Bile acids and their derivatives as potential modifiers of drug release and pharmacokinetic profiles

N Pavlović, S Goločorbin-Kon, M Ðanić… - Frontiers in …, 2018 - frontiersin.org
Bile acids have received considerable interest in the drug delivery research due to their
peculiar physicochemical properties and biocompatibility. The main advantage of bile acids …

[HTML][HTML] Intestinal absorption of bile acids in health and disease

AL Ticho, P Malhotra, PK Dudeja, RK Gill… - Comprehensive …, 2019 - ncbi.nlm.nih.gov
The intestinal reclamation of bile acids is crucial for the maintenance of their enterohepatic
circulation. The majority of bile acids are actively absorbed via specific transport proteins …

Overcoming the intestinal barrier: a look into targeting approaches for improved oral drug delivery systems

Y Xu, N Shrestha, V Préat, A Beloqui - Journal of controlled release, 2020 - Elsevier
Oral drug administration is one of the most preferred and simplest routes among both
patients and formulation scientists. Nevertheless, orally delivery of some of the most widely …

Structural basis of sodium-dependent bile salt uptake into the liver

K Goutam, FS Ielasi, E Pardon, J Steyaert, N Reyes - Nature, 2022 - nature.com
The liver takes up bile salts from blood to generate bile, enabling absorption of lipophilic
nutrients and excretion of metabolites and drugs. Human Na+–taurocholate co-transporting …

Physiology and physical chemistry of bile acids

MC Di Gregorio, J Cautela, L Galantini - International journal of molecular …, 2021 - mdpi.com
Bile acids (BAs) are facial amphiphiles synthesized in the body of all vertebrates. They
undergo the enterohepatic circulation: they are produced in the liver, stored in the …

Bile acid transporter-mediated oral drug delivery

F Deng, YH Bae - Journal of Controlled Release, 2020 - Elsevier
Bile acids are synthesized in the liver, stored in the gallbladder, and secreted into the
duodenum at meals. Apical sodium-dependent bile acid transporter (ASBT), an ileal Na+ …

Carrier-mediated cellular uptake of pharmaceutical drugs: an exception or the rule?

PD Dobson, DB Kell - Nature reviews Drug discovery, 2008 - nature.com
It is generally thought that many drug molecules are transported across biological
membranes via passive diffusion at a rate related to their lipophilicity. However, the types of …

Recent advances in ligand-based drug design: relevance and utility of the conformationally sampled pharmacophore approach

C Acharya, A Coop, JE Polli… - Current computer-aided …, 2011 - ingentaconnect.com
In the absence of three-dimensional (3D) structures of potential drug targets, ligand-based
drug design is one of the popular approaches for drug discovery and lead optimization. 3D …

Transporter-mediated drug delivery

G Gyimesi, MA Hediger - Molecules, 2023 - mdpi.com
Transmembrane transport of small organic and inorganic molecules is one of the
cornerstones of cellular metabolism. Among transmembrane transporters, solute carrier …

Role of the intestinal bile acid transporters in bile acid and drug disposition

PA Dawson - Drug transporters, 2011 - Springer
Membrane transporters expressed by the hepatocyte and enterocyte play critical roles in
maintaining the enterohepatic circulation of bile acids, an effective recycling and …