
-
Functional role of P-glycoprotein in limiting intestinal absorption of drugs: Contribution of passive permeability to P-glycoprotein mediated efflux transport
-
Varma MV, Sateesh K, Panchagnula R. 2005. Functional role of P-glycoprotein in limiting intestinal absorption of drugs: Contribution of passive permeability to P-glycoprotein mediated efflux transport. Mol Pharm 2:12-21.
-
(2005)
Mol Pharm
, vol.2
, pp. 12-21
-
-
Varma, M.V.1
Sateesh, K.2
Panchagnula, R.3
-
76
-
-
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
-
77
-
-
21644489142
-
Short term Caco-2/TC7 cell culture: Comparison between conventional 21-d and a commercially available 3-d system
-
Da VG, Zerrouk N, Richard I, Frendo JL, Zhiri A, Li-Khuan R, Tricottet V, Provot G, Chaumeil JC, Arnaud P. 2004. Short term Caco-2/TC7 cell culture: Comparison between conventional 21-d and a commercially available 3-d system. Biol Pharm Bull 27:1986-1992.
-
(2004)
Biol Pharm Bull
, vol.27
, pp. 1986-1992
-
-
Da, V.G.1
Zerrouk, N.2
Richard, I.3
Frendo, J.L.4
Zhiri, A.5
Li-Khuan, R.6
Tricottet, V.7
Provot, G.8
Chaumeil, J.C.9
Arnaud, P.10
-
78
-
-
53849088940
-
Simulation of absorption, metabolism, and bioavailability
-
van de Waterbeemd H, Lennernas H, Artursson P, editors. 18th edition. Weinheim: Wiley-VCH Verlag GmbH & Co
-
Bolger MB, Agoram B, Fraczkiewicz R, Steere B. 2003. Simulation of absorption, metabolism, and bioavailability. In: van de Waterbeemd H, Lennernas H, Artursson P, editors. Drug bioavailability, methods and principles in medicinal chemistry series, 18th edition. Weinheim: Wiley-VCH Verlag GmbH & Co. pp 420-443.
-
(2003)
Drug Bioavailability, Methods and Principles in Medicinal Chemistry Series
, pp. 420-443
-
-
Bolger, M.B.1
Agoram, B.2
Fraczkiewicz, R.3
Steere, B.4
-
79
-
-
0035214120
-
Interaction of omeprazole, lansoprazole and pantoprazole with P-glycoprotein
-
Pauli-Magnus C, Rekersbrink S, Klotz U, Fromm MF. 2001. Interaction of omeprazole, lansoprazole and pantoprazole with P-glycoprotein. Naunyn Schmiedebergs Arch Pharmacol 364:551-557.
-
(2001)
Naunyn Schmiedebergs Arch Pharmacol
, vol.364
, pp. 551-557
-
-
Pauli-Magnus, C.1
Rekersbrink, S.2
Klotz, U.3
Fromm, M.F.4
-
80
-
-
0041309866
-
Reversal of breast cancer resistance protein-mediated drug resistance by estrogen antagonists and agonists
-
Sugimoto Y, Tsukahara S, Imai Y, Sugimoto Y, Ueda K, Tsuruo T. 2003. Reversal of breast cancer resistance protein-mediated drug resistance by estrogen antagonists and agonists. Mol Cancer Ther 2:105-112.
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 105-112
-
-
Sugimoto, Y.1
Tsukahara, S.2
Imai, Y.3
Sugimoto, Y.4
Ueda, K.5
Tsuruo, T.6
-
81
-
-
2442719906
-
Unmasking the dynamic interplay between efflux transporters and metabolic enzymes
-
Benet LZ, Cummins CL, Wu CY. 2004. Unmasking the dynamic interplay between efflux transporters and metabolic enzymes. Int J Pharm 277:3-9.
-
(2004)
Int J Pharm
, vol.277
, pp. 3-9
-
-
Benet, L.Z.1
Cummins, C.L.2
Wu, C.Y.3
-
82
-
-
20444403742
-
Classification of substrates and inhibitors of P-glycoprotein using unsupervised machine learning approach
-
Wang YH, Li Y, Yang SL, Yang L. 2005. Classification of substrates and inhibitors of P-glycoprotein using unsupervised machine learning approach. J Chem Inf Model 45: 750-757.
-
(2005)
J Chem Inf Model
, vol.45
, pp. 750-757
-
-
Wang, Y.H.1
Li, Y.2
Yang, S.L.3
Yang, L.4
-
83
-
-
33746427894
-
Apparent active transport of MDMA is not mediated by P-glycoprotein: A comparison with MDCK and Caco-2 monolayers
-
Bertelsen KM, Greenblatt DJ, von Moltke LL. 2006. Apparent active transport of MDMA is not mediated by P-glycoprotein: A comparison with MDCK and Caco-2 monolayers. Biopharm Drug Dispos 27:219-227.
-
(2006)
Biopharm Drug Dispos
, vol.27
, pp. 219-227
-
-
Bertelsen, K.M.1
Greenblatt, D.J.2
Von Moltke, L.L.3
-
84
-
-
33751003834
-
Presentation of a structurally diverse and commercially available drug data set for correlation and benchmarking studies
-
Skold C, Winiwarter S, Wernevik J, Bergstrom F, Engstrom L, Allen R, Box K, Comer J, Mole J, Hallberg A, Lennernas H, Lundstedt T, Ungell AL, Karlen 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
-
-
Skold, C.1
Winiwarter, S.2
Wernevik, J.3
Bergstrom, F.4
Engstrom, L.5
Allen, R.6
Box, K.7
Comer, J.8
Mole, J.9
Hallberg, A.10
Lennernas, H.11
Lundstedt, T.12
Ungell, A.L.13
Karlen, A.14
-
85
-
-
0028324534
-
Uptake and transepithelial transport of the orally absorbed cephalosporin cephalexin, in the human intestinal cell line, Caco-2
-
Gochoco CH, Ryan FM, Miller J, Smith PL, Hidalgo IJ. 1994. Uptake and transepithelial transport of the orally absorbed cephalosporin cephalexin, in the human intestinal cell line, Caco-2. Int J Pharm 104:187-202.
-
(1994)
Int J Pharm
, vol.104
, pp. 187-202
-
-
Gochoco, C.H.1
Ryan, F.M.2
Miller, J.3
Smith, P.L.4
Hidalgo, I.J.5
-
86
-
-
0033973754
-
Caco-2 versus Caco-2/HT29-MTX co-cultured cell lines: Permeabilities via diffusion inside- And outside-directed carrier-mediated transport
-
Hilgendorf C, Spahn-Langguth H, Regardh CG, Lipka E, Amidon GL, Langguth P. 2000. Caco-2 versus Caco-2/HT29-MTX co-cultured cell lines: Permeabilities via diffusion, inside- and outside-directed carrier-mediated transport. J Pharm Sci 89:63-75.
-
(2000)
J Pharm Sci
, vol.89
, pp. 63-75
-
-
Hilgendorf, C.1
Spahn-Langguth, H.2
Regardh, C.G.3
Lipka, E.4
Amidon, G.L.5
Langguth, P.6
-
87
-
-
0029897299
-
Investigation of nifedipine absorption in different regions of the human gastrointestinal (GI) tract after simultaneous administration of 13C- And 12C-nifedipine
-
Bode H, Brendel E, Ahr G, Fuhr U, Harder S, Staib AH. 1996. Investigation of nifedipine absorption in different regions of the human gastrointestinal (GI) tract after simultaneous administration of 13C- and 12C-nifedipine. Eur J Clin Pharmacol 50:195-201.
-
(1996)
Eur J Clin Pharmacol
, vol.50
, pp. 195-201
-
-
Bode, H.1
Brendel, E.2
Ahr, G.3
Fuhr, U.4
Harder, S.5
Staib, A.H.6
-
88
-
-
33644674142
-
Computational models for identifying potential P-glycoprotein substrates and inhibitors
-
Crivori P, Reinach B, Pezzetta D, Poggesi I. 2006. Computational models for identifying potential P-glycoprotein substrates and inhibitors. Mol Pharm 3:33-44.
-
(2006)
Mol Pharm
, vol.3
, pp. 33-44
-
-
Crivori, P.1
Reinach, B.2
Pezzetta, D.3
Poggesi, I.4
-
89
-
-
33745624809
-
A novel tool to characterize paracellular transport: TheAPTS-dextran ladder
-
Neuhaus W, Bogner E, Wirth M, Trzeciak J, Lachmann B, Gabor F, Noe CR. 2006. A novel tool to characterize paracellular transport: TheAPTS-dextran ladder. PharmRes 23:1491-1501.
-
(2006)
PharmRes
, vol.23
, pp. 1491-1501
-
-
Neuhaus, W.1
Bogner, E.2
Wirth, M.3
Trzeciak, J.4
Lachmann, B.5
Gabor, F.6
Noe, C.R.7
-
90
-
-
13044249156
-
A multidrug resistance transporter from human MCF-7 breast cancer cells
-
Doyle LA, Yang W, Abruzzo LV, Krogmann T, Gao Y, Rishi AK, Ross DD. 1998. A multidrug resistance transporter from human MCF-7 breast cancer cells. Proc Natl Acad Sci USA 95:15665-15670.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 15665-15670
-
-
Doyle, L.A.1
Yang, W.2
Abruzzo, L.V.3
Krogmann, T.4
Gao, Y.5
Rishi, A.K.6
Ross, D.D.7
-
91
-
-
0033636283
-
Mechanisms of transport and structure-permeability relationship of sulfasalazine and its analogs in Caco-2 cell monolayers
-
Liang E, Proudfoot J, Yazdanian M. 2000. Mechanisms of transport and structure-permeability relationship of sulfasalazine and its analogs in Caco-2 cell monolayers. Pharm Res 17:1168-1174.
-
(2000)
Pharm Res
, vol.17
, pp. 1168-1174
-
-
Liang, E.1
Proudfoot, J.2
Yazdanian, M.3
-
92
-
-
0141815941
-
Wild-type breast cancer resistance protein (BCRP/ABCG2) is a methotrexate polyglutamate transporter
-
Volk EL, Schneider E. 2003. Wild-type breast cancer resistance protein (BCRP/ABCG2) is a methotrexate polyglutamate transporter. Cancer Res 63:5538-5543.
-
(2003)
Cancer Res
, vol.63
, pp. 5538-5543
-
-
Volk, E.L.1
Schneider, E.2
-
93
-
-
33745231761
-
Involvement of transporters in the hepatic uptake and biliary excretion of valsartan, a selective antagonist of the angiotensin II AT1-receptor, in humans
-
DOI 10.1124/dmd.105.008938
-
Yamashiro W, Maeda K, Hirouchi M, Adachi Y, Hu Z, Sugiyama Y. 2006. Involvement of transporters in the hepatic uptake and biliary excretion of valsartan, a selective antagonist of the angiotensin II AT1-receptor, in humans. Drug Metab Dispos 34:1247-1254. (Pubitemid 43920885)
-
(2006)
Drug Metabolism and Disposition
, vol.34
, Issue.7
, pp. 1247-1254
-
-
Yamashiro, W.1
Maeda, K.2
Hirouchi, M.3
Adachi, Y.4
Hu, Z.5
Sugiyama, Y.6
-
94
-
-
0033014877
-
Net secretion of furosemide is subject to indomethacin inhibition, as observed in Caco-2 monolayers and excised rat jejunum
-
Flanagan SD, Benet LZ. 1999. Net secretion of furosemide is subject to indomethacin inhibition, as observed in Caco-2 monolayers and excised rat jejunum. Pharm Res 16:221-224.
-
(1999)
Pharm Res
, vol.16
, pp. 221-224
-
-
Flanagan, S.D.1
Benet, L.Z.2
-
95
-
-
33645108568
-
Breast cancer resistance protein (BCRP/ ABCG2) transports fluoroquinolone antibiotics and affects their oral availability, pharmacokinetics, and milk secretion
-
Merino G, Alvarez AI, Pulido MM, Molina AJ, Schinkel AH, Prieto JG. 2006. Breast cancer resistance protein (BCRP/ ABCG2) transports fluoroquinolone antibiotics and affects their oral availability, pharmacokinetics, and milk secretion. Drug Metab Dispos 34:690-695.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 690-695
-
-
Merino, G.1
Alvarez, A.I.2
Pulido, M.M.3
Molina, A.J.4
Schinkel, A.H.5
Prieto, J.G.6
-
96
-
-
0041402720
-
Efflux ratio cannot assess P-glycoprotein-mediated attenuation of absorptive transport: Asymmetric effect of P-glycoprotein on absorptive and secretory transport across Caco-2 cell monolayers
-
Troutman MD, Thakker DR. 2003. Efflux ratio cannot assess P-glycoprotein-mediated attenuation of absorptive transport: Asymmetric effect of P-glycoprotein on absorptive and secretory transport across Caco-2 cell monolayers. Pharm Res 20:1200-1209.
-
(2003)
Pharm Res
, vol.20
, pp. 1200-1209
-
-
Troutman, M.D.1
Thakker, D.R.2
-
97
-
-
0034789387
-
Functional characterization of the human multidrug transporter, ABCG2, expressed in insect cells
-
DOI 10.1006/bbrc.2001.5130
-
Ozvegy C, Litman T, Szakacs G, Nagy Z, Bates S, Varadi A, Sarkadi B. 2001. Functional characterization of the human multidrug transporter, ABCG2, expressed in insect cells. Biochem Biophys Res Commun 285:111-117. (Pubitemid 32912517)
-
(2001)
Biochemical and Biophysical Research Communications
, vol.285
, Issue.1
, pp. 111-117
-
-
Ozvegy, C.1
Litman, T.2
Szakacs, G.3
Nagy, Z.4
Bates, S.5
Varadi, A.6
Sarkadi, B.7
-
98
-
-
0031890094
-
2-antagonists
-
DOI 10.1023/A:1011944602662
-
Gan LS, Yanni S, Thakker DR. 1998. Modulation of the tight junctions of the Caco-2 cell monolayers by H2-antagonists. Pharm Res 15:53-57. (Pubitemid 28080866)
-
(1998)
Pharmaceutical Research
, vol.15
, Issue.1
, pp. 53-57
-
-
Gan, L.-S.L.1
Yanni, S.2
Thakker, D.R.3
-
99
-
-
0030990079
-
In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in man - Fact or myth
-
Yee S. 1997. In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in man - Fact or myth. Pharm Res 14:763-766.
-
(1997)
Pharm Res
, vol.14
, pp. 763-766
-
-
Yee, S.1
-
100
-
-
0030030387
-
1and Caco-2 cell lines as models for studying intestinal paracellular drug absorption
-
DOI 10.1023/A:1016082829111
-
Collett A, Sims E, Walker D, He YL, Ayrton J, Rowland M, Warhurst G. 1996. Comparison of HT29-18-C1 and Caco-2 cell lines as models for studying intestinal paracellular drug absorption. Pharm Res 13:216-221. (Pubitemid 26072141)
-
(1996)
Pharmaceutical Research
, vol.13
, Issue.2
, pp. 216-221
-
-
Collett, A.1
Sims, E.2
Walker, D.3
He, Y.-L.4
Ayrton, J.5
Rowland, M.6
Warhurst, G.7
-
101
-
-
70349414560
-
Multiple efflux. Pumps are involved in the transepithelial transport of colchicine: Combined effect of P-gp and MRP2 leads to decreased intestinal absorption throughout the entire small intestine
-
Dahan A, Sabit H, Amidon GL. 2009. Multiple efflux. Pumps are involved in the transepithelial transport of colchicine: Combined effect of P-gp and MRP2 leads to decreased intestinal absorption throughout the entire small intestine. Drug Metab Dispos 10:2028-2036.
-
(2009)
Drug Metab Dispos
, vol.10
, pp. 2028-2036
-
-
Dahan, A.1
Sabit, H.2
Amidon, G.L.3
-
102
-
-
0027275566
-
Physiological parameters in laboratory animals and humans
-
DOI 10.1023/A:1018943613122
-
Davies B, Morris T. 1993. Physiological parameters in laboratory animals and humans. Pharm Res 10:1093-1095. (Pubitemid 23211439)
-
(1993)
Pharmaceutical Research
, vol.10
, Issue.7
, pp. 1093-1095
-
-
Davies, B.1
Morris, T.2
|