[HTML][HTML] Pharmacokinetic drug interactions in liver disease: an update

P Palatini, S De Martin - World Journal of Gastroenterology, 2016 - ncbi.nlm.nih.gov
Inhibition and induction of drug-metabolizing enzymes are the most frequent and dangerous
drug-drug interactions. They are an important cause of serious adverse events that have …

How can drug metabolism and transporter genetics inform psychotropic prescribing?

B Carvalho Henriques, EH Yang, D Lapetina… - Frontiers in …, 2020 - frontiersin.org
Many genetic variants in drug metabolizing enzymes and transporters have been shown to
be relevant for treating psychiatric disorders. Associations are strong enough to feature on …

How common are drug and gene interactions? Prevalence in a sample of 1143 patients with CYP2C9, CYP2C19 and CYP2D6 genotyping

P Verbeurgt, T Mamiya, J Oesterheld - Pharmacogenomics, 2014 - Taylor & Francis
Aim: Drug–drug interactions (DDIs) are a widely recognized major cause of adverse drug
reactions, but two other newly described important types of interactions also exist: drug …

In silico ADME profiling of salubrinal and its analogues

PV Zadorozhnii, VV Kiselev, AV Kharchenko - Future Pharmacology, 2022 - mdpi.com
This work reports on a complex in silico assessment of the ADME properties of Salubrinal
(S1) and 54 of its structural analogues containing a cinnamic acid residue (S2–S40) or a …

Identification of drug-drug interactions using chemical interactions

L Chen, C Chu, YH Zhang, M Zheng… - Current …, 2017 - ingentaconnect.com
Background: One drug can affect the activity of another when they are administered
together, which can cause adverse drug reactions or sometimes improve therapeutic effects …

Utility of non-human primates in drug development: Comparison of non-human primate and human drug-metabolizing cytochrome P450 enzymes

Y Uno, S Uehara, H Yamazaki - Biochemical pharmacology, 2016 - Elsevier
Cynomolgus monkeys (Macaca fascicularis, an Old World Monkey) have been widely used
as a non-human primate model in preclinical studies because of their genetic and …

Identifying potential drug interactions in chronic kidney disease patients

AB Marquito, NMS Fernandes… - Brazilian Journal of …, 2014 - SciELO Brasil
In clinical practice, multiple drugs are often combined in the treatment of patients with
chronic diseases. These associations generally produce drug interactions (DI) with expected …

Lost in modelling and simulation?

K Sugano - ADMET and DMPK, 2021 - hrcak.srce.hr
Sažetak Over the past few decades, physiologically-based pharmacokinetic modelling
(PBPK) has been anticipated to be a powerful tool to improve the productivity of drug …

Reappraisal and perspectives of clinical drug–drug interaction potential of α-glucosidase inhibitors such as acarbose, voglibose and miglitol in the treatment of type 2 …

RP Dash, RJ Babu, NR Srinivas - Xenobiotica, 2018 - Taylor & Francis
Amidst the new strategies being developed for the management of type 2 diabetes mellitus
(T2DM) with both established and newer therapies, alpha glucosidase inhibitors (AGIs) have …

Pharmacointeraction network models predict unknown drug-drug interactions

A Cami, S Manzi, A Arnold, BY Reis - PloS one, 2013 - journals.plos.org
Drug-drug interactions (DDIs) can lead to serious and potentially lethal adverse events. In
recent years, several drugs have been withdrawn from the market due to interaction-related …