TY - JOUR
T1 - Enhanced properties of poly(ε-caprolactone)/polyvinylpyrrolidone electrospun scaffolds fabricated using 1,1,1,3,3,3-hexafluoro-2-propanol
AU - Goreninskii, Semen
AU - Danilenko, Nadezhda
AU - Bolbasov, Evgeniy
AU - Evtina, Anastasia
AU - Buldakov, Mikhail
AU - Cherdyntseva, Nadezhda
AU - Saqib, Muhammad
AU - Beshchasna, Natalia
AU - Opitz, Joerg
AU - Filimonov, Victor
AU - Tverdokhlebov, Sergei
N1 - Funding Information:
Fabrication of the described materials was financially supported by the Tomsk Polytechnic University Competitiveness Enhancement Program. Physicochemical and biological studies were performed in Tomsk Polytechnic University and were financially supported by RFBR and Tomsk region according to the research project 19‐43‐703020. Degradation studies were performed in Fraunhofer Institute for Ceramic Technologies and Systems IKTS. UV‐spectrophotometry was carried out using the core facilities of TPU's “Physicochemical methods of analysis”. Additional cell studies were performed in Cancer Research Institute, Tomsk National Research Medical Center and funded by State assignment, Project № 0550‐2019‐0004.
Publisher Copyright:
© 2021 Wiley Periodicals LLC.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021
Y1 - 2021
N2 - Poly(ε-caprolactone)/polyvinylpyrrolidone (PCL/PVP) scaffolds with various composition were fabricated from 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) solution using the same electrospinning parameters in order to reveal the effect of polymer ratio on the material properties. The obtained materials were characterized using scanning electron microscopy, contact angle measurements, X-ray diffraction, Fourier-transformed infrared spectroscopy, and tensile testing. The strengthening effect of PVP was observed: Young modulus of PCL/PVP scaffold with 50/50 polymer ratio was found at 105.4 ± 8.4 MPa which is six times higher comparing to those of PCL scaffold. PVP-containing scaffolds were extremely hydrophilic with PVP concentration of 5 wt% (vs. 25 wt% in previous reports) leading to full wetting of the material. in vitro studies showed an improved viability of HeLa cells cultured with the composites containing higher concentrations of PVP. Owing to the application of HFIP, PCL-based materials were loaded with cyclophosphamide for the first time and the PVP-containing materials demonstrated the intensified initial release of the model compound. Utilizing HFIP for the fabrication of PCL/PVP scaffolds significantly widens their application for drug delivery systems due to a good solubility of proteins, drugs, and other biologically active compounds in this solvent.
AB - Poly(ε-caprolactone)/polyvinylpyrrolidone (PCL/PVP) scaffolds with various composition were fabricated from 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) solution using the same electrospinning parameters in order to reveal the effect of polymer ratio on the material properties. The obtained materials were characterized using scanning electron microscopy, contact angle measurements, X-ray diffraction, Fourier-transformed infrared spectroscopy, and tensile testing. The strengthening effect of PVP was observed: Young modulus of PCL/PVP scaffold with 50/50 polymer ratio was found at 105.4 ± 8.4 MPa which is six times higher comparing to those of PCL scaffold. PVP-containing scaffolds were extremely hydrophilic with PVP concentration of 5 wt% (vs. 25 wt% in previous reports) leading to full wetting of the material. in vitro studies showed an improved viability of HeLa cells cultured with the composites containing higher concentrations of PVP. Owing to the application of HFIP, PCL-based materials were loaded with cyclophosphamide for the first time and the PVP-containing materials demonstrated the intensified initial release of the model compound. Utilizing HFIP for the fabrication of PCL/PVP scaffolds significantly widens their application for drug delivery systems due to a good solubility of proteins, drugs, and other biologically active compounds in this solvent.
KW - biodegradable polymers
KW - controllable release
KW - drug delivery
KW - electrospinning
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U2 - 10.1002/app.50535
DO - 10.1002/app.50535
M3 - Article
AN - SCOPUS:85100496197
JO - Journal of Applied Polymer Science
JF - Journal of Applied Polymer Science
SN - 0021-8995
ER -