Biocompatibility and drug release behavior of scaffolds prepared by coaxial electrospinning of poly(butylene succinate) and polyethylene glycol

• Published in: Materials Science & Engineering C Vol. 49; pp. 472 - 484
• Main Authors: Llorens, E., Ibañez, H., del Valle, L.J., Puiggalí, J.
• Format: Journal Article Publication
• Language: English
• Published: Netherlands Elsevier B.V 01.04.2015
• Subjects: Animals; Antiinfectives and antibacterials; Biocompatibility; Biocompatible Materials; Butylene Glycols - chemistry; Cells, Cultured; Cercopithecus aethiops; Chemical composition; Coaxial electrospinning; curcumin; delivery; Drug release; Electrospinning; Enginyeria química; Ethyl alcohol; Fibers; Humans; mixtures; morphology; Poly(butylene succinate); Poly(ethylene glycol); Polyethylene Glycols - chemistry; polylactide; polymer nanofibers; Polymers; Polymers - chemistry; Polímers; Scaffolds; surfaces; Texture; Tissue Scaffolds; Àrees temàtiques de la UPC; Drug release; Poly(butylene succinate); Scaffolds; Coaxial electrospinning; Poly(ethylene glycol)
• ISSN: 0928-4931; 1873-0191
• DOI: 10.1016/j.msec.2015.01.039

Scaffolds constituted by electrospun microfibers of poly(ethylene glycol) (PEG) and poly(butylene succinate) (PBS) were studied. Specifically, coaxial microfibers having different core–shell distributions and compositions were considered as well as uniaxial micro/nanofibers prepared from mixtures of both polymers. Processing conditions were optimized for all geometries and compositions and resulting morphologies (i.e. diameter and surface texture) characterized by scanning electron microscopy. Chemical composition, molecular interactions and thermal properties were evaluated by FTIR, NMR, XPS and differential scanning calorimetry. The PEG component of electrospun fibers could be solubilized by immersion of scaffolds in aqueous medium, giving rise to high porosity and hydrophobic samples. Nevertheless, a small amount of PEG was retained in the PBS matrix, suggesting some degree of mixing. Solubilization was slightly dependent on fiber structure; specifically, the distribution of PEG in the core or shell of coaxial fibers led to higher or lower retention levels, respectively. Scaffolds could be effectively loaded with hydrophobic drugs having antibacterial and anticarcinogenic activities like triclosan and curcumin, respectively. Their release was highly dependent on their chemical structure and medium composition. Thus, low and high release rates were observed in phosphate buffer saline (SS) and SS/ethanol (30:70 v/v), respectively. Slight differences in the release of triclosan were found depending on fiber distribution and composition. Antibacterial activity and biocompatibility were evaluated for both loaded and unloaded scaffolds. •Coaxial microfibers with different hydrophobicities were studied.•The surface morphology of the coaxial fiber shows the distribution of polymers.•Coaxial fiber microstructure favors the polymer molecular orientation.•These hybrid materials have greater advantages for loading and drug release.•PEG removing from the coaxial fiber was handled as sacrificial polymer.