Inflammatory inert poly(ethylene glycol)–protein wound dressing improves healing responses in partial‐ and full‐thickness wounds

In this study, a novel soft hydrogel system based on the poly(ethylene glycol)–protein conjugates was evaluated as an occlusive wound dressing material. The hydrogel material, referred by the name of BioAquacare™, contains up to 96% of the liquid and is formulated with phosphate‐buffered saline and safe preservative to control bacterial load in the open wounds. Performance of the BioAquacare™ as a wound dressing material was assessed in partial‐ and full‐thickness wounds in pigs. Wound analysis comprised macroscopic determination of the wound size, histological examination of the healing tissues and biochemical characterisation of wound exudates. The wounds treated with BioAquacare™ healed without any signs of inflammation, skin irritation, oedema or erythema. Cellular composition of the reepithelialised wounds was very similar to that of the normal skin, with a well‐developed stratum corneum and epithelial layer. It was observed that BioAquacare™ plays the role of a liquid compartment, which provides pronounced hydration effect and helps maintain a natural moist environment of the healing tissues. BioAquacare™ showed relatively low protein‐absorbing activity, absorbing predominantly low‐molecular‐weight molecules, including interleukin (IL)‐1β, IL‐6, transforming growth factor‐β1 and products of haemoglobin degradation. It is concluded that application of the moist BioAquacare™ dressing promotes fast reepithelialisation by creating favourable environment for keratinocytes proliferation and it also reduces scarring. The results show that BioAquacare™ can be considered as a safe, biocompatible and inflammatory inert wound dressing material.

[1]  M. Faure,et al.  Structure-property relationships in poly(ethylene glycol)-protein hydrogel systems made from various proteins. , 2005, Biomacromolecules.

[2]  L. Manfield,et al.  Modulation of Macrophage Phenotype by Soluble Product(s) Released from Neutrophils1 , 2005, The Journal of Immunology.

[3]  T. Ohshima,et al.  The dynamics of inflammatory cytokines in the healing process of mouse skin wound: A preliminary study for possible wound age determination , 2005, International Journal of Legal Medicine.

[4]  M. Ishii,et al.  Superiority of water application to water sealing in burn wound healing. , 2004, Osaka city medical journal.

[5]  S. Werner,et al.  Regulation of wound healing by growth factors and cytokines. , 2003, Physiological reviews.

[6]  N. Mukaida,et al.  Accelerated wound healing in tumor necrosis factor receptor p55‐deficient mice with reduced leukocyte infiltration , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[7]  W. Eaglstein,et al.  THE PIG AS A MODEL FOR HUMAN WOUND HEALING , 2001, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[8]  W. Eaglstein,et al.  Moist Wound Healing with Occlusive Dressings: A Clinical Focus , 2001, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

[9]  M. Stacey,et al.  Mitogenic activity and cytokine levels in non‐healing and healing chronic leg ulcers , 2001, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[10]  M. Luster,et al.  Impaired cutaneous wound healing in interleukin‐6‐deficient and immunosuppressed mice , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[11]  T. Crombleholme,et al.  Diminished interleukin 6 (IL-6) production during scarless human fetal wound repair. , 2000, Cytokine.

[12]  V. Ivanov,et al.  Proteolytic degradation of hemoglobin in vivo. Role in formation of tissue specific peptide pool , 1998 .

[13]  Paul Martin,et al.  Wound Healing--Aiming for Perfect Skin Regeneration , 1997, Science.

[14]  N. Dagouassat,et al.  Generation of VV‐hemorphin‐7 from globin by peritoneal macrophages , 1996, FEBS letters.

[15]  S. Gordon,et al.  Macrophage recruitment during limb development and wound healing in the embryonic and foetal mouse. , 1994, Journal of cell science.

[16]  T. Chvapil,et al.  Inert wound dressing is not desirable. , 1991, The Journal of surgical research.

[17]  M. Mitchell,et al.  Production of Interleukin-6 by Fetal and Maternal Cells in Vivo during Intraamniotic Infection and in Vitro after Stimulation with Interleukin-1 , 1991, Pediatric Research.

[18]  W. Eaglstein,et al.  Interleukin-1 enhances epidermal wound healing. , 1990, Lymphokine research.

[19]  W. Eaglstein,et al.  "Inert" vehicles do affect wound healing. , 1980, The Journal of investigative dermatology.

[20]  I. A. Holder,et al.  Control of surface wound infection: skin versus synthetic grafts. , 1973, Applied microbiology.

[21]  C. O. Heocha The formation of bile pigments. , 1968, Biochemical Society Symposium.

[22]  G. Winter,et al.  Formation of the Scab and the Rate of Epithelization of Superficial Wounds in the Skin of the Young Domestic Pig , 1962, Nature.

[23]  Rich Ar THE FORMATION OF BILE PIGMENT , 1925 .