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Research Project
CICECO-Aveiro Institute of Materials
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Publications
Dried blood spots in clinical lipidomics: optimization and recent findings
Publication . Ferreira, Helena Beatriz; Guerra, Inês M.S.; Melo, Tânia; Rocha, Hugo; Moreira, Ana S.P.; Paiva, Artur; Domingues, M. Rosário
Dried blood spots (DBS) are being considered as an alternative sampling method of blood collection that can be used in combination with lipidomic and other omic analysis. DBS are successfully used in the clinical context to collect samples for newborn screening for the measurement of specific fatty acid derivatives, such as acylcarnitines, and lipids from whole blood for diagnostic purposes. However, DBS are scarcely used for lipidomic analysis and investigations. Lipidomic studies using DBS are starting to emerge as a powerful method for sampling and storage in clinical lipidomic analysis, but the major research work is being done in the pre- and analytical steps and procedures, and few in clinical applications. This review presents a description of the impact factors and variables that can affect DBS lipidomic analysis, such as the type of DBS card, haematocrit, homogeneity of the blood drop, matrix/chromatographic effects, and the chemical and physical properties of the analyte. Additionally, a brief overview of lipidomic studies using DBS to unveil their application in clinical scenarios is also presented, considering the studies of method development and validation and, to a less extent, for clinical diagnosis using clinical lipidomics. DBS combined with lipidomic approaches proved to be as effective as whole blood samples, achieving high levels of sensitivity and specificity during MS and MS/MS analysis, which could be a useful tool for biomarker identification. Lipidomic profiling using MS/MS platforms enables significant insights into physiological changes, which could be useful in precision medicine.
Insights into corrosion behaviour of uncoated Mg alloys for biomedical applications in different aqueous media
Publication . Neves, C.S.; Sousa, I.; Freitas, M.A.; Moreira, L.; Costa, C.; Teixeira, J.P.; Fraga, S.; Pinto, E.; Almeida, A.; Scharnagl, N.; Zheludkevich, M.L.; Ferreira, M.G.S.; Tedim, J.
MgCa and MgGd series of alloys are often reported as promising candidates for biomedical
applications. In the present study, cytotoxicity and corrosion behavior of Mg1Ca and
Mg10Gd alloys in different electrolytes (NaCl, PBS, MEM) have been investigated in order to
make a direct comparison and understand the mechanisms behind their performance.
Potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) were
employed to analyze corrosion processes depending on media composition, whereas X-Ray
diffraction (XRD) and scanning electron microscopy (SEM) were used to evaluate crystalline
structure, phase composition and surface morphology of the corroded substrates after
immersion in the different electrolytes. Moreover, cytotoxicity of the Mg alloys was
assessed using the WST-1 reduction and lactate dehydrogenase (LDH) release assays in
L929 mouse fibroblasts. The electrochemical results showed that Mg1Ca has a lower
degradation rate when compared to Mg10Gd, due to the lower microgalvanic effects and
the presence of Ca as an alloying element. Furthermore, the corrosion activity is reduced in
MEM, for both alloys, when compared to NaCl and PBS. The cytotoxicity assays revealed
that Mg10Gd was cytotoxic in all the conditions tested, while the toxicity of Mg1Ca was
low. Overall, these findings show that Mg1Ca alloy presents a higher corrosion resistance
and biocompatibility and is a promising material to be used in biomedical implants.
Co-exposure with CeO2NPs results in an antagonistic effect on the cytotoxicity and genotoxicity of TiO2NP on A549 cells
Publication . Rosário, Fernanda; Vilaça, Cláudia; Costa, Carla; Lopes, Cláudia B.; Estrada, Ana C.; Tavares, Daniela S.; Teixeira, João Paulo; Reis, Ana Teresa
Objective: Assess the CYTOTOXIC and GENOTOXIC POTENTIAL resulting
from titanium dioxide nanoparticles (TiO2NP) and cerium oxide
nanoparticles (CeO2NP) co-exposure in human lung epithelial cell line
A549.
In Vitro Hepatotoxic and Neurotoxic Effects of Titanium and Cerium Dioxide Nanoparticles, Arsenic and Mercury Co-Exposure
Publication . Rosário, Fernanda; Costa, Carla; Lopes, Cláudia B.; Estrada, Ana C.; Tavares, Daniela S.; Pereira, Eduarda; Teixeira, João Paulo; Reis, Ana Teresa
Considering the increasing emergence of new contaminants, such as nanomaterials, mixing with legacy contaminants, including metal(loid)s, it becomes imperative to understand the toxic profile resulting from these interactions. This work aimed at assessing and comparing the individual and combined hepatotoxic and neurotoxic potential of titanium dioxide nanoparticles (TiO2NPs 0.75-75 mg/L), cerium oxide nanoparticles (CeO2NPs 0.075-10 μg/L), arsenic (As 0.01-2.5 mg/L), and mercury (Hg 0.5-100 mg/L) on human hepatoma (HepG2) and neuroblastoma (SH-SY5Y) cells. Viability was assessed through WST-1 (24 h) and clonogenic (7 days) assays and it was affected in a dose-, time- and cell-dependent manner. Higher concentrations caused greater toxicity, while prolonged exposure caused inhibition of cell proliferation, even at low concentrations, for both cell lines. Cell cycle progression, explored by flow cytometry 24 h post-exposure, revealed that TiO2NPs, As and Hg but not CeO2NPs, changed the profiles of SH-SY5Y and HepG2 cells in a dose-dependent manner, and that the cell cycle was, overall, more affected by exposure to mixtures. Exposure to binary mixtures revealed either potentiation or antagonistic effects depending on the composition, cell type and time of exposure. These findings prove that joint toxicity of contaminants cannot be disregarded and must be further explored.
Integrated Use of Bioaccumulation, Genotoxic, and Haematological Endpoints to Assess the Effect of Water Remediation Strategies on Fish Health: A Complementary Study
Publication . Mieiro, Cláudia; Coelho, João; Reis, Ana Teresa; Castro, Diana; Figueira, Paula; Martinho, Filipe; Pardal, Miguel; Pereira, Eduarda; Pacheco, Mário; Lopes, Cláudia
Biosorption successfully remediates saline water contaminated with legacy contaminants, but its effects on the health of marine organisms remain unclear. Therefore, our aim was to address this knowledge gap with data on the accumulation ability, as well as the cytogenetic and biochemical effects in turbot (Scophthalmus maximus). To this end, we exposed turbot for seven days to a mixture of remediated metals (Rem treatments: Cd, Hg, and Pb), with and without the presence of nanoparticles (NP), and compared them with the maximum allowable concentrations (MAC treatment) for effluent discharges. We determined the metal accumulation in the blood and kidney and evaluated haematological changes (red blood cell count, haemoglobin, and mean cell haemoglobin (MCH)) and genotoxicity (erythrocytic nuclear abnormalities assay) in the blood. The results showed that remediation with non-living macroalgae significantly reduced the metallic blood and kidney burdens in the Rem treatments. Furthermore, no genotoxic potential occurred in the Rem and MAC treatments in parallel with the reduction in MCH levels in the Rem treatments, which would reflect hematopoietic disturbances in the MAC. Our results validate biosorption remediation as we achieved a considerable reduction in metal loads while maintaining the health status of fish, highlighting the importance of testing water remediation methods in the biota.
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Funding agency
Fundação para a Ciência e a Tecnologia
Funding programme
6817 - DCRRNI ID
Funding Award Number
UIDP/50011/2020
