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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...
Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention

Improving a drug's stability in the gastrointestinal (GI) tract is paramount for enhancing its bioavailability and therapeutic effectiveness. Various strategies are employed to protect the drug from the harsh gastric milieu and to ensure its release and absorption at the desired site within the GI tract.Polymer coatings are one such method used to shield drugs from the stomach's acidic environment. By preventing premature drug release, these coatings improve the bioavailability of unstable...
Modified-Release Drug Delivery Systems: Stimuli-Activated01:30

Modified-Release Drug Delivery Systems: Stimuli-Activated

Stimuli-activated drug delivery systems are designed to release drugs in response to specific physical, chemical, or biological stimuli. These systems often utilize hydrogels—three-dimensional, hydrophilic polymer networks capable of swelling in aqueous environments and retaining significant fluid volumes. Upon exposure to particular stimuli, these hydrogels undergo structural transitions that allow the embedded drug to be released. Due to this adaptive behavior, such systems are also called...

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Related Experiment Video

Updated: Jun 5, 2026

Fabrication of Small Caliber Stent-grafts Using Electrospinning and Balloon Expandable Bare Metal Stents
06:55

Fabrication of Small Caliber Stent-grafts Using Electrospinning and Balloon Expandable Bare Metal Stents

Published on: October 26, 2016

Polymers for drug eluting stents.

Ted Parker1, Vipul Davé, Robert Falotico

  • 1Cordis Corporation Warren NJ, USA. Tparker1@its.jnj.com

Current Pharmaceutical Design
|January 7, 2011
PubMed
Summary

Drug-eluting stents (DES) utilize polymers to control drug release for vascular tissue. Newer bioabsorbable polymers offer a promising alternative, degrading over time to leave a bare metal stent.

Area of Science:

  • Biomaterials Science
  • Cardiovascular Engineering
  • Polymer Chemistry

Background:

  • Drug-eluting stents (DES) are crucial in treating coronary artery disease.
  • Current DES employ biostable polymers to bind and control drug elution from metallic scaffolds.
  • These polymers are critical for stent performance and vascular tissue interaction.

Purpose of the Study:

  • To review the essential requirements for polymers used in drug-eluting stents.
  • To analyze the characteristics of currently marketed DES and their polymer coatings.
  • To explore the potential of next-generation bioabsorbable polymers in DES technology.

Main Methods:

  • Review of polymer properties, stability, drug compatibility, biocompatibility, and drug release control.

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Ferromagnetic Bare Metal Stent for Endothelial Cell Capture and Retention
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Ferromagnetic Bare Metal Stent for Endothelial Cell Capture and Retention

Published on: September 18, 2015

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Last Updated: Jun 5, 2026

Fabrication of Small Caliber Stent-grafts Using Electrospinning and Balloon Expandable Bare Metal Stents
06:55

Fabrication of Small Caliber Stent-grafts Using Electrospinning and Balloon Expandable Bare Metal Stents

Published on: October 26, 2016

Design of a Biocompatible Drug-Eluting Tracheal Stent in Mice with Laryngotracheal Stenosis
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Design of a Biocompatible Drug-Eluting Tracheal Stent in Mice with Laryngotracheal Stenosis

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Ferromagnetic Bare Metal Stent for Endothelial Cell Capture and Retention
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Ferromagnetic Bare Metal Stent for Endothelial Cell Capture and Retention

Published on: September 18, 2015

  • In-depth analysis of polymer structure, coating design, drug-polymer morphology, and elution profiles of four marketed DES.
  • Examination of bioabsorbable polymer composition, degradation, and drug release kinetics in new DES platforms.
  • Main Results:

    • Key polymer requirements for DES include physical properties, stability, drug compatibility, biocompatibility, and controlled release.
    • Detailed analysis of four major DES (CYPHER, Taxus, XIENCE V/Promus, Endeavor Resolute) reveals diverse polymer strategies.
    • Emerging bioabsorbable polymers, like those in the NEVO stent, show potential for improved long-term outcomes by degrading over time.

    Conclusions:

    • Polymers are integral to DES function, dictating drug delivery and vascular response.
    • Understanding polymer-drug interactions and degradation is vital for optimizing DES performance.
    • Bioabsorbable polymers represent a significant advancement, potentially leading to stents that leave no permanent foreign material in the vasculature.