Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/114007
Title: Lipid and Peptide-Oligonucleotide Conjugates for Therapeutic Purposes: From Simple Hybrids to Complex Multifunctional Assemblies
Authors: Fàbrega, Carme
Aviñó, Anna
Navarro, Natalia
Jorge, Andreia F. 
Grijalvo, Santiago
Eritja, Ramon
Keywords: antisense oligonucleotides; siRNA; lipid-oligonucleotide conjugates; peptide-oligonucleotide conjugates
Issue Date: 18-Jan-2023
Publisher: MDPI
Project: Spanish Ministerio de Ciencia e Innovación (CTQ2017-84415-R, CTQ2014-61758-EXP; BIO2017-92113-EXP; PID2020-118145RB-I100), 7th Framework Programme (NMP2007-213382, NMP-LA-2011-262943, COST Action CA17103) and CIBER-BBN an initiative funded by the VI National R + D + I Plan, Iniciativa Ingenio, Consolider Program 
Serial title, monograph or event: Pharmaceutics
Volume: 15
Issue: 2
Abstract: Antisense and small interfering RNA (siRNA) oligonucleotides have been recognized as powerful therapeutic compounds for targeting mRNAs and inducing their degradation. However, a major obstacle is that unmodified oligonucleotides are not readily taken up into tissues and are susceptible to degradation by nucleases. For these reasons, the design and preparation of modified DNA/RNA derivatives with better stability and an ability to be produced at large scale with enhanced uptake properties is of vital importance to improve current limitations. In the present study, we review the conjugation of oligonucleotides with lipids and peptides in order to produce oligonucleotide conjugates for therapeutics aiming to develop novel compounds with favorable pharmacokinetics.
URI: https://hdl.handle.net/10316/114007
ISSN: 1999-4923
DOI: 10.3390/pharmaceutics15020320
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
I&D CQC - Artigos em Revistas Internacionais

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