These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 25448073)

  • 1. Floating lipid beads for the improvement of bioavailability of poorly soluble basic drugs: in-vitro optimization and in-vivo performance in humans.
    Abouelatta SM; Aboelwafa AA; Khalil RM; ElGazayerly ON
    Eur J Pharm Biopharm; 2015 Jan; 89():82-92. PubMed ID: 25448073
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Utilization of ionotropic gelation technique for bioavailability enhancement of cinnarizine: in-vitro optimization and in-vivo performance in human.
    Abouelatta SM; Aboelwafa AA; Khalil RM; El-Gazayerly ON
    Drug Deliv; 2016 Oct; 23(8):2736-2746. PubMed ID: 26165421
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The effect of administered dose of lipid-based formulations on the in vitro and in vivo performance of cinnarizine as a model poorly water-soluble drug.
    Lee KW; Porter CJ; Boyd BJ
    J Pharm Sci; 2013 Feb; 102(2):565-78. PubMed ID: 23242691
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fed and fasted state gastro-intestinal in vitro lipolysis: In vitro in vivo relations of a conventional tablet, a SNEDDS and a solidified SNEDDS.
    Christophersen PC; Christiansen ML; Holm R; Kristensen J; Jacobsen J; Abrahamsson B; Müllertz A
    Eur J Pharm Sci; 2014 Jun; 57():232-9. PubMed ID: 24056027
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pluronic-Functionalized Silica-Lipid Hybrid Microparticles: Improving the Oral Delivery of Poorly Water-Soluble Weak Bases.
    Rao S; Richter K; Nguyen TH; Boyd BJ; Porter CJ; Tan A; Prestidge CA
    Mol Pharm; 2015 Dec; 12(12):4424-33. PubMed ID: 26523928
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Design and development of novel lipid based gastroretentive delivery system: response surface analysis, in-vivo imaging and pharmacokinetic study.
    Ahmed Abdelbary A; Elsayed I; Hassen Elshafeey A
    Drug Deliv; 2015 Jan; 22(1):37-49. PubMed ID: 24350634
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Encapsulation of poorly soluble basic drugs into enteric microparticles: a novel approach to enhance their oral bioavailability.
    Alhnan MA; Murdan S; Basit AW
    Int J Pharm; 2011 Sep; 416(1):55-60. PubMed ID: 21679756
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multi-Layer Self-Nanoemulsifying Pellets: an Innovative Drug Delivery System for the Poorly Water-Soluble Drug Cinnarizine.
    Shahba AA; Ahmed AR; Alanazi FK; Mohsin K; Abdel-Rahman SI
    AAPS PharmSciTech; 2018 Jul; 19(5):2087-2102. PubMed ID: 29696614
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transformation of poorly water-soluble drugs into lipophilic ionic liquids enhances oral drug exposure from lipid based formulations.
    Sahbaz Y; Williams HD; Nguyen TH; Saunders J; Ford L; Charman SA; Scammells PJ; Porter CJ
    Mol Pharm; 2015 Jun; 12(6):1980-91. PubMed ID: 25905624
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synergistic role of solid lipid and porous silica in improving the oral delivery of weakly basic poorly water soluble drugs.
    Yasmin R; Rao S; Bremmell K; Prestidge C
    Eur J Pharm Sci; 2017 Jan; 96():508-514. PubMed ID: 27793717
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In vitro release kinetics and bioavailability of gastroretentive cinnarizine hydrochloride tablet.
    Nagarwal RC; Ridhurkar DN; Pandit JK
    AAPS PharmSciTech; 2010 Mar; 11(1):294-303. PubMed ID: 20182827
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Formulation of Cinnarizine for Stabilization of Its Physiologically Generated Supersaturation.
    Maghsoodi M; Nokhodchi A; Oskuei MA; Heidari S
    AAPS PharmSciTech; 2019 Mar; 20(3):139. PubMed ID: 30868302
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Preparation and in vitro characterization of a non-effervescent floating drug delivery system for poorly soluble drug, glipizide.
    Meka VS; Pillai S; Dharmalingham SR; Sheshala R; Gorajana A
    Acta Pol Pharm; 2015; 72(1):193-204. PubMed ID: 25850215
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Design of innovated lipid-based floating beads loaded with an antispasmodic drug: in-vitro and in-vivo evaluation.
    Adel S; ElKasabgy NA
    J Liposome Res; 2014 Jun; 24(2):136-49. PubMed ID: 24236529
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison across Three Hybrid Lipid-Based Drug Delivery Systems for Improving the Oral Absorption of the Poorly Water-Soluble Weak Base Cinnarizine.
    Joyce P; Yasmin R; Bhatt A; Boyd BJ; Pham A; Prestidge CA
    Mol Pharm; 2017 Nov; 14(11):4008-4018. PubMed ID: 28950059
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A lipid-based liquid crystalline matrix that provides sustained release and enhanced oral bioavailability for a model poorly water soluble drug in rats.
    Boyd BJ; Khoo SM; Whittaker DV; Davey G; Porter CJ
    Int J Pharm; 2007 Aug; 340(1-2):52-60. PubMed ID: 17467935
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lipid-based systems as a promising approach for enhancing the bioavailability of poorly water-soluble drugs.
    Cerpnjak K; Zvonar A; Gašperlin M; Vrečer F
    Acta Pharm; 2013 Dec; 63(4):427-45. PubMed ID: 24451070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel gastro-floating multiparticulate system for dipyridamole (DIP) based on a porous and low-density matrix core: in vitro and in vivo evaluation.
    Li Z; Xu H; Li S; Li Q; Zhang W; Ye T; Yang X; Pan W
    Int J Pharm; 2014 Jan; 461(1-2):540-8. PubMed ID: 24368104
    [TBL] [Abstract][Full Text] [Related]  

  • 19. In Vitro Digestion-In Situ Absorption Setup Employing a Physiologically Relevant Value of the Membrane Surface Area/Volume Ratio for Evaluating Performance of Lipid-Based Formulations: A Comparative Study with an In Vitro Digestion-Permeation Model.
    Tanaka Y; Arai H; Hidaka A; Noda S; Imai K; Tsujisawa F; Yagi H; Sakuma S
    Mol Pharm; 2024 Jul; 21(7):3459-3470. PubMed ID: 38809159
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 96():464-471. PubMed ID: 27773836
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.