-
1
-
-
34547128386
-
In vitro and in vivo evaluation of a fast-disintegrating lyophilized dry emulsion tablet containing griseofulvin
-
DOI 10.1016/j.ejps.2007.05.114, PII S0928098707002564
-
I.S. Ahmed, and M.H. Aboul-Einien In vitro and in vivo evaluation of a fast-disintegrating lyophilized dry emulsion tablet containing griseofulvin Eur. J. Pharm. Sci. 32 1 2007 58 68 (Pubitemid 47102190)
-
(2007)
European Journal of Pharmaceutical Sciences
, vol.32
, Issue.1
, pp. 58-68
-
-
Ahmed, I.S.1
Aboul-Einien, M.H.2
-
2
-
-
0028948839
-
A theoretical basis for a biopharmaceutical drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
G.L. Amidon, H. Lennernas, V.P. Shah, and J.R.A. Crison A theoretical basis for a biopharmaceutical 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.A.4
-
3
-
-
34548134519
-
Cyclodextrins as pharmaceutical solubilizers
-
DOI 10.1016/j.addr.2007.05.012, PII S0169409X07000841
-
M.E. Brewster, and T. Loftsson Cyclodextrins as pharmaceutical solubilizers Adv. Drug Deliv. Rev. 59 2007 645 666 (Pubitemid 47299263)
-
(2007)
Advanced Drug Delivery Reviews
, vol.59
, Issue.7
, pp. 645-666
-
-
Brewster, M.E.1
Loftsson, T.2
-
4
-
-
35248822616
-
The utility of cyclodextrins for enhancing oral bioavailability
-
DOI 10.1016/j.jconrel.2007.07.018, PII S0168365907004129
-
R.L. Carrier, L.A. Miller, and I. Ahmed The utility of cyclodextrins for enhancing oral bioavailability J. Control. Rel. 123 2007 78 99 (Pubitemid 47566400)
-
(2007)
Journal of Controlled Release
, vol.123
, Issue.2
, pp. 78-99
-
-
Carrier, R.L.1
Miller, L.A.2
Ahmed, I.3
-
5
-
-
84859432248
-
Solid dispersions of itraconazole for inhalation with enhanced dissolution, solubility and dispersion properties
-
C. Duret, N. Wauthoz, T. Sebti, F. Vanderbist, and K. Amighi Solid dispersions of itraconazole for inhalation with enhanced dissolution, solubility and dispersion properties Int. J. Pharm. 428 2012 103 113
-
(2012)
Int. J. Pharm.
, vol.428
, pp. 103-113
-
-
Duret, C.1
Wauthoz, N.2
Sebti, T.3
Vanderbist, F.4
Amighi, K.5
-
6
-
-
64649100465
-
Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions: An overview
-
D.T. Friesen, R. Shanker, M. Crew, D.T. Smithey, W.J. Curatolo, and J.A.S. Nightingale Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions: an overview Mol. Pharm. 5 6 2008 1003 1019
-
(2008)
Mol. Pharm.
, vol.5
, Issue.6
, pp. 1003-1019
-
-
Friesen, D.T.1
Shanker, R.2
Crew, M.3
Smithey, D.T.4
Curatolo, W.J.5
Nightingale, J.A.S.6
-
7
-
-
0036844753
-
Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules
-
DOI 10.1023/A:1020905412654
-
M.K. Gupta, Y.C. Tseng, D. Goldman, and R.H. Bogner Hydrogen bonding with adsorbent during storage governs drug dissolution from solid-dispersion granules Pharm. Res. 19 11 2002 1663 1672 (Pubitemid 35305518)
-
(2002)
Pharmaceutical Research
, vol.19
, Issue.11
, pp. 1663-1672
-
-
Gupta, M.K.1
Tseng, Y.-C.2
Goldman, D.3
Bogner, R.H.4
-
8
-
-
1842684453
-
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
-
DOI 10.1016/j.biopha.2004.02.001, PII S0753332204000319
-
R.N. Gursoy, and S. Benita Self emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs Biomed. Pharmacother. 58 2004 173 182 (Pubitemid 38479922)
-
(2004)
Biomedicine and Pharmacotherapy
, vol.58
, Issue.3
, pp. 173-182
-
-
Gursoy, R.N.1
Benita, S.2
-
9
-
-
79960161186
-
Enhanced dissolution and bioavailability of biochanin A via the preparation of solid dispersion: In vitro and in vivo evaluation
-
H.K. Han, B.J. Lee, and H.K. Lee Enhanced dissolution and bioavailability of biochanin A via the preparation of solid dispersion: in vitro and in vivo evaluation Int. J. Pharm. 415 2011 89 94
-
(2011)
Int. J. Pharm.
, vol.415
, pp. 89-94
-
-
Han, H.K.1
Lee, B.J.2
Lee, H.K.3
-
10
-
-
0036176196
-
Production and characterization of a budesonide nanosuspension for pulmonary administration
-
DOI 10.1023/A:1014276917363
-
C. Jacobs, and R.H. Müller Production and characterization of a budesonide nanosuspension for pulmonary administration Pharm. Res. 19 2 2002 189 194 (Pubitemid 34165405)
-
(2002)
Pharmaceutical Research
, vol.19
, Issue.2
, pp. 189-194
-
-
Jacobs, C.1
Muller, R.H.2
-
11
-
-
67349158352
-
Spray drying from complex solvent systems broadens the applicability of Kollicoat IR as a carrier in the formulation of solid dispersions
-
S. Janssens, M. Anné, P. Rombaut, and G. Van den Mooter Spray drying from complex solvent systems broadens the applicability of Kollicoat IR as a carrier in the formulation of solid dispersions Eur. J. Pharm. Sci. 35 2009 241 248
-
(2009)
Eur. J. Pharm. Sci.
, vol.35
, pp. 241-248
-
-
Janssens, S.1
Anné, M.2
Rombaut, P.3
Van Den Mooter, G.4
-
12
-
-
77957017430
-
Stable nimodipine tablets with high bioavailability containing NM-SD prepared by hot-melt extrusion
-
F. Jijun, Z. Lili, G. Tingting, T. Xing, and H. Haibing Stable nimodipine tablets with high bioavailability containing NM-SD prepared by hot-melt extrusion Powder Technol. 204 2010 214 221
-
(2010)
Powder Technol.
, vol.204
, pp. 214-221
-
-
Jijun, F.1
Lili, Z.2
Tingting, G.3
Xing, T.4
Haibing, H.5
-
14
-
-
69749103682
-
Nanocrystal technology, drug delivery and clinical applications
-
J.A.H. Junghanns, and R.H. Müller Nanocrystal technology, drug delivery and clinical applications Int. J. Nanomed. 3 3 2008 295 309
-
(2008)
Int. J. Nanomed.
, vol.3
, Issue.3
, pp. 295-309
-
-
Junghanns, J.A.H.1
Müller, R.H.2
-
15
-
-
84859598844
-
Application of mixtures of polymeric carriers for dissolution enhancement of fenofibrate using hot-melt extrusion
-
A. Kalivoda, M. Fischbach, and P. Kleinebudde Application of mixtures of polymeric carriers for dissolution enhancement of fenofibrate using hot-melt extrusion Int. J. Pharm. 429 2012 58 68
-
(2012)
Int. J. Pharm.
, vol.429
, pp. 58-68
-
-
Kalivoda, A.1
Fischbach, M.2
Kleinebudde, P.3
-
16
-
-
75449106350
-
Novel crystalline solid dispersion of tranilast with high photostability and improved oral bioavailability
-
Y. Kawabata, K. Yamamoto, K. Debari, S. Onoue, and S. Yamada Novel crystalline solid dispersion of tranilast with high photostability and improved oral bioavailability Eur. J. Pharm. Sci. 39 2010 256 262
-
(2010)
Eur. J. Pharm. Sci.
, vol.39
, pp. 256-262
-
-
Kawabata, Y.1
Yamamoto, K.2
Debari, K.3
Onoue, S.4
Yamada, S.5
-
17
-
-
34249790272
-
Application of nanoparticles in oral delivery of immediate release formulations
-
DOI 10.2174/157341307780619251
-
F. Kesisoglou, S. Panmai, and Y. Wu Application of nanoparticles in oral delivery of immediate release formulations Curr. Nanosci. 3 2007 183 190 (Pubitemid 46845725)
-
(2007)
Current Nanoscience
, vol.3
, Issue.2
, pp. 183-190
-
-
Kesisoglou, F.1
Panmai, S.2
Wu, Y.3
-
18
-
-
67650806122
-
Particle characterization poorly water-soluble drugs using a spray freeze drying technique
-
M. Kondo, T. Niwa, and K. Danjo Particle characterization poorly water-soluble drugs using a spray freeze drying technique Chem. Pharm. Bull. 57 7 2009 657 662
-
(2009)
Chem. Pharm. Bull.
, vol.57
, Issue.7
, pp. 657-662
-
-
Kondo, M.1
Niwa, T.2
Danjo, K.3
-
19
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
DOI 10.1016/S0939-6411(00)00076-X, PII S093964110000076X
-
C. Leuner, and J.B. Dressman Improving drug solubility for oral delivery using solid dispersion Eur. J. Pharm. Sci. 50 2000 47 60 (Pubitemid 30326688)
-
(2000)
European Journal of Pharmaceutics and Biopharmaceutics
, vol.50
, Issue.1
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
20
-
-
0034461768
-
Drug-like properties and the causes of poor solubility and poor permeability
-
DOI 10.1016/S1056-8719(00)00107-6, PII S1056871900001076
-
C.A. Lipinski Drug-like properties and the causes of poor solubility and poor permeability J. Pharmacol. Toxicol. Meth. 44 2000 235 249 (Pubitemid 32239479)
-
(2000)
Journal of Pharmacological and Toxicological Methods
, vol.44
, Issue.1
, pp. 235-249
-
-
Lipinski, C.A.1
-
21
-
-
0036742053
-
Poor aqueous solubility an industry wide problem in drug discovery
-
C.A. Lipinski Poor aqueous solubility an industry wide problem in drug discovery Am. Pharm. Rev. 5 2002 82 85
-
(2002)
Am. Pharm. Rev.
, vol.5
, pp. 82-85
-
-
Lipinski, C.A.1
-
22
-
-
41949100244
-
Drug nanoparticles: Formulating poorly water soluble compounds
-
E.M. Merisko-Liversidge, and G.G. Liversidge Drug nanoparticles: formulating poorly water soluble compounds Toxicol. Pathol. 36 2008 43 48
-
(2008)
Toxicol. Pathol.
, vol.36
, pp. 43-48
-
-
Merisko-Liversidge, E.M.1
Liversidge, G.G.2
-
24
-
-
77952887486
-
Different modes of dynamic image analysis in monitoring of pharmaceutical dry milling process
-
V.R. Nalluri, P. Schirg, X. Gao, A. Virdis, G. Imanidis, and M. Kuentz Different modes of dynamic image analysis in monitoring of pharmaceutical dry milling process Inter. J. Pharm. 391 2010 107 114
-
(2010)
Inter. J. Pharm.
, vol.391
, pp. 107-114
-
-
Nalluri, V.R.1
Schirg, P.2
Gao, X.3
Virdis, A.4
Imanidis, G.5
Kuentz, M.6
-
25
-
-
70350211854
-
Design of porous microparticles with single-micron size by novel spray freeze-drying technique using four-fluid nozzle
-
T. Niwa, H. Shimabara, M. Kondo, and K. Danjo Design of porous microparticles with single-micron size by novel spray freeze-drying technique using four-fluid nozzle Int. J. Pharm. 382 2009 88 97
-
(2009)
Int. J. Pharm.
, vol.382
, pp. 88-97
-
-
Niwa, T.1
Shimabara, H.2
Kondo, M.3
Danjo, K.4
-
26
-
-
76149106514
-
Novel spray freeze-drying technique using four-fluid nozzle - Development of organic solvent system to expand its application to poorly water soluble drugs
-
T. Niwa, H. Shimabara, M. Kondo, and K. Danjo Novel spray freeze-drying technique using four-fluid nozzle - development of organic solvent system to expand its application to poorly water soluble drugs Chem. Pharm. Bull. 58 2 2010 195 200
-
(2010)
Chem. Pharm. Bull.
, vol.58
, Issue.2
, pp. 195-200
-
-
Niwa, T.1
Shimabara, H.2
Kondo, M.3
Danjo, K.4
-
27
-
-
79151476729
-
Universal wet-milling technique to prepare oral nanosuspension focused on discovery and preclinical animal studies - Development of particle design method
-
T. Niwa, S. Miura, and K. Danjo Universal wet-milling technique to prepare oral nanosuspension focused on discovery and preclinical animal studies - development of particle design method Int. J. Pharm. 405 2011 218 227
-
(2011)
Int. J. Pharm.
, vol.405
, pp. 218-227
-
-
Niwa, T.1
Miura, S.2
Danjo, K.3
-
28
-
-
80054759755
-
Design of dry nanosuspension with highly spontaneous dispersible characteristics to develop solubilized formulation for poorly water-soluble drugs
-
T. Niwa, S. Miura, and K. Danjo Design of dry nanosuspension with highly spontaneous dispersible characteristics to develop solubilized formulation for poorly water-soluble drugs Pharm. Res. 28 9 2011 2339 2349
-
(2011)
Pharm. Res.
, vol.28
, Issue.9
, pp. 2339-2349
-
-
Niwa, T.1
Miura, S.2
Danjo, K.3
-
29
-
-
84884526862
-
Design of porous microparticles by spray freeze-drying (SFD) technique and effect of particle density on dry powder inhalation behaviors
-
T. Niwa, D. Mizutani, and K. Danjo Design of porous microparticles by spray freeze-drying (SFD) technique and effect of particle density on dry powder inhalation behaviors J. Soc. Powder Technol. Japan. 49 8 2012 608 613
-
(2012)
J. Soc. Powder Technol. Japan.
, vol.49
, Issue.8
, pp. 608-613
-
-
Niwa, T.1
Mizutani, D.2
Danjo, K.3
-
30
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
A.A. Noyes, and W.R. Whitney The rate of solution of solid substances in their own solutions J. Am. Chem. Soc. 19 1897 930 934
-
(1897)
J. Am. Chem. Soc.
, vol.19
, pp. 930-934
-
-
Noyes, A.A.1
Whitney, W.R.2
-
31
-
-
39549094916
-
Formulation mechanism of colloidal nanoparticles obtained from probucol/PVP/SDS ternary ground mixture
-
A. Pongpeerapat, C. Wanawongthai, Y. Tozuka, K. Moribe, and K. Yamamoto Formulation mechanism of colloidal nanoparticles obtained from probucol/PVP/SDS ternary ground mixture Int. J. Pharm. 352 2008 309 316
-
(2008)
Int. J. Pharm.
, vol.352
, pp. 309-316
-
-
Pongpeerapat, A.1
Wanawongthai, C.2
Tozuka, Y.3
Moribe, K.4
Yamamoto, K.5
-
32
-
-
0033805858
-
Lipid formulations for oral administration of drugs: Non-emulsifying, self-emulsifying and "self-microemulsifying" drug delivery systems
-
C.W. Pouton Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and "self-microemulsifying" drug delivery systems Eur. J. Pharm. Sci. 11 2000 93 98
-
(2000)
Eur. J. Pharm. Sci.
, vol.11
, pp. 93-98
-
-
Pouton, C.W.1
-
33
-
-
84868545732
-
The use of amorphous solid dispersions: A formulation strategy to overcome poor solubility and dissolution rate
-
G. Van den Mooter The use of amorphous solid dispersions: a formulation strategy to overcome poor solubility and dissolution rate Drug Disc. Today Technol. 9 2012 79 85
-
(2012)
Drug Disc. Today Technol.
, vol.9
, pp. 79-85
-
-
Van Den Mooter, G.1
-
34
-
-
34249039982
-
Characterization of physico-chemical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti-HIV agent loviride prepared by media milling
-
DOI 10.1016/j.ijpharm.2007.02.005, PII S0378517307001573
-
B. Van Eerdenbrugh, L. Froyen, J.A. Martens, N. Blaton, P. Augustijns, M. Brewster, and G. Van den Mooter Characterization of physico-chemical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti-HIV agent loviride prepared by media Int. J. Pharm. 338 2007 198 206 (Pubitemid 46779149)
-
(2007)
International Journal of Pharmaceutics
, vol.338
, Issue.1-2
, pp. 198-206
-
-
Van Eerdenbrugh, B.1
Froyen, L.2
Martens, J.A.3
Blaton, N.4
Augustijns, P.5
Brewster, M.6
Van Den Mooter, G.7
-
35
-
-
48849111481
-
Drying of crystalline drug nanosuspensions - The importance of surface hydrophobicity on dissolution behavior upon redispersion
-
B. Van Eerdenbrugh, L. Froyen, J. Van Humbeeck, J.A. Martens, P. Van Augustijns, and G. den Mooter Drying of crystalline drug nanosuspensions - the importance of surface hydrophobicity on dissolution behavior upon redispersion Eur. J. Pharm. Sci. 35 2008 127 135
-
(2008)
Eur. J. Pharm. Sci.
, vol.35
, pp. 127-135
-
-
Van Eerdenbrugh, B.1
Froyen, L.2
Van Humbeeck, J.3
Martens, J.A.4
Van Augustijns, P.5
Den Mooter, G.6
-
36
-
-
53849109902
-
Alternative matrix formers for nanosuspension solidification: Dissolution performance and X-ray microanalysis as an evaluation tool for powder dispersion
-
B. Van Eerdenbrugh, L. Froyen, J. Van Humbeeck, J.A. Martens, P. Van Augustijns, and G. den Mooter Alternative matrix formers for nanosuspension solidification: dissolution performance and X-ray microanalysis as an evaluation tool for powder dispersion Eur. J. Pharm. Sci. 35 2008 344 353
-
(2008)
Eur. J. Pharm. Sci.
, vol.35
, pp. 344-353
-
-
Van Eerdenbrugh, B.1
Froyen, L.2
Van Humbeeck, J.3
Martens, J.A.4
Van Augustijns, P.5
Den Mooter, G.6
-
37
-
-
15244352260
-
Progress in drying technology for nanomaterials
-
DOI 10.1081/DRT-200047900
-
B.H. Wang, W.B. Zhang, W. Zhang, A.S. Mujumdar, and L.X. Huang Progress in drying technology for nanomaterials Dry. Technol. 23 2005 7 32 (Pubitemid 40390262)
-
(2005)
Drying Technology
, vol.23
, Issue.1-2 SPEC. ISS.
, pp. 7-32
-
-
Wang, B.1
Zhang, W.2
Zhang, W.3
Mujumdar, A.S.4
Huang, L.5
-
38
-
-
84863545483
-
Use of the co-grinding method to enhance the dissolution behavior of a poorly water-soluble drug: Generation of solvent-free drug-polymer solid dispersions
-
C. Yang, X. Xu, J. Wang, and A. An Use of the co-grinding method to enhance the dissolution behavior of a poorly water-soluble drug: generation of solvent-free drug-polymer solid dispersions Chem. Pharm. Bull. 60 7 2012 837 845
-
(2012)
Chem. Pharm. Bull.
, vol.60
, Issue.7
, pp. 837-845
-
-
Yang, C.1
Xu, X.2
Wang, J.3
An, A.4
|