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Martin Brandl

University of Southern Denmark

Research Interests

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Articles (20)

Collaborators (5)

Christos Reppas

National and Kapodistrian University of Athens

Ann-Christin Jacobsen

Kiel University

Poul Nielsen

University of Southern Denmark

Bartłomiej Milanowski

Assistant Professor

Poznan University of Medical Sciences

Aleksei Kabedev

Uppsala University

ApplyKite TwinLearns as you apply

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Martin Brandl

Research Interests

Make your next move.

Explore related searches

Articles (20)

Collaborators (5)

Christos Reppas

Ann-Christin Jacobsen

Poul Nielsen

Bartłomiej Milanowski

Aleksei Kabedev

Make your next move.

Martin Brandl

Research Interests

Make your next move.

Explore related searches

Articles (20)

Synthesis, in vitro characterization and biopharmaceutical evaluation of a novel phosphate prodrug of sorafenib

Dissolution-microdialysis predicts oral bioavailability from phospholipid-based amorphous solid dispersions

Microdialysis during in vitro lipolysis explains enhanced permeation of indomethacin from phospholipid-based amorphous solid dispersions

Can an absorptive sink improve the predictivity of biomimetic two-stage dissolution testing? Comparative IVIVC of various formulations of the poorly soluble drug emodepside

Indomethacin forms elusive nanoparticles with calcium in situ causing enhanced permeation across a biomimetic barrier

Looking behind the Solubilization Curtain

A novel combined lipolysis-permeation screening approach in 96-well format: Method development using type I lipid-based formulations

Dissolution / Permeation of Amorphous Solid Dispersions of Fenofibrate & Hydrogenated Phospholipid - Spontaneous Formation of Colloids: Nanofiltration & Particle Size Analysis

Untangling “dissolved” drug species from various formulations of a poorly soluble drug: Sampling methods, mechanistic insights, and IVIVC

Can the pH-Stat Lipolysis Model be used to Assess the Performance of Supersaturated Lipid-Based Type I Formulations?

A high-throughput micro-scale workflow to quantify molecularly dissolved drug concentrations under solubilizing conditions

The Impact of Volume of Dissolution Medium for Biopredictive Dissolution/Permeation Studies of Enabling Formulations

Melt-extruded formulations of fenofibrate with various grades of hydrogenated phospholipid exhibit promising in-vitro biopharmaceutical behavior

Oral absorption from surfactant-based drug formulations

Using molecularly dissolved drug concentrations in PBBMs improves the prediction of oral absorption from supersaturating formulations

Drug Dissolution in Oral Drug Absorption: Workshop Report

Impact of prandial state on luminal and permeation-behavior of fosamprenavir oral suspension studied by in vitro tools

Hydrogenated phospholipid, a promising excipient in amorphous solid dispersions of fenofibrate for oral delivery

Combining in vitro dissolution/permeation with microdialysis sampling

In vitro dissolution/permeation tools for amorphous solid dispersions bioavailability forecasting I: Experimental design for PermeaLoop™

Collaborators (5)

Christos Reppas

Ann-Christin Jacobsen

Poul Nielsen

Bartłomiej Milanowski

Aleksei Kabedev

Make your next move.