Effect of curcumin-encapsulated Pluronic(R) F-127 over duo-species biofilm of Streptococcus mutans and Candida albicans

被引:12
|
作者
Lopes dos Santos, Diego Dantas [1 ]
Besegato, Joao Felipe [2 ]
Gobbo de Melo, Priscila Borges [2 ]
Oshiro Junior, Joao Augusto [3 ,4 ]
Chorilli, Marlus [3 ]
Deng, Dongmei [5 ,6 ]
Bagnato, Vanderlei Salvador [7 ]
de Souza Rastelli, Alessandra Nara [2 ]
机构
[1] Sao Paulo State Univ UNESP, Sch Dent, Dept Dent Mat & Prosthodont, BR-14801903 Araraquara, SP, Brazil
[2] Sao Paulo State Univ UNESP, Sch Dent, Dept Restorat Dent, 1680 Humaita St,MailBox 331, BR-14801903 Araraquara, SP, Brazil
[3] Sao Paulo State Univ UNESP, Sch Pharmaceut Sci, Dept Drugs & Med, BR-14800903 Araraquara, SP, Brazil
[4] State Univ Paraiba UEPB, Grad Program Pharceut Sci, BR-58429500 Campina Grande, Paraiba, Brazil
[5] Univ Amsterdam, Acad Ctr Dent Amsterdam ACTA, Dept Prevent Dent, Amsterdam, Netherlands
[6] Vrije Univ Amsterdam, Amsterdam, Netherlands
[7] Univ Sao Paulo, Phys Inst Sao Carlos IFSC, Dept Phys & Mat Sci, BR-13566590 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Curcumin; Micelles; Photochemotherapy; Biofilms; Streptococcus mutans; Candida albicans; DRUG-DELIVERY; BLOCK-COPOLYMERS; MICELLES; NANOCONTAINERS; SOLUBILIZATION; SENSITIZERS;
D O I
10.1007/s10103-021-03432-9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
To assess the effect of curcumin-encapsulated Pluronic(R) F-127 (Cur-Plu) during antimicrobial photodynamic therapy (aPDT) over duo-species biofilm of Streptococcus mutans and Candida albicans. Thermal analysis, optical absorption, and fluorescence spectroscopy were evaluated. Minimum inhibitory concentration (MIC) and minimum bactericidal/fungal concentration were obtained. The biofilms were cultured for 48 h at 37 degrees C and treated according to the groups: P + M + L + (photosensitizer encapsulated with Pluronic(R) F-127 + light); P + D + L + (photosensitizer incorporated in 1% DMSO + light); P - M + L + (no Pluronic(R) F-127 + light); P - D + L + (1% DMSO + light); P - L + (Milli-Q water + light); P + M + L - (photosensitizer encapsulated with Pluronic(R) F-127 no light); P + D + L - (photosensitizer in 1% DMSO, no light); P - M + L - (Pluronic(R) F-127 no light); P - D + L - (1% DMSO, no light); P - L - (Milli-Q water, no light; negative control group); CHX (0.2% chlorhexidine, positive control group); and NYS (Nystatin). Dark incubation of 5 min was used. The groups that received aPDT were irradiated by blue LED (460 nm, 15 J/cm(2)). Cell viability of the biofilms was performed by colony-forming units (CFU/mL) and confocal microscopy. Two-way ANOVA followed by Tukey's post hoc test was used at a significance level of 5%. P + D + L + and P + M + L + groups exhibited better log-reduction for both Candida albicans and Streptococcus mutans biofilms than P - M + L + , P - L + , and P - D + L + experimental groups. Furthermore, P + M + L + and P + D + L + showed greater reduction for Candida albicans than for Streptococcus mutans. aPDT mediated by Cur-Plu can be a potential strategy for biofilm control against duo-species biofilm of Streptococcus mutans and Candida albicans.
引用
收藏
页码:1775 / 1786
页数:12
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