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 …
foreign to the human body. Several endogenous molecules, however, such as steroids and …
ABC transporter-mediated multidrug-resistant cancer
ATP-binding cassette (ABC) transporters are involved in active pumping of many diverse
substrates through the cellular membrane. The transport mediated by these proteins …
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
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 …
effectiveness, ease of administration, and high patient compliance. However, the absorption …
A novel chemometric method for the prediction of human oral bioavailability
Orally administered drugs must overcome several barriers before reaching their target site.
Such barriers depend largely upon specific membrane transport systems and intracellular …
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 …
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
Highly potent, but poorly water-soluble, drug candidates are common outcomes of
contemporary drug discovery programmes and present a number of challenges to drug …
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 …
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
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 …
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. 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 …
transporters in humans, is encoded by the ABCB1/MDR1 gene. Recent insights into the …