AI Article Synopsis

  • Maxillofacial bone defects can be treated using autografting or synthetic materials, with electrospun nanobiomaterials gaining traction due to their ease of use.
  • A study tested a new cotton-like fiber made from β-TCP and PLLA/PGA in a rat model to evaluate its effectiveness in bone regeneration.
  • Results showed that both β-TCP/PLLA/PGA and β-TCP promoted similar bone regeneration, but β-TCP/PLLA/PGA had higher osteogenic cell accumulation and better biomarker expression, suggesting it is a promising option for treating maxillofacial bone defects.

Article Abstract

Maxillofacial bone defects are treated by autografting or filling with synthetic materials in various forms and shapes. Electrospun nanobiomaterials are becoming popular due to their easy placement and handling; combining ideal biomaterials extrapolates better outcomes. We used a novel electrospun cotton-like fiber made from two time-tested bioresorbable materials, β-TCP and PLLA/PGA, to check the feasibility of its application to maxillofacial bone defects through an in vivo rat mandibular bone defect model. Novel β-TCP/PLLA/PGA and pure β-TCP blocks were evaluated for new bone regeneration through assessment of bone volume, inner defect diameter reduction, and bone mineral density. Bioactive/osteoconductivity was checked by scoring the levels of Runt-related transcription factor x, Leptin Receptor, Osteocalcin, and Periostin biomarkers. Bone regeneration in both β-TCP/PLLA/PGA and β-TCP was comparable at initial timepoints. Osteogenic cell accumulation was greater in β-TCP/PLLA/PGA than in β-TCP at initial as well as late phases. Periostin expression was more marked in β-TCP/PLLA/PGA. This study demonstrated comparable results between β-TCP/PLLA/PGA and β-TCP in terms of bone regeneration and bioactivity, even with a small material volume of β-TCP/PLLA/PGA and a decreased percentage of β-TCP. Electrospun β-TCP/PLLA/PGA is an ideal nanobiomaterial for inducing bone regeneration through osteoconductivity and bioresorbability in bony defects of the maxillofacial region.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10780666PMC
http://dx.doi.org/10.3390/nano14010091DOI Listing

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