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Evaluation of Indocyanine-Mediated Photodynamic Therapy Cytotoxicity in Human Osteoblast-Like Cells: An in Vitro Study; [Оценка Цитотоксичности Индоцианинопосредованной Фотодинамической Терапии В Остеобластоподобных Клетках Человека: Исследование in Vitro] Publisher Pubmed



Aghayan S1 ; Yazdanfar A2 ; Seyedjafari E3 ; Noroozian M4 ; Bordea RI5 ; Chiniforush N6
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Authors Affiliations
  1. 1. Department of Periodontics, Faculty of Dentistry, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
  2. 2. Faculty of Dentistry, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
  3. 3. Department of Biotechnology, University of Tehran, Tehran, Iran
  4. 4. Orthodontics Department, Dental School, Ilam University of Medical Sciences, Ilam, Iran
  5. 5. Department of Oral Rehabilitation, Faculty of Dentistry, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania
  6. 6. Laser Research Center of Dentistry, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Folia Medica Published:2022


Abstract

Introduction: Antimicrobial photodynamic therapy (aPDT) is an adjunctive non-invasive procedure for the management of periodontal tissue infection and deep periodontal pocket decontamination. However, the effects of this procedure on periodontal cells like osteoblasts that play a role in periodontal tissue repair and regeneration is not yet clear. Aim: This study aimed to investigate aPDT based on indocyanine green (ICG) on MG-63 osteoblast-like cells in vitro. Materials and methods: MG-63 cells were treated in 9 different groups: 1) Control (untreated cells), 2) ICG alone at a concentration of 1000 µg/mL, 3) ICG alone at a concentration of 2000 µg/mL, 4) diode laser irradiation alone for 30 s, 5) laser irradiation for 30 s combined with ICG with a concentration of 1000 µg/mL, 6) laser irradiation for 30 s combined with ICG at a concentration of 2000 µg/mL, 7) laser irradiation alone for 60 s, 8) laser irradiation for 60 s combined with ICG at a concentration of 1000 µg/mL, and 9) laser irradiation for 60 s combined with ICG at a concentration of 2000 µg/mL. Cell viability was assessed by MTT assay in different groups. Results: In groups that were treated with 2000 µg/mL of ICG or diode laser irradiation at fluency of 39 J/cm2 for 60 s alone or in combination during ICG-aPDT, osteoblast-like cells viability decreased, remarkably. Conclusions: IGC-mediated aPDT with 1000 µg/mL of ICG combined with diode laser irradiation at fluency of 39 J/cm2 for 30 s is safe for MG-63 human osteoblast-like cells; however, higher concentration of ICG or laser irradiation time will increase cells death. There is still a need for more in vivo studies. Copyright by authors.
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