TY - JOUR
T1 - Toughening mechanisms for the attachment of architectured materials
T2 - The mechanics of the tendon enthesis
AU - Golman, Mikhail
AU - Abraham, Adam C.
AU - Kurtaliaj, Iden
AU - Marshall, Brittany P.
AU - Hu, Yizhong Jenny
AU - Schwartz, Andrea G.
AU - Edward Guo, X.
AU - Birman, Victor
AU - Thurner, Philipp J.
AU - Genin, Guy M.
AU - Thomopoulos, Stavros
N1 - Publisher Copyright:
Copyright © 2021 The Authors, some rights reserved.
PY - 2021/11
Y1 - 2021/11
N2 - Architectured materials offer tailored mechanical properties but are limited in engineering applications due to challenges in maintaining toughness across their attachments. The enthesis connects tendon and bone, two vastly different architectured materials, and exhibits toughness across a wide range of loadings. Understanding the mechanisms by which this is achieved could inform the development of engineered attachments. Integrating experiments, simulations, and previously unexplored imaging that enabled simultaneous observation of mineralized and unmineralized tissues, we identified putative mechanisms of enthesis toughening in a mouse model and then manipulated these mechanisms via in vivo control of mineralization and architecture. Imaging uncovered a fibrous architecture within the enthesis that controls trade-offs between strength and toughness. In vivo models of pathology revealed architectural adaptations that optimize these trade-offs through cross-scale mechanisms including nanoscale protein denaturation, milliscale load-sharing, and macroscale energy absorption. Results suggest strategies for optimizing architecture for tough bimaterial attachments in medicine and engineering.
AB - Architectured materials offer tailored mechanical properties but are limited in engineering applications due to challenges in maintaining toughness across their attachments. The enthesis connects tendon and bone, two vastly different architectured materials, and exhibits toughness across a wide range of loadings. Understanding the mechanisms by which this is achieved could inform the development of engineered attachments. Integrating experiments, simulations, and previously unexplored imaging that enabled simultaneous observation of mineralized and unmineralized tissues, we identified putative mechanisms of enthesis toughening in a mouse model and then manipulated these mechanisms via in vivo control of mineralization and architecture. Imaging uncovered a fibrous architecture within the enthesis that controls trade-offs between strength and toughness. In vivo models of pathology revealed architectural adaptations that optimize these trade-offs through cross-scale mechanisms including nanoscale protein denaturation, milliscale load-sharing, and macroscale energy absorption. Results suggest strategies for optimizing architecture for tough bimaterial attachments in medicine and engineering.
UR - http://www.scopus.com/inward/record.url?scp=85120384044&partnerID=8YFLogxK
U2 - 10.1126/sciadv.abi5584
DO - 10.1126/sciadv.abi5584
M3 - Article
C2 - 34826240
AN - SCOPUS:85120384044
SN - 2375-2548
VL - 7
JO - Science Advances
JF - Science Advances
IS - 48
M1 - eabi5584
ER -