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...

You might also read

Related Articles

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

Sort by
Same author

CCL17-neutralizing and esterase-responsive core-shell microgels for endogenous Tregs recruitment and functional enhancement in myocardial infarction.

Bioactive materials·2026
Same author

Dynamic feedback BacGuard anchors microbial metabolism to host symbiosis in real-time ulcerative colitis therapy.

Bioactive materials·2026
Same author

Osteoclast-regulatory biomaterials: Direct cellular intervention and indirect microenvironment modulation.

Biomaterials·2026
Same author

Ionic thermoelectrics goes epidermal theranostics.

National science review·2026
Same author

Low-modulus hydrogels reduce scar formation in wound healing.

Acta biomaterialia·2026
Same author

Theoretical quantitative model and clinical outcome predictions of conductive cardiac patches for electrophysiological treatments.

Nature biomedical engineering·2026
Same journal

AI-Derived Smart Microneedle Systems for Advanced Wound Management: From Intelligent Sensing to Closed-Loop Therapy.

Macromolecular bioscience·2026
Same journal

A Novel Chitosan-Gelatin Scaffold and Cell Spray Therapy for Treating Limbal Stem Cell Deficiency.

Macromolecular bioscience·2026
Same journal

Electroconductive Soft Microcarriers for Suspension Culture of Skeletal Muscle Cells.

Macromolecular bioscience·2026
Same journal

Dual-Responsive Chitosan-Grafted PNIPAAm Hydrogel Eye Drop Incorporating Insulin-Imprinted Microgels for Dry Eye Syndrome Treatment.

Macromolecular bioscience·2026
Same journal

Levan Inspired Hybrid Composites Materials: Bridging Natural Polysaccharides with Biomedical Technology.

Macromolecular bioscience·2026
Same journal

Anion-Specific Mechanisms in Fibrinogen Self-Assembly: Contrasting Effects of Phosphates and Chlorides in Nanofiber Formation.

Macromolecular bioscience·2026
See all related articles

Related Experiment Video

Updated: Jun 27, 2026

PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS
12:48

PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS

Published on: December 27, 2013

Polyelectrolyte coated PLGA nanoparticles: templation and release behavior.

Jie Zhou1, Sergio Moya, Lie Ma

  • 1Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, China.

Macromolecular Bioscience
|December 18, 2008
PubMed
Summary
This summary is machine-generated.

Poly[(D,L-lactide)-co-glycolide] (PLGA) nanoparticles were surface-modified using layer-by-layer assembly. This method enhanced nanoparticle properties for controlled drug delivery applications.

More Related Videos

Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique
06:47

Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique

Published on: September 20, 2011

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
09:11

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release

Published on: February 13, 2016

Related Experiment Videos

Last Updated: Jun 27, 2026

PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS
12:48

PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS

Published on: December 27, 2013

Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique
06:47

Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique

Published on: September 20, 2011

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
09:11

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release

Published on: February 13, 2016

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Polymer Chemistry

Background:

  • Poly[(D,L-lactide)-co-glycolide] (PLGA) nanoparticles are widely used for drug delivery.
  • Surface modification is crucial for controlling nanoparticle behavior and drug release.

Purpose of the Study:

  • To prepare and characterize PLGA nanoparticles surface-modified with polyethyleneimine and poly(acrylic acid) multilayers.
  • To investigate the effect of crosslinking and poly(ethylene glycol) (PEG) grafting on nanoparticle properties and drug release.

Main Methods:

  • Emulsification-solvent evaporation method for nanoparticle preparation.
  • Layer-by-layer (LBL) assembly for surface modification.
  • Quartz crystal microbalance with dissipation monitoring (QCM-D), zeta-potential, flow cytometry, and transmission electron microscopy (TEM) for characterization.
  • Carbodiimide condensation for crosslinking and PEG grafting.
  • Drug release studies at 37°C and 60°C.

Main Results:

  • Successful fabrication of multilayer-coated PLGA nanoparticles.
  • Demonstrated control over surface properties through LBL assembly, crosslinking, and PEGylation.
  • Investigated the release kinetics of incorporated model drugs (Rhodamine 6G, 5(6)-carboxyfluorescein, fluorescein).

Conclusions:

  • Surface-modified PLGA nanoparticles offer tunable properties for advanced drug delivery systems.
  • Crosslinking and PEGylation can modulate drug release profiles.
  • The developed methodology provides a versatile platform for creating functional nanoparticles.