메뉴 건너뛰기




Volumn 15, Issue 4, 2008, Pages 28-34

Comparison of in vitro dissolution profiles of oxcarbazepine-HP β-CD tablet formulations with marketed oxcarbazepine tablets

Author keywords

[No Author keywords available]

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; CARBOXYMETHYLCELLULOSE; MACROGOL 6000; MAGNESIUM STEARATE; MICROCRYSTALLINE CELLULOSE; OXCARBAZEPINE; POVIDONE DERIVATIVE; STARCH; TALC;

EID: 77955835300     PISSN: 1521298X     EISSN: None     Source Type: Journal    
DOI: 10.14227/DT150408P28     Document Type: Article
Times cited : (38)

References (20)
  • 1
    • 42149156011 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 5
    • 0030926727 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.