Avaliação da efetividade de uma capacitação docente em consciência fonológica

Esta pesquisa teve como objetivo identificar o que os docentes que atuam no processo de alfabetização sabem sobre consciência fonológica, bem como verificar a eficácia da Capacitação Docente em Consciência Fonológica na ampliação desses conhecimentos. Este estudo se caracteriza por ser de campo, do tipo ensaio prospectivo e de cunho quantitativo analítico e contou com a participação de 19 educadores que atuam no programa Conectando Saberes da Secretaria de Educação da cidade de Esteio/RS. Os resultados obtidos neste estudo sugerem pouca ampliação do conhecimento geral dos professores sobre consciência fonológica após a Capacitação Docente em Consciência Fonológica. Mesmo após a formação, os educadores apresentaram dificuldades para responder perguntas específicas sobre o tema, principalmente quando relacionadas à prática em sala de aula. São necessárias intervenções de carga horária maior para que se possa obter modificações significativas no conhecimento e prática pedagógica dos alfabetizadores.Palavras-chave: fonoaudiologia, consciência fonológica, docentes, promoção da saúd

Is aggregated synthetic amorphous silica toxicologically relevant?

The regulatory definition(s) of nanomaterials (NMs) frequently uses the term 'agglomerates and aggregates' (AA) despite the paucity of evidence that AA are significantly relevant from a nanotoxicological perspective. This knowledge gap greatly affects the safety assessment and regulation of NMs, such as synthetic amorphous silica (SAS). SAS is used in a large panel of industrial applications. They are primarily produced as nano-sized particles (1-100 nm in diameter) and considered safe as they form large aggregates (> 100 nm) during the production process. So far, it is indeed believed that large aggregates represent a weaker hazard compared to their nano counterpart. Thus, we assessed the impact of SAS aggregation on in vitro cytotoxicity/biological activity to address the toxicological relevance of aggregates of different sizes

Moving Pharmacogenetics Into Practice: It’s All About the Evidence!

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/169310/1/cpt2327.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/169310/2/cpt2327_am.pd

Design of a mechanism for sample approach and alignment of a metrological atomic force microscope

In order to obtain the high accuracy required for a metrological atomic force microscope, the sample approach mechanism meets strict specifications. The design presented in this paper offers a stiff construction, which limits the influences of floor vibrations on the measurement. Next to this, thermal considerations in the design decrease the uncertainties introduced by temperature variations of the environment. Uncertainties can also be caused by misalignment of the sample holder with respect to the measurement system of three interferometers. To limit these uncertainties, the approach mechanism provides sufficient alignment possibilities. The performance of the sample approach mechanism was evaluated by means of a finite element simulation of its dynamic stiffness. A series of experiments provide the unknown parameters to the simulation model. The dynamic stiffness lies around 395 Hz, which is sufficiently high to provide accurate measurements.status: publishe

Moving Pharmacogenetics into Practice: It’s All About the Evidence!

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/169310/1/cpt2327.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/169310/2/cpt2327_am.pd

Design of a sample holder for a metrological atomic force microscope

This paper describes the design of a sample holder for a metrological atomic force microscope. Most attention goes to the measures taken to improve its mechanical and thermal stability. Dynamic simulations show a high natural frequency of the sample holder, which reduces the influence of floor vibrations on the measurement. A sample placement mechanism gives the user the possibility to easily reach and place the sample.status: publishe

Is aggregated synthetic amorphous silica toxicologically relevant?

BACKGROUND: The regulatory definition(s) of nanomaterials (NMs) frequently uses the term 'agglomerates and aggregates' (AA) despite the paucity of evidence that AA are significantly relevant from a nanotoxicological perspective. This knowledge gap greatly affects the safety assessment and regulation of NMs, such as synthetic amorphous silica (SAS). SAS is used in a large panel of industrial applications. They are primarily produced as nano-sized particles (1-100 nm in diameter) and considered safe as they form large aggregates (> 100 nm) during the production process. So far, it is indeed believed that large aggregates represent a weaker hazard compared to their nano counterpart. Thus, we assessed the impact of SAS aggregation on in vitro cytotoxicity/biological activity to address the toxicological relevance of aggregates of different sizes. RESULTS: We used a precipitated SAS dispersed by different methods, generating 4 ad-hoc suspensions with different aggregate size distributions. Their effect on cell metabolic activity, cell viability, epithelial barrier integrity, total glutathione content and, IL-8 and IL-6 secretion were investigated after 24 h exposure in human bronchial epithelial (HBE), colon epithelial (Caco2) and monocytic cells (THP-1). We observed that the de-aggregated suspension (DE-AGGR), predominantly composed of nano-sized aggregates, induced stronger effects in all the cell lines than the aggregated suspension (AGGR). We then compared DE-AGGR with 2 suspensions fractionated from AGGR: the precipitated fraction (PREC) and the supernatant fraction (SuperN). Very large aggregates in PREC were found to be the least cytotoxic/biologically active compared to other suspensions. SuperN, which contains aggregates larger in size (> 100 nm) than in DE-AGGR but smaller than PREC, exhibited similar activity as DE-AGGR. CONCLUSION: Overall, aggregation resulted in reduced toxicological activity of SAS. However, when comparing aggregates of different sizes, it appeared that aggregates > 100 nm were not necessarily less cytotoxic than their nano-sized counterparts. This study suggests that aggregates of SAS are toxicologically relevant for the definition of NMs.status: publishe

Agglomeration of titanium dioxide nanoparticles increases toxicological responses in vitro and in vivo.

BACKGROUND: The terms agglomerates and aggregates are frequently used in the regulatory definition(s) of nanomaterials (NMs) and hence attract attention in view of their potential influence on health effects. However, the influence of nanoparticle (NP) agglomeration and aggregation on toxicity is poorly understood although it is strongly believed that smaller the size of the NPs greater the toxicity. A toxicologically relevant definition of NMs is therefore not yet available, which affects not only the risk assessment process but also hinders the regulation of nano-products. In this study, we assessed the influence of NP agglomeration on their toxicity/biological responses in vitro and in vivo. RESULTS: We tested two TiO2 NPs with different primary sizes (17 and 117 nm) and prepared ad-hoc suspensions composed of small or large agglomerates with similar dispersion medium composition. For in vitro testing, human bronchial epithelial (HBE), colon epithelial (Caco2) and monocytic (THP-1) cell lines were exposed to these suspensions for 24 h and endpoints such as cytotoxicity, total glutathione, epithelial barrier integrity, inflammatory mediators and DNA damage were measured. Large agglomerates of 17 nm TiO2 induced stronger responses than small agglomerates for glutathione depletion, IL-8 and IL-1β increase, and DNA damage in THP-1, while no effect of agglomeration was observed with 117 nm TiO2. In vivo, C57BL/6JRj mice were exposed via oropharyngeal aspiration or oral gavage to TiO2 suspensions and, after 3 days, biological parameters including cytotoxicity, inflammatory cell recruitment, DNA damage and biopersistence were measured. Mainly, we observed that large agglomerates of 117 nm TiO2 induced higher pulmonary responses in aspirated mice and blood DNA damage in gavaged mice compared to small agglomerates. CONCLUSION: Agglomeration of TiO2 NPs influences their toxicity/biological responses and, large agglomerates do not appear less active than small agglomerates. This study provides a deeper insight on the toxicological relevance of NP agglomerates and contributes to the establishment of a toxicologically relevant definition for NMs

Agglomeration of titanium dioxide nanoparticles increases toxicological responses in vitro and in vivo

BACKGROUND: The terms agglomerates and aggregates are frequently used in the regulatory definition(s) of nanomaterials (NMs) and hence attract attention in view of their potential influence on health effects. However, the influence of nanoparticle (NP) agglomeration and aggregation on toxicity is poorly understood although it is strongly believed that smaller the size of the NPs greater the toxicity. A toxicologically relevant definition of NMs is therefore not yet available, which affects not only the risk assessment process but also hinders the regulation of nano-products. In this study, we assessed the influence of NP agglomeration on their toxicity/biological responses in vitro and in vivo. RESULTS: We tested two TiO2 NPs with different primary sizes (17 and 117 nm) and prepared ad-hoc suspensions composed of small or large agglomerates with similar dispersion medium composition. For in vitro testing, human bronchial epithelial (HBE), colon epithelial (Caco2) and monocytic (THP-1) cell lines were exposed to these suspensions for 24 h and endpoints such as cytotoxicity, total glutathione, epithelial barrier integrity, inflammatory mediators and DNA damage were measured. Large agglomerates of 17 nm TiO2 induced stronger responses than small agglomerates for glutathione depletion, IL-8 and IL-1β increase, and DNA damage in THP-1, while no effect of agglomeration was observed with 117 nm TiO2. In vivo, C57BL/6JRj mice were exposed via oropharyngeal aspiration or oral gavage to TiO2 suspensions and, after 3 days, biological parameters including cytotoxicity, inflammatory cell recruitment, DNA damage and biopersistence were measured. Mainly, we observed that large agglomerates of 117 nm TiO2 induced higher pulmonary responses in aspirated mice and blood DNA damage in gavaged mice compared to small agglomerates. CONCLUSION: Agglomeration of TiO2 NPs influences their toxicity/biological responses and, large agglomerates do not appear less active than small agglomerates. This study provides a deeper insight on the toxicological relevance of NP agglomerates and contributes to the establishment of a toxicologically relevant definition for NMs.status: publishe