The Effect of Whitlockite as an Osteoconductive Synthetic Bone Substitute Material in Animal Bony Defect Model

This study aimed to evaluate the biomechanical properties in vitro and the bone regeneration of whitlockite (WH) compared with hydroxyapatite (HA) or β-tricalcium phosphate (β-TCP)-based material. We investigated the morphology and phase composition of the bone grafts using a scanning electron microscope and X-ray diffractometer patterns and tested the compressive strength. Four circular defects of 8 mm in diameter were created on the calvaria of twelve rabbits. One defect was left empty, and each of the other defects was filled with WH, HA, and β-TCP. At 4 and 8 weeks, the specimens were harvested to evaluate for the new bone formation and the remaining bone grafts. Regarding the biomechanical properties, the three grafts had a similar micropore size, and WH showed nanopores. The compressive strength of WH was higher than HA and β-TCP without statistical significance. The radiological and histomorphometric analyses demonstrated that the new bone formation was similar among the groups. The remaining bone graft of the WH group was greater than that of the HA and β-TCP groups at 4 weeks (p < 0.05), and the total bone area of the WH, HA, and β-TCP groups was greater than that of the other (p < 0.01). WH has excellent volumetric stability and osteoconductivity compared with HA and β-TCP.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:15

Enthalten in:

Materials (Basel, Switzerland) - 15(2022), 5 vom: 04. März

Sprache:

Englisch

Beteiligte Personen:

Ku, Jeong-Kui [VerfasserIn]
Kim, Il-Hyung [VerfasserIn]
Shim, Jung Hee [VerfasserIn]
Kim, Yu Ha [VerfasserIn]
Kim, Baek Hyun [VerfasserIn]
Kim, Young-Kyun [VerfasserIn]
Yun, Pil-Young [VerfasserIn]

Links:

Volltext

Themen:

Beta-tricalcium phosphate
Biphasic calcium phosphate
Hydroxyapatite
Journal Article
Whitlockite

Anmerkungen:

Date Revised 08.03.2023

published: Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.3390/ma15051921

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM33800002X