메뉴 건너뛰기




Volumn 10, Issue 4, 2005, Pages 467-477

Characteristics of rofecoxib-polyethylene glycol 4000 solid dispersions and tablets based on solid dispersions

Author keywords

Anti inflammatory activity; Dissolution rate; Mean dissolution time; PEG 4000; Rofecoxib; Solid dispersions; Solubility; Tablets

Indexed keywords

AEROSIL; LACTOSE; MACROGOL 4000; MAGNESIUM STEARATE; MICROCRYSTALLINE CELLULOSE; ROFECOXIB; STARCH; WATER;

EID: 28844465151     PISSN: 10837450     EISSN: 10979867     Source Type: Journal    
DOI: 10.1080/10837450500299701     Document Type: Article
Times cited : (41)

References (31)
  • 1
    • 0013795160 scopus 로고
    • Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures I - Theoretical consideration and discussion of the literature
    • Goldberg, A.H.; Gibaldi, M.; Kanig, J.L. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures I - theoretical consideration and discussion of the literature. J. Pharm. Sci. 1965, 54, 1145-1148.
    • (1965) J. Pharm. Sci. , vol.54 , pp. 1145-1148
    • Goldberg, A.H.1    Gibaldi, M.2    Kanig, J.L.3
  • 2
    • 84984082270 scopus 로고
    • Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures II - Experimental evaluation of a eutectic mixture: Ureaacetaminophen system
    • Goldberg, A.H.; Gibaldi, M.; Kanig, J.L. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures II - experimental evaluation of a eutectic mixture: ureaacetaminophen system. J. Pharm. Sci. 1966, 55, 482-487.
    • (1966) J. Pharm. Sci. , vol.55 , pp. 482-487
    • Goldberg, A.H.1    Gibaldi, M.2    Kanig, J.L.3
  • 3
    • 0013920636 scopus 로고
    • Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures IV - Chloramphenicol-urea system
    • Goldberg, A.M.; Gibaldi, M.; Kanig, J.L.; Mayersohn, M. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures IV - chloramphenicol-urea system. J. Pharm. Sci. 1966, 55, 581-583.
    • (1966) J. Pharm. Sci. , vol.55 , pp. 581-583
    • Goldberg, A.M.1    Gibaldi, M.2    Kanig, J.L.3    Mayersohn, M.4
  • 5
    • 0038768850 scopus 로고    scopus 로고
    • Influence of physiochemical properties on dissolution of drugs in the gastrointestinal tract
    • Hoerter, D.; Dressman, J.B. Influence of physiochemical properties on dissolution of drugs in the gastrointestinal tract. Adv. Drug Deliv. Rev. 1997, 25, 3-14.
    • (1997) Adv. Drug Deliv. Rev. , vol.25 , pp. 3-14
    • Hoerter, D.1    Dressman, J.B.2
  • 6
    • 0030638567 scopus 로고    scopus 로고
    • Characteristics and significance of the amorphous state in pharmaceutical systems
    • Hancock, B.C.; Zografi, G. Characteristics and significance of the amorphous state in pharmaceutical systems. J. Pharm. Sci. 1997, 86, 1-12.
    • (1997) J. Pharm. Sci. , vol.86 , pp. 1-12
    • Hancock, B.C.1    Zografi, G.2
  • 7
    • 0029819323 scopus 로고    scopus 로고
    • Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization
    • Loftsson, T.; Brewster, M.E. Pharmaceutical applications of cyclodextrins. 1. Drug solubilization and stabilization. J. Pharm. Sci. 1996, 85, 1017-1025.
    • (1996) J. Pharm. Sci. , vol.85 , pp. 1017-1025
    • Loftsson, T.1    Brewster, M.E.2
  • 8
    • 0015124656 scopus 로고
    • Pharmaceutical applications of solid dispersions
    • Chiou, W.L.; Riegelman, S. Pharmaceutical applications of solid dispersions. J. Pharm. Sci. 1971, 60, 1281-1302.
    • (1971) J. Pharm. Sci. , vol.60 , pp. 1281-1302
    • Chiou, W.L.1    Riegelman, S.2
  • 9
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • Leuner, C.; Dressman, J. Improving drug solubility for oral delivery using solid dispersions. Eur. J. Pharm. Biopharm. 2000, 50, 47-60.
    • (2000) Eur. J. Pharm. Biopharm. , vol.50 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 10
    • 0022650603 scopus 로고
    • The current status of solid dispersions
    • Ford, J.L. The current status of solid dispersions. Pharm. Acta Helv. 1986, 61, 69-88.
    • (1986) Pharm. Acta Helv. , vol.61 , pp. 69-88
    • Ford, J.L.1
  • 11
    • 0037074108 scopus 로고    scopus 로고
    • The mechanisms of drug release from solid dispersions in water-soluble polymers
    • Craig, D.Q.M. The mechanisms of drug release from solid dispersions in water-soluble polymers. Int. J. Pharm. 2002, 231, 131-144.
    • (2002) Int. J. Pharm. , vol.231 , pp. 131-144
    • Craig, D.Q.M.1
  • 13
    • 0002488303 scopus 로고
    • Polyethylene glycol
    • The Pharmaceutical Press: Washington
    • Price, J.L. Polyethylene glycol. In Handbook of Pharmaceutical Excipients; The Pharmaceutical Press: Washington, 1994; 35-361.
    • (1994) Handbook of Pharmaceutical Excipients , pp. 35-361
    • Price, J.L.1
  • 14
    • 0029586490 scopus 로고
    • Enhancement of dissolution of glyburide by solid dispersion and liophilization techniques
    • Betageri, G.V.; Makarla, K.R. Enhancement of dissolution of glyburide by solid dispersion and liophilization techniques. Int. J. Pharm. 1995, 126, 155-160.
    • (1995) Int. J. Pharm. , vol.126 , pp. 155-160
    • Betageri, G.V.1    Makarla, K.R.2
  • 15
    • 0016539272 scopus 로고
    • Dissolution of acetylsalicylic acid from acetylsalicylic acid-polyethylene glycol 6000 coprecipitates
    • Asker, A.F. ; Whitworth, C.W. Dissolution of acetylsalicylic acid from acetylsalicylic acid-polyethylene glycol 6000 coprecipitates. Pharmazie 1975, 30, 530-531.
    • (1975) Pharmazie , vol.30 , pp. 530-531
    • Asker, A.F.1    Whitworth, C.W.2
  • 17
    • 0042307682 scopus 로고    scopus 로고
    • Solubility of rofecoxib in the presence of methanol, ethanol and sodium lauryl sulfate at (298.15, 303.15 and 308.15) K
    • Desai, K.G.; Kulkarni, A.R.; Aminabhavi, T.M. Solubility of rofecoxib in the presence of methanol, ethanol and sodium lauryl sulfate at (298.15, 303.15 and 308.15) K. J. Chem. Eng. Data 2003, 48, 942-945.
    • (2003) J. Chem. Eng. Data , vol.48 , pp. 942-945
    • Desai, K.G.1    Kulkarni, A.R.2    Aminabhavi, T.M.3
  • 18
    • 7644238120 scopus 로고    scopus 로고
    • Enhanced skin permeation of rofecoxib using topical microemulsion gel
    • Desai, K.G. Enhanced skin permeation of rofecoxib using topical microemulsion gel. Drug Dev. Res. 2004, 63 (1), 33-40.
    • (2004) Drug Dev. Res. , vol.63 , Issue.1 , pp. 33-40
    • Desai, K.G.1
  • 19
    • 9744273197 scopus 로고    scopus 로고
    • Solubility of valdecoxib in the presence of ethanol and sodium lauryl sulfate at (298.15, 303.15, and 308.15) K
    • Liu, C.; Desai, K.G.; Liu, C. Solubility of valdecoxib in the presence of ethanol and sodium lauryl sulfate at (298.15, 303.15, and 308.15) K. J. Chem. Eng. Data 2004, 49, 1847-1850.
    • (2004) J. Chem. Eng. Data , vol.49 , pp. 1847-1850
    • Liu, C.1    Desai, K.G.2    Liu, C.3
  • 20
    • 7644228338 scopus 로고    scopus 로고
    • Solubility studies on valdecoxib in the presence of carriers, cosolvents and surfactants
    • Desai, K.G.; Park, H.J. Solubility studies on valdecoxib in the presence of carriers, cosolvents and surfactants. Drug Dev. Res. 2004, 62, 41-48.
    • (2004) Drug Dev. Res. , vol.62 , pp. 41-48
    • Desai, K.G.1    Park, H.J.2
  • 21
    • 12844253104 scopus 로고    scopus 로고
    • Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000
    • Liu, C.; Desai, K.G.; Liu, C. Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000. Drug Dev. Ind. Pharm. 2005, 31 (1), 1-10.
    • (2005) Drug Dev. Ind. Pharm. , vol.31 , Issue.1 , pp. 1-10
    • Liu, C.1    Desai, K.G.2    Liu, C.3
  • 22
    • 12344329667 scopus 로고    scopus 로고
    • Solubility of valdecoxib in the presence of polyethylene glycol 4000, polyethylene glycol 6000, polyethylene glycol 8000, and polyethylene glycol 10 000 at (298.15, 303.15, and 308.15) K
    • Liu, C.; Desai, K.G.; Liu, C. Solubility of valdecoxib in the presence of polyethylene glycol 4000, polyethylene glycol 6000, polyethylene glycol 8000, and polyethylene glycol 10 000 at (298.15, 303.15, and 308.15) K. J. Chem. Eng. Data 2004, 50 (1), 278-282.
    • (2004) J. Chem. Eng. Data , vol.50 , Issue.1 , pp. 278-282
    • Liu, C.1    Desai, K.G.2    Liu, C.3
  • 23
    • 15844411900 scopus 로고    scopus 로고
    • Solubility of rofecoxib in the presence of mannitol, poly (ethylene glycol). 4000, poly (ethylene glycol) 6000, poly (vinyl pyrrolidone) K30, and urea at (298.15, 303.15, and 308.15) K
    • Liu, C.; Desai, K.G.; Liu, C. Solubility of rofecoxib in the presence of mannitol, poly (ethylene glycol). 4000, poly (ethylene glycol) 6000, poly (vinyl pyrrolidone) K30, and urea at (298.15, 303.15, and 308.15) K. J. Chem. Eng. Data 2005, 50 (2), 661-665.
    • (2005) J. Chem. Eng. Data , vol.50 , Issue.2 , pp. 661-665
    • Liu, C.1    Desai, K.G.2    Liu, C.3
  • 25
    • 0034032146 scopus 로고    scopus 로고
    • Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14
    • Damian, F.; Blaton, N.; Naesens, L.; Balzarini, J.; Kinget, R.; Augustinjns, P.; Mooter, G.V. Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14. Eur. J. Pharm. Sci. 2000, 10, 311-322.
    • (2000) Eur. J. Pharm. Sci. , vol.10 , pp. 311-322
    • Damian, F.1    Blaton, N.2    Naesens, L.3    Balzarini, J.4    Kinget, R.5    Augustinjns, P.6    Mooter, G.V.7
  • 26
    • 0026783391 scopus 로고
    • Characterization of solid dispersion of piroxicam/polyethylene glycol 4000
    • Fernandez, 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
    • Fernandez, M.1    Rodriguez, I.C.2    Margarit, M.V.3    Cerezo, A.4
  • 27
    • 0028340095 scopus 로고
    • Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000
    • Margarit, M.V.; Rodriguez, I.C.; Cerezo, A. Physical characteristics and dissolution kinetics of solid dispersions of ketoprofen and polyethylene glycol 6000. Int. J. Pharm. 1994, 108, 101-107.
    • (1994) Int. J. Pharm. , vol.108 , pp. 101-107
    • Margarit, M.V.1    Rodriguez, I.C.2    Cerezo, A.3
  • 28
    • 0024506012 scopus 로고
    • Characterization of a diflunisal polyethylene glycol solid dispersion system
    • Najib, N.M.; Suleiman, M.S. Characterization of a diflunisal polyethylene glycol solid dispersion system. Int. J. Pharm. 1989, 51, 225-232.
    • (1989) Int. J. Pharm. , vol.51 , pp. 225-232
    • Najib, N.M.1    Suleiman, M.S.2
  • 29
    • 12244253962 scopus 로고
    • Dissolution enhancement of furosemide from ground mixtures with chitin or chitosan
    • Shin, S.C.; Oh, I.J.; Lee, K.C.; Lee, Y.B.; Koh, I.B. Dissolution enhancement of furosemide from ground mixtures with chitin or chitosan. J. Korean Pharm. Sci. 1987, 17, 175-181.
    • (1987) J. Korean Pharm. Sci. , vol.17 , pp. 175-181
    • Shin, S.C.1    Oh, I.J.2    Lee, K.C.3    Lee, Y.B.4    Koh, I.B.5
  • 31
    • 0037472364 scopus 로고    scopus 로고
    • Physicochemical characterization of solid dispersion of furosemide with TPGS
    • Shin, S.C.; Kim, J. Physicochemical characterization of solid dispersion of furosemide with TPGS. Int. J. Pharm. 2003, 251, 79-84.
    • (2003) Int. J. Pharm. , vol.251 , pp. 79-84
    • Shin, S.C.1    Kim, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.