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Journal Abstract Search

296 related items for PubMed ID: 25673042

  • 1.
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  • 2. Use of the Flory-Huggins theory to predict the solubility of nifedipine and sulfamethoxazole in the triblock, graft copolymer Soluplus.
    Altamimi MA, Neau SH.
    Drug Dev Ind Pharm; 2016 Mar; 42(3):446-455. PubMed ID: 26266965
    [Abstract] [Full Text] [Related]

  • 3. Amorphous solid dispersions of piroxicam and Soluplus(®): Qualitative and quantitative analysis of piroxicam recrystallization during storage.
    Lust A, Strachan CJ, Veski P, Aaltonen J, Heinämäki J, Yliruusi J, Kogermann K.
    Int J Pharm; 2015 Mar; 486(1-2):306-14. PubMed ID: 25843761
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  • 4. An investigation into the role of polymeric carriers on crystal growth within amorphous solid dispersion systems.
    Tian Y, Jones DS, Andrews GP.
    Mol Pharm; 2015 Apr 06; 12(4):1180-92. PubMed ID: 25692314
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  • 5. On the inherent properties of Soluplus and its application in ibuprofen solid dispersions generated by microwave-quench cooling technology.
    Shi NQ, Lai HW, Zhang Y, Feng B, Xiao X, Zhang HM, Li ZQ, Qi XR.
    Pharm Dev Technol; 2018 Jul 06; 23(6):573-586. PubMed ID: 27824281
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  • 8. Improvement in the water solubility of drugs with a solid dispersion system by spray drying and hot-melt extrusion with using the amphiphilic polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer and d-mannitol.
    Ogawa N, Hiramatsu T, Suzuki R, Okamoto R, Shibagaki K, Fujita K, Takahashi C, Kawashima Y, Yamamoto H.
    Eur J Pharm Sci; 2018 Jan 01; 111():205-214. PubMed ID: 28893625
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  • 9. FTIR spectroscopic study of poly(ethylene glycol)-nifedipine dispersion stability in different relative humidities.
    Iqbal WS, Chan KL.
    J Pharm Sci; 2015 Jan 01; 104(1):280-4. PubMed ID: 25410816
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  • 10. Phase behavior, intermolecular interaction, and solid state characterization of amorphous solid dispersion of Febuxostat.
    Kini A, Patel SB.
    Pharm Dev Technol; 2017 Feb 01; 22(1):45-57. PubMed ID: 26853838
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  • 12. Molecular interaction between glimepiride and Soluplus®-PEG 4000 hybrid based solid dispersions: Characterisation and anti-diabetic studies.
    Reginald-Opara JN, Attama A, Ofokansi K, Umeyor C, Kenechukwu F.
    Int J Pharm; 2015 Dec 30; 496(2):741-50. PubMed ID: 26581773
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  • 13. Dissolution enhancement of felodipine by amorphous nanodispersions using an amphiphilic polymer: insight into the role of drug-polymer interactions on drug dissolution.
    Pandey MM, Jaipal A, Charde SY, Goel P, Kumar L.
    Pharm Dev Technol; 2016 Dec 30; 21(4):463-74. PubMed ID: 25777532
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  • 14. Solid-state characterization of nifedipine solid dispersions.
    Vippagunta SR, Maul KA, Tallavajhala S, Grant DJ.
    Int J Pharm; 2002 Apr 02; 236(1-2):111-23. PubMed ID: 11891075
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  • 15. Non-invasive insight into the release mechanisms of a poorly soluble drug from amorphous solid dispersions by confocal Raman microscopy.
    Punčochová K, Vukosavljevic B, Hanuš J, Beránek J, Windbergs M, Štěpánek F.
    Eur J Pharm Biopharm; 2016 Apr 02; 101():119-25. PubMed ID: 26861928
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  • 18. Drug-polymer interaction and its significance on the physical stability of nifedipine amorphous dispersion in microparticles of an ammonio methacrylate copolymer and ethylcellulose binary blend.
    Huang J, Wigent RJ, Schwartz JB.
    J Pharm Sci; 2008 Jan 02; 97(1):251-62. PubMed ID: 17724668
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  • 19. Characterization and stability of solid dispersions based on PEG/polymer blends.
    Bley H, Fussnegger B, Bodmeier R.
    Int J Pharm; 2010 May 10; 390(2):165-73. PubMed ID: 20132875
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  • 20. Miscibility of nifedipine and hydrophilic polymers as measured by (1)H-NMR spin-lattice relaxation.
    Aso Y, Yoshioka S, Miyazaki T, Kawanishi T, Tanaka K, Kitamura S, Takakura A, Hayashi T, Muranushi N.
    Chem Pharm Bull (Tokyo); 2007 Aug 10; 55(8):1227-31. PubMed ID: 17666850
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