Nanofibers made by blending natural and synthetic biopolymers have shown promise for better mechanical stability, ECM morphology mimicry, and cellular interaction of such materials. With the evolution of production methods of nanofibers, alternating field electrospinning (a.k.a. alternating current (AC) electrospinning) demonstrates a strong potential for scalable and sustainable fabrication of nanofibrous materials. This study focuses on AC‐electrospinning of poorly miscible blends of gelatin from cold water fish skin (FGEL) and polycaprolactone (PCL) in a range of FGEL/PCL mass ratios from 0.9:0.1 to 0.4:0.6 in acetic acid single‐solvent system. The nanofiber productivity rates of 7.8–19.0 g/h were obtained using a single 25 mm diameter dish‐like spinneret, depending on the precursor composition. The resulting nanofibrous meshes had 94%–96% porosity and revealed the nanofibers with 200–750 nm diameters and smooth surface morphology. The results of FTIR, XRD, and water contact angle analyses have shown the effect of FGEL/PCL mass ratio on the changes in the material wettability, PCL crystallinity and orientation of PCL crystalline regions, and secondary structure of FGEL in as‐spun and thermally crosslinked materials. Preliminary in vitro tests with 3 T3 mouse fibroblasts confirmed favorable and tunable cell attachment, proliferation, and spreading on all tested FGEL/PCL nanofibrous meshes.
With the increasing interest in biopolymer nanofibers for diverse applications, the characterization of these materials in the physiological environment has become of equal interest and importance. This study performs first‐time simulated body fluid (SBF) degradation and tensile mechanical analyses of blended fish gelatin (FGEL) and polycaprolactone (PCL) nanofibrous meshes prepared by a high‐throughput free‐surface alternating field electrospinning. The thermally crosslinked FGEL/PCL nanofibrous materials with 84–96% porosity and up to 60 wt% PCL fraction demonstrate mass retention up to 88.4% after 14 days in SBF. The trends in the PCL crystallinity and FGEL secondary structure modification during the SBF degradation are analyzed by Fourier transform infrared spectroscopy. Tensile tests of such porous, 0.1–2.2 mm thick FGEL/PCL nanofibrous meshes in SBF reveal the ultimate tensile strength, Young's modulus, and elongation at break within the ranges of 60–105 kPa, 0.3–1.6 MPa, and 20–70%, respectively, depending on the FGEL/PCL mass ratio. The results demonstrate that FGEL/PCL nanofibrous materials prepared from poorly miscible FGEL and PCL can be suitable for selected biomedical applications such as scaffolds for skin, cranial cruciate ligament, articular cartilage, or vascular tissue repair.
more » « less- Award ID(s):
- 1852207
- NSF-PAR ID:
- 10441876
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Macromolecular Materials and Engineering
- Volume:
- 308
- Issue:
- 10
- ISSN:
- 1438-7492
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Blended nanofibrous biomaterials from natural and synthetic sources show promise for better biointegration. This study explores high-yield alternating field electrospinning (AFES) of blended cold-water fish skin gelatin (FGEL) and polycaprolactone (PCL) nanofibrous meshes with up to 30 wt% PCL at 7.8–14.4 g/h fiber productivity, depending on the composition. FGEL/PCL nanofibers reveal smooth surface morphology and 237–313 nm average diameters after thermal crosslinking. FTIR analysis indicated little FGEL/PCL interaction and notable changes in PCL crystallinity in the crosslinked nanofibers. A 14-days in-vitro analysis shows good cellular viability and nanofibrous FGEL/PCL mesh stability. Results demonstrate that AFES provides efficient, scalable production of blended FGEL/PCL nanofibrous biomaterials with suitable characteristics.more » « less
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