Tunability of collagen matrix mechanical properties via multiple modes of mineralization
Author(s) -
Lester J. Smith,
Alix Deymier,
John J. Boyle,
Zhen Li,
Stephen W. Linderman,
Jill Dill Pasteris,
Younan Xia,
Guy M. Genin,
Stavros Thomopoulos
Publication year - 2015
Publication title -
interface focus
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.1
H-Index - 49
eISSN - 2042-8901
pISSN - 2042-8898
DOI - 10.1098/rsfs.2015.0070
Subject(s) - mineralization (soil science) , soft tissue , extracellular matrix , mineralized tissues , collagen fibril , tendon , chemistry , scaffold , biomedical engineering , stiffness , bone matrix , type i collagen , fetuin , toughness , materials science , biophysics , composite material , anatomy , biochemistry , pathology , glycoprotein , dentin , biology , endocrinology , engineering , medicine , cartilage , organic chemistry , nitrogen
Functionally graded, mineralized collagen tissues exist at soft-to-hard material attachments throughout the body. However, the details of how collagen and hydroxyapatite mineral (HA) interact are not fully understood, hampering efforts to develop tissue-engineered constructs that can assist with repair of injuries at the attachments of soft tissues to bone. In this study, spatial control of mineralization was achieved in collagen matrices using simulated body fluids (SBFs). Based upon previous observations of poor bonding between reconstituted collagen and HA deposited using SBF, we hypothesized that mineralizing collagen in the presence of fetuin (which inhibits surface mineralization) would lead to more mineral deposition within the scaffold and therefore a greater increase in stiffness and toughness compared with collagen mineralized without fetuin. We tested this hypothesis through integrated synthesis, mechanical testing and modelling of graded, mineralized reconstituted collagen constructs. Results supported the hypothesis, and further suggested that mineralization on the interior of reconstituted collagen constructs, as promoted by fetuin, led to superior bonding between HA and collagen. The results provide us guidance for the development of mineralized collagen scaffolds, with implications for bone and tendon-to-bone tissue engineering.
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