氯己定缓释复合抗菌树脂的体外研究。

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Flávia Gonçalves, Larissa Sampaio Tavares Silva, Julia Noborikawa Roschel, Greca de Souza, Luiza de Paiva Mello Campos, Gustavo Henrique Varca, Duclerc Parra, Mirko Ayala Perez, Antonio Carlos Gordilho, William Cunha Brandt, Leticia Boaro
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引用次数: 0

摘要

背景:在牙体修复材料中加入氯己定是一种很有前景的减少龋病复发的方法。然而,主要的挑战是开发具有长期抗菌活性的材料。目的:研究氯己定载体蒙脱土颗粒(MMT/CHX)复合树脂的填充类型和浓度对其化学、物理及短期和长期抗菌性能的影响。材料:实验复合材料分别以钡玻璃/胶体二氧化硅的70/30和80/20两种比例(0、30和60%)和5 wt% MMT/CHX的填充剂合成。转换用近傅里叶变换红外光谱法测定。通过干燥和浸泡前后样品的重量来测定吸附和溶解度。弯曲强度(FS)和弹性模量(E)在通用试验机上进行了三次弯曲试验。监测氯己定释放50 d。所有微生物学检测均采用变形链球菌UA159。抑制晕试验进行了12个月,也进行了标本和菌落形成单位(CFU)的生物膜生长。采用显微硬度Knoop和cfu测定修复牙再矿化试验。结果:填料类型和浓度对转化率、吸附性和溶解度均无影响。FS和E随填料浓度的增加而增加,与填料类型无关。氯己定在15 d内均有显著释放,填充剂浓度的增加使其释放度降低。以70/30的比例添加60 wt%填料的材料,观察到光晕抑制时间较长(12个月)。此外,60 wt%的填充物,与填充物比例无关,与对照组相比,CFU从8个月减少到12个月。在再矿化实验中,除了各组之间硬度没有差异外,生物膜生长后,添加60%填料的材料的CFU也显着降低。结论:60%填料、70%玻璃钡和30%二氧化硅优先、5% MMT/CHX颗粒的材料具有长期抗菌活性,有效时间可达12个月。此外,与其他材料相比,该配方具有更高的机械性能和相似的转化、吸附和溶解度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antibacterial Resin Composites with Sustained Chlorhexidine Release: One-Year In Vitro Study.

Antibacterial Resin Composites with Sustained Chlorhexidine Release: One-Year In Vitro Study.

Antibacterial Resin Composites with Sustained Chlorhexidine Release: One-Year In Vitro Study.

Antibacterial Resin Composites with Sustained Chlorhexidine Release: One-Year In Vitro Study.

Background: The addition of chlorhexidine in dental restorative materials is a promising strategy to reduce the recurrence of tooth decay lesions. However, the main challenge is to develop materials with antimicrobial activity in the long term. Objective: This study analyses the effect of filler type and concentration of resin composites supplemented with chlorhexidine loaded in carrier montmorillonite particles (MMT/CHX) regarding their chemical, physical, and short- and long-term antimicrobial proprieties. Materials: Experimental composites were synthesized with 0, 30, or 60% filler in two ratios, 70/30 and 80/20, of barium glass/colloidal silica, respectively, and 5 wt% MMT/CHX. Conversion was measured using near Fourier-transform infrared spectrometry. Sorption and solubility were determined by specimen weight before and after drying and immersing in water. Flexural strength (FS) and elastic modulus (E) were determined by three bending tests using a universal test machine. Chlorhexidine release was monitored for 50 days. Streptococcus mutans UA159 was used in all microbiological assays. Inhibition halo assay was performed for 12 months and, also, biofilm growth for the specimens and colony-forming unit (CFU). Remineralization assay was used on restored teeth using measurements of microhardness Knoop and CFUs. Results: Conversion, sorption, and solubility were not affected by filler type and concentration. FS and E increase with the filler concentration, independent from filler type. Chlorhexidine was significantly released for 15 days for all experimental materials, and the increase in filler concentration decreased its release. Halo inhibition was observed for a longer time (12 months) in materials with 60 wt% filler at 70/30 proportion. Also, 60 wt% filler materials, independent from the filler ratio, reduced the CFU in relation to the control group from 8 to 12 months. In the remineralization assay, besides the absence of differences in hardness among the groups, after biofilm growth, the CFU was also significantly lower in materials with 60 wt% filler. Conclusions: Materials with 60% filler, preferentially with 70% barium glass and 30% silica, and 5% MMT/CHX particles demonstrated long-term antimicrobial activity, reaching 12 months of effectiveness. Also, this formulation was associated with higher mechanical properties and similar conversion, sorption, and solubility compared to the other materials.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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