-
1
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability
-
Amidon G.L., Lunnernas 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
Lunnernas, H.2
Shah, V.P.3
Crison, J.R.4
-
2
-
-
0343527392
-
Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards
-
Amidon G.L., and Löbenberg R. Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. Eur. J. Pharm. Biopharm. 50 (2000) 3-12
-
(2000)
Eur. J. Pharm. Biopharm.
, vol.50
, pp. 3-12
-
-
Amidon, G.L.1
Löbenberg, R.2
-
3
-
-
0037020474
-
Applying the biopharmaceutics classification system to veterinary pharmaceutical products. Part I. Biopharmaceutics and formulation considerations
-
Martinez M., Augsburger L., Johnston T., and Jones W.W. Applying the biopharmaceutics classification system to veterinary pharmaceutical products. Part I. Biopharmaceutics and formulation considerations. Adv. Drug Deliv. Rev. 54 (2002) 805-824
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 805-824
-
-
Martinez, M.1
Augsburger, L.2
Johnston, T.3
Jones, W.W.4
-
4
-
-
33947487639
-
The rate of solution of solid substances in their own solutions
-
Noyes A.S., and Whitney W.R. 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.S.1
Whitney, W.R.2
-
5
-
-
0037223728
-
Micronization of anti-inflammatory drugs for pulmonary delivery by a controlled crystallization process
-
Rasenack N., Steckel H., and Müller B.W. Micronization of anti-inflammatory drugs for pulmonary delivery by a controlled crystallization process. J. Pharm. Sci. 92 (2003) 35-44
-
(2003)
J. Pharm. Sci.
, vol.92
, pp. 35-44
-
-
Rasenack, N.1
Steckel, H.2
Müller, B.W.3
-
6
-
-
0037467170
-
Microcrystals for dissolution rate enhancement of poorly water-soluble drugs
-
Rasenack N., Hartenhauer H., and Müller B.W. Microcrystals for dissolution rate enhancement of poorly water-soluble drugs. Int. J. Pharm. 254 (2003) 137-145
-
(2003)
Int. J. Pharm.
, vol.254
, pp. 137-145
-
-
Rasenack, N.1
Hartenhauer, H.2
Müller, B.W.3
-
7
-
-
0036849433
-
A novel particle engineering technology to enhance dissolution of poorly water soluble drugs: spray-freezing into liquid
-
Rogers T.L., Nelsen A.C., Hu J., Brown J.N., Sakrari M., Young T.J., Johnston K.P., and Williams III R.O. A novel particle engineering technology to enhance dissolution of poorly water soluble drugs: spray-freezing into liquid. Eur. J. Pharm. Biopharm. 54 (2002) 271-280
-
(2002)
Eur. J. Pharm. Biopharm.
, vol.54
, pp. 271-280
-
-
Rogers, T.L.1
Nelsen, A.C.2
Hu, J.3
Brown, J.N.4
Sakrari, M.5
Young, T.J.6
Johnston, K.P.7
Williams III, R.O.8
-
10
-
-
34547674483
-
-
B. Kühn, Verfahren und Vorrichtung zur In-Situ-Formulierung einer Arzneistofflösung zur parenteralen Applikation, German Patent No. WO 99/32175 A1 (1999).
-
-
-
-
11
-
-
25144515860
-
A new formulation concept with drugs with poor water soloubility for parenteral application
-
Jürgens K., and Müller B.W. A new formulation concept with drugs with poor water soloubility for parenteral application. Pharmazie 60 (2005) 665-670
-
(2005)
Pharmazie
, vol.60
, pp. 665-670
-
-
Jürgens, K.1
Müller, B.W.2
-
12
-
-
0028200490
-
Hydrosols-alternatives for the parenteral application of poorly water soluble drugs
-
Gassmann P., List M., Schweitzer A., and Sucker H. Hydrosols-alternatives for the parenteral application of poorly water soluble drugs. Eur. J. Pharm. Biopharm. 40 (1994) 64-72
-
(1994)
Eur. J. Pharm. Biopharm.
, vol.40
, pp. 64-72
-
-
Gassmann, P.1
List, M.2
Schweitzer, A.3
Sucker, H.4
-
13
-
-
33646836468
-
Nano- and micro-particulate formulations of poorly water-soluble drugs by using a novel optimized technique
-
Douroumis D., and Fahr A. Nano- and micro-particulate formulations of poorly water-soluble drugs by using a novel optimized technique. Eur. J. Pharm. Biophys. 63 (2006) 173-175
-
(2006)
Eur. J. Pharm. Biophys.
, vol.63
, pp. 173-175
-
-
Douroumis, D.1
Fahr, A.2
-
15
-
-
34547664660
-
-
P.H. Stahl, Novartis-Pharmaceutische Entwicklung, 1972.
-
-
-
-
16
-
-
0036913259
-
Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs
-
Rasenack N., and Müller B.W. Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs. Pharm. Res. 19 (2002) 1894-1900
-
(2002)
Pharm. Res.
, vol.19
, pp. 1894-1900
-
-
Rasenack, N.1
Müller, B.W.2
-
17
-
-
0001619795
-
The surface tension of aqueous hydroxypropyl cellulose solutions
-
Chang S.A., and Gray D.G. The surface tension of aqueous hydroxypropyl cellulose solutions. J. Colloid Interface Sci. 67 (1978) 255-1265
-
(1978)
J. Colloid Interface Sci.
, vol.67
, pp. 255-1265
-
-
Chang, S.A.1
Gray, D.G.2
-
18
-
-
0020534130
-
Absorption of non-anionic water soluble cellulose polymers at the solid water interface and their effect on suspension stability
-
Law S.L., and Kayes J.B. Absorption of non-anionic water soluble cellulose polymers at the solid water interface and their effect on suspension stability. Int. J. Pharm. 15 (1983) 251-260
-
(1983)
Int. J. Pharm.
, vol.15
, pp. 251-260
-
-
Law, S.L.1
Kayes, J.B.2
-
19
-
-
0029867284
-
Albumine nanospheres as carriers for passive drug targeting: an optimized manufacturing technique
-
Müller B.J., Leuenberger H., and Kissel T. Albumine nanospheres as carriers for passive drug targeting: an optimized manufacturing technique. Pharm. Res. 13 (1996) 32-37
-
(1996)
Pharm. Res.
, vol.13
, pp. 32-37
-
-
Müller, B.J.1
Leuenberger, H.2
Kissel, T.3
-
20
-
-
0022969997
-
Preparation and in vitro evaluation of polylactic acidmitomycin C microscapsules
-
Tsai D.C., Howard S.A., Hogan T.F., Malanga C.J., Kandzari S.J., and Ma J.K.H. Preparation and in vitro evaluation of polylactic acidmitomycin C microscapsules. J. Microencapsul. 3 (1986) 191-193
-
(1986)
J. Microencapsul.
, vol.3
, pp. 191-193
-
-
Tsai, D.C.1
Howard, S.A.2
Hogan, T.F.3
Malanga, C.J.4
Kandzari, S.J.5
Ma, J.K.H.6
-
21
-
-
0037241588
-
Preparation and characterization of sterile sub-200 nm meso-tetra(4-hydroxylphenyl)porphyrin-loaded nanoparticles for photodynamic therapy
-
Konan Y.N., Cerny R., Favet J., Berton M., Gurnya R., and Allemann E. Preparation and characterization of sterile sub-200 nm meso-tetra(4-hydroxylphenyl)porphyrin-loaded nanoparticles for photodynamic therapy. Eur. J. Pharm. Biopharm. 55 (2003) 115-124
-
(2003)
Eur. J. Pharm. Biopharm.
, vol.55
, pp. 115-124
-
-
Konan, Y.N.1
Cerny, R.2
Favet, J.3
Berton, M.4
Gurnya, R.5
Allemann, E.6
-
22
-
-
33947495741
-
Evaluation of in vitro-in vivo correlation and anticonvulsive effectof carbamazepine after cogrinding with microcrystalline cellulose
-
Barzegar-Jalali M., Nayebi A.M., Valizadeh1 H., Hanaee J., Barzegar-Jalali A., Adibkia K., Anoush M., and Sistanizad M. Evaluation of in vitro-in vivo correlation and anticonvulsive effectof carbamazepine after cogrinding with microcrystalline cellulose. J. Pharm. Pharm. Sci. 9 (2006) 307-316
-
(2006)
J. Pharm. Pharm. Sci.
, vol.9
, pp. 307-316
-
-
Barzegar-Jalali, M.1
Nayebi, A.M.2
Valizadeh1, H.3
Hanaee, J.4
Barzegar-Jalali, A.5
Adibkia, K.6
Anoush, M.7
Sistanizad, M.8
-
23
-
-
0000640463
-
Infrared spectra of crystalline polysaccharides
-
Liang C.Y., and Marchessault R.H. Infrared spectra of crystalline polysaccharides. J. Polym. Sci. 39 (1959) 269-278
-
(1959)
J. Polym. Sci.
, vol.39
, pp. 269-278
-
-
Liang, C.Y.1
Marchessault, R.H.2
-
24
-
-
24644474682
-
Miscibility behaviour and formation mechanism of stabilized felodipine-polyvinylpyrrolidone amorphous solid dispersions
-
Karavas E., Ktistis G., Xenakis A., and Georgarakis E. Miscibility behaviour and formation mechanism of stabilized felodipine-polyvinylpyrrolidone amorphous solid dispersions. Drug Dev. Ind. Pharm. 31 (2005) 473-489
-
(2005)
Drug Dev. Ind. Pharm.
, vol.31
, pp. 473-489
-
-
Karavas, E.1
Ktistis, G.2
Xenakis, A.3
Georgarakis, E.4
|