TY - JOUR
T1 - Development of low-cost bacterial cellulose-pomegranate peel extract-based antibacterial composite for potential biomedical applications
AU - Ul-Islam, Mazhar
AU - Alhajaim, Wafa
AU - Fatima, Atiya
AU - Yasir, Sumayia
AU - Kamal, Tahseen
AU - Abbas, Yawar
AU - Khan, Shaukat
AU - Khan, Abdul Hakim
AU - Manan, Sehrish
AU - Ullah, Muhammad Wajid
AU - Yang, Guang
N1 - Funding Information:
This research work was funded by Institutional Fund Projects under grant no. IFPIP: 1660-961-1443 . The authors gratefully acknowledge the technical and financial support provided by the Ministry of Education and King Abdulaziz University , DSR, Jeddah, Saudi Arabia.
Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/3/15
Y1 - 2023/3/15
N2 - This study was aimed to develop low-cost bacterial cellulose (BC)-based antibacterial composite with pomegranate (Punica granatum L.) peel extract (PGPE) for potential biomedical applications. BC was cost-effectively produced by utilizing food wastes, and PGPE was ex situ impregnated into its hydrogel. Field-emission scanning electron microscopic (FE-SEM) observation showed a nanofibrous and microporous morphology of pristine BC and confirmed the development of BC-PGPE composite. Fourier transform infrared (FTIR) spectroscopy indicated the chemical interaction of PGPE with BC nanofibers. BC-PGPE composite held 97 % water of its dry weight and retained it for more than 48 h. The BC-PGPE composite exhibited better reswelling capabilities than pristine BC after three consecutive re-wetting cycles. The antibacterial activity of the BC-PGPE composite was determined via minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), disc diffusion, and plate count methods. The PGPE extract showed good antimicrobial activity against Staphylococcus aureus (Gram-positive) and Escherichia coli (Gram-negative), both in the form of extract and composite with BC, with relatively better activity against the former. The BC-PGPE composite produced a 17 mm zone of inhibition against S. aureus, while no inhibition zone was formed against E. coli. Furthermore, BC-PGPE composite caused a 100 % and 50 % reduction in the growth of S. aureus and E. coli, respectively. The findings of this study indicate that BC-PGPE composite could be a promising antibacterial wound dressing material.
AB - This study was aimed to develop low-cost bacterial cellulose (BC)-based antibacterial composite with pomegranate (Punica granatum L.) peel extract (PGPE) for potential biomedical applications. BC was cost-effectively produced by utilizing food wastes, and PGPE was ex situ impregnated into its hydrogel. Field-emission scanning electron microscopic (FE-SEM) observation showed a nanofibrous and microporous morphology of pristine BC and confirmed the development of BC-PGPE composite. Fourier transform infrared (FTIR) spectroscopy indicated the chemical interaction of PGPE with BC nanofibers. BC-PGPE composite held 97 % water of its dry weight and retained it for more than 48 h. The BC-PGPE composite exhibited better reswelling capabilities than pristine BC after three consecutive re-wetting cycles. The antibacterial activity of the BC-PGPE composite was determined via minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), disc diffusion, and plate count methods. The PGPE extract showed good antimicrobial activity against Staphylococcus aureus (Gram-positive) and Escherichia coli (Gram-negative), both in the form of extract and composite with BC, with relatively better activity against the former. The BC-PGPE composite produced a 17 mm zone of inhibition against S. aureus, while no inhibition zone was formed against E. coli. Furthermore, BC-PGPE composite caused a 100 % and 50 % reduction in the growth of S. aureus and E. coli, respectively. The findings of this study indicate that BC-PGPE composite could be a promising antibacterial wound dressing material.
KW - Antimicrobial activity
KW - Bacterial cellulose
KW - BC-PEPG composite
KW - Pomegranate peel extract
UR - http://www.scopus.com/inward/record.url?scp=85146692163&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2023.123269
DO - 10.1016/j.ijbiomac.2023.123269
M3 - Article
C2 - 36649873
AN - SCOPUS:85146692163
SN - 0141-8130
VL - 231
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
M1 - 123269
ER -