Abstract
Ultrathin electrospun nanofibrous membranes (NfMs) based on poly(γ-benzyl-L-glutamate) (PBLG) were prepared. Scanning electron microscopy analysis revealed the production of a high-quality, bead-free nanofibrous membrane. The membrane thicknesses, ranging from 1.7 to 4.5μm, were found to correlate directly with membrane porosity. Raman scattering analysis was utilized to investigate the conformation of the PBLG nanofibrous membrane and to assess the effects of addition of 1 wt. % trifluoroacetic acid (TFA) into the PBLG solutions, as well as the impact of annealing at 70 °C. In addition, x-ray photoelectron spectroscopy (XPS) characterization was performed to elucidate the chemical composition of the PBLG nanofibrous membrane. The Raman and Fourier-transform infrared spectroscopy spectra indicated the characteristic α-helical conformation in both the PBLG solution and the PBLG nanofibrous membrane. Furthermore, a comparative analysis of Raman band profiles proved the absence of TFA after annealing, supporting the hypothesis of TFA evaporation post-annealing, which was subsequently confirmed by the XPS results. In addition, the results from the small punch test revealed a significant correlation between membrane thickness and stiffness, indicating that increased thickness enhances stiffness. This comprehensive study provides valuable insights into the structural and compositional properties of PBLG NfMs, laying the groundwork for future investigations into their potential applications in the field of tissue engineering.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
