Introduction: The present study aimed to establish the staining protocol for quantification of elastic fibers and muscle fibers in arterial vessels through the Verhoeff method adapted with eosin in Chelonia mydas. Materials and Methods: Aorta and pulmonary arteries of 11 individuals of the species Chelonia mydas were used. The fragments were fixed in formaldehyde solution buffered 10% for 24 hours, subjected to routine histological processing and staining technique to be adapted Verhoeff, take the photografies and analyzed by Image Pro Plus Software. Results: The combination of ferric hematoxylin Verhoeff use blushed black elastic arteries blades, already eosin stained muscle fibers and collagen, allowing the tissue quantification through distinction staining by software. Conclusion: The protocol is a low-cost alternative that facilitate the acquisition of morphometric data for research with turtles.

Objectives To evaluate the effects of the surface modification of 316L stainless steel (SS) by lowtemperature plasma nitriding on endothelial cells for stent applications. Results X-ray diffraction (XRD) confirmed the incorporation of nitrogen into the treated steel. The surface treatment significantly increased SS roughness and hydrophilic characteristics. After 4 h the cells adhered to the nitride surfaces and formed clusters. During the 24 h incubation period, cell viability on the nitrided surface was higher compared to the polished surface. Nitriding reduced late apoptosis of rabbit aorta endothelial cell (RAEC) on the SS surface. Conclusion Low temperature plasma nitriding improved the biocompatible of stainless steel for use in stents.

A titanium surface nitrided by plasma contains nitrogen ions that guarantee resistance to corrosion and biocompatibility. Despite this, no descriptions concerning the influence of the expression of cell adhesion proteins and their influence on osteogenic cell differentiation are available. Thus, the present study aimed to assess the response of murine pre‐osteoblastic cells (MC3T3‐E1) cultured on nitrided titanium surfaces. Pre‐osteoblastic cells were grown on polished titanium discs, used as controls, and on previously characterized plasma‐nitrided titanium discs. Cells from both groups were submitted to the MTT cell viability test. The expressions of α5, α2, and β1 integrin were assessed by flow cytometry and immunofluorescence, while osteocalcin expression was assessed by flow cytometry. The nitrided surface presented higher α2 and β1 integrin expressions, as well as osteocalcin expression, when compared to the polished surface, with no alterations in cell viability. These findings seem to suggest that the plasma nitriding treatment produces a titanium surface with the potential for effective in vitro osseointegration.

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