Christel Bergström
Professor at Department of Pharmacy; Molecular Pharmaceutics
- Telephone:
- +46 18 471 41 18
- Mobile phone:
- +46 73 469 76 22
- E-mail:
- christel.bergstrom@uu.se
- Visiting address:
- Biomedicinskt Centrum BMC, Husargatan 3
- Postal address:
- Box 580
751 23 UPPSALA
- CV:
- Download CV
Short presentation
I make use of knowledge of physiological pathways to improve delivery of pharmacologically active compounds to the site of action. With a strong background in pharmaceutics, material sciences, physical chemistry and physiology, I focus on making use of the right tech with a clinical translation in mind from day one. I make use of advanced computational modelling, develop novel in vitro tools and design new drug carriers in my quest for personalized medicines transforming the current healthcare.
Keywords
- drug delivery
- solubility
- computational pharmaceutics
- virtual intestine
- enabling formulations
- personalised medicines
- digestion
- absorption

Publications
Recent publications
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Lipid packing contributes to the confinement of caveolae to the plasma membrane
Part of eLIFE, 2026
- DOI for Lipid packing contributes to the confinement of caveolae to the plasma membrane
- Download full text (pdf) of Lipid packing contributes to the confinement of caveolae to the plasma membrane
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Part of Journal of Colloid and Interface Science, 2026
- DOI for Double emulsions enable in situ generation of permeation enhancers for oral delivery of macromolecules
- Download full text (pdf) of Double emulsions enable in situ generation of permeation enhancers for oral delivery of macromolecules
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Exploration of Colonic Mucus as A Dissolution Compartment for Orally Administered Drugs
Part of AAPS Journal, 2026
- DOI for Exploration of Colonic Mucus as A Dissolution Compartment for Orally Administered Drugs
- Download full text (pdf) of Exploration of Colonic Mucus as A Dissolution Compartment for Orally Administered Drugs
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Part of Drug Delivery, 2026
- DOI for Mechanics of small intestine motility for oral macromolecular delivery: modelling segmentation versus peristalsis
- Download full text (pdf) of Mechanics of small intestine motility for oral macromolecular delivery: modelling segmentation versus peristalsis
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Part of Colloids and Surfaces B, 2026
- DOI for Molecular dynamics simulations of a hexagonal liquid crystal phase to study drug partitioning and release mechanisms
- Download full text (pdf) of Molecular dynamics simulations of a hexagonal liquid crystal phase to study drug partitioning and release mechanisms
All publications
Articles in journal
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Lipid packing contributes to the confinement of caveolae to the plasma membrane
Part of eLIFE, 2026
- DOI for Lipid packing contributes to the confinement of caveolae to the plasma membrane
- Download full text (pdf) of Lipid packing contributes to the confinement of caveolae to the plasma membrane
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Part of Journal of Colloid and Interface Science, 2026
- DOI for Double emulsions enable in situ generation of permeation enhancers for oral delivery of macromolecules
- Download full text (pdf) of Double emulsions enable in situ generation of permeation enhancers for oral delivery of macromolecules
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Exploration of Colonic Mucus as A Dissolution Compartment for Orally Administered Drugs
Part of AAPS Journal, 2026
- DOI for Exploration of Colonic Mucus as A Dissolution Compartment for Orally Administered Drugs
- Download full text (pdf) of Exploration of Colonic Mucus as A Dissolution Compartment for Orally Administered Drugs
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Part of Drug Delivery, 2026
- DOI for Mechanics of small intestine motility for oral macromolecular delivery: modelling segmentation versus peristalsis
- Download full text (pdf) of Mechanics of small intestine motility for oral macromolecular delivery: modelling segmentation versus peristalsis
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Part of Colloids and Surfaces B, 2026
- DOI for Molecular dynamics simulations of a hexagonal liquid crystal phase to study drug partitioning and release mechanisms
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Part of International Journal of Pharmaceutics, 2026
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Part of Journal of Controlled Release, 2025
- DOI for Impact of chemical structure, lipidation and formulation on luminal stability and intestinal absorption of GLP-1 analogues
- Download full text (pdf) of Impact of chemical structure, lipidation and formulation on luminal stability and intestinal absorption of GLP-1 analogues
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Part of Journal of Nanobiotechnology, 2025
- DOI for Machine learning framework for investigating nano- and micro-scale particle diffusion in colonic mucus
- Download full text (pdf) of Machine learning framework for investigating nano- and micro-scale particle diffusion in colonic mucus
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Part of Journal of Cheminformatics, 2025
- DOI for Improved estimation of intrinsic solubility of drug-like molecules through multi-task graph transformer
- Download full text (pdf) of Improved estimation of intrinsic solubility of drug-like molecules through multi-task graph transformer
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Part of Journal of Colloid and Interface Science, p. 287-300, 2025
- DOI for Liquid crystal nanoparticles for oral combination antibiotic therapies: A strategy towards protecting commensal gut bacteria during treatment
- Download full text (pdf) of Liquid crystal nanoparticles for oral combination antibiotic therapies: A strategy towards protecting commensal gut bacteria during treatment
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Optimizing amorphous multidrug formulations: A particle engineering approach through spray drying
Part of European Journal of Pharmaceutical Sciences, 2025
- DOI for Optimizing amorphous multidrug formulations: A particle engineering approach through spray drying
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Part of Molecular Pharmaceutics, p. 4032-4045, 2025
- DOI for Optimized Artificial Colonic Mucus Enabling Physiologically Relevant Diffusion Studies of Drugs, Particles, and Delivery Systems
- Download full text (pdf) of Optimized Artificial Colonic Mucus Enabling Physiologically Relevant Diffusion Studies of Drugs, Particles, and Delivery Systems
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Impact of surfactants on solution behavior and membrane transport of amorphous solid dispersions
Part of Journal of Pharmaceutical Sciences, p. 458-467, 2025
- DOI for Impact of surfactants on solution behavior and membrane transport of amorphous solid dispersions
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Part of Molecular Pharmaceutics, p. 313-324, 2024
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Part of Molecular Pharmaceutics, p. 5261-5271, 2024
- DOI for Effect of Data Quality and Data Quantity on the Estimation of Intrinsic Solubility: Analysis Based on a Single-Source Data Set
- Download full text (pdf) of Effect of Data Quality and Data Quantity on the Estimation of Intrinsic Solubility: Analysis Based on a Single-Source Data Set
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Development of a canine artificial colonic mucus model for drug diffusion studies
Part of European Journal of Pharmaceutical Sciences, 2024
- DOI for Development of a canine artificial colonic mucus model for drug diffusion studies
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Part of Chemistry and Physics of Lipids, 2024
- DOI for Molecular dynamics simulations of lipid composition and its impact on structural and dynamic properties of skin membrane
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Part of Journal of Controlled Release, 2024
- DOI for Drug solubilization in dog intestinal fluids with and without administration of lipid-rich formulations
- Download full text (pdf) of Drug solubilization in dog intestinal fluids with and without administration of lipid-rich formulations
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Part of International Journal of Pharmaceutics, 2024
- DOI for Estimation of the concentration boundary layer adjacent to a flat surface using computational fluid dynamics
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Part of International Journal of Pharmaceutics, 2024
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Benefits of combining supersaturating and solubilizing formulations - Is two better than one?
Part of International Journal of Pharmaceutics, 2024
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Part of Journal of Medicinal Chemistry, p. 1008-1023, 2024
- DOI for Design, Synthesis, and Evaluation of New 1H-Benzo[d]imidazole Based PqsR Inhibitors as Adjuvant Therapy for Pseudomonas aeruginosa Infections
- Download full text (pdf) of Design, Synthesis, and Evaluation of New 1H-Benzo[d]imidazole Based PqsR Inhibitors as Adjuvant Therapy for Pseudomonas aeruginosa Infections
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Part of European Journal of Pharmaceutical Sciences, 2024
- DOI for Development and characterization of solid lipid-based formulations (sLBFs) of ritonavir utilizing a lipolysis and permeation assay
- Download full text (pdf) of Development and characterization of solid lipid-based formulations (sLBFs) of ritonavir utilizing a lipolysis and permeation assay
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Part of Journal of Computer-Aided Molecular Design, 2024
- DOI for Molecular dynamics study on micelle-small molecule interactions: developing a strategy for an extensive comparison
- Download full text (pdf) of Molecular dynamics study on micelle-small molecule interactions: developing a strategy for an extensive comparison
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Part of European Journal of Pharmaceutical Sciences, 2024
- DOI for Analysis of stabilization mechanisms in β-lactoglobulin-based amorphous solid dispersions by experimental and computational approaches
- Download full text (pdf) of Analysis of stabilization mechanisms in β-lactoglobulin-based amorphous solid dispersions by experimental and computational approaches
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Part of Journal of Colloid and Interface Science, p. 1253-1264, 2023
- DOI for Synergistic stabilization of emulsion gel by nanoparticles and surfactant enables 3D printing of lipid-rich solid oral dosage forms
- Download full text (pdf) of Synergistic stabilization of emulsion gel by nanoparticles and surfactant enables 3D printing of lipid-rich solid oral dosage forms
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Part of International Journal of Biological Macromolecules, 2023
- DOI for Numerical simulation of peristalsis to study co-localization and intestinal distribution of a macromolecular drug and permeation enhancer
- Download full text (pdf) of Numerical simulation of peristalsis to study co-localization and intestinal distribution of a macromolecular drug and permeation enhancer
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Part of Molecular Pharmaceutics, p. 451-460, 2023
- DOI for Molecular Dynamics Simulations of Self-Assembling Colloids in Fed-State Human Intestinal Fluids and Their Solubilization of Lipophilic Drugs
- Download full text (pdf) of Molecular Dynamics Simulations of Self-Assembling Colloids in Fed-State Human Intestinal Fluids and Their Solubilization of Lipophilic Drugs
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Part of European Journal of Pharmaceutical Sciences, 2023
- DOI for Exploring the use of modified in vitro digestion assays for the evaluation of ritonavir loaded solid lipid-based formulations
- Download full text (pdf) of Exploring the use of modified in vitro digestion assays for the evaluation of ritonavir loaded solid lipid-based formulations
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Intrinsic lipolysis rate for systematic design of lipid-based formulations
Part of Drug Delivery and Translational Research, p. 1288-1304, 2023
- DOI for Intrinsic lipolysis rate for systematic design of lipid-based formulations
- Download full text (pdf) of Intrinsic lipolysis rate for systematic design of lipid-based formulations
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Evaluation in pig of an intestinal administration device for oral peptide delivery
Part of Journal of Controlled Release, p. 792-801, 2023
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Part of International Journal of Pharmaceutics, 2023
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Part of European Journal of Pharmaceutical Sciences, 2023
- DOI for Development and validation of a porcine artificial colonic mucus model reflecting the properties of native colonic mucus in pigs
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Part of Journal of Pharmaceutical Sciences, p. 175-184, 2022
- DOI for Comparison of cellular monolayers and an artificial membrane as absorptive membranes in the in vitro lipolysis-permeation assay
- Download full text (pdf) of Comparison of cellular monolayers and an artificial membrane as absorptive membranes in the in vitro lipolysis-permeation assay
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Membrane insertion mechanism of the caveola coat protein Cavin1
Part of Proceedings of the National Academy of Sciences of the United States of America, 2022
- DOI for Membrane insertion mechanism of the caveola coat protein Cavin1
- Download full text (pdf) of Membrane insertion mechanism of the caveola coat protein Cavin1
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Part of ACS Applied Materials and Interfaces, p. 21978-21988, 2022
- DOI for Hyperthermia-Induced In Situ Drug Amorphization by Superparamagnetic Nanoparticles in Oral Dosage Forms
- Download full text (pdf) of Hyperthermia-Induced In Situ Drug Amorphization by Superparamagnetic Nanoparticles in Oral Dosage Forms
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Part of Molecular Pharmaceutics, p. 200-212, 2022
- DOI for Impact of Intestinal Concentration and Colloidal Structure on the Permeation-Enhancing Efficiency of Sodium Caprate in the Rat
- Download full text (pdf) of Impact of Intestinal Concentration and Colloidal Structure on the Permeation-Enhancing Efficiency of Sodium Caprate in the Rat
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Gastrointestinal mucus in dog: Physiological characteristics, composition, and structural properties
Part of European journal of pharmaceutics and biopharmaceutics, p. 92-102, 2022
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Part of Biomedicine and Pharmacotherapy, p. 112576-112576, 2022
- DOI for Manipulations and age-appropriateness of oral medications in pediatric oncology patients in Sweden: Need for personalized dosage forms
- Download full text (pdf) of Manipulations and age-appropriateness of oral medications in pediatric oncology patients in Sweden: Need for personalized dosage forms
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Part of Molecular Pharmaceutics, p. 2564-2572, 2022
- DOI for Intestinal Absorption of FITC-Dextrans and Macromolecular Model Drugs in the Rat Intestinal Instillation Model
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Bioavailability of Celecoxib Formulated with Mesoporous Magnesium Carbonate: An In Vivo Evaluation
Part of Molecules, 2022
- DOI for Bioavailability of Celecoxib Formulated with Mesoporous Magnesium Carbonate: An In Vivo Evaluation
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Stabilizing Mechanisms of β-Lactoglobulin in Amorphous Solid Dispersions of Indomethacin
Part of Molecular Pharmaceutics, p. 3922-3933, 2022
- DOI for Stabilizing Mechanisms of β-Lactoglobulin in Amorphous Solid Dispersions of Indomethacin
- Download full text (pdf) of Stabilizing Mechanisms of β-Lactoglobulin in Amorphous Solid Dispersions of Indomethacin
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Part of International Journal of Pharmaceutics, 2022
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UNGAP best practice for improving solubility data quality of orally administered drugs
Part of European Journal of Pharmaceutical Sciences, 2022
- DOI for UNGAP best practice for improving solubility data quality of orally administered drugs
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Part of Molecular Pharmaceutics, p. 4079-4089, 2021
- DOI for Impact of Simulated Intestinal Fluids on Dissolution, Solution Chemistry, and Membrane Transport of Amorphous Multidrug Formulations
- Download full text (pdf) of Impact of Simulated Intestinal Fluids on Dissolution, Solution Chemistry, and Membrane Transport of Amorphous Multidrug Formulations
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Part of Journal of Pharmaceutical Sciences, p. 239-250, 2021
- DOI for Proteomics-Informed Identification of Luminal Targets For In Situ Diagnosis of Inflammatory Bowel Disease
- Download full text (pdf) of Proteomics-Informed Identification of Luminal Targets For In Situ Diagnosis of Inflammatory Bowel Disease
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3D-printing of solid lipid tablets from emulsion gels
Part of International Journal of Pharmaceutics, 2021
- DOI for 3D-printing of solid lipid tablets from emulsion gels
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Physiological properties, composition and structural profiling of porcine gastrointestinal mucus
Part of European journal of pharmaceutics and biopharmaceutics, p. 156-167, 2021
- DOI for Physiological properties, composition and structural profiling of porcine gastrointestinal mucus
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Synergistic Computational Modeling Approaches as Team Players in the Game of Solubility Predictions
Part of Journal of Pharmaceutical Sciences, p. 22-34, 2021
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Part of Journal of Pharmaceutical Sciences, p. 176-185, 2021
- DOI for Molecular dynamics simulations reveal membrane interactions for poorly water-soluble drugs: impact of bile solubilization and drug aggregation
- Download full text (pdf) of Molecular dynamics simulations reveal membrane interactions for poorly water-soluble drugs: impact of bile solubilization and drug aggregation
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Part of Journal of Pharmaceutical Sciences, p. 228-238, 2021
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Part of Journal of Pharmaceutical Sciences, p. 2-11, 2021
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Part of Angewandte Chemie International Edition, p. 2069-2073, 2021
- DOI for TIRF Microscopy‐Based Monitoring of Drug Permeation Across a Lipid Membrane Supported on Mesoporous Silica
- Download full text (pdf) of TIRF Microscopy‐Based Monitoring of Drug Permeation Across a Lipid Membrane Supported on Mesoporous Silica
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Part of Molecules, 2021
- DOI for Increasing the Transport of Celecoxib over a Simulated Intestine Cell Membrane Model Using Mesoporous Magnesium Carbonate
- Download full text (pdf) of Increasing the Transport of Celecoxib over a Simulated Intestine Cell Membrane Model Using Mesoporous Magnesium Carbonate
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Part of ACS - Infectious Diseases, p. 2666-2685, 2021
- DOI for Design and Evaluation of New Quinazolin-4(3H)-one Derived PqsR Antagonists as Quorum Sensing Quenchers in Pseudomonas aeruginosa
- Download full text (pdf) of Design and Evaluation of New Quinazolin-4(3H)-one Derived PqsR Antagonists as Quorum Sensing Quenchers in Pseudomonas aeruginosa
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Part of Molecular Pharmaceutics, p. 2254-2262, 2021
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Part of Journal of Pharmaceutical Sciences, p. 217-227, 2021
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Part of Langmuir, p. 10200-10213, 2021
- DOI for Investigation of Self-Emulsifying Drug-Delivery System Interaction with a Biomimetic Membrane under Conditions Relevant to the Small Intestine
- Download full text (pdf) of Investigation of Self-Emulsifying Drug-Delivery System Interaction with a Biomimetic Membrane under Conditions Relevant to the Small Intestine
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Part of International Journal of Pharmaceutics, 2021
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Celebrating Women in the Pharmaceutical Sciences
Part of Molecular Pharmaceutics, p. 1487-1490, 2021
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Part of ADMET & DMPK, p. 176-179, 2020
- DOI for Strategies of solubility enhancement and perspectives in solubility measurements of pharmaceutical compounds
- Download full text (pdf) of Strategies of solubility enhancement and perspectives in solubility measurements of pharmaceutical compounds
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Part of Frontiers in Chemistry, 2020
- DOI for Hit Identification of New Potent PqsR Antagonists as Inhibitors of Quorum Sensing in Planktonic and Biofilm Grown Pseudomonas aeruginosa
- Download full text (pdf) of Hit Identification of New Potent PqsR Antagonists as Inhibitors of Quorum Sensing in Planktonic and Biofilm Grown Pseudomonas aeruginosa
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Insights into Dissolution and Solution Chemistry of Multidrug Formulations of Antihypertensive Drugs
Part of Molecular Pharmaceutics, p. 4018-4028, 2020
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Part of Pharmaceutics, 2020
- DOI for 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
- Download full text (pdf) of 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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Part of Pharmaceutics, 2020
- DOI for In Vitro Performance and Chemical Stability of Lipid-Based Formulations Encapsulated in a Mesoporous Magnesium Carbonate Carrier
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Part of Pharmaceutics, 2020
- DOI for Intrinsic Dissolution Rate Profiling of Poorly Water-Soluble Compounds in Biorelevant Dissolution Media
- Download full text (pdf) of Intrinsic Dissolution Rate Profiling of Poorly Water-Soluble Compounds in Biorelevant Dissolution Media
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Selection of In Vivo Predictive Dissolution Media Using Drug Substance and Physiological Properties
Part of AAPS Journal, 2020
- DOI for Selection of In Vivo Predictive Dissolution Media Using Drug Substance and Physiological Properties
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Part of Molecular Pharmaceutics, p. 3837-3844, 2020
- DOI for Molecular Dynamics Simulations on Interindividual Variability of Intestinal Fluids: Impact on Drug Solubilization
- Download full text (pdf) of Molecular Dynamics Simulations on Interindividual Variability of Intestinal Fluids: Impact on Drug Solubilization
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Suitability of Artificial Membranes in Lipolysis-Permeation Assays of Oral Lipid-Based Formulations
Part of Pharmaceutical research, 2020
- DOI for Suitability of Artificial Membranes in Lipolysis-Permeation Assays of Oral Lipid-Based Formulations
- Download full text (pdf) of Suitability of Artificial Membranes in Lipolysis-Permeation Assays of Oral Lipid-Based Formulations
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Influence of Bile Composition on Membrane Incorporation of Transient Permeability Enhancers
Part of Molecular Pharmaceutics, p. 4226-4240, 2020
- DOI for Influence of Bile Composition on Membrane Incorporation of Transient Permeability Enhancers
- Download full text (pdf) of Influence of Bile Composition on Membrane Incorporation of Transient Permeability Enhancers
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Part of ACS Omega, p. 25733-25746, 2020
- DOI for Model-Informed Drug Discovery and Development in Pulmonary Delivery: Biopharmaceutical Pharmacometric Modeling for Formulation Evaluation of Pulmonary Suspensions
- Download full text (pdf) of Model-Informed Drug Discovery and Development in Pulmonary Delivery: Biopharmaceutical Pharmacometric Modeling for Formulation Evaluation of Pulmonary Suspensions
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An in vitro dissolution–digestion–permeation assay for the study of advanced drug delivery systems
Part of European journal of pharmaceutics and biopharmaceutics, p. 21-29, 2020
- DOI for An in vitro dissolution–digestion–permeation assay for the study of advanced drug delivery systems
- Download full text (pdf) of An in vitro dissolution–digestion–permeation assay for the study of advanced drug delivery systems
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Part of Molecular Pharmaceutics, p. 1458-1469, 2020
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Part of Pharmaceutics, 2019
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Supersaturation Potential of Amorphous Active Pharmaceutical Ingredients after Long-Term Storage
Part of Molecules, 2019
- DOI for Supersaturation Potential of Amorphous Active Pharmaceutical Ingredients after Long-Term Storage
- Download full text (pdf) of Supersaturation Potential of Amorphous Active Pharmaceutical Ingredients after Long-Term Storage
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Part of AAPS PharmSciTech, 2019
- DOI for Aggregation Behavior of Medium Chain Fatty Acids Studied by Coarse-Grained Molecular Dynamics Simulation
- Download full text (pdf) of Aggregation Behavior of Medium Chain Fatty Acids Studied by Coarse-Grained Molecular Dynamics Simulation
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Part of Journal of Controlled Release, p. 90-100, 2019
- DOI for Effect of lipids on absorption of carvedilol in dogs: Is coadministration of lipids as efficient as a lipid-based formulation?
- Download full text (pdf) of Effect of lipids on absorption of carvedilol in dogs: Is coadministration of lipids as efficient as a lipid-based formulation?
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Part of Molecular Pharmaceutics, p. 4636-4650, 2019
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Part of European Journal of Pharmaceutical Sciences, 2019
- DOI for Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems
- Download full text (pdf) of 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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Does the Intake of Ethanol Affect Oral Absorption of Poorly Soluble Drugs?
Part of Journal of Pharmaceutical Sciences, p. 1765-1771, 2019
- DOI for Does the Intake of Ethanol Affect Oral Absorption of Poorly Soluble Drugs?
- Download full text (pdf) of Does the Intake of Ethanol Affect Oral Absorption of Poorly Soluble Drugs?
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Lipolysis-Permeation Setup for Simultaneous Study of Digestion and Absorption in Vitro
Part of Molecular Pharmaceutics, p. 921-930, 2019
- DOI for Lipolysis-Permeation Setup for Simultaneous Study of Digestion and Absorption in Vitro
- Download full text (pdf) of Lipolysis-Permeation Setup for Simultaneous Study of Digestion and Absorption in Vitro
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Part of Journal of Pharmaceutical Sciences, p. 2-7, 2019
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Molecular Drivers of Crystallization Kinetics for Drugs in Supersaturated Aqueous Solutions
Part of Journal of Pharmaceutical Sciences, p. 252-259, 2019
- DOI for Molecular Drivers of Crystallization Kinetics for Drugs in Supersaturated Aqueous Solutions
- Download full text (pdf) of Molecular Drivers of Crystallization Kinetics for Drugs in Supersaturated Aqueous Solutions
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Part of Journal of Pharmaceutical Sciences, p. 630-640, 2019
- DOI for Model-Based Drug Development in Pulmonary Delivery: Pharmacokinetic Analysis of Novel Drug Candidates for Treatment of Pseudomonas aeruginosa Lung Infection
- Download full text (pdf) of Model-Based Drug Development in Pulmonary Delivery: Pharmacokinetic Analysis of Novel Drug Candidates for Treatment of Pseudomonas aeruginosa Lung Infection
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Automated assays for thermodynamic (equilibrium) solubility determination.
Part of Drug Discovery Today, p. 11-19, 2018
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Part of AAPS Journal, 2018
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Part of AAPS PharmSciTech, p. 2859-2865, 2018
- DOI for A Modified In Situ Method to Determine Release from a Complex Drug Carrier in Particle-Rich Suspensions
- Download full text (pdf) of A Modified In Situ Method to Determine Release from a Complex Drug Carrier in Particle-Rich Suspensions
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Part of Molecular Pharmaceutics, p. 4733-4744, 2018
- DOI for Impact of Drug Physicochemical Properties on Lipolysis-Triggered Drug Supersaturation and Precipitation from Lipid-Based Formulations
- Download full text (pdf) of Impact of Drug Physicochemical Properties on Lipolysis-Triggered Drug Supersaturation and Precipitation from Lipid-Based Formulations
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Caco-2 Cell Conditions Enabling Studies of Drug Absorption from Digestible Lipid-Based Formulations
Part of Pharmaceutical research, 2018
- DOI for Caco-2 Cell Conditions Enabling Studies of Drug Absorption from Digestible Lipid-Based Formulations
- Download full text (pdf) of Caco-2 Cell Conditions Enabling Studies of Drug Absorption from Digestible Lipid-Based Formulations
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Part of International Journal of Pharmaceutics, p. 515-521, 2018
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Part of International Journal of Pharmaceutics, p. 183-190, 2017
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Part of Journal of Physical Chemistry B, p. 10869-10881, 2017
- DOI for Characterization of Solubilizing Nanoaggregates Present in Different Versions of Simulated Intestinal Fluid
- Download full text (pdf) of Characterization of Solubilizing Nanoaggregates Present in Different Versions of Simulated Intestinal Fluid
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Substrate and method dependent inhibition of three ABC-transporters (MDR1, BCRP, and MRP2)
Part of European Journal of Pharmaceutical Sciences, p. 70-76, 2017
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Part of Pharmaceutical research, p. 1805-1816, 2017
- DOI for Controlled Suspensions Enable Rapid Determinations of Intrinsic Dissolution Rate and Apparent Solubility of Poorly Water-Soluble Compounds
- Download full text (pdf) of Controlled Suspensions Enable Rapid Determinations of Intrinsic Dissolution Rate and Apparent Solubility of Poorly Water-Soluble Compounds
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Part of Journal of Controlled Release, p. 193-202, 2017
- DOI for Mechanism-based selection of stabilization strategy for amorphous formulations: Insights into crystallization pathways
- Download full text (pdf) of Mechanism-based selection of stabilization strategy for amorphous formulations: Insights into crystallization pathways
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Part of Molecular Pharmaceutics, p. 4145-4153, 2017
- DOI for Molecular Structuring and Phase Transition of Lipid-Based Formulations upon Water Dispersion: A Coarse-Grained Molecular Dynamics Simulation Approach
- Download full text (pdf) of Molecular Structuring and Phase Transition of Lipid-Based Formulations upon Water Dispersion: A Coarse-Grained Molecular Dynamics Simulation Approach
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Part of Molecular Pharmaceutics, p. 4161-4169, 2017
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Part of Journal of Pharmaceutical Sciences, p. 2864-2872, 2016
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Understanding the Challenge of Beyond-Rule-of-5 Compounds Preface
Part of Advanced Drug Delivery Reviews, p. 1-5, 2016
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Compromised in vitro dissolution and membrane transport of multidrug amorphous formulations.
Part of Journal of Controlled Release, p. 172-182, 2016
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Tools for Early Prediction of Drug Loading in Lipid-Based Formulations
Part of Molecular Pharmaceutics, p. 251-261, 2016
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Diffusion-Controlled Drug Release from the Mesoporous Magnesium Carbonate Upsalite®
Part of Journal of Pharmaceutical Sciences, p. 657-663, 2016
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Rapid determination of drug solubilization versus supersaturation in natural and digested lipids
Part of International Journal of Pharmaceutics, p. 164-174, 2016
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Lipophilicity in Drug Development: Too Much or Not Enough?
Part of AAPS Journal, p. 1095-1100, 2016
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Part of Langmuir, p. 12732-12740, 2016
- DOI for Partitioning into Colloidal Structures of Fasted State Intestinal Fluid Studied by Molecular Dynamics Simulations
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Supersaturation of poorly soluble drugs induced by mesoporous magnesium carbonate
Part of European Journal of Pharmaceutical Sciences, p. 468-474, 2016
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Computational Prediction of Drug Solubility in Fasted Simulated and Aspirated Human Intestinal Fluid
Part of Pharmaceutical research, p. 578-589, 2015
- DOI for Computational Prediction of Drug Solubility in Fasted Simulated and Aspirated Human Intestinal Fluid
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Computational modeling to predict the functions and impact of drug transporters
Part of In silico pharmacology, 2015
- DOI for Computational modeling to predict the functions and impact of drug transporters
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Models for Predicting Drug Absorption From Oral Lipid-Based Formulations
Part of Current molecular biology reports, p. 141-147, 2015
- DOI for Models for Predicting Drug Absorption From Oral Lipid-Based Formulations
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Part of International Journal of Pharmaceutics, p. 312-317, 2015
- DOI for Physical stability of drugs after storage above and below the glass transition temperature: Relationship to glass-forming ability
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Concomitant intake of alcohol may increase the absorption of poorly soluble drugs
Part of European Journal of Pharmaceutical Sciences, p. 12-20, 2015
- DOI for Concomitant intake of alcohol may increase the absorption of poorly soluble drugs
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Experimental and Computational Prediction of Glass Transition Temperature of Drugs
Part of JOURNAL OF CHEMICAL INFORMATION AND MODELING, p. 3396-3403, 2014
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Part of PLOS ONE, 2014
- DOI for Formulation of the Microbicide INP0341 for In Vivo Protection against a Vaginal Challenge by Chlamydia trachomatis
- Download full text (pdf) of Formulation of the Microbicide INP0341 for In Vivo Protection against a Vaginal Challenge by Chlamydia trachomatis
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Pyridyl Benzamides as a Novel Class of Potent Inhibitors for the Kinetoplastid Trypanosoma brucei
Part of Journal of Medicinal Chemistry, p. 6393-6402, 2014
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Computational predictions of glass-forming ability and crystallization tendency of drug molecules
Part of Molecular Pharmaceutics, p. 3123-3132, 2014
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Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs
Part of European Journal of Pharmaceutical Sciences, p. 173-199, 2014
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Is the full potential of the biopharmaceutics classification system reached?
Part of European Journal of Pharmaceutical Sciences, p. 224-231, 2014
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Part of Toxicological Sciences, p. 328-343, 2013
- DOI for Early Identification of Clinically Relevant Drug Interactions with the Human Bile Salt Export Pump (BSEP; ABCB11)
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Part of Journal of Medicinal Chemistry, p. 2690-2694, 2013
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Part of Bulletin Technique Gattefossé, p. 50-57, 2013
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Part of Molecular Pharmaceutics, p. 2823-2848, 2013
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Computational Prediction of Drug Solubility in Lipid Based Formulation Excipients
Part of Pharmaceutical research, p. 3225-3237, 2013
- DOI for Computational Prediction of Drug Solubility in Lipid Based Formulation Excipients
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Early drug development predictions of glass-forming ability and physical stability of drugs
Part of European Journal of Pharmaceutical Sciences, p. 323-332, 2013
- DOI for Early drug development predictions of glass-forming ability and physical stability of drugs
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Computational Prediction of CNS Drug Exposure Based on a Novel In Vivo Dataset
Part of Pharmaceutical research, p. 3131-3142, 2012
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Ethanol Effects on Apparent Solubility of Poorly Soluble Drugs in Simulated Intestinal Fluid
Part of Molecular Pharmaceutics, p. 1942-1952, 2012
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Part of Pharmaceutical research, p. 411-426, 2012
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Part of Molecular Pharmaceutics, p. 498-506, 2011
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Part of Journal of Pharmaceutical Sciences, p. 3763-3772, 2011
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A Modified Physiological BCS for Prediction of Intestinal Absorption in Drug Discovery
Part of Molecular pharmaceutics, p. 1478-1487, 2010
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Dissolution Rate and Apparent Solubility of Poorly Soluble Drugs in Biorelevant Dissolution Media
Part of Molecular pharmaceutics, p. 1419-1430, 2010
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Part of Drug metabolism reviews (Softcover ed.), p. 304-305, 2010
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Part of European Journal of Pharmaceutical Sciences, p. 556-563, 2009
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Part of Pharmaceutical research, p. 1816-1831, 2009
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Part of Journal of Medicinal Chemistry, p. 3275-3287, 2008
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Part of Journal of Medicinal Chemistry, p. 5932-5942, 2008
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Molecular characteristics for solid-state limited solubility
Part of Journal of Medicinal Chemistry, p. 3035-3039, 2008
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Poorly soluble marketed drugs display solvation limited solubility
Part of Journal of Medicinal Chemistry, p. 5858-5862, 2007
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Photoinduced Formation of N2 Molecules in Ammonium Compounds
Part of Journal of Physical Chemistry A, p. 9662-9669, 2007
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Part of Journal of Pharmacology and Experimental Therapeutics, p. 19-30, 2007
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Contribution of solid-state properties to the aqueous solubility of drugs.
Part of Eur J Pharm Sci, p. 294-305, 2006
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Prediction of ADMET Properties.
Part of ChemMedChem, p. 920-937, 2006
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Computational models to predict aqueous drug solubility, permeability and intestinal absorption
Part of Expert opinion on drug metabolism & toxicology, p. 613-627, 2005
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X-ray yield and selectively excited X-ray emission spectra of atenolol and nadolol.
Part of J Electr Spectr, p. 283-285, 2005
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Theoretical predictions of drug absorption in drug discovery and development
Part of Clinical Pharmacokinetics, p. 877-899, 2002
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Pickering emulsion gel enables 3D printing of lipid-rich solid oral dosage forms
Articles, review/survey
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Contemporary formulation development for inhaled pharmaceuticals
Part of Journal of Pharmaceutical Sciences, p. 66-86, 2021
- DOI for Contemporary formulation development for inhaled pharmaceuticals
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Part of European journal of pharmaceutics and biopharmaceutics, p. 46-55, 2019
- DOI for Molecular simulation as a computational pharmaceutics tool to predict drug solubility, solubilization processes and partitioning
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Part of International Journal of Pharmaceutics, p. 264-281, 2019
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Part of European journal of pharmaceutics and biopharmaceutics, p. 101-114, 2019
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Perspectives in solubility measurement and interpretation
Part of ADMET AND DMPK, p. 88-105, 2019
- DOI for Perspectives in solubility measurement and interpretation
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Part of International Journal of Pharmaceutics, p. 185-193, 2018
- DOI for Computational prediction of drug solubility in water-based systems: qualitative and quantitative approaches used in the current drug discovery and development setting
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The Need for Restructuring the Disordered Science of Amorphous Drug Formulations
Part of Pharmaceutical Research, p. 1754-1772, 2017
- DOI for The Need for Restructuring the Disordered Science of Amorphous Drug Formulations
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50 years of oral lipid-based formulations: Provenance, progress and future perspectives
Part of Advanced Drug Delivery Reviews, p. 167-194, 2016
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Computational prediction of formulation strategies for beyond-rule-of-5 compounds
Part of Advanced Drug Delivery Reviews, p. 6-21, 2016
- DOI for Computational prediction of formulation strategies for beyond-rule-of-5 compounds
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Part of Therapeutic delivery, p. 935-959, 2015
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Prediction of ADMET Properties
Part of ChemMedChem, p. 920-937, 2006
Chapters in book
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How Physicochemical Properties of Drugs Affect Their Metabolism and Clearance
Part of New Horizons in Predictive Drug Metabolism and Pharmacokinetics, p. 1-26, Royal Society of Chemistry, 2016
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Computational absorption prediction
Part of Drug bioavailability, p. 409-432, Wiley-VCH, 2008
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Prediction of ADMET Properties
Part of Chemical Biology, p. 1003-1044, Wiley-VCH, 2007
Conference papers
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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
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Synthesis of amorphous magnesium carbonate nanoparticles for biomedical applications
Part of Bioceramics 29 ISCM 2017, 2017
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A new method that enables in situ measurement of drug release from complex carrier-mediated systems
Part of 6th FIP Pharmaceutical Sciences World Congress2017., 2017
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Part of pION Fiber Optic Advanced Training Course. Uppsala, June 14-15, 2016., 2016
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Diffusion controlled drug release from Mesoprous Magnesium Carbonate
2016