-
1
-
-
0030657836
-
Preparation and evaluation of sustained release solid dispersions of drugs with Eudragit polymers
-
Ammar H.O., Khalil R.M. Preparation and evaluation of sustained release solid dispersions of drugs with Eudragit polymers. Drug Dev. Ind. Pharm. 23:1997;1043-1054.
-
(1997)
Drug Dev. Ind. Pharm.
, vol.23
, pp. 1043-1054
-
-
Ammar, H.O.1
Khalil, R.M.2
-
2
-
-
0001777594
-
Biodegredable microspheres: Advances in production technology
-
Benita, S. (Ed.). Marcel Dekker, New York
-
Benoit, J.P., Marchais, H., Rolland, H., Velde, V.V., 1996. Biodegredable microspheres: advances in production technology. In: Benita, S. (Ed.), Microencapsulation Methods and Industrial Applications. Marcel Dekker, New York, pp. 35-72.
-
(1996)
Microencapsulation Methods and Industrial Applications
, pp. 35-72
-
-
Benoit, J.P.1
Marchais, H.2
Rolland, H.3
Velde, V.V.4
-
3
-
-
0028960948
-
Effect of varying drug loading on particle size distribution and drug release kinetics of verapamil hydrochloride microspheres prepared with cellulose esters
-
Bhardwaj S.B., Shukla A.J., Collins C.C. Effect of varying drug loading on particle size distribution and drug release kinetics of verapamil hydrochloride microspheres prepared with cellulose esters. J. Microencapsul. 12:1995;71-81.
-
(1995)
J. Microencapsul.
, vol.12
, pp. 71-81
-
-
Bhardwaj, S.B.1
Shukla, A.J.2
Collins, C.C.3
-
4
-
-
0025813293
-
Eudragit E microspheres containing bacampicillin: Preparation by solvent removal methods
-
Bogataj M., Mrhar A., Kristl A., Kozjek F. Eudragit E microspheres containing bacampicillin: preparation by solvent removal methods. J. Microencapsul. 8:1991;401-406.
-
(1991)
J. Microencapsul.
, vol.8
, pp. 401-406
-
-
Bogataj, M.1
Mrhar, A.2
Kristl, A.3
Kozjek, F.4
-
5
-
-
0028202433
-
Formulation, preparation and dissolution characteristics of propranolol hydrochloride microspheres
-
Chiao C.S.L., Price J.C. Formulation, preparation and dissolution characteristics of propranolol hydrochloride microspheres. J. Microencapsul. 11:1994;153-159.
-
(1994)
J. Microencapsul.
, vol.11
, pp. 153-159
-
-
Chiao, C.S.L.1
Price, J.C.2
-
6
-
-
0019378948
-
Superiority of stable isotope techniques in the assessment of the bioavailability of drugs undergoing extensive first pass elimination
-
Eichelbaum M., Dengler H.J., Somogyi A., Von Unruh G.E. Superiority of stable isotope techniques in the assessment of the bioavailability of drugs undergoing extensive first pass elimination. Eur. J. Clin. Pharmacol. 19:1981;127-131.
-
(1981)
Eur. J. Clin. Pharmacol.
, vol.19
, pp. 127-131
-
-
Eichelbaum, M.1
Dengler, H.J.2
Somogyi, A.3
Von Unruh, G.E.4
-
7
-
-
0012771244
-
-
Industrial Products Division, Röhm Pharma GmbH, Weiterstadt, Germany
-
Eudragit Data Sheets, Industrial Products Division, Röhm Pharma GmbH, Weiterstadt, Germany.
-
Eudragit Data Sheets
-
-
-
9
-
-
0026608368
-
Biopharmaceutical comparison of oral multiple-unit and single-unit sustained-release dosage forms
-
Follonier N., Doelker E. Biopharmaceutical comparison of oral multiple-unit and single-unit sustained-release dosage forms. S.T.P. Pharma. Sci. 2:1992;141-158.
-
(1992)
S.T.P. Pharma. Sci.
, vol.2
, pp. 141-158
-
-
Follonier, N.1
Doelker, E.2
-
10
-
-
0014138173
-
Establishment of sink conditions in dissolution rate determinations. Theoretical considerations and application to non-disintegrating dosage forms
-
Gibaldi M., Feldman S. Establishment of sink conditions in dissolution rate determinations. Theoretical considerations and application to non-disintegrating dosage forms. J. Pharm. Sci. 56:1967;1238-1242.
-
(1967)
J. Pharm. Sci.
, vol.56
, pp. 1238-1242
-
-
Gibaldi, M.1
Feldman, S.2
-
11
-
-
0028883320
-
Physical characterization and dissolution properties of verapamil HCl coprecipitates
-
Goracinova K., Klisarova L.J., Simov A. Physical characterization and dissolution properties of verapamil HCl coprecipitates. Drug Dev. Ind. Pharm. 21:1995;383-391.
-
(1995)
Drug Dev. Ind. Pharm.
, vol.21
, pp. 383-391
-
-
Goracinova, K.1
Klisarova, L.J.2
Simov, A.3
-
12
-
-
0022826259
-
Eudragit RS and RL (acrylic resins) microcapsules as pH insensitive and sustained release preparations of ketoprofen
-
Goto S., Kawata M., Nakamura M., Maekawa K., Aoyama T. Eudragit RS and RL (acrylic resins) microcapsules as pH insensitive and sustained release preparations of ketoprofen. J. Microencapsul. 3:1986a;293-304.
-
(1986)
J. Microencapsul.
, vol.3
, pp. 293-304
-
-
Goto, S.1
Kawata, M.2
Nakamura, M.3
Maekawa, K.4
Aoyama, T.5
-
13
-
-
0022839358
-
Eudragit E, L and S (acrylic resins) microcapsules as pH sensitive release preparations of ketoprofen
-
Goto S., Kawata M., Nakamura M., Maekawa K., Aoyama T. Eudragit E, L and S (acrylic resins) microcapsules as pH sensitive release preparations of ketoprofen. J. Microencapsul. 3:1986b;305-316.
-
(1986)
J. Microencapsul.
, vol.3
, pp. 305-316
-
-
Goto, S.1
Kawata, M.2
Nakamura, M.3
Maekawa, K.4
Aoyama, T.5
-
15
-
-
0344893332
-
Mechanism of sustained-action medication: Theoretical analysis of rate of release of solid drug dispersed in solid matrices
-
Higuchi T. Mechanism of sustained-action medication: theoretical analysis of rate of release of solid drug dispersed in solid matrices. J. Pharm. Sci. 52:1963;1145-1149.
-
(1963)
J. Pharm. Sci.
, vol.52
, pp. 1145-1149
-
-
Higuchi, T.1
-
16
-
-
0022445026
-
Preparation and dissolution pattern of Eudragit RS microcapsules containing ketoprofen
-
Kawata M., Nakamura M., Goto S., Aoyama T. Preparation and dissolution pattern of Eudragit RS microcapsules containing ketoprofen. Chem. Pharm. Bull. 34:1986;2618-2623.
-
(1986)
Chem. Pharm. Bull.
, vol.34
, pp. 2618-2623
-
-
Kawata, M.1
Nakamura, M.2
Goto, S.3
Aoyama, T.4
-
17
-
-
0004188123
-
-
American Pharmaceutical Association and Pharmaceutical Press, Washington, DC
-
Kibbe, A.H., 2000. Handbook of Pharmaceutical Excipients, 3rd ed. American Pharmaceutical Association and Pharmaceutical Press, Washington, DC, pp. 401-406.
-
(2000)
Handbook of Pharmaceutical Excipients, 3rd Ed.
, pp. 401-406
-
-
Kibbe, A.H.1
-
18
-
-
0028329379
-
Preparation and evaluation of sustained release microspheres of terbutaline sulfate
-
Kim C.K., Kim M.J., Oh K.H. Preparation and evaluation of sustained release microspheres of terbutaline sulfate. Int. J. Pharm. 106:1994;213-219.
-
(1994)
Int. J. Pharm.
, vol.106
, pp. 213-219
-
-
Kim, C.K.1
Kim, M.J.2
Oh, K.H.3
-
19
-
-
0001960774
-
Biopharmaceutical aspects of multiparticulates
-
Ghebre-Sellasie, I. (Ed.). Marcel Dekker, New York
-
Kramer, J., Blume, H., 1994. Biopharmaceutical aspects of multiparticulates. In: Ghebre-Sellasie, I. (Ed.), Multiparticulate Oral Drug Delivery. Marcel Dekker, New York, pp. 307-332.
-
(1994)
Multiparticulate Oral Drug Delivery
, pp. 307-332
-
-
Kramer, J.1
Blume, H.2
-
20
-
-
0015453518
-
Linearization of dissolution rate curves by the Weibull distribution
-
Langenbucher F. Linearization of dissolution rate curves by the Weibull distribution. J. Pharm. Pharmacol. 24:1972;979-981.
-
(1972)
J. Pharm. Pharmacol.
, vol.24
, pp. 979-981
-
-
Langenbucher, F.1
-
21
-
-
0025854599
-
Nonlinear pharmacokinetics clinical implications
-
Lunden M.T. Nonlinear pharmacokinetics clinical implications. Clin. Pharmacokinet. 20:1991;429-446.
-
(1991)
Clin. Pharmacokinet.
, vol.20
, pp. 429-446
-
-
Lunden, M.T.1
-
22
-
-
0025146415
-
Controlled release indomethacin microspheres prepared by using an emulsion solvent-diffusion technique
-
Malamataris S., Avgerinos A. Controlled release indomethacin microspheres prepared by using an emulsion solvent-diffusion technique. Int. J. Pharm. 62:1990;105-111.
-
(1990)
Int. J. Pharm.
, vol.62
, pp. 105-111
-
-
Malamataris, S.1
Avgerinos, A.2
-
23
-
-
0022005501
-
Pharmacokinetics of sustained-release verapamil after a single administration and at steady state
-
Mattila J., Mäntylä R., Taskinen J., Männistö P. Pharmacokinetics of sustained-release verapamil after a single administration and at steady state. Eur. J. Drug Metab. Pharmacokinet. 10:1985;133-138.
-
(1985)
Eur. J. Drug Metab. Pharmacokinet.
, vol.10
, pp. 133-138
-
-
Mattila, J.1
Mäntylä, R.2
Taskinen, J.3
Männistö, P.4
-
24
-
-
0024363416
-
Verapamil an updated review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension
-
McTavish D., Sorkin E.M. Verapamil an updated review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension. Drugs. 38:1989;19-76.
-
(1989)
Drugs
, vol.38
, pp. 19-76
-
-
McTavish, D.1
Sorkin, E.M.2
-
25
-
-
0012762952
-
Packaging of multiparticulate dosage forms materials and equipment
-
Ghebre-Sellassie, I. (Ed.). Marcel Dekker, New York
-
Murthy, K.S., Reiterer, F., Wendt, J., 1994. Packaging of multiparticulate dosage forms materials and equipment. In: Ghebre-Sellassie, I. (Ed.), Multiparticulate Oral Drug Delivery. Marcel Dekker, New York, pp. 405-456.
-
(1994)
Multiparticulate Oral Drug Delivery
, pp. 405-456
-
-
Murthy, K.S.1
Reiterer, F.2
Wendt, J.3
-
26
-
-
0021697156
-
Preparation and evaluation of controlled release indomethacin microspheres
-
Pongpaibul Y., Price J.C., Whitworth C.W. Preparation and evaluation of controlled release indomethacin microspheres. Drug Dev. Ind. Pharm. 10:1984;1597-1616.
-
(1984)
Drug Dev. Ind. Pharm.
, vol.10
, pp. 1597-1616
-
-
Pongpaibul, Y.1
Price, J.C.2
Whitworth, C.W.3
-
27
-
-
0023009535
-
Preparation and in vitro dissolution characteristics of propranolol microcapsules
-
Pongpaibul Y., Whitworth C.W. Preparation and in vitro dissolution characteristics of propranolol microcapsules. Int. J. Pharm. 33:1986;243-248.
-
(1986)
Int. J. Pharm.
, vol.33
, pp. 243-248
-
-
Pongpaibul, Y.1
Whitworth, C.W.2
-
29
-
-
0034870405
-
Development of hollow microspheres as floating controlled-release systems for cardiovascular drugs: Preparation and release characteristics
-
Soppimath K.S., Kulkarni A.R., Aminabhavi T.J. Development of hollow microspheres as floating controlled-release systems for cardiovascular drugs: preparation and release characteristics. Drug Dev. Ind. Pharm. 27:2001;507-515.
-
(2001)
Drug Dev. Ind. Pharm.
, vol.27
, pp. 507-515
-
-
Soppimath, K.S.1
Kulkarni, A.R.2
Aminabhavi, T.J.3
-
30
-
-
0002725227
-
Formation of degradable drug-loaded microparticles by in-liquid drying processes
-
Donbrow, M. (Ed.). CRC Press, London, pp. 47-71.
-
Thies, C., 1992. Formation of degradable drug-loaded microparticles by in-liquid drying processes. In: Donbrow, M. (Ed.), Microcapsules and Nanoparticles in Medicine and Pharmacy. CRC Press, London, pp. 47-71.
-
(1992)
Microcapsules and Nanoparticles in Medicine and Pharmacy
-
-
Thies, C.1
-
31
-
-
0012771245
-
-
US Pharmacopeial Convention, Rockville, MD
-
US Pharmacopeia 24, 2000. US Pharmacopeial Convention, Rockville, MD, pp. 2477-2478 and 1945-1946.
-
(2000)
US Pharmacopeia
, vol.24
, pp. 2477-2478
-
-
-
32
-
-
0021713528
-
Stereoselective first-pass metabolism of highly cleared drugs: Studies of the bioavailability of L- and D-verapamil examined with a stable isotope technique
-
Vogelgesang B., Echizen H., Schmidt E., Eichelbaum M. Stereoselective first-pass metabolism of highly cleared drugs: studies of the bioavailability of L- and D-verapamil examined with a stable isotope technique. Br. J. Clin. Pharmacol. 18:1984;733-740.
-
(1984)
Br. J. Clin. Pharmacol.
, vol.18
, pp. 733-740
-
-
Vogelgesang, B.1
Echizen, H.2
Schmidt, E.3
Eichelbaum, M.4
-
33
-
-
0001147914
-
Calcium antagonists
-
Kist, K. (Ed.). Wolfe Publishing Ltd., London
-
Wingard, L.B., Brody, T.M., Larner, J., Schwartz, A., 1991. Calcium antagonists. In: Kist, K. (Ed.), Human Pharmacology Molecular-to-Clinical. Wolfe Publishing Ltd., London, pp. 212-222.
-
(1991)
Human Pharmacology Molecular-to-Clinical
, pp. 212-222
-
-
Wingard, L.B.1
Brody, T.M.2
Larner, J.3
Schwartz, A.4
-
34
-
-
0030729177
-
Preparation of polymeric microspheres by the solvent evaporation method using sucrose stearate as droplet stabilizer
-
Yüksel N., Baykara T. Preparation of polymeric microspheres by the solvent evaporation method using sucrose stearate as droplet stabilizer. J. Microencapsul. 14:1997;725-733.
-
(1997)
J. Microencapsul.
, vol.14
, pp. 725-733
-
-
Yüksel, N.1
Baykara, T.2
-
35
-
-
0034687583
-
Comparison of in vitro dissolution profiles by ANOVA-based, model dependent and independent methods
-
Yüksel N., Kanik A.E., Baykara T. Comparison of in vitro dissolution profiles by ANOVA-based, model dependent and independent methods. Int. J. Pharm. 209:2000;57-67.
-
(2000)
Int. J. Pharm.
, vol.209
, pp. 57-67
-
-
Yüksel, N.1
Kanik, A.E.2
Baykara, T.3
|