Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 156685 - 156685
Опубликована: Окт. 1, 2024
Язык: Английский
Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 156685 - 156685
Опубликована: Окт. 1, 2024
Язык: Английский
Journal of Nanobiotechnology, Год журнала: 2025, Номер 23(1)
Опубликована: Апрель 7, 2025
In the field of large-area trauma flap transplantation, preventing avascular necrosis remains a critical challenge. Key mechanisms for improving viability include angiogenesis promotion, oxidative stress inhibition, and cell death prevention. Recently, two-dimensional ultrathin Ti3C2TX (MXene) nanosheets have gained attention their potential contributions to these processes, though MXene's physiological impact on survival had not been previously investigated. This study is first confirm biological effects ischaemic microenvironment post-skin transplantation. Findings indicated that MXene significantly decreased necrotic area in flaps (37.96% ± 2.00%), with reductions 30.40% 1.86% at 1 mg/mL 20.19% 2.11% 2 concentration-dependent manner. Mechanistically, facilitated situ angiogenesis, mitigated stress, suppressed pro-inflammatory pyroptosis, activated PI3K-Akt pathway, particularly influencing vascular endothelial cells. Comparative transcriptome analysis skin tissues without treatment provided additional evidence, highlighting such as ROS metabolic proliferation regulation, signaling pathway activation. Overall, demonstrated activity, effectively promoting presenting novel strategy addressing flaps.
Язык: Английский
Процитировано
0ACS Biomaterials Science & Engineering, Год журнала: 2025, Номер unknown
Опубликована: Апрель 15, 2025
Backgrounds: The buildup of reactive oxygen species (ROS) in infected wounds triggers an excessive inflammatory response, while the overuse antibiotics has contributed to increased bacterial resistance. Therefore, developing wound dressings that effectively eliminate ROS and inhibit growth is crucial. Methods: Inspired by mussel-derived proteins, we developed a polydopamine (PDA)-grafted MXene (PDA@MXene) 3,4-dihydroxyphenylalanine-PonG1 (DOPA-PonG1)-modified photosensitive poly(vinyl alcohol) (PVA) hydrogel as dressing. PDA@MXene was synthesized through dopamine self-polymerization on surface, tyrosine hydroxylation used introduce DOPA into antibacterial peptide ponericin G1 (PonG1). its components were characterized, their morphology examined. hydrogel's hemostatic ability, mechanical properties, conductivity evaluated. In vitro studies systematically evaluated antioxidative effects, activity, biocompatibility, expression tissue regeneration-related factors. An full-thickness skin defect model established vivo, different treatments applied. wound-healing rate then measured, followed histological analysis using hematoxylin eosin, Masson, Sirius Red, immunofluorescence staining investigate healing mechanism. Results: sequence enhanced PonG1 stability leading sustained ability. significantly improved strength. Notably, combined effects DOPA-PonG1 ROS-scavenging properties. vivo findings demonstrated DOPA-PonG1/PDA@MXene/PVA accelerated promoting angiogenesis collagen deposition reducing inflammation. This study presents innovative approach for treating defects holds promise clinical applications.
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 163026 - 163026
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0Journal of Controlled Release, Год журнала: 2024, Номер 377, С. 37 - 53
Опубликована: Ноя. 17, 2024
Язык: Английский
Процитировано
3Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 156685 - 156685
Опубликована: Окт. 1, 2024
Язык: Английский
Процитировано
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