Related Experiment Video
Updated: Mar 12, 2026

Synthesis, Functionalization, and Characterization of Fusogenic Porous Silicon Nanoparticles for Oligonucleotide Delivery
Published on: April 16, 2019
Enhanced liver-targeted delivery with ribofuranose-based GalNAc conjugates
Sai Pallavi Pradeep1, Ruchi Ruchi1, Raman Bahal1
1Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269, USA.
Small geometric changes to GalNAc enhance siRNA stability and delivery. This modified N-acetylgalactosamine (GalNAc) scaffold shows promise for treating liver diseases by improving drug exposure and safety.
Area of Science:
- Biochemistry
- Pharmacology
- Drug Delivery
Background:
- N-acetylgalactosamine (GalNAc) conjugates are crucial for targeted delivery of small interfering RNA (siRNA) to hepatocytes.
- Improving the metabolic stability and pharmacokinetics of siRNA is essential for effective therapeutic applications.
- The 2'-O-methyl modification in the ribofuranose ring of siRNA enhances stability but its impact within GalNAc requires further investigation.
More Related Videos
08:46Regioselective O-Glycosylation of Nucleosides via the Temporary 2',3'-Diol Protection by a Boronic Ester for the Synthesis of Disaccharide Nucleosides
Published on: July 26, 2018
09:02Author Spotlight: Innovative Cancer Therapies with Iron Oxide Nanoparticles for Glioblastoma Treatment
Published on: September 27, 2024
Related Concept Videos
Modified-Release Drug Delivery Systems: Site-Targeted
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention
Hepatic Drug Clearance: Role of Transporters
Drug Metabolism: Phase II Reactions
Site-Targeted Drug Delivery Systems: Polymeric Carriers
Phase II Reactions: Glucuronidation