These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

61 related items for PubMed ID: 24956839

  • 1. [Study on preparation of ginkgolides component solid dispersions micro pill drug release unit].
    Liu D, Zhang ZH, Chen XY, Jia XB.
    Zhongguo Zhong Yao Za Zhi; 2014 Mar; 39(6):1002-6. PubMed ID: 24956839
    [Abstract] [Full Text] [Related]

  • 2. [Preparation and characterization of solid dispersions of ginkgolides].
    Ma L, Han L, Zhang Z, Wang J.
    Zhongguo Zhong Yao Za Zhi; 2009 Jun; 34(11):1368-72. PubMed ID: 19771864
    [Abstract] [Full Text] [Related]

  • 3. [Study on preparation and in vitro characteristics of ginsenoside Rg3 binary solid dispersion].
    Liu QY, Zhang ZH, Jin X, Yu ZH, Jia XB.
    Zhongguo Zhong Yao Za Zhi; 2013 Dec; 38(24):4298-302. PubMed ID: 24791534
    [Abstract] [Full Text] [Related]

  • 4. Preparation of Ginkgolide Solid Dispersions with Low-Molecular-Weight Chitosan and Assessment of their Protective Effect on Isoproterenol- Induced Myocardial Injury.
    Zhang L, Xia Z, Liu B, Cui L, Ding W, Liu D.
    Curr Drug Deliv; 2020 Dec; 17(8):711-719. PubMed ID: 32621716
    [Abstract] [Full Text] [Related]

  • 5. Use of highly compressible Ceolus™ microcrystalline cellulose for improved dosage form properties containing a hydrophilic solid dispersion.
    Dinunzio JC, Schilling SU, Coney AW, Hughey JR, Kaneko N, McGinity JW.
    Drug Dev Ind Pharm; 2012 Feb; 38(2):180-9. PubMed ID: 21774741
    [Abstract] [Full Text] [Related]

  • 6. [Evaluation of drug release behavior in vitro of ginkgolides component drug release unit].
    Liu D, Zhang ZH, Chen XY, Jia XB.
    Zhongguo Zhong Yao Za Zhi; 2014 Apr; 39(8):1426-9. PubMed ID: 25039176
    [Abstract] [Full Text] [Related]

  • 7. 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; 64(2):200-5. PubMed ID: 16750355
    [Abstract] [Full Text] [Related]

  • 8. Development of prednisone:polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters.
    Leonardi D, Barrera MG, Lamas MC, Salomón CJ.
    AAPS PharmSciTech; 2007 Dec 14; 8(4):E108. PubMed ID: 18181529
    [Abstract] [Full Text] [Related]

  • 9. Development and in-vivo assessment of the bioavailability of oridonin solid dispersions by the gas anti-solvent technique.
    Li S, Liu Y, Liu T, Zhao L, Zhao J, Feng N.
    Int J Pharm; 2011 Jun 15; 411(1-2):172-7. PubMed ID: 21511016
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. [Study on andrographolide solid dispersion vectored by hydroxyapatite].
    Hu SY, Zhang ZH, Jia XB.
    Zhongguo Zhong Yao Za Zhi; 2013 Feb 10; 38(3):341-5. PubMed ID: 23668005
    [Abstract] [Full Text] [Related]

  • 12. [Preparation of water-soluble chitosan solid dispersion of daidzein].
    Ge Y, Wang X, Guo W, Xie X.
    Zhongguo Zhong Yao Za Zhi; 2010 Feb 10; 35(3):293-6. PubMed ID: 20422991
    [Abstract] [Full Text] [Related]

  • 13. Investigation of griseofulvin and hydroxypropylmethyl cellulose acetate succinate miscibility in ball milled solid dispersions.
    Al-Obaidi H, Lawrence MJ, Al-Saden N, Ke P.
    Int J Pharm; 2013 Feb 25; 443(1-2):95-102. PubMed ID: 23299082
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. [Influence of solid dispersion technique combination on dissolution of tanshinone IIA].
    Yuan J, Mao S, Shen Q, Hou S, He Y.
    Zhongguo Zhong Yao Za Zhi; 2009 Mar 01; 34(6):685-9. PubMed ID: 19624004
    [Abstract] [Full Text] [Related]

  • 16. Application of novel chitosan derivatives in dissolution enhancement of a poorly water soluble drug.
    Aiedeh KM, Khatib HA, Taha MO, Al-Zoubi N.
    Pharmazie; 2006 Apr 01; 61(4):306-11. PubMed ID: 16649543
    [Abstract] [Full Text] [Related]

  • 17. Stochiometrically governed molecular interactions in drug: poloxamer solid dispersions.
    Ali W, Williams AC, Rawlinson CF.
    Int J Pharm; 2010 May 31; 391(1-2):162-8. PubMed ID: 20214957
    [Abstract] [Full Text] [Related]

  • 18. Preparation and physicochemical evaluation of a new tacrolimus tablet formulation for sublingual administration.
    Srinarong P, Pham BT, Holen M, van der Plas A, Schellekens RC, Hinrichs WL, Frijlink HW.
    Drug Dev Ind Pharm; 2012 Apr 31; 38(4):490-500. PubMed ID: 21961909
    [Abstract] [Full Text] [Related]

  • 19. 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 31; 24(5):455-62. PubMed ID: 9876608
    [Abstract] [Full Text] [Related]

  • 20. Effect of the solid-dispersion method on the solubility and crystalline property of tacrolimus.
    Joe JH, Lee WM, Park YJ, Joe KH, Oh DH, Seo YG, Woo JS, Yong CS, Choi HG.
    Int J Pharm; 2010 Aug 16; 395(1-2):161-6. PubMed ID: 20580799
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.