Synthetic methods for azaheterocyclic phosphonates and their biological activity
K Moonen, I Laureyn, CV Stevens - Chemical reviews, 2004 - ACS Publications
Despite the importance in synthetic, agrochemical, and medicinal chemistry, to the best of
our knowledge, no overview has been made on the synthetic methods and the field of …
our knowledge, no overview has been made on the synthetic methods and the field of …
Targeted prodrug design to optimize drug delivery
HK Han, GL Amidon - Aaps Pharmsci, 2000 - Springer
Classical prodrug design often represents a nonspecific chemical approach to mask
undesirable drug properties such as limited bioavailability, lack of site specificity, and …
undesirable drug properties such as limited bioavailability, lack of site specificity, and …
Overcoming the intestinal barrier: a look into targeting approaches for improved oral drug delivery systems
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 …
patients and formulation scientists. Nevertheless, orally delivery of some of the most widely …
Intestinal drug transporters: an overview
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 …
become increasingly evident [1]. While much research has been conducted focusing the role …
Expression and function of efflux drug transporters in the intestine
M Takano, R Yumoto, T Murakami - Pharmacology & therapeutics, 2006 - Elsevier
A variety of drug transporters expressed in the body control the fate of drugs by affecting
absorption, distribution, and elimination processes. In the small intestine, transporters …
absorption, distribution, and elimination processes. In the small intestine, transporters …
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 …
cornerstones of cellular metabolism. Among transmembrane transporters, solute carrier …
Transport of valganciclovir, a ganciclovir prodrug, via peptide transporters PEPT1 and PEPT2
M Sugawara, W Huang, YJ Fei, FH Leibach… - Journal of …, 2000 - Elsevier
In clinical trials, valganciclovir, the valyl ester of ganciclovir, has been shown to enhance the
bioavailability of ganciclovir when taken orally by patients with cytomegalovirus infection …
bioavailability of ganciclovir when taken orally by patients with cytomegalovirus infection …
Administration routes and delivery systems of bisphosphonates for the treatment of bone resorption
A Ezra, G Golomb - Advanced drug delivery reviews, 2000 - Elsevier
Geminal bisphosphonates (BPs) are a class of drugs considered to be stable analogs of
pyrophosphate (P–O–P), a physiological regulator of calcification and bone resorption. A …
pyrophosphate (P–O–P), a physiological regulator of calcification and bone resorption. A …
5′-Amino acid esters of antiviral nucleosides, acyclovir, and AZT are absorbed by the intestinal PEPT1 peptide transporter
H Han, RLA De Vrueh, JK Rhie, KMY Covitz… - Pharmaceutical …, 1998 - Springer
Purpose. General use of nucleoside analogues in the treatment of viral infections and
cancer is often limited by poor oral absorption. Valacyclovir, a water soluble amino acid …
cancer is often limited by poor oral absorption. Valacyclovir, a water soluble amino acid …
Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies
Clinical development of orally active peptide drugs has been restricted by their unfavorable
physicochemical properties, which limit their intestinal mucosal permeation and their lack of …
physicochemical properties, which limit their intestinal mucosal permeation and their lack of …