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Updated: Jul 9, 2026

A Comparative Study of Drug Delivery Methods Targeted to the Mouse Inner Ear: Bullostomy Versus Transtympanic Injection
Published on: March 8, 2017
EVA implants for controlled drug delivery to the inner ear
Y Bedulho das Lages1, N Milanino1, J Verin1
1Univ. Lille, Inserm, CHU Lille, U1008, F-59000 Lille, France.
Poly(ethylene vinyl acetate) (EVA) copolymers show promise for controlled drug delivery to the inner ear. These novel implants offer tunable drug release rates and stable mechanical properties for potential clinical use.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Cochlear Drug Delivery
Background:
- The blood-cochlea barrier impedes effective drug delivery to the inner ear.
- Miniaturized implants are needed for localized and controlled therapeutic administration.
Purpose of the Study:
- To evaluate poly(ethylene vinyl acetate) (EVA) copolymers as matrix formers for controlled inner ear drug delivery.
- To investigate the impact of vinyl acetate content and implant diameter on drug release characteristics.
Main Methods:
- EVA implants containing dexamethasone were fabricated using hot melt extrusion.
- Drug release was quantified in artificial perilymph.
- Extensive material characterization was performed (microscopy, DSC, X-ray diffraction, microtomography, texture analysis).
Main Results:
- EVA implants exhibited higher dexamethasone release rates compared to silicone implants.
- Decreasing vinyl acetate content increased copolymer crystallinity and reduced drug release.
- Dexamethasone was homogeneously distributed as microcrystals within the EVA matrix.
- Implants showed minimal swelling/shrinking over 10 months and possessed suitable mechanical properties.
Conclusions:
- EVA copolymers are effective matrix formers for controlled inner ear drug delivery.
- Tunable drug release profiles can be achieved by adjusting vinyl acetate content.
- EVA implants demonstrate stability and appropriate mechanical characteristics for inner ear administration.
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