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Volumn 4, Issue 5, 2007, Pages 794-802

Molecular and thermodynamic aspects of solubility advantage from solid dispersions

Author keywords

Amorphous; Entropy; Etoricoxib; Interactions; Solid dispersions; Solubility; Solution thermodynamics; Valdecoxib

Indexed keywords

ETORICOXIB; POVIDONE; VALDECOXIB;

EID: 35548944559     PISSN: 15438384     EISSN: 15438392     Source Type: Journal    
DOI: 10.1021/mp7000796     Document Type: Article
Times cited : (35)

References (30)
  • 1
    • 0035289779 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Delivery Rev. 2001, 46, 3-26.
    • (2001) Adv. Drug Delivery Rev , vol.46 , pp. 3-26
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 2
    • 5144219871 scopus 로고    scopus 로고
    • Amorphous drug delivery systems: Molecular aspects, design and performance
    • Kaushal, A. M.; Gupta, P.; Bansal, A. K. Amorphous drug delivery systems: molecular aspects, design and performance. Crit. Rev. Ther. Drug Carrier Syst. 2004, 21, 133-193.
    • (2004) Crit. Rev. Ther. Drug Carrier Syst , vol.21 , pp. 133-193
    • Kaushal, A.M.1    Gupta, P.2    Bansal, A.K.3
  • 3
  • 4
    • 0036913471 scopus 로고    scopus 로고
    • Enthalpy relaxation studies of celecoxib amorphous mixtures
    • Kakumanu, V. K.; Bansal, A. K. Enthalpy relaxation studies of celecoxib amorphous mixtures. Pharm. Res. 2002, 19, 1873-1878.
    • (2002) Pharm. Res , vol.19 , pp. 1873-1878
    • Kakumanu, V.K.1    Bansal, A.K.2
  • 5
    • 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
  • 6
    • 0035826241 scopus 로고    scopus 로고
    • Supercooled liquids and the glass transition
    • Debendetti, P. G.; Stillinger, F. H. Supercooled liquids and the glass transition. Nature 2001, 410, 259-267.
    • (2001) Nature , vol.410 , pp. 259-267
    • Debendetti, P.G.1    Stillinger, F.H.2
  • 7
    • 1042287180 scopus 로고    scopus 로고
    • Drug polymorphism and dosage form design: A practical perspective
    • Singhal, D.; Curatolo, W. Drug polymorphism and dosage form design: a practical perspective. Adv. Drug Delivery Rev. 2004, 56, 335-347.
    • (2004) Adv. Drug Delivery Rev , vol.56 , pp. 335-347
    • Singhal, D.1    Curatolo, W.2
  • 8
    • 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
  • 9
    • 6344247455 scopus 로고    scopus 로고
    • Stability and solubility of celecoxib-PVP amorphous dispersions: A molecular perspective
    • Gupta, P.; Kakumanu, V. K.; Bansal, A. K. Stability and solubility of celecoxib-PVP amorphous dispersions: a molecular perspective. Pharm. Res. 2004, 21, 1762-1769.
    • (2004) Pharm. Res , vol.21 , pp. 1762-1769
    • Gupta, P.1    Kakumanu, V.K.2    Bansal, A.K.3
  • 10
    • 0017235421 scopus 로고
    • Dissolution rates of high energy sulfathiazole-povidone co-precipitates II: Characterization of form of drug controlling its dissolution rate via solubility studies
    • Simonelli, A. P.; Mehta, S. C.; Higuchi, W. I. Dissolution rates of high energy sulfathiazole-povidone co-precipitates II: characterization of form of drug controlling its dissolution rate via solubility studies. J. Pharm. Sci. 1976, 65, 355-361.
    • (1976) J. Pharm. Sci , vol.65 , pp. 355-361
    • Simonelli, A.P.1    Mehta, S.C.2    Higuchi, W.I.3
  • 11
    • 0029831538 scopus 로고    scopus 로고
    • How does residual water affect the solid state degradation of drugs in the amorphous state
    • Shalaev, E. Y.; Zografi, G. How does residual water affect the solid state degradation of drugs in the amorphous state. J. Pharm. Sci. 1996, 85, 1137-1141.
    • (1996) J. Pharm. Sci , vol.85 , pp. 1137-1141
    • Shalaev, E.Y.1    Zografi, G.2
  • 12
    • 0037142202 scopus 로고    scopus 로고
    • Influence of polyethylene glycol and povidone on the polymorphic transformation and solubility of carbamazepine
    • Nair, R.; Gonen, S.; Hoag, S. W. Influence of polyethylene glycol and povidone on the polymorphic transformation and solubility of carbamazepine. Int. J. Pharm. 2002, 240, 11-22.
    • (2002) Int. J. Pharm , vol.240 , pp. 11-22
    • Nair, R.1    Gonen, S.2    Hoag, S.W.3
  • 13
    • 33646850912 scopus 로고    scopus 로고
    • Effect of hydrogen bonding interactions on the release mechanism of felodipine from nanodispersions with polyvinylpyrrolidone
    • Karavas, E.; Ktistis, G.; Xenakis, A.; Georgarakis, E. Effect of hydrogen bonding interactions on the release mechanism of felodipine from nanodispersions with polyvinylpyrrolidone. Eur J. Pharm. Biopharm. 2006, 63, 103-114.
    • (2006) Eur J. Pharm. Biopharm , vol.63 , pp. 103-114
    • Karavas, E.1    Ktistis, G.2    Xenakis, A.3    Georgarakis, E.4
  • 14
    • 0000901912 scopus 로고
    • The glass-liquid transition of hyperquenched water
    • Johari, G. P.; Hallbrucker, A.; Mayer, E. The glass-liquid transition of hyperquenched water. Nature 1987, 330, 552-553.
    • (1987) Nature , vol.330 , pp. 552-553
    • Johari, G.P.1    Hallbrucker, A.2    Mayer, E.3
  • 15
    • 17644414570 scopus 로고    scopus 로고
    • Phase behavior of amorphous molecular dispersions I: Determination of the degree and mechanism of solid solubility
    • Vasanthavada, M.; Tong, W. T.; Joshi, Y.; Kislalioglu, M. S. Phase behavior of amorphous molecular dispersions I: determination of the degree and mechanism of solid solubility. Pharm. Res. 2004, 21, 1598-1606.
    • (2004) Pharm. Res , vol.21 , pp. 1598-1606
    • Vasanthavada, M.1    Tong, W.T.2    Joshi, Y.3    Kislalioglu, M.S.4
  • 16
    • 0035997888 scopus 로고    scopus 로고
    • Disordered drug delivery: Destiny, dynamics and the Deborah number
    • Hancock, B. C. Disordered drug delivery: destiny, dynamics and the Deborah number. J. Pharm. Pharmacol. 2002, 54, 737-746.
    • (2002) J. Pharm. Pharmacol , vol.54 , pp. 737-746
    • Hancock, B.C.1
  • 17
    • 4444300929 scopus 로고    scopus 로고
    • Stability study of amorphous valdecoxib
    • Ambike, A. A.; Mahadik, K. R.; Paradkar, A. Stability study of amorphous valdecoxib. Int. J. Pharm. 2004, 282, 151-162.
    • (2004) Int. J. Pharm , vol.282 , pp. 151-162
    • Ambike, A.A.1    Mahadik, K.R.2    Paradkar, A.3
  • 19
    • 27744532687 scopus 로고    scopus 로고
    • Preparation and characterization of etoricoxib solid dispersions using lipid carriers by spray drying technique
    • Chauhan, B.; Shimpi, S.; Paradkar, A. Preparation and characterization of etoricoxib solid dispersions using lipid carriers by spray drying technique. AAPS PharmSciTech 2005, 6, E405-E412.
    • (2005) AAPS PharmSciTech , vol.6
    • Chauhan, B.1    Shimpi, S.2    Paradkar, A.3
  • 20
    • 14644406137 scopus 로고    scopus 로고
    • Molecular interactions in celecoxib-PVP- meglumine amorphous system
    • Gupta, P.; Bansal, A. K. Molecular interactions in celecoxib-PVP- meglumine amorphous system. J. Pharm. Pharmacol. 2005, 57, 303-310.
    • (2005) J. Pharm. Pharmacol , vol.57 , pp. 303-310
    • Gupta, P.1    Bansal, A.K.2
  • 21
    • 0023039336 scopus 로고
    • Retardation of polymeric carrier dissolution by dispersed drugs: Factors influencing the dissolution of solid dispersions containing polyethylene glycols
    • Corrigan, O. I. Retardation of polymeric carrier dissolution by dispersed drugs: factors influencing the dissolution of solid dispersions containing polyethylene glycols. Drug Dev. Ind. Pharm. 1986, 12, 1777-1793.
    • (1986) Drug Dev. Ind. Pharm , vol.12 , pp. 1777-1793
    • Corrigan, O.I.1
  • 22
    • 49049135337 scopus 로고
    • An investigation into the mechanisms of dissolution of alkyl p-aminobenzoates from polyethylene glycol solid dispersions
    • Saers, E. S.; Craig, D. Q. M. An investigation into the mechanisms of dissolution of alkyl p-aminobenzoates from polyethylene glycol solid dispersions. Int. J. Pharm. 1992, 83, 211-219.
    • (1992) Int. J. Pharm , vol.83 , pp. 211-219
    • Saers, E.S.1    Craig, D.Q.M.2
  • 23
    • 0021873176 scopus 로고
    • Mechanisms of dissolution of fast release solid dispersions
    • Corrigan, O. I. Mechanisms of dissolution of fast release solid dispersions. Drug Dev. Ind. Pharm. 1985, 11, 697-724.
    • (1985) Drug Dev. Ind. Pharm , vol.11 , pp. 697-724
    • Corrigan, O.I.1
  • 24
    • 0021801507 scopus 로고
    • Similarities in the release rates of different drugs from polyethylene glycol 6000 solid dispersions
    • Dubois, J. L.; Ford, J. L. Similarities in the release rates of different drugs from polyethylene glycol 6000 solid dispersions. J. Pharm. Pharmacol. 1985, 37, 494-496.
    • (1985) J. Pharm. Pharmacol , vol.37 , pp. 494-496
    • Dubois, J.L.1    Ford, J.L.2
  • 25
    • 0019967104 scopus 로고
    • Mechanism of drug dissolution rate enhancements from b cyclodextrin drug systems
    • Corrigan, O. I.; Stanley, C. T. Mechanism of drug dissolution rate enhancements from b cyclodextrin drug systems. J. Pharm. Pharmacol. 1982, 34, 621-626.
    • (1982) J. Pharm. Pharmacol , vol.34 , pp. 621-626
    • Corrigan, O.I.1    Stanley, C.T.2
  • 26
    • 0015359870 scopus 로고
    • Solubility of non electrolytes in polar solvents
    • Yalkowski, S. H.; Flynn, G. L.; Amidon, G. L. Solubility of non electrolytes in polar solvents. J. Pharm. Sci. 1972, 61, 983-984.
    • (1972) J. Pharm. Sci , vol.61 , pp. 983-984
    • Yalkowski, S.H.1    Flynn, G.L.2    Amidon, G.L.3
  • 27
    • 35548960046 scopus 로고    scopus 로고
    • Hodge, I. M. Adam-Gibbs formulation of enthalpy relaxation near the glass transition. J. Res. Natl. Inst. Stand. Technol. 1997, 102, 195-205.
    • Hodge, I. M. Adam-Gibbs formulation of enthalpy relaxation near the glass transition. J. Res. Natl. Inst. Stand. Technol. 1997, 102, 195-205.
  • 28
    • 0021234228 scopus 로고
    • Thermodynamics of aqueous solutions of alkyl p-aminobenzoate
    • Paruta, A. N. Thermodynamics of aqueous solutions of alkyl p-aminobenzoate. Drug Dev. Ind. Pharm. 1984, 10, 453-465.
    • (1984) Drug Dev. Ind. Pharm , vol.10 , pp. 453-465
    • Paruta, A.N.1
  • 29
    • 12844253104 scopus 로고    scopus 로고
    • Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000
    • Liu, C.; Liu, C.; Desai, K. G. H. Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000. Drug Dev. Ind. Pharm. 2005, 1, 1-10.
    • (2005) Drug Dev. Ind. Pharm , vol.1 , pp. 1-10
    • Liu, C.1    Liu, C.2    Desai, K.G.H.3
  • 30
    • 25144499290 scopus 로고    scopus 로고
    • Physical stability and solubility advantage from amorphous celecoxib: The role of thermodynamic quantities and molecular mobility
    • Gupta, P.; Chawla, G.; Bansal, A. K. Physical stability and solubility advantage from amorphous celecoxib: the role of thermodynamic quantities and molecular mobility. Mol. Pharmaceutics 2004, 1, 406-413.
    • (2004) Mol. Pharmaceutics , vol.1 , pp. 406-413
    • Gupta, P.1    Chawla, G.2    Bansal, A.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.