List of works - Christel A. S. Bergström

A global drug inhibition pattern for the human ATP-binding cassette transporter breast cancer resistance protein (ABCG2).

scientific article

A modified physiological BCS for prediction of intestinal absorption in drug discovery.

scientific article published on September 2010

Absorption classification of oral drugs based on molecular surface properties

scientific article published on 01 February 2003

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

scientific article published on 24 April 2020

Accuracy of calculated pH-dependent aqueous drug solubility.

scientific article

Amorphous magnesium carbonate nanoparticles with strong stabilizing capability for amorphous ibuprofen

scholarly article by Jiaojiao Yang et al published September 2018 in International Journal of Pharmaceutics

Caco-2 Cell Conditions Enabling Studies of Drug Absorption from Digestible Lipid-Based Formulations.

scientific article published on 26 February 2018

Computational prediction of CNS drug exposure based on a novel in vivo dataset.

scientific article published on 29 June 2012

Computational prediction of drug solubility in lipid based formulation excipients.

scientific article published on 15 June 2013

Dissolution rate and apparent solubility of poorly soluble drugs in biorelevant dissolution media.

scientific article published on 24 June 2010

Early drug development predictions of glass-forming ability and physical stability of drugs

scientific article published on 02 April 2013

Early identification of clinically relevant drug interactions with the human bile salt export pump (BSEP/ABCB11).

scientific article published on 06 September 2013

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

scientific article

Effect of lipids on absorption of carvedilol in dogs: Is coadministration of lipids as efficient as a lipid-based formulation?

scientific article published on 29 April 2019

Ethanol effects on apparent solubility of poorly soluble drugs in simulated intestinal fluid.

scientific article

Evaluation of the structural determinants of polymeric precipitation inhibitors using solvent shift methods and principle component analysis.

scientific article published on 2 July 2013

Experimental and computational screening models for prediction of aqueous drug solubility

scientific article published on 01 February 2002

Exploring the role of different drug transport routes in permeability screening.

scientific article published on January 2005

Global and Local Computational Models for Aqueous Solubility Prediction of Drug-Like Molecules

scientific article published on 01 July 2004

Hyperthermia-Induced In Situ Drug Amorphization by Superparamagnetic Nanoparticles in Oral Dosage Forms

scientific article published on 22 April 2022

Identification of novel specific and general inhibitors of the three major human ATP-binding cassette transporters P-gp, BCRP and MRP2 among registered drugs.

scientific article

In Vitro and In Silico Strategies to Identify OATP1B1 Inhibitors and Predict Clinical Drug–Drug Interactions ⬇️

scientific article published on August 23, 2011

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

scientific article published on 28 May 2020

Is the full potential of the biopharmaceutics classification system reached?

scientific article

Mechanism-based selection of stabilization strategy for amorphous formulations: Insights into crystallization pathways

scientific article published on 12 April 2017

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

scientific article published on 06 April 2020

Molecular Descriptors Influencing Melting Point and Their Role in Classification of Solid Drugs

scientific article published on 01 July 2003

Optimizing solubility and permeability of a biopharmaceutics classification system (BCS) class 4 antibiotic drug using lipophilic fragments disturbing the crystal lattice.

scientific article

Photoinduced Formation of N2Molecules in Ammonium Compounds

scientific article published on 12 September 2007

Poorly soluble marketed drugs display solvation limited solubility

scientific article published on 11 October 2007

Prediction and identification of drug interactions with the human ATP-binding cassette transporter multidrug-resistance associated protein 2 (MRP2; ABCC2).

scientific article

Prediction of ADMET Properties.

scientific article published on September 2006

Structural requirements for drug inhibition of the liver specific human organic cation transport protein 1.

scientific article published on 13 September 2008

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

scientific article published on 20 May 2020

Supersaturation Potential of Amorphous Active Pharmaceutical Ingredients after Long-Term Storage

scientific article published on 27 July 2019

The Permeation of Acamprosate Is Predominantly Caused by Paracellular Diffusion across Caco-2 Cell Monolayers: A Paracellular Modeling Approach

scientific article published on 17 October 2019

The importance of gel properties for mucoadhesion measurements: a multivariate data analysis approach

scientific article

TowardIn SilicoPrediction of Glass-Forming Ability from Molecular Structure Alone: A Screening Tool in Early Drug Development

article

List of works by Christel A. S. Bergström

A global drug inhibition pattern for the human ATP-binding cassette transporter breast cancer resistance protein (ABCG2).

A modified physiological BCS for prediction of intestinal absorption in drug discovery.

Absorption classification of oral drugs based on molecular surface properties

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

Accuracy of calculated pH-dependent aqueous drug solubility.

Amorphous magnesium carbonate nanoparticles with strong stabilizing capability for amorphous ibuprofen

Caco-2 Cell Conditions Enabling Studies of Drug Absorption from Digestible Lipid-Based Formulations.

Computational prediction of CNS drug exposure based on a novel in vivo dataset.

Computational prediction of drug solubility in lipid based formulation excipients.

Dissolution rate and apparent solubility of poorly soluble drugs in biorelevant dissolution media.

Early drug development predictions of glass-forming ability and physical stability of drugs

Early identification of clinically relevant drug interactions with the human bile salt export pump (BSEP/ABCB11).

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

Effect of lipids on absorption of carvedilol in dogs: Is coadministration of lipids as efficient as a lipid-based formulation?

Ethanol effects on apparent solubility of poorly soluble drugs in simulated intestinal fluid.

Evaluation of the structural determinants of polymeric precipitation inhibitors using solvent shift methods and principle component analysis.

Experimental and computational screening models for prediction of aqueous drug solubility

Exploring the role of different drug transport routes in permeability screening.

Global and Local Computational Models for Aqueous Solubility Prediction of Drug-Like Molecules

Hyperthermia-Induced In Situ Drug Amorphization by Superparamagnetic Nanoparticles in Oral Dosage Forms

Identification of novel specific and general inhibitors of the three major human ATP-binding cassette transporters P-gp, BCRP and MRP2 among registered drugs.

In Vitro and In Silico Strategies to Identify OATP1B1 Inhibitors and Predict Clinical Drug–Drug Interactions ⬇️

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

Is the full potential of the biopharmaceutics classification system reached?

Mechanism-based selection of stabilization strategy for amorphous formulations: Insights into crystallization pathways

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

Molecular Descriptors Influencing Melting Point and Their Role in Classification of Solid Drugs

Optimizing solubility and permeability of a biopharmaceutics classification system (BCS) class 4 antibiotic drug using lipophilic fragments disturbing the crystal lattice.

Photoinduced Formation of N2Molecules in Ammonium Compounds

Poorly soluble marketed drugs display solvation limited solubility

Prediction and identification of drug interactions with the human ATP-binding cassette transporter multidrug-resistance associated protein 2 (MRP2; ABCC2).

Prediction of ADMET Properties.

Structural requirements for drug inhibition of the liver specific human organic cation transport protein 1.

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

Supersaturation Potential of Amorphous Active Pharmaceutical Ingredients after Long-Term Storage

The Permeation of Acamprosate Is Predominantly Caused by Paracellular Diffusion across Caco-2 Cell Monolayers: A Paracellular Modeling Approach

The importance of gel properties for mucoadhesion measurements: a multivariate data analysis approach

TowardIn SilicoPrediction of Glass-Forming Ability from Molecular Structure Alone: A Screening Tool in Early Drug Development

X-ray yield and selectively excited X-ray emission spectra of atenolol and nadolol