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The Effect of Rainbow Trout (Oncorhynchus mykiss) Collagen Incorporated with Exo-Polysaccharides Derived from Rhodotorula mucilaginosa sp. on Burn Healing.

Tayyeb GhadimiSoheila Naderi GharahgheshlaghNoorahmad LatifiAhmad HivechiVahid Hosseinpour SarmadiSiamak Farokh ForghaniNaser AminiPeiman B MilanFatemeh LatifiMasoud HamidiGhazaleh LarijaniSeyed Mohammad Amin HaramshahiMotahareh AbdollahiFatemeh GhadimiSaeed Nezari
Published in: Macromolecular bioscience (2023)
Burn is one of the physically debilitating injuries that can be potentially fatal; therefore, providing appropriate coverage in order to reduce possible mortality risk and accelerate wound healing is mandatory. In this study, collagen/exo-polysaccharide (Col/EPS 1-3%) scaffolds are synthesized from rainbow trout (Oncorhynchus mykiss) skins incorporated with Rhodotorula mucilaginosa sp. GUMS16, respectively, for promoting Grade 3 burn wound healing. Physicochemical characterizations and, consequently, biological properties of the Col/EPS scaffolds are tested. The results show that the presence of EPS does not affect the minimum porosity dimensions, while raising the EPS amount significantly reduces the maximum porosity dimensions. Thermogravimetric analysis (TGA), FTIR, and tensile property results confirm the successful incorporation of the EPS into Col scaffolds. Furthermore,the biological results show that the increasing EPS does not affect Col biodegradability and cell viability, and the use of Col/EPS 1% on rat models displays a faster healing rate. Finally, histopathological examination reveals that the Col/EPS 1% treatment accelerates wound healing, through greater re-epithelialization and dermal remodeling, more abundant fibroblast cells and Col accumulation. These findings suggest that Col/EPS 1% promotes dermal wound healing via antioxidant and anti-inflammatory activities, which can be a potential medical process in the treatment of burn wounds.
Keyphrases
  • wound healing
  • anti inflammatory
  • healthcare
  • tissue engineering
  • induced apoptosis
  • cell proliferation
  • endoplasmic reticulum stress
  • cell cycle arrest
  • replacement therapy