TY - JOUR
T1 - A hydrogen generator composed of poly (lactic-co-glycolic acid) nanofibre membrane loaded iron nanoparticles for infectious diabetic wound repair
AU - Zhang, Xiangqi
AU - Yu, Wei
AU - Zhang, Yihui
AU - Zhang, Wenkai
AU - Wang, Jiayu
AU - Gu, Muge
AU - Cheng, Sulin
AU - Ren, Guogang
AU - Zhao, Bo
AU - Yuan, Wei En
N1 - © 2024 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2024/5/31
Y1 - 2024/5/31
N2 - Diabetic wound, which is chronic skin disease, poses a significant challenge in clinical practice because of persistent inflammation and impaired angiogenesis. Recently, hydrogen has emerged as a novel therapeutic agent due to its superior antioxidant and anti-inflammatory properties. In this study, we engineered a poly (lactic-co-glycolic acid) (PLGA) electrospun nanofibre membrane loaded with citric acid (CA) and iron (Fe) nanoparticles, referred to as Fe@PLGA + CA. Our in vitro assays demonstrated that the Fe@PLGA + CA membrane continuously generated and released hydrogen molecules via a chemical reaction between Fe and CA in an acidic microenvironment created by CA. We also discovered that hydrogen can ameliorate fibroblast migration disorders by reducing the levels of matrix metalloproteinase 9 (MMP9). Furthermore, we confirmed that hydrogen can scavenge or biochemically neutralise accumulated reactive oxygen species (ROS), inhibit pro-inflammatory responses, and induce anti-inflammatory reactions. This, in turn, promotes vessel formation, wound-healing and accelerates skin regeneration. These findings open new possibilities for using elemental iron in skin dressings and bring us one step closer to implementing hydrogen-releasing biomedical materials in clinical practice.
AB - Diabetic wound, which is chronic skin disease, poses a significant challenge in clinical practice because of persistent inflammation and impaired angiogenesis. Recently, hydrogen has emerged as a novel therapeutic agent due to its superior antioxidant and anti-inflammatory properties. In this study, we engineered a poly (lactic-co-glycolic acid) (PLGA) electrospun nanofibre membrane loaded with citric acid (CA) and iron (Fe) nanoparticles, referred to as Fe@PLGA + CA. Our in vitro assays demonstrated that the Fe@PLGA + CA membrane continuously generated and released hydrogen molecules via a chemical reaction between Fe and CA in an acidic microenvironment created by CA. We also discovered that hydrogen can ameliorate fibroblast migration disorders by reducing the levels of matrix metalloproteinase 9 (MMP9). Furthermore, we confirmed that hydrogen can scavenge or biochemically neutralise accumulated reactive oxygen species (ROS), inhibit pro-inflammatory responses, and induce anti-inflammatory reactions. This, in turn, promotes vessel formation, wound-healing and accelerates skin regeneration. These findings open new possibilities for using elemental iron in skin dressings and bring us one step closer to implementing hydrogen-releasing biomedical materials in clinical practice.
KW - Anti-inflammation
KW - Diabetic wound
KW - Hydrogen
KW - Iron
KW - MMP-9
KW - Reactive oxygen species
KW - Skin dressing
UR - http://www.scopus.com/inward/record.url?scp=85195077354&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2024.05.222
DO - 10.1016/j.jcis.2024.05.222
M3 - Article
AN - SCOPUS:85195077354
SN - 0021-9797
VL - 672
SP - 266
EP - 278
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -