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PUBMED FOR HANDHELDS

Journal Abstract Search

184 related items for PubMed ID: 26238806

  • 21.
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  • 22. Formulation and evaluation of self-emulsifying orlistat tablet to enhance drug release and in vivo performance: factorial design approach.
    Gade MM, Hurkadale PJ.
    Drug Deliv Transl Res; 2016 Jun; 6(3):276-88. PubMed ID: 27037924
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  • 23. Enhanced stability and oral bioavailability of erlotinib by solid self nano emulsifying drug delivery systems.
    Jain S, Dongare K, Nallamothu B, Parkash Dora C, Kushwah V, Katiyar SS, Sharma R.
    Int J Pharm; 2022 Jun 25; 622():121852. PubMed ID: 35618179
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  • 24. Preparation and pharmaceutical evaluation of new tacrolimus-loaded solid self-emulsifying drug delivery system.
    Seo YG, Kim DW, Cho KH, Yousaf AM, Kim DS, Kim JH, Kim JO, Yong CS, Choi HG.
    Arch Pharm Res; 2015 Feb 25; 38(2):223-8. PubMed ID: 25134927
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  • 25. Preparation and evaluation of a self-nanoemulsifying drug delivery system loaded with Akebia saponin D-phospholipid complex.
    Shen J, Bi J, Tian H, Jin Y, Wang Y, Yang X, Yang Z, Kou J, Li F.
    Int J Nanomedicine; 2016 Feb 25; 11():4919-4929. PubMed ID: 27713630
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  • 26. Enhancing in vitro dissolution and in vivo bioavailability of fenofibrate by solid self-emulsifying matrix combined with SBA-15 mesoporous silica.
    Quan G, Wu Q, Zhang X, Zhan Z, Zhou C, Chen B, Zhang Z, Li G, Pan X, Wu C.
    Colloids Surf B Biointerfaces; 2016 May 01; 141():476-482. PubMed ID: 26896653
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  • 27. Effects of spray-drying and choice of solid carriers on concentrations of Labrasol® and Transcutol® in solid self-microemulsifying drug delivery systems (SMEDDS).
    Li L, Yi T, Lam CW.
    Molecules; 2013 Jan 02; 18(1):545-60. PubMed ID: 23282540
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  • 34. Self-emulsifying drug delivery system (SEDDS) of Ibuprofen: formulation, in vitro and in vivo evaluation.
    Penjuri SCB, Damineni S, Ravouru N, Poreddy SR.
    Ceska Slov Farm; 2017 Jan 02; 66(1):23-34. PubMed ID: 28569515
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  • 35. The novel formulation design of self-emulsifying drug delivery systems (SEDDS) type O/W microemulsion I: enhancing effects on oral bioavailability of poorly water soluble compounds in rats and beagle dogs.
    Araya H, Nagao S, Tomita M, Hayashi M.
    Drug Metab Pharmacokinet; 2005 Aug 02; 20(4):244-56. PubMed ID: 16141604
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  • 36. Role of excipients in successful development of self-emulsifying/microemulsifying drug delivery system (SEDDS/SMEDDS).
    Rahman MA, Hussain A, Hussain MS, Mirza MA, Iqbal Z.
    Drug Dev Ind Pharm; 2013 Jan 02; 39(1):1-19. PubMed ID: 22372916
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  • 37. Self emulsifying drug delivery system (SEDDS) for phytoconstituents: a review.
    Chouhan N, Mittal V, Kaushik D, Khatkar A, Raina M.
    Curr Drug Deliv; 2015 Jan 02; 12(2):244-53. PubMed ID: 25335929
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  • 38. Insights into Novel Excipients of Self-Emulsifying Drug Delivery Systems and Their Significance: An Updated Review.
    Rani ER, Radha GV.
    Crit Rev Ther Drug Carrier Syst; 2021 Jan 02; 38(2):27-74. PubMed ID: 33639067
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  • 39. Enhanced dissolution and oral bioavailability of nifedipine by spontaneous emulsifying powders: effect of solid carriers and dietary state.
    Weerapol Y, Limmatvapirat S, Jansakul C, Takeuchi H, Sriamornsak P.
    Eur J Pharm Biopharm; 2015 Apr 02; 91():25-34. PubMed ID: 25615879
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  • 40. Characterization and evaluation of self-nanoemulsifying sustained-release pellet formulation of ziprasidone with enhanced bioavailability and no food effect.
    Miao Y, Chen G, Ren L, Pingkai O.
    Drug Deliv; 2016 Sep 02; 23(7):2163-2172. PubMed ID: 25148542
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