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Journal Abstract Search

825 related items for PubMed ID: 30553058

  • 1. Enhancement of the apparent solubility and bioavailability of Tadalafil nanoparticles via antisolvent precipitation.
    Rao Q, Qiu Z, Huang D, Lu T, Zhang ZJ, Luo D, Pan P, Zhang L, Liu Y, Guan S, Li Q.
    Eur J Pharm Sci; 2019 Feb 01; 128():222-231. PubMed ID: 30553058
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  • 5. 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 Feb 01; 9():4269-77. PubMed ID: 26345723
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  • 6. Comparing various techniques to produce micro/nanoparticles for enhancing the dissolution of celecoxib containing PVP.
    Homayouni A, Sadeghi F, Varshosaz J, Garekani HA, Nokhodchi A.
    Eur J Pharm Biopharm; 2014 Sep 01; 88(1):261-74. PubMed ID: 24952357
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  • 7. Antisolvent precipitation technique: A very promising approach to crystallize curcumin in presence of polyvinyl pyrrolidon for solubility and dissolution enhancement.
    Sadeghi F, Ashofteh M, Homayouni A, Abbaspour M, Nokhodchi A, Garekani HA.
    Colloids Surf B Biointerfaces; 2016 Nov 01; 147():258-264. PubMed ID: 27518458
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  • 8. Physicochemical properties of direct compression tablets with spray dried and ball milled solid dispersions of tadalafil in PVP-VA.
    Wlodarski K, Tajber L, Sawicki W.
    Eur J Pharm Biopharm; 2016 Dec 01; 109():14-23. PubMed ID: 27658987
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  • 9. Preparation and characterization of betulin nanoparticles for oral hypoglycemic drug by antisolvent precipitation.
    Zhao X, Wang W, Zu Y, Zhang Y, Li Y, Sun W, Shan C, Ge Y.
    Drug Deliv; 2014 Sep 01; 21(6):467-79. PubMed ID: 24479653
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  • 10. The influence of amorphization methods on the apparent solubility and dissolution rate of tadalafil.
    Wlodarski K, Sawicki W, Paluch KJ, Tajber L, Grembecka M, Hawelek L, Wojnarowska Z, Grzybowska K, Talik E, Paluch M.
    Eur J Pharm Sci; 2014 Oct 01; 62():132-40. PubMed ID: 24907679
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  • 11. Preparation and characterization of micronized ellagic acid using antisolvent precipitation for oral delivery.
    Li Y, Zhao X, Zu Y, Zhang Y, Ge Y, Zhong C, Wu W.
    Int J Pharm; 2015 Oct 01; 486(1-2):207-16. PubMed ID: 25841566
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  • 12. 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
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  • 17. 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 01; 69(2):454-65. PubMed ID: 18359211
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  • 18. Development of an amorphous nanosuspension by sonoprecipitation-formulation and process optimization using design of experiment methodology.
    Gajera BY, Shah DA, Dave RH.
    Int J Pharm; 2019 Mar 25; 559():348-359. PubMed ID: 30721724
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  • 19. In vitro dissolution enhancement of micronized l-nimodipine by antisolvent re-crystallization from its crystal form H.
    Zu Y, Li N, Zhao X, Li Y, Ge Y, Wang W, Wang K, Liu Y.
    Int J Pharm; 2014 Apr 10; 464(1-2):1-9. PubMed ID: 24456674
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  • 20. Characterization and pharmacokinetic study of itraconazole solid dispersions prepared by solvent-controlled precipitation and spray-dry methods.
    Sim T, Lim C, Lee JW, Kim DW, Kim Y, Kim M, Choi S, Choi HG, Lee ES, Kim KS, Kang W, Oh KT.
    J Pharm Pharmacol; 2017 Dec 10; 69(12):1707-1715. PubMed ID: 28872678
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