Masterarbeit, 2012
96 Seiten, Note: A
1. CHAPTER 1: INTRODUCTION
2. CHAPTER 2: LITERATURE REVIEW
2.1 INTRODUCTION
2.2 DENTAL COMPOSITES
2.2.1 COMPOSITION AND STRUCTURE
2.2.2 RESIN/ORGANIC MATRIX
2.2.3 FILLER
2.2.4 COUPLING AGENT
2.2.5 INTIATORS AND ACCELERATORS
2.2.6 CLASSIFICATION OF COMPOSITES
2.2.7 PACKABLE COMPOSITES
2.2.8 POLYMERIZATION REACTION
2.3 PHYSICAL PROPERTIES OF DENTAL COMPOSITES
2.3.1 Working and setting time:
2.3.2 Polymerization Shrinkage
2.3.3 Thermal Properties
2.3.4 Water Sorption.
2.3.5 Solubility
2.3.6 Colour and Colour Stability
2.4 MECHANICAL PROPERTIES
2.4.1 Strength and Modulus
2.4.2 Hardness
2.4.3 Bond Strength and Dental Substrates (Ceramics, Alloys, etc….)
2.5 CLINICAL PROPERTIES
2.5.1 Depth of cure for light-cured composites
2.5.2 Radiopacity
2.5.3 Wear Rates
2.5.4 Biocompatibility
2.6 DENTAL ADHESIVES
2.7 FLOWABLE COMPOSITES
2.7.1 PROPERTIES OF FLOWABLE COMPOSITES
2.7.2 VERTISE FLOW
2.7.3 GRANDIO FLOW
2.7.4 PREMISE FLOWABLE
2.7.5 HYDROXYETHYL METHACRYLATE (HEMA) Figure 2.6
3. CHAPTER 3: AIMS AND OBJECTIVES
3.1 AIM
3.2 OBJECTIVES
4. CHAPTER 4: MATERIAL AND METHODS
4.1 COMPOSITE MATERIALS
4.2 IMMERSION SOLUTIONS
4.3 METHODOLOGY FOR WATER ABSORPTION AND DESORPTION
4.3.1 SAMPLE PREPARATION
4.3.2 ABSORPTION
4.3.3 LONG-TERM IMMERSION
4.3.4 DESORPTION
4.3.5 DIFFUSION THEORY AND FICK’S LAW
4.3.6 CALCULATING DIFFUSION COEEFICIENT
4.3.7 CALCULATING SOLUBILITY
4.3.8 CALCULATING REAL UPTAKE
4.4 COMPOSITE RESIN DEGREE OF CONVERSION
4.4.1 METHODOLOGY FOR COMPOSITE DEGREE OF CONVERSION
4.5 POLYMERIZATION EXOTHERM
4.5.1 METHODOLOGY FOR EXOTHERM MEAUREMENTS
4.6 DEPTH OF CURE OF LIGHT CURED COMPOSITES
4.6.1 METHODOLOGY FOR DEPTH OF CURE
4.7 STATISTICAL METHODOLOGY
5. CHAPTER 5: RESULTS
5.1WATER UPTAKE OF COMPOSITES
5.1.1 Vertise TM Flow
5.1.2 AVERAGE OF VERTISE TM FLOW, GRANDIO FLOW and PREMISE FLOWABLE IN DISTILLED WATER AND ARTIFICAL SALIVA
5.2 DESORPTION OF COMPOSITES
5.2.1 THREE MONTHS CONTINOUS UPTAKE OF FLOWABLE COMPOSITE (VF, GF & PF) IN ARTIFICIAL SALIVA
5.3 DIFFUSION COEEFICIENT FOR ABSORPTION AND DESORPTION AND SOLUBILTY %
5.4 DEGREE OF CONVERSION
5.5 POLYMERISATION EXOTHERM
5.6 DEPTH OF CURE
6. CHAPTER 6: DISCUSSION
6.1: IMMERSION SOLUTIONS
6.2: WATER ABSORPTION AND DESORPTION PROFILE AFTER IMMERSION IN DISTILLED WATER AND ARTIFICIAL SALIVA
6.3: SOLUBILITY OF THE COMPOSITES
6.4 DIFFUSION COEEFICIENT OF THE COMPOSITES.
6.5: DEGREE OF CONVERSION
6.6: POLYMERISATION EXOTHERM
6.7: DEPTH OF CURE
7. CHAPTER 7: CONCLUSIONS
This thesis aims to assess the physical and mechanical characteristics of the self-adhesive flowable composite Vertise™ Flow by comparing it against two conventional market alternatives, Grandio Flow and Premise Flowable, through the analysis of water interaction and polymerization behavior.
2.2.2 RESIN/ORGANIC MATRIX
Primarily, in a fluid monomer form, the resin is the chemically active element, which gets converted to a rigid polymer, by a free radical polymerization reaction. Due to its ability to convert from a plastic to rigid form it is favorable to be used for restorations (van Noort, 2007). These fluid resins (monomers) are viscous liquids and their viscosity is reduced, to a useful clinical level, by adding diluent monomers (Powers & Sakaguchi, 2006)
The most common monomers used in dental composites are dimethacrylates amongst which 2, 2-bis [4(2-hydroxy-3 methacryloyloxy-propyloxy)-phenyl) 1] propane (Bis-GMA) (Figure 2.1), which is derived from reacting bis-phenol-A and glycidylmethacrylate; it is referred to as Bowens-resin, after its inventor. The other monomer which is used in a number of composites, in place of Bis-GMA, is Urethane Dimethacrylate (UDMA figure 2.2) (van Noort. 2007)
Both Bis-GMA and UDMA contain carbon-carbon double bonds at each chain of their chemical structures, which undergo addition polymerization (Powers and Sakaguchi, 2006). Due to their high molecular weight, even a small addition of filler results in a composite with a viscosity that is inappropriate for clinical use. (van Noort, 2007) Bis-GMA and UDMA (Figure 2.2) are highly viscous fluids (Patel, 2012) due to the hydrogen bonding interactions between hydroxyl group and monomer molecules,(Chen, 2010).Thus low viscosity diluents such as tri-ethylene, glycol dimethacrylate (Figure 2.3) are added by the manufacturers (Powers and Sakaguchi, 2006).
CHAPTER 1: INTRODUCTION: Provides an overview of restorative dentistry and the evolution of flowable composites, specifically introducing Vertise™ Flow and its dual adhesion mechanism.
CHAPTER 2: LITERATURE REVIEW: Examines the composition, physical properties, and clinical behavior of dental composites, with a specific focus on the role of HEMA and light-curing technology.
CHAPTER 3: AIMS AND OBJECTIVES: Defines the research goal to compare Vertise™ Flow with standard flowable composites regarding water interaction, solubility, and curing performance.
CHAPTER 4: MATERIAL AND METHODS: Details the experimental procedures, including sample preparation, immersion tests in distilled water and artificial saliva, and spectroscopic methods for analysis.
CHAPTER 5: RESULTS: Presents the findings regarding water uptake, desorption, degree of conversion, polymerization exotherm, and depth of cure for the tested composites.
CHAPTER 6: DISCUSSION: Interprets the experimental results, linking the presence of HEMA to increased water absorption and polymerization exotherms compared to non-HEMA materials.
CHAPTER 7: CONCLUSIONS: Summarizes that while Vertise™ Flow offers specific adhesive benefits, its higher water uptake and polymerization exotherm represent critical factors for clinical application.
Flowable composites, Vertise™ Flow, HEMA, Water absorption, Solubility, Polymerization exotherm, Depth of cure, FTIR, Dental materials, Adhesive dentistry, Resin matrix, Diffusion coefficient, Biocompatibility, Microleakage, Composite restoration.
The thesis evaluates the physical and mechanical properties of the self-adhesive flowable composite Vertise™ Flow (VF) compared to conventional products like Grandio Flow and Premise Flowable.
The work covers dental composite chemistry, water sorption behavior, polymerization kinetics, and clinical performance metrics like depth of cure and exotherm measurements.
The primary aim is to analyze how the inclusion of hydrophilic monomers like HEMA in Vertise™ Flow influences its interaction with external media compared to non-HEMA flowable composites.
The study employed gravimetric analysis for water absorption/desorption, FTIR spectroscopy for evaluating the degree of conversion, and K-type thermocouples for measuring polymerization exotherms.
The main body investigates the composition of resin matrices, the physics of water sorption, the mechanics of polymerization, and provides a comparative experimental analysis of three commercial flowable composites.
Key terms include flowable composites, water absorption, HEMA, degree of conversion, polymerization exotherm, and dental restoration longevity.
The presence of HEMA, a hydrophilic hydrogel, leads to significantly higher water uptake and a higher polymerization exotherm in Vertise™ Flow compared to the other tested composites.
Due to its high polymerization exotherm, the author does not recommend using Vertise™ Flow in close proximity to the tooth pulp to avoid potential thermal trauma.
No, the study found no statistically significant difference in the degree of conversion between the bottom surfaces of the three tested flowable composite materials.
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