Renal drug transporters and drug interactions

A Ivanyuk, F Livio, J Biollaz, T Buclin - Clinical pharmacokinetics, 2017 - Springer
Transporters in proximal renal tubules contribute to the disposition of numerous drugs.
Furthermore, the molecular mechanisms of tubular secretion have been progressively …

Assessing the performance of amorphous solid dispersions

A Newman, G Knipp, G Zografi - Journal of pharmaceutical sciences, 2012 - Elsevier
The characterization and performance of stable amorphous solid dispersion systems were
evaluated in 40 research papers reporting active pharmaceutical ingredient (API) dissolution …

Intestinal drug transporters: an overview

M Estudante, JG Morais, G Soveral, LZ Benet - Advanced drug delivery …, 2013 - Elsevier
The importance of drug transporters as one of the determinants of pharmacokinetics has
become increasingly evident [1]. While much research has been conducted focusing the role …

[HTML][HTML] Disease-drug and drug-drug interaction in COVID-19: Risk and assessment

D Kumar, N Trivedi - Biomedicine & Pharmacotherapy, 2021 - Elsevier
COVID-19 is announced as a global pandemic in 2020. Its mortality and morbidity rate are
rapidly increasing, with limited medications. The emergent outbreak of COVID-19 prompted …

[HTML][HTML] Pharmacogenomics implications of using herbal medicinal plants on African populations in health transition

NE Thomford, K Dzobo, D Chopera, A Wonkam… - Pharmaceuticals, 2015 - mdpi.com
The most accessible points of call for most African populations with respect to primary health
care are traditional health systems that include spiritual, religious, and herbal medicine. This …

Canalicular ABC transporters and liver disease

M Nicolaou, EJ Andress, JK Zolnerciks… - The Journal of …, 2012 - Wiley Online Library
Bile is a complex mixture that includes bile salts, the membrane phospholipid
phosphatidylcholine (PC), cholesterol and various endobiotic and xenobiotic toxins, each of …

[HTML][HTML] 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 …

A critical analysis of the interplay between cytochrome P450 3A and P-glycoprotein: recent insights from knockout and transgenic mice

RAB van Waterschoot, AH Schinkel - Pharmacological reviews, 2011 - ASPET
CYP3A is one of the most important drug-metabolizing enzymes, determining the first-pass
metabolism, oral bioavailability, and elimination of many drugs. It is also an important …

Antiviral drug delivery system for enhanced bioactivity, better metabolism and pharmacokinetic characteristics

R Chen, T Wang, J Song, D Pu, D He, J Li… - International journal …, 2021 - Taylor & Francis
Antiviral drugs (AvDs) are the primary resource in the global battle against viruses, including
the recent fight against corona virus disease 2019 (COVID-19). Most AvDs require multiple …

The dual role of pharmacogenetics in HIV treatment: mutations and polymorphisms regulating antiretroviral drug resistance and disposition

V Michaud, T Bar-Magen, J Turgeon, D Flockhart… - Pharmacological …, 2012 - ASPET
Significant intra-and interindividual variability has been observed in response to use of
pharmacological agents in treatment of HIV infection. Treatment of HIV infection is limited by …