Launch week offerEnds in00h00m00s

annual Promonthly Pro

Martin Kuentz

University of Applied Sciences and Arts Northwestern Switzerland

Research Interests

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Explore related searches

Articles (27)

Collaborators (6)

Karl G. Wagner

University of Bonn

Patrick O'Dwyer

Lecturer in Pharmaceutics

University College Cork

René Holm

University of Southern Denmark

Lorraine Bateman

Lecturer in Pharmaceutical Chemistry & NMR Spectroscopist

University College Cork

Brendan Griffin

Professor of Pharmaceutics

University College Cork

Niklas Koehl

University College Cork National University of Ireland

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Martin Kuentz

Research Interests

Make your next move.

Explore related searches

Articles (27)

Collaborators (6)

Karl G. Wagner

Patrick O'Dwyer

René Holm

Lorraine Bateman

Brendan Griffin

Niklas Koehl

Make your next move.

Martin Kuentz

Research Interests

Make your next move.

Explore related searches

Articles (27)

Combined second harmonic and linear light scattering as a tool for solubility and aggregation screening

Using mixtures of linoleic acid, a long-chain polyunsaturated fatty acid, and its monoglyceride in lipid-based formulations to increase drug loading and enhance aqueous microemulsification

Progressing conformational analysis to drug-excipient interactions - a study of co-amorphous systems with macrocycles

Establishing experimental parameters for biphasic transfer in vitro lipolysis model

Formulation of amorphous solid dispersion of clofazimine, an extremely water-insoluble basic drug, via hot-melt extrusion by applying acid-base supersolubilization principle

Deep eutectic systems as enabling pharmaceutical formulations: mechanisms and applications

pH-stat versus pH-shift lipolysis model: Exploring in vitro-in vivo relationships for lipid-based formulations of nilotinib

Mechanistic Investigation into the Phase Separation Behavior of Soluplus in the Presence of Biorelevant Media

Approaching drug release performance from mesoporous silica formulations by modeling of chemical potentials

High-throughput analysis of aqueous drug solubility, supersaturation, and aggregation behaviour using second harmonic light scattering

Guiding excipient selection for amorphous solid dispersions by combining an in vitro-in-silico approach – II: Supersaturation and drug release

Guiding excipient selection for physically stable amorphous solid dispersions: A combined in-vitro in-silico approach

Ranking of apparent drug affinity to mesoporous silica utilizing a chromatographic screening method and a tree-based prediction model

Highly increasing solubility of clofazimine, an extremely water-insoluble basic drug, in lipid-based SEDDS using digestion products of long-chain lipids

Discovery of Cilnidipine Cocrystals with Enhanced Dissolution by the Use of Computational Tools and Semiautomatic High-Throughput Screening

Exploring co-milling of poorly water-soluble drugs with swellable polymers to enhance the dissolution rate

Hydrophobic deep eutectic solvent (HDES) as oil phase in lipid-based drug formulations

Comparative Analysis of Chemical Descriptors by Machine Learning Reveals Atomistic Insights into Solute–Lipid Interactions

A study of hydrophobic domain formation of polymeric drug precipitation inhibitors in aqueous solution

Amorphous solid dispersion of a binary formulation with felodipine and HPMC for 3D printed floating tablets

High loading of lipophilic compounds in mesoporous silica for improved solubility and dissolution performance

Effects of Different Weak Small Organic Acids on Clofazimine Solubility in Aqueous Media

Study of Disordered Mesoporous Silica Regarding Intrinsic Compound Affinity to the Carrier and Drug-Accessible Surface Area

Comparative Drug Solubility Studies Using Shake-Flask Versus a Laser-Based Robotic Method

Physiological Buffer Effects in Drug Supersaturation - A Mechanistic Study of Hydroxypropyl Cellulose as Precipitation Inhibitor

Exploring the Cocrystal Landscape of Posaconazole by Combining High-Throughput Screening Experimentation with Computational Chemistry

Hydroxypropyl Cellulose for Drug Precipitation Inhibition: From the Potential of Molecular Interactions to Performance Considering Microrheology

Collaborators (6)

Karl G. Wagner

Patrick O'Dwyer

René Holm

Lorraine Bateman

Brendan Griffin

Niklas Koehl

Make your next move.