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Updated: Jan 28, 2026

Design of a Biocompatible Drug-Eluting Tracheal Stent in Mice with Laryngotracheal Stenosis
Published on: January 21, 2020
Controlled Release Ultrasonic-Coated Drug-Eluting Stent with Multilayers of Chitosan and Curcumin
Jeremia Frandy Apitalau1, Dyah Listyarifah1,2, Adhyatmika -3
1Biomedical Engineering Program, Graduate School, Universitas Gadjah Mada, Yogyakarta, Indonesia.
This study developed a multilayer drug-eluting stent using genipin-crosslinked chitosan and curcumin to prevent initial burst release (IBR). The novel system demonstrates controlled drug release without IBR, reducing restenosis risk.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Polymer Chemistry
Background:
- Commercial drug-eluting stents often exhibit initial burst release (IBR), increasing restenosis risk.
- A multilayer strategy using genipin-crosslinked chitosan and curcumin was employed to overcome IBR limitations.
Purpose of the Study:
- To develop and evaluate a novel multilayer drug-eluting stent system.
- To prevent initial burst release (IBR) and achieve controlled drug delivery.
Main Methods:
- Ultrasonic coating technique used to create uniform layers at varying speeds (7, 8, 9 mm/s).
- Characterization via scanning electron microscopy (SEM).
- Drug release studies analyzed using Korsmeyer-Peppas and Peppas-Sahlin models; analytical method validated with UV-Vis spectrophotometry.
Main Results:
- Release data modeled by Korsmeyer-Peppas indicated Super Case II transport (relaxation/erosion).
- Peppas-Sahlin model showed Fickian diffusion dominating the initial 6-7 days, followed by polymer relaxation.
- Higher speeds (9 mm/s) extended Fickian diffusion duration compared to lower speeds.
Conclusions:
- The multilayer system effectively prevents initial burst release by maintaining matrix integrity.
- Drug release mechanism transitions from diffusion to polymer relaxation, avoiding burst release.
- The system exhibits a controlled-release profile, validated by zero-order model fit.
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