Abstract

Age and diabetes related slow-healing or chronic wounds may result in morbidity and mortality through persistent biofilms infections and prolonged inflammatory phase. Nano-materials [metal/metal oxide NPs (39%), lipid vehicles (21%), polymer NPs (19%), ceramic nanoparticles (NPs) (14%), and carbon nanomaterials (NMs) (7%)] can be introduced as a possible next-generation therapy because of either their intrinsic wound healing activity or via carrying bioactive compounds including, antibiotics, antioxidants, growth factor or stem cell. The nanomaterials have been shown to implicate in all four stages of wound healing including hemostasis (polymer NPs, ceramic NPs, nanoceria-6.1%), inflammation (liposome/vesicles/solid lipid NPs/polymer NPs/ceramic NPs/silver NPs/gold NPs/nanoceria/fullerenes/carbon-based NPs-32.7%), proliferation (vesicles/liposome/solid lipid NPs/gold NPs/silver NPs/iron oxide NPs/ceramic NPs/copper NPs/self-assembling elastin-like NPs/nanoceria/micelle/dendrimers/polymer NPs-57.1%), remodeling (iron oxide NPs/nanoceria-4.1%). Natural compounds from alkaloids, flavonoids, retinoids, volatile oil, terpenes, carotenoids, or polyphenolic compounds with proven antioxidant, anti-inflammatory, immunomodulatory, or antimicrobial characteristics are also well known for their potential to accelerate the wound healing process. In the current paper, we survey the potential and properties of nanomaterials and microbial compounds in improving the process of wound and scar healing. Finally, we review the potential biocompounds for incorporation to nano-material in perspective to designate more effective or multivalent wound healing natural or nano-based drugs.

Highlights

  • Wounding disrupts the typical structure and function of the tissues and causes hemorrhage, vessel contraction via blood coagulation, activation of complement, and inflammation (Robson et al, 2001)

  • If healing processes is compromised or cannot be completed in the organized normal healing process, the postponed wound repairing or hard to heal chronic wound may occur owing to extension or discontinuation of each phase, which leads to chronic wounds (Szycher and Lee, 1992; Robson et al, 2001)

  • The interaction of these cells with each other and extracellular matrix (ECM) are tightly controlled by some bioactive molecules and mediators such as the interleukin family, multiple growth factors, chemokines, and cytokines specified for every phase

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Summary

Nanomaterials Versus The Microbial Compounds With Wound Healing Property

Reviewed by: Mubarak A Mujawar, Florida International University, United States Yiqun Zhou, University of Miami, United States Alina Maria Holban, University of Bucharest, Romania. Nanomaterials [metal/metal oxide NPs (39%), lipid vehicles (21%), polymer NPs (19%), ceramic nanoparticles (NPs) (14%), and carbon nanomaterials (NMs) (7%)] can be introduced as a possible next-generation therapy because of either their intrinsic wound healing activity or via carrying bioactive compounds including, antibiotics, antioxidants, growth factor or stem cell. Natural compounds from alkaloids, flavonoids, retinoids, volatile oil, terpenes, carotenoids, or polyphenolic compounds with proven antioxidant, anti-inflammatory, immunomodulatory, or antimicrobial characteristics are well known for their potential to accelerate the wound healing process. We survey the potential and properties of nanomaterials and microbial compounds in improving the process of wound and scar healing. We review the potential biocompounds for incorporation to nano-material in perspective to designate more effective or multivalent wound healing natural or nano-based drugs

INTRODUCTION
TYPES OF WOUNDS
SKIN WOUND HEALING PROCESS
Hemostatic Events
Proliferative Stage
Current Wound Repair Regimes
INVOLVED TARGETS IN THE WOUND HEALING PROCESS
WOUND HEALING USING MICROORGANISMS
Wound healing model in diabetic mice model
NANOMATERIAL AND WOUND HEALING
Zn SODs in the wound area
Proliferation and inflammation phases All phases
In vitro egg yolk angiogenesis and endothelial cell migration assay
Nanoparticles loaded by opioids
Inflammatory and proliferation phases
Leads to better drug release in wound sites
In vivo model of dorsal skin wound repair
Nanofiber Graft copolymer
Hemostasis phase Hemostasis phase Hemostasis phase Not reported
In vitro blood clotting test using rabbit blood
BIOCOMPOUNDS INCORPORATED INTO NANOMATERIALS FOR WOUND HEALING
Findings
FUTURE PERSPECTIVE

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