[HTML][HTML] Synergistic mechanisms of constituents in herbal extracts during intestinal absorption: Focus on natural occurring nanoparticles
The systematic separation strategy has long and widely been applied in the research and
development of herbal medicines. However, the pharmacological effects of many bioactive …
development of herbal medicines. However, the pharmacological effects of many bioactive …
Applications of targeted proteomics in systems biology and translational medicine
Biological systems are composed of numerous components of which proteins are of
particularly high functional significance. Network models are useful abstractions for studying …
particularly high functional significance. Network models are useful abstractions for studying …
[HTML][HTML] An update on the role of intestinal cytochrome P450 enzymes in drug disposition
F Xie, X Ding, QY Zhang - Acta Pharmaceutica Sinica B, 2016 - Elsevier
Oral administration is the most commonly used route for drug treatment. Intestinal
cytochrome P450 (CYP)-mediated metabolism can eliminate a large proportion of some …
cytochrome P450 (CYP)-mediated metabolism can eliminate a large proportion of some …
Large‐scale multiplex absolute protein quantification of drug‐metabolizing enzymes and transporters in human intestine, liver, and kidney microsomes by SWATH‐MS …
K Nakamura, M Hirayama‐Kurogi, S Ito, T Kuno… - …, 2016 - Wiley Online Library
The purpose of the present study was to examine simultaneously the absolute protein
amounts of 152 membrane and membrane‐associated proteins, including 30 metabolizing …
amounts of 152 membrane and membrane‐associated proteins, including 30 metabolizing …
Predicting drug extraction in the human gut wall: assessing contributions from drug metabolizing enzymes and transporter proteins using preclinical models
SA Peters, CR Jones, AL Ungell, OJD Hatley - Clinical pharmacokinetics, 2016 - Springer
Intestinal metabolism can limit oral bioavailability of drugs and increase the risk of drug
interactions. It is therefore important to be able to predict and quantify it in drug discovery …
interactions. It is therefore important to be able to predict and quantify it in drug discovery …
Tramadol metabolism to O-desmethyl tramadol (M1) and N-desmethyl tramadol (M2) by dog liver microsomes: species comparison and identification of responsible …
TE Perez, KL Mealey, TL Grubb, SA Greene - Drug Metabolism and …, 2016 - ASPET
Tramadol is widely used to manage mild to moderately painful conditions in dogs. However,
this use is controversial, since clinical efficacy studies in dogs showed conflicting results …
this use is controversial, since clinical efficacy studies in dogs showed conflicting results …
In silico resources to assist in the development and evaluation of physiologically-based kinetic models
Since their inception in pharmaceutical applications, physiologically-based kinetic (PBK)
models are increasingly being used across a range of sectors, such as safety assessment of …
models are increasingly being used across a range of sectors, such as safety assessment of …
Comparison of canine and human physiological factors: understanding interspecies differences that impact drug pharmacokinetics
This review is a summary of factors affecting the drug pharmacokinetics (PK) of dogs versus
humans. Identifying these interspecies differences can facilitate canine-human PK …
humans. Identifying these interspecies differences can facilitate canine-human PK …
Novel cytochrome P450 2C94 functionally metabolizes diclofenac and omeprazole in dogs
Y Uno, S Morikuni, M Shiraishi, A Asano… - Drug Metabolism and …, 2023 - ASPET
Cytochromes P450 (P450s or CYPs) are important drug-metabolizing enzymes. Because
dogs are frequently used in drug metabolism studies, knowledge of dog CYP2C enzymes is …
dogs are frequently used in drug metabolism studies, knowledge of dog CYP2C enzymes is …
In vitro–in vivo extrapolation scaling factors for intestinal P-glycoprotein and breast cancer resistance protein: part I: a cross-laboratory comparison of transporter …
Over the last 5 years the quantification of transporter-protein absolute abundances has
dramatically increased in parallel to the expanded use of in vitro–in vivo extrapolation …
dramatically increased in parallel to the expanded use of in vitro–in vivo extrapolation …