Nano Biomedicine
ORIGINAL ARTICLE

Cytotoxicity Test of Five Commercially Tooth-surface-polishing Agents by Three-dimensional Culture Technique using Type I Collagen

Tomoko MATSUNAMI1, Koichi IMAI2, and Ayuko MAESOMA3

1Graduate School of Health Sciences, 2Department of Tissue Engineering, School of Dentistry,
3Department of Oral Health Sciences, Faculty of Health Sciences,
Osaka Dental University, Osaka, Japan

Nano Biomed 2024; 16(2): 73-78, (Dec 30, Nano Biomedicine)

Synopsis
Tooth-surface-polishing agents are a material for tooth surface polishing for dental hygienists to use after removing plaque, exogenous deposit, and tartar that cannot be removed by patient self-care. We performed cytotoxicity tests of 5 products among clinically available products. As a result, when a tooth-cleaning agent was mixed with the assay medium as a 1/5-concentration sample, cell viability reduced in proportion to sample addition. As there were marked differences in cell viabil-ity among the products used in this experiment, dental hygienists should understand the characteris-tics of a tooth-cleaning agent before use. They are routinely used in current dental clinical practice, but few studies have reported their biological influence.
Chinese-hamster-derived V79 cells and Dulbecco's Modified Eagle's Medium (DMEM) con-taining 10 % fetal bovine serum as an assay medium were used. Cell viability was investigated us-ing the three-dimensional culture method with collagen and MTT assay. The results showed marked differences in cell viability among the samples after cell exposure to each tooth-surface-polishing agents at a 1/5 concentration. It is necessary to understand the characteristics of various tooth-surface-polishing agents and select the most appropriate one for each purpose.

Key words: tooth-surface-polishing agent, cytotoxicity, cell viability, three-dimensional culture, PMTC

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DOI: 10.11344/nano.16.73

Matsunami T, Imai K, Maesoma A. Cytotoxicity test of five commercially tooth-surface-polishing agents by three-dimensional culture technique using type I collagen. Nano Biomed 2004; 16(2): 73-78.