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Journal Abstract Search

167 related items for PubMed ID: 25404856

  • 1. Fabrication and evaluation of valsartan-polymer- surfactant composite nanoparticles by using the supercritical antisolvent process.
    Kim MS, Baek IH.
    Int J Nanomedicine; 2014; 9():5167-76. PubMed ID: 25404856
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  • 2. Improved pH-independent dissolution and oral absorption of valsartan via the preparation of solid dispersion.
    Park YJ, Lee HK, Im YB, Lee W, Han HK.
    Arch Pharm Res; 2010 Aug; 33(8):1235-40. PubMed ID: 20803127
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  • 3. Development of megestrol acetate solid dispersion nanoparticles for enhanced oral delivery by using a supercritical antisolvent process.
    Ha ES, Kim JS, Baek IH, Yoo JW, Jung Y, Moon HR, Kim MS.
    Drug Des Devel Ther; 2015 Aug; 9():4269-77. PubMed ID: 26345723
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  • 7. Development of valsartan-loaded gelatin microcapsule without crystal change using hydroxypropylmethylcellulose as a stabilizer.
    Li DX, Yan YD, Oh DH, Yang KY, Seo YG, Kim JO, Kim YI, Yong CS, Choi HG.
    Drug Deliv; 2010 Jul; 17(5):322-9. PubMed ID: 20367177
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  • 11. Formulation, characterization, and in vivo evaluation of celecoxib-PVP solid dispersion nanoparticles using supercritical antisolvent process.
    Ha ES, Choo GH, Baek IH, Kim MS.
    Molecules; 2014 Dec 04; 19(12):20325-39. PubMed ID: 25486246
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  • 13. Preparation, characterization and in vivo evaluation of amorphous atorvastatin calcium nanoparticles using supercritical antisolvent (SAS) process.
    Kim MS, Jin SJ, Kim JS, Park HJ, Song HS, Neubert RH, Hwang SJ.
    Eur J Pharm Biopharm; 2008 Jun 04; 69(2):454-65. PubMed ID: 18359211
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  • 14. Enhanced dissolution and oral bioavailability of valsartan solid dispersions prepared by a freeze-drying technique using hydrophilic polymers.
    Xu WJ, Xie HJ, Cao QR, Shi LL, Cao Y, Zhu XY, Cui JH.
    Drug Deliv; 2016 Jun 04; 23(1):41-8. PubMed ID: 24735247
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  • 15. Enhanced oral bioavailability of novel mucoadhesive pellets containing valsartan prepared by a dry powder-coating technique.
    Cao QR, Liu Y, Xu WJ, Lee BJ, Yang M, Cui JH.
    Int J Pharm; 2012 Sep 15; 434(1-2):325-33. PubMed ID: 22688251
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  • 17. Microparticles-entrapped micelles: a novel delivery system to improve solubility and dissolution rate of poorly water-soluble valsartan.
    Parvataneni DM, Devraj R, Mangamoori LN.
    J Microencapsul; 2013 Sep 15; 30(8):805-16. PubMed ID: 23631386
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  • 18. Dissolution-enhancing mechanism of alkalizers in poloxamer-based solid dispersions and physical mixtures containing poorly water-soluble valsartan.
    Ha NS, Tran TT, Tran PH, Park JB, Lee BJ.
    Chem Pharm Bull (Tokyo); 2011 Sep 15; 59(7):844-50. PubMed ID: 21720034
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  • 19. Improved oral absorption of tacrolimus by a solid dispersion with hypromellose and sodium lauryl sulfate.
    Jung HJ, Ahn HI, Park JY, Ho MJ, Lee DR, Cho HR, Park JS, Choi YS, Kang MJ.
    Int J Biol Macromol; 2016 Feb 15; 83():282-7. PubMed ID: 26642839
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  • 20. Nanostructured Valsartan Microparticles with Enhanced Bioavailability Produced by High-Throughput Electrohydrodynamic Room-Temperature Atomization.
    Prieto C, Evtoski Z, Pardo-Figuerez M, Hrakovsky J, Lagaron JM.
    Mol Pharm; 2021 Aug 02; 18(8):2947-2958. PubMed ID: 34181413
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