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Journal Abstract Search

232 related items for PubMed ID: 21219991

  • 21. The dissolution enhancement of piroxicam in its physical mixtures and solid dispersion formulations using gluconolactone and glucosamine hydrochloride as potential carriers.
    Al-Hamidi H, Obeidat WM, Nokhodchi A.
    Pharm Dev Technol; 2015 Jan; 20(1):74-83. PubMed ID: 24392858
    [Abstract] [Full Text] [Related]

  • 22. Synthesis of novel core-shell structured dual-mesoporous silica nanospheres and their application for enhancing the dissolution rate of poorly water-soluble drugs.
    Wu C, Sun X, Zhao Z, Zhao Y, Hao Y, Liu Y, Gao Y.
    Mater Sci Eng C Mater Biol Appl; 2014 Nov; 44():262-7. PubMed ID: 25280705
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  • 23. Enhanced dissolution of ibuprofen using solid dispersion with poloxamer 407.
    Newa M, Bhandari KH, Oh DH, Kim YR, Sung JH, Kim JO, Woo JS, Choi HG, Yong CS.
    Arch Pharm Res; 2008 Nov; 31(11):1497-507. PubMed ID: 19023548
    [Abstract] [Full Text] [Related]

  • 24. Preparation and physicochemical characterizations of tanshinone IIA solid dispersion.
    Zhao X, Liu X, Gan L, Zhou C, Mo J.
    Arch Pharm Res; 2011 Jun; 34(6):949-59. PubMed ID: 21725816
    [Abstract] [Full Text] [Related]

  • 25. Novel scheme for rapid synthesis of hollow mesoporous silica nanoparticles (HMSNs) and their application as an efficient delivery carrier for oral bioavailability improvement of poorly water-soluble BCS type II drugs.
    Li T, Geng T, Md A, Banerjee P, Wang B.
    Colloids Surf B Biointerfaces; 2019 Apr 01; 176():185-193. PubMed ID: 30616109
    [Abstract] [Full Text] [Related]

  • 26. Impact of surface area of silica particles on dissolution rate and oral bioavailability of poorly water soluble drugs: a case study with aceclofenac.
    Kumar D, Sailaja Chirravuri SV, Shastri NR.
    Int J Pharm; 2014 Jan 30; 461(1-2):459-68. PubMed ID: 24368106
    [Abstract] [Full Text] [Related]

  • 27. The investigation of MCM-48-type and MCM-41-type mesoporous silica as oral solid dispersion carriers for water insoluble cilostazol.
    Wang Y, Sun L, Jiang T, Zhang J, Zhang C, Sun C, Deng Y, Sun J, Wang S.
    Drug Dev Ind Pharm; 2014 Jun 30; 40(6):819-28. PubMed ID: 23594300
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  • 28. Application of miscibility analysis and determination of Soluplus solubility map for development of carvedilol-loaded nanofibers.
    Kaljević O, Djuris J, Čalija B, Lavrič Z, Kristl J, Ibrić S.
    Int J Pharm; 2017 Nov 30; 533(2):445-454. PubMed ID: 28495583
    [Abstract] [Full Text] [Related]

  • 29. Preparation, characterization, and dissolution studies of ibuprofen solid dispersions using polyethylene glycol (PEG), talc, and PEG-talc as dispersion carriers.
    Khan GM, Jiabi Z.
    Drug Dev Ind Pharm; 1998 May 30; 24(5):455-62. PubMed ID: 9876608
    [Abstract] [Full Text] [Related]

  • 30. [Compared with colloidal silica and porous silica as baicalin solid dispersion carrier].
    Yan HM, Ding DM, Wang J, Sun E, Jia XB, Zhang ZH.
    Zhongguo Zhong Yao Za Zhi; 2014 Jul 30; 39(13):2484-8. PubMed ID: 25276968
    [Abstract] [Full Text] [Related]

  • 31. Effects of particle morphology, pore size and surface coating of mesoporous silica on Naproxen dissolution rate enhancement.
    Guo Z, Liu XM, Ma L, Li J, Zhang H, Gao YP, Yuan Y.
    Colloids Surf B Biointerfaces; 2013 Jan 01; 101():228-35. PubMed ID: 23010024
    [Abstract] [Full Text] [Related]

  • 32. Drug loading into porous calcium carbonate microparticles by solvent evaporation.
    Preisig D, Haid D, Varum FJ, Bravo R, Alles R, Huwyler J, Puchkov M.
    Eur J Pharm Biopharm; 2014 Aug 01; 87(3):548-58. PubMed ID: 24568926
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  • 33. Preparation and evaluation of glibenclamide-polyglycolized glycerides solid dispersions with silicon dioxide by spray drying technique.
    Chauhan B, Shimpi S, Paradkar A.
    Eur J Pharm Sci; 2005 Oct 01; 26(2):219-30. PubMed ID: 16087324
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  • 34. Raman and thermal analysis of indomethacin/PVP solid dispersion enteric microparticles.
    Fini A, Cavallari C, Ospitali F.
    Eur J Pharm Biopharm; 2008 Sep 01; 70(1):409-20. PubMed ID: 18621516
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  • 35. Formulation and delivery of improved amorphous fenofibrate solid dispersions prepared by thin film freezing.
    Zhang M, Li H, Lang B, O'Donnell K, Zhang H, Wang Z, Dong Y, Wu C, Williams RO.
    Eur J Pharm Biopharm; 2012 Nov 01; 82(3):534-44. PubMed ID: 22974985
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  • 36. Evaluation and correlation of the physicochemical properties of carvedilol.
    Alves JM, Prado LD, Rocha HV.
    Pharm Dev Technol; 2016 Nov 01; 21(7):856-866. PubMed ID: 26336079
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  • 37. Improvement in oral bioavailability and dissolution of tanshinone IIA by preparation of solid dispersions with porous silica.
    Yan HM, Sun E, Cui L, Jia XB, Jin X.
    J Pharm Pharmacol; 2015 Sep 01; 67(9):1207-14. PubMed ID: 25944009
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  • 38. Dissolution behaviour of nalidixic acid solid dispersions using water soluble dispersion carriers.
    Mallick S, Sahu A, Pal K.
    Acta Pol Pharm; 2004 Sep 01; 61(1):21-30. PubMed ID: 15259854
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  • 39. Solid molecular dispersions of poorly water-soluble drugs in poly(2-hydroxyethyl methacrylate) hydrogels.
    Zahedi P, Lee PI.
    Eur J Pharm Biopharm; 2007 Mar 01; 65(3):320-8. PubMed ID: 17182231
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  • 40. Physicochemical and dissolution studies of simvastatin solid dispersions with Pluronic F127.
    Karolewicz B, Gajda M, Owczarek A, Pluta J, Górniak A.
    Pharmazie; 2014 Aug 01; 69(8):589-94. PubMed ID: 25158569
    [Abstract] [Full Text] [Related]

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