메뉴 건너뛰기




Volumn 63, Issue 4, 2004, Pages 181-189

Enhancement of dissolution rate of rofecoxib using solid dispersions with urea

Author keywords

Dissolution rate; MDT; Rofecoxib; Solid dispersion; Solubility; Urea

Indexed keywords

DRUG CARRIER; MACROGOL 4000; MANNITOL; POVIDONE; POVIDONE K30; ROFECOXIB; UNCLASSIFIED DRUG; UREA; WATER;

EID: 16344362340     PISSN: 02724391     EISSN: None     Source Type: Journal    
DOI: 10.1002/ddr.10412     Document Type: Article
Times cited : (22)

References (33)
  • 2
    • 0020017145 scopus 로고
    • Solid dispersion of chlothalidone in urea phase diagram and dissolution characteristics
    • Bloch DW, Elegakey MA, Speiser PP. 1982. Solid dispersion of chlothalidone in urea phase diagram and dissolution characteristics. Pharm Act Helv 57:231-235.
    • (1982) Pharm Act Helv , vol.57 , pp. 231-235
    • Bloch, D.W.1    Elegakey, M.A.2    Speiser, P.P.3
  • 3
    • 0031921289 scopus 로고    scopus 로고
    • Scientific rationale for specific inhibition of COX-2
    • Bolten WW. 1998. Scientific rationale for specific inhibition of COX-2. J Rheumatol 25:2-7.
    • (1998) J Rheumatol , vol.25 , pp. 2-7
    • Bolten, W.W.1
  • 4
    • 0015124656 scopus 로고
    • Pharmaceutical applications of solid dispersions
    • Chiou WL, Riegelman S. 1971. Pharmaceutical applications of solid dispersions. J Pharm Sci 60:1281-1302.
    • (1971) J Pharm Sci , vol.60 , pp. 1281-1302
    • Chiou, W.L.1    Riegelman, S.2
  • 5
    • 0033735234 scopus 로고    scopus 로고
    • Effect of water-soluble carriers on dissolution characteristics of nifedipine solid dispersions
    • Chutimaworapan S, Ritthidej GC, Yonemochi E, Oguchi T, Yamamoto K. 2000. Effect of water-soluble carriers on dissolution characteristics of nifedipine solid dispersions. Drug Dev Ind Pharm 26:1141-1150.
    • (2000) Drug Dev Ind Pharm , vol.26 , pp. 1141-1150
    • Chutimaworapan, S.1    Ritthidej, G.C.2    Yonemochi, E.3    Oguchi, T.4    Yamamoto, K.5
  • 6
    • 0034032146 scopus 로고    scopus 로고
    • Physico-chemical 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 GV 2000. Physico-chemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14. Eur J Pharm Sci 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
  • 7
    • 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 KGH, Kulkarni AR, Aminabhavi TM. 2003. 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 48:942-945.
    • (2003) J Chem Eng Data , vol.48 , pp. 942-945
    • Desai, K.G.H.1    Kulkarni, A.R.2    Aminabhavi, T.M.3
  • 8
    • 6044274282 scopus 로고    scopus 로고
    • Coxibs and cardiovascular disease
    • FitzGerald GA 2004. Coxibs and cardiovascular disease. New Engl J Med 351:1709-1711.
    • (2004) New Engl J Med , vol.351 , pp. 1709-1711
    • FitzGerald, G.A.1
  • 9
    • 0022650603 scopus 로고
    • The current status of solid dispersions
    • Ford JL, 1986. The current status of solid dispersions. Pharm Act Helv 61:69-88.
    • (1986) Pharm Act Helv , vol.61 , pp. 69-88
    • Ford, J.L.1
  • 10
    • 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 AH, Gibaldi M, Kanig JL. 1965. 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 54:1145-1148.
    • (1965) J Pharm Sci , vol.54 , pp. 1145-1148
    • Goldberg, A.H.1    Gibaldi, M.2    Kanig, J.L.3
  • 11
    • 84984082270 scopus 로고
    • Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. II: Experimental evaluation of a eutectic mixture: Urea-acetarninophen system
    • Goldberg AH, Gibaldi M, Kanig JL. 1966a. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. II: Experimental evaluation of a eutectic mixture: urea-acetarninophen system. J Pharm Sci 55:482-487.
    • (1966) J Pharm Sci , vol.55 , pp. 482-487
    • Goldberg, A.H.1    Gibaldi, M.2    Kanig, J.L.3
  • 12
    • 84984082270 scopus 로고
    • Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. III: Experimental evaluation of griseofulvin-succinic acid solid solution
    • Goldberg AH, Gibaldi M, Kanig JL. 1966b. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. III: Experimental evaluation of griseofulvin-succinic acid solid solution. J Pharm Sci 55:482-487.
    • (1966) J Pharm Sci , vol.55 , pp. 482-487
    • Goldberg, A.H.1    Gibaldi, M.2    Kanig, J.L.3
  • 13
    • 0013920636 scopus 로고
    • Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. IV: Chloramphenicol-urea system
    • Goldberg AH, Gibaldi M, Kanig JL, Mayersohn M, 1966c. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. IV: Chloramphenicol-urea system. J Pharm Sci 55:581-583.
    • (1966) J Pharm Sci , vol.55 , pp. 581-583
    • Goldberg, A.H.1    Gibaldi, M.2    Kanig, J.L.3    Mayersohn, M.4
  • 14
    • 0030638567 scopus 로고    scopus 로고
    • Characteristics and significance of the amorphous state in pharmaceutical systems
    • Hancock BC, Zographi G. 1997. Characteristics and significance of the amorphous state in pharmaceutical systems. J Pharm Sci 86:1-12.
    • (1997) J Pharm Sci , vol.86 , pp. 1-12
    • Hancock, B.C.1    Zographi, G.2
  • 16
    • 16344386554 scopus 로고    scopus 로고
    • Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract
    • Hoerter D, Dressman JB. 1997. Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract (review). J Pharm Sci 86:1-12.
    • (1997) J Pharm Sci , vol.86 , pp. 1-12
    • Hoerter, D.1    Dressman, J.B.2
  • 17
    • 0029928882 scopus 로고    scopus 로고
    • Oral absorption improvement of poorly soluble drug using solid dispersion technique
    • Kai T, Akiyama Y, Nomura S, Sato M. 1996. Oral absorption improvement of poorly soluble drug using solid dispersion technique. Chem Pharm Bull 44:568-571.
    • (1996) Chem Pharm Bull , vol.44 , pp. 568-571
    • Kai, T.1    Akiyama, Y.2    Nomura, S.3    Sato, M.4
  • 18
    • 0028326530 scopus 로고
    • Effect of polyvinylpyrrolidone on the crystallinity and dissolution rate of solid dispersions of the anti-inflammatory Ci-987
    • Kearney AS, Gabriel DW, Mehta SC, Radebaugh GW. 1994. Effect of polyvinylpyrrolidone on the crystallinity and dissolution rate of solid dispersions of the anti-inflammatory Ci-987. Int J Pharm 104:169-174.
    • (1994) Int J Pharm , vol.104 , pp. 169-174
    • Kearney, A.S.1    Gabriel, D.W.2    Mehta, S.C.3    Radebaugh, G.W.4
  • 19
    • 0031748005 scopus 로고    scopus 로고
    • Preparation, characterization, and dissolution studies of ibuprofen solid dispersions using polyethylene glycol (PEG), talc, and PEG-talc as dispersion carriers
    • Khan GM, Zhu JB. 1998. Preparation, characterization, and dissolution studies of ibuprofen solid dispersions using polyethylene glycol (PEG), talc, and PEG-talc as dispersion carriers. Drug Dev Ind Pharm 24:455-462.
    • (1998) Drug Dev Ind Pharm , vol.24 , pp. 455-462
    • Khan, G.M.1    Zhu, J.B.2
  • 20
    • 0036875661 scopus 로고    scopus 로고
    • Preparation and characterization of drug-loaded polymethacrylic microspheres by an emulsion solvent evaporation method
    • Kim BK, Hwang SJ, Park JB, Park HJ. 2002. Preparation and characterization of drug-loaded polymethacrylic microspheres by an emulsion solvent evaporation method. J Microencapsulation 19:811-822.
    • (2002) J Microencapsulation , vol.19 , pp. 811-822
    • Kim, B.K.1    Hwang, S.J.2    Park, J.B.3    Park, H.J.4
  • 21
    • 0037027849 scopus 로고    scopus 로고
    • Preparation and characterization of chitosan microparticles intended for controlled drug delivery
    • Ko JA, Park HJ, Hwang SJ, Park JB, Lee JS. 2002. Preparation and characterization of chitosan microparticles intended for controlled drug delivery. Int J Pharm 249:165-174.
    • (2002) Int J Pharm , vol.249 , pp. 165-174
    • Ko, J.A.1    Park, H.J.2    Hwang, S.J.3    Park, J.B.4    Lee, J.S.5
  • 22
    • 0037370959 scopus 로고    scopus 로고
    • Preparation and release characteristics of polymer-coated and blended alginate microspheres
    • Lee DW, Hwang SJ, Park JB, Park HJ. 2003. Preparation and release characteristics of polymer-coated and blended alginate microspheres. J Microencapsulation 20:179-192.
    • (2003) J Microencapsulation , vol.20 , pp. 179-192
    • Lee, D.W.1    Hwang, S.J.2    Park, J.B.3    Park, H.J.4
  • 23
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • Leuner C, Dressman J. 2000. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 50:47-60.
    • (2000) Eur J Pharm Biopharm , vol.50 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 24
    • 0030829359 scopus 로고    scopus 로고
    • The discovery and function of COX-2
    • Needleman P, Isakson PC. 1997. The discovery and function of COX-2. J Rheumatol 49:6-8.
    • (1997) J Rheumatol , vol.49 , pp. 6-8
    • Needleman, P.1    Isakson, P.C.2
  • 27
  • 28
    • 0025269652 scopus 로고
    • Improved dissolution of poorly water-soluble drug from solid dispersions in polyethylene: Polysorbate 80 mixture
    • Serajuddin ATM, Sheen PC, Augustine MA. 1990. Improved dissolution of poorly water-soluble drug from solid dispersions in polyethylene: polysorbate 80 mixture. J Pharm Sci 79:463-464.
    • (1990) J Pharm Sci , vol.79 , pp. 463-464
    • Serajuddin, A.T.M.1    Sheen, P.C.2    Augustine, M.A.3
  • 29
    • 85008071016 scopus 로고
    • Studies on absorption of eutectic mixtures. I. A comparison of the behavior of eutectic mixtures of sulphathiazole and that of ordinary sulphathiazole in man
    • Sekiguchi K, Obi N. 1961. Studies on absorption of eutectic mixtures. I. A comparison of the behavior of eutectic mixtures of sulphathiazole and that of ordinary sulphathiazole in man. Chem Pharm Bull 9:866-872.
    • (1961) Chem Pharm Bull , vol.9 , pp. 866-872
    • Sekiguchi, K.1    Obi, N.2
  • 30
    • 0025135012 scopus 로고
    • Solubilization of salicylamide and acetaminophen by antihistamines in aqueous solution
    • Shah SP, Flanagan DR. 1990. Solubilization of salicylamide and acetaminophen by antihistamines in aqueous solution. J Pharm Sci 79:889-892.
    • (1990) J Pharm Sci , vol.79 , pp. 889-892
    • Shah, S.P.1    Flanagan, D.R.2
  • 31
    • 0037472364 scopus 로고    scopus 로고
    • Physicochemical characterization of solid dispersion of furosemide with TPGS
    • Shim SC, Kim J. 2003. Physicochemical characterization of solid dispersion of furosemide with TPGS. Int J Pharm 251:79-84.
    • (2003) Int J Pharm , vol.251 , pp. 79-84
    • Shim, S.C.1    Kim, J.2
  • 32
    • 12244253962 scopus 로고
    • Dissolution enhancement of furosemide from ground mixtures with chitin or chitosan
    • Shin SC, Oh IJ, Lee KC, Lee YB, Koh IB. 1987. Dissolution enhancement of furosemide from ground mixtures with chitin or chitosan. J Kor Pharm Sci 17:175-181.
    • (1987) J Kor 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
  • 33
    • 0035660775 scopus 로고    scopus 로고
    • Evaluation and selection of bio-relevant dissolution media for a poorly water soluble new chemical entity
    • Tang L, Khan SU, Muhammad NA. 2001. Evaluation and selection of bio-relevant dissolution media for a poorly water soluble new chemical entity. Pharm Dev Tech 6:531-540.
    • (2001) Pharm Dev Tech , vol.6 , pp. 531-540
    • Tang, L.1    Khan, S.U.2    Muhammad, N.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.