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 ∼ 1) on polished dentin, and the second is the demonstrable effect of
Immunocytochemical identification of type I collagen in acid-etched dentin
✍ Scribed by Lorenzo Breschi; Jorge Perdigão; Pietro Gobbi; Giovanni Mazzotti; Mirella Falconi; Manuela Lopes
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 378 KB
- Volume
- 66A
- Category
- Article
- ISSN
- 1549-3296
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✦ Synopsis
Abstract
The hypothesis tested in this study is that the application of phosphoric acid prevents collagen fibrils (CF) from maintaining their structural morphology, as assessed by their immunochemical antigenicity. Dentin was conditioned with EDTA and with 35% H~3~PO~4~ for 15, 30, and 60 s. For a control there was no treatment. A pre‐embedding immunohistochemical procedure was evaluated under high‐resolution SEM and a postembedding immunolocalization technique was performed on ultrathin sections at TEM level. Conditioning with EDTA resulted in a weaker labeling signal than for dentin conditioned with H~3~PO~4~. The most intense labeling was observed after dentin had been etched with H~3~PO~4~ for 15 s. The least intensive labeling was evident when the acid was applied for 30 s or for 60 s. A very weak signal was detected on the untreated dentin surface. These results provide evidence that a 15‐s application of 35% H~3~PO~4~ causes mineral dissolution of the crystals enveloping the superficial CF without damaging the ultrastructure of the CF while longer applications of 35% H~3~PO~4~ cause alterations in the CF that decrease their antigenicity. © 2003 Wiley Periodicals, Inc. J Biomed Mater Res 66A: 764–769, 2003
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Procollagen (Type I) contains a noncollagenous COOH-terminal propeptide (C-propeptide) hypothesized to be important in directing chain association and alignment during assembly. We previously expressed human pro-␣2(I) cDNA in rat liver epithelial cells, W8, that produce only pro-␣1(I) trimer collage