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

27
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...
27
Modified-Release Drug Delivery Systems: Site-Targeted01:24

Modified-Release Drug Delivery Systems: Site-Targeted

24
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.
24

You might also read

Related Articles

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

Sort by
Same author

<i>Fusobacterium nucleatum-</i>derived succinic acid aggravates colitis by triggering macrophage pro-inflammatory phenotypic transformation via SUCNR1/NF-κB axis.

Gut microbes·2026
Same author

Job Crafting Through the Lens of Paradoxical Leadership: The Role of Positive Psychological Capital and Promotive Voice.

Behavioral sciences (Basel, Switzerland)·2026
Same author

Development and internal validation of a nomogram for predicting short-term functional improvement after pharmacological treatment in severe symptomatic lumbar disk herniation.

Frontiers in medicine·2026
Same author

A Chemically Defined Four-Component Self-Adjuvanting Tn Vaccine Activating Mincle, FcγR, and CD206 for Enhanced Antitumor Immunity.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Decoupling pitch and angle of attack with a variable-incidence wing extends quadrotor flight endurance.

Scientific reports·2026
Same author

Reconceptualizing Aplastic Anemia-Seed, Worm, Soil.

Journal of clinical laboratory analysis·2026

Related Experiment Video

Updated: Feb 17, 2026

Evaluation of Polymeric Gene Delivery Nanoparticles by Nanoparticle Tracking Analysis and High-throughput Flow Cytometry
08:51

Evaluation of Polymeric Gene Delivery Nanoparticles by Nanoparticle Tracking Analysis and High-throughput Flow Cytometry

Published on: March 1, 2013

16.8K

Long Circulating Polymeric Nanoparticles for Gene/Drug Delivery.

Jiaming Hu1, Yan Sheng2, Junfeng Shi1

  • 1Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.

Current Drug Metabolism
|December 9, 2017
PubMed
Summary

Developing long-circulating polymeric nanoparticles is crucial for effective gene/drug delivery. Surface modification strategies, including PEGylation, are key to enhancing nanoparticle circulation time for improved therapeutic outcomes.

Keywords:
Long circulationbiodistributiongene/drug deliverymononuclear phagocyte systemopsonizationpolymeric nanoparticles.

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

8.0K
Assembly and Characterization of Polyelectrolyte Complex Micelles
08:44

Assembly and Characterization of Polyelectrolyte Complex Micelles

Published on: March 2, 2020

11.6K

Related Experiment Videos

Last Updated: Feb 17, 2026

Evaluation of Polymeric Gene Delivery Nanoparticles by Nanoparticle Tracking Analysis and High-throughput Flow Cytometry
08:51

Evaluation of Polymeric Gene Delivery Nanoparticles by Nanoparticle Tracking Analysis and High-throughput Flow Cytometry

Published on: March 1, 2013

16.8K
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

8.0K
Assembly and Characterization of Polyelectrolyte Complex Micelles
08:44

Assembly and Characterization of Polyelectrolyte Complex Micelles

Published on: March 2, 2020

11.6K

Area of Science:

  • Nanotechnology
  • Biomedical Engineering
  • Materials Science

Background:

  • Prolonged nanoparticle circulation is essential for targeted gene/drug delivery.
  • Current methods like PEGylation offer limited circulation times for clinical needs.

Purpose of the Study:

  • To review recent advances in designing polymeric nanoparticles for extended blood circulation.
  • To discuss factors influencing nanoparticle surface characteristics and modifications.

Main Methods:

  • Review of literature on polymeric nanoparticle design and fabrication.
  • Analysis of surface modification techniques and their impact on circulation time.

Main Results:

  • Particle size, surface charge, and hydrophilicity significantly influence nanoparticle circulation.
  • Surface modifications using PEG and polysaccharides are common strategies.
  • Stimuli-responsive modifications can enhance targeting strategies.

Conclusions:

  • Novel coating materials are needed to further improve long-circulating polymer-based nanoparticles.
  • Optimizing nanoparticle properties is critical for successful clinical translation of nanomedicines.