Composites Part B Engineering, Год журнала: 2024, Номер 291, С. 111976 - 111976
Опубликована: Ноя. 16, 2024
Язык: Английский
Composites Part B Engineering, Год журнала: 2024, Номер 291, С. 111976 - 111976
Опубликована: Ноя. 16, 2024
Язык: Английский
Composites Part B Engineering, Год журнала: 2025, Номер unknown, С. 112163 - 112163
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
1Composites Part B Engineering, Год журнала: 2025, Номер unknown, С. 112192 - 112192
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
1Composites Part B Engineering, Год журнала: 2024, Номер 291, С. 111970 - 111970
Опубликована: Ноя. 12, 2024
Язык: Английский
Процитировано
5Composites Part B Engineering, Год журнала: 2024, Номер 280, С. 111481 - 111481
Опубликована: Апрель 24, 2024
With the increasing incidence of osteoarthritis (OA) in elderly patients and challenges posed by its multifaceted pathogenesis developing effective treatments, this study explores protein loading mode Progranulin (PGRN) therapeutic potential for treating OA. GelMA hydrogels prepared with different concentrations PGRN, employing AC-PEG-NHS as a crosslinking agent drug encapsulation, were used to test sustained release effect composite hydrogel delivery system. Additionally, we conducted vitro assays investigate regulatory effects on rat bone marrow mesenchymal atromal cells (BMSCs), chondrocytes, mouse macrophages - focusing cell proliferation, differentiation. For vivo studies, histological staining techniques utilized assess inflammatory polarization cartilage repair knee injury model. The results demonstrated that PGRN-loaded significantly accelerated enhance differentiation BMSCs into maintained healthy chondrocyte phenotype, induce M2-type while inhibiting M1-type macrophages. Histological analyses also showed markedly improved tissue group treated GelMA–NHS–PGRN hydrogels. As result, these present promising approach OA, potentially mitigating chronic inflammation facilitating through controlled PGRN. Osteoarthritis, Anti-inflammatory hydrogels, Cartilage regeneration.
Язык: Английский
Процитировано
4Materials Today Bio, Год журнала: 2025, Номер 31, С. 101494 - 101494
Опубликована: Янв. 13, 2025
Osteochondral defects are still facing a significant challenge in clinical surgery, making post-trauma repair difficult. Tissue engineering has provided promising approach to solving these defects. However, existing scaffolds cannot replicate the complex biphasic cartilage-bone microenvironment with accuracy. We aimed develop biomimetic scaffold regionally regulated vascularization that promoted chondrogenesis and osteogenesis through bidirectional regulation of endochondral ossification. This consisted pre-chondrogenic microspheres (PCMs) decalcified bone frame prepared by decalcifying cartilage layer varying degrees. Incorporation PCMs into created regeneration while axitinib was modified inhibit enhance regeneration. The ossification facilitated repair. In vitro studies have shown axitinib-modified layers significantly VEGF expression cells, powder from promotes PCMs. vivo experiments indicated this controls regionalized angiogenesis, promoting integrated reconstruction osteochondral rabbit knee joints. These results suggest our designed demineralized can precisely engineer microenvironment, providing theoretical guidance for anisotropic tissue injuries.
Язык: Английский
Процитировано
0Biomaterials Science, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Cartilage tissue engineering based on the combination of biomaterials, adult or stem cells and bioactive factors is a challenging approach for regenerative medicine with aim achieving formation functional neotissue stable in long term. Various 3D scaffolds have been developed to mimic extracellular matrix environment promote cartilage repair. In addition, extensively employed induce maintain phenotype. However, spatiotemporal control factor release remains critical maximizing potential multipotent cells, such as mesenchymal stromal (MSCs), efficient chondrogenesis sustained homeostasis, which are essential repair hyaline cartilage. Despite advances, effective delivery limited by challenges insufficient retention at site injury loss therapeutic efficacy due uncontrolled drug release. These limitations prompted research biomolecule-scaffold interactions develop advanced systems that provide controlled bioavailability biological factors, thereby improving outcomes. This review focuses specifically biomaterials (natural, hybrid synthetic) biomolecules (molecules, proteins, nucleic acids) interest engineering. Herein, we detail approaches their release, chemical nature structure, through steric, non-covalent and/or covalent interactions, view application
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 162441 - 162441
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0Composites Part B Engineering, Год журнала: 2024, Номер 291, С. 111976 - 111976
Опубликована: Ноя. 16, 2024
Язык: Английский
Процитировано
2