-
1
-
-
25844469583
-
Drug metabolism and pharmacokinetics, the blood-brain barrier, and central nervous system drug discovery
-
10.1602/neurorx.2.4.554 16489365
-
Alavijeh MS, Chishty M, Qaiser MZ, Palmer AM. Drug metabolism and pharmacokinetics, the blood-brain barrier, and central nervous system drug discovery. NeuroRx. 2005;2:554-71.
-
(2005)
NeuroRx
, vol.2
, pp. 554-571
-
-
Alavijeh, M.S.1
Chishty, M.2
Qaiser, M.Z.3
Palmer, A.M.4
-
2
-
-
0034713376
-
A simple model for the prediction of blood-brain partitioning
-
1:CAS:528:DC%2BD3cXktlSlurg%3D 10.1016/S0378-5173(00)00422-1 10878329
-
Feher M, Sourial E, Schmidt JM. A simple model for the prediction of blood-brain partitioning. Int J Pharm. 2000;201:239-47.
-
(2000)
Int J Pharm
, vol.201
, pp. 239-247
-
-
Feher, M.1
Sourial, E.2
Schmidt, J.M.3
-
3
-
-
77951963113
-
Prediction of passive blood-brain partitioning: Straightforward and effective classification models based on in silico derived physicochemical descriptors
-
1:CAS:528:DC%2BC3cXmtFChs7g%3D 10.1016/j.jmgm.2010.03.010 20427217
-
Vilar S, Chakrabarti M, Costanzi S. Prediction of passive blood-brain partitioning: straightforward and effective classification models based on in silico derived physicochemical descriptors. J Mol Graph Model. 2010;28:899-903.
-
(2010)
J Mol Graph Model
, vol.28
, pp. 899-903
-
-
Vilar, S.1
Chakrabarti, M.2
Costanzi, S.3
-
4
-
-
0035440324
-
Correlation and prediction of a large blood-brain distribution data set - An LFER study
-
1:CAS:528:DC%2BD3MXnvVSjtb0%3D 10.1016/S0223-5234(01)01269-7 11672881
-
Platts JA, Abraham MH, Zhao YH, Hersey A, Ijaz L, Butina D. Correlation and prediction of a large blood-brain distribution data set - an LFER study. Eur J Med Chem. 2001;36:719-30.
-
(2001)
Eur J Med Chem
, vol.36
, pp. 719-730
-
-
Platts, J.A.1
Abraham, M.H.2
Zhao, Y.H.3
Hersey, A.4
Ijaz, L.5
Butina, D.6
-
5
-
-
1842635478
-
Log(BB), PS products and in silico models of drug brain penetration
-
10.1016/S1359-6446(04)03065-X 15081955
-
Pardridge WM. Log(BB), PS products and in silico models of drug brain penetration. Drug Discov Today. 2004;9:392-3.
-
(2004)
Drug Discov Today
, vol.9
, pp. 392-393
-
-
Pardridge, W.M.1
-
6
-
-
79251504066
-
Brain availability is the key parameter for optimising the permeability of central nervous system drugs
-
10.2174/157018010789869316
-
Boriss H. Brain availability is the key parameter for optimising the permeability of central nervous system drugs. Drug Discov. 2010;7:57-60.
-
(2010)
Drug Discov
, vol.7
, pp. 57-60
-
-
Boriss, H.1
-
7
-
-
70449526541
-
Assessment of the blood-brain barrier in CNS drug discovery
-
1:CAS:528:DC%2BD1MXhsVGms7jN 10.1016/j.nbd.2009.07.033 19664709
-
Jeffrey P, Summerfield S. Assessment of the blood-brain barrier in CNS drug discovery. Neurobiol Dis. 2010;37:33-7.
-
(2010)
Neurobiol Dis
, vol.37
, pp. 33-37
-
-
Jeffrey, P.1
Summerfield, S.2
-
8
-
-
78649706279
-
The effect of plasma protein binding on in vivo efficacy: Misconceptions in drug discovery
-
1:CAS:528:DC%2BC3cXhsV2jurfI 10.1038/nrd3287 21119731
-
Smith DA, Di L, Kerns EH. The effect of plasma protein binding on in vivo efficacy: misconceptions in drug discovery. Nat Rev Drug Discov. 2010;9:929-39.
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 929-939
-
-
Smith, D.A.1
Di, L.2
Kerns, E.H.3
-
9
-
-
70350054854
-
Structure-brain exposure relationships in rat and human using a novel data set of unbound drug concentrations in brain interstitial and cerebrospinal fluids
-
10.1021/jm901036q 19764786 1:CAS:528:DC%2BD1MXhtFCqtbzM
-
Fridén M, Winiwarter S, Jerndal G, Bengtsson O, Wan H, Bredberg U, et al. Structure-brain exposure relationships in rat and human using a novel data set of unbound drug concentrations in brain interstitial and cerebrospinal fluids. J Med Chem. 2009;52:6233-43.
-
(2009)
J Med Chem
, vol.52
, pp. 6233-6243
-
-
Fridén, M.1
Winiwarter, S.2
Jerndal, G.3
Bengtsson, O.4
Wan, H.5
Bredberg, U.6
-
10
-
-
1642579680
-
Development of a computational approach to predict blood-brain barrier permeability
-
1:CAS:528:DC%2BD2cXnsFWqs7k%3D 10.1124/dmd.32.1.132 14709630
-
Liu X, Tu M, Kelly RS, Chen C, Smith BJ. Development of a computational approach to predict blood-brain barrier permeability. Drug Metab Dispos. 2004;32:132-9.
-
(2004)
Drug Metab Dispos
, vol.32
, pp. 132-139
-
-
Liu, X.1
Tu, M.2
Kelly, R.S.3
Chen, C.4
Smith, B.J.5
-
11
-
-
73449088412
-
Physiologically based pharmacokinetics (PBPK)
-
10.1080/10837450902891360 19601719 1:CAS:528:DC%2BD1MXosV2mt7w%3D
-
Espié P, Tytgat D, Sargentini-Maier M-L, Poggesi I, Watelet J-B. Physiologically based pharmacokinetics (PBPK). Drug Metab Rev. 2009;41:391-407.
-
(2009)
Drug Metab Rev
, vol.41
, pp. 391-407
-
-
Espié, P.1
Tytgat, D.2
Sargentini-Maier, M.-L.3
Poggesi, I.4
Watelet, J.-B.5
-
12
-
-
70449529433
-
Structure and function of the blood-brain barrier
-
1:CAS:528:DC%2BD1MXhsVGms73P 10.1016/j.nbd.2009.07.030 19664713
-
Abbott NJ, Patabendige AAK, Dolman DEM, Yusof SR, Begley DJ. Structure and function of the blood-brain barrier. Neurobiol Dis. 2010;37:13-25.
-
(2010)
Neurobiol Dis
, vol.37
, pp. 13-25
-
-
Abbott, N.J.1
Patabendige, A.A.K.2
Dolman, D.E.M.3
Yusof, S.R.4
Begley, D.J.5
-
13
-
-
84866740453
-
Translational CNS medicines research
-
1:CAS:528:DC%2BC38XnslKru7s%3D 10.1016/j.drudis.2012.05.001 22580061
-
Palmer AM, Alavijeh MS. Translational CNS medicines research. Drug Discov Today. 2012;17:1068-78.
-
(2012)
Drug Discov Today
, vol.17
, pp. 1068-1078
-
-
Palmer, A.M.1
Alavijeh, M.S.2
-
14
-
-
84875485383
-
Confounding parameters in preclinical assessment of blood-brain barrier permeation: An overview with emphasis on species differences and effect of disease states
-
10.1021/mp300570z 23256608
-
Deo AK, Theil F-P, Nicolas J-M. Confounding parameters in preclinical assessment of blood-brain barrier permeation: an overview with emphasis on species differences and effect of disease states. Mol Pharm. 2013. doi: 10.1021/mp300570z.
-
(2013)
Mol Pharm
-
-
Deo, A.K.1
Theil, F.-P.2
Nicolas, J.-M.3
-
15
-
-
84880747634
-
Applications of minimal physiologically-based pharmacokinetic models
-
1:CAS:528:DC%2BC38XhvVSktbfN 10.1007/s10928-012-9280-2 23179857
-
Cao Y, Jusko WJ. Applications of minimal physiologically-based pharmacokinetic models. J Pharmacokinet Pharmacodyn. 2012;39:711-23.
-
(2012)
J Pharmacokinet Pharmacodyn
, vol.39
, pp. 711-723
-
-
Cao, Y.1
Jusko, W.J.2
-
16
-
-
33644900716
-
The role of blood-brain barrier studies in the pharmaceutical industry
-
1:CAS:528:DC%2BD28Xht1Oms7o%3D 10.2174/138920006775541525 16472107
-
Reichel A. The role of blood-brain barrier studies in the pharmaceutical industry. Curr Drug Metab. 2006;7:183-203.
-
(2006)
Curr Drug Metab
, vol.7
, pp. 183-203
-
-
Reichel, A.1
-
17
-
-
4744353974
-
Principles and applicability of CSF sampling for the assessment of CNS drug delivery and pharmacodynamics
-
1:CAS:528:DC%2BD2cXnslOhsrg%3D 10.1016/j.addr.2004.07.011 15381336
-
Shen DD, Artru AA, Adkison KK. Principles and applicability of CSF sampling for the assessment of CNS drug delivery and pharmacodynamics. Adv Drug Deliv Rev. 2004;56:1825-57.
-
(2004)
Adv Drug Deliv Rev
, vol.56
, pp. 1825-1857
-
-
Shen, D.D.1
Artru, A.A.2
Adkison, K.K.3
-
18
-
-
0036349375
-
Considerations in the use of cerebrospinal fluid pharmacokinetics to predict brain target concentrations in the clinical setting: Implications of the barriers between blood and brain
-
10.2165/00003088-200241100-00001 12162757
-
De Lange ECM, Danhof M. Considerations in the use of cerebrospinal fluid pharmacokinetics to predict brain target concentrations in the clinical setting: implications of the barriers between blood and brain. Clin Pharmacokinet. 2002;41:691-703.
-
(2002)
Clin Pharmacokinet
, vol.41
, pp. 691-703
-
-
De Lange, E.C.M.1
Danhof, M.2
-
19
-
-
38849136513
-
CSF as a surrogate for assessing CNS exposure: An industrial perspective
-
1:CAS:528:DC%2BD1cXhsFSitbo%3D 10.2174/138920008783331077 18220571
-
Lin JH. CSF as a surrogate for assessing CNS exposure: an industrial perspective. Curr Drug Metab. 2008;9:46-59.
-
(2008)
Curr Drug Metab
, vol.9
, pp. 46-59
-
-
Lin, J.H.1
-
20
-
-
79960159776
-
Preclinical prediction of human brain target site concentrations: Considerations in extrapolating to the clinical setting
-
1:CAS:528:DC%2BC3MXosFehtbY%3D 10.1002/jps.22604 21544824
-
Westerhout J, Danhof M, De Lange ECM. Preclinical prediction of human brain target site concentrations: considerations in extrapolating to the clinical setting. J Pharm Sci. 2011;100:3577-93.
-
(2011)
J Pharm Sci
, vol.100
, pp. 3577-3593
-
-
Westerhout, J.1
Danhof, M.2
De Lange, E.C.M.3
-
21
-
-
33747860858
-
Evaluation of cerebrospinal fluid concentration and plasma free concentration as a surrogate measurement for brain free concentration
-
1:CAS:528:DC%2BD28Xpt1Sksrc%3D 10.1124/dmd.105.008201 16760229
-
Liu X, Smith BJ, Chen C, Callegari E, Becker SL, Chen X, et al. Evaluation of cerebrospinal fluid concentration and plasma free concentration as a surrogate measurement for brain free concentration. Drug Metab Dispos. 2006;34:1443-7.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 1443-1447
-
-
Liu, X.1
Smith, B.J.2
Chen, C.3
Callegari, E.4
Becker, S.L.5
Chen, X.6
-
22
-
-
84878763676
-
Utility of CSF in translational neuroscience
-
10.1007/s10928-013-9301-9
-
De Lange ECM. Utility of CSF in translational neuroscience. J Pharmacokinet Pharmacodyn. 2013. doi: 10.1007/s10928-013-9301-9.
-
(2013)
J Pharmacokinet Pharmacodyn
-
-
De Lange, E.C.M.1
-
23
-
-
81555210969
-
Quantitative evaluation of the impact of active efflux by p-glycoprotein and breast cancer resistance protein at the blood-brain barrier on the predictability of the unbound concentrations of drugs in the brain using cerebrospinal fluid concentration as a
-
1:CAS:528:DC%2BC38XjtVSksbo%3D 10.1124/jpet.111.180398 21934030
-
Kodaira H, Kusuhara H, Fujita T, Ushiki J, Fuse E, Sugiyama Y. Quantitative evaluation of the impact of active efflux by p-glycoprotein and breast cancer resistance protein at the blood-brain barrier on the predictability of the unbound concentrations of drugs in the brain using cerebrospinal fluid concentration as a. J Pharmacol Exp Ther. 2011;339:935-44.
-
(2011)
J Pharmacol Exp Ther
, vol.339
, pp. 935-944
-
-
Kodaira, H.1
Kusuhara, H.2
Fujita, T.3
Ushiki, J.4
Fuse, E.5
Sugiyama, Y.6
-
24
-
-
84863380559
-
Cerebrospinal fluid can be used as a surrogate to assess brain exposures of breast cancer resistance protein and P-glycoprotein substrates
-
1:CAS:528:DC%2BC38XkvVOhsb8%3D 10.1124/dmd.111.043703 22266779
-
Xiao G, Black C, Hetu G, Sands E, Wang J, Caputo R, et al. Cerebrospinal fluid can be used as a surrogate to assess brain exposures of breast cancer resistance protein and P-glycoprotein substrates. Drug Metab Dispos. 2012;40:779-87.
-
(2012)
Drug Metab Dispos
, vol.40
, pp. 779-787
-
-
Xiao, G.1
Black, C.2
Hetu, G.3
Sands, E.4
Wang, J.5
Caputo, R.6
-
25
-
-
67649392513
-
A framework for assessing inter-individual variability in pharmacokinetics using virtual human populations and integrating general knowledge of physical chemistry, biology, anatomy, physiology and genetics: A tale of "bottom-up" vs "top-down" recognition
-
1:CAS:528:DC%2BD1MXks1Whu7o%3D 10.2133/dmpk.24.53 19252336
-
Jamei M, Dickinson GL, Rostami-Hodjegan A. A framework for assessing inter-individual variability in pharmacokinetics using virtual human populations and integrating general knowledge of physical chemistry, biology, anatomy, physiology and genetics: a tale of "bottom-up" vs "top-down" recognition. Drug Metab Pharmacokinet. 2009;24:53-75.
-
(2009)
Drug Metab Pharmacokinet
, vol.24
, pp. 53-75
-
-
Jamei, M.1
Dickinson, G.L.2
Rostami-Hodjegan, A.3
-
26
-
-
0019783061
-
Methods for quantifying the transport of drugs across brain barrier systems
-
1:CAS:528:DyaL38XksFKrtw%3D%3D 10.1016/0163-7258(81)90062-0 7031708
-
Fenstermacher JD, Blasberg RG, Patlak CS. Methods for quantifying the transport of drugs across brain barrier systems. Pharmacol Ther. 1981;14:217-48.
-
(1981)
Pharmacol Ther
, vol.14
, pp. 217-248
-
-
Fenstermacher, J.D.1
Blasberg, R.G.2
Patlak, C.S.3
-
27
-
-
0017704173
-
Distribution of methotrexate in the cerebrospinal fluid and brain after intraventricular administration
-
1:CAS:528:DyaE2sXltFWhs70%3D 406996
-
Blasberg RG, Patlak CS, Shapiro WR. Distribution of methotrexate in the cerebrospinal fluid and brain after intraventricular administration. Cancer Treat Rep. 1977;61:633-41.
-
(1977)
Cancer Treat Rep
, vol.61
, pp. 633-641
-
-
Blasberg, R.G.1
Patlak, C.S.2
Shapiro, W.R.3
-
28
-
-
0018237164
-
Lower limits of cerebrovascular permeability to nonelectrolytes in the conscious rat
-
1:CAS:528:DyaE1cXmtFals7s%3D 696840
-
Ohno K, Pettigrew KD, Rapoport SI. Lower limits of cerebrovascular permeability to nonelectrolytes in the conscious rat. Am J Physiol. 1978;235:H299-307.
-
(1978)
Am J Physiol
, vol.235
, pp. 299-307
-
-
Ohno, K.1
Pettigrew, K.D.2
Rapoport, S.I.3
-
29
-
-
0018398457
-
Drug entry into the brain
-
1:CAS:528:DyaE1MXls1yitb4%3D 10.1016/0006-8993(79)90546-8 466480
-
Rapoport SI, Ohno K, Pettigrew KD. Drug entry into the brain. Brain Res. 1979;172:354-9.
-
(1979)
Brain Res
, vol.172
, pp. 354-359
-
-
Rapoport, S.I.1
Ohno, K.2
Pettigrew, K.D.3
-
30
-
-
0020826160
-
Distributed model for drug delivery to CSF and brain tissue
-
1:CAS:528:DyaL3sXlsFWksrY%3D 6614201
-
Collins JM, Dedrick RL. Distributed model for drug delivery to CSF and brain tissue. Am J Physiol. 1983;245:R303-10.
-
(1983)
Am J Physiol
, vol.245
, pp. 303-310
-
-
Collins, J.M.1
Dedrick, R.L.2
-
31
-
-
84995367368
-
Application of in vivo brain microdialysis to the study of blood-brain barrier transport of drugs
-
1:CAS:528:DC%2BD3sXhtFanuro%3D 10.2133/dmpk.17.395 15618691
-
Deguchi Y. Application of in vivo brain microdialysis to the study of blood-brain barrier transport of drugs. Drug Metab Pharmacokinet. 2002;17:395-407.
-
(2002)
Drug Metab Pharmacokinet
, vol.17
, pp. 395-407
-
-
Deguchi, Y.1
-
32
-
-
0030898087
-
Drug equilibration across the blood-brain barrier-pharmacokinetic considerations based on the microdialysis method
-
1:CAS:528:DyaK2sXitFyrsbc%3D 10.1023/A:1012080106490 9090698
-
Hammarlund-Udenaes M, Paalzow LK, De Lange EC. Drug equilibration across the blood-brain barrier-pharmacokinetic considerations based on the microdialysis method. Pharm Res. 1997;14:128-34.
-
(1997)
Pharm Res
, vol.14
, pp. 128-134
-
-
Hammarlund-Udenaes, M.1
Paalzow, L.K.2
De Lange, E.C.3
-
33
-
-
0029876793
-
The simultaneous estimation of the influx and efflux blood-brain barrier permeabilities of gabapentin using a microdialysis-pharmacokinetic approach
-
1:CAS:528:DyaK28XhvVOiurY%3D 10.1023/A:1016092525901 8692732
-
Wang Y, Welty DF. The simultaneous estimation of the influx and efflux blood-brain barrier permeabilities of gabapentin using a microdialysis- pharmacokinetic approach. Pharm Res. 1996;13:398-403.
-
(1996)
Pharm Res
, vol.13
, pp. 398-403
-
-
Wang, Y.1
Welty, D.F.2
-
34
-
-
0029013672
-
Zidovudine transport in the rabbit brain during intravenous and intracerebroventricular infusion
-
1:CAS:528:DyaK2MXmt12lur0%3D 10.1002/jps.2600840717 7562440
-
Wang Y, Sawchuk RJ. Zidovudine transport in the rabbit brain during intravenous and intracerebroventricular infusion. J Pharm Sci. 1995;84:871-6.
-
(1995)
J Pharm Sci
, vol.84
, pp. 871-876
-
-
Wang, Y.1
Sawchuk, R.J.2
-
35
-
-
0031473836
-
Zidovudine transport within the rabbit brain during intracerebroventricular administration and the effect of probenecid
-
1:CAS:528:DyaK2sXnt1Ohtr0%3D 10.1021/js950330v 9423165
-
Wang Y, Wei Y, Sawchuk RJ. Zidovudine transport within the rabbit brain during intracerebroventricular administration and the effect of probenecid. J Pharm Sci. 1997;86:1484-90.
-
(1997)
J Pharm Sci
, vol.86
, pp. 1484-1490
-
-
Wang, Y.1
Wei, Y.2
Sawchuk, R.J.3
-
36
-
-
0343554785
-
Role of efflux transport across the blood-brain barrier and blood-cerebrospinal fluid barrier on the disposition of xenobiotics in the central nervous system
-
1:CAS:528:DyaK2sXjsVKht7g%3D 10.1016/S0169-409X(97)00503-6
-
Suzuki H, Terasaki T, Sugiyama Y. Role of efflux transport across the blood-brain barrier and blood-cerebrospinal fluid barrier on the disposition of xenobiotics in the central nervous system. Adv Drug Deliv Rev. 1997;25:257-85.
-
(1997)
Adv Drug Deliv Rev
, vol.25
, pp. 257-285
-
-
Suzuki, H.1
Terasaki, T.2
Sugiyama, Y.3
-
37
-
-
11144243288
-
An integrated model for the analysis of pharmacokinetic data from microdialysis experiments
-
1:CAS:528:DC%2BD2cXnsFOquro%3D 10.1023/B:PHAM.0000041468.00587.c6 15497699
-
Tunblad K, Hammarlund-Udenaes M, Jonsson EN. An integrated model for the analysis of pharmacokinetic data from microdialysis experiments. Pharm Res. 2004;21:1698-707.
-
(2004)
Pharm Res
, vol.21
, pp. 1698-1707
-
-
Tunblad, K.1
Hammarlund-Udenaes, M.2
Jonsson, E.N.3
-
38
-
-
33644812284
-
Toward the prediction of CNS drug-effect profiles in physiological and pathological conditions using microdialysis and mechanism-based pharmacokinetic-pharmacodynamic modeling
-
10.1208/aapsj070354 16353931 1:CAS:528:DC%2BD2MXhtlSrtbbP
-
De Lange ECM, Ravenstijn PGM, Groenendaal D, Van Steeg TJ. Toward the prediction of CNS drug-effect profiles in physiological and pathological conditions using microdialysis and mechanism-based pharmacokinetic- pharmacodynamic modeling. AAPS J. 2005;7:E532-43.
-
(2005)
AAPS J
, vol.7
, pp. 532-543
-
-
De Lange, E.C.M.1
Ravenstijn, P.G.M.2
Groenendaal, D.3
Van Steeg, T.J.4
-
39
-
-
0034293553
-
Pharmacokinetic-pharmacodynamic modelling of morphine transport across the blood-brain barrier as a cause of the antinociceptive effect delay in rats-A microdialysis study
-
1:CAS:528:DC%2BD3MXit1Wk 10.1023/A:1026414713509 11145227
-
Bouw MR, Gårdmark M, Hammarlund-Udenaes M. Pharmacokinetic- pharmacodynamic modelling of morphine transport across the blood-brain barrier as a cause of the antinociceptive effect delay in rats-A microdialysis study. Pharm Res. 2000;17:1220-7.
-
(2000)
Pharm Res
, vol.17
, pp. 1220-1227
-
-
Bouw, M.R.1
Gårdmark, M.2
Hammarlund-Udenaes, M.3
-
40
-
-
0034527760
-
Modelling of the blood-brain barrier transport of morphine-3-glucuronide studied using microdialysis in the rat: Involvement of probenecid-sensitive transport
-
1:CAS:528:DC%2BD3MXjtVGrsw%3D%3D 10.1038/sj.bjp.0703759 11139459
-
Xie R, Bouw MR, Hammarlund-Udenaes M. Modelling of the blood-brain barrier transport of morphine-3-glucuronide studied using microdialysis in the rat: involvement of probenecid-sensitive transport. Br J Pharmacol. 2000;131:1784-92.
-
(2000)
Br J Pharmacol
, vol.131
, pp. 1784-1792
-
-
Xie, R.1
Bouw, M.R.2
Hammarlund-Udenaes, M.3
-
41
-
-
0035679267
-
Blood-brain barrier transport and brain distribution of morphine-6-glucuronide in relation to the antinociceptive effect in rats-pharmacokinetic/pharmacodynamic modelling
-
1:CAS:528:DC%2BD38XkvFSj 10.1038/sj.bjp.0704406 11739257
-
Bouw MR, Xie R, Tunblad K, Hammarlund-Udenaes M. Blood-brain barrier transport and brain distribution of morphine-6-glucuronide in relation to the antinociceptive effect in rats-pharmacokinetic/pharmacodynamic modelling. Br J Pharmacol. 2001;134:1796-804.
-
(2001)
Br J Pharmacol
, vol.134
, pp. 1796-1804
-
-
Bouw, M.R.1
Xie, R.2
Tunblad, K.3
Hammarlund-Udenaes, M.4
-
42
-
-
33747816123
-
In vivo blood-brain barrier transport of oxycodone in the rat: Indications for active influx and implications for pharmacokinetics/ pharmacodynamics
-
10.1124/dmd.106.009746 16763013 1:CAS:528:DC%2BD28Xpt1Sksb4%3D
-
Boström E, Simonsson USH, Hammarlund-Udenaes M. In vivo blood-brain barrier transport of oxycodone in the rat: indications for active influx and implications for pharmacokinetics/pharmacodynamics. Drug Metab Dispos. 2006;34:1624-31.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 1624-1631
-
-
Boström, E.1
Simonsson, U.S.H.2
Hammarlund-Udenaes, M.3
-
43
-
-
39749132196
-
Blood-brain barrier transport helps to explain discrepancies in in vivo potency between oxycodone and morphine
-
10.1097/ALN.0b013e318164cf9e 18292687 1:CAS:528:DC%2BD1cXit1Okur8%3D
-
Boström E, Hammarlund-Udenaes M, Simonsson USH. Blood-brain barrier transport helps to explain discrepancies in in vivo potency between oxycodone and morphine. Anesthesiology. 2008;108:495-505.
-
(2008)
Anesthesiology
, vol.108
, pp. 495-505
-
-
Boström, E.1
Hammarlund-Udenaes, M.2
Simonsson, U.S.H.3
-
44
-
-
84866452633
-
Microdialysis evaluation of clozapine and N-desmethylclozapine pharmacokinetics in rat brain
-
1:CAS:528:DC%2BC38XhsFSmsbvI 10.1124/dmd.112.045682 22736307
-
Cremers TIFH, Flik G, Hofland C, Stratford RE. Microdialysis evaluation of clozapine and N-desmethylclozapine pharmacokinetics in rat brain. Drug Metab Dispos. 2012;40:1909-16.
-
(2012)
Drug Metab Dispos
, vol.40
, pp. 1909-1916
-
-
Cremers, T.1
Flik, G.2
Hofland, C.3
Stratford, R.E.4
-
45
-
-
45949107902
-
On the rate and extent of drug delivery to the brain
-
1:CAS:528:DC%2BD1cXot1Whsb8%3D 10.1007/s11095-007-9502-2 18058202
-
Hammarlund-Udenaes M, Fridén M, Syvänen S, Gupta A. On the rate and extent of drug delivery to the brain. Pharm Res. 2008;25:1737-50.
-
(2008)
Pharm Res
, vol.25
, pp. 1737-1750
-
-
Hammarlund-Udenaes, M.1
Fridén, M.2
Syvänen, S.3
Gupta, A.4
-
46
-
-
43349096961
-
Pharmacokinetic modeling of non-linear brain distribution of fluvoxamine in the rat
-
1:CAS:528:DC%2BD1cXkt1Snsbw%3D 10.1007/s11095-007-9390-5 17710515
-
Geldof M, Freijer J, Van Beijsterveldt L, Danhof M. Pharmacokinetic modeling of non-linear brain distribution of fluvoxamine in the rat. Pharm Res. 2008;25:792-804.
-
(2008)
Pharm Res
, vol.25
, pp. 792-804
-
-
Geldof, M.1
Freijer, J.2
Van Beijsterveldt, L.3
Danhof, M.4
-
47
-
-
84857630809
-
Alteration in P-glycoprotein functionality affects intrabrain distribution of quinidine more than brain entry-A study in rats subjected to status epilepticus by kainate
-
10.1208/s12248-011-9318-1 22215264 1:CAS:528:DC%2BC38XjtVGhur8%3D
-
Syvänen S, Schenke M, Van den Berg D-J, Voskuyl RA, De Lange EC. Alteration in P-glycoprotein functionality affects intrabrain distribution of quinidine more than brain entry-A study in rats subjected to status epilepticus by kainate. AAPS J. 2012;14:87-96.
-
(2012)
AAPS J
, vol.14
, pp. 87-96
-
-
Syvänen, S.1
Schenke, M.2
Van Den Berg, D.-J.3
Voskuyl, R.A.4
De Lange, E.C.5
-
48
-
-
0030799004
-
Kinetic evidence for active efflux transport across the blood-brain barrier of quinolone antibiotics
-
1:CAS:528:DyaK2sXmslCltbw%3D 9336336
-
Ooie T, Terasaki T, Suzuki H, Sugiyama Y. Kinetic evidence for active efflux transport across the blood-brain barrier of quinolone antibiotics. J Pharmacol Exp Ther. 1997;283:293-304.
-
(1997)
J Pharmacol Exp Ther
, vol.283
, pp. 293-304
-
-
Ooie, T.1
Terasaki, T.2
Suzuki, H.3
Sugiyama, Y.4
-
49
-
-
0030954863
-
Distributed model analysis of 3′-azido-3′-deoxythymidine and 2′,3′-dideoxyinosine distribution in brain tissue and cerebrospinal fluid
-
1:CAS:528:DyaK2sXmsVGlur0%3D 9316866
-
Takasawa K, Terasaki T, Suzuki H, Ooie T, Sugiyama Y. Distributed model analysis of 3′-azido-3′-deoxythymidine and 2′,3′- dideoxyinosine distribution in brain tissue and cerebrospinal fluid. J Pharmacol Exp Ther. 1997;282:1509-17.
-
(1997)
J Pharmacol Exp Ther
, vol.282
, pp. 1509-1517
-
-
Takasawa, K.1
Terasaki, T.2
Suzuki, H.3
Ooie, T.4
Sugiyama, Y.5
-
50
-
-
0036498117
-
Comparison of in vitro BBMEC permeability and in vivo CNS uptake by microdialysis sampling
-
1:CAS:528:DC%2BD38XhtVKktrg%3D 10.1016/S0731-7085(01)00542-8 11836058
-
Hansen DK, Scott DO, Otis KW, Lunte SM. Comparison of in vitro BBMEC permeability and in vivo CNS uptake by microdialysis sampling. J Pharm Biomed Anal. 2002;27:945-58.
-
(2002)
J Pharm Biomed Anal
, vol.27
, pp. 945-958
-
-
Hansen, D.K.1
Scott, D.O.2
Otis, K.W.3
Lunte, S.M.4
-
51
-
-
22944452799
-
Neuropharmacokinetics of a new alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) modulator, S18986 [(S)-2,3-dihydro-[3,4]cyclopentano-1,2, 4-benzothiadiazine-1,1-dioxide], in the rat
-
1:CAS:528:DC%2BD2MXntVamsL4%3D 10.1124/dmd.105.004424 15860654
-
Bourasset F, Bernard K, Muñoz C, Genissel P, Scherrmann J. Neuropharmacokinetics of a new alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) modulator, S18986 [(S)-2,3-dihydro-[3,4]cyclopentano-1,2, 4-benzothiadiazine-1,1-dioxide], in the rat. Drug Metab Dispos. 2005;33:1137-43.
-
(2005)
Drug Metab Dispos
, vol.33
, pp. 1137-1143
-
-
Bourasset, F.1
Bernard, K.2
Muñoz, C.3
Genissel, P.4
Scherrmann, J.5
-
52
-
-
33645391312
-
Carrier-mediated processes at several rat brain interfaces determine the neuropharmacokinetics of morphine and morphine-6-beta-D-glucuronide
-
1:CAS:528:DC%2BD28XjtFamsr4%3D 10.1016/j.lfs.2005.09.043 16309712
-
Bourasset F, Scherrmann J-M. Carrier-mediated processes at several rat brain interfaces determine the neuropharmacokinetics of morphine and morphine-6-beta-D-glucuronide. Life Sci. 2006;78:2302-14.
-
(2006)
Life Sci
, vol.78
, pp. 2302-2314
-
-
Bourasset, F.1
Scherrmann, J.-M.2
-
53
-
-
34248680469
-
Physiologically based pharmacokinetics in drug development and regulatory science: A workshop report (Georgetown University, Washington, DC, May 29-30, 2002)
-
18465258
-
Rowland M, Balant L, Peck C. Physiologically based pharmacokinetics in drug development and regulatory science: a workshop report (Georgetown University, Washington, DC, May 29-30, 2002). AAPS J. 2004;6:56-67.
-
(2004)
AAPS J
, vol.6
, pp. 56-67
-
-
Rowland, M.1
Balant, L.2
Peck, C.3
-
54
-
-
79951765993
-
Physiologically-based pharmacokinetics in drug development and regulatory science
-
1:CAS:528:DC%2BC3MXisFOjurw%3D 10.1146/annurev-pharmtox-010510-100540 20854171
-
Rowland M, Peck C, Tucker G. Physiologically-based pharmacokinetics in drug development and regulatory science. Annu Rev Pharmacol Toxicol. 2011;51:45-73.
-
(2011)
Annu Rev Pharmacol Toxicol
, vol.51
, pp. 45-73
-
-
Rowland, M.1
Peck, C.2
Tucker, G.3
-
55
-
-
78951482203
-
Applications of physiologically based pharmacokinetic (PBPK) modeling and simulation during regulatory review
-
1:STN:280:DC%2BC3M7ivFKisw%3D%3D 10.1038/clpt.2010.298 21191381
-
Zhao P, Zhang L, Grillo JA, Liu Q, Bullock JM, Moon YJ, et al. Applications of physiologically based pharmacokinetic (PBPK) modeling and simulation during regulatory review. Clin Pharmacol Ther. 2011;89:259-67.
-
(2011)
Clin Pharmacol Ther
, vol.89
, pp. 259-267
-
-
Zhao, P.1
Zhang, L.2
Grillo, J.A.3
Liu, Q.4
Bullock, J.M.5
Moon, Y.J.6
-
56
-
-
84858699365
-
Physiologically based pharmacokinetic (PBPK) modelling tools: How to fit with our needs?
-
1:CAS:528:DC%2BC38Xht1ynsL0%3D 10.1002/bdd.1767 22228149
-
Bouzom F, Ball K, Perdaems N, Walther B. Physiologically based pharmacokinetic (PBPK) modelling tools: how to fit with our needs? Biopharm Drug Dispos. 2012;33:55-71.
-
(2012)
Biopharm Drug Dispos
, vol.33
, pp. 55-71
-
-
Bouzom, F.1
Ball, K.2
Perdaems, N.3
Walther, B.4
-
57
-
-
21144451475
-
Use of a physiologically based pharmacokinetic model to study the time to reach brain equilibrium: An experimental analysis of the role of blood-brain barrier permeability, plasma protein binding, and brain tissue binding
-
1:CAS:528:DC%2BD2MXkslektbs%3D 10.1124/jpet.104.079319 15743928
-
Liu X, Smith BJ, Chen C, Callegari E, Becker SL, Chen X, et al. Use of a physiologically based pharmacokinetic model to study the time to reach brain equilibrium: an experimental analysis of the role of blood-brain barrier permeability, plasma protein binding, and brain tissue binding. J Pharmacol Exp Ther. 2005;313:1254-62.
-
(2005)
J Pharmacol Exp Ther
, vol.313
, pp. 1254-1262
-
-
Liu, X.1
Smith, B.J.2
Chen, C.3
Callegari, E.4
Becker, S.L.5
Chen, X.6
-
58
-
-
84859907548
-
Exploratory translational modeling approach in drug development to predict human brain pharmacokinetics and pharmacologically relevant clinical doses
-
1:CAS:528:DC%2BC38Xmt1Kgu7o%3D 10.1124/dmd.111.043554 22287668
-
Kielbasa W, Stratford RE. Exploratory translational modeling approach in drug development to predict human brain pharmacokinetics and pharmacologically relevant clinical doses. Drug Metab Dispos. 2012;40:877-83.
-
(2012)
Drug Metab Dispos
, vol.40
, pp. 877-883
-
-
Kielbasa, W.1
Stratford, R.E.2
-
59
-
-
58149467009
-
Microdialysis evaluation of atomoxetine brain penetration and central nervous system pharmacokinetics in rats
-
1:CAS:528:DC%2BD1MXhsVSlsA%3D%3D 10.1124/dmd.108.023119 18936112
-
Kielbasa W, Kalvass JC, Stratford R. Microdialysis evaluation of atomoxetine brain penetration and central nervous system pharmacokinetics in rats. Drug Metab Dispos. 2009;37:137-42.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 137-142
-
-
Kielbasa, W.1
Kalvass, J.C.2
Stratford, R.3
-
60
-
-
84862768064
-
Physiologically based pharmacokinetic modeling to investigate regional brain distribution kinetics in rats
-
1:CAS:528:DC%2BC38XptFWit7w%3D 10.1208/s12248-012-9366-1 22588644
-
Westerhout J, Ploeger B, Smeets J, Danhof M, De Lange ECM. Physiologically based pharmacokinetic modeling to investigate regional brain distribution kinetics in rats. AAPS J. 2012;14:543-53.
-
(2012)
AAPS J
, vol.14
, pp. 543-553
-
-
Westerhout, J.1
Ploeger, B.2
Smeets, J.3
Danhof, M.4
De Lange, E.C.M.5
-
61
-
-
63349101281
-
Assessing drug distribution in tissues expressing P-glycoprotein through physiologically based pharmacokinetic modeling: Model structure and parameters determination
-
10.1186/1742-4682-6-2 19146691 1:CAS:528:DC%2BD1MXhvVWhtbk%3D
-
Fenneteau F, Turgeon J, Couture L, Michaud V, Li J, Nekka F. Assessing drug distribution in tissues expressing P-glycoprotein through physiologically based pharmacokinetic modeling: model structure and parameters determination. Theor Biol Med Model. 2009;6:2.
-
(2009)
Theor Biol Med Model
, vol.6
, pp. 2
-
-
Fenneteau, F.1
Turgeon, J.2
Couture, L.3
Michaud, V.4
Li, J.5
Nekka, F.6
-
62
-
-
3543025187
-
Predicting P-glycoprotein effects on oral absorption: Correlation of transport in caco-2 with drug pharmacokinetics in wild-type and mdr1a(-/-) mice in vivo
-
1:CAS:528:DC%2BD2cXjs1Kju7o%3D 10.1023/B:PHAM.0000026434.82855.69 15180340
-
Collett A, Tanianis-Hughes J, Hallifax D, Warhurst G. Predicting P-glycoprotein effects on oral absorption: correlation of transport in caco-2 with drug pharmacokinetics in wild-type and mdr1a(-/-) mice in vivo. Pharm Res. 2004;21:819-26.
-
(2004)
Pharm Res
, vol.21
, pp. 819-826
-
-
Collett, A.1
Tanianis-Hughes, J.2
Hallifax, D.3
Warhurst, G.4
-
63
-
-
0025329190
-
Comparison of in vitro and in vivo models of drug transcytosis through the blood-brain barrier
-
1:CAS:528:DyaK3cXktFOnsr8%3D 2338660
-
Pardridge WM, Triguero D, Yang J, Cancilla PA. Comparison of in vitro and in vivo models of drug transcytosis through the blood-brain barrier. J Pharmacol Exp Ther. 1990;253:884-91.
-
(1990)
J Pharmacol Exp Ther
, vol.253
, pp. 884-891
-
-
Pardridge, W.M.1
Triguero, D.2
Yang, J.3
Cancilla, P.A.4
-
64
-
-
72349089667
-
Assessing drug distribution in tissues expressing P-glycoprotein using physiologically based pharmacokinetic modeling: Identification of important model parameters through global sensitivity analysis
-
1:CAS:528:DC%2BD1MXhsV2jt7zF 10.1007/s10928-009-9134-8 19847628
-
Fenneteau F, Li J, Nekka F. Assessing drug distribution in tissues expressing P-glycoprotein using physiologically based pharmacokinetic modeling: identification of important model parameters through global sensitivity analysis. J Pharmacokinet Pharmacodyn. 2009;36:495-522.
-
(2009)
J Pharmacokinet Pharmacodyn
, vol.36
, pp. 495-522
-
-
Fenneteau, F.1
Li, J.2
Nekka, F.3
-
65
-
-
0031412578
-
Physiologically based pharmacokinetic modeling of a homologous series of barbiturates in the rat: A sensitivity analysis
-
1:CAS:528:DyaK1cXis1OjsLk%3D 10.1023/A:1025740909016 9561487
-
Nestorov IA, Aarons LJ, Rowland M. Physiologically based pharmacokinetic modeling of a homologous series of barbiturates in the rat: a sensitivity analysis. J Pharmacokinet Biopharm. 1997;25:413-47.
-
(1997)
J Pharmacokinet Biopharm
, vol.25
, pp. 413-447
-
-
Nestorov, I.A.1
Aarons, L.J.2
Rowland, M.3
-
66
-
-
84866354603
-
Development of a physiologically based pharmacokinetic model for the rat central nervous system and determination of an in vitro-in vivo scaling methodology for the blood-brain barrier permeability of two transporter substrates, morphine and oxycodone
-
1:CAS:528:DC%2BC38XhtFahtr3J 10.1002/jps.23266 22864977
-
Ball K, Bouzom F, Scherrmann J, Walther B, Declèves X. Development of a physiologically based pharmacokinetic model for the rat central nervous system and determination of an in vitro-in vivo scaling methodology for the blood-brain barrier permeability of two transporter substrates, morphine and oxycodone. J Pharm Sci. 2012;101:4277-92.
-
(2012)
J Pharm Sci
, vol.101
, pp. 4277-4292
-
-
Ball, K.1
Bouzom, F.2
Scherrmann, J.3
Walther, B.4
Declèves, X.5
-
67
-
-
84862619047
-
Physiologically based pharmacokinetics joined with in vitro-in vivo extrapolation of ADME: A marriage under the arch of systems pharmacology
-
1:CAS:528:DC%2BC38XptVGmtbo%3D 10.1038/clpt.2012.65 22644330
-
Rostami-Hodjegan A. Physiologically based pharmacokinetics joined with in vitro-in vivo extrapolation of ADME: a marriage under the arch of systems pharmacology. Clin Pharmacol Ther. 2012;92:50-61.
-
(2012)
Clin Pharmacol Ther
, vol.92
, pp. 50-61
-
-
Rostami-Hodjegan, A.1
-
68
-
-
0036805724
-
Comparison of human duodenum and Caco-2 gene expression profiles for 12,000 gene sequences tags and correlation with permeability of 26 drugs
-
1:CAS:528:DC%2BD38XnsFSgsLg%3D 10.1023/A:1020483911355 12425456
-
Sun D, Lennernas H, Welage LS, Barnett JL, Landowski CP, Foster D, et al. Comparison of human duodenum and Caco-2 gene expression profiles for 12,000 gene sequences tags and correlation with permeability of 26 drugs. Pharm Res. 2002;19:1400-16.
-
(2002)
Pharm Res
, vol.19
, pp. 1400-1416
-
-
Sun, D.1
Lennernas, H.2
Welage, L.S.3
Barnett, J.L.4
Landowski, C.P.5
Foster, D.6
-
69
-
-
84865191410
-
Use of mechanistic modeling to assess interindividual variability and interspecies differences in active uptake in human and rat hepatocytes
-
10.1124/dmd.112.046193 22665271 1:CAS:528:DC%2BC38XhtlShtbnI
-
Ménochet K, Kenworthy KE, Houston JB, Galetin A. Use of mechanistic modeling to assess interindividual variability and interspecies differences in active uptake in human and rat hepatocytes. Drug Metab Dispos. 2012;40:1744-56.
-
(2012)
Drug Metab Dispos
, vol.40
, pp. 1744-1756
-
-
Ménochet, K.1
Kenworthy, K.E.2
Houston, J.B.3
Galetin, A.4
-
70
-
-
84871294584
-
Why we need proper PBPK models to examine intestine and liver oral drug absorption
-
1:CAS:528:DC%2BC3sXjvFOmur0%3D 10.2174/138920013804545124 22935069
-
Chow ECY, Pang KS. Why we need proper PBPK models to examine intestine and liver oral drug absorption. Curr Drug Metab. 2013;14:57-79.
-
(2013)
Curr Drug Metab
, vol.14
, pp. 57-79
-
-
Chow, E.C.Y.1
Pang, K.S.2
-
71
-
-
0141923651
-
New approaches to in vitro models of blood-brain barrier drug transport
-
1:CAS:528:DC%2BD3sXnvFSiu7s%3D 10.1016/S1359-6446(03)02858-7 14554158
-
Terasaki T, Ohtsuki S, Hori S, Takanaga H, Nakashima E, Hosoya K. New approaches to in vitro models of blood-brain barrier drug transport. Drug Discov Today. 2003;8:944-54.
-
(2003)
Drug Discov Today
, vol.8
, pp. 944-954
-
-
Terasaki, T.1
Ohtsuki, S.2
Hori, S.3
Takanaga, H.4
Nakashima, E.5
Hosoya, K.6
-
72
-
-
84858826144
-
Efflux transporters in the blood-brain interfaces - In vitro and in vivo methods and correlations
-
1:CAS:528:DC%2BC38XksVOrsL0%3D 10.1517/17425255.2012.668184 22394316
-
Krajcsi P, Jani M, Tóth B, Erdo F, Kis E, Beéry E, et al. Efflux transporters in the blood-brain interfaces - in vitro and in vivo methods and correlations. Expert Opin Drug Metab Toxicol. 2012;8:419-31.
-
(2012)
Expert Opin Drug Metab Toxicol
, vol.8
, pp. 419-431
-
-
Krajcsi, P.1
Jani, M.2
Tóth, B.3
Erdo, F.4
Kis, E.5
Beéry, E.6
-
73
-
-
33751100685
-
Porcine brain microvessel endothelial cells as an in vitro model to predict in vivo blood-brain barrier permeability
-
1:CAS:528:DC%2BD28XhtFGqt7nE 10.1124/dmd.105.006437 16896068
-
Zhang Y, Li CSW, Ye Y, Johnson K, Poe J, Johnson S, et al. Porcine brain microvessel endothelial cells as an in vitro model to predict in vivo blood-brain barrier permeability. Drug Metab Dispos. 2006;34:1935-43.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 1935-1943
-
-
Zhang, Y.1
Li, C.S.W.2
Ye, Y.3
Johnson, K.4
Poe, J.5
Johnson, S.6
-
74
-
-
34248173562
-
A functional in vitro model of rat blood-brain barrier for molecular analysis of efflux transporters
-
10.1016/j.brainres.2007.02.091 17434463 1:CAS:528:DC%2BD2sXlt1Cjsb0%3D
-
Perrière N, Yousif S, Cazaubon S, Chaverot N, Bourasset F, Cisternino S, et al. A functional in vitro model of rat blood-brain barrier for molecular analysis of efflux transporters. Brain Res. 2007;1150:1-13.
-
(2007)
Brain Res
, vol.1150
, pp. 1-13
-
-
Perrière, N.1
Yousif, S.2
Cazaubon, S.3
Chaverot, N.4
Bourasset, F.5
Cisternino, S.6
-
75
-
-
34547645047
-
Modelling of the blood-brain barrier in drug discovery and development
-
1:CAS:528:DC%2BD2sXotl2qtLc%3D 10.1038/nrd2368 17667956
-
Cecchelli R, Berezowski V, Lundquist S, Culot M, Renftel M, Dehouck M-P, et al. Modelling of the blood-brain barrier in drug discovery and development. Nat Rev Drug Discov. 2007;6:650-61.
-
(2007)
Nat Rev Drug Discov
, vol.6
, pp. 650-661
-
-
Cecchelli, R.1
Berezowski, V.2
Lundquist, S.3
Culot, M.4
Renftel, M.5
Dehouck, M.-P.6
-
76
-
-
55849128943
-
The human brain endothelial cell line hCMEC/D3 as a human blood-brain barrier model for drug transport studies
-
1:CAS:528:DC%2BD1cXhsV2mtbvJ 10.1111/j.1471-4159.2008.05730.x 19013850
-
Poller B, Gutmann H, Krähenbühl S, Weksler B, Romero I, Couraud P-O, et al. The human brain endothelial cell line hCMEC/D3 as a human blood-brain barrier model for drug transport studies. J Neurochem. 2008;107:1358-68.
-
(2008)
J Neurochem
, vol.107
, pp. 1358-1368
-
-
Poller, B.1
Gutmann, H.2
Krähenbühl, S.3
Weksler, B.4
Romero, I.5
Couraud, P.-O.6
-
77
-
-
78650678061
-
Murine in vitro model of the blood-brain barrier for evaluating drug transport
-
1:CAS:528:DC%2BC3cXhs1agtLnO 10.1016/j.ejps.2010.11.005 21078386
-
Shayan G, Choi YS, Shusta EV, Shuler ML, Lee KH. Murine in vitro model of the blood-brain barrier for evaluating drug transport. Eur J Pharm Sci. 2011;42:148-55.
-
(2011)
Eur J Pharm Sci
, vol.42
, pp. 148-155
-
-
Shayan, G.1
Choi, Y.S.2
Shusta, E.V.3
Shuler, M.L.4
Lee, K.H.5
-
78
-
-
84871343030
-
Hurdles with using in vitro models to predict human blood-brain barrier drug permeability: A special focus on transporters and metabolizing enzymes
-
1:CAS:528:DC%2BC3sXjvFOmurY%3D 10.2174/138920013804545232 23215812
-
Shawahna R, Decleves X, Scherrmann J-M. Hurdles with using In vitro models to predict human blood-brain barrier drug permeability: a special focus on transporters and metabolizing enzymes. Curr Drug Metab. 2013;14:120-36.
-
(2013)
Curr Drug Metab
, vol.14
, pp. 120-136
-
-
Shawahna, R.1
Decleves, X.2
Scherrmann, J.-M.3
-
79
-
-
79960279229
-
Development of a three-dimensional, all-human in vitro model of the blood-brain barrier using mono-, co-, and tri-cultivation transwell models
-
10.1016/j.jneumeth.2011.05.012 21609734
-
Hatherell K, Couraud P-O, Romero IA, Weksler B, Pilkington GJ. Development of a three-dimensional, all-human in vitro model of the blood-brain barrier using mono-, co-, and tri-cultivation transwell models. J Neurosci Methods. 2011;199:223-9.
-
(2011)
J Neurosci Methods
, vol.199
, pp. 223-229
-
-
Hatherell, K.1
Couraud, P.-O.2
Romero, I.A.3
Weksler, B.4
Pilkington, G.J.5
-
80
-
-
79952599989
-
In vitro models of the blood-cerebrospinal fluid barrier and their use in neurotoxicological research
-
1:CAS:528:DC%2BC3MXmtFansLg%3D 10.1007/978-1-61779-077-5-8
-
Strazielle N, Ghersi-Egea J-F. In vitro models of the blood-cerebrospinal fluid barrier and their use in neurotoxicological research. Neuromethods. 2011;56:161-84.
-
(2011)
Neuromethods
, vol.56
, pp. 161-184
-
-
Strazielle, N.1
Ghersi-Egea, J.-F.2
-
81
-
-
84962359573
-
High throughput artificial membrane permeability assay for blood-brain barrier
-
1:CAS:528:DC%2BD3sXitlKju7c%3D 10.1016/S0223-5234(03)00012-6 12667689
-
Di L, Kerns EH, Fan K, McConnell OJ, Carter GT. High throughput artificial membrane permeability assay for blood-brain barrier. Eur J Med Chem. 2003;38:223-32.
-
(2003)
Eur J Med Chem
, vol.38
, pp. 223-232
-
-
Di, L.1
Kerns, E.H.2
Fan, K.3
McConnell, O.J.4
Carter, G.T.5
-
82
-
-
84867848663
-
Comparison of brain capillary endothelial cell-based and epithelial (MDCK-MDR1, Caco-2, and VB-Caco-2) cell-based surrogate blood-brain barrier penetration models
-
1:CAS:528:DC%2BC38XhtlCiur7F 10.1016/j.ejpb.2012.07.020 22906709
-
Hellinger E, Veszelka S, Tóth AE, Walter F, Kittel A, Bakk ML, et al. Comparison of brain capillary endothelial cell-based and epithelial (MDCK-MDR1, Caco-2, and VB-Caco-2) cell-based surrogate blood-brain barrier penetration models. Eur J Pharm Biopharm. 2012;82:340-51.
-
(2012)
Eur J Pharm Biopharm
, vol.82
, pp. 340-351
-
-
Hellinger, E.1
Veszelka, S.2
Tóth, A.E.3
Walter, F.4
Kittel, A.5
Bakk, M.L.6
-
83
-
-
67049114278
-
Comparison of blood-brain barrier permeability assays: In situ brain perfusion, MDR1-MDCKII and PAMPA-BBB
-
1:CAS:528:DC%2BD1MXltlelurs%3D 10.1002/jps.21580 18837012
-
Di L, Kerns EH, Bezar IF, Petusky SL, Huang Y. Comparison of blood-brain barrier permeability assays: in situ brain perfusion, MDR1-MDCKII and PAMPA-BBB. J Pharm Sci. 2009;98:1980-91.
-
(2009)
J Pharm Sci
, vol.98
, pp. 1980-1991
-
-
Di, L.1
Kerns, E.H.2
Bezar, I.F.3
Petusky, S.L.4
Huang, Y.5
-
84
-
-
79952485977
-
Physicochemical selectivity of the BBB microenvironment governing passive diffusion-matching with a porcine brain lipid extract artificial membrane permeability model
-
1:CAS:528:DC%2BC3cXht1yrs7vF 10.1007/s11095-010-0280-x 20945153
-
Tsinman O, Tsinman K, Sun N, Avdeef A. Physicochemical selectivity of the BBB microenvironment governing passive diffusion-matching with a porcine brain lipid extract artificial membrane permeability model. Pharm Res. 2011;28:337-63.
-
(2011)
Pharm Res
, vol.28
, pp. 337-363
-
-
Tsinman, O.1
Tsinman, K.2
Sun, N.3
Avdeef, A.4
-
85
-
-
34250744722
-
Central nervous system drug disposition: The relationship between in situ brain permeability and brain free fraction
-
1:CAS:528:DC%2BD2sXntl2jt7g%3D 10.1124/jpet.107.121525 17405866
-
Summerfield SG, Read K, Begley DJ, Obradovic T, Hidalgo IJ, Coggon S, et al. Central nervous system drug disposition: the relationship between in situ brain permeability and brain free fraction. J Pharmacol Exp Ther. 2007;322:205-13.
-
(2007)
J Pharmacol Exp Ther
, vol.322
, pp. 205-213
-
-
Summerfield, S.G.1
Read, K.2
Begley, D.J.3
Obradovic, T.4
Hidalgo, I.J.5
Coggon, S.6
-
86
-
-
38749087222
-
In vitro P-glycoprotein assays to predict the in vivo interactions of P-glycoprotein with drugs in the central nervous system
-
1:CAS:528:DC%2BD1cXht1yktbc%3D 10.1124/dmd.107.017434 17962372
-
Feng B, Mills JB, Davidson RE, Mireles RJ, Janiszewski JS, Troutman MD, et al. In vitro P-glycoprotein assays to predict the in vivo interactions of P-glycoprotein with drugs in the central nervous system. Drug Metab Dispos. 2008;36:268-75.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 268-275
-
-
Feng, B.1
Mills, J.B.2
Davidson, R.E.3
Mireles, R.J.4
Janiszewski, J.S.5
Troutman, M.D.6
-
87
-
-
33644756715
-
Improving the in vitro prediction of in vivo central nervous system penetration: Integrating permeability, P-glycoprotein efflux, and free fractions in blood and brain
-
1:CAS:528:DC%2BD28Xit1SgsL0%3D 10.1124/jpet.105.092916 16330496
-
Summerfield SG, Stevens AJ, Cutler L, Del Carmen Osuna M, Hammond B, Tang S, et al. Improving the in vitro prediction of in vivo central nervous system penetration: integrating permeability, P-glycoprotein efflux, and free fractions in blood and brain. J Pharmacol Exp Ther. 2006;316:1282-90.
-
(2006)
J Pharmacol Exp Ther
, vol.316
, pp. 1282-1290
-
-
Summerfield, S.G.1
Stevens, A.J.2
Cutler, L.3
Del Carmen Osuna, M.4
Hammond, B.5
Tang, S.6
-
88
-
-
79958273257
-
In vitro primary human and animal cell-based blood-brain barrier models as a screening tool in drug discovery
-
1:CAS:528:DC%2BC3MXkslGktLc%3D 10.1021/mp1004614 21438632
-
Lacombe O, Videau O, Chevillon D, Guyot A-C, Contreras C, Blondel S, et al. In vitro primary human and animal cell-based blood-brain barrier models as a screening tool in drug discovery. Mol Pharm. 2011;8:651-63.
-
(2011)
Mol Pharm
, vol.8
, pp. 651-663
-
-
Lacombe, O.1
Videau, O.2
Chevillon, D.3
Guyot, A.-C.4
Contreras, C.5
Blondel, S.6
-
89
-
-
13844299532
-
In vitro models for the blood-brain barrier
-
1:CAS:528:DC%2BD2MXhtlCrurg%3D 10.1016/j.tiv.2004.06.011 15713540
-
Garberg P, Ball M, Borg N, Cecchelli R, Fenart L, Hurst RD, et al. In vitro models for the blood-brain barrier. Toxicol In Vitro. 2005;19:299-334.
-
(2005)
Toxicol in Vitro
, vol.19
, pp. 299-334
-
-
Garberg, P.1
Ball, M.2
Borg, N.3
Cecchelli, R.4
Fenart, L.5
Hurst, R.D.6
-
90
-
-
78349311922
-
Comparison of in vitro cell models in predicting in vivo brain entry of drugs
-
1:CAS:528:DC%2BC3cXhsVWhu7%2FF 10.1016/j.ijpharm.2010.09.016 20920560
-
Hakkarainen JJ, Jalkanen AJ, Kääriäinen TM, Keski-Rahkonen P, Venäläinen T, Hokkanen J, et al. Comparison of in vitro cell models in predicting in vivo brain entry of drugs. Int J Pharm. 2010;402:27-36.
-
(2010)
Int J Pharm
, vol.402
, pp. 27-36
-
-
Hakkarainen, J.J.1
Jalkanen, A.J.2
Kääriäinen, T.M.3
Keski-Rahkonen, P.4
Venäläinen, T.5
Hokkanen, J.6
-
91
-
-
80054720200
-
Quinidine as an ABCB1 probe for testing drug interactions at the blood-brain barrier: An in vitro in vivo correlation study
-
10.1177/1087057111414896 21832259 1:CAS:528:DC%2BC3MXht1yitrjE
-
Sziráki I, Erdo F, Beéry E, Molnár PM, Fazakas C, Wilhelm I, et al. Quinidine as an ABCB1 probe for testing drug interactions at the blood-brain barrier: an in vitro in vivo correlation study. J Biomol Screen. 2011;16:886-94.
-
(2011)
J Biomol Screen
, vol.16
, pp. 886-894
-
-
Sziráki, I.1
Erdo, F.2
Beéry, E.3
Molnár, P.M.4
Fazakas, C.5
Wilhelm, I.6
-
92
-
-
77949269469
-
Model analysis of the concentration-dependent permeability of P-gp substrates
-
1:CAS:528:DC%2BC3cXhsFGhs7o%3D 10.1007/s11095-009-0026-9 20135207
-
Tachibana T, Kitamura S, Kato M, Mitsui T, Shirasaka Y, Yamashita S, et al. Model analysis of the concentration-dependent permeability of P-gp substrates. Pharm Res. 2010;27:442-6.
-
(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
-
93
-
-
79956337554
-
How well can in vitro brain microcapillary endothelial cell models predict rodent in vivo blood-brain barrier permeability?
-
1:CAS:528:DC%2BC3MXmvFSkt70%3D 10.1016/j.ejps.2011.04.001 21514381
-
Avdeef A. How well can in vitro brain microcapillary endothelial cell models predict rodent in vivo blood-brain barrier permeability? Eur J Pharm Sci. 2011;43:109-24.
-
(2011)
Eur J Pharm Sci
, vol.43
, pp. 109-124
-
-
Avdeef, A.1
-
94
-
-
77949267657
-
Leakiness and size exclusion of paracellular channels in cultured epithelial cell monolayers-interlaboratory comparison
-
1:CAS:528:DC%2BC3cXksVequg%3D%3D 10.1007/s11095-009-0036-7 20069445
-
Avdeef A. Leakiness and size exclusion of paracellular channels in cultured epithelial cell monolayers-interlaboratory comparison. Pharm Res. 2010;27:480-9.
-
(2010)
Pharm Res
, vol.27
, pp. 480-489
-
-
Avdeef, A.1
-
95
-
-
77952035631
-
How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability?
-
1:CAS:528:DC%2BC3cXksVamsLw%3D 10.1021/jm901846t 20373811
-
Avdeef A, Tam KY. How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability? J Med Chem. 2010;53:3566-84.
-
(2010)
J Med Chem
, vol.53
, pp. 3566-3584
-
-
Avdeef, A.1
Tam, K.Y.2
-
96
-
-
14144250264
-
Caco-2 permeability of weakly basic drugs predicted with the double-sink PAMPA pKa(flux) method
-
1:CAS:528:DC%2BD2MXhslWmsbw%3D 10.1016/j.ejps.2004.11.011 15734300
-
Avdeef A, Artursson P, Neuhoff S, Lazorova L, Gråsjö J, Tavelin S. Caco-2 permeability of weakly basic drugs predicted with the double-sink PAMPA pKa(flux) method. Eur J Pharm Sci. 2005;24:333-49.
-
(2005)
Eur J Pharm Sci
, vol.24
, pp. 333-349
-
-
Avdeef, A.1
Artursson, P.2
Neuhoff, S.3
Lazorova, L.4
Gråsjö, J.5
Tavelin, S.6
-
97
-
-
52949145587
-
Involvement of the pyrilamine transporter, a putative organic cation transporter, in blood-brain barrier transport of oxycodone
-
1:CAS:528:DC%2BD1cXhtF2jtLbI 10.1124/dmd.108.022087 18606742
-
Okura T, Hattori A, Takano Y, Sato T, Hammarlund-Udenaes M, Terasaki T, et al. Involvement of the pyrilamine transporter, a putative organic cation transporter, in blood-brain barrier transport of oxycodone. Drug Metab Dispos. 2008;36:2005-13.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 2005-2013
-
-
Okura, T.1
Hattori, A.2
Takano, Y.3
Sato, T.4
Hammarlund-Udenaes, M.5
Terasaki, T.6
-
98
-
-
79961096875
-
Transcriptomic and quantitative proteomic analysis of transporters and drug metabolizing enzymes in freshly isolated human brain microvessels
-
1:CAS:528:DC%2BC3MXos1WhtLY%3D 10.1021/mp200129p 21707071
-
Shawahna R, Uchida Y, Declèves X, Ohtsuki S, Yousif S, Dauchy S, et al. Transcriptomic and quantitative proteomic analysis of transporters and drug metabolizing enzymes in freshly isolated human brain microvessels. Mol Pharm. 2011;8:1332-41.
-
(2011)
Mol Pharm
, vol.8
, pp. 1332-1341
-
-
Shawahna, R.1
Uchida, Y.2
Declèves, X.3
Ohtsuki, S.4
Yousif, S.5
Dauchy, S.6
-
99
-
-
79960116572
-
Quantitative targeted absolute proteomics-based ADME research as a new path to drug discovery and development: Methodology, advantages, strategy, and prospects
-
1:CAS:528:DC%2BC3MXosFegt7c%3D 10.1002/jps.22612 21560129
-
Ohtsuki S, Uchida Y, Kubo Y, Terasaki T. Quantitative targeted absolute proteomics-based ADME research as a new path to drug discovery and development: methodology, advantages, strategy, and prospects. J Pharm Sci. 2011;100:3547-59.
-
(2011)
J Pharm Sci
, vol.100
, pp. 3547-3559
-
-
Ohtsuki, S.1
Uchida, Y.2
Kubo, Y.3
Terasaki, T.4
-
100
-
-
43049114146
-
Quantitative atlas of membrane transporter proteins: Development and application of a highly sensitive simultaneous LC/MS/MS method combined with novel in-silico peptide selection criteria
-
1:CAS:528:DC%2BD1cXltFCjsLs%3D 10.1007/s11095-008-9532-4 18219561
-
Kamiie J, Ohtsuki S, Iwase R, Ohmine K, Katsukura Y, Yanai K, et al. Quantitative atlas of membrane transporter proteins: development and application of a highly sensitive simultaneous LC/MS/MS method combined with novel in-silico peptide selection criteria. Pharm Res. 2008;25:1469-83.
-
(2008)
Pharm Res
, vol.25
, pp. 1469-1483
-
-
Kamiie, J.1
Ohtsuki, S.2
Iwase, R.3
Ohmine, K.4
Katsukura, Y.5
Yanai, K.6
-
101
-
-
79953718797
-
Quantitative membrane protein expression at the blood-brain barrier of adult and younger cynomolgus monkeys
-
1:CAS:528:DC%2BC3MXosFentb4%3D 10.1002/jps.22487 21254069
-
Ito K, Uchida Y, Ohtsuki S, Aizawa S, Kawakami H, Katsukura Y, et al. Quantitative membrane protein expression at the blood-brain barrier of adult and younger cynomolgus monkeys. J Pharm Sci. 2011;100:3939-50.
-
(2011)
J Pharm Sci
, vol.100
, pp. 3939-3950
-
-
Ito, K.1
Uchida, Y.2
Ohtsuki, S.3
Aizawa, S.4
Kawakami, H.5
Katsukura, Y.6
-
102
-
-
79953686193
-
Quantitative targeted absolute proteomics of human blood-brain barrier transporters and receptors
-
1:CAS:528:DC%2BC3MXltFGhsr0%3D 10.1111/j.1471-4159.2011.07208.x 21291474
-
Uchida Y, Ohtsuki S, Katsukura Y, Ikeda C, Suzuki T, Kamiie J, et al. Quantitative targeted absolute proteomics of human blood-brain barrier transporters and receptors. J Neurochem. 2011;117:333-45.
-
(2011)
J Neurochem
, vol.117
, pp. 333-345
-
-
Uchida, Y.1
Ohtsuki, S.2
Katsukura, Y.3
Ikeda, C.4
Suzuki, T.5
Kamiie, J.6
-
103
-
-
84881609722
-
Quantitative atlas of blood-brain barrier transporters, receptors, and tight junction proteins in rats and common marmoset
-
doi: 10.1002/jps.23575
-
Hoshi Y, Uchida Y, Tachikawa M, Inoue T, Ohtsuki S, Terasaki T. Quantitative atlas of blood-brain barrier transporters, receptors, and tight junction proteins in rats and common marmoset. J Pharm Sci. 2013. doi: 10.1002/jps.23575.
-
(2013)
J Pharm Sci
-
-
Hoshi, Y.1
Uchida, Y.2
Tachikawa, M.3
Inoue, T.4
Ohtsuki, S.5
Terasaki, T.6
-
104
-
-
80054792485
-
Blood-brain barrier (BBB) pharmacoproteomics: Reconstruction of in vivo brain distribution of 11 P-glycoprotein substrates based on the BBB transporter protein concentration, in vitro intrinsic transport activity, and unbound fraction in plasma and brain
-
1:CAS:528:DC%2BC3MXhsFehtbrK 10.1124/jpet.111.184200 21828264
-
Uchida Y, Ohtsuki S, Kamiie J, Terasaki T. Blood-brain barrier (BBB) pharmacoproteomics: reconstruction of in vivo brain distribution of 11 P-glycoprotein substrates based on the BBB transporter protein concentration, in vitro intrinsic transport activity, and unbound fraction in plasma and brain. J Pharmacol Exp Ther. 2011;339:579-88.
-
(2011)
J Pharmacol Exp Ther
, vol.339
, pp. 579-588
-
-
Uchida, Y.1
Ohtsuki, S.2
Kamiie, J.3
Terasaki, T.4
-
105
-
-
59649115878
-
An unexpected synergist role of P-glycoprotein and breast cancer resistance protein on the central nervous system penetration of the tyrosine kinase inhibitor lapatinib (N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[5- ({[2-(methylsulfonyl)ethyl]amino}meth
-
1:CAS:528:DC%2BD1MXhs1Krtro%3D 10.1124/dmd.108.024646 19056914
-
Polli JW, Olson KL, Chism JP, John-Williams LS, Yeager RL, Woodard SM, et al. An unexpected synergist role of P-glycoprotein and breast cancer resistance protein on the central nervous system penetration of the tyrosine kinase inhibitor lapatinib (N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[5-({[2- (methylsulfonyl)ethyl]amino}meth. Drug Metab Dispos. 2009;37:439-42.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 439-442
-
-
Polli, J.W.1
Olson, K.L.2
Chism, J.P.3
John-Williams, L.S.4
Yeager, R.L.5
Woodard, S.M.6
-
106
-
-
59049091078
-
The effect of P-gp (Mdr1a/1b), BCRP (Bcrp1) and P-gp/BCRP inhibitors on the in vivo absorption, distribution, metabolism and excretion of imatinib
-
1:CAS:528:DC%2BD1cXhsFejt77F 10.1007/s10637-008-9138-z 18449471
-
Oostendorp RL, Buckle T, Beijnen JH, Van Tellingen O, Schellens JHM. The effect of P-gp (Mdr1a/1b), BCRP (Bcrp1) and P-gp/BCRP inhibitors on the in vivo absorption, distribution, metabolism and excretion of imatinib. Invest New Drugs. 2009;27:31-40.
-
(2009)
Invest New Drugs
, vol.27
, pp. 31-40
-
-
Oostendorp, R.L.1
Buckle, T.2
Beijnen, J.H.3
Van Tellingen, O.4
Schellens, J.H.M.5
-
107
-
-
65249151331
-
Brain accumulation of dasatinib is restricted by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) and can be enhanced by elacridar treatment
-
1:CAS:528:DC%2BD1MXjvVWlurg%3D 10.1158/1078-0432.CCR-08-2253 19276246
-
Lagas JS, Van Waterschoot RA, Van Tilburg VA, Hillebrand MJ, Lankheet N, Rosing H, et al. Brain accumulation of dasatinib is restricted by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) and can be enhanced by elacridar treatment. Clin Cancer Res. 2009;15:2344-51.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 2344-2351
-
-
Lagas, J.S.1
Van Waterschoot, R.A.2
Van Tilburg, V.A.3
Hillebrand, M.J.4
Lankheet, N.5
Rosing, H.6
-
108
-
-
77953783419
-
Distribution of gefitinib to the brain is limited by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2)-mediated active efflux
-
1:CAS:528:DC%2BC3cXos1KltL8%3D 10.1124/jpet.110.167601 20421331
-
Agarwal S, Sane R, Gallardo JL, Ohlfest JR, Elmquist WF. Distribution of gefitinib to the brain is limited by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2)-mediated active efflux. J Pharmacol Exp Ther. 2010;334:147-55.
-
(2010)
J Pharmacol Exp Ther
, vol.334
, pp. 147-155
-
-
Agarwal, S.1
Sane, R.2
Gallardo, J.L.3
Ohlfest, J.R.4
Elmquist, W.F.5
-
109
-
-
77952393660
-
Kinetic analysis of the cooperation of P-glycoprotein (P-gp/Abcb1) and breast cancer resistance protein (Bcrp/Abcg2) in limiting the brain and testis penetration of erlotinib, flavopiridol, and mitoxantrone
-
1:CAS:528:DC%2BC3cXmvFClsLs%3D 10.1124/jpet.109.162321 20304939
-
Kodaira H, Kusuhara H, Ushiki J, Fuse E, Sugiyama Y. Kinetic analysis of the cooperation of P-glycoprotein (P-gp/Abcb1) and breast cancer resistance protein (Bcrp/Abcg2) in limiting the brain and testis penetration of erlotinib, flavopiridol, and mitoxantrone. J Pharmacol Exp Ther. 2010;333:788-96.
-
(2010)
J Pharmacol Exp Ther
, vol.333
, pp. 788-796
-
-
Kodaira, H.1
Kusuhara, H.2
Ushiki, J.3
Fuse, E.4
Sugiyama, Y.5
-
110
-
-
78650785470
-
The role of the breast cancer resistance protein (ABCG2) in the distribution of sorafenib to the brain
-
1:CAS:528:DC%2BC3MXls1eqtg%3D%3D 10.1124/jpet.110.175034 20952483
-
Agarwal S, Sane R, Ohlfest JR, Elmquist WF. The role of the breast cancer resistance protein (ABCG2) in the distribution of sorafenib to the brain. J Pharmacol Exp Ther. 2011;336:223-33.
-
(2011)
J Pharmacol Exp Ther
, vol.336
, pp. 223-233
-
-
Agarwal, S.1
Sane, R.2
Ohlfest, J.R.3
Elmquist, W.F.4
-
111
-
-
79955032486
-
Differential impact of P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) on axitinib brain accumulation and oral plasma pharmacokinetics
-
1:CAS:528:DC%2BC3MXls1OjtLo%3D 10.1124/dmd.110.037317 21282407
-
Poller B, Iusuf D, Sparidans RW, Wagenaar E, Beijnen JH, Schinkel AH. Differential impact of P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) on axitinib brain accumulation and oral plasma pharmacokinetics. Drug Metab Dispos. 2011;39:729-35.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 729-735
-
-
Poller, B.1
Iusuf, D.2
Sparidans, R.W.3
Wagenaar, E.4
Beijnen, J.H.5
Schinkel, A.H.6
-
112
-
-
66449110827
-
The effect of breast cancer resistance protein and P-glycoprotein on the brain penetration of flavopiridol, imatinib mesylate (Gleevec), prazosin, and 2-methoxy-3-(4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)phenyl)propanoic acid (PF-407288) in mice
-
1:CAS:528:DC%2BD1MXlsVWitLo%3D 10.1124/dmd.108.024489 19225039
-
Zhou L, Schmidt K, Nelson FR, Zelesky V, Troutman MD, Feng B. The effect of breast cancer resistance protein and P-glycoprotein on the brain penetration of flavopiridol, imatinib mesylate (Gleevec), prazosin, and 2-methoxy-3-(4-(2- (5-methyl-2-phenyloxazol-4-yl)ethoxy)phenyl)propanoic acid (PF-407288) in mice. Drug Metab Dispos. 2009;37:946-55.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 946-955
-
-
Zhou, L.1
Schmidt, K.2
Nelson, F.R.3
Zelesky, V.4
Troutman, M.D.5
Feng, B.6
-
113
-
-
79251492055
-
Brain tissue binding of drugs: Evaluation and validation of solid supported porcine brain membrane vesicles (TRANSIL) as a novel high-throughput method
-
1:CAS:528:DC%2BC3MXhslKmtr0%3D 10.1124/dmd.110.036095 21071520
-
Longhi R, Corbioli S, Fontana S, Vinco F, Braggio S, Helmdach L, et al. Brain tissue binding of drugs: evaluation and validation of solid supported porcine brain membrane vesicles (TRANSIL) as a novel high-throughput method. Drug Metab Dispos. 2011;39:312-21.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 312-321
-
-
Longhi, R.1
Corbioli, S.2
Fontana, S.3
Vinco, F.4
Braggio, S.5
Helmdach, L.6
-
114
-
-
34548071206
-
In vitro methods for estimating unbound drug concentrations in the brain interstitial and intracellular fluids
-
10.1124/dmd.107.015222 17591680 1:CAS:528:DC%2BD2sXpslKqsLg%3D
-
Fridén M, Gupta A, Antonsson M, Bredberg U, Hammarlund-Udenaes M. In vitro methods for estimating unbound drug concentrations in the brain interstitial and intracellular fluids. Drug Metab Dispos. 2007;35:1711-9.
-
(2007)
Drug Metab Dispos
, vol.35
, pp. 1711-1719
-
-
Fridén, M.1
Gupta, A.2
Antonsson, M.3
Bredberg, U.4
Hammarlund-Udenaes, M.5
-
115
-
-
63849149894
-
Unbound drug concentration in brain homogenate and cerebral spinal fluid at steady state as a surrogate for unbound concentration in brain interstitial fluid
-
1:CAS:528:DC%2BD1MXktVSku7s%3D 10.1124/dmd.108.024125 19116265
-
Liu X, Van Natta K, Yeo H, Vilenski O, Weller PE, Worboys PD, et al. Unbound drug concentration in brain homogenate and cerebral spinal fluid at steady state as a surrogate for unbound concentration in brain interstitial fluid. Drug Metab Dispos. 2009;37:787-93.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 787-793
-
-
Liu, X.1
Van Natta, K.2
Yeo, H.3
Vilenski, O.4
Weller, P.E.5
Worboys, P.D.6
-
116
-
-
33645821904
-
Evaluation of the utility of brain slice methods to study brain penetration
-
1:CAS:528:DC%2BD28Xks1Skt78%3D 10.1124/dmd.105.007914 16501003
-
Becker S, Liu X. Evaluation of the utility of brain slice methods to study brain penetration. Drug Metab Dispos. 2006;34:855-61.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 855-861
-
-
Becker, S.1
Liu, X.2
-
117
-
-
66649119187
-
Development of a high-throughput brain slice method for studying drug distribution in the central nervous system
-
10.1124/dmd.108.026377 19299522 1:CAS:528:DC%2BD1MXmslamu70%3D
-
Fridén M, Ducrozet F, Middleton B, Antonsson M, Bredberg U, Hammarlund-Udenaes M. Development of a high-throughput brain slice method for studying drug distribution in the central nervous system. Drug Metab Dispos. 2009;37:1226-33.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 1226-1233
-
-
Fridén, M.1
Ducrozet, F.2
Middleton, B.3
Antonsson, M.4
Bredberg, U.5
Hammarlund-Udenaes, M.6
-
118
-
-
79951865101
-
Measurement of unbound drug exposure in brain: Modeling of pH partitioning explains diverging results between the brain slice and brain homogenate methods
-
10.1124/dmd.110.035998 21149540 1:CAS:528:DC%2BC3MXivVWitLs%3D
-
Fridén M, Bergström F, Wan H, Rehngren M, Ahlin G, Hammarlund-Udenaes M, et al. Measurement of unbound drug exposure in brain: modeling of pH partitioning explains diverging results between the brain slice and brain homogenate methods. Drug Metab Dispos. 2011;39:353-62.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 353-362
-
-
Fridén, M.1
Bergström, F.2
Wan, H.3
Rehngren, M.4
Ahlin, G.5
Hammarlund-Udenaes, M.6
-
119
-
-
34648813134
-
High-throughput screening of drug-brain tissue binding and in silico prediction for assessment of central nervous system drug delivery
-
1:CAS:528:DC%2BD2sXps1Kntb8%3D 10.1021/jm070375w 17725338
-
Wan H, Rehngren M, Giordanetto F, Bergström F, Tunek A. High-throughput screening of drug-brain tissue binding and in silico prediction for assessment of central nervous system drug delivery. J Med Chem. 2007;50:4606-15.
-
(2007)
J Med Chem
, vol.50
, pp. 4606-4615
-
-
Wan, H.1
Rehngren, M.2
Giordanetto, F.3
Bergström, F.4
Tunek, A.5
-
120
-
-
56749183619
-
Toward an improved prediction of human in vivo brain penetration
-
1:CAS:528:DC%2BD1cXhsVWmur7E 10.1080/00498250802499459 18979396
-
Summerfield SG, Lucas AJ, Porter RA, Jeffrey P, Gunn RN, Read KR, et al. Toward an improved prediction of human in vivo brain penetration. Xenobiotica. 2008;38:1518-35.
-
(2008)
Xenobiotica
, vol.38
, pp. 1518-1535
-
-
Summerfield, S.G.1
Lucas, A.J.2
Porter, R.A.3
Jeffrey, P.4
Gunn, R.N.5
Read, K.R.6
-
121
-
-
79959417881
-
Species independence in brain tissue binding using brain homogenates
-
1:CAS:528:DC%2BC3MXosFWktrg%3D 10.1124/dmd.111.038778 21474681
-
Di L, Umland JP, Chang G, Huang Y, Lin Z, Scott DO, et al. Species independence in brain tissue binding using brain homogenates. Drug Metab Dispos. 2011;39:1270-7.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 1270-1277
-
-
Di, L.1
Umland, J.P.2
Chang, G.3
Huang, Y.4
Lin, Z.5
Scott, D.O.6
-
122
-
-
35748977617
-
Challenges for blood-brain barrier (BBB) screening
-
1:CAS:528:DC%2BD2sXht1ahu7vE 10.1080/00498250701570285 17968740
-
Jeffrey P, Summerfield SG. Challenges for blood-brain barrier (BBB) screening. Xenobiotica. 2007;37:1135-51.
-
(2007)
Xenobiotica
, vol.37
, pp. 1135-1151
-
-
Jeffrey, P.1
Summerfield, S.G.2
-
123
-
-
84867669201
-
An evaluation of using rat-derived single-dose neuropharmacokinetic parameters to project accurately large animal unbound brain drug concentrations
-
1:CAS:528:DC%2BC38XhsFKkt7rI 10.1124/dmd.112.046391 22899853
-
Doran AC, Osgood SM, Mancuso JY, Shaffer CL. An evaluation of using rat-derived single-dose neuropharmacokinetic parameters to project accurately large animal unbound brain drug concentrations. Drug Metab Dispos. 2012;40:2162-73.
-
(2012)
Drug Metab Dispos
, vol.40
, pp. 2162-2173
-
-
Doran, A.C.1
Osgood, S.M.2
Mancuso, J.Y.3
Shaffer, C.L.4
-
124
-
-
84863914345
-
In vivo microdialysis in pharmacological studies of antibacterial agents in the brain
-
1:CAS:528:DC%2BC38XhtVOjt7fL 10.1093/bja/aes216 22745353
-
Notkina N, Dahyot-Fizelier C, Gupta AK. In vivo microdialysis in pharmacological studies of antibacterial agents in the brain. Br J Anaesth. 2012;109:155-60.
-
(2012)
Br J Anaesth
, vol.109
, pp. 155-160
-
-
Notkina, N.1
Dahyot-Fizelier, C.2
Gupta, A.K.3
-
125
-
-
77957998294
-
Using PET studies of P-gp function to elucidate mechanisms underlying the disposition of drugs
-
10.2174/156802610792927997 20645912
-
Syvänen S, Hammarlund-Udenaes M. Using PET studies of P-gp function to elucidate mechanisms underlying the disposition of drugs. Curr Top Med Chem. 2010;10:1799-809.
-
(2010)
Curr Top Med Chem
, vol.10
, pp. 1799-1809
-
-
Syvänen, S.1
Hammarlund-Udenaes, M.2
-
126
-
-
33645881089
-
Verapamil P-glycoprotein transport across the rat blood-brain barrier: Cyclosporine, a concentration inhibition analysis, and comparison with human data
-
1:CAS:528:DC%2BD28XktFamurg%3D 10.1124/jpet.105.097931 16415090
-
Hsiao P, Sasongko L, Link JM, Mankoff DA, Muzi M, Collier AC, et al. Verapamil P-glycoprotein transport across the rat blood-brain barrier: cyclosporine, a concentration inhibition analysis, and comparison with human data. J Pharmacol Exp Ther. 2006;317:704-10.
-
(2006)
J Pharmacol Exp Ther
, vol.317
, pp. 704-710
-
-
Hsiao, P.1
Sasongko, L.2
Link, J.M.3
Mankoff, D.A.4
Muzi, M.5
Collier, A.C.6
-
127
-
-
40849145621
-
In vitro-to-in vivo prediction of P-glycoprotein-based drug interactions at the human and rodent blood-brain barrier
-
1:CAS:528:DC%2BD1cXjt1arsL4%3D 10.1124/dmd.107.018176 18057117
-
Hsiao P, Bui T, Ho RJY, Unadkat JD. In vitro-to-in vivo prediction of P-glycoprotein-based drug interactions at the human and rodent blood-brain barrier. Drug Metab Dispos. 2008;36:481-4.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 481-484
-
-
Hsiao, P.1
Bui, T.2
Ho, R.J.Y.3
Unadkat, J.D.4
-
128
-
-
20444480695
-
Imaging P-glycoprotein transport activity at the human blood-brain barrier with positron emission tomography
-
1:CAS:528:DC%2BD2MXlt1Gqt70%3D 10.1016/j.clpt.2005.01.022 15961982
-
Sasongko L, Link JM, Muzi M, Mankoff DA, Yang X, Collier AC, et al. Imaging P-glycoprotein transport activity at the human blood-brain barrier with positron emission tomography. Clin Pharmacol Ther. 2005;77:503-14.
-
(2005)
Clin Pharmacol Ther
, vol.77
, pp. 503-514
-
-
Sasongko, L.1
Link, J.M.2
Muzi, M.3
Mankoff, D.A.4
Yang, X.5
Collier, A.C.6
-
129
-
-
34249943356
-
Polyspecific organic cation transporters: Structure, function, physiological roles, and biopharmaceutical implications
-
1:CAS:528:DC%2BD2sXnt1Clu7Y%3D 10.1007/s11095-007-9254-z 17473959
-
Koepsell H, Lips K, Volk C. Polyspecific organic cation transporters: structure, function, physiological roles, and biopharmaceutical implications. Pharm Res. 2007;24:1227-51.
-
(2007)
Pharm Res
, vol.24
, pp. 1227-1251
-
-
Koepsell, H.1
Lips, K.2
Volk, C.3
-
130
-
-
61449118888
-
Species differences in blood-brain barrier transport of three positron emission tomography radioligands with emphasis on P-glycoprotein transport
-
10.1124/dmd.108.024745 19047468 1:CAS:528:DC%2BD1MXislamtbo%3D
-
Syvänen S, Lindhe O, Palner M, Kornum BR, Rahman O, Långström B, et al. Species differences in blood-brain barrier transport of three positron emission tomography radioligands with emphasis on P-glycoprotein transport. Drug Metab Dispos. 2009;37:635-43.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 635-643
-
-
Syvänen, S.1
Lindhe, O.2
Palner, M.3
Kornum, B.R.4
Rahman, O.5
Långström, B.6
-
131
-
-
42049115452
-
11C-loperamide and its N-desmethyl radiometabolite are avid substrates for brain permeability-glycoprotein efflux
-
1:CAS:528:DC%2BD1cXltl2gtb8%3D 10.2967/jnumed.107.047308 18344435
-
Zoghbi SS, Liow J-S, Yasuno F, Hong J, Tuan E, Lazarova N, et al. 11C-loperamide and its N-desmethyl radiometabolite are avid substrates for brain permeability-glycoprotein efflux. J Nucl Med. 2008;49:649-56.
-
(2008)
J Nucl Med
, vol.49
, pp. 649-656
-
-
Zoghbi, S.S.1
Liow, J.-S.2
Yasuno, F.3
Hong, J.4
Tuan, E.5
Lazarova, N.6
-
132
-
-
66149123753
-
Human brain imaging and radiation dosimetry of 11C-N-desmethyl- loperamide, a PET radiotracer to measure the function of P-glycoprotein
-
1:CAS:528:DC%2BD1MXmtV2hsrs%3D 10.2967/jnumed.108.058453 19372478
-
Seneca N, Zoghbi SS, Liow J-S, Kreisl W, Herscovitch P, Jenko K, et al.
-
(2009)
J Nucl Med
, vol.50
, pp. 807-813
-
-
Seneca, N.1
Zoghbi, S.S.2
Liow, J.-S.3
Kreisl, W.4
Herscovitch, P.5
Jenko, K.6
-
133
-
-
77950952797
-
P-glycoprotein function at the blood-brain barrier in humans can be quantified with the substrate radiotracer 11C-N-desmethyl-loperamide
-
1:CAS:528:DC%2BC3cXls12gur8%3D 10.2967/jnumed.109.070151 20237038
-
Kreisl WC, Liow J-S, Kimura N, Seneca N, Zoghbi SS, Morse CL, et al. P-glycoprotein function at the blood-brain barrier in humans can be quantified with the substrate radiotracer 11C-N-desmethyl-loperamide. J Nucl Med. 2010;51:559-66.
-
(2010)
J Nucl Med
, vol.51
, pp. 559-566
-
-
Kreisl, W.C.1
Liow, J.-S.2
Kimura, N.3
Seneca, N.4
Zoghbi, S.S.5
Morse, C.L.6
-
134
-
-
84875851139
-
Retrospective analysis of p-glycoprotein-mediated drug-drug interactions at the blood-brain barrier in humans
-
1:CAS:528:DC%2BC3sXkslSktr8%3D 10.1124/dmd.112.049577 23340958
-
Sugimoto H, Hirabayashi H, Amano N, Moriwaki T. Retrospective analysis of p-glycoprotein-mediated drug-drug interactions at the blood-brain barrier in humans. Drug Metab Dispos. 2013;41:683-8.
-
(2013)
Drug Metab Dispos
, vol.41
, pp. 683-688
-
-
Sugimoto, H.1
Hirabayashi, H.2
Amano, N.3
Moriwaki, T.4
-
135
-
-
84879415192
-
Why clinical inhibition of efflux transport at the blood-brain barrier is unlikely: The ITC evidence-based position
-
10.1038/clpt.2013.34
-
Kalvass JC, Polli JW, Bourdet DL, Feng B, Huang S-M, Smith QR, et al. Why clinical inhibition of efflux transport at the blood-brain barrier is unlikely: the ITC evidence-based position. Clin Pharmacol Ther. 2013. doi: 10.1038/clpt.2013.34.
-
(2013)
Clin Pharmacol Ther
-
-
Kalvass, J.C.1
Polli, J.W.2
Bourdet, D.L.3
Feng, B.4
Huang, S.-M.5
Smith, Q.R.6
|