Effect of Chloroaluminium phthalocyanine in cationic nanoemulsion on photoinactivation of multispecies biofilm

Author(s)

Trigo-Gutierrez, Jeffersson Krishan ^[1] ; Sanita, Paula Volpato ^[1] ; Tedesco, Antonio Claudio ^[2] ; Pavarina, Ana Claudia ^[1] ; de Oliveira Mima, Ewerton Garcia ^[1]

Affiliation

^[1] Sao Paulo State Univ Unesp, Sch Dent, Dept Dent Mat & Prosthodont, Sao Paulo - Brazil

^[2] FECLRP Sao Paulo Univ, Photobiol & Photomed Res Grp, Ctr Nanotechnol & Tissue Engineers, Sao Paulo - Brazil

• Document type: Journal article
• Source: Photodiagnosis and Photodynamic Therapy; v. 24, p. 212-219, DEC 2018.
• Web of Science Citations: 2

Abstract

Background: Photosensitizers in nanocarriers have been investigated for antimicrobial Photodynamic Therapy (aPDT). However, most studies are focused against microorganisms in planktonic or monospecies biofilm. Thus, this in vitro study evaluated the effect of aPDT using Chloroaluminium phthalocyanine (ClAlPc) in cationic nanoemulsion (NE) against Candida albicans, Candida glabrata and Streptococcus mutans grown as multispecies biofilm. Methods: Standard suspensions of each microorganism were added into wells of a microtiter plate for biofilm growth for 48 h in a candle jar. The biofilms were incubated with ClAlPc in cationic NE at 31.8 mu M for 30 min and illuminated with red light fluence of 39.3 J/cm(2) (P + L + group). Additional samples were treated only with photosensitizer (P +L-) or red light (P-L + ) or neither (P-L-, control group). aPDT efficacy was assessed by colony quantification, biofilm's metabolic activity, total biomass, and confocal microscopy. Data were analyzed by ANOVA/Welch and post-hoc Tukey/Games-Howell tests (alpha = 0.05). Results: aPDT (P + L + ) reduced the colony count in 1.30 to 2.24 lg(10) and the metabolic activity in 53.7% compared with the control group (P-L-). The total biomass showed no statistical difference among the groups. The confocal microscopy analyzes showed uptake of the PS in the biofilm, and dead cells were observed in the biofilm treated with aPDT. Conclusion: aPDT mediated by ClAlPc in cationic NE promoted photoinactivation of the multispecies biofilm, which was confirmed by colony quantification, metabolic activity, and confocal microscopy. However, the total biomass of the biofilm was not affected by the treatment. (AU)

• FAPESP's process: 13/07276-1 - CEPOF - Optics and Photonic Research Center
• Grantee: Vanderlei Salvador Bagnato
• Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC