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Related Concept Videos

siRNA - Small Interfering RNAs02:30

siRNA - Small Interfering RNAs

Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the ATP-dependent...
Experimental RNAi02:15

Experimental RNAi

RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
RNA Interference01:23

RNA Interference

RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
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Related Experiment Video

Updated: May 8, 2026

Porous Silicon Microparticles for Delivery of siRNA Therapeutics
08:31

Porous Silicon Microparticles for Delivery of siRNA Therapeutics

Published on: January 15, 2015

Chitosan-based siRNA delivery systems.

Héloïse Ragelle1, Gaëlle Vandermeulen1, Véronique Préat1

  • 1Pharmaceutics and Drug Delivery Group, Louvain Drug Research Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.

Journal of Controlled Release : Official Journal of the Controlled Release Society
|August 23, 2013
PubMed
Summary

Chitosan nanoparticles offer a promising platform for delivering small interfering RNA (siRNA) therapeutics. Recent advancements address key challenges like stability and endosomal escape, enhancing in vivo delivery efficiency.

Keywords:
ChitosanDelivery barriersLigandNanoparticlesRNA interferencesiRNA

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Last Updated: May 8, 2026

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Chitosan/Interfering RNA Nanoparticle Mediated Gene Silencing in Disease Vector Mosquito Larvae
08:36

Chitosan/Interfering RNA Nanoparticle Mediated Gene Silencing in Disease Vector Mosquito Larvae

Published on: March 25, 2015

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Gene Therapy

Background:

  • Chitosan's cationic nature facilitates complexation with small interfering RNA (siRNA), forming nanoparticles.
  • Its biocompatibility and biodegradability make it suitable for in vivo applications.
  • Current chitosan-based siRNA delivery systems face efficiency limitations.

Purpose of the Study:

  • To review major barriers hindering chitosan-based siRNA delivery efficiency.
  • To discuss solutions for overcoming these barriers.
  • To explore parameters for designing improved delivery systems, including ligand grafting.

Main Methods:

  • Literature review of recent advancements in chitosan-based siRNA delivery systems.
  • Analysis of challenges such as biological fluid stability and endosomal escape.
  • Examination of strategies for enhancing in vivo therapeutic applications.

Main Results:

  • Identified stability and endosomal escape as critical barriers.
  • Highlighted solutions involving system optimization and ligand functionalization.
  • Reviewed successful local and systemic in vivo delivery systems.

Conclusions:

  • Recent improvements have overcome previous limitations in chitosan-siRNA systems.
  • Optimized systems are paving the way for a new generation of siRNA therapeutics.
  • Further development promises enhanced in vivo efficacy for gene silencing applications.