Artificial intelligence and machine learning in computational nanotoxicology: unlocking and empowering nanomedicine

AV Singh, MHD Ansari, D Rosenkranz… - Advanced …, 2020 - Wiley Online Library
Advances in nanomedicine, coupled with novel methods of creating advanced materials at
the nanoscale, have opened new perspectives for the development of healthcare and …

Food, gastrointestinal pH, and models of oral drug absorption

AY Abuhelwa, DB Williams, RN Upton… - European journal of …, 2017 - Elsevier
This article reviews the major physiological and physicochemical principles of the effect of
food and gastrointestinal (GI) pH on the absorption and bioavailability of oral drugs, and the …

ADMET in silico modelling: towards prediction paradise?

H Van De Waterbeemd, E Gifford - Nature reviews Drug discovery, 2003 - nature.com
Following studies in the late 1990s that indicated that poor pharmacokinetics and toxicity
were important causes of costly late-stage failures in drug development, it has become …

In silico ADME-Tox modeling: progress and prospects

S Alqahtani - Expert opinion on drug metabolism & toxicology, 2017 - Taylor & Francis
Introduction: Although significant progress has been made in high-throughput screening of
absorption, distribution, metabolism and excretion, and toxicity (ADME-Tox) properties in …

Towards a platform PBPK model to characterize the plasma and tissue disposition of monoclonal antibodies in preclinical species and human

DK Shah, AM Betts - Journal of pharmacokinetics and pharmacodynamics, 2012 - Springer
The objectives of the following investigation were (1) development of a physiologically
based pharmacokinetic (PBPK) model capable of characterizing the plasma and tissue …

Physiological‐based pharmacokinetic modeling trends in pharmaceutical drug development over the last 20‐years; in‐depth analysis of applications, organizations …

E El‐Khateeb, S Burkhill, S Murby… - … & Drug Disposition, 2021 - Wiley Online Library
We assess the advancement of physiologically based pharmacokinetic (PBPK) modeling
and simulation (M&S) over the last 20 years (start of 2000 to end of 2019) focusing on the …

Pectin-based systems for colon-specific drug delivery via oral route

LS Liu, ML Fishman, J Kost, KB Hicks - Biomaterials, 2003 - Elsevier
Pectin-derived matrices are now being examined and tested for controlled drug delivery.
Pectin is intact in the upper gastrointestinal tract and degraded by colonic microflora. The …

The Caco-2 cell monolayer: usefulness and limitations

H Sun, ECY Chow, S Liu, Y Du… - Expert opinion on drug …, 2008 - Taylor & Francis
Background: The Caco-2 monolayer has been used extensively for the high-throughput
screening of drug permeability and identification of substrates, inhibitors, and inducers of …

High throughput solubility measurement in drug discovery and development

J Alsenz, M Kansy - Advanced drug delivery reviews, 2007 - Elsevier
Measurement of drug solubility in various solvents is one of the key elements of compound
characterization during the whole discovery and development process. This review …

Oral absorption of poorly water-soluble drugs: computer simulation of fraction absorbed in humans from a miniscale dissolution test

R Takano, K Sugano, A Higashida, Y Hayashi… - Pharmaceutical …, 2006 - Springer
Purpose The purpose of this study was to develop a new system for computer simulation to
predict fraction absorbed (F a) of Biopharmaceutical Classification System (BCS) class II …