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Journal Abstract Search

186 related items for PubMed ID: 32298758

  • 1. Effect of supersaturation on absorption of indomethacin and tadalafil in a single pass intestinal perfusion rat model, in the absence and presence of a precipitation inhibitor.
    Strindberg S, Plum J, Stie MB, Christiansen ML, Hagner Nielsen L, Rades T, Müllertz A.
    Eur J Pharm Biopharm; 2020 Jun; 151():108-115. PubMed ID: 32298758
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  • 4. In vitro-in vivo correlation of the effect of supersaturation on the intestinal absorption of BCS Class 2 drugs.
    Higashino H, Hasegawa T, Yamamoto M, Matsui R, Masaoka Y, Kataoka M, Sakuma S, Yamashita S.
    Mol Pharm; 2014 Mar 03; 11(3):746-54. PubMed ID: 24460473
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  • 5. Comparison of induction methods for supersaturation: Amorphous dissolution versus solvent shift.
    Plum J, Bavnhøj CG, Eliasen JN, Rades T, Müllertz A.
    Eur J Pharm Biopharm; 2020 Jul 03; 152():35-43. PubMed ID: 32376371
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  • 7. Ordered mesoporous silica induces pH-independent supersaturation of the basic low solubility compound itraconazole resulting in enhanced transepithelial transport.
    Mellaerts R, Mols R, Kayaert P, Annaert P, Van Humbeeck J, Van den Mooter G, Martens JA, Augustijns P.
    Int J Pharm; 2008 Jun 05; 357(1-2):169-79. PubMed ID: 18325700
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  • 8. Effects of absorption-modifying excipients on jejunal drug absorption in simulated fasted and fed luminal conditions.
    Roos C, Dahlgren D, Sjögren E, Sjöblom M, Hedeland M, Lennernäs H.
    Eur J Pharm Biopharm; 2019 Sep 05; 142():387-395. PubMed ID: 31306752
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  • 9. Polymeric Precipitation Inhibitors Promote Fenofibrate Supersaturation and Enhance Drug Absorption from a Type IV Lipid-Based Formulation.
    Suys EJA, Chalmers DK, Pouton CW, Porter CJH.
    Mol Pharm; 2018 Jun 04; 15(6):2355-2371. PubMed ID: 29659287
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  • 10. Solvent shift method for anti-precipitant screening of poorly soluble drugs using biorelevant medium and dimethyl sulfoxide.
    Yamashita T, Ozaki S, Kushida I.
    Int J Pharm; 2011 Oct 31; 419(1-2):170-4. PubMed ID: 21840385
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  • 11. Investigation of supersaturation and in vitro permeation of the poorly water soluble drug ezetimibe.
    Alhayali A, Selo MA, Ehrhardt C, Velaga S.
    Eur J Pharm Sci; 2018 May 30; 117():147-153. PubMed ID: 29408604
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  • 13. Prediction of oral absorption of cinnarizine--a highly supersaturating poorly soluble weak base with borderline permeability.
    Berlin M, Przyklenk KH, Richtberg A, Baumann W, Dressman JB.
    Eur J Pharm Biopharm; 2014 Nov 30; 88(3):795-806. PubMed ID: 25195981
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  • 14. Interaction with biliary and pancreatic fluids drives supersaturation and drug absorption from lipid-based formulations of low (saquinavir) and high (fenofibrate) permeability poorly soluble drugs.
    Suys EJA, Brundel DHS, Chalmers DK, Pouton CW, Porter CJH.
    J Control Release; 2021 Mar 10; 331():45-61. PubMed ID: 33450318
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  • 15. Polymer/lipid interplay in altering in vitro supersaturation and plasma concentration of a model poorly soluble drug.
    Peng R, Huang J, He L, Zhao L, Wang C, Wei W, Xia T, Mao Y, Wen Y, Wang L, Yang J.
    Eur J Pharm Sci; 2020 Apr 15; 146():105262. PubMed ID: 32060005
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  • 16. Supersaturation in human gastric fluids.
    Bevernage J, Hens B, Brouwers J, Tack J, Annaert P, Augustijns P.
    Eur J Pharm Biopharm; 2012 May 15; 81(1):184-9. PubMed ID: 22342777
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  • 17. Transient Supersaturation Supports Drug Absorption from Lipid-Based Formulations for Short Periods of Time, but Ongoing Solubilization Is Required for Longer Absorption Periods.
    Crum MF, Trevaskis NL, Pouton CW, Porter CJ.
    Mol Pharm; 2017 Feb 06; 14(2):394-405. PubMed ID: 28002666
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  • 18. Excipient-mediated supersaturation stabilization in human intestinal fluids.
    Bevernage J, Forier T, Brouwers J, Tack J, Annaert P, Augustijns P.
    Mol Pharm; 2011 Apr 04; 8(2):564-70. PubMed ID: 21268663
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  • 19. Supersaturated polymeric micelles for oral cyclosporine A delivery.
    Yu H, Xia D, Zhu Q, Zhu C, Chen D, Gan Y.
    Eur J Pharm Biopharm; 2013 Nov 04; 85(3 Pt B):1325-36. PubMed ID: 23954511
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  • 20. In vivo evaluation of supersaturation/precipitation/re-dissolution behavior of cinnarizine, a lipophilic weak base, in the gastrointestinal tract: the key process of oral absorption.
    Tanaka Y, Kawakami A, Nanimatsu A, Horio M, Matsuoka J, Wada T, Kasaoka S, Yoshikawa H.
    Eur J Pharm Sci; 2017 Jan 01; 96():464-471. PubMed ID: 27773836
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