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Evaluation of the bleached human enamel by Scanning Electron Microscopy
Carolina Baptista Miranda1, Clovis Pagani, Ana Raquel Benetti
1São José dos Campos School of Dentistry, UNESP.
Journal of Applied Oral Science : Revista FOB
|October 7, 2010
Summary
In-office bleaching with peroxides can cause enamel erosion and surface damage. Dentists should use these agents cautiously to protect dental hard tissues.
Area of Science:
- Dental materials science
- Biomaterials research
- Oral health diagnostics
Background:
- Tooth bleaching is a popular cosmetic procedure.
- The effects of bleaching peroxides on dental hard tissues are of significant research interest.
- Understanding these effects is crucial for safe clinical application.
Purpose of the Study:
- To qualitatively analyze human enamel morphology after in-office bleaching.
- To evaluate the effects of carbamide peroxide and hydrogen peroxide on enamel structure.
- To utilize Scanning Electron Microscopy (SEM) for detailed surface examination.
Main Methods:
- Human third molars were divided into four groups: control, 35% carbamide peroxide (2h and 8h total exposure), and light-activated 35% hydrogen peroxide (40min total exposure).
- Specimens were prepared using gold sputter coating under vacuum.
- Enamel surfaces were examined using SEM at 500x and 2000x magnification.
Main Results:
- Both 35% carbamide peroxide and 35% hydrogen peroxide caused morphological alterations on the enamel surface.
- Surface porosities indicative of an erosive process were observed.
- Depressions, crater formation, and exposed enamel rods were detected.
Conclusions:
- In-office bleaching agents can lead to varying degrees of enamel damage.
- Adverse effects on enamel morphology were randomly distributed across the surface.
- Caution is advised when using in-office bleaching materials due to potential enamel damage.
Related Concept Videos
Scanning Electron Microscopy
A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
Fundamental Principles
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Fundamental Principles
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Overview of Electron Microscopy
The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.

