BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 30663770)

  • 1. Baicalin reduces ciclosporin bioavailability by inducing intestinal p-glycoprotein in rats.
    Tian X; Chang Y; Wei J; Liu R; Wang L; Zhang J; Zhang X
    J Pharm Pharmacol; 2019 May; 71(5):788-796. PubMed ID: 30663770
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dextran sulfate sodium-induced colitis and ginseng intervention altered oral pharmacokinetics of cyclosporine A in rats.
    Yang Y; Hu N; Gao XJ; Li T; Yan ZX; Wang PP; Wei B; Li S; Zhang ZJ; Li SL; Yan R
    J Ethnopharmacol; 2021 Jan; 265():113251. PubMed ID: 32810615
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Baicalin pharmacokinetic profile of absorption process using novel in-vitro model: cytochrome P450 3A4-induced Caco-2 cell monolayers combined with rat intestinal rinse fluids.
    Morisaki T; Hou XL; Takahashi K; Takahashi K
    J Pharm Pharmacol; 2013 Oct; 65(10):1526-35. PubMed ID: 24028620
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effects of sinapic acid on hepatic cytochrome P450 3A2, 2C11, and intestinal P-glycoprotein on the pharmacokinetics of oral carbamazepine in rats: Potential food/herb-drug interaction.
    Raish M; Ahmad A; Ansari MA; Alkharfy KM; Ahad A; Al-Jenoobi FI; Al-Mohizea AM; Khan A; Ali N
    Epilepsy Res; 2019 Jul; 153():14-18. PubMed ID: 30927680
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Decrease in oral bioavailability of ciclosporin by intravenous pulse of methylprednisolone succinate in rats.
    Konishi H; Sumi M; Shibata N; Takada K; Minouchi T; Yamaji A
    J Pharm Pharmacol; 2004 Oct; 56(10):1259-66. PubMed ID: 15482640
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An antioxidant Trolox restores decreased oral absorption of cyclosporine A after liver ischemia-reperfusion through distinct mechanisms between CYP3A and P-glycoprotein in the small intestine.
    Ikemura K; Inoue K; Mizutani H; Oka H; Iwamoto T; Okuda M
    Eur J Pharmacol; 2012 Sep; 690(1-3):192-201. PubMed ID: 22749977
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Effects of myricetin on the bioavailability of doxorubicin for oral drug delivery in rats: possible role of CYP3A4 and P-glycoprotein inhibition by myricetin.
    Choi SJ; Shin SC; Choi JS
    Arch Pharm Res; 2011 Feb; 34(2):309-15. PubMed ID: 21380815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Decreased oral absorption of cyclosporine A after liver ischemia-reperfusion injury in rats: the contribution of CYP3A and P-glycoprotein to the first-pass metabolism in intestinal epithelial cells.
    Ikemura K; Urano K; Matsuda H; Mizutani H; Iwamoto T; Okuda M
    J Pharmacol Exp Ther; 2009 Jan; 328(1):249-55. PubMed ID: 18842703
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Effects of cyclosporine A and itraconazole on permeability, biliary excretion and pharmacokinetics of amlodipine.
    Ni L; Yu X; Yu Q; Chen X; Jia L
    Drug Metab Lett; 2008 Aug; 2(3):163-8. PubMed ID: 19356088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. In situ and in vivo efficacy of peroral absorption enhancers in rats and correlation to in vitro mechanistic studies.
    Sharma P; Varma MV; Chawla HP; Panchagnula R
    Farmaco; 2005; 60(11-12):874-83. PubMed ID: 16243320
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Effects of nifedipine on the pharmacokinetics of repaglinide in rats: possible role of CYP3A4 and P-glycoprotein inhibition by nifedipine.
    Choi JS; Choi I; Choi DH
    Pharmacol Rep; 2013; 65(5):1422-30. PubMed ID: 24399740
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of the Role of P-glycoprotein (P-gp)-Mediated Efflux in the Intestinal Absorption of Common Substrates with Elacridar, a P-gp Inhibitor, in Rats.
    Suzuki K; Taniyama K; Aoyama T; Watanabe Y
    Eur J Drug Metab Pharmacokinet; 2020 Jun; 45(3):385-392. PubMed ID: 32078103
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Effects of roxithromycin on the pharmacokinetics of loratadine after oral and intravenous administration of loratadine in rats.
    Li C; Kim CS; Yang JY; Park YJ; Choi JS
    Eur J Drug Metab Pharmacokinet; 2008; 33(4):231-6. PubMed ID: 19230596
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of quercetin‑induced changes in drug‑metabolizing enzyme and transporter expression on the pharmacokinetics of cyclosporine in rats.
    Liu Y; Luo X; Yang C; Yang T; Zhou J; Shi S
    Mol Med Rep; 2016 Oct; 14(4):3073-85. PubMed ID: 27510982
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High-dose etoposide formulations do not saturate intestinal P-glycoprotein: Development, stability, and pharmacokinetics in Sprague-Dawley rats.
    Al-Ali AAA; Sandra L; Versweyveld D; Pijpers I; Dillen L; Vermeulen A; Snoeys J; Holm R; Nielsen CU
    Int J Pharm; 2020 Jun; 583():119399. PubMed ID: 32376439
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Baicalin Enhanced Oral Bioavailability of Sorafenib in Rats by Inducing Intestine Absorption.
    Wei J; Liu R; Zhang J; Liu S; Yan D; Wen X; Tian X
    Front Pharmacol; 2021; 12():761763. PubMed ID: 34819863
    [No Abstract]   [Full Text] [Related]  

  • 17. Quercetin significantly decreased cyclosporin oral bioavailability in pigs and rats.
    Hsiu SL; Hou YC; Wang YH; Tsao CW; Su SF; Chao PD
    Life Sci; 2002 Dec; 72(3):227-35. PubMed ID: 12427482
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Possible roles of intestinal P-glycoprotein and cytochrome P450 3A on the limited oral absorption of irinotecan.
    Yamasaki K; Hidaka M; Kawano Y; Furuya Y; Ono H; Arimori K
    J Pharm Pharmacol; 2021 Mar; 73(2):178-184. PubMed ID: 33793796
    [TBL] [Abstract][Full Text] [Related]  

  • 19. In vivo effects of cyclosporin A and ketoconazole on the pharmacokinetics of representative substrates for P-glycoprotein and cytochrome P450 (CYP) 3A in rats.
    Kageyama M; Namiki H; Fukushima H; Ito Y; Shibata N; Takada K
    Biol Pharm Bull; 2005 Feb; 28(2):316-22. PubMed ID: 15684491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Modulation of mdr1a and CYP3A gene expression in the intestine and liver as possible cause of changes in the cyclosporin A disposition kinetics by dexamethasone.
    Yokogawa K; Shimada T; Higashi Y; Itoh Y; Masue T; Ishizaki J; Asahi M; Miyamoto K
    Biochem Pharmacol; 2002 Feb; 63(4):777-83. PubMed ID: 11992648
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.