-
1
-
-
0035024266
-
Comparison of impact of the different hydrophilic carriers on the properties of piperazine-containing drug
-
Ahmed MO (2001) Comparison of impact of the different hydrophilic carriers on the properties of piperazine-containing drug. Bur J Pharm Biopharm 51: 221-226.
-
(2001)
Bur J Pharm Biopharm
, vol.51
, pp. 221-226
-
-
Ahmed, M.O.1
-
2
-
-
0028948839
-
A theoretical basis for biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon GL, Lennernäs H, Shah VP, Crison JR (1995) A theoretical basis for biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 12: 413-420.
-
(1995)
Pharm Res
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernäs, H.2
Shah, V.P.3
Crison, J.R.4
-
3
-
-
0037407282
-
Human jejunal permeability of cyclosporin A: Influence of surfactants on P-glycoprotein efflux in Caco-2 cells
-
Chiu YY, Higaki K, Neudeck BL, Barnett JL, Welage LS, Amidon GL (2003) Human jejunal permeability of cyclosporin A: influence of surfactants on P-glycoprotein efflux in Caco-2 cells. Pharm Res 20: 749-756.
-
(2003)
Pharm Res
, vol.20
, pp. 749-756
-
-
Chiu, Y.Y.1
Higaki, K.2
Neudeck, B.L.3
Barnett, J.L.4
Welage, L.S.5
Amidon, G.L.6
-
4
-
-
0037074108
-
The mechanisms of drug release from solid dispersions in water-soluble polymers
-
Craig DQM (2002) The mechanisms of drug release from solid dispersions in water-soluble polymers. Jut J Pharm 231: 131-144.
-
(2002)
Jut J Pharm
, vol.231
, pp. 131-144
-
-
Craig, D.Q.M.1
-
5
-
-
0024976004
-
Cyclosporine
-
Kahan BD (1989) Cyclosporine. N Engl J Med 321: 1725-1738.
-
(1989)
N Engl J Med
, vol.321
, pp. 1725-1738
-
-
Kahan, B.D.1
-
6
-
-
0019298791
-
Comparison of polyethylene glycol and polyoxyethylene stearate as excipients for solid dispersion systems of Griseofulvin and Tolbutamide II: Dissolution and solubility studies
-
Kaur V, Grant DJW, Eaves T (1980) Comparison of polyethylene glycol and polyoxyethylene stearate as excipients for solid dispersion systems of Griseofulvin and Tolbutamide II: dissolution and solubility studies. J Pharm Sci 69: 1321-1326.
-
(1980)
J Pharm Sci
, vol.69
, pp. 1321-1326
-
-
Kaur, V.1
Grant, D.J.W.2
Eaves, T.3
-
7
-
-
0035821352
-
Bioavailability of cyclosporine A dispersed in sodium lauryl sulfate-dextrin based solid microspheres
-
Lee EJ, Lee SW, Choi HG, Kim CK (2001) Bioavailability of cyclosporine A dispersed in sodium lauryl sulfate-dextrin based solid microspheres. Int J Pharm 218: 125-131.
-
(2001)
Int J Pharm
, vol.218
, pp. 125-131
-
-
Lee, E.J.1
Lee, S.W.2
Choi, H.G.3
Kim, C.K.4
-
8
-
-
0034601240
-
Improving drug solubility for oral delivery using solid dispersions
-
Leuner C, Dressman J (2000) Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 50: 47-60.
-
(2000)
Eur J Pharm Biopharm
, vol.50
, pp. 47-60
-
-
Leuner, C.1
Dressman, J.2
-
9
-
-
0030926727
-
Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets
-
Polli JE, Rekhi GS, Augsburger LL, Shah VP (1997) Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets. J Pharm Sci 86: 690-700.
-
(1997)
J Pharm Sci
, vol.86
, pp. 690-700
-
-
Polli, J.E.1
Rekhi, G.S.2
Augsburger, L.L.3
Shah, V.P.4
-
10
-
-
0037026283
-
Evaluation of controlled-release polar lipid microparticles
-
Savolainen M, Khoo C, Glad H, Dahlqvist C, Juppo AM (2002) Evaluation of controlled-release polar lipid microparticles. Int J Pharm 244: 151-161.
-
(2002)
Int J Pharm
, vol.244
, pp. 151-161
-
-
Savolainen, M.1
Khoo, C.2
Glad, H.3
Dahlqvist, C.4
Juppo, A.M.5
-
11
-
-
0027141121
-
Solvent dependent conformation and hydrogen bounding capacity of cyclosporin A: Evidence from partition coefficient and molecular dynamic simulations
-
Taylor NE, Mark AE, Vallat P, Brunne RM, Testa B, Van Gunteren WF (1993) Solvent dependent conformation and hydrogen bounding capacity of cyclosporin A: evidence from partition coefficient and molecular dynamic simulations. J Med Chem 36: 3753-3764.
-
(1993)
J Med Chem
, vol.36
, pp. 3753-3764
-
-
Taylor, N.E.1
Mark, A.E.2
Vallat, P.3
Brunne, R.M.4
Testa, B.5
Van Gunteren, W.F.6
-
12
-
-
1842611878
-
Physicochemical Characterization of solid dispersions of Indomethacin with PEG 6000, Myrj 52, Lactose, Sorbitol, Dextrin, and Eudragit® E100
-
Valizadeh H, Nokhodchi A, Qarakhani N, Zakeri-Milani P, Azarmi S, Hassanzadeh D, Löbenberg R (2004) Physicochemical Characterization of solid dispersions of Indomethacin with PEG 6000, Myrj 52, Lactose, Sorbitol, Dextrin, and Eudragit® E100, Drug Dev Ind Pharm 30: 303-317.
-
(2004)
Drug Dev Ind Pharm
, vol.30
, pp. 303-317
-
-
Valizadeh, H.1
Nokhodchi, A.2
Qarakhani, N.3
Zakeri-Milani, P.4
Azarmi, S.5
Hassanzadeh, D.6
Löbenberg, R.7
|