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PUBMED FOR HANDHELDS

Journal Abstract Search


414 related items for PubMed ID: 21975808

  • 1.
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  • 2. Formulation of sustained-release dosage form of verapamil hydrochloride by solid dispersion technique using Eudragit RLPO or Kollidon SR.
    Sahoo J, Murthy PN, Biswal S, Manik.
    AAPS PharmSciTech; 2009; 10(1):27-33. PubMed ID: 19145487
    [Abstract] [Full Text] [Related]

  • 3. Modulation of drug release by utilizing pH-independent matrix system comprising water soluble drug verapamil hydrochloride.
    Baviskar D, Sharma R, Jain D.
    Pak J Pharm Sci; 2013 Jan; 26(1):137-44. PubMed ID: 23261739
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  • 6. 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; 59(5):645-53. PubMed ID: 17524229
    [Abstract] [Full Text] [Related]

  • 7. Selection of the suitable polymer for supercritical fluid assisted preparation of carvedilol solid dispersions.
    Djuris J, Milovanovic S, Medarevic D, Dobricic V, Dapčević A, Ibric S.
    Int J Pharm; 2019 Jan 10; 554():190-200. PubMed ID: 30414899
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  • 8. Controlled poorly soluble drug release from solid self-microemulsifying formulations with high viscosity hydroxypropylmethylcellulose.
    Yi T, Wan J, Xu H, Yang X.
    Eur J Pharm Sci; 2008 Aug 07; 34(4-5):274-80. PubMed ID: 18541418
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  • 10. Formulation performance and processability window for manufacturing a dual-polymer amorphous solid dispersion via hot-melt extrusion and strand pelletization.
    Hörmann TR, Jäger N, Funke A, Mürb RK, Khinast JG, Paudel A.
    Int J Pharm; 2018 Dec 20; 553(1-2):408-421. PubMed ID: 30326284
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  • 11. Characterization and drug release investigation of amorphous drug-hydroxypropyl methylcellulose composites made via supercritical carbon dioxide assisted impregnation.
    Gong K, Rehman IU, Darr JA.
    J Pharm Biomed Anal; 2008 Dec 01; 48(4):1112-9. PubMed ID: 18922658
    [Abstract] [Full Text] [Related]

  • 12. Mid-infrared spectroscopy as a polymer selection tool for formulating amorphous solid dispersions.
    Wegiel LA, Mauer LJ, Edgar KJ, Taylor LS.
    J Pharm Pharmacol; 2014 Feb 01; 66(2):244-55. PubMed ID: 24433425
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  • 13. 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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  • 14. Raman and thermal analysis of indomethacin/PVP solid dispersion enteric microparticles.
    Fini A, Cavallari C, Ospitali F.
    Eur J Pharm Biopharm; 2008 Sep 10; 70(1):409-20. PubMed ID: 18621516
    [Abstract] [Full Text] [Related]

  • 15. Application of Solid Dispersion Technique to Improve Solubility and Sustain Release of Emamectin Benzoate.
    Huang BB, Liu DX, Liu K, Wu G.
    Molecules; 2019 Nov 26; 24(23):. PubMed ID: 31779169
    [Abstract] [Full Text] [Related]

  • 16. Application of PVP/HPMC miscible blends with enhanced mucoadhesive properties for adjusting drug release in predictable pulsatile chronotherapeutics.
    Karavas E, Georgarakis E, Bikiaris D.
    Eur J Pharm Biopharm; 2006 Aug 26; 64(1):115-26. PubMed ID: 16675210
    [Abstract] [Full Text] [Related]

  • 17. To enhance dissolution rate of poorly water-soluble drugs: glucosamine hydrochloride as a potential carrier in solid dispersion formulations.
    Al-Hamidi H, Edwards AA, Mohammad MA, Nokhodchi A.
    Colloids Surf B Biointerfaces; 2010 Mar 01; 76(1):170-8. PubMed ID: 19945828
    [Abstract] [Full Text] [Related]

  • 18. Novel valsartan-loaded solid dispersion with enhanced bioavailability and no crystalline changes.
    Yan YD, Sung JH, Kim KK, Kim DW, Kim JO, Lee BJ, Yong CS, Choi HG.
    Int J Pharm; 2012 Jan 17; 422(1-2):202-10. PubMed ID: 22085435
    [Abstract] [Full Text] [Related]

  • 19. Preparation of a solid dispersion of felodipine using a solvent wetting method.
    Kim EJ, Chun MK, Jang JS, Lee IH, Lee KR, Choi HK.
    Eur J Pharm Biopharm; 2006 Oct 17; 64(2):200-5. PubMed ID: 16750355
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  • 20. Investigation and correlation of physical stability, dissolution behaviour and interaction parameter of amorphous solid dispersions of telmisartan: a drug development perspective.
    Dukeck R, Sieger P, Karmwar P.
    Eur J Pharm Sci; 2013 Jul 16; 49(4):723-31. PubMed ID: 23684913
    [Abstract] [Full Text] [Related]


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