Open AccessAssessment of structural, biological and drug release properties of electro-sprayed poly lactic acid-dexamethasone coating for biomedical applications
Author(s) -
Mostafa Rahvar,
Gholamreza Ahmadi Lakalayeh,
Niloofar Nazeri,
Bahereh T. Marouf,
Mahdieh Shirzad,
Azar Najafi Tireh Shabankareh,
Hossein Ghanbari
Publication year - 2021
Publication title -
biomedical engineering letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.709
H-Index - 26
eISSN - 2093-985X
pISSN - 2093-9868
DOI - 10.1007/s13534-021-00205-9
Subject(s) - materials science , coating , differential scanning calorimetry , scanning electron microscope , crystallinity , spin coating , surface roughness , poloxamer , contact angle , chemical engineering , nuclear chemistry , biomedical engineering , polymer , composite material , chemistry , medicine , copolymer , physics , engineering , thermodynamics
The efficacy of an implant is highly depends on its coating characteristics mainly determined by polymer properties and coating technique. Electro-spraying is an inexpensive and versatile coating technique with various advantages for biomedical application. In this study, the efficacy of electro-sprayed (ES) poly lactic acid (PLA)-dexamethasone (DEX) coatings for medical implants was evaluated and compared with spin-coated samples as control. Structural properties of coatings were investigated using X-ray diffraction (XRD) and differential scanning calorimetry (DSC). Confocal and scanning electron microscopy (SEM), contact angle measurement and nanoindentation tests were used to study surface properties. Coating degradation rate and drug release profile were studied for 40 days. Cell viability experiments were also performed on human endothelial (HUVEC) and smooth muscle cells (HUASMC) using MTT assay and SEM. XRD and DSC analysis showed electro-spraying significantly reduce PLA and DEX crystallinity. Surface studies showed ES coatings has significantly higher hydrophobicity and roughness with microbead-nanofiber morphology vs. micro-nanoporous structure of spin-coated samples. Initial burst release of DEX was 22% and 10% after 6 h and total release was 71% and 46% after 40 days for ES and spin-coated samples, respectively. HUVEC viability of ES samples was higher than spin-coated ones after 1 and 4 days. However, dexamethasone release profile reduced HUASMC proliferation in ES PLA-DEX samples in comparison to spin-coated after 1 and 3 days. In conclusion, in vitro results showed potential of ES PLA-DEX as a biocompatible and efficient anti-inflammatory coating with suitable drug release profile for future applications such as coronary drug eluting stents.