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基于聚赖氨酸的牙科复合材料的合成、单体转化率和力学性能。

Synthesis, monomer conversion, and mechanical properties of polylysine based dental composites.

机构信息

Department of Dental Materials, Rashid Latif Dental College, Lahore, Pakistan.

Interdisciplinary Research Centre in Biomedical Materials, COMSATS University Islamabad, Lahore Campus, Lahore, Pakistan.

出版信息

J Mech Behav Biomed Mater. 2024 Mar;151:106398. doi: 10.1016/j.jmbbm.2024.106398. Epub 2024 Jan 14.

DOI:10.1016/j.jmbbm.2024.106398
PMID:38237205
Abstract

OBJECTIVE

The aim of this study was to synthesize a new bioactive and antibacterial composite by incorporating reactive calcium phosphate and antibacterial polylysine into a resin matrix and evaluate the effect of these fillers on structural analysis, degree of monomer conversion, mechanical properties, and bioactivity of these newly developed polypropylene based dental composites.

METHODOLOGY

Stock monomers were prepared by mixing urethane dimethacrylate and polypropylene glycol dimethacrylate and combined with 40 wt% silica to make experimental control (E-C). The other three experimental groups contained a fixed percentage of silica (40 wt%), monocalcium phosphate monohydrate, and β-tri calcium phosphate (5 wt% each) with varying amounts of polylysine (PL). These groups include E-CCP0 (0 wt% PL), E-CCP5 (5 wt% PL) and E-CCP10 (10 wt% PL). The commercial control used was Filtek™ Z250 3M ESPE. The degree of conversion was assessed by using Fourier transform infrared spectroscopy (FTIR). Compressive strength and Vicker's micro hardness testing were evaluated after 24 h of curing the samples. For bioactivity, prepared samples were placed in simulated body fluid for 0, 1, 7, and 28 days and were analyzed using a scanning electron microscope (SEM). SPSS 23 was used to analyze the data and one-way ANOVA and post hoc tukey's test were done, where the significant level was set ≤0.05.

RESULTS

Group E-C showed better mechanical properties than other experimental and commercial control groups. Group E-C showed the highest degree of conversion (72.72 ± 1.69%) followed by E-CCP0 (72.43 ± 1.47%), Z250 (72.26 ± 1.75%), E-CCP10 (71.07 ± 0.19%), and lowest value was shown by E-CCP5 (68.85 ± 7.23%). In shear bond testing the maximum value was obtained by E-C. The order in decreasing value of bond strength is E-C (8.13 ± 3.5 MPa) > Z250 (2.15 ± 1.1 MPa) > E-CCP10 (2.08 ± 2.1 MPa) > E-CCP5 (0.94 ± 0.8 MPa) > E-CCP0 (0.66 ± 0.2 MPa). In compressive testing, the maximum strength was observed by commercial control i.e., Z250 (210.36 ± 18 MPa) and E-C (206.55 ± 23 MPa), followed by E-CCP0 (108.06 ± 19 MPa), E-CCP5 (94.16 ± 9 MPa), and E-CCP10 (80.80 ± 13 MPa). The maximum number of hardness was shown by E-C (93.04 ± 8.23) followed by E-CCP0 (38.93 ± 9.21) > E-CCP10 (35.21 ± 12.31) > E-CCP5 (34.34 ± 12.49) > Z250 (25 ± 2.61). SEM images showed that the maximum apatite layer as shown by E-CCP10 and the order followed as E-CCP10 > E-CCP5 > E-CCP0 >Z250> E-C.

CONCLUSION

The experimental formulation showed an optimal degree of conversion with compromised mechanical properties when the polylysine percentage was increased. Apatite layer formation and polylysine at the interface may result in remineralization and ultimately lead to the prevention of secondary caries formation.

摘要

目的

本研究的目的是通过将反应性磷酸钙和抗菌聚赖氨酸掺入树脂基质中合成一种新的生物活性和抗菌复合材料,并评估这些填料对结构分析、单体转化率、机械性能和这些新开发的基于聚丙烯牙科复合材料的生物活性的影响。

方法

通过混合异佛尔酮二甲基丙烯酸酯和聚丙二醇二甲基丙烯酸酯来制备基质单体,并将其与 40wt%二氧化硅结合制成实验对照(E-C)。另外三个实验组包含固定百分比的二氧化硅(40wt%)、一水合单磷酸钙和β-三磷酸钙(各 5wt%),并含有不同量的聚赖氨酸(PL)。这些组包括 E-CCP0(0wt%PL)、E-CCP5(5wt%PL)和 E-CCP10(10wt%PL)。使用的商业对照物是 Filtek™Z250 3M ESPE。通过傅里叶变换红外光谱(FTIR)评估转化率。在样品固化 24 小时后,评估压缩强度和维氏硬度测试。为了进行生物活性评估,将制备的样品置于模拟体液中 0、1、7 和 28 天,并使用扫描电子显微镜(SEM)进行分析。使用 SPSS 23 分析数据,并进行单向方差分析和事后 Tukey's 检验,显著水平设为≤0.05。

结果

组 E-C 显示出比其他实验组和商业对照组更好的机械性能。组 E-C 显示出最高的转化率(72.72±1.69%),其次是 E-CCP0(72.43±1.47%)、Z250(72.26±1.75%)、E-CCP10(71.07±0.19%),转化率最低的是 E-CCP5(68.85±7.23%)。在剪切结合测试中,E-C 获得了最大值。结合强度值的降低顺序为 E-C(8.13±3.5MPa)>Z250(2.15±1.1MPa)>E-CCP10(2.08±2.1MPa)>E-CCP5(0.94±0.8MPa)>E-CCP0(0.66±0.2MPa)。在压缩测试中,商业对照物 Z250 表现出最大强度(210.36±18MPa)和 E-C(206.55±23MPa),其次是 E-CCP0(108.06±19MPa)、E-CCP5(94.16±9MPa)和 E-CCP10(80.80±13MPa)。硬度值最大的是 E-C(93.04±8.23),其次是 E-CCP0(38.93±9.21)>E-CCP10(35.21±12.31)>E-CCP5(34.34±12.49)>Z250(25±2.61)。SEM 图像显示,E-CCP10 显示出最大的磷灰石层,其次是 E-CCP10>E-CCP5>E-CCP0>Z250>E-C。

结论

当聚赖氨酸的百分比增加时,实验配方表现出最佳的转化率和妥协的机械性能。磷灰石层的形成和聚赖氨酸在界面处的形成可能导致再矿化,并最终导致继发性龋齿的形成得到预防。

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