A. Müllertz

发表

Enhancing Stability and Tooth Bleaching Activity of Carbamide Peroxide by Electrospun Nanofibrous Film

T. Rades, Mingshi Yang, S. Okonogi, 2020, Pharmaceuticals.

INFOGEST inter-laboratory recommendations for assaying gastric and pancreatic lipases activities prior to in vitro digestion studies

T. Grauwet, A. Brodkorb, S. N. El, 2021, Journal of Functional Foods.

Evaluation Of Self-Emulsifying Drug Delivery Systems For Oral Insulin Delivery Using An In Vitro Model Simulating The Intestinal Proteolysis.

Jingying Liu, A. Müllertz, H. Mu, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

In vitro digestion models to evaluate lipid based drug delivery systems; present status and current trends.

T. Rades, A. Müllertz, R. Berthelsen, 2019, Advanced drug delivery reviews.

Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems.

Christel A. S. Bergström, M. Brandl, M. Kuentz, 2019, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Comparison of lipases for in vitro models of gastric digestion: lipolysis using two infant formulas as model substrates.

T. Rades, A. Müllertz, H. Mu, 2016, Food & function.

Survival of Lactobacillus acidophilus NCFM® and Bifidobacterium lactis HN019 encapsulated in chocolate during in vitro simulated passage of the upper gastrointestinal tract

D. Nielsen, D. Zielińska, A. Müllertz, 2016 .

A dynamic in vitro lipolysis model. II: Evaluation of the model.

H. Kristensen, A. Müllertz, N. H. Zangenberg, 2001, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Toward the establishment of standardized in vitro tests for lipid-based formulations, part 1: method parameterization and comparison of in vitro digestion profiles across a range of representative formulations.

A. Müllertz, C. Pouton, C. Porter, 2012, Journal of pharmaceutical sciences.

Toward the establishment of standardized in vitro tests for lipid-based formulations. 2. The effect of bile salt concentration and drug loading on the performance of type I, II, IIIA, IIIB, and IV formulations during in vitro digestion.

A. Müllertz, C. Pouton, C. Porter, 2012, Molecular pharmaceutics.

Biorelevant media simulating fed state intestinal fluids: colloid phase characterization and impact on solubilization capacity.

A. Müllertz, Karen Kleberg, F. Jacobsen, 2010, Journal of pharmaceutical sciences.

Characterising the behaviour of poorly water soluble drugs in the intestine: application of biorelevant media for solubility, dissolution and transport studies

A. Müllertz, Karen Kleberg, J. Jacobsen, 2010, The Journal of pharmacy and pharmacology.

Precipitation of a poorly soluble model drug during in vitro lipolysis: characterization and dissolution of the precipitate.

T. Rades, A. Müllertz, P. Sassene, 2010, Journal of pharmaceutical sciences.

In vitro lipolysis models as a tool for the characterization of oral lipid and surfactant based drug delivery systems.

A. Müllertz, P. Sassene, A. Larsen, 2011, International journal of pharmaceutics.

Optimization of self nanoemulsifying drug delivery system for poorly water-soluble drug using response surface methodology

A. Müllertz, H. Mu, Shan Ren, 2013, Drug development and industrial pharmacy.

From concept to in vivo testing: Microcontainers for oral drug delivery

Anja Boisen, Anette Müllertz, Stephan Sylvest Keller, 2017, Journal of controlled release : official journal of the Controlled Release Society.

Effect of composition of simulated intestinal media on the solubility of poorly soluble compounds investigated by design of experiments

Kung-I Feng, T. Rades, A. Müllertz, 2018, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

A Comparison of the Solubility of Danazol in Human and Simulated Gastrointestinal Fluids

Anette Müllertz, Henning Gjelstrup Kristensen, H. Brøndsted, 2000, Pharmaceutical Research.

Spatial confinement can lead to increased stability of amorphous indomethacin.

Anja Boisen, Thomas Rades, Anette Müllertz, 2012, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Dissolution of solid lipid extrudates in biorelevant media.

P. Kleinebudde, A. Müllertz, Venkata-Rangarao Kanikanti, 2012, International journal of pharmaceutics.

High-Throughput Lipolysis in 96-Well Plates for Rapid Screening of Lipid-Based Drug Delivery Systems.

T. Rades, A. Müllertz, H. Mu, 2017, Journal of pharmaceutical sciences.

Evaluating Oral Drug Delivery Systems: Digestion Models

T. Rades, A. Müllertz, R. Berthelsen, 2016 .

In vitro models for the prediction of in vivo performance of oral dosage forms.

Anette Müllertz, Patrick Augustijns, Bertil Abrahamsson, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Property profiling of biosimilar mucus in a novel mucus-containing in vitro model for assessment of intestinal drug absorption.

H. M. Nielsen, A. Müllertz, S. Baldursdóttir, 2014, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Adsorption of pharmaceutical excipients onto microcrystals of siramesine hydrochloride: effects on physicochemical properties.

A. Müllertz, L. Hovgaard, A. Millqvist-Fureby, 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Effect of liquid volume and food intake on the absolute bioavailability of danazol, a poorly soluble drug.

Anette Müllertz, Henning Gjelstrup Kristensen, H. Kristensen, 2005, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

The Influence of Solidification on the in vitro Solubilisation of Blonanserin Loaded Supersaturated Lipid-Based Oral Formulations.

C. Prestidge, A. Müllertz, H. B. Schultz, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Using biorelevant dissolution to obtain IVIVC of solid dosage forms containing a poorly-soluble model compound.

A. Müllertz, T. Magnussen, F. S. Nielsen, 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Lipids in oral controlled release drug delivery

A. Müllertz, B. Boyd, Tri-Hung Nguyen, 2011 .

Exploring the impact of intestinal fluid components on the solubility and supersaturation of danazol.

T. Rades, B. Hens, A. Müllertz, 2021, Journal of pharmaceutical sciences.

Exploring the utility of the Chasing Principle: influence of drug-free SNEDDS composition on solubilization of carvedilol, cinnarizine and R3040 in aqueous suspension

T. Rades, A. Müllertz, H. Mu, 2018, Acta pharmaceutica Sinica. B.

Solution or suspension – Does it matter for lipid based systems? In vivo studies of chase dosing lipid vehicles with aqueous suspensions of a poorly soluble drug

A. Müllertz, R. Holm, A. Larsen, 2017, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Effect of food intake and co-administration of placebo self-nanoemulsifying drug delivery systems on the absorption of cinnarizine in healthy human volunteers.

B. Abrahamsson, A. Müllertz, J. R. Andersen, 2016, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Supersaturation of zafirlukast in fasted and fed state intestinal media with and without precipitation inhibitors.

T. Rades, A. Müllertz, B. Boyd, 2016, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Structural features of colloidal species in the human fasted upper small intestine

A. Müllertz, D. Fatouros, C. Reppas, 2015, The Journal of pharmacy and pharmacology.

Development of Self‐Emulsifying Drug Delivery Systems (SEDDS) for Oral Bioavailability Enhancement of Poorly Soluble Drugs

A. Müllertz, D. Fatouros, 2013 .

Physicochemical Characterization of Simulated Intestinal Fed-State Fluids Containing Lyso-Phosphatidylcholine and Cholesterol

B. Bergenståhl, A. Müllertz, D. Fatouros, 2009 .

In vitro and in vivo evaluations of the performance of an indirubin derivative, formulated in four different self‐emulsifying drug delivery systems

Xinlai Cheng, G. Eisenbrand, A. Müllertz, 2014, The Journal of pharmacy and pharmacology.

Self-nanoemulsifying drug delivery systems for oral insulin delivery: in vitro and in vivo evaluations of enteric coating and drug loading.

H. M. Nielsen, C. Prestidge, A. Müllertz, 2014, International journal of pharmaceutics.

SEDDS for intestinal absorption of insulin: Application of Caco‐2 and Caco‐2/HT29 co‐culture monolayers and intra‐jejunal instillation in rats

Jingying Liu, A. Müllertz, H. Mu, 2019, International journal of pharmaceutics.

Impact of Lipid-Based Drug Delivery Systems on the Transport and Uptake of Insulin Across Caco-2 Cell Monolayers.

H. M. Nielsen, A. Müllertz, Ping Li, 2016, Journal of pharmaceutical sciences.

Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 3: Understanding Supersaturation Versus Precipitation Potential During the In Vitro Digestion of Type I, II, IIIA, IIIB and IV Lipid-Based Formulations

A. Müllertz, C. Pouton, C. Porter, 2013, Pharmaceutical Research.

In vivo evaluation of lipid-based formulations for oral delivery of apomorphine and its diester prodrugs.

Mingshi Yang, A. Müllertz, R. Holm, 2016, International journal of pharmaceutics.

Bioavailability of Seocalcitol IV: Evaluation of Lymphatic Transport in Conscious Rats

A. Müllertz, G. Pedersen, M. Grove, 2006, Pharmaceutical Research.

Formulation of co-amorphous systems from naproxen and naproxen sodium and in situ monitoring of physicochemical state changes during dissolution testing by Raman spectroscopy.

T. Rades, A. Müllertz, J. Østergaard, 2020, International journal of pharmaceutics.

Predicting oral absorption of fenofibrate in lipid-based drug delivery systems by combining in vitro lipolysis with the mucus-PVPA permeability model.

A. Müllertz, R. Berthelsen, M. Klitgaard, 2020, Journal of pharmaceutical sciences.

Lipophilic prodrugs of apomorphine I: preparation, characterisation, and in vitro enzymatic hydrolysis in biorelevant media.

Mingshi Yang, A. Müllertz, R. Holm, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Comparison of total oral bioavailability and the lymphatic transport of halofantrine from three different unsaturated triglycerides in lymph-cannulated conscious rats.

H. Kristensen, A. Müllertz, C. Høy, 2001, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Ex vivo correlation of the permeability of metoprolol across human and porcine buccal mucosa.

A. Pedersen, A. Müllertz, R. Holm, 2014, Journal of pharmaceutical sciences.

Structured Triglyceride Vehicles for Oral Delivery of Halofantrine: Examination of Intestinal Lymphatic Transport and Bioavailability in Conscious Rats

H. Kristensen, A. Müllertz, C. Porter, 2002, Pharmaceutical Research.

Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 6: Effects of Varying Pancreatin and Calcium Levels

A. Müllertz, C. Pouton, C. Porter, 2014, The AAPS Journal.

In Vitro Model Simulating Gastro-Intestinal Digestion in the Pediatric Population (Neonates and Young Infants)

A. Müllertz, R. Berthelsen, P. Sassene, 2016, AAPS PharmSciTech.

Studying furosemide solubilization using an in vitro model simulating gastrointestinal digestion and drug solubilization in neonates and young infants

A. Müllertz, R. Berthelsen, M. Klitgaard, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Using resin to generate a non-invasive intestinal bile-depleted rat model was unsuccessful.

A. Müllertz, R. Holm, Janne Z Hesselkilde, 2012, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Increased concentration of plasminogen activator inhibitor type-1 in plasma after intake of fish oil.

J. Grøndahl‐Hansen, A. Müllertz, G. Hølmer, 1990 .

Investigating the effect of graphene oxide in chitosan/alginate-based foams on the release and antifungal activity of clotrimazole in vitro.

H. M. Nielsen, A. Müllertz, S. Larsen, 2022, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Kolliphor surfactants affect solubilization and bioavailability of fenofibrate. Studies of in vitro digestion and absorption in rats.

B. Abrahamsson, A. Müllertz, R. Holm, 2015, Molecular pharmaceutics.

Elucidating Pathway and Anesthetic Mechanism of Action of Clove Oil Nanoformulations in Fish

T. Rades, L. Jørgensen, S. Okonogi, 2022, Pharmaceutics.

In vivo anesthetic effect and mechanism of action of active compounds from Alpinia galanga oil on Cyprinus carpio (koi carp)

S. Okonogi, A. Müllertz, S. Pikulkaew, 2018, Aquaculture.

Amorphous is not always better-A dissolution study on solid state forms of carbamazepine.

T. Rades, B. Abrahamsson, A. Müllertz, 2017, International journal of pharmaceutics.

Towards analyzing the potential of exosomes to deliver microRNA therapeutics

A. Müllertz, Konstantina Psatha, M. Aivaliotis, 2020, Journal of cellular physiology.

Influence of the Type of Surfactant and the Degree of Dispersion on the Lymphatic Transport of Halofantrine in Conscious Rats

H. Kristensen, A. Müllertz, R. Holm, 2004, Pharmaceutical Research.

Efficacy of oral lipid‐based formulations of apomorphine and its diester in a Parkinson's disease rat model

Mingshi Yang, A. Müllertz, R. Holm, 2017, The Journal of pharmacy and pharmacology.

Additive Manufacturing of Solid Products for Oral Drug Delivery Using Binder Jetting Three-Dimensional Printing

J. Rantanen, A. Müllertz, Yingya Wang, 2022, AAPS PharmSciTech.

Universitet Analysis of 3 D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging

J. Rantanen, T. Rades, J. Bøtker, 2017 .

Analysis of 3D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging

J. Rantanen, T. Rades, J. Bøtker, 2016, Pharmaceutical Research.

Cinnarizine food-effects in beagle dogs can be avoided by administration in a Self Nano Emulsifying Drug Delivery System (SNEDDS).

B. Abrahamsson, A. Müllertz, R. Holm, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Development of gastro-resistant coated probiotic granulates and evaluation of viability and release during simulated upper gastrointestinal transit

D. Nielsen, A. Müllertz, Martín S Marcial-Coba, 2021, LWT.

Achieving delayed release of freeze-dried probiotic strains by extrusion, spheronization and fluid bed coating - evaluated using a three-step in vitro model.

A. Müllertz, Daniel Bar-Shalom, Natashia Mai Yde Jacobsen, 2020, International journal of pharmaceutics.

Characterization of fasted human gastric fluid for relevant rheological parameters and gastric lipase activities.

P. Vilmann, A. Müllertz, S. Baldursdóttir, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Development and characterization of clove oil nanoemulsions and self-microemulsifying drug delivery systems

T. Rades, S. Okonogi, A. Müllertz, 2018, Journal of Drug Delivery Science and Technology.

In vitro and in vivo comparison of microcontainers and microspheres for oral drug delivery.

A. Boisen, A. Müllertz, Sophie Strindberg, 2021, International journal of pharmaceutics.

Milk osteopontin retains integrin-binding activity after in vitro gastrointestinal transit.

A. Müllertz, M. S. Ostenfeld, B. Christensen, 2019, Journal of dairy science.

Estimating the Oral Absorption from Self-Nanoemulsifying Drug Delivery Systems Using an In Vitro Lipolysis-Permeation Method

A. Müllertz, R. Berthelsen, M. Klitgaard, 2021, Pharmaceutics.

Enzyme supplementation of wheat-based diets for broilers

A. Müllertz, M. Hammershøj, S. Steenfeldt, 1998 .

Enzyme supplementation of wheat-based diets for broilers 1. Effect on growth performance and intestinal viscosity

A. Müllertz, S. Steenfeldt, J. F. Jensen, 1998 .

Development of a Microgram Scale Video-Microscopic Method to Investigate Dissolution Behavior of Poorly Water-Soluble Drugs

T. Rades, A. Müllertz, E. Spillum, 2022, AAPS PharmSciTech.

Bioinspired Layer-by-Layer Microcapsules Based on Cellulose Nanofibers with Switchable Permeability.

A. Müllertz, A. Svagan, Kun Yao, 2017, Biomacromolecules.

Formulation, characterization and in-vitro evaluation of self-nanoemulsifying drug delivery system containing rhamnolipid biosurfactant

A. Müllertz, S. Khan, Nisar-ur Rahman, 2022, Journal of Drug Delivery Science and Technology.

Improving the Drug Load and in vitro Performance of Supersaturated Self-Nanoemulsifying Drug Delivery Systems (Super-SNEDDS) using Polymeric Precipitation Inhibitors.

T. Rades, A. Müllertz, K. Löbmann, 2019, International journal of pharmaceutics.

A New Approach to Dissolution Testing by UV Imaging and Finite Element Simulations

J. Rantanen, J. Boetker, T. Rades, 2013, Pharmaceutical Research.

In Vitro, Ex Vivo and In Vivo Evaluation of Microcontainers for Oral Delivery of Insulin

H. M. Nielsen, A. Boisen, T. Rades, 2020, Pharmaceutics.

Solid lipid particles for oral delivery of peptide and protein drugs I--elucidating the release mechanism of lysozyme during lipolysis.

H. M. Nielsen, Mingshi Yang, A. Müllertz, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Comparison of induction methods for supersaturation: pH shift versus solvent shift.

T. Rades, A. Müllertz, L. Pérez-Alós, 2019, International journal of pharmaceutics.

New perspectives on lipid and surfactant based drug delivery systems for oral delivery of poorly soluble drugs

Shan Ren, Thomas Rades, Anette Müllertz, 2010, The Journal of pharmacy and pharmacology.

Monoacyl phosphatidylcholine inhibits the formation of lipid multilamellar structures during in vitro lipolysis of self‐emulsifying drug delivery systems

T. Rades, H. Amenitsch, A. Müllertz, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Towards the development of Self-Nano-Emulsifying Drug Delivery Systems (SNEDDS) containing trimethyl chitosan for the oral delivery of amphotericin B: In vitro assessment and cytocompatibility studies

H. Gika, A. Müllertz, D. Fatouros, 2020 .

Bile salts and their importance for drug absorption.

A. Müllertz, R. Holm, H. Mu, 2013, International journal of pharmaceutics.

Toward the establishment of standardized in vitro tests for lipid-based formulations, part 4: proposing a new lipid formulation performance classification system.

Anette Müllertz, Hywel D Williams, Philip Sassene, 2014, Journal of pharmaceutical sciences.

Analytical Techniques in the Pharmaceutical Sciences

T. Rades, A. Müllertz, Y. Perrie, 2016, Advances in Delivery Science and Technology.

Characterization and Physical Stability of Spray Dried Solid Dispersions of Probucol and PVP-K30

B. Pedersen, A. Müllertz, R. Holm, 2008, Pharmaceutical development and technology.

Development of Self-Nanoemulsifying Drug Delivery Systems Containing 4-Allylpyrocatechol for Treatment of Oral Infections Caused by Candida albicans.

T. Rades, S. Okonogi, A. Müllertz, 2021, Pharmaceutics.

Hydrolysed pea proteins mitigate in vitro wheat starch digestibility

A. Blennow, A. Müllertz, L. Saaby, 2018, Food Hydrocolloids.

Insights into the early dissolution events of amlodipine using UV imaging and Raman spectroscopy.

Claus Cornett, Thomas Rades, Jukka Rantanen, 2011, Molecular pharmaceutics.

Amphotericin B and monoacyl-phosphatidylcholine form a stable amorphous complex that can facilitate oral administration of amphotericin B.

A. Müllertz, R. Berthelsen, J. Doutch, 2023, International journal of pharmaceutics.

Newer Trends in In Situ Gelling Systems for Controlled Ocular Drug Delivery

A. Müllertz, Dharmendra Jain, H. Singh, 2016 .

SNEDDS Containing Poorly Water Soluble Cinnarizine; Development and in Vitro Characterization of Dispersion, Digestion and Solubilization

B. Abrahamsson, A. Müllertz, J. Østergaard, 2012, Pharmaceutics.

Formulation optimization, anesthetic activity, skin permeation, and transportation pathway of Alpinia galanga oil SNEDDS in zebrafish (Danio rerio).

T. Rades, S. Okonogi, A. Müllertz, 2021, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Towards the understanding of complex fluids in pharmaceutical sciences

P. Vilmann, A. Müllertz, J. Pajander, 2013 .

Bioavailability of seocalcitol II: development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides.

Anette Müllertz, A. Müllertz, Mette Grove, 2006, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides.

G. Edwards, H. Kristensen, A. Müllertz, 2003, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Influence of the Solid Form of Siramesine Hydrochloride on its Behavior in Aqueous Environments

Jukka Rantanen, Anette Müllertz, J. Rantanen, 2009, Pharmaceutical Research.

Effect of centrifugation speed on the measured equilibrium solubility of poorly water-soluble compounds in viscous solvents

A. Müllertz, R. Berthelsen, Xiaona Liu, 2020 .

Preparation and characterization of insulin-surfactant complexes for loading into lipid-based drug delivery systems.

H. M. Nielsen, A. Müllertz, M. Fanø, 2013, Journal of pharmaceutical sciences.

Intestinal lymphatic transport of halofantrine in rats assessed using a chylomicron flow blocking approach: the influence of polysorbate 60 and 80.

A. Müllertz, R. Holm, M. Lind, 2008, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

In Vitro Evaluation of Self-Nano-Emulsifying Drug Delivery Systems (SNEDDS) Containing Room Temperature Ionic Liquids (RTILs) for the Oral Delivery of Amphotericin B

H. Gika, A. Müllertz, D. Fatouros, 2020, Pharmaceutics.

Supersaturated Self-Nanoemulsifying Drug Delivery Systems (super-SNEDDS)

R Holm, A Müllertz, T. Rades, 2012 .

Bioavailability of probucol from lipid and surfactant based formulations in minipigs: influence of droplet size and dietary state.

A. Müllertz, K. Petersen, F. S. Nielsen, 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Characterization of prototype self-nanoemulsifying formulations of lipophilic compounds.

J. S. Pedersen, L. Arleth, A. Müllertz, 2007, Journal of pharmaceutical sciences.

Investigating the correlation between in vivo absorption and in vitro release of fenofibrate from lipid matrix particles in biorelevant medium.

Mingshi Yang, A. Müllertz, R. Holm, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Biorelevant dissolution media: aggregation of amphiphiles and solubility of estradiol.

H. Kristensen, A. Müllertz, David Ilardia-Arana, 2006, Journal of pharmaceutical sciences.

Biorelevant intrinsic dissolution profiling in early drug development: Fundamental, methodological, and industrial aspects.

Thomas Rades, Anette Müllertz, Wayne Matthews, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

In vivo in vitro correlations for a poorly soluble drug, danazol, using the flow-through dissolution method with biorelevant dissolution media.

Anette Müllertz, Henning Gjelstrup Kristensen, B. Pedersen, 2005, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Studying the Propensity of Compounds to Supersaturate: A Practical and Broadly Applicable Approach.

Thomas Rades, Anette Müllertz, T. Rades, 2016, Journal of pharmaceutical sciences.

Oral delivery of peptides and proteins using lipid-based drug delivery systems

Anette Müllertz, Hanne Mørck Nielsen, Ping Li, 2012, Expert opinion on drug delivery.

Graphene oxide as a functional excipient in buccal films for delivery of clotrimazole: effect of molecular interactions on drug release and antifungal activity in vitro.

H. M. Nielsen, A. Müllertz, M. van de Weert, 2020, International journal of pharmaceutics.

Comparison of drug transporter gene expression and functionality in Caco-2 cells from 10 different laboratories.

P. Artursson, R. Hayeshi, A. Ungell, 2008, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Dissolution Model Development: Formulation Effects and Filter Complications

B. Abrahamsson, A. Müllertz, R. Holm, 2016 .

Solid cellulose nanofiber based foams - Towards facile design of sustained drug delivery systems.

A. Müllertz, L. Wågberg, K. Löbmann, 2016, Journal of controlled release : official journal of the Controlled Release Society.

Combining in vitro and in silico methods for better prediction of surfactant effects on the absorption of poorly water soluble drugs-a fenofibrate case example.

B. Abrahamsson, A. Müllertz, R. Holm, 2014, International journal of pharmaceutics.

Influence of drug load and physical form of cinnarizine in new SNEDDS dosing regimens: in vivo and in vitro evaluations

T. Rades, A. Müllertz, H. Mu, 2017, The AAPS Journal.

Characterising Lipid Lipolysis and Its Implication in Lipid-Based Formulation Development

Thomas Rades, Anette Müllertz, Nicky Thomas, 2012, The AAPS Journal.

Cellulose Nanopaper and Nanofoam for Patient‐Tailored Drug Delivery

A. Müllertz, L. Wågberg, J. Wohlert, 2017 .

Bioavailability of Cinnarizine in Dogs: Effect of SNEDDS Loading Level and Correlation with Cinnarizine Solubilization During In Vitro Lipolysis

Anna Juréus, B. Abrahamsson, A. Müllertz, 2013, Pharmaceutical Research.

A dynamic in vitro lipolysis model. I. Controlling the rate of lipolysis by continuous addition of calcium.

A Müllertz, H. Kristensen, A. Müllertz, 2001, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Exploring the fate of liposomes in the intestine by dynamic in vitro lipolysis.

T. Rades, A. Müllertz, G. Fricker, 2012, International journal of pharmaceutics.

Biodegradable microcontainers - towards real life applications of microfabricated systems for oral drug delivery.

A. Boisen, S. Keller, C. Gundlach, 2019, Lab on a chip.

Polymeric microcontainers improve oral bioavailability of furosemide.

A. Boisen, S. Keller, T. Rades, 2016, International journal of pharmaceutics.

Phase transformations of amlodipine besylate solid forms.

J. Rantanen, M. Allesø, A. Müllertz, 2011, Journal of pharmaceutical sciences.

Biorelevant Dissolution Media

A. Müllertz, 2007 .

Drug solubilization during simulated pediatric gastro-intestinal digestion.

A. Müllertz, R. Berthelsen, A. Selen, 2021, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Colloidal Structures in Media Simulating Intestinal Fed State Conditions with and Without Lipolysis Products

Anette Müllertz, B. Bergenståhl, A. Müllertz, 2009, Pharmaceutical Research.

Investigation of Mucoadhesion and Degradation of PCL and PLGA Microcontainers for Oral Drug Delivery

A. Boisen, A. Müllertz, Zarmeena Abid, 2019, Polymers.

Ex vivo intestinal perfusion model for investigating mucoadhesion of microcontainers.

A. Boisen, A. Müllertz, A. J. Andersen, 2019, International journal of pharmaceutics.

Real-time dissolution behavior of furosemide in biorelevant media as determined by UV imaging

Jukka Rantanen, Anette Müllertz, Arzu Selen, 2013, Pharmaceutical development and technology.

Application of a Salt Coformer in a Co-Amorphous Drug System Dramatically Enhances the Glass Transition Temperature: A Case Study of the Ternary System Carbamazepine, Citric Acid, and l-Arginine.

T. Rades, A. Müllertz, Wenqi Wu, 2018, Molecular pharmaceutics.

Impact of gastrointestinal physiology on drug absorption in special populations - An UNGAP review.

Christine M. Madla, A. Basit, Cordula Stillhart, 2020, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Evaluation of the use of Göttingen minipigs to predict food effects on the oral absorption of drugs in humans.

B. Abrahamsson, A. Müllertz, R. Holm, 2015, Journal of pharmaceutical sciences.

In vitro models for the prediction of in vivo performance of oral dosage forms: Recent progress from partnership through the IMI OrBiTo collaboration

Anette Müllertz, Filippos Kesisoglou, Christos Reppas, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Current challenges and future perspectives in oral absorption research: An opinion of the UNGAP network.

Clive G. Wilson, B. Griffin, P. Artursson, 2021, Advanced drug delivery reviews.

Solid Lipid Particles for Oral Delivery of Peptide and Protein Drugs III — the Effect of Fed State Conditions on the In Vitro Release and Degradation of Desmopressin

H. M. Nielsen, Mingshi Yang, A. Müllertz, 2014, The AAPS Journal.

Lipid-based Formulations for Danazol Containing a Digestible Surfactant, Labrafil M2125CS: In Vivo Bioavailability and Dynamic In Vitro Lipolysis

Anette Müllertz, René Holm, A. Müllertz, 2008, Pharmaceutical Research.

Combining lipid based drug delivery and amorphous solid dispersions for improved oral drug absorption of a poorly water-soluble drug.

Francis S. Romanski, T. Rades, A. Müllertz, 2022, Journal of controlled release : official journal of the Controlled Release Society.

Self-emulsifying drug delivery systems (SEDDS) - The splendid comeback of an old technology.

T. Rades, A. Müllertz, A. Bernkop‐Schnürch, 2019, Advanced drug delivery reviews.

Influence of bile on the absorption of halofantrine from lipid-based formulations.

A. Müllertz, R. Holm, E. Jørgensen, 2012, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

A novel excipient, 1-perfluorohexyloctane shows limited utility for the oral delivery of poorly water-soluble drugs.

P. Holm, A. Müllertz, R. Holm, 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

In vitro and in vivo performance of monoacyl phospholipid‐based self‐emulsifying drug delivery systems

Thomas Rades, Anette Müllertz, Thuy Tran, 2017, Journal of controlled release : official journal of the Controlled Release Society.

Formulation and characterization of self-nanoemulsifying drug delivery systems containing monoacyl phosphatidylcholine.

T. Rades, A. Müllertz, T. Tran, 2016, International journal of pharmaceutics.

The Binding of Alpinia galanga Oil and Its Nanoemulsion to Mammal GABAA Receptors Using Rat Cortical Membranes and an In Silico Modeling Platform

T. Rades, S. Okonogi, A. Müllertz, 2022, Pharmaceutics.

Binding effects of Alpinia galanga oil and its nanoemulsion 1 to GABAA receptors in rat cortical membranes

T. Rades, S. Okonogi, A. Müllertz, 2021 .

Miniaturized approach for excipient selection during the development of oral solid dosage form.

J. Rantanen, A. Müllertz, C. Cornett, 2014, Journal of pharmaceutical sciences.

Impact of oral gavage technique of drug-containing microcontainers on the gastrointestinal transit and absorption in rats.

A. Boisen, T. Rades, A. Müllertz, 2022, International journal of pharmaceutics.

Comparison of the Lymphatic Transport of Halofantrine Administered in Disperse Systems Containing Three Different Unsaturated Fatty Acids

H. Kristensen, A. Müllertz, R. Holm, 2001, Pharmaceutical Research.

Optimizing Clinical Drug Product Performance: Applying Biopharmaceutics Risk Assessment Roadmap (BioRAM) and the BioRAM Scoring Grid.

Talia Flanagan, Anette Müllertz, Filippos Kesisoglou, 2016, Journal of pharmaceutical sciences.

The biopharmaceutics risk assessment roadmap for optimizing clinical drug product performance.

Anette Müllertz, Arzu Selen, Hans Lennernäs, 2014, Journal of pharmaceutical sciences.

Lipid-based formulations for oral administration of poorly water-soluble drugs.

Anette Müllertz, Huiling Mu, René Holm, 2013, International journal of pharmaceutics.

Bioavailability of Cinnarizine in Dogs: Effect of SNEDDS Loading Level and Correlation with Cinnarizine Solubilization During In Vitro Lipolysis

Anna Juréus, B. Abrahamsson, A. Müllertz, 2013, Pharmaceutical Research.

Insights into Amlodipine Besilate Dissolution Behavior Using UV Imaging

J. Rantanen, T. Rades, J. Bøtker, 2011 .

pH-triggered drug release from biodegradable microwells for oral drug delivery

Anja Boisen, Thomas Rades, Anette Müllertz, 2015, Biomedical microdevices.

Anhydrate to hydrate solid-state transformations of carbamazepine and nitrofurantoin in biorelevant media studied in situ using time-resolved synchrotron X-ray diffraction.

J. Rantanen, J. Boetker, T. Rades, 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

pH-triggered drug release from biodegradable microwells for oral drug delivery

A. Boisen, S. Keller, T. Rades, 2015, Biomedical Microdevices.

Biorelevant characterisation of amorphous furosemide salt exhibits conversion to a furosemide hydrate during dissolution.

Thomas Rades, Anette Müllertz, Jesper Østergaard, 2013, International journal of pharmaceutics.

A New Approach to Dissolution Testing by UV Imaging and Finite Element Simulations

J. Rantanen, J. Boetker, T. Rades, 2013, Pharmaceutical Research.

Integrated Multi-stakeholder Systems Thinking Strategy: Decision-making with Biopharmaceutics Risk Assessment Roadmap (BioRAM) to Optimize Clinical Performance of Drug Products

Talia Flanagan, Filippos Kesisoglou, Arzu Selen, 2020, The AAPS Journal.

In vivo Models and Decision Trees for Formulation Development in Early Drug Development: A Review of Current Practices and Recommendations for Biopharmaceutical Development.

P Zane, P Langguth, A Müllertz, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations. 5. Lipolysis of Representative Formulations by Gastric Lipase

Anette Müllertz, Vincent Jannin, Christopher J. H. Porter, 2014, Pharmaceutical Research.

Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations, Part 6: Effects of Varying Pancreatin and Calcium Levels

A. Müllertz, C. Pouton, C. Porter, 2014, The AAPS Journal.

Direct visualizing of paracetamol immediate release tablet disintegration in vivo and in vitro.

A. Müllertz, R. Berthelsen, Camilla Di Meo, 2022, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Floating solid cellulose nanofibre nanofoams for sustained release of the poorly soluble model drug furosemide

A. Müllertz, K. Löbmann, A. Svagan, 2017, The Journal of pharmacy and pharmacology.

Six years of progress in the oral biopharmaceutics area - a summary from the IMI OrBiTo project.

H Lennernäs, A Lindahl, E Sjögren, 2020, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

The Influence of Polymers on the Supersaturation Potential of Poor and Good Glass Formers

T. Rades, A. Müllertz, K. Löbmann, 2018, Pharmaceutics.

Fasted and fed state human duodenal fluids: Characterization, drug solubility, and comparison to simulated fluids and with human bioavailability.

H. Lennernäs, P. Hellström, A. Müllertz, 2021, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Stability and intrinsic dissolution of vacuum compression molded amorphous solid dispersions of efavirenz.

T. Rades, A. Müllertz, M. Rischer, 2022, International journal of pharmaceutics.

Solid Forms of Amlodipine Besylate: Physicochemical, Structural, and Thermodynamic Characterization

J. Rantanen, A. Bond, A. Müllertz, 2010 .

X-ray Imaging for Gastrointestinal Tracking of Microscale Oral Drug Delivery Devices.

A. Boisen, T. Rades, C. Gundlach, 2021, ACS biomaterials science & engineering.

Polymeric Lids for Microcontainers for Oral Protein Delivery.

A. Boisen, C. Gundlach, A. Müllertz, 2019, Macromolecular bioscience.

Design of a self-unfolding delivery concept for oral administration of macromolecules.

H. M. Nielsen, A. Boisen, T. Rades, 2020, Journal of controlled release : official journal of the Controlled Release Society.

Assessing acute colitis induced by dextran sulfate sodium in rats and its impact on gastrointestinal fluids

T. Rades, A. Müllertz, R. Berthelsen, 2023, Drug Delivery and Translational Research.

Developing a predictive in vitro dissolution model based on gastrointestinal fluid characterisation in rats.

A. Müllertz, C. Janfelt, Sophie Strindberg, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

In Vivo Precipitation of Poorly Soluble Drugs from Lipid-Based Drug Delivery Systems.

A Müllertz, T. Rades, A. Müllertz, 2016, Molecular pharmaceutics.

Lymphatic fatty acids in canines dosed with pharmaceutical formulations containing structured triacylglycerols

G. Edwards, H. Kristensen, A. Müllertz, 2006 .

Absorption of triglycerides with defined or random structure by rats with biliary and pancreatic diversion

A. Müllertz, C. Høy, M. S. Christensen, 1995, Lipids.

Bovine Milk-Derived Emulsifiers Increase Triglyceride Absorption in Newborn Formula-Fed Pigs

A. Müllertz, Christine Heerup, Xiaolu Geng, 2021, Nutrients.

Hot punching for loading of biodegradable microcontainers with budesonide-Soluplus film

A. Boisen, S. Keller, A. Müllertz, 2021, Biomedical Microdevices.

Stabilisation of amorphous furosemide increases the oral drug bioavailability in rats.

T. Rades, A. Müllertz, L. Nielsen, 2015, International journal of pharmaceutics.

Enzymatic characterization of lipid-based drug delivery systems.

Anette Müllertz, Emma Troedsson, A. Müllertz, 2005, International journal of pharmaceutics.

Fed and fasted state gastro-intestinal in vitro lipolysis: In vitro in vivo relations of a conventional tablet, a SNEDDS and a solidified SNEDDS.

Anette Müllertz, Bertil Abrahamsson, Jakob Kristensen, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Effects of recombinant human gastric lipase and pancreatin during in vitro pediatric gastro-intestinal digestion.

A. Müllertz, Christine Heerup, R. Berthelsen, 2021, Food & function.

Oral biopharmaceutics tools - time for a new initiative - an introduction to the IMI project OrBiTo.

H Lennernäs, A Lindahl, B Abrahamsson, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Image Analytical Approach for Needle-Shaped Crystal Counting and Length Estimation

J. Rantanen, T. Rades, A. Müllertz, 2015 .

Effect of different surfactants in biorelevant medium on the secretion of a lipophilic compound in lipoproteins using Caco-2 cell culture.

Anette Müllertz, René Holm, Jette Jacobsen, 2006, Journal of pharmaceutical sciences.

From Molecule to Dose Form – Accelerated Bioavailability Enhancement for Early Phase Molecules

J. Veuthey, C. Strachan, T. Rades, 2015 .

Preparation of an amorphous sodium furosemide salt improves solubility and dissolution rate and leads to a faster Tmax after oral dosing to rats.

T. Rades, A. Müllertz, R. Holm, 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Impact of physiologically relevant viscosity on intrinsic dissolution rate of poorly soluble compounds in simulated gastric media

A. Müllertz, S. Baldursdóttir, P. Pedersen, 2012 .

Using Potentiometric Free Drug Sensors to Determine the Free Concentration of Ionizable Drugs in Colloidal Systems.

Claus Cornett, Thomas Rades, Anette Müllertz, 2018, Journal of pharmaceutical sciences.

Are phytosomes a superior nanodelivery system for the antioxidant rutin?

T. Rades, A. Müllertz, S. Hook, 2018, International journal of pharmaceutics.

A fast and novel internal calibration method for quantitative Raman measurements on aqueous solutions

Anette Müllertz, Jan C. Petersen, Mark R. Pollard, 2018 .

Effect of supersaturation on absorption of indomethacin and tadalafil in a single pass intestinal perfusion rat model, in the absence and presence of a precipitation inhibitor.

T. Rades, A. Müllertz, Sophie Strindberg, 2020, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Development of a Video-Microscopic Tool To Evaluate the Precipitation Kinetics of Poorly Water Soluble Drugs: A Case Study with Tadalafil and HPMC.

T. Rades, A. Müllertz, L. Nielsen, 2017, Molecular pharmaceutics.

Oral bioavailability of cinnarizine in dogs: relation to SNEDDS droplet size, drug solubility and in vitro precipitation.

B. Abrahamsson, A. Müllertz, P. Dickinson, 2013, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Development of simulated intestinal fluids containing nutrients as transport media in the Caco-2 cell culture model: assessment of cell viability, monolayer integrity and transport of a poorly aqueous soluble drug and a substrate of efflux mechanisms.

A. Müllertz, R. Holm, M. Lind, 2007, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Solid Lipid Particles for Oral Delivery of Peptide and Protein Drugs II – The Digestion of Trilaurin Protects Desmopressin from Proteolytic Degradation

H. M. Nielsen, Mingshi Yang, A. Müllertz, 2014, Pharmaceutical Research.

Development of a high-throughput in vitro intestinal lipolysis model for rapid screening of lipid-based drug delivery systems.

Thomas Rades, Anette Müllertz, Huiling Mu, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Bioavailability of seocalcitol III. Administration of lipid-based formulations to minipigs in the fasted and fed state.

A. Müllertz, G. Pedersen, M. Grove, 2007, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Development of a μDissolution-Permeation model with in situ drug concentration monitoring

B. Abrahamsson, A. Müllertz, R. Holm, 2016 .

Azone® decreases the buccal mucosal permeation of diazepam in a concentration-dependent manner via a reservoir effect.

A. Müllertz, C. Janfelt, R. Holm, 2014, Journal of pharmaceutical sciences.

Impact of sodium dodecyl sulphate on the dissolution of poorly soluble drug into biorelevant medium from drug-surfactant discs.

P. Bertelsen, A. Müllertz, J. Ostergaard, 2014, International journal of pharmaceutics.

In Vitro Lipolysis Data Does Not Adequately Predict the In Vivo Performance of Lipid-Based Drug Delivery Systems Containing Fenofibrate

T. Rades, Katharina Richter, A. Müllertz, 2014, The AAPS Journal.

Feasibility of Capsule Endoscopy for Direct Imaging of Drug Delivery Systems in the Fasted Upper-Gastrointestinal Tract

P. Vilmann, A. Müllertz, S. Baldursdóttir, 2014, Pharmaceutical Research.

Insights into intermediate phases of human intestinal fluids visualized by atomic force microscopy and cryo-transmission electron microscopy ex vivo.

Anette Müllertz, Christos Reppas, Dimitrios G Fatouros, 2012, Molecular pharmaceutics.

Supersaturated Self-Nanoemulsifying Drug Delivery Systems (Super-SNEDDS) Enhance the Bioavailability of the Poorly Water-Soluble Drug Simvastatin in Dogs

T. Rades, A. Müllertz, R. Holm, 2012, The AAPS Journal.

Design and optimization of self-nanoemulsifying drug delivery systems of clove oil for efficacy enhancement in fish anesthesia

T. Rades, L. Jørgensen, S. Okonogi, 2021 .

Formulation of self-nanoemulsifying drug delivery systems containing monoacyl phosphatidylcholine and Kolliphor® RH40 using experimental design

T. Rades, A. Müllertz, T. Tran, 2017, Asian journal of pharmaceutical sciences.

Physico-chemical characterization of aspirated human and simulated human gastric fluids to study their influence on the intrinsic dissolution rate of cinnarizine.

P. Vilmann, T. Rades, A. Müllertz, 2022, International journal of pharmaceutics.

Comparison of induction methods for supersaturation: amorphous dissolution versus solvent shift.

T. Rades, A. Müllertz, Jakob Plum, 2020, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Interlaboratory Validation of Small-Scale Solubility and Dissolution Measurements of Poorly Water-Soluble Drugs.

Thomas Rades, Anette Müllertz, Jan Bevernage, 2016, Journal of pharmaceutical sciences.

Recent developments in oral lipid-based drug delivery

T. Rades, A. Müllertz, N. Thomas, 2013 .

Comparison of the lymphatic transport of a lipophilic drug from vehicles containing α‐tocopherol and/or triglycerides in rats

H. Kristensen, A. Müllertz, P. Nielsen, 2001, The Journal of pharmacy and pharmacology.

Dissolution of Hydrocortisone in Human and Simulated Intestinal Fluids

Anette Müllertz, Hans Lennernäs, Henning Gjelstrup Kristensen, 2000, Pharmaceutical Research.

Investigation of the Intra- and Interlaboratory Reproducibility of a Small Scale Standardized Supersaturation and Precipitation Method.

Thomas Rades, Anette Müllertz, Jan Bevernage, 2017, Molecular pharmaceutics.

Effect of bile on the oral absorption of halofantrine in polyethylene glycol 400 and polysorbate 80 formulations dosed to bile duct cannulated rats

Anette Müllertz, Huiling Mu, René Holm, 2011, The Journal of pharmacy and pharmacology.

Visualizing the Journey of Fenofibrate through the Rat Gastrointestinal Tract by Matrix-Assisted Laser Desorption/Ionization-Mass Spectrometry Imaging.

A. Müllertz, C. Janfelt, Sophie Strindberg, 2021, Molecular pharmaceutics.

Determination of surface-adsorbed excipients of various types on drug particles prepared by antisolvent precipitation using HPLC with evaporative light scattering detection.

A. Müllertz, L. Hovgaard, A. Zimmermann, 2007, Journal of pharmaceutical and biomedical analysis.

Fenofibrate oral absorption from SNEDDS and super-SNEDDS is not significantly affected by lipase inhibition in rats.

T. Rades, A. Müllertz, K. Wasan, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

The ability of two in vitro lipolysis models reflecting the human and rat gastro‐intestinal conditions to predict the in vivo performance of SNEDDS dosing regimens

T. Rades, A. Müllertz, H. Mu, 2018, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

The Effect of Digestion and Drug Load on Halofantrine Absorption from Self-nanoemulsifying Drug Delivery System (SNEDDS)

T. Rades, A. Müllertz, K. Wasan, 2015, The AAPS Journal.

Mapping the intermediate digestion phases of human healthy intestinal contents from distal ileum and caecum at fasted and fed state conditions

A. Müllertz, D. Fatouros, C. Reppas, 2017, The Journal of pharmacy and pharmacology.

Unravelling the ultrastructure of ascending colon fluids from patients with ulcerative colitis by cryogenic transmission electron microscopy

A. Müllertz, D. Fatouros, C. Reppas, 2013, The Journal of pharmacy and pharmacology.

Exploring Porcine Gastric and Intestinal Fluids using Microscopic and Solubility Estimates: Impact of Placebo Self-Emulsifying Drug Delivery System Administration to Inform Bio-Predictive in vitro Tools.

Niklas J. Koehl, B. Griffin, A. Müllertz, 2021, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Mucosal drug delivery: barriers, in vitro models and formulation strategies

H. M. Nielsen, A. Müllertz, C. Foged, 2013 .

A. Müllertz, C. Pouton, C. Porter, 2013, Pharmaceutical Research.

Dairy-Derived Emulsifiers in Infant Formula Show Marginal Effects on the Plasma Lipid Profile and Brain Structure in Preterm Piglets Relative to Soy Lecithin

Christer S. Ejsing, S. Eskildsen, C. Ejsing, 2021, Nutrients.

The Influence of Blonanserin Supersaturation in Liquid and Silica Stabilised Self-Nanoemulsifying Drug Delivery Systems on In Vitro Solubilisation

C. Prestidge, A. Müllertz, P. Joyce, 2023, Pharmaceutics.

Structured approach for designing drug-loaded solid products by binder jetting 3D printing.

J. Rantanen, A. Müllertz, Yingya Wang, 2022, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

In vitro-in vivo relationship for amorphous solid dispersions using a double membrane dissolution-permeation setup.

T. Rades, A. Müllertz, M. Rischer, 2023, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Coating of primary powder particles improves the quality of binder jetting 3D printed oral solid products.

J. Rantanen, A. Müllertz, N. Genina, 2022, Journal of pharmaceutical sciences.

Influence of lipid composition and drug load on the In Vitro performance of self-nanoemulsifying drug delivery systems.

T. Rades, A. Müllertz, N. Thomas, 2012, Journal of pharmaceutical sciences.

SOLUPLUS® FOR MODIFYING THE RELEASE OF HIGHLY WATER SOLUBLE APIs

J. Rantanen, J. Boetker, T. Rades, 2012 .

Evaluating side‐by‐side diffusion models for studying drug supersaturation in an absorptive environment: a case example of fenofibrate and felodipine

A. Müllertz, R. Berthelsen, J. Eliasen, 2019, The Journal of pharmacy and pharmacology.

Using in vitro lipolysis and SPECT/CT in vivo imaging to understand oral absorption of fenofibrate from lipid-based drug delivery systems.

T. Rades, U. Häfeli, A. Müllertz, 2019, Journal of controlled release : official journal of the Controlled Release Society.

The effect of α-tocopherol on the in vitro solubilisation of lipophilic drugs

H. Kristensen, A. Müllertz, P. Nielsen, 2001 .

Characterising Lipid Lipolysis and Its Implication in Lipid-Based Formulation Development

T. Rades, A. Müllertz, R. Holm, 2012, The AAPS Journal.

Microcontainers for oral insulin delivery - in vitro studies of permeation enhancement.

A. Boisen, T. Rades, A. Müllertz, 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Adding a gastric step to the intestinal in vitro digestion model improves the prediction of pharmacokinetic data in beagle dogs of two lipid based drug delivery systems.

A. Müllertz, R. Berthelsen, M. Klitgaard, 2020, Molecular pharmaceutics.

Elucidating the Molecular Interactions Occurring during Drug Precipitation of Weak Bases from Lipid-Based Formulations: A Case Study with Cinnarizine and a Long Chain Self-Nanoemulsifying Drug Delivery System.

Thomas Rades, Anette Müllertz, Huiling Mu, 2015, Molecular pharmaceutics.

Toward the Establishment of Standardized In Vitro Tests for Lipid-Based Formulations. 5. Lipolysis of Representative Formulations by Gastric Lipase

A. Müllertz, C. Pouton, C. Porter, 2015, Pharmaceutical Research.

Characterization of the Hydrodynamics in a Miniaturized Dissolution Apparatus.

Thomas Rades, Anette Müllertz, T. Rades, 2017, Journal of pharmaceutical sciences.

Steric and interactive barrier properties of intestinal mucus elucidated by particle diffusion and peptide permeation.

H. M. Nielsen, A. Müllertz, M. García-Díaz, 2015, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Microfabricated devices for oral drug delivery.

A. Boisen, S. Keller, T. Rades, 2018, Lab on a chip.

Polymer-filled microcontainers for oral delivery loaded using supercritical impregnation.

Anja Boisen, Anette Müllertz, A. Boisen, 2014, Journal of controlled release : official journal of the Controlled Release Society.

Development and Rheological Profiling of Biosimilar Mucus

H. M. Nielsen, A. Müllertz, S. Baldursdóttir, 2013 .

Polymer Selection for Simulation of Rheological Properties of Human Gastric Fluid

P. Vilmann, A. Müllertz, S. Baldursdóttir, 2013 .

Apomorphine and its esters: Differences in Caco-2 cell permeability and chylomicron affinity.

Mingshi Yang, A. Müllertz, R. Holm, 2016, International journal of pharmaceutics.

A slow cooling rate of indomethacin melt spatially confined in microcontainers increases the physical stability of the amorphous drug without influencing its biorelevant dissolution behaviour

A. Boisen, S. Keller, T. Rades, 2014, Drug Delivery and Translational Research.