Vanadium-Binding Protein in Marine Plankton from Tropical South Atlantic Ocean

We investigated the role of plankton in the vanadium (V) cycle at Cabo Frio, Rio de Janeiro state, Brazil, a region with high V concentration in the atmospheric particles due to marine aerosol. The concentrations of V in plankton vary from 0.08 to 20.9 µg g-1 (zooplankton), 0.1 to 28.4 µg g-1 (phytoplankton &gt; 64 µm) and < 0.0005 to 49.0 µg g-1 (small phytoplankton &gt; 20 µm). The V speciation in biomolecules was performed by the use of two strategies: (i) coupling of size exclusion chromatography (SEC) for the fractionation of species with inductively coupled plasma mass spectrometry (ICP-MS) and (ii) with size exclusion anionic exchange chromatography with UV-Vis detector coupled to inductively coupled plasma mass spectrometry (SEC-AE-UV-Vis-ICP-MS). The results showed a single fraction containing V associated with a biomolecule in the range of 8 to 16 kDa, with isoeletric points above 8. The preliminary analyses using matrix-assisted laser desorption-ionization-time of flight (MALDI-TOF) do not permit to identify such biomolecule, considering the broader size range of the proteins obtained

Ion release and local effects of titanium metal particles from dental implants: an experimental study in rats

Background: The objective of this study was to evaluate the accumulation of ions in blood and organs caused by Ti metal particles in a mandibular defect in rats, together with a description of the local reaction of oral tissues to these titanium alloy debris. Methods: Twenty Sprague-Dawley rats were randomly distributed into three groups: an experimental group with a mandibular bone defect filled with metallic debris obtained by implantoplasty; a positive control group; and a negative control group. Thirty days after surgery, the rats were euthanized and perilesional tissue surrounding the mandibular defect was removed, together with the lungs, spleen, liver and brain. Two blood samples were collected: immediately before surgery and before euthanasia. The perilesional tissue was histologically analyzed using hematoxylin-eosin staining, and titanium, aluminum and vanadium ion concentrations in blood and organs were measured by TQ-ICP-MS. Descriptive and bivariate analyses of the data were performed. Results: All rats with implanted metal debris showed metal particles and a bone fracture callus on the osseous defect. The metal particles were surrounded by a foreign body reaction characterized by the presence of histiocytes and multinucleated giant cells. The experimental group had a significant higher concentration of Ti ions in all studied organs except lung tissue (p < 0.05). In addition, there were more V ions in the brain in the experimental group (p = 0.008). Conclusions: Although further studies are required to confirm the clinical relevance of these results, Ti metal particles in the jaw might increase the concentration of metal ions in vital organs and induce a foreign body reaction. This article is protected by copyright. All rights reserved. Keywords: Ion release; Ti6Al4V; implantoplasty; metal particles; peri-implantitis; titanium

Capabilities of Single Cell ICP-MS for the Analysis of Cell Suspensions from Solid Tissues

Single cell elemental (SC) analysis of isogenic cell cultures can be done using inductively coupled plasma (ICP-MS) detection. However, 2D cell cultures are just models to simplify the complexity of real tissue samples. Here, we show for the first time the capabilities of the technique (SC-ICP-MS) to analyze single cell suspensions of isolated cells from tissues. An optimized cocktail of proteolytic and collagenolytic enzymes was applied in a single preparation step with cellular yields up to 28% using 0.5 g of fresh rat spleen and liver, respectively. The retrieved cells revealed adequate morphology and stability to be examined by SC-ICP-MS. Quantitative elemental analysis of P, S, Cu, and Fe from disaggregated cells from rat spleen and liver tissues revealed levels of Fe of 7–16 fg/cell in the spleen and 8–12 fg/cell in the liver, while Cu was about 3–5 fg/cell in the spleen and 1.5–2.5 fg/cell in the liver. Evaluation of the transmembrane protein transferrin receptor 1 (TfR1) expression levels in disaggregated cells was also conducted by using a Nd-labelled antibody against this cell surface biomarker. Quantitative results showed significantly lower expression in the disaggregated cells than in the cell model HepG2, in agreement with the overexpression of this biomarker in tumor cells. In this proof of concept study, the tissue disaggregation protocol has shown to maintain the elemental intracellular content of cells as well as the presence of relevant antigens. This opens a completely new area of research for SC-ICP-MS in tissue samples as a complementary strategy with validation capabilities