59 research outputs found
Psychological Indicators and Perceptions of Adolescents in Residential Care
Abstract The institutionalization of adolescents has been mentioned in the literature with positive and negative aspects. This study investigated 61 adolescents in residential care aiming to evaluate psychological problems and perceptions related to the care, using interviews and the YSR. Data was evaluated using quantitative and qualitative analysis, using gender, age and length of institutionalization as variables. Results indicated clinical scores for psychological problems, except for externalizing problems, in younger girls recently taken into care and older boys institutionalized for longer periods. The perceptions about the care were negative or indifferent; elements of positivity were expressed by adolescents institutionalized for longer periods. Instability in the permanence in the care service and the reasons for having been taken into care were manifested with psychological distress. There were few contacts with the family of origin; the adolescents mentioned the importance of their families and the desire to leave the institution. Members of the institutional teams were indicated as sources of care and protection. This study reflects the challenges for the positive development of this population
Germinação e crescimento inicial da muda de orelha-de-macaco (Enterolobium contortisiliqunn (Vell.) Morong): efeito de tratamentos químicos e luminosidade
The multidimensional evaluation and treatment of anxiety in children and adolescents: rationale, design, methods and preliminary findings
A versatile reagent to synthesize diverse ionic liquids ranging from small molecules and dendrimers to functionalized proteins
An ionic liquid “reagent” bearing a succinimidyl activated ester is reported that can be used to synthesize a variety of small molecule and macromolecular ionic liquids. In addition, the ionic liquid reagent was used to modify lysozyme, and the protein retained its structure and function after modification. This study describes a facile and reliable route to new ionic liquid compositions
Real time imaging of supramolecular assembly formation via programmed nucleolipid recognition
Immobilized Hydrogels for Screening of Molecular Interactions
Spatially arrayed, high-density microarrays enable the
rapid assessment of biological recognition events, and this
information is of widespread interest for those working
in basic research laboratories as well as in the clinic.
Today, one can find DNA, protein, or small molecule
arrays. Limitations with these systems include covalent
modification of the target complement to the array substrate, array- and target-dependent setup conditions,
multiple steps, and loss of hydration at the surface. To
overcome these limitations, we have designed, prepared,
and evaluated immobilized hydrogels as general screening
chambers for small molecule−protein, protein−protein,
and nucleic acid−nucleic acid interactions. This biomaterial-based approach is facile, rapid, requires only one
setup protocol, and physically entraps the target complement within the polymer network and thus offers advantages over the conventional chips
Diphosphonium Ionic Liquids as Broad-Spectrum Antimicrobial Agents
PURPOSE: One of the most disturbing trends in recent years is the growth of resistant strains of bacteria with the simultaneous dearth of new antimicrobial agents. Thus, new antimicrobial agents for use on the ocular surface are needed. METHODS: We synthesized a variety of ionic liquid compounds, which possess two positively charged phosphonium groups separated by ten methylene units in a “bola” type configuration. We tested these compounds for antimicrobial activity versus a variety of ocular pathogens, as well as their cytoxicity in vitro in a corneal cell line and in vivo in mice. RESULTS: The ionic liquid Di-Hex C10 demonstrated broad in vitro antimicrobial activity at the low micromolar concentrations versus Gram-negative and Gram-positive organisms, including methicillin-resistant Staphylococcus aureus strains, as well as ocular fungal pathogens. Treatment with Di-Hex C10 resulted in bacterial killing in as little as 15 minutes in vitro. Di-Hex C10 showed little cytotoxicity at 1 μM versus a corneal epithelial cell line or at 10 μM in a mouse corneal wound model. We also show that this bis-phosphonium ionic liquid structure is key, as a comparable mono phosphonium ionic liquid is cytotoxic to both bacteria and corneal epithelial cells. CONCLUSIONS: Here we report the first use of dicationic bis-phosphonium ionic liquids as antimicrobial agents. Our data suggest that diphosphonium ionic liquids may represent a new class of broad-spectrum antimicrobial agents for use on the ocular surface
Study on agglutinating factors from flocculent Saccharomyces cerevisiae strains
International audienceThe lectin-like theory suggest that yeast flocculation is mediated by an aggregating lectinic factor. In this study we isolated an agglutinating factor, which corresponds to lectin, from whole cells by treating the flocculent wild-type Saccharomyces cerevisiae NCYC 625 strain and its weakly flocculent mutant [rho°] with EDTA and two non-ionic surfactants (Hecameg and HTAC). The dialysed crude extracts obtained in this way agglutinated erythrocytes and this hemagglutination was specifically inhibited by mannose and mannose derivatives. However, SDS-PAGE profiles showed that the three reagents had different effects on the yeast cells. The non-ionic surfactants appeared to be the most efficient, as their extracts possessed the highest specific agglutinating activity. The products released by the wild-type strain presented a higher specific agglutinating activity than those released by the [rho°] mutant. Purification of the agglutinating factor from extracts of both strains by affinity chromatography revealed two active bands of relative mass of 26 and 47 kDa on SDS-PAGE. Mass spectrometry analysis by MALDI-TOF, identified a 26 kDa band as the triose phosphate isomerase (TPI) whereas a 47 kDa band was identical to enolase. Edman degradation showed that the N-terminal sequences of these proteins were similar to TPI and enolase, respectively. The difference in the flocculation behaviour of the two strains is due to changes in the protein composition of the cell wall and in the protein structure involved in cell-cell recognition
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