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This multicenter study evaluated the effect of harmonizing spectrophotometric (d/8°) color measurements by using actual dental materials of clinically relevant thickness and translucency as "calibration tiles." Ten tooth‐colored, 1‐mm thick, resin‐ and ceramic‐based materials were tested at the coordinating center (CC) and six research sites (RS). Correction factors were calculated for each material and each site to obtain the corrected reflection spectra from the non‐corrected data set. Non‐corrected (NC) and corrected (C) reflection values were converted into CIEDE2000 and CIELAB color parameters for the following comparisons: CC vs RSNC and CC vs RSC, between RSNC vs RSNC and RSC vs RSC pairs, and among RS separately (α = 0.05). Mean color differences for CC vs RSNC and corresponding CC vs RSC values were ΔE00 = 4.2 (2.6) and ΔE00 = 0.7 (0.6), respectively. Corresponding values for RSNC vs RSNC and RSC vs RSC specimen pairs were ΔE00 = 5.9 (2.9) and ΔE00 = 1.0 (0.5), respectively. The CIEDE2000 NC vs C comparison for each research site separately ranged from 0.5 to 8.5. Color differences of CC vs RSC and RSC vs RSC pairs decreased 83% to 84.5% as compared with respective color differences for non‐corrected research site measurements and was RS dependent (P <.001). The obtained results validated the proposed method of harmonizing color measurements for dental application as a reliable quality control tool for dental research laboratories and industry. [ABSTRACT FROM AUTHOR]

Objective To evaluate in vitro the fluorescence properties of extracted human teeth whitened with 40% hydrogen peroxide. Materials and Methods A total of 28 extracted human teeth were pumiced for 1 minute using a low-speed dental handpiece and a disposable rubber cup. Pre-whitening fluorescence measurements (T0), maximum excitation (Exmax), maximum emission (Emmax), and maximum intensity ( Imax108), were performed using a spectrofluorometer. After T0 measurements, the teeth were whitened using the in-office method with 40% hydrogen peroxide, three times for 20 minutes. The fluorescence parameters were measured under the same conditions 7 and 14 days after bleaching (T1 and T2, respectively). Results Exmax exhibited a broader range 7 days after whitening and decreased after 14 days. The Emmax and Imax108 displayed a narrower range after whitening. The mean Exmax differed significantly between the time points ( F = 20.09. P < .001). The corresponding analysis for the mean Emmax differed significantly between the time points ( F = 16.69, P < .001). The same was true for the mean Imax108 ( F = 9.69, P < .001). Conclusions Within the limitations of this study, whitening provoked statistically significant changes in fluorescence of the intact teeth in vitro. Clinical significance The appearance of human teeth and dental materials and their changes upon aging and exposure to different agents (staining, whitening) is a topic of great relevance to esthetic dentistry. While some appearance parameters, such as color, translucency, and gloss, have been thoroughly studied, fluorescence and its influence on overall tooth appearance is still not well understood, yet it has influenced the development of fluorescence emitting restorative materials. [ABSTRACT FROM AUTHOR]