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Volumn 84, Issue 1, 2013, Pages 228-237

Preparation of carbamazepine-Soluplus® solid dispersions by hot-melt extrusion, and prediction of drug-polymer miscibility by thermodynamic model fitting

Author keywords

Carbamazepine; Flory Huggins; Hansen solubility parameter; Hot melt extrusion; Solid dispersion; Soluplus

Indexed keywords

CARBAMAZEPINE; PLASTICIZER; POLYETHYLENEGLYCOL POLYVINYL CAPROLACTAM POLYVINYL ACETATE GRAFTED COPOLYMER; POLYMER; UNCLASSIFIED DRUG;

EID: 84876933684     PISSN: 09396411     EISSN: 18733441     Source Type: Journal    
DOI: 10.1016/j.ejpb.2012.12.018     Document Type: Article
Times cited : (171)

References (45)
  • 1
    • 85111386879 scopus 로고    scopus 로고
    • Hot-melt extrusion technique: A review
    • R. Chokshi, and H. Zia Hot-melt extrusion technique: a review Iran. J. Pharm. Res. 3 2004 3 16
    • (2004) Iran. J. Pharm. Res. , vol.3 , pp. 3-16
    • Chokshi, R.1    Zia, H.2
  • 2
    • 1842865536 scopus 로고    scopus 로고
    • Melt extrusion: From process to drug delivery technology
    • J. Breitenbach Melt extrusion: from process to drug delivery technology Eur. J. Pharm. Biopharm. 54 2002 107 117
    • (2002) Eur. J. Pharm. Biopharm. , vol.54 , pp. 107-117
    • Breitenbach, J.1
  • 4
    • 30544436192 scopus 로고    scopus 로고
    • Characterization of physico-mechanical properties of indomethacin and polymers to assess their suitability for hot-melt extrusion process as a means to manufacture solid dispersion/solution
    • R.J. Chokshi, H.K. Sandhu, R.M. Iyer, N.H. Shah, A.W. Malick, and H. Zia Characterization of physico-mechanical properties of indomethacin and polymers to assess their suitability for hot-melt extrusion process as a means to manufacture solid dispersion/solution J. Pharm. Sci. 94 11 2005 2463 2474
    • (2005) J. Pharm. Sci. , vol.94 , Issue.11 , pp. 2463-2474
    • Chokshi, R.J.1    Sandhu, H.K.2    Iyer, R.M.3    Shah, N.H.4    Malick, A.W.5    Zia, H.6
  • 5
    • 0034601240 scopus 로고    scopus 로고
    • Improving drug solubility for oral delivery using solid dispersions
    • C. Leuner, and J. Dressman Improving drug solubility for oral delivery using solid dispersions Eur. J. Pharm. Biopharm. 50 1 2000 47 60
    • (2000) Eur. J. Pharm. Biopharm. , vol.50 , Issue.1 , pp. 47-60
    • Leuner, C.1    Dressman, J.2
  • 6
    • 0028287352 scopus 로고
    • Evaluation of hot-melt extrusion as a new technique for the production of polymer-based pellets for sustained release capsules containing high loadings of freely soluble drugs
    • N. Follonier, E. Doelker, and E.T. Cole Evaluation of hot-melt extrusion as a new technique for the production of polymer-based pellets for sustained release capsules containing high loadings of freely soluble drugs Drug Dev. Ind. Pharm. 20 1994 1323 1339
    • (1994) Drug Dev. Ind. Pharm. , vol.20 , pp. 1323-1339
    • Follonier, N.1    Doelker, E.2    Cole, E.T.3
  • 8
    • 0036139891 scopus 로고    scopus 로고
    • Preparation of extruded carbamazepine and PEG 4000 as a potential rapid release dosage form
    • B. Perissutti, J.M. Newton, F. Podczeck, and F. Rubessa Preparation of extruded carbamazepine and PEG 4000 as a potential rapid release dosage form Eur. J. Pharm. Biopharm. 53 2002 125 132
    • (2002) Eur. J. Pharm. Biopharm. , vol.53 , pp. 125-132
    • Perissutti, B.1    Newton, J.M.2    Podczeck, F.3    Rubessa, F.4
  • 10
    • 33749442356 scopus 로고    scopus 로고
    • Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility
    • P.J. Marsac, S.L. Shamblin, and L.S. Taylor Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility Pharm. Res. 23 10 2006 2417 2426
    • (2006) Pharm. Res. , vol.23 , Issue.10 , pp. 2417-2426
    • Marsac, P.J.1    Shamblin, S.L.2    Taylor, L.S.3
  • 12
    • 0035845751 scopus 로고    scopus 로고
    • Selection of excipients for melt extrusion with two poorly water-soluble drugs by solubility parameter calculation and thermal analysis
    • A. Forster, J. Hempenstall, I. Tucker, and T. Rades Selection of excipients for melt extrusion with two poorly water-soluble drugs by solubility parameter calculation and thermal analysis Int. J. Pharm. 226 2001 147 161
    • (2001) Int. J. Pharm. , vol.226 , pp. 147-161
    • Forster, A.1    Hempenstall, J.2    Tucker, I.3    Rades, T.4
  • 13
    • 0035800245 scopus 로고    scopus 로고
    • A comparison of alternative polymer excipients and processing methods for making solid dispersions of a poorly water soluble drug
    • E. Broman, C. Khoo, and L.S. Taylor A comparison of alternative polymer excipients and processing methods for making solid dispersions of a poorly water soluble drug Int. J. Pharm. 222 2001 139 151
    • (2001) Int. J. Pharm. , vol.222 , pp. 139-151
    • Broman, E.1    Khoo, C.2    Taylor, L.S.3
  • 14
    • 4344664615 scopus 로고    scopus 로고
    • Physicochemical properties of the binary system glibenclamide and polyethylene glycol 4000
    • S.E. Bartsch, and U.J. Griesser Physicochemical properties of the binary system glibenclamide and polyethylene glycol 4000 J. Therm. Anal. Calorim. 77 2 2004 555 569
    • (2004) J. Therm. Anal. Calorim. , vol.77 , Issue.2 , pp. 555-569
    • Bartsch, S.E.1    Griesser, U.J.2
  • 15
    • 57749206650 scopus 로고    scopus 로고
    • Estimation of drug-polymer miscibility and solubility in amorphous solid dispersions using experimentally determined interaction parameters
    • P.J. Marsac, T.L. Li, and L.S. Taylor Estimation of drug-polymer miscibility and solubility in amorphous solid dispersions using experimentally determined interaction parameters Pharm. Res. 26 1 2009 139 151
    • (2009) Pharm. Res. , vol.26 , Issue.1 , pp. 139-151
    • Marsac, P.J.1    Li, T.L.2    Taylor, L.S.3
  • 17
    • 0014479469 scopus 로고
    • The universality of the solubility parameter
    • C.M. Hansen The universality of the solubility parameter Ind. Eng. Chem. Prod. Res. Dev. 8 1969 2 11
    • (1969) Ind. Eng. Chem. Prod. Res. Dev. , vol.8 , pp. 2-11
    • Hansen, C.M.1
  • 20
    • 0032726595 scopus 로고    scopus 로고
    • Solubility parameters as predictors of miscibility in solid dispersions
    • D. Greenhalgh, A. Williams, P. Timmins, and P. York Solubility parameters as predictors of miscibility in solid dispersions J. Pharm. Sci. 88 1999 1182 1190
    • (1999) J. Pharm. Sci. , vol.88 , pp. 1182-1190
    • Greenhalgh, D.1    Williams, A.2    Timmins, P.3    York, P.4
  • 21
    • 1242337285 scopus 로고    scopus 로고
    • Solubilizing excipients in oral and injectable formulations
    • G. Strickley Solubilizing excipients in oral and injectable formulations Pharm. Res. 21 2004 201 230
    • (2004) Pharm. Res. , vol.21 , pp. 201-230
    • Strickley, G.1
  • 23
    • 77951538902 scopus 로고    scopus 로고
    • Combining HME & solubilization: Soluplus®-The solid solution
    • H. Hardung, D. Djuric, and S. Ali Combining HME & solubilization: Soluplus®-The solid solution Drug Deliv. Technol. 10 3 2010
    • (2010) Drug Deliv. Technol. , vol.10 , Issue.3
    • Hardung, H.1    Djuric, D.2    Ali, S.3
  • 25
    • 36549042006 scopus 로고    scopus 로고
    • Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs
    • T. Vasconcelos, B. Sarmento, and P. Costa Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs Drug Discov. Today 12 2007 1068 1075
    • (2007) Drug Discov. Today , vol.12 , pp. 1068-1075
    • Vasconcelos, T.1    Sarmento, B.2    Costa, P.3
  • 26
    • 82255179553 scopus 로고    scopus 로고
    • Comparison of electrospun and extruded Soluplus®-based solid dosage forms of improved dissolution
    • Z.K. Nagy, A. Balogh, B. Vajna, A. Farkas, G. Patyi, A. Kramarics, and G. Marosi Comparison of electrospun and extruded Soluplus®-based solid dosage forms of improved dissolution J. Pharm. Sci. 101 1 2012 322 332
    • (2012) J. Pharm. Sci. , vol.101 , Issue.1 , pp. 322-332
    • Nagy, Z.K.1    Balogh, A.2    Vajna, B.3    Farkas, A.4    Patyi, G.5    Kramarics, A.6    Marosi, G.7
  • 29
    • 62649134312 scopus 로고    scopus 로고
    • Justification of biowaiver for carbamazepine, a low soluble high permeable compound, in solid dosage forms based on IVIVC and gastrointestinal simulation
    • I. Kovacevic, J. Parojcic, I. Homsek, M. Tubic-Grozdanis, and P. Langguth Justification of biowaiver for carbamazepine, a low soluble high permeable compound, in solid dosage forms based on IVIVC and gastrointestinal simulation Mol. Pharm. 6 1 2008 40 47
    • (2008) Mol. Pharm. , vol.6 , Issue.1 , pp. 40-47
    • Kovacevic, I.1    Parojcic, J.2    Homsek, I.3    Tubic-Grozdanis, M.4    Langguth, P.5
  • 30
    • 0023025587 scopus 로고
    • Polymorphic transitions of CBZ during grinding and compression
    • C. Lefebvre, and A.M. Guyot-Hermann Polymorphic transitions of CBZ during grinding and compression Drug Dev. Ind. Pharm. 12 11-13 1986 1913 1927
    • (1986) Drug Dev. Ind. Pharm. , vol.12 , Issue.1113 , pp. 1913-1927
    • Lefebvre, C.1    Guyot-Hermann, A.M.2
  • 31
    • 3543045038 scopus 로고    scopus 로고
    • Modeling and monitoring of polymorphic transformations during the drying phase of wet granulation
    • T.D. Davis, G.E. Peck, J.G. Stowell, K.R. Morris, and S.R. Byrn Modeling and monitoring of polymorphic transformations during the drying phase of wet granulation Pharm. Res. 21 5 2004 860 866
    • (2004) Pharm. Res. , vol.21 , Issue.5 , pp. 860-866
    • Davis, T.D.1    Peck, G.E.2    Stowell, J.G.3    Morris, K.R.4    Byrn, S.R.5
  • 32
    • 33750908727 scopus 로고    scopus 로고
    • Simultaneous quantification of carbamazepine crystal forms in ternary mixtures (I, III and IV) by diffuse reflectance FTIR spectroscopy (DRIFTS) and multivariate calibration
    • K. Kipouros, K. Kachrimanis, I. Nikolakakis, V. Tserki, and S. Malamataris Simultaneous quantification of carbamazepine crystal forms in ternary mixtures (I, III and IV) by diffuse reflectance FTIR spectroscopy (DRIFTS) and multivariate calibration J. Pharm. Sci. 95 11 2006 2419 2431
    • (2006) J. Pharm. Sci. , vol.95 , Issue.11 , pp. 2419-2431
    • Kipouros, K.1    Kachrimanis, K.2    Nikolakakis, I.3    Tserki, V.4    Malamataris, S.5
  • 33
    • 70349328788 scopus 로고    scopus 로고
    • 37th ed., Pharmaceutical Press, London (CD-Rom Version)
    • Martindale: The Complete Drug Reference, 37th ed., Pharmaceutical Press, London, 2007 (CD-Rom Version).
    • (2007) Martindale: The Complete Drug Reference
  • 35
    • 84876933806 scopus 로고    scopus 로고
    • Influence of the extrusion temperature on the physical properties of solid dispersions based on a new graft copolymer
    • Prague, Czech Republic
    • A.A. Foppoli, G. Loreti, E. Macchi, M. Cerea, A. Gazzaniga, Influence of the extrusion temperature on the physical properties of solid dispersions based on a new graft copolymer, in: Proceedings of the PharmSciFair, Prague, Czech Republic, 2011.
    • (2011) Proceedings of the PharmSciFair
    • Foppoli, A.A.1    Loreti, G.2    Macchi, E.3    Cerea, M.4    Gazzaniga, A.5
  • 37
    • 84862304361 scopus 로고    scopus 로고
    • Improving the chemical stability of amorphous solid dispersion with cocrystal technique by hot melt extrusion
    • X. Liu, M. Lu, Z. Guo, L. Huang, X. Feng, and C. Wu Improving the chemical stability of amorphous solid dispersion with cocrystal technique by hot melt extrusion Pharm. Res. 29 2012 806 817
    • (2012) Pharm. Res. , vol.29 , pp. 806-817
    • Liu, X.1    Lu, M.2    Guo, Z.3    Huang, L.4    Feng, X.5    Wu, C.6
  • 39
    • 0033512614 scopus 로고    scopus 로고
    • Quickly screen solvents for organic solids
    • T.C. Frank, J.R. Downey, and S.K. Gupta Quickly screen solvents for organic solids Chem. Eng. Prog. 95 12 1999 41 61
    • (1999) Chem. Eng. Prog. , vol.95 , Issue.12 , pp. 41-61
    • Frank, T.C.1    Downey, J.R.2    Gupta, S.K.3
  • 40
    • 0033988596 scopus 로고    scopus 로고
    • Physicochemical properties and bioavailability of carbamazepine polymorphs and dehydrate
    • Y. Kobayashi, S. Ito, S. Itai, and K. Yamamoto Physicochemical properties and bioavailability of carbamazepine polymorphs and dehydrate Int. J. Pharm. 193 2 2000 137 146
    • (2000) Int. J. Pharm. , vol.193 , Issue.2 , pp. 137-146
    • Kobayashi, Y.1    Ito, S.2    Itai, S.3    Yamamoto, K.4
  • 41
    • 0035107663 scopus 로고    scopus 로고
    • Interactions between carbamazepine and polyethylene glycol (PEG) 6000: Characterisations of the physical, solid dispersed and eutectic mixtures
    • N. Zerrouk, S. Toscani, J.M. Gines-Dorado, C. Chemtob, R. Ceólin, and J. Dugué Interactions between carbamazepine and polyethylene glycol (PEG) 6000: characterisations of the physical, solid dispersed and eutectic mixtures Eur. J. Pharm. Sci. 12 2001 395 404
    • (2001) Eur. J. Pharm. Sci. , vol.12 , pp. 395-404
    • Zerrouk, N.1    Toscani, S.2    Gines-Dorado, J.M.3    Chemtob, C.4    Ceólin, R.5    Dugué, J.6
  • 42
    • 0024382811 scopus 로고
    • Effect of type and extent of crystalline order on chemical and physical stability of carbamazepine
    • F.U. Krahn, and J.B. Mielck Effect of type and extent of crystalline order on chemical and physical stability of carbamazepine Int. J. Pharm. 53 1989 25 34
    • (1989) Int. J. Pharm. , vol.53 , pp. 25-34
    • Krahn, F.U.1    Mielck, J.B.2
  • 43
    • 0242322069 scopus 로고    scopus 로고
    • Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form i
    • A.L. Grzesiak, M. Lang, K. Kim, and A.J. Matzger Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I J. Pharm. Sci. 92 11 2003 2260 2271
    • (2003) J. Pharm. Sci. , vol.92 , Issue.11 , pp. 2260-2271
    • Grzesiak, A.L.1    Lang, M.2    Kim, K.3    Matzger, A.J.4
  • 44
    • 84876914783 scopus 로고    scopus 로고
    • Solubility enhancement of Efavirenz hydrochloride by hot melt technique
    • V. Deshmukh, S. Mulik, T. Deshmukh, and K. Kasat Solubility enhancement of Efavirenz hydrochloride by hot melt technique Curr. Pharm. Res. 1 4 2011 320 336
    • (2011) Curr. Pharm. Res. , vol.1 , Issue.4 , pp. 320-336
    • Deshmukh, V.1    Mulik, S.2    Deshmukh, T.3    Kasat, K.4
  • 45
    • 0030896467 scopus 로고    scopus 로고
    • The use of solubility parameters in pharmaceutical dosage form design
    • B.C. Hancock, P. York, and R. Raymond The use of solubility parameters in pharmaceutical dosage form design Int. J. Pharm. 148 1997 1 21
    • (1997) Int. J. Pharm. , vol.148 , pp. 1-21
    • Hancock, B.C.1    York, P.2    Raymond, R.3


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