Guido De Guidi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Guido De Guidi has a total of 33 co-authors. Here are the top co-authors by number of shared publications:
- Alfio Catalfo
C Department of Chemical Sciences , University of Catania , Catania , Italy
2 shared publications - Fabiana Vento
Department of Chemical Sciences and INSTM UdR of Catania, University of Catania, V.le A. Doria 6, I-95125 Catania, Italy
2 shared publications L.L. Costanzo
Dipartimento di Scienze Chimiche, Università di Catania, Catania, Italy
2 shared publications- Lidia Mezzina
Department of Chemical Sciences and INSTM UdR of Catania, University of Catania, V.le A. Doria 6, I-95125 Catania, Italy
2 shared publications - Placido Mineo
Department of Chemical Sciences, University of Catania, Viale A. Doria 6, 95125 Catania, Italy
2 shared publications - Salvatore Giuffrida
Department of Architecture, University of Palermo, 90133 Palermo, Italy
2 shared publications
Latest Publications
- 17 May 2022
- Published by Elsevier in Chemosphere
- Vol. 303 (Pt 1) , 134988
Solar light mediated anthracene abatement in aerated aqueous media using a thermoplastic nanocomposite photocatalyst
- 17 May 2022
- Published by Elsevier in Chemosphere
- Vol. 303 (Pt 1) , 134988
Solar light mediated anthracene abatement in aerated aqueous media using a thermoplastic nanocomposite photocatalyst
- Open Access
- 17 March 2022
- Published by MDPI AG in Nanomaterials
- Vol. 12 (6) , 996
Photosensitized Thermoplastic Nano-Photocatalysts Active in the Visible Light Range for Potential Applications Inside Extraterrestrial Facilities
Among different depollution methods, photocatalysis activated by solar light is promising for terrestrial outdoor applications. However, its use in underground structures and/or microgravity environments (e.g., extraterrestrial structures) is forbidden. In these cases, there are issues related to the energy emitted from the indoor lighting system because it is not high enough to promote the photocatalytic mechanism. Moreover, microgravity does not allow the recovery of the photocatalytic slurry from the depolluted solution. In this work, the synthesis of a filmable nanocomposite based on semiconductor nanoparticles supported by photosensitized copolyacrylates was performed through a bulk in situ radical copolymerization involving a photosensitizer macromonomer. The macromonomer and the nanocomposites were characterized through UV-Vis, fluorescence and NMR spectroscopies, gel permeation chromatography and thermogravimetric analysis. The photocatalytic activity of the sensitized nanocomposites was studied through photodegradation tests of common dyes and recalcitrant xenobiotic pollutants, employing UV-Vis and visible range (λ > 390 nm) light radiations. The sensitized nanocomposite photocatalytic performances increased about two times that of the unsensitized nanocomposite and that of visible range light radiation alone (>390 nm). The experimental data have shown that these new systems, applied as thin films, have the potential for use in indoor deep underground and extraterrestrial structures.
- 17 March 2022
- Published by MDPI AG in Nanomaterials
- Vol. 12 (6) , 996
Open AccessPhotosensitized Thermoplastic Nano-Photocatalysts Active in the Visible Light Range for Potential Applications Inside Extraterrestrial Facilities
Among different depollution methods, photocatalysis activated by solar light is promising for terrestrial outdoor applications. However, its use in underground structures and/or microgravity environments (e.g., extraterrestrial structures) is forbidden. In these cases, there are issues related to the energy emitted from the indoor lighting system because it is not high enough to promote the photocatalytic mechanism. Moreover, microgravity does not allow the recovery of the photocatalytic slurry from the depolluted solution. In this work, the synthesis of a filmable nanocomposite based on semiconductor nanoparticles supported by photosensitized copolyacrylates was performed through a bulk in situ radical copolymerization involving a photosensitizer macromonomer. The macromonomer and the nanocomposites were characterized through UV-Vis, fluorescence and NMR spectroscopies, gel permeation chromatography and thermogravimetric analysis. The photocatalytic activity of the sensitized nanocomposites was studied through photodegradation tests of common dyes and recalcitrant xenobiotic pollutants, employing UV-Vis and visible range (λ > 390 nm) light radiations. The sensitized nanocomposite photocatalytic performances increased about two times that of the unsensitized nanocomposite and that of visible range light radiation alone (>390 nm). The experimental data have shown that these new systems, applied as thin films, have the potential for use in indoor deep underground and extraterrestrial structures.
- 6 April 2018
- Published by Taylor & Francis in Pharmaceutical Development and Technology
- Vol. 24 (2) , 222-234
Antioxidant activity and photostability assessment of trans-resveratrol acrylate microspheres
Trans-resveratrol (RSV) was microencapsulated in Eudragit® RS100 and RL100 resin blends. Lyophilized microspheres were characterized in the solid state for their micromeritic properties and drug loading. FT-IR, PXRD, and DSC analyzes suggested that RSV formed an intimate microcrystalline dispersion within the polymer network, also confirmed by SEM analysis. This produced a reduced degradation of RSV after storage at 40 °C, compared to the neat drug, and a protection of the drug from UV light-induced trans-cis isomerization (60% intact drug was found after 60 s irradiation at 350 nm, compared to 37% for the pure drug). Solubility and in vitro dissolution studies indicated that microencapsulation did not improve the dissolution pattern of RSV in simulated gastric and intestinal aqueous fluids. Evaluation of the in vitro antioxidant activity showed that, compared to the neat drug in aqueous solution, RSV loaded in the microspheres retained for a longer time, up to 22 days of incubation, the initial ORAC capacity. The present study thus demonstrated that Eudragit® Retard resins can be used to easily produce micro-sized solid dispersions with RSV, for potential oral administration, contributing to ameliorate the physico-chemical stability and antioxidant activity of this compound.
- 6 April 2018
- Published by Taylor & Francis in Pharmaceutical Development and Technology
- Vol. 24 (2) , 222-234
Antioxidant activity and photostability assessment of trans-resveratrol acrylate microspheres
Trans-resveratrol (RSV) was microencapsulated in Eudragit® RS100 and RL100 resin blends. Lyophilized microspheres were characterized in the solid state for their micromeritic properties and drug loading. FT-IR, PXRD, and DSC analyzes suggested that RSV formed an intimate microcrystalline dispersion within the polymer network, also confirmed by SEM analysis. This produced a reduced degradation of RSV after storage at 40 °C, compared to the neat drug, and a protection of the drug from UV light-induced trans-cis isomerization (60% intact drug was found after 60 s irradiation at 350 nm, compared to 37% for the pure drug). Solubility and in vitro dissolution studies indicated that microencapsulation did not improve the dissolution pattern of RSV in simulated gastric and intestinal aqueous fluids. Evaluation of the in vitro antioxidant activity showed that, compared to the neat drug in aqueous solution, RSV loaded in the microspheres retained for a longer time, up to 22 days of incubation, the initial ORAC capacity. The present study thus demonstrated that Eudragit® Retard resins can be used to easily produce micro-sized solid dispersions with RSV, for potential oral administration, contributing to ameliorate the physico-chemical stability and antioxidant activity of this compound.
- 1 August 2012
- Published by Taylor & Francis in Polycyclic Aromatic Compounds
- Vol. 32 (4) , 439-456
The PAH and Nitro-PAH Concentration Profiles in Size-Segregated Urban Particulate Matter and Soil in Traffic-Related Sites in Catania, Italy
Polycyclic aromatic hydrocarbons (PAHs) and nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) were identified from both air particulate matter and soils. For air sampling, a six-stage cascade impactor was situated in an urban area (Catania, Italy) that is recognized for its high traffic volume. The soil samples were collected every 1.5 km from under the grass by the side of the median of a Catania road along its full length (8.2 km). HPLC in electrochemical-fluorescence detection mode was used for selective separation, identification and quantification of analytes in air and soil samples, providing both good selectivity and sensitivity. The seasonal trends, effects of urban traffic, and source profiles are discussed herein. Higher PM10 concentrations were observed for summer (43 μg m−3) in comparison to winter (24 μg m−3). Conversely, the PAHs contained in PM10 were higher in winter (0.48 ng m−3 for fluoranthene) than in summer (0.14 ng m−3 for fluoranthene). Analysis of the size-segregated urban particulate matter showed that the amount of PM0.5 (stage 6) was always higher than the amount of other particles (stages 1–5). Furthermore, the PM0.5 was always higher in summer (about 40%, m/m) than in winter (about 30%, m/m). Finally, the amounts of PAH and nitro-PAH in PM0.5 (stage 6) were always higher, by a maximum of one order of magnitude, than that of other particles (stages 1–5). This result is crucial because ultrafine particles have a tendency to move into the blood through the alveolar epithelial barrier. Moreover, the air and soil pollution levels agree with those found in other cities with similar levels of pollution. Supplemental materials are available for this article. Go to the publisher's online edition of Polycyclic Aromatic Compounds to view the supplemental file.
- 1 August 2012
- Published by Taylor & Francis in Polycyclic Aromatic Compounds
- Vol. 32 (4) , 439-456
The PAH and Nitro-PAH Concentration Profiles in Size-Segregated Urban Particulate Matter and Soil in Traffic-Related Sites in Catania, Italy
Polycyclic aromatic hydrocarbons (PAHs) and nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) were identified from both air particulate matter and soils. For air sampling, a six-stage cascade impactor was situated in an urban area (Catania, Italy) that is recognized for its high traffic volume. The soil samples were collected every 1.5 km from under the grass by the side of the median of a Catania road along its full length (8.2 km). HPLC in electrochemical-fluorescence detection mode was used for selective separation, identification and quantification of analytes in air and soil samples, providing both good selectivity and sensitivity. The seasonal trends, effects of urban traffic, and source profiles are discussed herein. Higher PM10 concentrations were observed for summer (43 μg m−3) in comparison to winter (24 μg m−3). Conversely, the PAHs contained in PM10 were higher in winter (0.48 ng m−3 for fluoranthene) than in summer (0.14 ng m−3 for fluoranthene). Analysis of the size-segregated urban particulate matter showed that the amount of PM0.5 (stage 6) was always higher than the amount of other particles (stages 1–5). Furthermore, the PM0.5 was always higher in summer (about 40%, m/m) than in winter (about 30%, m/m). Finally, the amounts of PAH and nitro-PAH in PM0.5 (stage 6) were always higher, by a maximum of one order of magnitude, than that of other particles (stages 1–5). This result is crucial because ultrafine particles have a tendency to move into the blood through the alveolar epithelial barrier. Moreover, the air and soil pollution levels agree with those found in other cities with similar levels of pollution. Supplemental materials are available for this article. Go to the publisher's online edition of Polycyclic Aromatic Compounds to view the supplemental file.
- 1 September 1996
- Published by Elsevier in Journal of Inorganic Biochemistry
- Vol. 63 (4) , 253-263
Molecular mechanism of drug photosensitization: VIII. Effect of inorganic ions on membrane damage photosensitized by naproxen
- 1 September 1996
- Published by Elsevier in Journal of Inorganic Biochemistry
- Vol. 63 (4) , 253-263
Molecular mechanism of drug photosensitization: VIII. Effect of inorganic ions on membrane damage photosensitized by naproxen
- 1 December 1993
- Published by Elsevier in Journal of Photochemistry and Photobiology A: Chemistry
- Vol. 76 (1-2) , 127-133
Effect of cyclodextrin inclusion on the photoisomerization of arylethylenethioamides
- 1 December 1993
- Published by Elsevier in Journal of Photochemistry and Photobiology A: Chemistry
- Vol. 76 (1-2) , 127-133
Effect of cyclodextrin inclusion on the photoisomerization of arylethylenethioamides
- 1 January 1990
- Published by Elsevier in Biochemical Pharmacology
- Vol. 39 (2) , 285-291
Modulation of mediator release from human basophils and pulmonary mast cells and macrophages by auranofin
- 1 January 1990
- Published by Elsevier in Biochemical Pharmacology
- Vol. 39 (2) , 285-291
Modulation of mediator release from human basophils and pulmonary mast cells and macrophages by auranofin