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Journal Abstract Search

152 related items for PubMed ID: 17223289

  • 1. Effect of n-scCO(2) on crystalline to amorphous conversion of carbamazepine.
    Ugaonkar S, Nunes AC, Needham TE.
    Int J Pharm; 2007 Mar 21; 333(1-2):152-61. PubMed ID: 17223289
    [Abstract] [Full Text] [Related]

  • 2. Solid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methods.
    Sethia S, Squillante E.
    Int J Pharm; 2004 Mar 19; 272(1-2):1-10. PubMed ID: 15019063
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  • 3. Adsorption onto Mesoporous Silica Using Supercritical Fluid Technology Improves Dissolution Rate of Carbamazepine-a Poorly Soluble Compound.
    Gandhi AV, Thipsay P, Kirthivasan B, Squillante E.
    AAPS PharmSciTech; 2017 Nov 19; 18(8):3140-3150. PubMed ID: 28534299
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  • 4. Solubility and partitioning of carbamazepine in a two-phase supercritical carbon dioxide/polyvinylpyrrolidone system.
    Ugaonkar S, Needham TE, Bothun GD.
    Int J Pharm; 2011 Jan 17; 403(1-2):96-100. PubMed ID: 20971172
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  • 5. Physicochemical characterization of solid dispersions of carbamazepine formulated by supercritical carbon dioxide and conventional solvent evaporation method.
    Sethia S, Squillante E.
    J Pharm Sci; 2002 Sep 17; 91(9):1948-57. PubMed ID: 12210042
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  • 9. Evaluation of physico-mechanical properties of drug-excipients agglomerates obtained by crystallization.
    Maghsoodi M, Tajalli Bakhsh AS.
    Pharm Dev Technol; 2011 Jun 17; 16(3):243-9. PubMed ID: 20175665
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  • 11. Amino acids as co-amorphous stabilizers for poorly water soluble drugs--Part 1: preparation, stability and dissolution enhancement.
    Löbmann K, Grohganz H, Laitinen R, Strachan C, Rades T.
    Eur J Pharm Biopharm; 2013 Nov 17; 85(3 Pt B):873-81. PubMed ID: 23537574
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  • 12. Physicochemical characterization of solid dispersions of three antiepileptic drugs prepared by solvent evaporation method.
    Douroumis D, Bouropoulos N, Fahr A.
    J Pharm Pharmacol; 2007 May 17; 59(5):645-53. PubMed ID: 17524229
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  • 13. Stable carbamazepine colloidal systems using the cosolvent technique.
    Douroumis D, Fahr A.
    Eur J Pharm Sci; 2007 Apr 17; 30(5):367-74. PubMed ID: 17234395
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  • 14. Glucosamine HCl as a new carrier for improved dissolution behaviour: effect of grinding.
    Al-Hamidi H, Edwards AA, Mohammad MA, Nokhodchi A.
    Colloids Surf B Biointerfaces; 2010 Nov 01; 81(1):96-109. PubMed ID: 20674291
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  • 15. Solubility of small-molecule crystals in polymers: D-mannitol in PVP, indomethacin in PVP/VA, and nifedipine in PVP/VA.
    Tao J, Sun Y, Zhang GG, Yu L.
    Pharm Res; 2009 Apr 01; 26(4):855-64. PubMed ID: 19052850
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  • 17. Preparation of an amorphous sodium furosemide salt improves solubility and dissolution rate and leads to a faster Tmax after oral dosing to rats.
    Nielsen LH, Gordon S, Holm R, Selen A, Rades T, Müllertz A.
    Eur J Pharm Biopharm; 2013 Nov 01; 85(3 Pt B):942-51. PubMed ID: 24075980
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  • 18. Comparing various techniques to produce micro/nanoparticles for enhancing the dissolution of celecoxib containing PVP.
    Homayouni A, Sadeghi F, Varshosaz J, Garekani HA, Nokhodchi A.
    Eur J Pharm Biopharm; 2014 Sep 01; 88(1):261-74. PubMed ID: 24952357
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  • 19. Crystallization pathways and kinetics of carbamazepine-nicotinamide cocrystals from the amorphous state by in situ thermomicroscopy, spectroscopy, and calorimetry studies.
    Seefeldt K, Miller J, Alvarez-Núñez F, Rodríguez-Hornedo N.
    J Pharm Sci; 2007 May 01; 96(5):1147-58. PubMed ID: 17455346
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  • 20. Stabilization of low glass transition temperature indomethacin formulations: impact of polymer-type and its concentration.
    Chokshi RJ, Shah NH, Sandhu HK, Malick AW, Zia H.
    J Pharm Sci; 2008 Jun 01; 97(6):2286-98. PubMed ID: 17879977
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