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Journal Abstract Search
1860 related items for PubMed ID: 17182231
1. Solid molecular dispersions of poorly water-soluble drugs in poly(2-hydroxyethyl methacrylate) hydrogels. Zahedi P, Lee PI. Eur J Pharm Biopharm; 2007 Mar; 65(3):320-8. PubMed ID: 17182231 [Abstract] [Full Text] [Related]
2. Enhanced kinetic solubility profiles of indomethacin amorphous solid dispersions in poly(2-hydroxyethyl methacrylate) hydrogels. Sun DD, Ju TC, Lee PI. Eur J Pharm Biopharm; 2012 May; 81(1):149-58. PubMed ID: 22233548 [Abstract] [Full Text] [Related]
3. Preparation and evaluation of solid dispersions of piroxicam and Eudragit S100 by spherical crystallization technique. Maghsoodi M, Sadeghpoor F. Drug Dev Ind Pharm; 2010 Aug; 36(8):917-25. PubMed ID: 20180658 [Abstract] [Full Text] [Related]
7. 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]
8. Phase behavior of poly(vinylpyrrolidone) containing amorphous solid dispersions in the presence of moisture. Rumondor AC, Marsac PJ, Stanford LA, Taylor LS. Mol Pharm; 2009 Mar 01; 6(5):1492-505. PubMed ID: 19634917 [Abstract] [Full Text] [Related]
10. Effect of water soluble carrier on dissolution profiles of diclofenac sodium. Cwiertnia B. Acta Pol Pharm; 2013 Mar 01; 70(4):721-6. PubMed ID: 23923395 [Abstract] [Full Text] [Related]
13. Influence of cyclodextrin complexation on piroxicam gel formulations. Jug M, Bećirević-Laćan M, Kwokal A, Cetina-Cizmek B. Acta Pharm; 2005 Sep 01; 55(3):223-36. PubMed ID: 16375834 [Abstract] [Full Text] [Related]
14. 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 [Abstract] [Full Text] [Related]
18. Evaluation of Inutec SP1 as a new carrier in the formulation of solid dispersions for poorly soluble drugs. Van den Mooter G, Weuts I, De Ridder T, Blaton N. Int J Pharm; 2006 Jun 19; 316(1-2):1-6. PubMed ID: 16563676 [Abstract] [Full Text] [Related]