Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

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...
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 levelĀ 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...
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.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Programmable Peptide Nanofibers Enable Effective MRSA Biofilm Eradication and Infection Control.

ACS applied bio materialsĀ·2026
Same author

Distinct Biodistribution of Natural Killer Cell-Derived Exosomes in an Orthotopic A549 Lung Cancer Mouse Model: Implications for Potent Targeted Drug Delivery.

Life (Basel, Switzerland)Ā·2026
Same author

Adipocyte-driven STAT3-ANGPT2-PTGIS axis promotes cutaneous metastasis in breast cancer and represents a targetable pathway.

NPJ precision oncologyĀ·2026
Same author

Coordination-Enabled Resolution of Inherently Chiral 1,5-Naphthiporphyrin.

Inorganic chemistryĀ·2025
Same author

Stroma-targeted gene delivery for efficient immunogene therapy against pancreatic cancer.

Molecular therapy : the journal of the American Society of Gene TherapyĀ·2025
Same author

Cryogel-Based Dendritic Cell Immunotherapy for Post-Surgical Breast Cancer Treatment.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)Ā·2025

Related Experiment Video

Updated: May 20, 2026

Porous Silicon Microparticles for Delivery of siRNA Therapeutics
08:31

Porous Silicon Microparticles for Delivery of siRNA Therapeutics

Published on: January 15, 2015

Recent progress in copolymer-mediated siRNA delivery.

Zong-Wei Wu1, Chih-Te Chien, Chia-Yeh Liu

  • 1Center for Nanomedicine Research, National Health Research Institutes, Zhunan, Taiwan.

Journal of Drug Targeting
|July 5, 2012
PubMed
Summary
This summary is machine-generated.

Copolymer-based vehicles show promise for delivering short interfering RNA (siRNA) to treat diseases. These advanced materials offer improved in vivo delivery compared to older methods.

More Related Videos

Preparation of Neutrally-charged, pH-responsive Polymeric Nanoparticles for Cytosolic siRNA Delivery
09:09

Preparation of Neutrally-charged, pH-responsive Polymeric Nanoparticles for Cytosolic siRNA Delivery

Published on: May 2, 2019

Assembly and Characterization of Polyelectrolyte Complex Micelles
08:44

Assembly and Characterization of Polyelectrolyte Complex Micelles

Published on: March 2, 2020

Related Experiment Videos

Last Updated: May 20, 2026

Porous Silicon Microparticles for Delivery of siRNA Therapeutics
08:31

Porous Silicon Microparticles for Delivery of siRNA Therapeutics

Published on: January 15, 2015

Preparation of Neutrally-charged, pH-responsive Polymeric Nanoparticles for Cytosolic siRNA Delivery
09:09

Preparation of Neutrally-charged, pH-responsive Polymeric Nanoparticles for Cytosolic siRNA Delivery

Published on: May 2, 2019

Assembly and Characterization of Polyelectrolyte Complex Micelles
08:44

Assembly and Characterization of Polyelectrolyte Complex Micelles

Published on: March 2, 2020

Area of Science:

  • Biotechnology
  • Polymer Science
  • Gene Therapy

Background:

  • RNA interference (RNAi) uses short interfering RNA (siRNA) to silence disease-causing genes.
  • Developing effective in vivo siRNA delivery vehicles remains a significant challenge.
  • Copolymer-based vectors offer advantages over homopolymer vectors for siRNA delivery.

Purpose of the Study:

  • To review recent advancements in copolymer-mediated siRNA delivery systems.
  • To highlight essential components for effective siRNA delivery vehicles.
  • To provide insights into overcoming challenges for in vivo applications.

Main Methods:

  • Review of literature on copolymer-based siRNA delivery systems.
  • Analysis of essential building blocks: cationic segments, organelle-escape units, and degradable fragments.
  • Comparison of copolymer vs. homopolymer vector performance.

Main Results:

  • Copolymer vectors are less immunogenic and more efficient at cellular uptake than homopolymer vectors.
  • Cationic segments (e.g., polyamines) protect siRNA and aid endosomal escape.
  • Degradable fragments are crucial for releasing siRNA in the cytoplasm.

Conclusions:

  • Copolymer-based systems are a promising strategy for efficient in vitro and in vivo siRNA delivery.
  • Careful selection of building blocks is key to optimizing copolymer vehicle performance.
  • Further research into copolymer design can address current limitations in gene therapy delivery.