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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Cytotoxicity of adhesive systems of different hydrophilicities on cultured odontoblast-like cells

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Author(s):
Bianchi, Luciana [1] ; Dias Ribeiro, Ana Paula [2] ; de Oliveira Carrilho, Marcela Rocha [3] ; Pashley, David H. [4] ; de Souza Costa, Carlos Alberto [5] ; Hebling, Josimeri [1]
Total Authors: 6
Affiliation:
[1] UNESP Univ Estadual Paulista, Araraquara Sch Dent, Dept Pediat Dent & Orthodont, Sao Paulo - Brazil
[2] Univ Brasilia, Dept Dent, Brasilia, DF - Brazil
[3] Univ Western Ontario, Schulich Sch Med & Dent, London, ON - Canada
[4] Georgia Hlth Sci Univ, Dept Oral Biol, Coll Dent Med, Augusta, GA - USA
[5] UNESP Univ Estadual Paulista, Araraquara Sch Dent, Dept Physiol & Pathol, Sao Paulo - Brazil
Total Affiliations: 5
Document type: Journal article
Source: JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS; v. 101, n. 8, p. 1498-1507, NOV 2013.
Web of Science Citations: 4
Abstract

This study evaluated the cytotoxicity of experimental adhesive systems (EASs) on odontoblast-like cells. Paper discs (n=132) were impregnated with 10 mu L of each EASR1, R2, R3, R4, and R5 (in an ascending order of hydrophilicity), followed by photoactivation. R1 and R2 are nonsolvated hydrophobic blends, R3 represents a simplified etch-and-rinse adhesive system, and R4 and R5 represent simplified self-etch adhesive systems. Discs were immersed in Dulbecco's modified Eagle's medium for 24 h to obtain eluates applied on MDPC-23 cell cultures. No material was applied on discs used as control (R0). Cell viability {[}3-(4,5-dimethythiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay], total protein (TP) production, alkaline phosphatase (ALP) activity, type of cell death, and degree of monomer conversion Fourier transform infrared (%DC-FTIR) were evaluated. Data were analyzed by Kruskal-Wallis and Mann-Whitney tests (=0.05). Considering R0 (control) as having 100% of cell viability, R1, R2, R3, R4, and R5 reduced the metabolic activity of cells by 36.4, 3.1, 0.2, 21.5, and 65.7%, respectively, but only R1 and R5 differed from R0. Comparing with R0, lower TP production was observed for R1, R4, and R5, while ALP activity decreased for R1 and R5. Necrotic cell death was predominant for all EASs, but only R1, R4, and R5 differed from R0. Only R5 presented a different apoptotic cell death ratio from R0. R1 presented the lowest %DC (ca. 37%), whereas R4 and R5 presented the highest (ca. 56%). In conclusion, R2 and R3 were not toxic to the MDPC-23 cells, suggesting that the degree of hydrophilicity or %DC of the EASs alone were not responsible for their cytopathic effects. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 101B: 1498-1507, 2013. (AU)

FAPESP's process: 09/06446-5 - Transdentinal cytotoxicity of adhesive systems of different hydrophilicity on ethanol-impregnated dentin.
Grantee:Luciana Bianchi
Support Opportunities: Scholarships in Brazil - Master