Alveolar Bone Preservation Using a Combination of Nanocrystalline Hydroxyapatite and Injectable Platelet-Rich Fibrin: A Study in Rats

被引:1
|
作者
Pascawinata, Andries [1 ]
Revilla, Gusti [2 ]
Sahputra, Roni Eka [3 ]
Arief, Syukri [4 ]
机构
[1] Andalas Univ, Fac Med, Padang 25163, Indonesia
[2] Andalas Univ, Fac Med, Dept Anat, Padang 25163, Indonesia
[3] Andalas Univ, Fac Med, Dept Surg, Orthopaed Div, Padang 25163, Indonesia
[4] Andalas Univ, Fac Math & Nat Sci, Dept Chem, Padang 25163, Indonesia
关键词
nanocrystalline hydroxyapatite; injectable platelet-rich fibrin; TRAP; ALP; OCN; new bone; post-extraction healing;
D O I
10.3390/cimb45070377
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alveolar bone resorption is a post-extraction complication wherein there is a reduction in the dimensions and quality of the alveolar bone. This study aimed to examine the effects of implantation of a combination of nanocrystalline hydroxyapatite (nHA) and injectable platelet-rich fibrin (IPRF) on the expression of tartrate-resistant acid phosphatase (TRAP), alkaline phosphatase (ALP), osteocalcin (OCN), and new bone formation. A total of 32 male rats had their upper right incisors extracted under general anesthesia and were then divided into a control group, nHA group, IPRF group, and nHA-IPRF group. Decapitation was carried out on day 14 and day 28 in each group and the jaws of each rat were subjected to immunohistochemical and histological analysis. The results showed a decrease in TRAP expression in the nHA-IPRF group compared with the control group on day 14 (p = 0.074) and day 28 (p = 0.017). The study also showed an increase in ALP and OCN in the HA-IPRF group on day 14 and day 28 compared with the control group. New bone formation suggested a significant increase in the nHA-IPRF group compared with the control group on day 14 (p = 0.001) and day 28 (p = 0.001). nHA-IPRF implantation can suppress alveolar bone resorption, which is indicated by decreased TRAP expression, and it can increase bone growth, as indicated by increased expression of ALP, OCN, and new bone formation.
引用
收藏
页码:5967 / 5980
页数:14
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