3D scaffold induces efficient bone repair: in vivo studies of ultra-structural architecture at the interface. Issue 96 (30th September 2016)

• Record Type: Journal Article
• Authors: Sagar, Nitin; Singh, Atul Kumar; Temgire, Mayur K.; Vijayalakshmi, S.; Dhawan, Alok; Kumar, Ashutosh; Chattopadhyay, Naibedya; Bellare, Jayesh R.
• Is Part Of: RSC advances. Volume 6:Issue 96(2016)
• Page Start: 93768
• Page End: 93776
• Publication Date: 2016-09-30
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra20420a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Biodegradable designer 3D scaffold bridges critical size defect and induces new bone formation as revealed by ssNMR, SEM, EDX and μ-CT in rabbit tibial model during healing. No growth factor was needed due to chemical and microstructural cues. Abstract : The repair of critical bone loss remains a challenge to orthopaedic surgeons. Various artificial scaffolds have been intensively evaluated to provide an alternative solution for the repair and regeneration of bone defects; however, the inconsistent clinical performances of available materials have prompted the development of reactive 3D scaffolds for bone tissue engineering. We have studied the ability of a functionally designed 3D scaffold to bridge critical size defects and induce new bone formation in a New Zealand white rabbit tibial model, and have evaluated its ultra-structural properties using a combination of techniques, such as solid-state nuclear magnetic resonance (ssNMR), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) and micro-computed tomography (μ-CT) with MIMICS® (Materialise's Interactive Medical Image Control System). ssNMR showed the structural similarity of the synthetic biomaterial to naturally occurring human bone. SEM studies showed an increase in Ca/P ratio with time, the progressively uniform distribution of elements in healed bones, and increased new bone formation, finally resembling native (intact) bone. μ-CT and MIMICS® demonstrated the pattern and morphology of new bone formed, with a noticeable shift in the HU unit towards compact bone, from week 2 to 25. The results suggest that in the critical size bone defect, the scaffold enhanced the formation of new bone having biomaterial composition, ultra-structure and quality resembling that of native bone, thus suggesting significant improvement in guided bone regeneration. This research provides a promising new avenue for orthopaedic implant design that safely biodegrades while promoting new bone growth.