Electrospun Poly(acrylic acid-<i>co</i>-4-styrene sulfonate) as Potential Drug-Eluting Scaffolds for Targeted Chemotherapeutic Delivery Systems on Gastric (AGS) and Breast (MDA-Mb-231) Cancer Cell Lines
Andrónico Neira-Carrillo,
Ignacio A. Zárate,
Eddie Nieto,
Nicole Butto-Miranda,
Lorena Lobos-González,
Matias Del Campo-Smith,
Daniel A. Palacio,
Bruno F. Urbano
Affiliations
Andrónico Neira-Carrillo
Department of Biological and Animal Sciences, Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, La Pintana, Santiago 8820808, Chile
Ignacio A. Zárate
Department of Biological and Animal Sciences, Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, La Pintana, Santiago 8820808, Chile
Eddie Nieto
Department of Biological and Animal Sciences, Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, La Pintana, Santiago 8820808, Chile
Nicole Butto-Miranda
Department of Biological and Animal Sciences, Faculty of Veterinary and Animal Sciences, University of Chile, Santa Rosa 11735, La Pintana, Santiago 8820808, Chile
Lorena Lobos-González
Advanced Center for Chronic Diseases (ACCDIS), Santiago 380492, Chile
Matias Del Campo-Smith
Advanced Center for Chronic Diseases (ACCDIS), Santiago 380492, Chile
Daniel A. Palacio
Department of Polymer Chemistry, Faculty of Chemical Science, University of Concepción, Concepción 3349001, Chile
Bruno F. Urbano
Department of Polymer Chemistry, Faculty of Chemical Science, University of Concepción, Concepción 3349001, Chile
Potential drug-eluting scaffolds of electrospun poly(acrylic acid-co-styrene sulfonate) P(AA-co-SS) in clonogenic assays using tumorigenic gastric and ovarian cancer cells were tested in vitro. Electrospun polymer nanofiber (EPnF) meshes of PAA and PSSNa homo- and P(AA-co-SS) copolymer composed of 30:70, 50:50, 70:30 acrylic acid (AA) and sodium 4-styrene sulfonate (SSNa) units were performed by electrospinning (ES). The synthesis, structural and morphological characterization of all EPnF meshes were analyzed by optical and electron microscopy (SEM-EDS), infrared spectroscopy (FTIR), contact angle, and X-ray diffraction (XRD) measurements. This study shows that different ratio of AA and SSNa of monomers in P(AA-co-SS) EPnF play a crucial role in clonogenic in vitro assays. We found that 50:50 P(AA-co-SS) EPnF mesh loaded with antineoplastic drugs can be an excellent suppressor of growth-independent anchored capacities in vitro assays and a good subcutaneous drug delivery system for chemotherapeutic medication in vivo model for surgical resection procedures in cancer research.