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Electrospray loading and release of hydrophobic gramicidin in polyester microparticles

Authors :
Carlos Alemán
Carlos Cativiela
Jordi Puiggalí
Silvana Maione
Maria M. Pérez-Madrigal
Luis J. del Valle
European Commission
Ministerio de Economía y Competitividad (España)
Gobierno de Aragón
Generalitat de Catalunya
Universitat Politècnica de Catalunya. Departament d'Enginyeria Química
Universitat Politècnica de Catalunya. PSEP - Polimers Sintètics: Estructura i Propietats. Polimers Biodegradables
Universitat Politècnica de Catalunya. IMEM - Innovació, Modelització i Enginyeria en (BIO) Materials
Universitat Politècnica de Catalunya. PSEP - Polimers Sintètics: Estructura i Propietats. Polimers Biodegradables.
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname, Zaguán. Repositorio Digital de la Universidad de Zaragoza, UPCommons. Portal del coneixement obert de la UPC, Universitat Politècnica de Catalunya (UPC), Recercat. Dipósit de la Recerca de Catalunya
Publication Year :
2016
Publisher :
Royal Society of Chemistry (RSC), 2016.

Abstract

Gramicidin (GA), a very hydrophobic pentadecapeptide with important biological activities (i.e. in addition to its well-known antimicrobial and antibiotic activities, GA has been recently identified as a potent therapeutic agent against different carcinomas), has been loaded by electrospraying in poly(tetramethylene succinate) (PE44), a biodegradable and biocompatible aliphatic polyester. Microspheres (average diameter: 5.0 ± 0.7 μm) were successfully obtained from the mixture of GA and PE44 solutions in ethanol and chloroform, respectively. The loading of the peptide, which has been proved by FTIR and X-ray photoelectron spectroscopies, essentially occurred at the surface of the microspheres, as was reflected by scanning electron microscopy micrographs and atomic force microscopy phase images. In spite of this, the thermal stability of the polyester matrix remained essentially unaltered, even though the wettability decreased. The release of GA in phosphate buffer saline (PBS) was limited by the very low solubility of the peptide in aqueous solution, a fast burst effect followed by the establishment of equilibrium after 5 days of being observed in this hydrophilic environment. The release behaviour was very different when the hydrophilicity of the medium was reduced by adding ethanol. In this case, a very fast but sustained release was identified during the first few hours. On the other hand, biological tests have demonstrated that GA retains its antimicrobial activity after loading and does not alter the biocompatibility of PE44. Our results prove that, despite its hydrophobicity and relatively large number of residues, the loading of GA in a polymeric matrix represents an alternative strategy for the release of this versatile peptide in cancer therapy.<br />Authors thank supports from MINECO and FEDER (MAT2015-69367-R, MAT2015-69547-R and CTQ2013-40855-R) and Gobierno de Aragón – Fondo Social Europeo (research group E40). Support for the research of C.A. was received through the prize “ICREA Academia” for excellence in research funded by the Generalitat de Catalunya.

Details

ISSN :
20462069 and 20156936
Volume :
6
Database :
OpenAIRE
Journal :
RSC Advances
Accession number :
edsair.doi.dedup.....e263b4dd4fc9c2c16cad3e0e7547b3cb
Full Text :
https://doi.org/10.1039/c6ra11056h