| 1. |
- Ali Malik, Muhammad, et al.
(author)
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Imaging fingerprinting of excitation emission matrices
- 2009
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In: Analytica Chimica Acta. - : Elsevier BV. - 0003-2670 .- 1873-4324. ; 635:2, s. 196-201
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Journal article (peer-reviewed)abstract
- The spectral fingerprinting of the excitation emission matrix (EEM) of fluorescent substances is demonstrated using polychromatic light sources and tri-chromatic image detectors. A model of the measured fingerprints explaining their features and classification performance, based on the polychromatic excitation of the indicators is proposed.Substantial amount of spectral information is retained in the fingerprints as corroborated by multivariate analysis and experimental conditions that favor such situation are identified.In average, for five different substances, the model shows a fitting goodness measured by the Pearsons r coefficient and the root mean square deviation of 0.8541 and 0.0247 respectively, while principal component classification patterns satisfactorily compare with the EEM spectroscopy classification and respectively explain 96% and 93% of the information in the fist two principal components.The measurements can be performed using regular computer screens as illumination and web cameras as detectors, which constitute ubiquitous and affordable platforms compatible with distributed evaluations, in contrast to regular instrumentation for EEM measurements.
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| 2. |
- Brinkman, Paul, et al.
(author)
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Identification and prospective stability of electronic nose (eNose)-derived inflammatory phenotypes in patients with severe asthma
- 2019
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In: Journal of Allergy and Clinical Immunology. - : Elsevier. - 0091-6749 .- 1097-6825. ; 143:5, s. 1811-1820.e7
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Journal article (peer-reviewed)abstract
- Background: Severe asthma is a heterogeneous condition, as shown by independent cluster analyses based on demographic, clinical, and inflammatory characteristics. A next step is to identify molecularly driven phenotypes using “omics” technologies. Molecular fingerprints of exhaled breath are associated with inflammation and can qualify as noninvasive assessment of severe asthma phenotypes.Objectives: We aimed (1) to identify severe asthma phenotypes using exhaled metabolomic fingerprints obtained from a composite of electronic noses (eNoses) and (2) to assess the stability of eNose-derived phenotypes in relation to withinpatient clinical and inflammatory changes.Methods: In this longitudinal multicenter study exhaled breath samples were taken from an unselected subset of adults with severe asthma from the U-BIOPRED cohort. Exhaled metabolites were analyzed centrally by using an assembly of eNoses. Unsupervised Ward clustering enhanced by similarity profile analysis together with K-means clustering was performed. For internal validation, partitioning around medoids and topological data analysis were applied. Samples at 12 to 18 months of prospective follow-up were used to assess longitudinal within-patient stability.Results: Data were available for 78 subjects (age, 55 years [interquartile range, 45-64 years]; 41% male). Three eNosedriven clusters (n = 26/33/19) were revealed, showing differences in circulating eosinophil (P = .045) and neutrophil (P = .017) percentages and ratios of patients using oral corticosteroids (P = .035). Longitudinal within-patient cluster stability was associated with changes in sputum eosinophil percentages (P = .045).Conclusions: We have identified and followed up exhaled molecular phenotypes of severe asthma, which were associated with changing inflammatory profile and oral steroid use. This suggests that breath analysis can contribute to the management of severe asthma.
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| 3. |
- Di Natale, Corrado, et al.
(author)
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Evaluation of the performance of sensors based on optical imaging of a chemically sensitive layer
- 2010
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In: ANALYTICAL AND BIOANALYTICAL CHEMISTRY. - : Springer Science Business Media. - 1618-2642 .- 1618-2650. ; 397:2, s. 613-621
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Journal article (peer-reviewed)abstract
- Interest in the use of the optical properties of chemical indicators is growing steadily. Among the optical methods that can be used to capture changes in sensing layers, those producing images of large-area devices are particularly interesting for chemical sensor array development. Until now, few studies addressed the characterization of image sensors from the point of view of their chemical sensor application. In this paper, a method to evaluate such performance is proposed. It is based on the simultaneous measurement of absorption events in a metalloporphyrin layer with an image sensor and a quartz microbalance (QMB). Exploiting the well-known behaviour of QMB, comparison of signals enables estimation of the minimum amount of absorbed molecules that the image sensor can detect. Results indicate that at the single pixel level a standard image sensor (for example a webcam) can easily detect femtomoles of absorbed molecules. It should therefore be possible to design sensor arrays in which the pixels of images of large-area sensing layers are regarded as individual chemical sensors providing a ready and simple method for large sensor array development.
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| 4. |
- Di Natale, Corrado, et al.
(author)
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Investigation of quartz microbalance and ChemFET transduction of molecular recognition events in a metalloporphyrin film
- 2009
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In: Sensors and actuators. B, Chemical. - : Elsevier BV. - 0925-4005. ; 135:2, s. 560-567
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Journal article (peer-reviewed)abstract
- Progresses of synthetic chemistry methodologies have allowed the preparation of a great variety of artificial receptors that are particularly appealing for chemical sensor development. In this paper, we investigate and compare the properties of gas sensors based on two types of devices, quartz microbalances (QMBs) and field effect transistors (FETs), which give the means to exploit the molecular recognition events occurring in non-conductive sensing layers formed by a thiol-modified cobalt tetraphenylporphyrin (CoTPPSH). Since QMB is sensitive to mass and FET is sensitive to electric dipoles, the resulting sensors are expected to exhibit different sensitivities and selectivities, although both based on the same sensing layer. In particular we show that the high sensitivity of CoTPPSH-coated FETs towards CO and NO is a consequence of the significant CoTPPSH electric dipole change after the gas coordination to the metal centre.
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| 5. |
- Di Natale, Corrado, et al.
(author)
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Multi-transduction of molecular recognition events in metalloporphyrin layers
- 2009
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In: Journal of Porphyrins and Phthalocyanines. - 1088-4246 .- 1099-1409. ; 13:11, s. 1123-1128
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Journal article (peer-reviewed)abstract
- Besides the design and synthesis of appropriate molecular recognition systems, the development of chemical sensors requires a careful selection of the transducer to allow conversion of the chemical interaction into an exploitable electric signal. Metalloporphyrins, which are characterized by manifold of interactions of different strength and selectivity, provide a good example of the complexity of such an issue. In this paper, an example of the different ways to capture interactions occurring in a metalloporphyrin layer is presented. In particular, the properties of mass ( quartz microbalance) and surface potential transducers (field effect transistor) are illustrated. Results suggest that field effect transistors are more suitable to preserve the interactions magnitude scale than to maintain the original selectivity of the molecular recognition system.
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| 6. |
- Dini, Francesca, et al.
(author)
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Chemical sensitivity of self-assembled porphyrin nano-aggregates
- 2009
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In: NANOTECHNOLOGY. - : IOP Publishing. - 0957-4484 .- 1361-6528. ; 20:5, s. 055502-
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Journal article (peer-reviewed)abstract
- Nanostructured molecular assemblies may provide additional sensing properties not found in other arrangements of the same basic constituents. Among three-dimensional structures, nanotubes are particularly appealing for applications as chemical sensors, because of the potential inclusion of different guests inside the cavity or the induced modification of the skeletal interaction after analyte binding. Porphyrins are a class of compounds characterized by brilliant sensing properties, appearing also in non-ordered solid-state aggregates. In recent years, it was reported that aggregation of oppositely charged porphyrins led to the formation of self-assembled nanotubes and in this paper their sensing properties, both in solution and in the solid state, have been investigated. The interactions of porphyrin nanotubes with guest molecules have been monitored by following the changes in their UV-vis spectra. The results obtained have been exploited to build up a sensing platform based on a computer screen as a light source and a digital camera as detector. Porphyrin nanostructures exhibited an enhanced sensitivity to different compounds with respect to those shown by single porphyrin subunits. The reason for the increased sensitivity may be likely found in an additional sensing mechanism related to the modulation of the strength of the forces that keep the supramolecular ensemble together.
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| 7. |
- Dini, Francesca, et al.
(author)
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Polymer matrices effects on the sensitivity and the selectivity of optical chemical sensors
- 2011
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In: SENSORS AND ACTUATORS B-CHEMICAL. - : Elsevier Science B.V., Amsterdam.. - 0925-4005. ; 154:2, s. 220-225
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Journal article (peer-reviewed)abstract
- Polymers are commonly used in optical chemical sensors as inert supports for indicator dyes keeping the molecules apart to allow for exposure to analytes and to maintain the peculiar optical properties of the sensitive dyes. However, the partitioning properties of polymers may play a significant role in determining the sensitivity of the sensors. Herewith, the properties of a single dye blended with different polymers have been studied through optical absorbance changes elicited by the exposure to organic vapors. Results show that the partitioning properties of polymers modulate the response of the dye and confer a combinatorial selectivity to the system, allowing for the recognition of vapors.
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| 8. |
- Dini, Francesca, et al.
(author)
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Polymers with embedded chemical indicators as an artificial olfactory mucosa
- 2010
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In: ANALYST. - : Royal Society of Chemistry. - 0003-2654. ; 135:6, s. 1245-1252
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Journal article (peer-reviewed)abstract
- Physiological investigations suggest that the olfactory mucosa probably plays an ancillary role in the recognition of odours introducing a sort of chromatographic separation that, together with the zonal distribution of olfactory receptors, gives place to selective spatio-temporal response patterns. It has been recently suggested that this behaviour may be simulated by chemical sensors embedded in continuous polymer layers. In this paper, in analogy to the biology of olfaction, a simple and compact platform able to separate and detect gases and vapours on the basis of their diffusion properties is proposed. In such a system, broadly selective colour indicators, such as metalloporphyrins, are embedded in continuous layers of polymers with different sorption properties. The exposure to various alcohols and amines shows that the porphyrins are mainly responsible for the recognition of the molecular family, while the occurring spatio-temporal signal patterns make possible the identification of the individual chemical species.
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| 9. |
- Filippini, Daniel, 1968-, et al.
(author)
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Chemical Sensing with Familiar Devices
- 2006
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In: Angewandte Chemie : : a journal of the Gesellschaft Deutscher Chemiker.. International edition. - : Wiley. ; 45:23, s. 3800-3803
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Journal article (peer-reviewed)
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| 10. |
- Filippini, Daniel, et al.
(author)
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Spectral fingerprinting of porphyrins for distributed chemical sensing
- 2009
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In: JOURNAL OF PORPHYRINS AND PHTHALOCYANINES. - 1088-4246. ; 13:1, s. 77-83
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Journal article (peer-reviewed)abstract
- Recent progress in spectral fingerprinting of fluorescent indicators using distributed instrumentation based on consumer electronic devices is reviewed. In particular, the evaluation of disposable assays using a computer screen photo-assisted technique (CSPT) is discussed. Sample identification and optimization strategies are analyzed as well as the underlying theoretical background for polychromatic spectral fingerprinting.
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