TY - JOUR
T1 - Strong and tough mineralized PLGA nanofibers for tendon-to-bone scaffolds
AU - Kolluru, Pavan V.
AU - Lipner, Justin
AU - Liu, Wenying
AU - Xia, Younan
AU - Thomopoulos, Stavros
AU - Genin, Guy M.
AU - Chasiotis, Ioannis
N1 - Funding Information:
The study was supported by the National Science Foundation (PECASE 0748120 to I.C. and CAREER 844607 to S.T.) and the National Institutes of Health ( R01 AR060820 to Y.X. and S.T.).
PY - 2013/12
Y1 - 2013/12
N2 - Engineering complex tissues such as the tendon-to-bone insertion sites require a strong and tough biomimetic material system that incorporates both mineralized and unmineralized tissues with different strengths and stiffnesses. However, increasing strength without degrading toughness is a fundamental challenge in materials science. Here, we demonstrate a promising nanofibrous polymer-hydroxyapatite system, in which, a continuous fibrous network must function as a scaffold for both mineralized and unmineralized tissues. It is shown that the high toughness of this material system could be maintained without compromising on the strength with the addition of hydroxyapatite mineral. Individual electrospun poly (lactide-co-glycolide) (PLGA) nanofibers demonstrated outstanding strain-hardening behavior and ductility when stretched uniaxially, even in the presence of surface mineralization. This highly desirable hardening behavior which results in simultaneous nanofiber strengthening and toughening was shown to depend on the initial cross-sectional morphology of the PLGA nanofibers. For pristine PLGA nanofibers, it was shown that ellipsoidal cross-sections provide the largest increase in fiber strength by almost 200% compared to bulk PLGA. This exceptional strength accompanied by 100% elongation was shown to be retained for thin and strongly bonded conformal mineral coatings, which were preserved on the nanofiber surface even for such very large extensions.
AB - Engineering complex tissues such as the tendon-to-bone insertion sites require a strong and tough biomimetic material system that incorporates both mineralized and unmineralized tissues with different strengths and stiffnesses. However, increasing strength without degrading toughness is a fundamental challenge in materials science. Here, we demonstrate a promising nanofibrous polymer-hydroxyapatite system, in which, a continuous fibrous network must function as a scaffold for both mineralized and unmineralized tissues. It is shown that the high toughness of this material system could be maintained without compromising on the strength with the addition of hydroxyapatite mineral. Individual electrospun poly (lactide-co-glycolide) (PLGA) nanofibers demonstrated outstanding strain-hardening behavior and ductility when stretched uniaxially, even in the presence of surface mineralization. This highly desirable hardening behavior which results in simultaneous nanofiber strengthening and toughening was shown to depend on the initial cross-sectional morphology of the PLGA nanofibers. For pristine PLGA nanofibers, it was shown that ellipsoidal cross-sections provide the largest increase in fiber strength by almost 200% compared to bulk PLGA. This exceptional strength accompanied by 100% elongation was shown to be retained for thin and strongly bonded conformal mineral coatings, which were preserved on the nanofiber surface even for such very large extensions.
KW - Bone
KW - Electrospinning, mechanical properties
KW - Tendon-to-bone insertion
KW - Tissue engineering
UR - https://www.scopus.com/pages/publications/84887136746
U2 - 10.1016/j.actbio.2013.07.042
DO - 10.1016/j.actbio.2013.07.042
M3 - Article
C2 - 23933048
AN - SCOPUS:84887136746
SN - 1742-7061
VL - 9
SP - 9442
EP - 9450
JO - Acta Biomaterialia
JF - Acta Biomaterialia
IS - 12
ER -