Personalised burn treatment: bedside electrospun nanofibre scaffold with cultured autologous keratinocytes: a case study

Author:

Segni Ayelet Di1,BenShoshan Marina1,Harats Moti2345,Melnikov Nir1,Barzilay Claudia M6,Dothan Daniel1,Liaani Adi1,Kornhaber Rachel27,Haik Josef12345

Affiliation:

1. The Green Skin Engineering Center, National Burn Center, Sheba Medical Center, Tel Hashomer, Israel

2. National Burn Center, Sheba Medical Center, Tel Hashomer, Israel

3. Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel

4. University of Notre Dame Australia, Fremantle, Western Australia, Australia

5. Talpiot Leadership Program, Sheba Medical Center, Tel Hashomer, Israel

6. Nanomedic Technologies Ltd. Lod, Israel

7. School of Nursing, Paramedicine and Healthcare Sciences, Charles Sturt University, NSW, Australia

Abstract

Nearly four decades after cultured epidermal autografts (CEA) were first used for the treatment of extensive burn wounds, the current gold standard treatment remains grafting healthy autologous skin from a donor site to the damaged areas, with current skin substitutes limited in their clinical use. We propose a novel treatment approach, using an electrospun polymer nanofibrous matrix (EPNM) applied on-site directly on the CEA-grafted areas. In addition, we propose a personalised treatment on hard-to-heal areas, in which we spray suspended autologous keratinocytes integrated with 3D EPNM applied on-site, directly onto the wound bed. This method enables the coverage of larger wound areas than possible with CEA. We present the case of a 26-year-old male patient with full-thickness burns covering 98% of his total body surface area (TBSA). We were able to show that this treatment approach resulted in good re-epithelialisation, seen as early as seven days post CEA grafting, with complete wound closure within three weeks, and to a lesser extent in areas treated with cell spraying. Moreover, in vitro experiments confirmed the feasibility of using keratinocytes embedded within the EPNM: cell and culture viability, identity, purity and potency were determined. These experiments show that the skin cells are viable and can proliferate within the EPNM. The results presented are of a promising novel strategy for the development of personalised wound treatment, integrating on-the-spot ‘printed’ EPNM with autologous skin cells, which will be applied at the bedside, over deep dermal wounds, to accelerate healing time and wound closure.

Publisher

Mark Allen Group

Subject

Nursing (miscellaneous),Fundamentals and skills

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