Rad Mehdi Rostami, Pourhajibagher Maryam, Rokn Amir Reza, Barikani Hamid Reza, Bahador Abbas
Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Front Dent. 2019 May-Jun;16(3):187-193. doi: 10.18502/fid.v16i3.1590. Epub 2019 Jun 29.
Eradication of (), as an opportunistic periodontopathogen, and inhibition of its virulence factor expression require a new adjunctive therapeutic method. In this study, we accessed the expression level of gene, as a virulence factor associated with biofilm formation, following treatment by antimicrobial photodynamic therapy (aPDT) using indocyanine green (ICG) doped with chitosan nanoparticles (CS-NPs@ICG).
CS-NPs@ICG was synthesized and examined using scanning electron microscopy (SEM). ATCC 33384 strain was treated with CS-NPs@ICG, as a photosensitizer, which was excited with a diode laser at the wavelength of 810 nm with the energy density of 31.2 J/cm2. Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to determine the changes in gene expression level.
Synthetized CS-NPs@ICG was confirmed via SEM. The results revealed that CS-NPs@ICG-mediated aPDT could significantly decrease gene expression to 13.2-fold (P<0.05). There was a remarkable difference between aPDT using CS-NPs@ICG and ICG (P<0.05). The diode laser, ICG, and CS-NPs@ICG were unable to significantly downregulate gene expression (P>0.05).
aPDT with CS-NPs@ICG leads to a decrease of the virulence factor of and can be used as an adjunct to routine treatments for successful periodontal therapy in vivo.
作为一种机会性牙周病原体,根除()并抑制其毒力因子表达需要一种新的辅助治疗方法。在本研究中,我们检测了使用负载壳聚糖纳米颗粒的吲哚菁绿(CS-NPs@ICG)进行抗菌光动力疗法(aPDT)治疗后,作为与生物膜形成相关的毒力因子的基因表达水平。
合成CS-NPs@ICG并使用扫描电子显微镜(SEM)进行检测。用CS-NPs@ICG作为光敏剂处理ATCC 33384菌株,用波长810nm、能量密度31.2J/cm²的二极管激光激发。进行定量实时聚合酶链反应(qRT-PCR)以确定基因表达水平的变化。
通过SEM确认合成了CS-NPs@ICG。结果显示,CS-NPs@ICG介导的aPDT可使基因表达显著降低至13.2倍(P<0.05)。使用CS-NPs@ICG的aPDT与ICG之间存在显著差异(P<0.05)。二极管激光、ICG和CS-NPs@ICG均无法显著下调基因表达(P>0.05)。
CS-NPs@ICG介导的aPDT可降低的毒力因子水平,可作为体内成功牙周治疗常规治疗的辅助手段。