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富血小板纤维蛋白、富血小板纤维蛋白+50wt%纳米羟基磷灰石、富血小板纤维蛋白+50wt%牙本质碎屑的射线不透性和细胞毒性的比较评估:一项研究。

Comparative evaluation of radiopacity and cytotoxicity of platelet-rich fibrin, platelet-rich fibrin + 50wt% nano-hydroxyapatite, platelet-rich fibrin + 50wt% dentin chips: An study.

作者信息

Mahendran Kavitha, Kottuppallil Girija, Sekar Velayudham

机构信息

Department of Conservative Dentistry Endodontics, Tamil Nadu Government Dental College and Hospital, Tamil Nadu Dr. M. G. R. Medical University, Chennai, Tamil Nadu, India.

出版信息

J Conserv Dent. 2019 Jan-Feb;22(1):28-33. doi: 10.4103/JCD.JCD_281_18.

Abstract

AIMS

The aim of this study is to impart radiopacity to platelet-rich fibrin (PRF) using two different bioactive agents (nano-hydroxyapatite [nHA] and dentin chips [DC]) and to assess the cell proliferation rate induced by the modified PRF.

SUBJECTS AND MATERIALS

PRF was modified with 50wt% of nHA (G bone-SHAG31, Surgiwear Company) and 50wt% of DC. The five samples of each group (Group 1 - dentin disc, Group 2 - PRF, Group 3 - PRF + 50wt% nHA, and Group 4-PRF + 50wt% DC) were digitally radiographed together with 8-mm aluminum stepwedge using DIGORA software (for Windows 2.9.113.490). The aluminum equivalent of radiopacity of the samples was compared with the dentin disc (control). Further cytotoxicity (on L929 mouse fibroblast cell lines) among the groups was assessed using methyl thiazolyl tetrazolium assay.

STATISTICAL ANALYSIS USED

One-way ANOVA with Tukey-honestly significant difference tests were applied to assess the significance among the various groups.

RESULTS

The mean aluminum equivalent radiopacity among each group showed statistically significant results with < 0.05. Group 3 (PRF + 50wt% nHA) can achieve an aluminum equivalent radiopacity (1.51 ± 0.089) better than Group 4 (0.97 ± 0.22 mmAl). The cell viability was >73% for all groups.

CONCLUSIONS

This study found that the addition of bioactive radiopacifiers into PRF was able to impart radiopacity and these biomaterials were proved to be noncytotoxic.

摘要

目的

本研究旨在使用两种不同的生物活性剂(纳米羟基磷灰石[nHA]和牙本质碎屑[DC])使富血小板纤维蛋白(PRF)具有射线不透性,并评估改良后的PRF诱导的细胞增殖率。

受试者和材料

PRF用50wt%的nHA(G bone-SHAG31,Surgiwear公司)和50wt%的DC进行改良。每组的五个样本(第1组 - 牙本质盘,第2组 - PRF,第3组 - PRF + 50wt% nHA,第4组 - PRF + 50wt% DC)与8毫米铝阶梯楔形块一起使用DIGORA软件(适用于Windows 2.9.113.490)进行数字射线照相。将样本的射线不透性的铝当量与牙本质盘(对照)进行比较。使用甲基噻唑基四氮唑法评估各组之间的进一步细胞毒性(对L929小鼠成纤维细胞系)。

使用的统计分析

应用单因素方差分析和Tukey真实显著差异检验来评估各组之间的显著性。

结果

每组的平均铝当量射线不透性显示出具有统计学意义的结果,P < 0.05。第3组(PRF + 50wt% nHA)的铝当量射线不透性(1.51 ± 0.089)优于第4组(0.97 ± 0.22 mmAl)。所有组的细胞活力均>73%。

结论

本研究发现,向PRF中添加生物活性射线不透剂能够赋予其射线不透性,并且这些生物材料被证明无细胞毒性。

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