BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 32011151)

  • 21. Improving Correlations Between Drug Solubilization and In Vitro Lipolysis by Monitoring the Phase Partitioning of Lipolytic Species for Lipid-Based Formulations.
    Dening TJ; Joyce P; Prestidge CA
    J Pharm Sci; 2019 Jan; 108(1):295-304. PubMed ID: 30257194
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Five-Stage Approach for a Systematic Screening and Development of Etravirine Amorphous Solid Dispersions by Hot-Melt Extrusion.
    Simões MF; Pereira A; Cardoso S; Cadonau S; Werner K; Pinto RMA; Simões S
    Mol Pharm; 2020 Feb; 17(2):554-568. PubMed ID: 31774685
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Use of in vitro lipid digestion data to explain the in vivo performance of triglyceride-based oral lipid formulations of poorly water-soluble drugs: studies with halofantrine.
    Porter CJ; Kaukonen AM; Taillardat-Bertschinger A; Boyd BJ; O'Connor JM; Edwards GA; Charman WN
    J Pharm Sci; 2004 May; 93(5):1110-21. PubMed ID: 15067688
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nanostructured lipid carriers versus microemulsions for delivery of the poorly water-soluble drug luteolin.
    Liu Y; Wang L; Zhao Y; He M; Zhang X; Niu M; Feng N
    Int J Pharm; 2014 Dec; 476(1-2):169-77. PubMed ID: 25280882
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Impact of Drug Physicochemical Properties on Lipolysis-Triggered Drug Supersaturation and Precipitation from Lipid-Based Formulations.
    Alskär LC; Keemink J; Johannesson J; Porter CJH; Bergström CAS
    Mol Pharm; 2018 Oct; 15(10):4733-4744. PubMed ID: 30142268
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Structural development of self nano emulsifying drug delivery systems (SNEDDS) during in vitro lipid digestion monitored by small-angle X-ray scattering.
    Fatouros DG; Deen GR; Arleth L; Bergenstahl B; Nielsen FS; Pedersen JS; Mullertz A
    Pharm Res; 2007 Oct; 24(10):1844-53. PubMed ID: 17458683
    [TBL] [Abstract][Full Text] [Related]  

  • 27. How relevant are assembled equilibrium samples in understanding structure formation during lipid digestion?
    Phan S; Salentinig S; Hawley A; Boyd BJ
    Eur J Pharm Biopharm; 2015 Oct; 96():117-24. PubMed ID: 26212786
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A closer look at the behaviour of milk lipids during digestion.
    Clulow AJ; Salim M; Hawley A; Boyd BJ
    Chem Phys Lipids; 2018 Mar; 211():107-116. PubMed ID: 29100945
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Effect of lipids on absorption of carvedilol in dogs: Is coadministration of lipids as efficient as a lipid-based formulation?
    Alskär LC; Parrow A; Keemink J; Johansson P; Abrahamsson B; Bergström CAS
    J Control Release; 2019 Jun; 304():90-100. PubMed ID: 31047962
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Drug solubilization behavior during in vitro digestion of simple triglyceride lipid solution formulations.
    Kaukonen AM; Boyd BJ; Porter CJ; Charman WN
    Pharm Res; 2004 Feb; 21(2):245-53. PubMed ID: 15032305
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Probing Pharmaceutical Mixtures during Milling: The Potency of Low-Frequency Raman Spectroscopy in Identifying Disorder.
    Walker G; Römann P; Poller B; Löbmann K; Grohganz H; Rooney JS; Huff GS; Smith GPS; Rades T; Gordon KC; Strachan CJ; Fraser-Miller SJ
    Mol Pharm; 2017 Dec; 14(12):4675-4684. PubMed ID: 29091447
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Computational Models of the Gastrointestinal Environment. 2. Phase Behavior and Drug Solubilization Capacity of a Type I Lipid-Based Drug Formulation after Digestion.
    Birru WA; Warren DB; Han S; Benameur H; Porter CJ; Pouton CW; Chalmers DK
    Mol Pharm; 2017 Mar; 14(3):580-592. PubMed ID: 27936778
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Addition of Cationic Surfactants to Lipid-Based Formulations of Poorly Water-Soluble Acidic Drugs Alters the Phase Distribution and the Solid-State Form of the Precipitate Upon In Vitro Lipolysis.
    Khan J; Rades T; Boyd BJ
    J Pharm Sci; 2018 Sep; 107(9):2420-2427. PubMed ID: 29859958
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Montmorillonite and Laponite Clay Materials for the Solidification of Lipid-Based Formulations for the Basic Drug Blonanserin: In Vitro and in Vivo Investigations.
    Dening TJ; Thomas N; Rao S; van Looveren C; Cuyckens F; Holm R; Prestidge CA
    Mol Pharm; 2018 Sep; 15(9):4148-4160. PubMed ID: 30067372
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Real time Raman imaging to understand dissolution performance of amorphous solid dispersions.
    Tres F; Treacher K; Booth J; Hughes LP; Wren SA; Aylott JW; Burley JC
    J Control Release; 2014 Aug; 188():53-60. PubMed ID: 24910191
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rapid determination of drug solubilization versus supersaturation in natural and digested lipids.
    Gautschi N; Bergström CA; Kuentz M
    Int J Pharm; 2016 Nov; 513(1-2):164-174. PubMed ID: 27609663
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Study of drug supersaturation for rational early formulation screening of surfactant/co-solvent drug delivery systems.
    Stillhart C; Cavegn M; Kuentz M
    J Pharm Pharmacol; 2013 Feb; 65(2):181-92. PubMed ID: 23278685
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Impact of gastrointestinal lipolysis on oral lipid-based formulations and bioavailability of lipophilic drugs.
    Carrière F
    Biochimie; 2016 Jun; 125():297-305. PubMed ID: 26607242
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ionic Liquid Forms of Weakly Acidic Drugs in Oral Lipid Formulations: Preparation, Characterization, in Vitro Digestion, and in Vivo Absorption Studies.
    Sahbaz Y; Nguyen TH; Ford L; McEvoy CL; Williams HD; Scammells PJ; Porter CJH
    Mol Pharm; 2017 Nov; 14(11):3669-3683. PubMed ID: 28954512
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phytantriol and glyceryl monooleate cubic liquid crystalline phases as sustained-release oral drug delivery systems for poorly water-soluble drugs II. In-vivo evaluation.
    Nguyen TH; Hanley T; Porter CJ; Larson I; Boyd BJ
    J Pharm Pharmacol; 2010 Jul; 62(7):856-65. PubMed ID: 20636873
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.