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    Proteomics-Informed Identification of Luminal Targets For In Situ Diagnosis of Inflammatory Bowel Disease

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    In Vitro and In Vivo Evaluation of 3D Printed Capsules with Pressure Triggered Release Mechanism for Oral Peptide Delivery

    Part of Journal of Pharmaceutical Sciences, p. 228-238, 2021.

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    Synergistic Computational Modeling Approaches as Team Players in the Game of Solubility Predictions

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    A Tribute to Professor Per Artursson - Scientist, Explorer, Mentor, Innovator, and Giant in Pharmaceutical Research

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    Molecular dynamics simulations reveal membrane interactions for poorly water-soluble drugs: impact of bile solubilization and drug aggregation

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    A comparison of chitosan, mesoporous silica and poly(lactic-co-glycolic) acid nanocarriers for optimising intestinal uptake of oral protein therapeutics

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    Influence of Proteome Profiles and Intracellular Drug Exposure on Differences in CYP Activity in Donor-Matched Human Liver Microsomes and Hepatocytes

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    Contemporary formulation development for inhaled pharmaceuticals

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    Expanding the Efflux In Vitro Assay Toolbox: A CRISPR-Cas9 Edited MDCK Cell Line with Human BCRP and Completely Lacking Canine MDR1

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    3D-printing of solid lipid tablets from emulsion gels

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    Global variability analysis of mRNA and protein concentrations across and within human tissues

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    A Comparative Analysis of Cytochrome P450 Activities in Paired Liver and Small Intestinal Samples from Patients with Obesity

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    Selection of In Vivo Predictive Dissolution Media Using Drug Substance and Physiological Properties

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    Exploiting loss of heterozygosity for allele-selective colorectal cancer chemotherapy

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    Model-Informed Drug Development in Pulmonary Delivery: Semimechanistic Pharmacokinetic-Pharmacodynamic Modeling for Evaluation of Treatments against Chronic Pseudomonas aeruginosa Lung Infections

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    Acamprosate Is a Substrate of the Human Organic Anion Transporter (OAT) 1 without OAT3 Inhibitory Properties: Implications for Renal Acamprosate Secretion and Drug-Drug Interactions

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    Hit Identification of New Potent PqsR Antagonists as Inhibitors of Quorum Sensing in Planktonic and Biofilm Grown Pseudomonas aeruginosa

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    Suitability of Artificial Membranes in Lipolysis-Permeation Assays of Oral Lipid-Based Formulations

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    Intrinsic Dissolution Rate Profiling of Poorly Water-Soluble Compounds in Biorelevant Dissolution Media

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    Cell-type-resolved proteomic analysis of the human liver

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    MkVsites: A tool for creating GROMACS virtual sites parameters to increase performance in all-atom molecular dynamics simulations.

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    Strategies of solubility enhancement and perspectives in solubility measurements of pharmaceutical compounds

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  • El Sayed, Mira; Alhalaweh, Amjad; Bergström, Christel A. S.

    Insights into Dissolution and Solution Chemistry of Multidrug Formulations of Antihypertensive Drugs

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    An in vitro dissolution–digestion–permeation assay for the study of advanced drug delivery systems

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    Model-Informed Drug Discovery and Development in Pulmonary Delivery: Biopharmaceutical Pharmacometric Modeling for Formulation Evaluation of Pulmonary Suspensions

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    Influence of Bile Composition on Membrane Incorporation of Transient Permeability Enhancers

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  • Parrow, Albin; Larsson, Per; Augustijns, Patrick; Bergström, Christel A. S.

    Molecular Dynamics Simulations on Interindividual Variability of Intestinal Fluids: Impact on Drug Solubilization

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    TIRF Microscopy‐Based Monitoring of Drug Permeation Across a Lipid Membrane Supported on Mesoporous Silica

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    Proteomics‐Informed Prediction of Rosuvastatin Plasma Profiles in Patients with a Wide Range of Body Weight

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    A new opening for orally taken peptide drugs

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    The Critical Role of Passive Permeability in Designing Successful Drugs

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    Model-Based Drug Development in Pulmonary Delivery: Pharmacokinetic Analysis of Novel Drug Candidates for Treatment of Pseudomonas aeruginosa Lung Infection

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  • Alhalaweh, Amjad; Alzghoul, Ahmad; Bergström, Christel A. S.

    Molecular Drivers of Crystallization Kinetics for Drugs in Supersaturated Aqueous Solutions

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  • Nies, A. T.; Handin, Niklas; Schaeffeler, E.; Haag, M. et al.

    Comprehensive drug uptake transporter proteomics and metabolomic profiling of human liver

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    Fifty-Eight Years and Counting: High-Impact Publishing in Computational Pharmaceutical Sciences and Mechanism-Based Modeling

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    Experimental approaches to understand intracellular based drug bioavailability

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    Improved predictions of time-dependent drug-drug interactions by determination of cytosolic drug concentrations

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    Lipolysis-Permeation Setup for Simultaneous Study of Digestion and Absorption in Vitro

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    A simple approach for restoration of differentiation and function in cryopreserved human hepatocytes

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    Perspectives in solubility measurement and interpretation

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    Image-based quantification of cell debris as a measure of apoptosis

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

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    Multiple-Enzyme-Digestion Strategy Improves Accuracy and Sensitivity of Label- and Standard-Free Absolute Quantification to a Level That Is Achievable by Analysis with Stable Isotope-Labeled Standard Spiking

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    The Biopharmaceutics Classification System (BCS) and the Biopharmaceutics Drug Disposition Classification System (BDDCS): Beyond guidelines

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    Does the Intake of Ethanol Affect Oral Absorption of Poorly Soluble Drugs?

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

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    Advanced methodologies to study in vitro digestion of a lipid-loaded mesoporous drug carrier

    Part of Preclinical Form and Formulation for Drug Discovery, Gordon Research Conference 2019, 2019.