RESUMEN
BACKGROUND/PURPOSE: Color errors associated with the visual color duplication approach for ceramic laminate veneers are still challenging in esthetic dentistry. The aim of this study is to evaluate color errors generated during traditional visual shade matching approach. MATERIALS AND METHODS: Eighteen stooth-shaped veneer discs (shade A2 and 0.7 mm in thickness) were fabricated using six veneer materials. The veneer specimens placed on five extracted teeth with nominal shade A2 formed veneer-tooth combinations. Color coordinates of the A2 shade tab, the extracted teeth, and the veneer-tooth combinations were measured using a spectrophotometer. Then, the veneers were reduced to 0.5 mm, and 0.3 mm in thickness consecutively. Color measurements were performed repeatedly. Color differences of the extracted teeth to veneer-tooth combinations (ΔEt-v), veneer-tooth combinations to shade tab (ΔEv-s), and translucency parameter (TP) values were calculated and analyzed using Two-way ANOVA. RESULTS: ΔEt-v ranged from 2.0937 to 5.0603 (mean of 3.1833±1.5485). Mean of ΔEv-s was 4.0103±1.8508. ΔEt-v and ΔEv-s values were significantly influenced by veneer material and thickness (P<0.05). TP values decreased gradually with the lessening of veneers thickness. CONCLUSION: Acceptable color duplication of ceramic veneers cannot be achieved by routine visual shade replica protocols, when the thickness of veneers is less than 0.7 mm. Specified color matching standards for the ceramic veneers are needed.
RESUMEN
Nucleus pulposus (NP) tissue engineering has been proposed as a novel biological treatment for early-stage intervertebral disc degeneration. In this study, a novel functional self-assembling peptide PKP was first designed by linking the short functional motif of bone morphogenetic protein-7 (BMP7) to the C-terminal of RADA16-I, and another new functional self-assembling peptide was obtained by mixing RKP with RADA16-I. Then, the biocompatibilities and bioactivities of RKP and RAD-RKP for human degenerated nucleus pulposus cells (hNPCs) were studied in vitro. Atomic force microscopy and scanning electron microscopy (SEM) confirmed that both RKP and RAD-RKP could self-assemble into three-dimensional (3D) nanofiber hydrogel scaffolds in a culture medium at 37°C. After the hNPCs were cultured in 3D scaffolds, both RKP and RAD-RKP exhibited reliable attachment and extremely low cytotoxicities (<14%), which were verified by SEM and cytotoxity assays, respectively. Our results also showed that the functional-based scaffolds could increase the proliferation and migration of hNPCs after 7 days compared with culture plates and pure RADA16-I. Quantitative real-time polymerase chain reaction demonstrated that the expressions of collagen II α1, Sox-9, and aggrecan were upregulated, while collagen I α1 was downregulated by functional-based scaffolds after 28 days. Furthermore, we also confirmed that RAD-RKP exhibited a higher hNPC proliferation, migration, and expression of Sox-9 and aggrecan compared with pure RKP. Therefore, the results of this study indicated that the BMP7 short motif-designed functional self-assembling peptide nanofiber hydrogels could be used as excellent scaffolds in NP tissue engineering, and RAD-RKP might have further potential application in human mild degenerated NP tissue regeneration.