-
1
-
-
0032948943
-
Prediction of dissolution–absorption relationships from a dissolution/Caco-2 system
-
Ginski M., Prediction of dissolution–absorption relationships from a dissolution/Caco-2 system. Int J Pharm 1999;177:117–25.
-
(1999)
Int J Pharm
, vol.177
, pp. 117-125
-
-
Ginski, M.1
-
2
-
-
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, et al. In vitro system to evaluate oral absorption of poorly water-soluble drugs:simultaneous analysis on dissolution and permeation of drugs. Pharm Res 2003;20:1674–80.
-
(2003)
Pharm Res
, vol.20
, pp. 1674-1680
-
-
Kataoka, M.1
Masaoka, Y.2
Yamazaki, Y.3
-
3
-
-
67049162366
-
IVIVC in oral absorption for fenofibrate immediate release tablets using a dissolution/permeation system
-
Buch P, Langguth P, Kataoka M, Yamashita S., IVIVC in oral absorption for fenofibrate immediate release tablets using a dissolution/permeation system. J Pharm Sci 2009;98:2001–9.
-
(2009)
J Pharm Sci
, vol.98
, pp. 2001-2009
-
-
Buch, P.1
Langguth, P.2
Kataoka, M.3
Yamashita, S.4
-
4
-
-
0035523263
-
Strategies for absorption screening in drug discovery and development
-
Bohets H, Annaert P, Mannens G, et al. Strategies for absorption screening in drug discovery and development. Curr Topics Med Chem 2001;1:367–83.
-
(2001)
Curr Topics Med Chem
, vol.1
, pp. 367-383
-
-
Bohets, H.1
Annaert, P.2
Mannens, G.3
-
5
-
-
0031750861
-
Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs
-
Galia E, Nicolaides E, Hörter D, et al. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm Res 1998;15:698–705.
-
(1998)
Pharm Res
, vol.15
, pp. 698-705
-
-
Galia, E.1
Nicolaides, E.2
Hörter, D.3
-
6
-
-
0033452575
-
Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data
-
Nicolaides E, Galia E, Efthymiopoulos C, et al. Forecasting the in vivo performance of four low solubility drugs from their in vitro dissolution data. Pharm Res 1999;16:1876–82.
-
(1999)
Pharm Res
, vol.16
, pp. 1876-1882
-
-
Nicolaides, E.1
Galia, E.2
Efthymiopoulos, C.3
-
7
-
-
33645006387
-
Use of simulated intestinal fluids with Caco-2 cells and rat ileum
-
Patel N, Forbes B, Eskola S, Murray J., Use of simulated intestinal fluids with Caco-2 cells and rat ileum. Drug Dev Ind Pharm 2006;32:151–61.
-
(2006)
Drug Dev Ind Pharm
, vol.32
, pp. 151-161
-
-
Patel, N.1
Forbes, B.2
Eskola, S.3
Murray, J.4
-
8
-
-
84919935669
-
Evaluation of fasted and fed state simulated and human intestinal fluids as solvent system in the Ussing chambers model to explore food effects on intestinal permeability
-
Wuyts B, Riethorst D, Brouwers J, et al. Evaluation of fasted and fed state simulated and human intestinal fluids as solvent system in the Ussing chambers model to explore food effects on intestinal permeability. Int J Pharm 2015;478:736–44.
-
(2015)
Int J Pharm
, vol.478
, pp. 736-744
-
-
Wuyts, B.1
Riethorst, D.2
Brouwers, J.3
-
9
-
-
0036849486
-
Effect of bovine serum albumin on drug permeability estimation across Caco-2 monolayers
-
Saha P, Kou JH., Effect of bovine serum albumin on drug permeability estimation across Caco-2 monolayers. Eur J Pharm Biopharm 2002;54:319–24.
-
(2002)
Eur J Pharm Biopharm
, vol.54
, pp. 319-324
-
-
Saha, P.1
Kou, J.H.2
-
10
-
-
84911997037
-
Nanoparticle structure development in the gastro-intestinal model fluid FaSSIF mod6.5 from several phospholipids at various water content relevant for oral drug administration
-
Khoshakhlagh P, Johnson R, Nawroth T, et al. Nanoparticle structure development in the gastro-intestinal model fluid FaSSIF mod6.5 from several phospholipids at various water content relevant for oral drug administration. Eur J Lipid Sci Technol 2014;116:1155–66.
-
(2014)
Eur J Lipid Sci Technol
, vol.116
, pp. 1155-1166
-
-
Khoshakhlagh, P.1
Johnson, R.2
Nawroth, T.3
-
11
-
-
84934998890
-
Fasted-state simulated intestinal fluid “FaSSIF-C”, a cholesterol containing intestinal model medium for in vitro drug delivery development
-
Khoshakhlagh P, Johnson R, Langguth P, et al. Fasted-state simulated intestinal fluid “FaSSIF-C”, a cholesterol containing intestinal model medium for in vitro drug delivery development. J Pharm Sci 2015;104:2213–24.
-
(2015)
J Pharm Sci
, vol.104
, pp. 2213-2224
-
-
Khoshakhlagh, P.1
Johnson, R.2
Langguth, P.3
-
12
-
-
84883002237
-
Mechanistic basis for unexpected bioavailability enhancement of polyelectrolyte complexes incorporating BCS class III drugs and carrageenans
-
Heinen C, Reuss S, Saaler-Reinhardt S, Langguth P., Mechanistic basis for unexpected bioavailability enhancement of polyelectrolyte complexes incorporating BCS class III drugs and carrageenans. Eur J Pharm Biopharm 2013;85:26–33.
-
(2013)
Eur J Pharm Biopharm
, vol.85
, pp. 26-33
-
-
Heinen, C.1
Reuss, S.2
Saaler-Reinhardt, S.3
Langguth, P.4
-
13
-
-
0032904840
-
Evaluation of viability of excised rat intestinal segments in the Ussing chamber: investigation of morphology, electrical parameters, and permeability characteristics
-
Polentarutti BI, Peterson AL, Sjöberg AK, et al. Evaluation of viability of excised rat intestinal segments in the Ussing chamber:investigation of morphology, electrical parameters, and permeability characteristics. Pharm Res 1999;16:446–54.
-
(1999)
Pharm Res
, vol.16
, pp. 446-454
-
-
Polentarutti, B.I.1
Peterson, A.L.2
Sjöberg, A.K.3
-
14
-
-
84857508129
-
Suitability of isolated rat jejunum model for demonstration of complete absorption in humans for bcs-based biowaiver request
-
Peternel L, Kristan K, Petruševska M, et al. Suitability of isolated rat jejunum model for demonstration of complete absorption in humans for bcs-based biowaiver request. J Pharm Sci 2012;101:1436–49.
-
(2012)
J Pharm Sci
, vol.101
, pp. 1436-1449
-
-
Peternel, L.1
Kristan, K.2
Petruševska, M.3
-
15
-
-
0031946994
-
Membrane transport of drugs in different regions of the intestinal tract of the rat
-
Ungell A, Nylander S, Bergstrand S, et al. Membrane transport of drugs in different regions of the intestinal tract of the rat. J Pharm Sci 1998;87:360–6.
-
(1998)
J Pharm Sci
, vol.87
, pp. 360-366
-
-
Ungell, A.1
Nylander, S.2
Bergstrand, S.3
-
16
-
-
0034042068
-
Mucosal in vitro permeability in the intestinal tract of the pig, the rat, and man: species- and region-related differences
-
Nejdfors MEBJ P., Mucosal in vitro permeability in the intestinal tract of the pig, the rat, and man:species- and region-related differences. Scand J Gastroenterol 2009;35:501–7.
-
(2009)
Scand J Gastroenterol
, vol.35
, pp. 501-507
-
-
Nejdfors MEBJ, P.1
-
17
-
-
59249108194
-
The role of membrane cholesterol in determining bile acid cytotoxicity and cytoprotection of ursodeoxycholic acid
-
Zhou Y, Doyen R, Lichtenberger LM., The role of membrane cholesterol in determining bile acid cytotoxicity and cytoprotection of ursodeoxycholic acid. Biochim Biophys Acta 2009;1788:507–13.
-
(2009)
Biochim Biophys Acta
, vol.1788
, pp. 507-513
-
-
Zhou, Y.1
Doyen, R.2
Lichtenberger, L.M.3
-
18
-
-
40349096749
-
Role of phosphatidylcholine saturation in preventing bile salt toxicity to gastrointestinal epithelia and membranes
-
Dial EJ, Rooijakkers SHM, Darling RL, et al. Role of phosphatidylcholine saturation in preventing bile salt toxicity to gastrointestinal epithelia and membranes. J Gastroenterol Hepatol 2008;23:430–6.
-
(2008)
J Gastroenterol Hepatol
, vol.23
, pp. 430-436
-
-
Dial, E.J.1
Rooijakkers, S.H.M.2
Darling, R.L.3
-
19
-
-
0035524138
-
Assessing the absorption of new pharmaceuticals
-
Hidalgo IJ., Assessing the absorption of new pharmaceuticals. Curr Topics Med Chem 2001;1:385–401.
-
(2001)
Curr Topics Med Chem
, vol.1
, pp. 385-401
-
-
Hidalgo, I.J.1
-
20
-
-
0022655086
-
Distribution of glycosphingolipids and ceramide of rat small intestinal mucosa
-
Dahiya R, Brasitus TA., Distribution of glycosphingolipids and ceramide of rat small intestinal mucosa. Lipids 1986;21:112–16.
-
(1986)
Lipids
, vol.21
, pp. 112-116
-
-
Dahiya, R.1
Brasitus, T.A.2
-
21
-
-
52949093858
-
An evaluation of the relative roles of the unstirred water layer and receptor sink in limiting the in-vitro intestinal permeability of drug compounds of varying lipophilicity
-
Katneni K, Charman SA, Porter CJH., An evaluation of the relative roles of the unstirred water layer and receptor sink in limiting the in-vitro intestinal permeability of drug compounds of varying lipophilicity. J Pharm Pharmacol 2008;60:1311–19.
-
(2008)
J Pharm Pharmacol
, vol.60
, pp. 1311-1319
-
-
Katneni, K.1
Charman, S.A.2
Porter, C.J.H.3
-
22
-
-
0034031969
-
Optimized conditions for prediction of intestinal drug permeability using Caco-2 cells
-
Yamashita S, Furubayashi T, Kataoka M, et al. Optimized conditions for prediction of intestinal drug permeability using Caco-2 cells. Eur J Pharm Sci 2000;10:195–204.
-
(2000)
Eur J Pharm Sci
, vol.10
, pp. 195-204
-
-
Yamashita, S.1
Furubayashi, T.2
Kataoka, M.3
-
23
-
-
0028335309
-
Transcellular permeability of chlorpromazine demonstrating the roles of protein-binding and membrane partitioning
-
Sawada GA, Ho NFH, Williams LR, et al. Transcellular permeability of chlorpromazine demonstrating the roles of protein-binding and membrane partitioning. Pharm Res 1994;11:665–73.
-
(1994)
Pharm Res
, vol.11
, pp. 665-673
-
-
Sawada, G.A.1
Ho, N.F.H.2
Williams, L.R.3
-
24
-
-
0037006601
-
Intestinal absorption characteristics of the low solubility thiocarboxanilide UC-781
-
Deferme S, van Gelder J, Ingels F, et al. Intestinal absorption characteristics of the low solubility thiocarboxanilide UC-781. Int J Pharm 2002;234:113–19.
-
(2002)
Int J Pharm
, vol.234
, pp. 113-119
-
-
Deferme, S.1
van Gelder, J.2
Ingels, F.3
-
25
-
-
0032150514
-
Effect of stabilising amino acids on the digestive absorption of heme and non-heme iron
-
Vaghefi N, Guillochon D, Bureau F, et al. Effect of stabilising amino acids on the digestive absorption of heme and non-heme iron. Reprod Nutr Dev1998;38:559–66.
-
(1998)
. Reprod Nutr Dev
, vol.38
, pp. 559-566
-
-
Vaghefi, N.1
Guillochon, D.2
Bureau, F.3
-
26
-
-
0033129537
-
Loperamide-simethicone vs loperamide alone, simethicone alone, and placebo in the treatment of acute diarrhea with gas-related abdominal discomfort: a randomized controlled trial
-
Kaplan MA., Loperamide-simethicone vs loperamide alone, simethicone alone, and placebo in the treatment of acute diarrhea with gas-related abdominal discomfort:a randomized controlled trial. Arch Family Med 1999;8:243–8.
-
(1999)
Arch Family Med
, vol.8
, pp. 243-248
-
-
Kaplan, M.A.1
-
27
-
-
20844446627
-
The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869: a Beagle dog model predicts improved bioavailability and diminished food effect on absorption in human
-
Wu Y, Loper A, Landis E, et al. The role of biopharmaceutics in the development of a clinical nanoparticle formulation of MK-0869:a Beagle dog model predicts improved bioavailability and diminished food effect on absorption in human. Int J Pharm 2004;285:135–46.
-
(2004)
Int J Pharm
, vol.285
, pp. 135-146
-
-
Wu, Y.1
Loper, A.2
Landis, E.3
-
28
-
-
51649116580
-
Rate-limiting steps of oral absorption for poorly watersoluble drugs in dogs; prediction from a Miniscale Dissolution Test and a physiologically-based computer simulation
-
Takano R, Furumoto K, Shiraki K, et al. Rate-limiting steps of oral absorption for poorly watersoluble drugs in dogs; prediction from a Miniscale Dissolution Test and a physiologically-based computer simulation. Pharm Res 2008;25:2334–44.
-
(2008)
Pharm Res
, vol.25
, pp. 2334-2344
-
-
Takano, R.1
Furumoto, K.2
Shiraki, K.3
|