Author/Authors :
Koochaki, Mahsa Department of Oral and Maxillofacial Disease - School of Dentistry - Tehran University of Medical Sciences, Tehran, Iran , Hendi, Amirreza Dental Sciences Research Center - Department of Prosthodontics - School of Dentistry - Guilan University of Medical Sciences, Rasht, Iran , Ghasemi, Mahmood Department of periodontics - Dental Faculty - Tehran Medical Sciences - Islamic Azad University tehran branch, Tehran, Iran , jafari, Ehsan Department of Biotechnology - College of Sciences - University of Tehran, Tehran, Iran , Hamidain, Mehdi Dental Faculty - Tehran Medical Sciences - Islamic Azad University tehran branch, Tehran, Iran , Chiniforush, Nasim Laser Research Center of Dentistry - Dentistry Research Institute - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Introduction: This study aimed to compare the effects of root biomodification by citric acid and
antimicrobial photodynamic therapy (aPDT) with LED and laser on the proliferation of human
gingival fibroblasts (HGFs).
Methods: This in vitro experimental study evaluated 60 single-rooted teeth extracted
due to periodontal disease. The teeth underwent scaling and root planing (SRP), and
then 5 × 5 mm blocks were prepared from the cervical area of the teeth 1 mm apical to
the cementoenamel junction. The blocks were divided into 4 groups (n=15 blocks): SRP alone
(control), SRP + citric acid, SRP + toluidine blue (TBO) + LED light, and SRP + TBO + laser. HGFs
were seeded on the surface of the samples, and the methyl thiazolyl tetrazolium (MTT) assay was
performed after 24, 48 and 72 hours. Group comparisons were performed using repeated measures
ANOVA, while pairwise comparisons of the time points were performed by an LSD test.
Results: Cell proliferation was higher in all experimental groups at 48 and 72 hours, compared with
24 hours (P<0.05). Cell proliferation was significantly different in the citric acid group at 24 hours
(P=0.016) and 48 hours (P=0.015), compared with other groups. However, cell proliferation was
not significantly different in the aPDT group with LED Photosan and a diode laser at 24 and 48
hours (P>0.05).
Conclusion: aPDT and citric acid can enhance the proliferation of HGFs on dentin blocks. Further
studies can pave the way for their future use in the clinical setting.
Keywords :
Antimicrobial photodynamic therapy , Laser , LED , Human gingival fibroblasts , Citric acid