TY - JOUR
T1 - Multifunctional Mesoporous Calcium-Aluminosilicate Nanoparticles Enable Heterogeneous Activation of Endogenous Transforming Growth Factor β1 and Rapid Hemostasis for Bone Repair
AU - Xu, Chun
AU - Chen, Qingxuan
AU - Chen, Hang
AU - Xu, Aoni
AU - Wen, Juan
AU - Li, Yiwei
AU - Dai, Huan
AU - Liu, Siyuan
AU - Cheng, Dan
AU - Song, Yaping
AU - Sun, Bing
AU - Tang, Jie
AU - Fan, Jie
AU - Lei, Chang
AU - Yu, Chengzhong
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/9/15
Y1 - 2026/9/15
N2 - The development of multifunctional biomaterials capable of simultaneously activating endogenous growth factors, promoting rapid hemostasis, and enhancing bone regeneration remains a significant challenge in regenerative medicine. Here, we report a rationally designed calcium-aluminosilicate dendritic mesoporous silica nanoparticle (CaAl-DMSN) that integrates heterogeneous catalytic growth factor activation with pro-coagulant and osteogenic functionalities in a single nanoscale platform. Featuring a four-coordinate aluminosilicate framework functionalized with calcium in a radial large-pore architecture, CaAl-DMSN generates a nanoconfined alkaline microenvironment via Ca2+ mediated hydroxide enrichment. This enables more than an order-of-magnitude higher activation efficiency of latent Transforming Growth Factor β1 (TGF-β1) compared to conventional homogeneous alkaline catalysis. Molecular dynamics simulations reveal a markedly reduced free-energy barrier for TGF-β1 dissociation, establishing a direct structure–function relationship between composition, nanostructure, and catalytic activity. Functionally, CaAl-DMSN induces rapid clot formation, enhances CD105+ CD73+ mesenchymal stromal cell recruitment, and promotes osteogenic differentiation via Smad signaling activation. In a rat critical-size calvarial defect model, CaAl-DMSN increases bone volume fraction by 80% compared with controls, while exhibiting excellent biocompatibility. Collectively, CaAl-DMSN couples interfacial chemistry, endogenous growth factor activation, hemostasis, and regenerative microenvironment modulation, offering a growth factor-free strategy for bone repair and broader tissue regeneration applications.
AB - The development of multifunctional biomaterials capable of simultaneously activating endogenous growth factors, promoting rapid hemostasis, and enhancing bone regeneration remains a significant challenge in regenerative medicine. Here, we report a rationally designed calcium-aluminosilicate dendritic mesoporous silica nanoparticle (CaAl-DMSN) that integrates heterogeneous catalytic growth factor activation with pro-coagulant and osteogenic functionalities in a single nanoscale platform. Featuring a four-coordinate aluminosilicate framework functionalized with calcium in a radial large-pore architecture, CaAl-DMSN generates a nanoconfined alkaline microenvironment via Ca2+ mediated hydroxide enrichment. This enables more than an order-of-magnitude higher activation efficiency of latent Transforming Growth Factor β1 (TGF-β1) compared to conventional homogeneous alkaline catalysis. Molecular dynamics simulations reveal a markedly reduced free-energy barrier for TGF-β1 dissociation, establishing a direct structure–function relationship between composition, nanostructure, and catalytic activity. Functionally, CaAl-DMSN induces rapid clot formation, enhances CD105+ CD73+ mesenchymal stromal cell recruitment, and promotes osteogenic differentiation via Smad signaling activation. In a rat critical-size calvarial defect model, CaAl-DMSN increases bone volume fraction by 80% compared with controls, while exhibiting excellent biocompatibility. Collectively, CaAl-DMSN couples interfacial chemistry, endogenous growth factor activation, hemostasis, and regenerative microenvironment modulation, offering a growth factor-free strategy for bone repair and broader tissue regeneration applications.
KW - alkaline activation
KW - bone repair
KW - heterogeneous catalysis
KW - nanomaterials
KW - stem cell recruitment
UR - https://www.scopus.com/pages/publications/105051074383
U2 - 10.1021/acsnano.6c05126
DO - 10.1021/acsnano.6c05126
M3 - 文章
AN - SCOPUS:105051074383
SN - 1936-0851
VL - 20
SP - 24656
EP - 24670
JO - ACS Nano
JF - ACS Nano
IS - 36
ER -