Sep 2026· International Journal of Nanomedicine· Vol 21, pp. 1-22· 0 citations· 153 references
Medicine
TL;DR
This review underscores smart nanomaterial reservoirs for bone regeneration, focusing on their capacity to remodel the hostile microenvironment and restore immune homeostasis by reprogramming intercellular communication and promoting M1-to-M2 macrophage polarization.
Abstract
Abstract Bone defects remain challenging due to microenvironment disruption and immune imbalance. Traditional grafts offer structural support; however, they do not actively modulate this pathological niche. This review underscores smart nanomaterial reservoirs for bone regeneration, focusing on their capacity to remodel the hostile microenvironment and restore immune homeostasis. Key pathophysiological barriers, including vascular disruption, macrophage imbalance, and oxidative stress-induced ferroptosis, are identified as therapeutic targets. Additionally, fundamental nanoscale building blocks (rigid inorganic, polymeric, and inorganic piezoelectric materials) are critically compared, with an expanded focus on emerging technologies such as versatile nanofibers and 3D-printable bio-ink formulations. These components can be assembled into smart reservoirs (hydrogels, exosomes, and 3D scaffolds), enabling stimuli-responsive therapeutic delivery (pH, reactive oxygen species, and enzymes). By reprogramming intercellular communication and promoting M1-to-M2 macrophage polarization, these reservoirs restore osteoimmune homeostasis and couple osteogenesis with angiogenesis. Finally, translational challenges and future directions toward dynamically adaptive nanomedicines are discussed.
The rapid evolution of smart biomaterials has opened new therapeutic avenues for complex bone defects, non-union fractures, and post-tumor resection reconstruction. Conventional bone substitutes often suffer from insufficient bioactivity, mechanical mismatch, and a lack of capacity to modulate the healing microenvironm...
Jin-Di Han, Bao-Jian Zhang, Jin-Yang Du et al.· Journal of Visualized Experi...· 0 citations
Complex bone defects caused by trauma, infection, tumor-related bone loss and metabolic disorders remain clinically challenging because an inflammatory imbalance, impaired vascularization and insufficient osteogenesis often coexist. Gelatin methacryloyl (GelMA) hydrogels are attractive matrices for bone regeneration ow...
Li Chen, Jing-Yao Tan, Mao-Lin Li et al.· Frontiers in Bioengineering...· 0 citations
Wound healing is a tightly orchestrated sequence of hemostatic, inflammatory, proliferative, and remodeling events, yet chronic wounds arise when this cascade is dysregulated by persistent infection, excessive oxidative stress, and biofilm formation. Such pathological conditions particularly in diabetic and vascular-co...
M. B. Habib, Laiba Arshad, Muhammad Kamran et al.· RSC Advances· 0 citations
Infected bone defects are not simply bone defects complicated by bacterial infection; they are dynamic pathological niches in which biofilms, intracellular bacterial persistence, oxidative stress, dysregulated immunity, vascular failure, and pathological bone remodeling are mutually reinforcing. This coupling explains...
Yuan-Hong Li, Zi-Yi Xu, Yue Wang et al.· Advanced Healthcare Material...· 0 citations
Abstract Large segmental bone defects resulting from trauma, tumor resection, infection, or congenital abnormalities often exceed the innate regenerative capacity of bone, necessitating effective therapeutic strategies. Conventional treatments, such as autografts and allografts, are associated with significant limitati...
G. Sabarees, Sivakumar Kanmani, S. Kowsalya et al.· International Journal of Pol...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.