MULLERTZ, ANETTE

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

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.

Are phytosomes a superior nanodelivery system for the antioxidant rutin?

Characterization of the Hydrodynamics in a Miniaturized Dissolution Apparatus

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

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

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

Hydrolysed pea proteins mitigate in vitro wheat starch digestibility

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

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

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

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

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

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

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

Cellulose Nanopaper and Nanofoam for Patient‐Tailored Drug Delivery

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

Dissolution enhancement of griseofulvin from griseofulvin-sodium dodecyl sulfate discs investigated by UV imaging

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

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

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

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

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

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

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

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

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

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

Self-microemulsifying drug delivery system and nanoemulsion for enhancing aqueous miscibility of Alpinia galanga oil

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

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

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

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

Buccal absorption of diazepam is improved when administered in bioadhesive tablets—An in vivo study in conscious Göttingen mini-pigs

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

Corrigendum to “Formulation and characterization of self-nanoemulsifying drug delivery systems containing monoacyl phosphatidylcholine” [Int. J. Pharm. 502 (1–2) (2016) 151–160]

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

Dissolution Model Development: Formulation Effects and Filter Complications

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

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

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

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

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

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

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

Polymeric microcontainers improve oral bioavailability of furosemide

Rhamnogalacturonan-I Based Microcapsules for Targeted Drug Release

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

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

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

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

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

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

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.

Evaluation of the Use of Göttingen Minipigs to Predict Food Effects on the Oral Absorption of Drugs in Humans

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

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

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

Stabilisation of amorphous furosemide increases the oral drug bioavailability in rats

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

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

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

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

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

Azone® Decreases the Buccal Mucosal Permeation of Diazepam in a Concentration‐Dependent Manner via a Reservoir Effect

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

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

Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs

Ex Vivo Correlation of the Permeability of Metoprolol Across Human and Porcine Buccal Mucosa

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

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

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

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

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

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

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

Miniaturized Approach for Excipient Selection During the Development of Oral Solid Dosage Form

Oral biopharmaceutics tools – Time for a new initiative – An introduction to the IMI project OrBiTo

Polymer-filled microcontainers for oral delivery loaded using supercritical impregnation

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

Refining stability and dissolution rate of amorphous drug formulations

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

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

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

The Biopharmaceutics Risk Assessment Roadmap for Optimizing Clinical Drug Product Performance

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

Toward the Establishment of Standardized In Vitro Tests for Lipid‐Based Formulations, Part 4: Proposing a New Lipid Formulation Performance Classification System

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MULLERTZ, ANETTE

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