Purpose: To compare the fracture strength of three-unit provisional partial fixed dental prostheses (FDPs) fabricated by an indirect-direct technique from poly(methylmethacrylate) (PMMA) through digital and conventional workflows, and FDPs fabricated by a direct technique using Bisacryl (BisA) and externally reinforced BisA.
Materials And Methods: Forty partially edentulous typodonts with a missing mandibular left first molar and standard preparations on mandibular left second premolar and molar were used to fabricate three-unit provisional FDPs. Two materials and two techniques were used to fabricate a total of forty provisional FDPs: (1) BisA; (2) BisA reinforced with glass fiber strips [BisA-GFR]; (3) conventionally fabricated PMMA shell relined with PMMA [C-PMMA]; (4) CAD/CAM fabricated PMMA shell relined with PMMA [CAD/CAM-PMMA].
Aim: The purpose of the present study was to evaluate noninstrumentation technology (NIT) for root-canal cleansing in vivo.
Methodology: A total of 22 teeth that were to be extracted in 18 patients were treated with NIT for 30 min with 3.0% NaOCl.
The purpose of the study was to determine the effect of electron beam sterilization on gutta-percha cones (GPCs) at different times after sterilization. An agar diffusion test was used with -one aerobic bacterium (Bacillus subtilis) and five oral anaerobic bacteria (Fusobacterium nucleatum, Peptostreptococcus micros, Porphyromonas gingivalis, Propionibacterium acnes, and Veillonella parvula). With each microorganism 30 agar plates were prepared, evenly distributed among three groups (group 1: unsterilized GPCs; groups 2 and 3: GPCs sterilized by electron beam irradiation 5 months and 5 yr before, respectively).
View Article and Find Full Text PDFThe aim of the present in vitro study was to evaluate the influence of sodium fluoride solutions on brushing abrasion of eroded dentin. Dentin specimens were prepared from 60 bovine incisors. The specimens were embedded in acrylic resin, ground flat, polished and subsequently covered with tape exposing an area of 1.
View Article and Find Full Text PDFThrough extensive serologic, chemical, and molecular studies involving monoclonal Ig proteins and B cell-related populations, we provide definitive evidence that the V lambda IV subgroup of human light (L) chains is separate and distinct from V lambda III and all other known V lambda gene families. lambda IV and lambda III L chains were differentiated immunochemically using well-characterized polyclonal and monoclonal anti-V lambda subgroup-specific Abs. Prototypic L chains, originally classified as lambda IV on the basis of distinctive framework region 1 residues, were distinguished serologically from lambda IIIa, lambda IIIb, and lambda IIIc proteins and also from lambda I, lambda II, lambda VI, and lambda VIII L chains.
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