-
1
-
-
0035478436
-
In vitro assessment of oral lipid based formulation
-
Porter C.J.H., and Charman W.N. In vitro assessment of oral lipid based formulation. Adv. Drug Deliv. Rev. 50 Suppl. 1 (2001) S127-S147
-
(2001)
Adv. Drug Deliv. Rev.
, vol.50
, Issue.SUPPL. 1
-
-
Porter, C.J.H.1
Charman, W.N.2
-
2
-
-
0027473738
-
Estimating the fraction dose absorbed from suspensions of poorly soluble compounds in human: a mathematical model
-
Doo-Man O., Curl R.L., and Amidon G.L. Estimating the fraction dose absorbed from suspensions of poorly soluble compounds in human: a mathematical model. Pharm. Res. 10 (1993) 264-270
-
(1993)
Pharm. Res.
, vol.10
, pp. 264-270
-
-
Doo-Man, O.1
Curl, R.L.2
Amidon, G.L.3
-
3
-
-
0242266530
-
Establishment of new preparation method of solid dispersion formulation of tacrolimus
-
Yamashita K., Nakate T., Okimoto K., Ohiki A., Tokunaga Y., Ibuki R., Higaki K., and Kimura T. Establishment of new preparation method of solid dispersion formulation of tacrolimus. Int. J. Pharm. 267 (2003) 79-91
-
(2003)
Int. J. Pharm.
, vol.267
, pp. 79-91
-
-
Yamashita, K.1
Nakate, T.2
Okimoto, K.3
Ohiki, A.4
Tokunaga, Y.5
Ibuki, R.6
Higaki, K.7
Kimura, T.8
-
4
-
-
33344478634
-
Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs
-
Jinno J., Kamada N., Miyake M., Yamada K., Mukai T., Odomi M., Toguchi H., Liversidge G.G., Higaki K., and Kimura T. Effect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogs. J. Control. Release 111 (2006) 56-64
-
(2006)
J. Control. Release
, vol.111
, pp. 56-64
-
-
Jinno, J.1
Kamada, N.2
Miyake, M.3
Yamada, K.4
Mukai, T.5
Odomi, M.6
Toguchi, H.7
Liversidge, G.G.8
Higaki, K.9
Kimura, T.10
-
5
-
-
0033816196
-
Intestinal permeation enhancers
-
Aungst B.J. Intestinal permeation enhancers. J. Pharm. Sci. 89 (2000) 429-442
-
(2000)
J. Pharm. Sci.
, vol.89
, pp. 429-442
-
-
Aungst, B.J.1
-
6
-
-
0036281181
-
Mechanisms of cytoprotective effect of amino acids on local toxicity caused by sodium laurate, a drug absorption enhancer, in intestinal epithelium
-
Endo Y., Hanada K., Miyake M., Ogawara K., Higaki K., and Kimura T. Mechanisms of cytoprotective effect of amino acids on local toxicity caused by sodium laurate, a drug absorption enhancer, in intestinal epithelium. J. Pharm. Sci. 91 (2002) 730-743
-
(2002)
J. Pharm. Sci.
, vol.91
, pp. 730-743
-
-
Endo, Y.1
Hanada, K.2
Miyake, M.3
Ogawara, K.4
Higaki, K.5
Kimura, T.6
-
7
-
-
33344468568
-
Novel oral formulation safely improving intestinal absorption of poorly absorbable drugs: utilization of polyamines and bile acids
-
Miyake M., Minami T., Hirota M., Toguchi H., Odomi M., Ogawara K., Higaki K., and Kimura T. Novel oral formulation safely improving intestinal absorption of poorly absorbable drugs: utilization of polyamines and bile acids. J. Control. Release 111 (2006) 27-34
-
(2006)
J. Control. Release
, vol.111
, pp. 27-34
-
-
Miyake, M.1
Minami, T.2
Hirota, M.3
Toguchi, H.4
Odomi, M.5
Ogawara, K.6
Higaki, K.7
Kimura, T.8
-
8
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon G.L., Lennernas H., Shah V.P., and Crison J.R. A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm. Res. 12 (1995) 413-420
-
(1995)
Pharm. Res.
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
9
-
-
0035997323
-
Biopharmaceutics classification system: the scientific basis for biowaiver extensions
-
Yu L.X., Amidon G.L., Polli J.E., Zhao H., Mehta M.U., Conner D.P., Shah V.P., Lesko L.J., Chen M.-L., Lee V.H.L., and Hussain A.S. Biopharmaceutics classification system: the scientific basis for biowaiver extensions. Pharm. Res. 19 (2002) 921-925
-
(2002)
Pharm. Res.
, vol.19
, pp. 921-925
-
-
Yu, L.X.1
Amidon, G.L.2
Polli, J.E.3
Zhao, H.4
Mehta, M.U.5
Conner, D.P.6
Shah, V.P.7
Lesko, L.J.8
Chen, M.-L.9
Lee, V.H.L.10
Hussain, A.S.11
-
10
-
-
3843097202
-
Classification of orally administered drugs on the World Health Organization model list of essential medicines according to the biopharmaceutics classification system
-
Lindenberg M., Kopp S., and Dressman J.B. Classification of orally administered drugs on the World Health Organization model list of essential medicines according to the biopharmaceutics classification system. Eur. J. Pharm. Biopharm. 58 (2004) 265-278
-
(2004)
Eur. J. Pharm. Biopharm.
, vol.58
, pp. 265-278
-
-
Lindenberg, M.1
Kopp, S.2
Dressman, J.B.3
-
11
-
-
0031750861
-
Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs
-
Galia E., Nicolaides E., Horter D., Lobenberg R., Reppas C., and Dressman J.B. Evaluation of various dissolution media for predicting in vivo performance of class I and II drugs. Pharm. Res. 15 (1998) 698-705
-
(1998)
Pharm. Res.
, vol.15
, pp. 698-705
-
-
Galia, E.1
Nicolaides, E.2
Horter, D.3
Lobenberg, R.4
Reppas, C.5
Dressman, J.B.6
-
12
-
-
0033805179
-
In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs
-
Dressman J.B., and Reppas C. In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs. Eur. J. Pharm. Sci. 11 Suppl. 2 (2000) S73-S80
-
(2000)
Eur. J. Pharm. Sci.
, vol.11
, Issue.SUPPL. 2
-
-
Dressman, J.B.1
Reppas, C.2
-
14
-
-
0028143513
-
Griseofulvin absorption from different sites in the human small intestine
-
Gramatte T. Griseofulvin absorption from different sites in the human small intestine. Biopharm. Drug Dispos. 15 (1994) 747-759
-
(1994)
Biopharm. Drug Dispos.
, vol.15
, pp. 747-759
-
-
Gramatte, T.1
-
15
-
-
0030928205
-
Prediction of the plasma concentration profiles of orally administered drugs in rats on the basis of gastrointestinal transit kinetics and absorbability
-
Sawamoto T., Haruta S., Kurosaki Y., Higaki K., and Kimura T. Prediction of the plasma concentration profiles of orally administered drugs in rats on the basis of gastrointestinal transit kinetics and absorbability. J. Pharm. Pharmacol. 49 (1997) 450-457
-
(1997)
J. Pharm. Pharmacol.
, vol.49
, pp. 450-457
-
-
Sawamoto, T.1
Haruta, S.2
Kurosaki, Y.3
Higaki, K.4
Kimura, T.5
-
16
-
-
0031680610
-
Absorption behavior of orally administered drugs in rats treated with propantheline
-
Haruta S., Iwasaki N., Ogawara K., Higaki K., and Kimura T. Absorption behavior of orally administered drugs in rats treated with propantheline. J. Pharm. Sci. 87 (1998) 1081-1085
-
(1998)
J. Pharm. Sci.
, vol.87
, pp. 1081-1085
-
-
Haruta, S.1
Iwasaki, N.2
Ogawara, K.3
Higaki, K.4
Kimura, T.5
-
17
-
-
0034009449
-
Analysis and prediction of absorption profile including hepatic first-pass metabolism of N-methyltyramine, a potent stimulant of gastrin release present in beer, after oral ingestion in rats by gastrointestinal-transit-absorption model
-
Kimura T., Iwasaki N., Yokoe J., Haruta S., Yokoo Y., Ogawara K., and Higaki K. Analysis and prediction of absorption profile including hepatic first-pass metabolism of N-methyltyramine, a potent stimulant of gastrin release present in beer, after oral ingestion in rats by gastrointestinal-transit-absorption model. Drug Metab. Dispos. 28 (2000) 577-581
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 577-581
-
-
Kimura, T.1
Iwasaki, N.2
Yokoe, J.3
Haruta, S.4
Yokoo, Y.5
Ogawara, K.6
Higaki, K.7
-
18
-
-
0036481691
-
Gastrointestinal transit and drug absorption
-
Kimura T., and Higaki K. Gastrointestinal transit and drug absorption. Biol. Pharm. Bull. 25 (2002) 149-164
-
(2002)
Biol. Pharm. Bull.
, vol.25
, pp. 149-164
-
-
Kimura, T.1
Higaki, K.2
-
19
-
-
0037449482
-
Analysis and prediction of absorption behavior of colon-targeted prodrug in rats by GI-transit-absorption model
-
Yokoe J., Iwasaki N., Haruta S., Kadono K., Ogawara K., Higaki K., and Kimura T. Analysis and prediction of absorption behavior of colon-targeted prodrug in rats by GI-transit-absorption model. J. Control. Release 86 (2003) 305-313
-
(2003)
J. Control. Release
, vol.86
, pp. 305-313
-
-
Yokoe, J.1
Iwasaki, N.2
Haruta, S.3
Kadono, K.4
Ogawara, K.5
Higaki, K.6
Kimura, T.7
-
20
-
-
0035070539
-
Evaluation of absorption kinetics of orally administered theophylline in rats based on gastrointestinal transit monitoring by gamma scintigraphy
-
Haruta S., Kawai K., Jinnouchi S., Ogawara K., Higaki K., Tamura S., Arimori K., and Kimura T. Evaluation of absorption kinetics of orally administered theophylline in rats based on gastrointestinal transit monitoring by gamma scintigraphy. J. Pharm. Sci. 90 (2001) 464-473
-
(2001)
J. Pharm. Sci.
, vol.90
, pp. 464-473
-
-
Haruta, S.1
Kawai, K.2
Jinnouchi, S.3
Ogawara, K.4
Higaki, K.5
Tamura, S.6
Arimori, K.7
Kimura, T.8
-
21
-
-
0037148655
-
Prediction plasma concentration-time curve of orally administered theophylline based on a scintigraphic monitoring of gastrointestinal transit in human volunteers
-
Haruta S., Kawai K., Nishii R., Jinnouchi S., Ogawara K., Higaki K., Tamura S., Arimori K., and Kimura T. Prediction plasma concentration-time curve of orally administered theophylline based on a scintigraphic monitoring of gastrointestinal transit in human volunteers. Int. J. Pharm. 233 (2002) 179-190
-
(2002)
Int. J. Pharm.
, vol.233
, pp. 179-190
-
-
Haruta, S.1
Kawai, K.2
Nishii, R.3
Jinnouchi, S.4
Ogawara, K.5
Higaki, K.6
Tamura, S.7
Arimori, K.8
Kimura, T.9
-
22
-
-
84982814204
-
Analysis and prediction of absorption behavior for theophylline orally administered as powders based on gastrointestinal-transit-absorption (GITA) model
-
Kadono K., Yokoe J., Ogawara K., Higaki K., and Kimura T. Analysis and prediction of absorption behavior for theophylline orally administered as powders based on gastrointestinal-transit-absorption (GITA) model. Drug Metab. Pharmacokinet. 17 (2002) 307-315
-
(2002)
Drug Metab. Pharmacokinet.
, vol.17
, pp. 307-315
-
-
Kadono, K.1
Yokoe, J.2
Ogawara, K.3
Higaki, K.4
Kimura, T.5
-
24
-
-
0014788109
-
Effect of bile salts on the gastrointestinal absorption of drugs. II. Mechanism of the enhancement of the intestinal absorption of sulfaguanidine by bile salts
-
Kakemi K., Sezaki H., Konishi R., Kimura T., and Okita A. Effect of bile salts on the gastrointestinal absorption of drugs. II. Mechanism of the enhancement of the intestinal absorption of sulfaguanidine by bile salts. Chem. Pharm. Bull. 18 (1970) 1034-1039
-
(1970)
Chem. Pharm. Bull.
, vol.18
, pp. 1034-1039
-
-
Kakemi, K.1
Sezaki, H.2
Konishi, R.3
Kimura, T.4
Okita, A.5
-
25
-
-
0031719454
-
Some relation ships between the physical properties of various 3-acyloxymethyl prodrugs of phenytoin to structure: potential in vivo performance implications
-
Stella V.J., Martodihardio S., Terada K., and Rao V.M. Some relation ships between the physical properties of various 3-acyloxymethyl prodrugs of phenytoin to structure: potential in vivo performance implications. J. Pharm. Sci. 87 (1998) 1235-1241
-
(1998)
J. Pharm. Sci.
, vol.87
, pp. 1235-1241
-
-
Stella, V.J.1
Martodihardio, S.2
Terada, K.3
Rao, V.M.4
-
26
-
-
0032795383
-
Aqueous solubility and dissolution rate dose not adequately predict in vivo performance: a probe utilizing some N-acylixymethyl phenytoin prodrugs
-
Stella V.J., Martodihardio S., and Rao V.M. Aqueous solubility and dissolution rate dose not adequately predict in vivo performance: a probe utilizing some N-acylixymethyl phenytoin prodrugs. J. Pharm. Sci. 88 (1998) 775-779
-
(1998)
J. Pharm. Sci.
, vol.88
, pp. 775-779
-
-
Stella, V.J.1
Martodihardio, S.2
Rao, V.M.3
-
29
-
-
0017084526
-
Plasma concentrations of griseofulvin in healthy volunteers and out-patients treated for onychomycosis
-
Hägermark Ö., Berlin A., Wallin I., and Boréus O.L. Plasma concentrations of griseofulvin in healthy volunteers and out-patients treated for onychomycosis. Acta Dermatovenerol. 56 (1976) 289-296
-
(1976)
Acta Dermatovenerol.
, vol.56
, pp. 289-296
-
-
Hägermark, Ö.1
Berlin, A.2
Wallin, I.3
Boréus, O.L.4
-
30
-
-
0020408449
-
Arterial and venous blood sampling in pharmacokinetic studies: griseofulvin
-
Chen M.-L., Lam G., Lee M.G., and Chiou W.L. Arterial and venous blood sampling in pharmacokinetic studies: griseofulvin. J. Pharm. Sci. 71 (1982) 1386-1389
-
(1982)
J. Pharm. Sci.
, vol.71
, pp. 1386-1389
-
-
Chen, M.-L.1
Lam, G.2
Lee, M.G.3
Chiou, W.L.4
-
31
-
-
0015124660
-
Absorption characteristics of solid dispersed and micronized griseofulvin in man
-
Chiou W.L., and Riegelman S. Absorption characteristics of solid dispersed and micronized griseofulvin in man. J. Pharm. Sci. 60 (1971) 1376-1380
-
(1971)
J. Pharm. Sci.
, vol.60
, pp. 1376-1380
-
-
Chiou, W.L.1
Riegelman, S.2
-
32
-
-
0019957357
-
Bioavailability of griseofulvin from tablets in beagle dogs and correlation rate and bioavailability in humans
-
Aoyagi N., Ogata H., Kaniwa N., Koibuchi M., Shibazaki T., Ejima A., Tamaki N., Kamimura H., Katougi Y., and Omi Y. Bioavailability of griseofulvin from tablets in beagle dogs and correlation rate and bioavailability in humans. J. Pharm. Sci. 71 (1982) 1169-1173
-
(1982)
J. Pharm. Sci.
, vol.71
, pp. 1169-1173
-
-
Aoyagi, N.1
Ogata, H.2
Kaniwa, N.3
Koibuchi, M.4
Shibazaki, T.5
Ejima, A.6
Tamaki, N.7
Kamimura, H.8
Katougi, Y.9
Omi, Y.10
-
33
-
-
0018154657
-
Intestinal absorption of griseofulvin from a triolein digestion mixture in rats
-
Grisafe J.A., and Hayton W.L. Intestinal absorption of griseofulvin from a triolein digestion mixture in rats. J. Pharm. Sci. 67 (1978) 895-899
-
(1978)
J. Pharm. Sci.
, vol.67
, pp. 895-899
-
-
Grisafe, J.A.1
Hayton, W.L.2
-
34
-
-
0000919395
-
Development of in vitro dissolution tests witch correlate quantitatively with dissolution rate-limited drug absorption in man
-
Levy G., Leeonards J.R., and Prockual J.A. Development of in vitro dissolution tests witch correlate quantitatively with dissolution rate-limited drug absorption in man. J. Pharm. Sci. 54 (1965) 1719-1722
-
(1965)
J. Pharm. Sci.
, vol.54
, pp. 1719-1722
-
-
Levy, G.1
Leeonards, J.R.2
Prockual, J.A.3
-
35
-
-
0014138173
-
Establishment of sink conditions in dissolution rate determinations: Theoretical considerations and application to nondisintegrating dosage forms
-
Gibaldi M., and Feldman S. Establishment of sink conditions in dissolution rate determinations: Theoretical considerations and application to nondisintegrating dosage forms. J. Pharm. Sci. 56 (1967) 1238-1242
-
(1967)
J. Pharm. Sci.
, vol.56
, pp. 1238-1242
-
-
Gibaldi, M.1
Feldman, S.2
|