-
1
-
-
0031913402
-
Dissolution testing as a pronostic tool for oral drug absorption: Immediate release dosage forms
-
Dressman J.B., Amidon G.L., Reppas C., Shad V.P. Dissolution testing as a pronostic tool for oral drug absorption: immediate release dosage forms. Pharm. Res. 15:1998;11-22.
-
(1998)
Pharm. Res.
, vol.15
, pp. 11-22
-
-
Dressman, J.B.1
Amidon, G.L.2
Reppas, C.3
Shad, V.P.4
-
2
-
-
0035659563
-
Bioavailability and bioequivalence: An FDA regulatory overview
-
Chen M.-L., Shad V., Patnaik R., Adams W., Hussain A., Conner D., Mehta M., Malinowski H., Lazor J., Huang S.-M., Hare D., Lesko L., Sporn D., Williams R. Bioavailability and bioequivalence: an FDA regulatory overview. Pharm. Res. 18:2001;1645-1650.
-
(2001)
Pharm. Res.
, vol.18
, pp. 1645-1650
-
-
Chen, M.-L.1
Shad, V.2
Patnaik, R.3
Adams, W.4
Hussain, A.5
Conner, D.6
Mehta, M.7
Malinowski, H.8
Lazor, J.9
Huang, S.-M.10
Hare, D.11
Lesko, L.12
Sporn, D.13
Williams, R.14
-
3
-
-
0031723063
-
Evaluation and comparison of dissolution data derived from different modified release dosage forms: An alternative method
-
Pillay V., Fassihi R. Evaluation and comparison of dissolution data derived from different modified release dosage forms: an alternative method. J. Control. Release. 55:1998;45-55.
-
(1998)
J. Control. Release
, vol.55
, pp. 45-55
-
-
Pillay, V.1
Fassihi, R.2
-
4
-
-
17344386713
-
Correlation between drug release kinetics from proteineous matrix and matrix structure: EPR and NMR study
-
Katzhendler I., Mäder K., Friedman M. Correlation between drug release kinetics from proteineous matrix and matrix structure: EPR and NMR study. J. Pharm. Sci. 89:2000;365-381.
-
(2000)
J. Pharm. Sci.
, vol.89
, pp. 365-381
-
-
Katzhendler, I.1
Mäder, K.2
Friedman, M.3
-
5
-
-
0032960417
-
The effect of excipients on the molecular mobility of lyophilized formulations, as measured by glass transition temperature and NMR relaxation-based critical mobility temperature
-
Yoshioka S., Aso Y., Kojima S. The effect of excipients on the molecular mobility of lyophilized formulations, as measured by glass transition temperature and NMR relaxation-based critical mobility temperature. Pharm. Res. 16:1999;135-140.
-
(1999)
Pharm. Res.
, vol.16
, pp. 135-140
-
-
Yoshioka, S.1
Aso, Y.2
Kojima, S.3
-
6
-
-
0004188123
-
-
The Pharmaceutical Press, London and American Pharmaceutical Association, Washington
-
A.H. Kibbe, Handbook of Pharmaceutical Excipients, Third ed., The Pharmaceutical Press, London and American Pharmaceutical Association, Washington, 2000.
-
(2000)
Handbook of Pharmaceutical Excipients, Third Ed.
-
-
Kibbe, A.H.1
-
7
-
-
0032897426
-
The influence of water content and drug solubility on the formulation of pellets by extrusion and spheronisation
-
Lustig-Gustafsson C., Johal H.K., Podczeck F., Newton J.M. The influence of water content and drug solubility on the formulation of pellets by extrusion and spheronisation. Eur. J. Pharm. Sci. 8:1999;147-152.
-
(1999)
Eur. J. Pharm. Sci.
, vol.8
, pp. 147-152
-
-
Lustig-Gustafsson, C.1
Johal, H.K.2
Podczeck, F.3
Newton, J.M.4
-
9
-
-
0035073301
-
Modeling and comparison of dissolution profiles
-
Costa P., Lobo J.M.S. Modeling and comparison of dissolution profiles. Eur. J. Pharm. Sci. 13:2001;123-133.
-
(2001)
Eur. J. Pharm. Sci.
, vol.13
, pp. 123-133
-
-
Costa, P.1
Lobo, J.M.S.2
-
10
-
-
0033638252
-
Investigating the structure and properties of hydrated hydroxypropyl methylcellulose and egg albumin matrices containing carbamazepine: EPR and NMR study
-
Katzhendler I., Mäder K., Azoury R., Friedman M. Investigating the structure and properties of hydrated hydroxypropyl methylcellulose and egg albumin matrices containing carbamazepine: EPR and NMR study. Pharm. Res. 17:2000;1299-1308.
-
(2000)
Pharm. Res.
, vol.17
, pp. 1299-1308
-
-
Katzhendler, I.1
Mäder, K.2
Azoury, R.3
Friedman, M.4
-
13
-
-
0030724408
-
Polymorphism in anhydrous theophylline - Implications on the dissolution rate of theophylline tablets
-
Phadnis N.V., Suryanarayanan R. Polymorphism in anhydrous theophylline - implications on the dissolution rate of theophylline tablets. J. Pharm. Sci. 86:1997;1256-1263.
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 1256-1263
-
-
Phadnis, N.V.1
Suryanarayanan, R.2
-
14
-
-
0037168237
-
Application of slurry bridging experiments at controlled water activities to predict the solid-state conversion between anhydrous and hydrated forms using theophylline as a model drug
-
Ticehurst M.D., Storey R.A., Watt C. Application of slurry bridging experiments at controlled water activities to predict the solid-state conversion between anhydrous and hydrated forms using theophylline as a model drug. Int. J. Pharm. 247:2002;1-10.
-
(2002)
Int. J. Pharm.
, vol.247
, pp. 1-10
-
-
Ticehurst, M.D.1
Storey, R.A.2
Watt, C.3
-
15
-
-
0032968130
-
Controlled-release hydrophilic tablets for individualized theophylline therapy
-
Sabnis S., Adeyeye C.M. Controlled-release hydrophilic tablets for individualized theophylline therapy. Drug Dev. Ind. Pharm. 25:1998;187-196.
-
(1998)
Drug Dev. Ind. Pharm.
, vol.25
, pp. 187-196
-
-
Sabnis, S.1
Adeyeye, C.M.2
-
16
-
-
0032894638
-
Studies on drug release kinetics from ibuprofen-carbomer hydrophilic matrix tablets: Influence of co-excipients on release rate of the drug
-
Khan G.M., Zhu J.-B. Studies on drug release kinetics from ibuprofen-carbomer hydrophilic matrix tablets: influence of co-excipients on release rate of the drug. J. Control. Release. 57:1999;197-203.
-
(1999)
J. Control. Release
, vol.57
, pp. 197-203
-
-
Khan, G.M.1
Zhu, J.-B.2
-
17
-
-
0031001487
-
The crystallite-gel-model for microcrystalline cellulose in wet-granulation, extrusion, and spheronization
-
Kleinebudde P. The crystallite-gel-model for microcrystalline cellulose in wet-granulation, extrusion, and spheronization. Pharm. Res. 14:1997;804-809.
-
(1997)
Pharm. Res.
, vol.14
, pp. 804-809
-
-
Kleinebudde, P.1
-
18
-
-
0032838893
-
Observation of swelling process and diffusion front position during swelling in hydroxypropyl methyl cellulose (HPMC) matrices containing a soluble drug
-
Colombo P., Bettini R., Peppas N.A. Observation of swelling process and diffusion front position during swelling in hydroxypropyl methyl cellulose (HPMC) matrices containing a soluble drug. J. Control. Release. 61:1999;83-91.
-
(1999)
J. Control. Release
, vol.61
, pp. 83-91
-
-
Colombo, P.1
Bettini, R.2
Peppas, N.A.3
-
19
-
-
0030911525
-
Studies on the interaction between water and (hydroxypropyl) methylcellulose
-
Nokhodchi A., Ford J.L., Rubinstein M.H. Studies on the interaction between water and (hydroxypropyl)methylcellulose. J. Pharm. Sci. 86:1997;608-615.
-
(1997)
J. Pharm. Sci.
, vol.86
, pp. 608-615
-
-
Nokhodchi, A.1
Ford, J.L.2
Rubinstein, M.H.3
-
20
-
-
0032904704
-
A new model describing the swelling and drug release kinetics from hydroxypropyl methylcellulose tablets
-
Siepmann J., Podual K., Sriwongjanya M., Peppas N.A., Bodmeier R. A new model describing the swelling and drug release kinetics from hydroxypropyl methylcellulose tablets. J. Pharm. Sci. 88:1999;65-72.
-
(1999)
J. Pharm. Sci.
, vol.88
, pp. 65-72
-
-
Siepmann, J.1
Podual, K.2
Sriwongjanya, M.3
Peppas, N.A.4
Bodmeier, R.5
-
22
-
-
0033997187
-
Modified drug release from inert matrix tablets prepared from formulations of identical composition but different organisations
-
Barra J., Falson-Rieg F., Doelker E. Modified drug release from inert matrix tablets prepared from formulations of identical composition but different organisations. J. Control. Release. 65:2000;419-428.
-
(2000)
J. Control. Release
, vol.65
, pp. 419-428
-
-
Barra, J.1
Falson-Rieg, F.2
Doelker, E.3
-
23
-
-
0035990554
-
Release characteristics of the matrices prepared from co-spray-dried powders of theophylline and ethylcellulose
-
Kulvanich P., Leesawat P., Patomchaiviwat V. Release characteristics of the matrices prepared from co-spray-dried powders of theophylline and ethylcellulose. Drug Dev. Ind. Pharm. 28:2002;727-739.
-
(2002)
Drug Dev. Ind. Pharm.
, vol.28
, pp. 727-739
-
-
Kulvanich, P.1
Leesawat, P.2
Patomchaiviwat, V.3
-
24
-
-
0032966414
-
The effect of the aqueous solubility of xanthine derivatives on the release mechanism from ethylcellulose matrix tablets
-
Neau S.H., Howard M.A., Claudius J.S., Howard D.R. The effect of the aqueous solubility of xanthine derivatives on the release mechanism from ethylcellulose matrix tablets. Int. J. Pharm. 179:1999;97-105.
-
(1999)
Int. J. Pharm.
, vol.179
, pp. 97-105
-
-
Neau, S.H.1
Howard, M.A.2
Claudius, J.S.3
Howard, D.R.4
-
25
-
-
0037203723
-
Comparative evaluations of powder and mechanical properties of low crystallinity celluloses, microcrystalline celluloses, and powdered celluloses
-
Kothari S.J., Kumar V., Banker G.S. Comparative evaluations of powder and mechanical properties of low crystallinity celluloses, microcrystalline celluloses, and powdered celluloses. Int. J. Pharm. 232:2002;69-80.
-
(2002)
Int. J. Pharm.
, vol.232
, pp. 69-80
-
-
Kothari, S.J.1
Kumar, V.2
Banker, G.S.3
-
26
-
-
0031556482
-
Investigation of hydrogel formation from hydroxypropylmethylcellulose (HPMC) by NMR spectroscopy and NMR imaging techniques
-
Fyfe C.A., Blazek A.I. Investigation of hydrogel formation from hydroxypropylmethylcellulose (HPMC) by NMR spectroscopy and NMR imaging techniques. Macromolecules. 30:1997;6230-6237.
-
(1997)
Macromolecules
, vol.30
, pp. 6230-6237
-
-
Fyfe, C.A.1
Blazek, A.I.2
-
27
-
-
0035897596
-
Chemical reactivity in solid-state pharmaceuticals: Formulation implications
-
Byrn S.R., Xu W., Newman A.W. Chemical reactivity in solid-state pharmaceuticals: formulation implications. Adv. Drug Deliv. Rev. 48:2001;115-136.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.48
, pp. 115-136
-
-
Byrn, S.R.1
Xu, W.2
Newman, A.W.3
|