-
1
-
-
0022359497
-
Improving the intestinal mucosal cell uptake of water insoluble compounds
-
G.L. Amidon Improving the intestinal mucosal cell uptake of water insoluble compounds J. Controlled Release 2 1985 13 26
-
(1985)
J. Controlled Release
, vol.2
, pp. 13-26
-
-
Amidon, G.L.1
-
2
-
-
33748778747
-
Inducing effect of liposomalization on the transdermal delivery of hydrocortisone: Creation of a drug supersaturated state
-
J.M. Barichello, H. Handa, M. Kisyku, T. Shibata, T. Ishida, and H. Kiwada Inducing effect of liposomalization on the transdermal delivery of hydrocortisone: creation of a drug supersaturated state J. Controlled Release 115 2006 94 102
-
(2006)
J. Controlled Release
, vol.115
, pp. 94-102
-
-
Barichello, J.M.1
Handa, H.2
Kisyku, M.3
Shibata, T.4
Ishida, T.5
Kiwada, H.6
-
3
-
-
68249128120
-
Supersaturating drug delivery systems: The answer to solubility-limited oral bioavailability?
-
J. Brouwers, M.E. Brewster, and P. Augustijns Supersaturating drug delivery systems: the answer to solubility-limited oral bioavailability? J. Pharm. Sci. 98 2009 2549 2572
-
(2009)
J. Pharm. Sci.
, vol.98
, pp. 2549-2572
-
-
Brouwers, J.1
Brewster, M.E.2
Augustijns, P.3
-
4
-
-
41349119990
-
Combination of pluronic/vitamin e TPGS as a potential inhibitor of drug precipitation
-
W. Dai, L.C. Dong, S. Li, and Z. Deng Combination of pluronic/vitamin E TPGS as a potential inhibitor of drug precipitation Int. J. Pharm. 355 2008 31 37
-
(2008)
Int. J. Pharm.
, vol.355
, pp. 31-37
-
-
Dai, W.1
Dong, L.C.2
Li, S.3
Deng, Z.4
-
5
-
-
79959603915
-
Liposomal solubilization of new 3-hydroxy-qionolinone derivatives with promising anticancer activity: A screening method to identify maximum incorporation capacity
-
M. Di Cagno, J. Styskala, J. Hlaváč, M. Brandl, A. Bauer-Brandl, and N. Skalko-Basnet Liposomal solubilization of new 3-hydroxy-qionolinone derivatives with promising anticancer activity: a screening method to identify maximum incorporation capacity J. Lipos. Res. 21 2011 272 278
-
(2011)
J. Lipos. Res.
, vol.21
, pp. 272-278
-
-
Di Cagno, M.1
Styskala, J.2
Hlaváč, J.3
Brandl, M.4
Bauer-Brandl, A.5
Skalko-Basnet, N.6
-
6
-
-
84858157244
-
Overcoming instability and low solubility of new cytostatic compounds: A comparison of two approaches
-
M. Di Cagno, P.C. Stein, J. Styskala, J. Hlaváč, N. Skalko-Basnet, and A. Bauer-Brandl Overcoming instability and low solubility of new cytostatic compounds: a comparison of two approaches Eur. J. Pharm. Biopharm. 80 2012 657 662
-
(2012)
Eur. J. Pharm. Biopharm.
, vol.80
, pp. 657-662
-
-
Di Cagno, M.1
Stein, P.C.2
Styskala, J.3
Hlaváč, J.4
Skalko-Basnet, N.5
Bauer-Brandl, A.6
-
8
-
-
34547864243
-
Drug delivery strategies for poorly water-soluble drugs
-
A. Fahr, and X. Liu Drug delivery strategies for poorly water-soluble drugs Expert Opin. Drug Deliv. 4 2007 403 416
-
(2007)
Expert Opin. Drug Deliv.
, vol.4
, pp. 403-416
-
-
Fahr, A.1
Liu, X.2
-
9
-
-
80054996010
-
Effect of the non-ionic surfactant Poloxamer 188 on passive permeability of poorly soluble drugs across caco-2 cell monolayers
-
S.M. Fischer, M. Brandl, and G. Fricker Effect of the non-ionic surfactant Poloxamer 188 on passive permeability of poorly soluble drugs across caco-2 cell monolayers Eur. J. Pharm. Biopharm. 79 2011 416 422
-
(2011)
Eur. J. Pharm. Biopharm.
, vol.79
, pp. 416-422
-
-
Fischer, S.M.1
Brandl, M.2
Fricker, G.3
-
10
-
-
84861211886
-
Impact of FaSSIF on the solubility and dissolution-/permeation rate of a poorly water-soluble compound
-
K.J. Frank, U. Westedt, K.M. Rosenblatt, P. Hölig, J. Rosenberg, M. Mägerlein, M. Brandl, and G. Fricker Impact of FaSSIF on the solubility and dissolution-/permeation rate of a poorly water-soluble compound Eur. J. Pharm. Sci. 47 2012 16 20
-
(2012)
Eur. J. Pharm. Sci.
, vol.47
, pp. 16-20
-
-
Frank, K.J.1
Westedt, U.2
Rosenblatt, K.M.3
Hölig, P.4
Rosenberg, J.5
Mägerlein, M.6
Brandl, M.7
Fricker, G.8
-
11
-
-
0021257379
-
Influence of liposomal drug entrapment on percutaneous absorption
-
M.G. Ganesan, N.D. Weiner, G.L. Flynn, and N.F.H. Ho Influence of liposomal drug entrapment on percutaneous absorption Int. J. Pharm. 20 1984 139 154
-
(1984)
Int. J. Pharm.
, vol.20
, pp. 139-154
-
-
Ganesan, M.G.1
Weiner, N.D.2
Flynn, G.L.3
Ho, N.F.H.4
-
12
-
-
0029760056
-
Nasal delivery. the use of animal models to predict performance in man
-
L. Illium Nasal delivery. The use of animal models to predict performance in man J. Drug Target. 3 1996 427 442
-
(1996)
J. Drug Target.
, vol.3
, pp. 427-442
-
-
Illium, L.1
-
13
-
-
33749987516
-
Permeability assessment of poorly water-soluble compounds under solubilizing conditions, the reciprocal permeability approach
-
K. Katneni, S.A. Charman, and C.J.H. Porter Permeability assessment of poorly water-soluble compounds under solubilizing conditions, the reciprocal permeability approach J. Pharm. Sci. 95 2006 2170 2185
-
(2006)
J. Pharm. Sci.
, vol.95
, pp. 2170-2185
-
-
Katneni, K.1
Charman, S.A.2
Porter, C.J.H.3
-
14
-
-
0342561507
-
The effect of water-soluble polymers on aqueous solubility of drugs
-
T. Loftsson, H. Fridriksdóttir, and T.K. Gudmundsdóttir The effect of water-soluble polymers on aqueous solubility of drugs Int. J. Pharm. 127 1996 293 296
-
(1996)
Int. J. Pharm.
, vol.127
, pp. 293-296
-
-
Loftsson, T.1
Fridriksdóttir, H.2
Gudmundsdóttir, T.K.3
-
16
-
-
0032927356
-
The effect of disordered structure on the solubility and dissolution rates of some hydrophilic, sparingly soluble drugs
-
M. Mosharraf, T. Sebhatu, and C. Nyström The effect of disordered structure on the solubility and dissolution rates of some hydrophilic, sparingly soluble drugs Int. J. Pharm. 177 1999 29 51
-
(1999)
Int. J. Pharm.
, vol.177
, pp. 29-51
-
-
Mosharraf, M.1
Sebhatu, T.2
Nyström, C.3
-
17
-
-
72449187503
-
Prodrug approaches for enhancing the bioavailability of drugs with low solubility
-
C.E. Muller Prodrug approaches for enhancing the bioavailability of drugs with low solubility Chem. Biodivers. 6 2009 2071 2083
-
(2009)
Chem. Biodivers.
, vol.6
, pp. 2071-2083
-
-
Muller, C.E.1
-
18
-
-
0034019525
-
Dissolution of hydrocortisone in human and simulated intestinal fluids
-
B.L. Pedersen, H. Brøndsted, H. Lennernäs, F.N. Christensen, A. Müllertz, and H.G. Kristensen Dissolution of hydrocortisone in human and simulated intestinal fluids Pharm. Res. 17 2000 183 189
-
(2000)
Pharm. Res.
, vol.17
, pp. 183-189
-
-
Pedersen, B.L.1
Brøndsted, H.2
Lennernäs, H.3
Christensen, F.N.4
Müllertz, A.5
Kristensen, H.G.6
-
21
-
-
0032484673
-
In vitro cell models to study nasal mucosal permeability and metabolism
-
M.C. Schmidt, H. Peter, S.R. Lang, G. Ditzinger, and H.P. Merkle In vitro cell models to study nasal mucosal permeability and metabolism Adv. Drug. Deliver. Rev. 29 1998 51 79
-
(1998)
Adv. Drug. Deliver. Rev.
, vol.29
, pp. 51-79
-
-
Schmidt, M.C.1
Peter, H.2
Lang, S.R.3
Ditzinger, G.4
Merkle, H.P.5
-
22
-
-
0037467195
-
Influence of micelle solubilization by tocopheryl polyethylene glycol succinate (TPGS) on solubility enhancement and percutaneous penetration of estradiol
-
M. Sheu, S. Chen, L. Chen, and H. Ho Influence of micelle solubilization by tocopheryl polyethylene glycol succinate (TPGS) on solubility enhancement and percutaneous penetration of estradiol J. Controlled Release 88 2003 355 368
-
(2003)
J. Controlled Release
, vol.88
, pp. 355-368
-
-
Sheu, M.1
Chen, S.2
Chen, L.3
Ho, H.4
-
23
-
-
0030574681
-
The role of percutaneous penetration enhancers
-
R.B. Walker, and E.W. Smith The role of percutaneous penetration enhancers Adv. Drug Deliv. Rev. 18 1996 295 301
-
(1996)
Adv. Drug Deliv. Rev.
, vol.18
, pp. 295-301
-
-
Walker, R.B.1
Smith, E.W.2
-
24
-
-
0033427847
-
Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability
-
L. Yu, A. Bridges, J. Polli, A. Vickers, S. Long, A. Roy, R. Winnike, and M. Coffin Vitamin E-TPGS increases absorption flux of an HIV protease inhibitor by enhancing its solubility and permeability Pharm. Res. 16 1999 1812 1817
-
(1999)
Pharm. Res.
, vol.16
, pp. 1812-1817
-
-
Yu, L.1
Bridges, A.2
Polli, J.3
Vickers, A.4
Long, S.5
Roy, A.6
Winnike, R.7
Coffin, M.8
|