1,721,149 research outputs found
Organically modified silica nanoparticles doped with new acridine-1,2-dioxetane analogues as thermochemiluminescence reagentless labels for ultrasensitive immunoassays
Doped organically modified silica nanoparticles (ORMOSIL NPs) with luminescent molecules represent a potent approach to signal amplification in biomolecule labeling. Herein, we report the synthesis of new ORMOSIL NPs incorporating thermochemiluminescent (TCL) 1,2-dioxetane derivatives to prepare TCL labels for ultrasensitive immunoassay, displaying a detectability comparable to those offered by other conventional luminescence-based systems. Amino-functionalized ORMOSIL NPs were synthesized for inclusion of acridine-containing 1,2-dioxetane derivatives with a fluorescence energy acceptor. The doped ORMOSIL NPs were further functionalized with biotin for binding to streptavidin-labeled species to be used as universal detection reagents for immunoassays. A quantitative non-competitive immunoassay for streptavidin has been developed by immobilizing anti-streptavidin antibody to capture streptavidin, then the antibody-bound streptavidin was detected by the biotinylated TCL ORMOSIL NPs. The analytical performance was similar to that obtained by chemiluminescent (CL) detection using horseradish peroxidase (HRP) as label, being the limits of detection 2.5-3.8 and 0.8 ng mL(-1) for TCL and CL detection, respectively. In addition, since the TCL emission is simply initiated by thermolysis of the label, chemical reagents were not required, thus allowing reagentless detection with a simplification of the analytical protocols. A compact mini dark box device based on the use of a cooled charge-coupled device (CCD) and a miniaturized heater has been developed and used to quantify the light emission after heat decomposition of the label at a temperature of 90-120 °C. These characteristics make TCL-doped ORMOSIL NPs ideal universal nanoprobes for ultrasensitive bioassays such as immuno- and DNA-based assay
A portable device for on site detection of chicken ovalbumin in artworks by chemiluminescent immunochemical contact imaging
The development of user-friendly devices for on site analysis and characterization of painting materials is one of the most challenging objectives in the diagnostics for cultural heritage. Thanks to the specificity of antigen-antibody reactions, immunological methods have been already successfully applied for the detection of proteins and for their localization within painting stratigraphies. Moreover, by combining the advantages of the immunological techniques with the high detectability offered by chemiluminescence detection, it has been possible to achieve good analytical performance and very low detection limits. This work was aimed at developing a portable analytical device for the detection of chicken ovalbumin (a protein found in egg tempera and in egg-based protective varnishes) in painting samples employing ready-to-use analytical cartridges and a thermoelectrically-cooled CCD camera as a chemiluminescence detector. The protein was extracted from using a simple procedure and revealed by a non-competitive immunoassay with chemiluminescence contact imaging detection. The assay was simple, fast and suitable for the detection of ovalbumin in small samples. This analytical system provided positive identification of ovalbumin in samples obtained from both fresh or artificially aged paint reconstructions and historical paintings. It might be easily employed in different contexts (such as small museums, restoration laboratories or even on site) by restorers to obtain prompt information during restoration actions, such as cleaning operations. In perspective this device could be also employed for the detection of other proteinaceous and organic painting component
METHOD FOR THE PRODUCTION OF THERMOCHEMILUMINESCENT SILICA NANOPARTICLES AND THEIR USE AS MARKERS IN BIOANALYTIC METHODS
The invention relates to thermochemiluminescent silica nanoparticles containing in dispersion in the silica matrix molecules of a thermochemiluminescent acridine-based 1,2-dioxetane and additional chemical species, such as a fluorescent energy acceptor with the function of improving the efficiency of the thermochemiluminescent reaction and/or modifying the emission wavelength, and a method for the synthesis thereof. The nanoparticles are functionalized on the surface with reactive groups (e.g. amines) and procedures are described for bonding them to biospecific probes (e.g. antibodies) and enabling their use as thermochemiluminescent markers in bioanalytical methods (e.g. immunometric methods) based on thermochemi luminescence measurements
Immunochemical Micro Imaging Analyses for the Detection of Proteins in Artworks
The present review is aimed at reporting on the most advanced and recent applications of immunochemical imaging techniques for the localization of proteins within complex and multilayered paint stratigraphies. Indeed, a paint sample is usually constituted by the superimposition of different layers whose characterization is fundamental in the evaluation of the state of conservation and for addressing proper restoration interventions. Immunochemical methods, which are based on the high selectivity of antigen–antibody reactions, were proposed some years ago in the field of cultural heritage. In addition to enzyme-linked immunosorbent assays for protein identification, immunochemical imaging methods have also been explored in the last decades, thanks to the possibility to localize the target analytes, thus increasing the amount of information obtained and thereby reducing the number of samples and/or analyses needed for a comprehensive characterization of the sample. In this review, chemiluminescent, spectroscopic and electrochemical imaging detection methods are discussed to illustrate potentialities and limits of advanced immunochemical imaging systems for the analysis of paint cross-sections
Chemiluminescent high-throughput microassay for evaluation of acetylcholinesterase inhibitors
Current drug therapies for Alzheimer’s disease are mainly based on acetylcholinesterase (AChE) inhibitors. However, such inhibitors may possess non-optimal pharmacological properties or cause adverse effects, therefore research for the development of new drugs is still in progress. In this paper a rapid and simple chemiluminescent assay for the in vitro evaluation of AChE inhibitors, in which the activity of AChE is measured through a series of coupled enzymatic reactions leading to light emission, is described. The assay is performed in microtiter plates, both in the 96- and 384-well formats. In the latter format up to 30 compounds can be simultaneously analyzed in a very short time (the chemiluminescence measurement lasts 5 minutes) and using small volumes of samples and reagents (the assay volume is less than 60 microL), thus allowing high throughput screening. The assay proved to be reliable, as demonstrated by the analysis of known AChE inhibitors, and the reproducibility of the results was satisfying for a screening assay (CV% in the order of 20%). It could therefore represent a valuable alternative to other methods for the preliminary evaluation of new potential AChE inhibitors
Engineering of Highly Luminescent Lanthanide Tags Suitable for Protein Labeling and Time Resolved Luminescence Imaging.
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Variations on the Author
“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
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