-
1
-
-
42149156011
-
Tablet formulation studies on an oxcarbazepine-β cyclodextrin binary system
-
Patel, N. V.; Chotai, N. P.; Patel, M. P. Tablet formulation studies on an oxcarbazepine-β cyclodextrin binary system. Die Pharmazie 2008, 63 (4), 275-281.
-
(2008)
Die Pharmazie
, vol.63
, Issue.4
, pp. 275-281
-
-
Patel, N.V.1
Chotai, N.P.2
Patel, M.P.3
-
2
-
-
0029916015
-
USP workshop on dissolution calibration and testing
-
Carrico, C. K. Workshop report AAPS: USP workshop on dissolution calibration and testing. Pharm. Res. 1996, 13, 6-9.
-
(1996)
Pharm. Res
, vol.13
, pp. 6-9
-
-
Carrico, C.K.1
-
3
-
-
84962052802
-
FDA Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms
-
Shah, V. P.; Lesko, L. J.; Fan, J.; Fleischer, N.; Handerson, J.; Malinowski, H.; Makary, M.; Ouderkirk, L.; Roy, S.; Sathe, P.; Singh, G. J. P.; Tillman, L.; Tsong, Y.; Williams, R. L. FDA Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms. Dissolution Technol. 1997, 4, 15-22.
-
(1997)
Dissolution Technol
, vol.4
, pp. 15-22
-
-
Shah, V.P.1
Lesko, L.J.2
Fan, J.3
Fleischer, N.4
Handerson, J.5
Malinowski, H.6
Makary, M.7
Ouderkirk, L.8
Roy, S.9
Sathe, P.10
Singh, G.J.P.11
Tillman, L.12
Tsong, Y.13
Williams R., L.14
-
4
-
-
0022538060
-
On the analysis of the dissolution data
-
Mauger, J. W.; Chilko, D.; Howard, S. On the analysis of the dissolution data. Drug Dev. Ind. Pharm. 1986, 12, 969-992.
-
(1986)
Drug Dev. Ind. Pharm
, vol.12
, pp. 969-992
-
-
Mauger, J.W.1
Chilko, D.2
Howard, S.3
-
5
-
-
0030926727
-
Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets
-
Polli, J. E.; Rekhi, G. S.; Augsburger, L. L.; Shah, V. P. Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets. J. Pharm. Sci. 1997, 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
-
6
-
-
0030472470
-
In vitro dissolution profile comparison: Statistics and analysis, model dependent approach
-
Sathe, P. M.; Tsong, Y.; Shah, V. P. In vitro dissolution profile comparison: statistics and analysis, model dependent approach. Pharm. Res. 1996, 13, 1799-1803.
-
(1996)
Pharm. Res
, vol.13
, pp. 1799-1803
-
-
Sathe, P.M.1
Tsong, Y.2
Shah, V.P.3
-
7
-
-
0027223963
-
Comparison of in vitro dissolution profiles by calculating mean dissolution time (MDT) or mean residence time (MRT)
-
Podczeck, F. Comparison of in vitro dissolution profiles by calculating mean dissolution time (MDT) or mean residence time (MRT). Int. J. Pharm. 1993, 97, 93-100.
-
(1993)
Int. J. Pharm
, vol.97
, pp. 93-100
-
-
Podczeck, F.1
-
8
-
-
2342652446
-
Mathematical comparison of dissolution profiles
-
Moore, J. W.; Flanner, H. H. Mathematical comparison of dissolution profiles. Pharm. Technol. 1996, 6, 64-74.
-
(1996)
Pharm. Technol
, vol.6
, pp. 64-74
-
-
Moore, J.W.1
Flanner, H.H.2
-
9
-
-
0031779119
-
In vitro dissolution profile comparison statistics and analysis of the similarity factor, f2
-
Shah, V. P.; Tsong, Y.; Sathe, P.; Liu, J.-P. In vitro dissolution profile comparison statistics and analysis of the similarity factor, f2. Pharm. Res. 1998, 15, 889-896.
-
(1998)
Pharm. Res
, vol.15
, pp. 889-896
-
-
Shah, V.P.1
Tsong, Y.2
Sathe, P.3
Liu J.-P4
-
10
-
-
0019967104
-
Mechanism of drug dissolution rate enhancement from bcyclodextrin drug systems
-
Corrigan, O. I.; Stanley, T. Mechanism of drug dissolution rate enhancement from bcyclodextrin drug systems. J. Pharm. Pharmacol. 1982, 34, 621-626.
-
(1982)
J. Pharm. Pharmacol
, vol.34
, pp. 621-626
-
-
Corrigan, O.I.1
Stanley, T.2
-
11
-
-
0034846201
-
Guidelines on dissolution profile comparison
-
Gudrun, F. Guidelines on dissolution profile comparison. Drug Inf. J. 2001, 35, 865-874.
-
(2001)
Drug Inf. J
, vol.35
, pp. 865-874
-
-
Gudrun, F.1
-
12
-
-
85036770573
-
Guidance for Industry; U.S. Department of Health and Human Services
-
Food and Drug Administration, Center for Drug Evaluation and Research (CDER), U.S. Government Printing Office: Washington, DC, accessed Sept 29, 2008
-
Dissolution Testing of Immediate Release Solid Oral Dosage Forms; Guidance for Industry; U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), U.S. Government Printing Office: Washington, DC, 1997. http://www.fda.gov/ cder/guidance/1713bp1.pdf (accessed Sept 29, 2008).
-
(1997)
Dissolution Testing of Immediate Release Solid Oral Dosage Forms
-
-
-
13
-
-
0015453518
-
Linearization of dissolution rate curves by the Weibull distribution
-
Langenbucher, F. Linearization of dissolution rate curves by the Weibull distribution. J. Pharm. Pharmacol. 1972, 24, 979-981.
-
(1972)
J. Pharm. Pharmacol
, vol.24
, pp. 979-981
-
-
Langenbucher, F.1
-
14
-
-
0014138173
-
Establishment of sink conditions of dissolution rate determinations
-
Gibaldi, M.; Feldman, S. Establishment of sink conditions of dissolution rate determinations. J. Pharm. Sci. 1967, 56, 1238-1242.
-
(1967)
J. Pharm. Sci
, vol.56
, pp. 1238-1242
-
-
Gibaldi, M.1
Feldman, S.2
-
15
-
-
0014592606
-
Interpretation of percent dissolved-time plots derived from in vitro testing of conventional tablets and capsules
-
Wagner, J. G. Interpretation of percent dissolved-time plots derived from in vitro testing of conventional tablets and capsules. J. Pharm. Sci. 1969, 58, 1253-1257.
-
(1969)
J. Pharm. Sci
, vol.58
, pp. 1253-1257
-
-
Wagner, J.G.1
-
16
-
-
36049039764
-
Merchant. Evaluation of drug release kinetics from ibuprofen matrix tablets using HPMC
-
Harris, M. S.; Jaweria, T.; Hamid, A.; Merchant. Evaluation of drug release kinetics from ibuprofen matrix tablets using HPMC. Pak. J. Pharm. Sci. 2006, 19 (2), 119-124.
-
(2006)
Pak. J. Pharm. Sci
, vol.19
, Issue.2
, pp. 119-124
-
-
Harris, M.S.1
Jaweria, T.2
Hamid, A.3
-
17
-
-
0035073301
-
Modeling and comparison of dissolution profiles
-
Coasta, P.; Sousa, L. J. M. Modeling and comparison of dissolution profiles. Eur. J. Pharm. Sci. 2001, 13, 123-133.
-
(2001)
Eur. J. Pharm. Sci
, vol.13
, pp. 123-133
-
-
Coasta, P.1
Sousa, L.J.M.2
-
18
-
-
85036726458
-
-
USP 23-NF 18; The United States Pharmacopeial Convention, Inc.: Rockville, MD
-
United States Pharmacopeia and National Formulary USP 23-NF 18; The United States Pharmacopeial Convention, Inc.: Rockville, MD, 1997.
-
(1997)
United States Pharmacopeia and National Formulary
-
-
-
19
-
-
0035806261
-
An alternative method to the evaluation of similarity factor in dissolution testing
-
Costa, P. An alternative method to the evaluation of similarity factor in dissolution testing. Int. J. Pharm. 2001, 220, 77-83.
-
(2001)
Int. J. Pharm
, vol.220
, pp. 77-83
-
-
Costa, P.1
-
20
-
-
0000052746
-
Dissolution rate studies II. Dissolution of particles under conditions of rapid agitation
-
Niebergall, P. J.; Milosovich, G.; Goyan, J. E. Dissolution rate studies II. Dissolution of particles under conditions of rapid agitation. J. Pharm. Sci. 1963, 52, 236-241
-
(1963)
J. Pharm. Sci
, vol.52
, pp. 236-241
-
-
Niebergall, P.J.1
Milosovich, G.2
Goyan, J.E.3
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