Bioactive peptide amphiphile nanofiber gels enhance burn wound healing. Issue 5 (August 2019)

• Record Type: Journal Article
• Authors: Zhou, Situo; Hokugo, Akishige; McClendon, Mark; Zhang, Zheyu; Bakshi, Reena; Wang, Lixin; Segovia, Luis Andres; Rezzadeh, Kameron; Stupp, Samuel I.; Jarrahy, Reza
• Is Part Of: Burns. Volume 45:Issue 5(2019)
• Page Start: 1112
• Page End: 1121
• Publication Date: 2019-08
• Subjects: Self-assembly -- Peptide amphiphile -- Nanofiber -- Thermally damaged cells -- Wound healing; Burns and scalds -- Periodicals; 617.11
• DOI: 10.1016/j.burns.2018.06.008
• Languages: English
• ISSNs: 0305-4179

Abstract

Highlights: This study investigates a novel bioactive nanofiber-based hydrogel biomaterial that can accelerate burn wound healing. Bioactive RGDS modified peptide amphiphilic gels stimulate cell proliferation of thermally damaged cells. The application of RGDS modified peptide amphiphilic gels accelerates the recovery of deep partial thickness burn wounds. Abstract: Background: Burns are physically debilitating and potentially fatal injuries. The standard-of-care for burn wounds is the coverage with gauze dressings designed to minimize trauma to the regenerating epidermis and dermis during dressing changes. However, deep partial- and full-thickness burns always heal slowly when standard wound care alone is performed. We have previously reported that peptide amphiphile (PA) gels, pH-induced self-assembling nanostructured fibrous scaffolds, promote cell proliferation and have great potential in regenerative medicine for rapid repair of tissues. In this study, we hypothesized that the PA gels are capable of accelerating wound healing in burn injury. Methods: Artificially generated thermally damaged fibroblasts and human umbilical vein endothelial cells were seeded onto the various PA nanofiber gels including bioactive and nonbioactive peptide sequences. Cell proliferation was assessed at different time points, and thermally damaged fibroblasts and HUVECs manifested increased proliferation with time when cultured with various PA gels. To determine in vivo effects, burn wounds of rats were treated with the bioactive Arg-Gly-Asp-Ser (RGDS)-modified gel that showed greater cell proliferation in vitro . The wound closure was observed, and skin samples were harvested for histologic evaluation. Results: Cell proliferation using the RGDS-PA gel was significantly higher than that observed in other gels. The RGDS-PA gel significantly enhanced re-epithelialization during the burn wound healing process between days 7 and 28. Application of PA gels accelerates the recovery of deep partial-thickness burn wounds by stimulation of fibroblasts and the creation of an environment conducive to epithelial cell proliferation and wound closure. Conclusions: This biomaterial represents a new therapeutic strategy to overcome current clinical challenges in the treatment of injuries resulting from burns.