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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

280 related items for PubMed ID: 31650430

  • 1. Simultaneous Evaluation of Dissolution and Permeation of Oral Drug Solid Formulations for Predicting Absorption Rate-Limiting Factors and In Vitro-In Vivo Correlations: Case Study Using a Poorly Soluble Weakly Basic Drug.
    Li Z, He X, Tian S, Feng G, Huang C, Xun M, Wu Z, Wang Y.
    AAPS PharmSciTech; 2019 Oct 24; 20(8):321. PubMed ID: 31650430
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  • 3. In vitro-in vivo correlations for three different commercial immediate-release indapamide tablets.
    Yaro P, He X, Liu W, Xun M, Ma Y, Li Z, Shi X.
    Drug Dev Ind Pharm; 2014 Dec 24; 40(12):1670-6. PubMed ID: 24102615
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  • 6. Development of a bionic system for the simultaneous prediction of the release/absorption characteristics of enteric-coated formulations.
    Liu W, He X, Li Z, Gao X, Ma Y, Xun M, Liu C.
    Pharm Res; 2013 Feb 24; 30(2):596-605. PubMed ID: 23135820
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  • 7. Application of an In Vitro Dissolution/Permeation System to Early Screening of Oral Formulations of Poorly Soluble, Weakly Basic Drugs Containing an Acidic pH-Modifier.
    Mizoguchi M, Kataoka M, Yokoyama K, Aihara R, Wada K, Yamashita S.
    J Pharm Sci; 2018 Sep 24; 107(9):2404-2410. PubMed ID: 29802932
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  • 8. Advantage of the Dissolution/Permeation System for Estimating Oral Absorption of Drug Candidates in the Drug Discovery Stage.
    Miyaji Y, Fujii Y, Takeyama S, Kawai Y, Kataoka M, Takahashi M, Yamashita S.
    Mol Pharm; 2016 May 02; 13(5):1564-74. PubMed ID: 27031624
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  • 9. Identify super quality markers from prototype-based pharmacokinetic markers of Tangzhiqing tablet (TZQ) based on in vitro dissolution/ permeation and in vivo absorption correlations.
    Li Z, Liu J, Li Y, Du X, Li Y, Wang R, Lv C, He X, Wang B, Huang Y, Zhang D.
    Phytomedicine; 2018 Jun 01; 45():59-67. PubMed ID: 29685365
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  • 10. IVIVC in oral absorption for fenofibrate immediate release tablets using a dissolution/permeation system.
    Buch P, Langguth P, Kataoka M, Yamashita S.
    J Pharm Sci; 2009 Jun 01; 98(6):2001-9. PubMed ID: 18855916
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  • 13. Biomimetic Dissolution: A Tool to Predict Amorphous Solid Dispersion Performance.
    Puppolo MM, Hughey JR, Dillon T, Storey D, Jansen-Varnum S.
    AAPS PharmSciTech; 2017 Nov 01; 18(8):2841-2853. PubMed ID: 28560506
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  • 14. Dissolution/permeation with PermeaLoop™: Experience and IVIVC exemplified by dipyridamole enabling formulations.
    Eriksen JB, Messerschmid R, Andersen ML, Wada K, Bauer-Brandl A, Brandl M.
    Eur J Pharm Sci; 2020 Nov 01; 154():105532. PubMed ID: 32871215
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  • 16. Application of an in vitro DDASS to evaluate oral absorption of two chemicals simultaneously: establishment of a level A in vitro-in vivo correlation.
    Hou J, He X, Xu X, Shi X, Xu Y, Liu C.
    Drug Dev Ind Pharm; 2012 Nov 01; 38(11):1305-12. PubMed ID: 22296178
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  • 18. Analysis of the enhanced oral bioavailability of fenofibrate lipid formulations in fasted humans using an in vitro-in silico-in vivo approach.
    Fei Y, Kostewicz ES, Sheu MT, Dressman JB.
    Eur J Pharm Biopharm; 2013 Nov 01; 85(3 Pt B):1274-84. PubMed ID: 23500116
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  • 19. Combining in vitro dissolution/permeation with microdialysis sampling: Capabilities and limitations for biopharmaceutical assessments of supersaturating drug formulations.
    Holzem FL, Jensen IH, Petrig Schaffland J, Stillhart C, Brandl M, Bauer-Brandl A.
    Eur J Pharm Sci; 2023 Sep 01; 188():106533. PubMed ID: 37480963
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