期刊
JOURNAL OF DENTAL RESEARCH
卷 90, 期 1, 页码 82-87出版社
SAGE PUBLICATIONS INC
DOI: 10.1177/0022034510385241
关键词
biomimetic; biomineralization; chemical phosphorylation; collagen; specific binding
资金
- NIDCR [R21 DE019213]
- NATIONAL INSTITUTE OF DENTAL &CRANIOFACIAL RESEARCH [R21DE019213] Funding Source: NIH RePORTER
Inability of chemical phosphorylation of sodium trimetaphosphate to induce intrafibrillar mineralization of type I collagen may be due to the failure to incorporate a biomimetic analog to stabilize amorphous calcium phosphates (ACP) as nanoprecursors. This study investigated adsorption/desorption characteristics of hydrolyzed and pH-adjusted sodium trimetaphosphate (HPA-Na3P3O9) to collagen. Based on those results, a 5-minute treatment time with 2.8 wt% HPA-Na3P3O9 was used in a single-layer reconstituted collagen model to confirm that both the ACP-stabilization analog and matrix phosphoprotein analog must be present for intrafibrillar mineralization. The results of that model were further validated by complete remineralization of phosphoric-acid-etched dentin treated with the matrix phosphoprotein analog and lined with a remineralizing lining composite, and with the ACP-stabilization analog supplied in simulated body fluid. An understanding of the basic processes involved in intrafibrillar mineralization of reconstituted collagen fibrils facilitates the design of novel tissue engineering materials for hard tissue repair and regeneration.
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