Multifunctional Coatings for Robotic Implanted Device.
Caterina CristalliniSerena DantiBahareh AzimiVeronika TempestiClaudio RicciLetizia VentrelliPatrizia CinelliNiccoletta BarbaniAndrea LazzeriPublished in: International journal of molecular sciences (2019)
The objective of this study was the preparation and physico-chemical, mechanical, biological, and functional characterization of a multifunctional coating for an innovative, fully implantable device. The multifunctional coating was designed to have three fundamental properties: adhesion to device, close mechanical resemblance to human soft tissues, and control of the inflammatory response and tissue repair process. This aim was fulfilled by preparing a multilayered coating based on three components: a hydrophilic primer to allow device adhesion, a poly(vinyl alcohol) hydrogel layer to provide good mechanical compliance with the human tissue, and a layer of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) fibers. The use of biopolymer fibers offered the potential for a long-term interface able to modulate the release of an anti-inflammatory drug (dexamethasone), thus contrasting acute and chronic inflammation response following device implantation. Two copolymers, poly(vinyl acetate-acrylic acid) and poly(vinyl alcohol-acrylic acid), were synthetized and characterized using thermal analysis (DSC, TGA), Fourier transform infrared spectroscopy (FT-IR chemical imaging), in vitro cell viability, and an adhesion test. The resulting hydrogels were biocompatible, biostable, mechanically compatible with soft tissues, and able to incorporate and release the drug. Finally, the multifunctional coating showed a good adhesion to titanium substrate, no in vitro cytotoxicity, and a prolonged and controlled drug release.
Keyphrases
- drug delivery
- drug release
- cancer therapy
- inflammatory response
- endothelial cells
- biofilm formation
- gene expression
- anti inflammatory
- oxidative stress
- cell migration
- low dose
- high resolution
- high dose
- lipopolysaccharide induced
- minimally invasive
- climate change
- liquid chromatography
- escherichia coli
- hyaluronic acid
- intensive care unit
- pluripotent stem cells
- human health
- adverse drug
- pseudomonas aeruginosa
- electronic health record