A tapping mode AFM study of collapse and denaturation in dentinal collagen.

OBJECTIVES: Tapping mode atomic force microscopy (AFM) was used to investigate the surface changes of collagen exposed to phosphoric acid treatment. We focus on denaturation and collapse following demineralization and exposure to air. METHODS: Unpolished dentin disks, obtained from freshly extracted human molars, were etched in 37% phosphoric acid for 15s, rinsed ultrasonically and gently blotted with soft paper; the specimens were then continuously observed using tapping mode AFM. RESULTS: Immediately after the removal of bulk water, the surface consisted of a porous network of banded collagen fibrils, having periodicities of 67nm. After approximately 8min of subsequent air-drying, the spacing between fibrils was lost, and the surface was observed to consist of a dense array of closely spaced fibrils. The banding periodicity was still observable. SIGNIFICANCE: The air drying of etched dentin results in the collapse of the collagen network, but not in the denaturation of the collagen fibrils. This study indicates that collapse and denaturation are separate phenomena. It further shows that water loss occurs rapidly, and disrupts the native conformation of the collagen network. This would have adverse effects on adhesion.

Moisture-dependent renaturation of collagen in phosphoric acid etched human dentin.

We used atomic force microscopy (AFM) to investigate the effects of acidic and aqueous treatments on human dentin. Two basic points were determined: the first is the ability of AFM to discriminate the effect of phosphoric acid (pH approximately equal to 1) on polished dentin, and the second is the demonstrable effect of moisture on fibrous collagen structure. AFM images confirmed that the polishing process led to the removal of both smear layer and smear plugs. Our AFM study of undried dentin, which was then acid treated and kept moist, revealed substantial morphological changes at the dentin surface. Collagen fibers, having a characteristic periodicity of 67 nm, were imaged in situ for the first time; these structures were absent in dentin treated by phosphoric acid and subsequently vacuum dried, even after prolonged reimmersion in water. The AFM technique permitted us to demonstrate the important roles that moisture and etching play in the determination of the structure of collagen fibrils. Such structure may also play an important role in the diffusibility of subsequently applied dental adhesion systems.