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. 2017 Jul 20;15(3):236–243. doi: 10.5301/jabfm.5000373

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© 2017 The Authors

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (http://www.creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Fig. 4 — Evaluation of MG63 (A, B) and SAOS-2 (C, D) cell proliferation on dentin (D) and enamel (E) particles subjected or not to demineralization process. MG63 and SAOS-2 cells cultured onto polystyrene plates were used as the internal reference (i.e., positive controls [CTRL] for cell growth; 100% cell viability). Data are expressed as arbitrary units (RFU) as well as percentage of cell viability with respect to the CTRL. Bio-Oss® was used as a positive control. Data are expressed as mean ± SD; D = dentin; dD = demineralized dentin; E = enamel; dE = demineralized enamel.

∗p<0.05.