Faculty Opinions recommendation of Acute Ultraviolet Radiation Perturbs Epithelialization but not the Biomechanical Strength of Full-thickness Cutaneous Wounds.

Author(s):  
Robert Knobler
2016 ◽  
Vol 92 (1) ◽  
pp. 187-192 ◽  
Author(s):  
Patricia L. Danielsen ◽  
Catharina M. Lerche ◽  
Hans Christian Wulf ◽  
Lars N. Jorgensen ◽  
Ann-Sofie H. Liedberg ◽  
...  

2013 ◽  
Vol 38 (2) ◽  
pp. 178-184 ◽  
Author(s):  
S. Sadigh-Eteghad ◽  
A. Dehnad ◽  
J. Mahmodi ◽  
H. Hoseyni ◽  
I. Khalili ◽  
...  

2021 ◽  
Vol 8 (6) ◽  
Author(s):  
Yangkun Liu ◽  
JinChuan Fan ◽  
MingQi Lv ◽  
Kepeng She ◽  
Jiale Sun ◽  
...  

Abstract Damage to the skin causes physiological and functional issues. The most effective treatment approach is the use of wound dressings. Silk fibroin (SF) is a promising candidate biomaterial for regulating wound healing; however, its antibacterial properties and biological activity must be further improved. In this study, a photocrosslinking hydrogel was developed to treat full-thickness cutaneous wounds. The composite hydrogel (Ag–AV–SF hydrogel) was prepared by introducing the silver nanoparticles (AgNPs) and aloe vera (AV) as the modifiers. In vitro study exhibited great antibacterial ability, biocompatibility and cell-proliferation and -migration-promoting capacities. It also showed the pH-response releasing properties which release more AgNPs in a simulated chronic infection environment. The healing effect evaluation in vivo showed the healing-promoting ability of the Ag–AV–SF hydrogel was stronger than the single-modifiers groups, and the healing rate of it reached 97.02% on Day 21, higher than the commercial wound dressing, silver sulfadiazine (SS) cream on sale. Additionally, the histological and protein expression results showed that the Ag–AV–SF hydrogel has a greater effect on the pro-healing regenerative phenotype with M2 macrophages at the early stage, reconstructing the blood vessels networks and inhibiting the formation of scars. In summary, the Ag–AV–SF hydrogel developed in this study had good physical properties, overwhelming antibacterial properties, satisfactory biocompatibility and significantly promoting effect on cell proliferation, migration and wound healing. Overall, our results suggest that the Ag–AV–SF hydrogel we developed has great potential for improving the wound healing in clinical treatment.


Cureus ◽  
2017 ◽  
Author(s):  
Matthew R MacEwan ◽  
Sarah MacEwan ◽  
Anna P Wright ◽  
Tamas R Kovacs ◽  
Joel Batts ◽  
...  

2013 ◽  
Vol 5 (6) ◽  
pp. 233-239 ◽  
Author(s):  
A.H. AL-Bayati ◽  
R.N. Al-Asadi ◽  
A.K. Mahdi ◽  
N.H. Al-Falahi

2016 ◽  
Vol 2016 ◽  
pp. 1-11
Author(s):  
Yssel Mendoza Marí ◽  
Maday Fernández Mayola ◽  
Ana Aguilera Barreto ◽  
Ariana García Ojalvo ◽  
Yilian Bermúdez Alvarez ◽  
...  

In addition to its cytoprotective effects, growth hormone-releasing peptide 6 (GHRP-6) proved to reduce liver fibrotic induration. CD36 as one of the GHRP-6 receptors appears abundantly represented in cutaneous wounds granulation tissue. The healing response in a scenario of CD36 agonistic stimulation had not been previously investigated. Excisional full-thickness wounds (6 mmØ) were created in the dorsum of Wistar rats and topically treated twice a day for 5 days. The universal model of rabbit’s ears hypertrophic scars was implemented and the animals were treated daily for 30 days. Treatments for both species were based on a CMC jelly composition containing GHRP-6 400 μg/mL. Wounds response characterization included closure dynamic, RT-PCR transcriptional profile, histology, and histomorphometric procedures. The rats experiment indicated that GHRP-6 pharmacodynamics involves attenuation of immunoinflammatory mediators, their effector cells, and the reduction of the expression of fibrotic cytokines. Importantly, in the hypertrophic scars rabbit’s model, GHRP-6 intervention dramatically reduced the onset of exuberant scars by activating PPARγ and reducing the expression of fibrogenic cytokines. GHRP-6 showed no effect on the reversion of consolidated lesions. This evidence supports the notion that CD36 is an active and pharmacologically approachable receptor to attenuate wound inflammation and accelerate its closure so as to improve wound esthetic.


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