{"title":"Topical application of lyophilized and powdered human amniotic membrane promotes diabetic ulcer healing","authors":"Anna Rodella , Michela Pozzobon , Matteo Rigon , Cinzia Franchin , Giorgio Arrigoni , Manuela Simonato , Emiliano Ghinelli , Luca Vedovelli","doi":"10.1016/j.wndm.2019.100171","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Amniotic membrane has been widely used in the treatment of several acute and chronic diseases, and surgical reconstructions. Here we report the successful application of a commercial lyophilized, powdered, amniotic membrane (AMX) to a patient with a treatment-refractory diabetic ulcer, with further investigations on AMX angiogenic and anti-inflammatory properties.</p></div><div><h3>Objective</h3><p>To investigate the topical, continuous, treatment with AMX on a chronic diabetic foot ulcer, along with its angiogenic <em>in vitro</em> properties and proteomic profile.</p></div><div><h3>Methods</h3><p>A 77-year old woman was treated with AMX 2–3 drops 4–6 times a day for 2 months. Amniotic fluid stem cells were tested for proliferation and angiogenesis potential with or without AMX. ELISA quantification was conducted on NGF, TGF-alpha, NT-3, and IL1-ra. Proteomic analysis was also performed on AMX.</p></div><div><h3>Results</h3><p>At 2-month follow-up, the ulcer was reduced by 60% and it remained steady after 3-months. At 4-month follow-up, the lesion showed signs of re-epithelization. Cells, with or without AMX, were prone to form endothelial tubules with similar characteristics. Proteomic analysis confirmed that AMX retains proteins involved in anti-inflammatory and angiogenesis pathways.</p></div><div><h3>Conclusions</h3><p>AMX ameliorated pain and extent of a chronic diabetic ulcer. The effect could be ascribed to angiogenesis and epithelium stimulation that was confirmed in <em>in vitro</em>. Multiple wound healing-involved proteins were detected but further studies are needed to assess their specific role.</p></div>","PeriodicalId":38278,"journal":{"name":"Wound Medicine","volume":"27 1","pages":"Article 100171"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.wndm.2019.100171","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Wound Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213909518300272","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 2
Abstract
Background
Amniotic membrane has been widely used in the treatment of several acute and chronic diseases, and surgical reconstructions. Here we report the successful application of a commercial lyophilized, powdered, amniotic membrane (AMX) to a patient with a treatment-refractory diabetic ulcer, with further investigations on AMX angiogenic and anti-inflammatory properties.
Objective
To investigate the topical, continuous, treatment with AMX on a chronic diabetic foot ulcer, along with its angiogenic in vitro properties and proteomic profile.
Methods
A 77-year old woman was treated with AMX 2–3 drops 4–6 times a day for 2 months. Amniotic fluid stem cells were tested for proliferation and angiogenesis potential with or without AMX. ELISA quantification was conducted on NGF, TGF-alpha, NT-3, and IL1-ra. Proteomic analysis was also performed on AMX.
Results
At 2-month follow-up, the ulcer was reduced by 60% and it remained steady after 3-months. At 4-month follow-up, the lesion showed signs of re-epithelization. Cells, with or without AMX, were prone to form endothelial tubules with similar characteristics. Proteomic analysis confirmed that AMX retains proteins involved in anti-inflammatory and angiogenesis pathways.
Conclusions
AMX ameliorated pain and extent of a chronic diabetic ulcer. The effect could be ascribed to angiogenesis and epithelium stimulation that was confirmed in in vitro. Multiple wound healing-involved proteins were detected but further studies are needed to assess their specific role.