Affiliations 

  • 1 Department of Biological Sciences, National University of Medical Sciences (NUMS), Rawalpindi 46000, Pakistan; School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia Nibong Tebal, Engineering Campus, 14300, Pulau Penang, Malaysia
  • 2 Department of Chemistry, Shaheed Benazir Bhutto Women University, Charsadda road Larama, 25000 Peshawar, Pakistan
  • 3 Department of Biological Sciences, National University of Medical Sciences (NUMS), Rawalpindi 46000, Pakistan
  • 4 Institute of Chemical Sciences, University of Peshawar, Pakistan
  • 5 Department of Chemistry, College of Science and Humanities, Prince Sattam bin Abdulaziz University, 16278 Al-Kharj, Saudi Arabia. Electronic address: drisraf@yahoo.com
  • 6 Department of Chemistry, College of Science and Humanities, Prince Sattam bin Abdulaziz University, 16278 Al-Kharj, Saudi Arabia
  • 7 Department of Clinical Pharmacy, college of pharmacy, Prince Sattam bin Abdulaziz University, 16278 Al-Kharj, Saudi Arabia
  • 8 Chemistry Department, Kohat University of Science and Technology Kohat, Pakistan
Int J Biol Macromol, 2023 Jan 05;230:123131.
PMID: 36610570 DOI: 10.1016/j.ijbiomac.2022.123131

Abstract

3-D Bioprinting is employed as a novel approach in biofabrication to promote skin regeneration following chronic-wounds and injury. A novel bioink composed of carbohydrazide crosslinked {polyethylene oxide-co- Chitosan-co- poly(methylmethacrylic-acid)} (PEO-CS-PMMA) laden with Nicotinamide and human dermal fibroblast was successfully synthesized via Free radical-copolymerization at 73 °C. The developed bioink was characterized in term of swelling, structural-confirmation by solid state 13C-Nuclear Magnetic Resonance (NMR), morphology, thermal, 3-D Bioprinting via extrusion, rheological and interaction with DNA respectively. The predominant rate of gelation was attributed to the electrostatic interactions between cationic CS and anionic PMMA pendant groups. The morphology of developed bioink presented a porous architecture satisfying the cell and growth-factor viability across the barrier. The thermal analysis revealed two-step degradation with 85 % weight loss in term of decomposition and molecular changes in the bioink moieties By applying low pressure in the range of 25-50 kPa, the optimum reproducibility and printability were determined at 37 °C in the viscosity range of 500-550 Pa. s. A higher survival rate of 92 % was observed for (PEO-CS-PMMA) in comparison to 67 % for pure chitosan built bioink. A binding constant of K ≈ 1.8 × 106 M-1 recognized a thermodynamically stable interaction of (PEO-CS-PMMA) with the Salmon-DNA. Further, the addition of PEO (5.0 %) was addressed with better self-healing and printability to produce skin-tissue constructs to replace the infected skin in human.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.