Abstract
The present report describes techniques of fixation and embedding suitable for studying the fine structure of odontoblasts without demineralization. The quality of the procedures employed was verified by comparing the ultrastructural preservation of the odontoblasts prepared by simple fixation and by the double-fixation method. Simple fixation by immersion in osmium tetroxide in vacuum preserves the longitudinal arrangement of the rough endoplasmic reticulum and Golgi apparatus, showing various vesicles which often contain filamentous threads of weak electron density aligned in parallel at repeating intervals typical of odontoblastic cells. The results obtained with this method are compared to previous descriptions of the ultrastructure of odontoblasts.