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AuthorSarrigiannidis S.O.
AuthorMoussa H.
AuthorDobre O.
AuthorDalby M.J.
AuthorTamimi F.
AuthorSalmeron-Sanchez M.
Available date2022-05-31T19:01:23Z
Publication Date2020
Publication NameACS Applied Bio Materials
ResourceScopus
Identifierhttp://dx.doi.org/10.1021/acsabm.0c00555
URIhttp://hdl.handle.net/10576/31835
AbstractBrushite cements are promising bone regeneration materials with limited biological and mechanical properties. Here, we engineer a mechanically improved brushite-collagen type I cement with enhanced biological properties by use of chiral chemistry; d- A nd l-tartaric acid were used to limit crystal growth and increase the mechanical properties of brushite-collagen cements. The impact of the chiral molecules on the cements was examined with Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM). A 3-point bend test was utilized to study the fracture toughness, and cell attachment and morphology studies were carried out to demonstrate biocompatibility. XRD and SEM analyses showed that l-, but not d-tartaric acid, significantly restrained brushite crystal growth by binding to the {010} plane of the mineral and increased brushite crystal packing and the collagen interaction area. l-Tartaric acid significantly improved fracture toughness compared to traditional brushite by 30%. Collagen significantly enhanced cell morphology and focal adhesion expression on l-tartaric acid-treated brushite cements.
Languageen
PublisherAmerican Chemical Society
SubjectBiocompatibility
Biomechanics
Bone
Bone cement
Collagen
Crystal growth
Crystallization
Fourier transform infrared spectroscopy
Morphology
Scanning electron microscopy
Stereochemistry
Tissue regeneration
X ray diffraction
Biological properties
Bone regeneration materials
Cell attachments
Chiral chemistry
Collagen type I
Crystal packings
Interaction area
L-tartaric acids
Fracture toughness
TitleChiral Tartaric Acid Improves Fracture Toughness of Bioactive Brushite-Collagen Bone Cements
TypeArticle
Pagination5056-5066
Issue Number8
Volume Number3
dc.accessType Abstract Only


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