Laser Nd:YAG patterning enhance human osteoblast behavior on zirconia implants

Zirconia has been regarded as a promising material for dental implants, and Nd:YAG laser treatment has been proposed as a potential strategy to improve its bioactivity. The main aim of the present study was to evaluate the in vitro behavior of human fetal osteoblasts in contact with laser-textured z...

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Veröffentlicht in:Lasers in medical science 2020-12, Vol.35 (9), p.2039-2048
Hauptverfasser: Fernandes, Beatriz Ferreira, da Cruz, Mariana Brito, Marques, Joana Faria, Madeira, Sara, Carvalho, Óscar, Silva, Filipe Samuel, da Mata, António Duarte Sola Pereira, Caramês, João Manuel Mendez
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Sprache:eng
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Zusammenfassung:Zirconia has been regarded as a promising material for dental implants, and Nd:YAG laser treatment has been proposed as a potential strategy to improve its bioactivity. The main aim of the present study was to evaluate the in vitro behavior of human fetal osteoblasts in contact with laser-textured zirconia implant surfaces assessing the effect of different texture patterns, spacing between laser passes and number of laser passes. Zirconia discs were produced and treated with Nd:YAG laser according to test group variables: texture (microgrooves and micropillar array), distance between surface features (25 μm, 30 μm and 35 μm), and laser passes [1, 2, 4, and 8]. Untextured sandblasted and acid-etched zirconia discs (SBAE) were used as controls. Human osteoblasts (hFOB 1.19) were cultured for 14 days on test and control samples. Morphology and cellular adhesion were observed using scanning electron microscopy (SEM). Cell viability and proliferation were evaluated at 1, 3, 7, and 14 days using a commercial resazurin-based method. Collagen type I was evaluated at 3 days using ELISA. Alkaline phosphatase (ALP) activity was evaluated at 7 days using a colorimetric enzymatic technique. Group comparisons were tested using ANOVA or Mann-Whitney test (Tukey’s post hoc) using statistical software, and significance was set at p  
ISSN:0268-8921
1435-604X
DOI:10.1007/s10103-020-03066-3