[Role of minocycline-loaded silica nanospheres in the regulation of periodontitis inflammation in rats].

Q4 Medicine
上海口腔医学 Pub Date : 2025-06-01
Jinxin Yang, Kexin Ding, Zhe Sun, Yawen Cui, Zongxiang Liu
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引用次数: 0

Abstract

Purpose: To investigate the effect of minocycline hydrochloride(MH) loaded nano-silica microspheres(MSNion) on the inflammatory regulation of periodontitis in rats.

Methods: Mesoporous silica(MSN) was prepared by classical St?ber method and MSNion was obtained by doping hydroxyapatite. MH was loaded into MSNion by magnetic stirring, and chitosan (COS), which had anti-inflammatory and antibacterial effect, was adsorbed on its surface by using charge interactions, forming MH@MSNion@COS microspheres. The microspheres were characterized by electron microscopy and X-ray diffraction. The experiments were divided into control, MH, MSNion@COS and MH@MSNion@COS groups. The cytotoxicity of each group was assessed using the CCK-8 cell assay and the optimal concentration was determined. The expression levels of inflammatory factors(TNF-α, IL-6, IL-1β, iNOS, IL-10) were determined in each group using ELISA kits. In periodontitis model, the rats were treated according to the grouping of cell experiments, periodontal probing depth (PD) and gingival index (GI) of the rats were measured at 0, 1, 2, 4 weeks. At 4 weeks of the experiment, the peripheral blood of each group of rats was collected, and the levels of inflammatory factors in serum were detected by ELISA kits.

Results: Nanoparticles with a particle size of about 110 nm were prepared and observed as regular spheres by electron microscopy. MH@MSNion@COS degraded into fragments with unclear structure at the 8th day. In vitro drug release assay showed a slow release of MH, and the MH release rate reached 80% at about the 15th day. In cell experiment, MH@MSNion@COS showed the best cell proliferation activity at 50 μg/mL (P<0.05), and the cell activity was higher than that of MH group and MSNion@COS group(P<0.05). There was no significant difference between MH group and MSNion@COS group. ELISA results showed that the expression of inflammatory factors in MH@MSNion@COS group was significantly lower than that in LPS group at the first day(P<0.01), and there was no significant difference between MH group and MSNion@COS group. At the 3rd day, the expression of M1 inflammatory factors in MH@MSNion@COS group was lower than that in control group, and the expression of M2 inflammatory factors was higher than that in control group(P<0.05). PD and GI of MH@MSNion@COS group were significantly decreased after administration compared with other groups(P<0.05), and the amount of inflammatory factors was lower than other groups(P<0.05).

Conclusions: MH@MSNion@COS has a good inflammatory regulation effect on experimental periodontitis in vitro and in vivo.

二甲胺四环素负载二氧化硅纳米球在大鼠牙周炎炎症调节中的作用。
目的:探讨盐酸米诺环素(MH)负载纳米二氧化硅微球(MSNion)对大鼠牙周炎的炎症调节作用。方法:采用经典St?她的方法和掺杂羟基磷灰石制备的MSNion。将MH通过磁搅拌加载到MSNion中,具有抗炎和抗菌作用的壳聚糖(COS)通过电荷相互作用吸附在其表面,形成MH@MSNion@COS微球。用电子显微镜和x射线衍射对微球进行了表征。实验分为对照组、MH组、MSNion@COS组和MH@MSNion@COS组。采用CCK-8细胞法测定各组细胞毒性,确定最佳浓度。采用ELISA试剂盒检测各组炎症因子(TNF-α、IL-6、IL-1β、iNOS、IL-10)的表达水平。在牙周炎模型中,按细胞实验分组处理大鼠,于0、1、2、4周测定大鼠牙周探诊深度(PD)和牙龈指数(GI)。实验第4周采集各组大鼠外周血,采用ELISA试剂盒检测血清炎症因子水平。结果:制备出粒径约为110 nm的纳米颗粒,电镜观察其为规则球体。MH@MSNion@COS在第8天降解为结构不清晰的碎片。体外释药试验显示,MH缓释,约15天释药率达80%。细胞实验中,MH@MSNion@COS在50 μg/mL时细胞增殖活性最佳(P<0.05),且细胞活性高于MH组和MSNion@COS组(P<0.05)。MH组与MSNion@COS组间无显著差异。ELISA结果显示,MH@MSNion@COS组第1天炎性因子表达量显著低于LPS组(P<0.01), MH组与MSNion@COS组间差异无统计学意义。第3天,MH@MSNion@COS组M1炎性因子的表达低于对照组,M2炎性因子的表达高于对照组(P<0.05)。MH@MSNion@COS组给药后PD、GI较其他组显著降低(P<0.05),炎症因子量低于其他组(P<0.05)。结论:MH@MSNion@COS对实验性牙周炎具有良好的体外和体内炎症调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
上海口腔医学
上海口腔医学 Medicine-Medicine (all)
CiteScore
0.30
自引率
0.00%
发文量
5299
期刊介绍: "Shanghai Journal of Stomatology (SJS)" is a comprehensive academic journal of stomatology directed by Shanghai Jiao Tong University and sponsored by the Ninth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine. The main columns include basic research, clinical research, column articles, clinical summaries, reviews, academic lectures, etc., which are suitable for reference by clinicians, scientific researchers and teaching personnel at all levels engaged in oral medicine.
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