Therapeutic Window of Photodynamic Treatment (PDT) in Conservative Periodontal Therapy -Analysis of Cell Migration Within A Three Dimensional Collagen Matrix-

Grimm Wd
{"title":"Therapeutic Window of Photodynamic Treatment (PDT) in Conservative Periodontal Therapy -Analysis of Cell Migration Within A Three Dimensional Collagen Matrix-","authors":"Grimm Wd","doi":"10.33552/ojdoh.2021.04.000595","DOIUrl":null,"url":null,"abstract":"the present study was to investigate the effect of low-level laser irradiation as photodynamic therapy (PDT) on proliferation and differentiation of a human fibroblast cell line, determining the therapeutic window of toluidine blue O (TBO) using the 3-D collagen matrix assay with fibroblasts. The collagen-based 3-D assay (MetaVi Germany) combines all the advantages of 3-D collagen matrix assays with the benefits of high-throughput, fully auto-mated (hands-off) tracking technology. Two sets of tests (MetaVì Labs 3-D collagen matrix assay) were performed with human dermal fibroblasts derived from PromoCell (Heidelberg, Germany). Cells do not need to be labelled with any dyes or tags that could interfere with cell motility or inter-act with substances being tested in the assay. Results: The sensitization of fibroblasts with a physiological concentration of 5% (v:v) TBO and exposure to light from a 810 nm diode laser (1 min, 0.3 W) did not reduce cell viability and migratory activity measured by migration dynamics in comparison to the not sensitized fibroblasts. Conclusion: The study provided evidence that PDT with a diode laser 810nm and the photosensitizer toluidine blue O does not influence locomotory behavior of human fibroblasts in vitro","PeriodicalId":361768,"journal":{"name":"Online Journal of Dentistry & Oral Health","volume":"12 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Online Journal of Dentistry & Oral Health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33552/ojdoh.2021.04.000595","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

the present study was to investigate the effect of low-level laser irradiation as photodynamic therapy (PDT) on proliferation and differentiation of a human fibroblast cell line, determining the therapeutic window of toluidine blue O (TBO) using the 3-D collagen matrix assay with fibroblasts. The collagen-based 3-D assay (MetaVi Germany) combines all the advantages of 3-D collagen matrix assays with the benefits of high-throughput, fully auto-mated (hands-off) tracking technology. Two sets of tests (MetaVì Labs 3-D collagen matrix assay) were performed with human dermal fibroblasts derived from PromoCell (Heidelberg, Germany). Cells do not need to be labelled with any dyes or tags that could interfere with cell motility or inter-act with substances being tested in the assay. Results: The sensitization of fibroblasts with a physiological concentration of 5% (v:v) TBO and exposure to light from a 810 nm diode laser (1 min, 0.3 W) did not reduce cell viability and migratory activity measured by migration dynamics in comparison to the not sensitized fibroblasts. Conclusion: The study provided evidence that PDT with a diode laser 810nm and the photosensitizer toluidine blue O does not influence locomotory behavior of human fibroblasts in vitro
光动力治疗(PDT)在保守牙周治疗中的治疗窗口-三维胶原基质中细胞迁移的分析
本研究旨在探讨低水平激光光动力治疗(PDT)对人成纤维细胞增殖和分化的影响,利用成纤维细胞三维胶原基质实验确定甲苯胺蓝O (TBO)的治疗窗口。基于胶原蛋白的3-D分析(MetaVi德国)结合了3-D胶原蛋白基质分析的所有优点和高通量、全自动(不干涉)跟踪技术的优点。用PromoCell(海德堡,德国)衍生的人真皮成纤维细胞进行了两组测试(MetaVì实验室3-D胶原基质测定)。细胞不需要用任何可能干扰细胞运动或与实验中被测物质相互作用的染料或标签进行标记。结果:与未致敏的成纤维细胞相比,生理浓度为5% (v:v) TBO并暴露于810 nm二极管激光(1分钟,0.3 W)下的成纤维细胞敏化并没有降低细胞活力和迁移活性(通过迁移动力学测量)。结论:810nm二极管激光PDT和光敏剂甲苯胺蓝O对体外人成纤维细胞的运动行为没有影响
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信