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Volumn 30, Issue 6, 2004, Pages 601-607

In vitro and in vivo evaluation of glibenclamide in solid dispersion systems

Author keywords

Gelucire ; Glibenclamide; In vitro dissolution; In vivo bioavailability; Polyethylene glycol 6000 (PEG 6000); Solid dispersion

Indexed keywords

GELUCIRE; GLIBENCLAMIDE; MACROGOL 6000;

EID: 3142754096     PISSN: 03639045     EISSN: None     Source Type: Journal    
DOI: 10.1081/DDC-120037491     Document Type: Article
Times cited : (48)

References (26)
  • 1
    • 0002096610 scopus 로고    scopus 로고
    • Insulin, oral hypoglycemic agents and the pharmacology of endocrine pancreas
    • Gilman, A.G., Ed.; McGraw-Hill: New York
    • Davis, S.N.; Granner, D.K. Insulin, oral hypoglycemic agents and the pharmacology of endocrine pancreas. In The Pharmacological Basis of Therapeutics, 9th Ed.; Gilman, A.G., Ed.; McGraw-Hill: New York, 1996; 1487-1518.
    • (1996) The Pharmacological Basis of Therapeutics, 9th Ed. , pp. 1487-1518
    • Davis, S.N.1    Granner, D.K.2
  • 3
    • 0015131941 scopus 로고
    • Increased dissolution rates of water-insoluble cardiac glycosides and steroids via solid dispersions in polyethylene glycol 6000
    • Chiou, W.L.; Riegelman, S. Increased dissolution rates of water-insoluble cardiac glycosides and steroids via solid dispersions in polyethylene glycol 6000. J. Pharm. Sci. 1971, 60 (10), 1569-1571.
    • (1971) J. Pharm. Sci. , vol.60 , Issue.10 , pp. 1569-1571
    • Chiou, W.L.1    Riegelman, S.2
  • 4
    • 0029037331 scopus 로고
    • Preparation and in vitro dissolution profiles of tolazamide-polyethylene glycol solid dispersion
    • Betageri, G.V.; Dipali, S.R. Preparation and in vitro dissolution profiles of tolazamide-polyethylene glycol solid dispersion. Drug Dev. Ind. Pharm. 1995, 21 (11), 1347-1352.
    • (1995) Drug Dev. Ind. Pharm. , vol.21 , Issue.11 , pp. 1347-1352
    • Betageri, G.V.1    Dipali, S.R.2
  • 5
    • 0026640050 scopus 로고
    • Studies on solid dispersions of nifedipine
    • Save, T.; Venkitachalam, P. Studies on solid dispersions of nifedipine. Drug Dev. Ind. Pharm. 1992, 18, 1663-1679.
    • (1992) Drug Dev. Ind. Pharm. , vol.18 , pp. 1663-1679
    • Save, T.1    Venkitachalam, P.2
  • 6
    • 0024804488 scopus 로고
    • Some properties of diazepam-polyethylene glycol solid dispersion and their modification in the presence of stearic acid or polysorbate 80
    • Fernandez, J.; Vila-Jato, J.L.; Banco, J.; Ford, J.L. Some properties of diazepam-polyethylene glycol solid dispersion and their modification in the presence of stearic acid or polysorbate 80. Drug Dev. Ind. Pharm. 1989, 15, 2491-2513.
    • (1989) Drug Dev. Ind. Pharm. , vol.15 , pp. 2491-2513
    • Fernandez, J.1    Vila-Jato, J.L.2    Banco, J.3    Ford, J.L.4
  • 7
    • 0026783391 scopus 로고
    • Characterization of solid dispersion of piroxicam/polyethylene glycol 4000
    • Fernanadez, M.; Rodriguez, I.C.; Margarit, M.V.; Cerezo, A. Characterization of solid dispersion of piroxicam/polyethylene glycol 4000. Int. J. Pharm. 1992, 84, 197-202.
    • (1992) Int. J. Pharm. , vol.84 , pp. 197-202
    • Fernanadez, M.1    Rodriguez, I.C.2    Margarit, M.V.3    Cerezo, A.4
  • 8
    • 0029047420 scopus 로고
    • Influence of the preparation method of solid dispersions on their dissolution rate: Study of trimetrene-D-mannitol system
    • Araias, M.J.; Gines, J.M.; Moyano, J.R.; Martinez, J.I.; Rabasco, A.M. Influence of the preparation method of solid dispersions on their dissolution rate: study of trimetrene-D-mannitol system. Int. J. Pharm. 1995, 123, 25-31.
    • (1995) Int. J. Pharm. , vol.123 , pp. 25-31
    • Araias, M.J.1    Gines, J.M.2    Moyano, J.R.3    Martinez, J.I.4    Rabasco, A.M.5
  • 9
    • 0025864425 scopus 로고
    • Preformulation studies on solid dispersions containing traimterene or temazepam in polyethylene glycols or gelucire 44/14 for liquid filling of hard gelatine capsules
    • Dordunoo, S.K.; Ford, J.L.; Rubinstein, M.H. Preformulation studies on solid dispersions containing traimterene or temazepam in polyethylene glycols or gelucire 44/14 for liquid filling of hard gelatine capsules. Drug Dev. Ind. Pharm. 1991, 17, 1685-1713.
    • (1991) Drug Dev. Ind. Pharm. , vol.17 , pp. 1685-1713
    • Dordunoo, S.K.1    Ford, J.L.2    Rubinstein, M.H.3
  • 11
    • 0025741318 scopus 로고
    • Bioavailability of poorly water-soluble drug for tablet and solid dispersion in human
    • Sheen, P.C.; Kim, E.I.; Petillo, J.J.; Serajuddin, A.T.M. Bioavailability of poorly water-soluble drug for tablet and solid dispersion in human. J. Pharm. Sci. 1991, 80 (7), 712-714.
    • (1991) J. Pharm. Sci. , vol.80 , Issue.7 , pp. 712-714
    • Sheen, P.C.1    Kim, E.I.2    Petillo, J.J.3    Serajuddin, A.T.M.4
  • 13
    • 0025962426 scopus 로고
    • Dissolution rate of diazepam from PEG 6000 solid dispersion
    • Rabasco, A.M.; Gines, J.M.; Fernandez, A.; Hogado, M.A. Dissolution rate of diazepam from PEG 6000 solid dispersion. Int. J. Pharm. 1991, 67, 201-205.
    • (1991) Int. J. Pharm. , vol.67 , pp. 201-205
    • Rabasco, A.M.1    Gines, J.M.2    Fernandez, A.3    Hogado, M.A.4
  • 14
    • 0028127826 scopus 로고
    • Characterization and dissolution of fenofibrate solid dispersion systems
    • Sheu, M.-T.; Yeh, C.-M.; Sokoloski, T.D. Characterization and dissolution of fenofibrate solid dispersion systems. Int. J. Pharm. 1994, 103, 137-246.
    • (1994) Int. J. Pharm. , vol.103 , pp. 137-246
    • Sheu, M.-T.1    Yeh, C.-M.2    Sokoloski, T.D.3
  • 16
    • 0031913402 scopus 로고    scopus 로고
    • Dissolution testing as aprognostic tool for oral drug absorption; Immediate release dosage forms
    • review
    • Dressman, J.B.; Amidon, G.L.; Reppas, C.; Shan, V.P. Dissolution testing as aprognostic tool for oral drug absorption; Immediate release dosage forms. Pharm. Res. 1998, 15 (1), 11-22, review.
    • (1998) Pharm. Res. , vol.15 , Issue.1 , pp. 11-22
    • Dressman, J.B.1    Amidon, G.L.2    Reppas, C.3    Shan, V.P.4
  • 17
    • 0032923660 scopus 로고    scopus 로고
    • Typical variability in drug dissolution testing: Study with USP and FDA calibrator tablets and a marketed drug (glibenclamide) product
    • Qureshi, S.; McGilveray, I. Typical variability in drug dissolution testing: study with USP and FDA calibrator tablets and a marketed drug (glibenclamide) product. Eur. J. Pharm. Sci. 1999, 7, 249-258.
    • (1999) Eur. J. Pharm. Sci. , vol.7 , pp. 249-258
    • Qureshi, S.1    McGilveray, I.2
  • 18
    • 0027772495 scopus 로고
    • Pharmaceutical quality of glibenclamide products: A multinational postmarketing comparative study
    • Blume, H.; Ali, S.; Siewert, M. Pharmaceutical quality of glibenclamide products: a multinational postmarketing comparative study. Drug Dev. Ind. Pharm. 1993, 19 (20), 2713-2741.
    • (1993) Drug Dev. Ind. Pharm. , vol.19 , Issue.20 , pp. 2713-2741
    • Blume, H.1    Ali, S.2    Siewert, M.3
  • 20
    • 0028118327 scopus 로고
    • High performance liquid chromatographic method for determination of glibenclamide in human plasma
    • Al-Kamis, K.; El-sayed, Y.; Al-Rashood, K.; Al-Yamani, M. High performance liquid chromatographic method for determination of glibenclamide in human plasma. Anal. lett. 1994, 27 (7), 1277-1293.
    • (1994) Anal. Lett. , vol.27 , Issue.7 , pp. 1277-1293
    • Al-Kamis, K.1    El-Sayed, Y.2    Al-Rashood, K.3    Al-Yamani, M.4
  • 21
    • 0015124656 scopus 로고
    • Pharmaceutical application of solid dispersion systems
    • Chiou, W.; Riegelman, S. Pharmaceutical application of solid dispersion systems. J. Pharm. Sci. 1971, 60 (9), 1281-1302.
    • (1971) J. Pharm. Sci. , vol.60 , Issue.9 , pp. 1281-1302
    • Chiou, W.1    Riegelman, S.2
  • 23
    • 0023637723 scopus 로고
    • Comparison of pharmacokinetics and pharmacodynamics of a conventional and a new rapidly dissolving glibenclamide preparation
    • Shaheen, O.; Othman; Sadeq; Jalal, I.; Awidi, A.; Al-Turk, W. Comparison of pharmacokinetics and pharmacodynamics of a conventional and a new rapidly dissolving glibenclamide preparation. Int. J. Pharm. 1987, 38, 123-131.
    • (1987) Int. J. Pharm. , vol.38 , pp. 123-131
    • Shaheen, O.1    Othman2    Sadeq3    Jalal, I.4    Awidi, A.5    Al-Turk, W.6
  • 25
    • 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
  • 26
    • 0343807478 scopus 로고
    • Dissolution testing and assessment of bioavailability/bioequivalence
    • Banker, U.V., Ed.; Marcel Dekker, Inc.: New York
    • Santosh, J.V. Dissolution testing and assessment of bioavailability/ bioequivalence. In Pharmaceutical Dissolution Testing; Banker, U.V., Ed.; Marcel Dekker, Inc.: New York, 1992; 391-411.
    • (1992) Pharmaceutical Dissolution Testing , pp. 391-411
    • Santosh, J.V.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.