Drug metabolism in the liver

OA Almazroo, MK Miah… - Clinics in liver …, 2017 - liver.theclinics.com
Drugs are typically small molecules that are generally classified as xenobiotics, which are
foreign to the human body. Several endogenous molecules, however, such as steroids and …

ABC transporter-mediated multidrug-resistant cancer

H Amawi, HM Sim, AK Tiwari, SV Ambudkar… - Drug transporters in …, 2019 - Springer
ATP-binding cassette (ABC) transporters are involved in active pumping of many diverse
substrates through the cellular membrane. The transport mediated by these proteins …

An overview of in vitro, ex vivo and in vivo models for studying the transport of drugs across intestinal barriers

Y Xu, N Shrestha, V Préat, A Beloqui - Advanced Drug Delivery Reviews, 2021 - Elsevier
Oral administration is the most commonly used route for drug delivery owing to its cost-
effectiveness, ease of administration, and high patient compliance. However, the absorption …

A novel chemometric method for the prediction of human oral bioavailability

X Xu, W Zhang, C Huang, Y Li, H Yu, Y Wang… - International journal of …, 2012 - mdpi.com
Orally administered drugs must overcome several barriers before reaching their target site.
Such barriers depend largely upon specific membrane transport systems and intracellular …

Developmental pharmacokinetics in pediatric populations

H Lu, S Rosenbaum - The Journal of Pediatric …, 2014 - meridian.allenpress.com
Information on drug absorption and disposition in infants and children has increased
considerably over the past 2 decades. However, the impact of specific age-related effects on …

Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs

CJH Porter, NL Trevaskis, WN Charman - Nature reviews Drug …, 2007 - nature.com
Highly potent, but poorly water-soluble, drug candidates are common outcomes of
contemporary drug discovery programmes and present a number of challenges to drug …

Induction of phase I, II and III drug metabolism/transport by xenobiotics

C Xu, CYT Li, ANT Kong - Archives of pharmacal research, 2005 - Springer
Drug metabolizing enzymes (DMEs) play central roles in the metabolism, elimination and
detoxification of xenobiotics and drugs introduced into the human body. Most of the tissues …

[HTML][HTML] Drug permeability profiling using cell-free permeation tools: Overview and applications

P Berben, A Bauer-Brandl, M Brandl, B Faller… - European Journal of …, 2018 - Elsevier
Cell-free permeation systems are gaining interest in drug discovery and development as
tools to obtain a reliable prediction of passive intestinal absorption without the …

Cyclodextrins in drug delivery systems and their effects on biological barriers

Á Haimhoffer, Á Rusznyák, K Réti-Nagy… - Scientia …, 2019 - mdpi.com
Cyclodextrins are widely used excipients, composed of glucopyranose units with a cyclic
structure. One of their most important properties, is that their inner cavity is hydrophobic …

Structure, function and regulation of P-glycoprotein and its clinical relevance in drug disposition

SF Zhou - Xenobiotica, 2008 - Taylor & Francis
1. P-glycoprotein (P-gp/MDR1), one of the most clinically important transmembrane
transporters in humans, is encoded by the ABCB1/MDR1 gene. Recent insights into the …