AI Article Synopsis

  • - The study develops polyvinyl alcohol-chitosan-loaded oleanolic acid nanofibers (PVA-CS-OLA-NFs) aimed at treating bacterial infections, with detailed characterization methods including SEM and FTIR revealing their consistent structure and effective drug loading.
  • - In vitro tests show that these nanofibers have a drug release rate of about 51.82% over 24 hours and are non-hemolytic, indicating they don't damage human blood cells.
  • - The PVA-CS-OLA-NFs exhibit strong antibacterial activity against S. aureus, promote enhanced wound healing compared to existing treatments, and their effectiveness is monitored via advanced imaging techniques that assess blood flow and oxygen levels.

Article Abstract

The present work focuses on the fabrication of polyvinyl alcohol-chitosan-loaded oleanolic acid-nanofibers (PVA-CS-OLA-NFs) for bacterial infection. The prepared PVA-CS-OLA-NFs were characterized for contact angle, SEM, AFM, XRD, FTIR, and TGA. The solid-state characterization and in vitro performance evaluation of nanofibers reveal consistent interconnection and diameters ranging from 102 ± 9.5 to 386 ± 11.6 nm. The nanofibers have a flat surface topography and exhibit efficient drug entrapment. Moreover, the in vitro release profile of PVA-CS-OLA-NFs was found to be 51.82 ± 1.49 % at 24 h. Furthermore, the hemocompatibility study showed that the developed PVA-CS-OLA-NFs are non-hemolytic to human blood. The PVA-CS-OLA-NFs demonstrate remarkable antibacterial capabilities, as evidenced by their MBC and MIC values, which range from 128 and 32 μg/mL, against the strains of S. aureus. The in-vivo fluorescence optical imaging showed the sustained PVA-CS-OLA-NFs release at the wound site infected with S. aureus for a longer duration of time. Moreover, the PVA-CS-OLA-NFs showed superior wound healing performance against S. aureus infected wounds compared to the marketed formulation. Further, the laser Doppler imaging system improved oxygen saturation, blood supply, and wound healing by providing real-time blood flow and oxygen saturation information.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2024.135532DOI Listing

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