Cavalcante Leonardo Lobo Ribeiro, Tedesco Antonio Claudio, Takahashi Luandra Aparecida Unten, Curylofo-Zotti Fabiana Almeida, Souza-Gabriel Aline Evangelista, Corona Silmara Aparecida Milori
Department of Restorative Dentistry, Ribeirão Preto School of Dentistry, University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil.
Department of Chemistry, Center of Nanotechnology and Tissue Engineers, Photobiology and Photomedicine Research Group, FFCLRP- University of São Paulo (USP), Ribeirão Preto, São Paulo, Brazil.
Photodiagnosis Photodyn Ther. 2020 Jun;30:101709. doi: 10.1016/j.pdpdt.2020.101709. Epub 2020 Apr 9.
Antimicrobial photodynamic therapy (aPDT) using chloroaluminium phthalocyanine (ClAlPc) has high oxidative power allowing for the control of biofilms, especially when the photosensitizer is administered in an appropriate release vehicle. This study aimed to develop/characterize the ClAlPc encapsulated in chitosan nanoparticles (CSNPs), and evaluate its antimicrobial properties against S. mutans biofilms.
CSNPs were prepared by ion gelation, and characterization studies included particle size, polydispersion index (IPd), zeta potential, accelerated stability, absorption spectrum and ClAlPc quantification. The S. mutans biofilms were formed in bovine dentin blocks at 37 °C for 48 h under microaerophilic conditions. 8 μM ClAlPc was combined with a diode laser (InGaAlP) at 660 nm and 100 J/cm. The aPDT toxicity was verified by dark phototoxicity. The antimicrobial activity was verified by CFU/mL and biofilm was analyzed by scanning electron microscopy (SEM). The number of viable bacteria was analyzed by ANOVA and Tukey HSD tests (α = 0.05).
The characterization revealed that the ClAlPc nanoparticles were found in nanometer-scale with adequate photophysical and photochemical properties. The aPDT mediated by ClAlPc + CSNPs nanoconjugate showed a significant reduction in the viability of S. mutans (1log10 CFU/mL) compared to the negative control (PBS, p < 0.05). The aPDT mediated by ClAlPc was similar to PBS (p > 0.05). SEM revealed change in biofilm morphology following the treatment of bacteria with aPDT ClAlPc + CSNPs. Cells were arranged as single or in shorted chains. Irregular shapes of S. mutans were found.
ClAlPc nanoparticles are considered stable and aPDT mediated by ClAlPc + CSNPs nanoconjugate was effective against S. mutans biofilm.
使用氯铝酞菁(ClAlPc)的抗菌光动力疗法(aPDT)具有高氧化能力,可用于控制生物膜,特别是当光敏剂以适当的缓释载体给药时。本研究旨在开发/表征包裹在壳聚糖纳米颗粒(CSNP)中的ClAlPc,并评估其对变形链球菌生物膜的抗菌性能。
通过离子凝胶法制备CSNP,表征研究包括粒径、多分散指数(IPd)、zeta电位、加速稳定性、吸收光谱和ClAlPc定量。在微需氧条件下,于37℃在牛牙本质块中形成变形链球菌生物膜48小时。将8μM ClAlPc与660nm、100J/cm²的二极管激光器(InGaAlP)联合使用。通过暗光毒性验证aPDT的毒性。通过CFU/mL验证抗菌活性,并通过扫描电子显微镜(SEM)分析生物膜。通过方差分析和Tukey HSD检验(α = 0.05)分析活菌数量。
表征显示ClAlPc纳米颗粒呈纳米级,具有适当的光物理和光化学性质。与阴性对照(PBS,p < 0.05)相比,由ClAlPc + CSNP纳米共轭物介导的aPDT使变形链球菌的活力显著降低(1log10 CFU/mL)。由ClAlPc介导的aPDT与PBS相似(p > 0.05)。SEM显示用aPDT ClAlPc + CSNP处理细菌后生物膜形态发生变化。细胞呈单个或短链排列。发现变形链球菌形状不规则。
ClAlPc纳米颗粒被认为是稳定的,由ClAlPc + CSNP纳米共轭物介导的aPDT对变形链球菌生物膜有效。