Cesar Filho

Dr. Cesar Filho

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Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 April 2020 in Polymers
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Journal Article
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CFCesar Filho
Cesar Filho
PBPedro V. A. Bueno
Pedro V. A. Bueno
AMAlan Matsushita
Alan Matsushita
Bruno Henrique VilsinskiBruno Henrique Vilsinski
Bruno Henrique Vilsinski
ARAdley F. Rubira
Adley F. Rubira
Artur ValenteArtur Valente
Artur Valente
Aromatic hydrocarbons are extensive environmental pollutants occurring in both water and air media, and their removal is a priority effort for a healthy environment. The use of adsorbents is among the several strategies used for the remediation of these compounds. In this paper, we aim the synthesis of an amphiphilic hydrogel with the potential for the simultaneous sorption of a set of monocyclic and polycyclic aromatic hydrocarbons associated with toxicity effects in humans. Thus, we start by the synthesis of a copolymer-based in chitosan and β-cyclodextrin previously functionalized with the maleic anhydride. The presence of β-cyclodextrin will confer the ability to interact with hydrophobic compounds. The resulting material is posteriorly incorporated in a cryogel of poly(vinyl alcohol) matrix. We aim to improve the amphiphilic ability of the hydrogel matrix. The obtained hydrogel was characterized by swelling water kinetics, thermogravimetric analysis, rheological measurements, and scanning electron microscopy. The sorption of aromatic hydrocarbons onto the gel is characterized by pseudo-first-order kinetics and Henry isotherm, suggesting a physisorption mechanism. The results show that the presence of maleic anhydride-β-cyclodextrin and chitosan into hydrogels leads to an increase in the removal efficiency of the aromatic compounds. Additionally, the capacity of this hydrogel for removing these pollutants from a fossil fuel sample has also been tested.

20 October 2022 in Biochem
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Journal Article
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Mariana MarquesMariana Marques
Mariana Marques
JNJoao Pedro Nunes
Joao Pedro Nunes
BUBárbara Ustymenko
Bárbara Ustymenko
LFLuísa Fialho
Luísa Fialho
LMLuís Martins
Luís Martins
Célia M. AntunesCélia M. Antunes
Célia M. Antunes
Skin is one of the organs most tested for toxicity and safety evaluation during the process of drug research and development and in the past has usually been performed in vivo using animals. Over the last few years, non-animal alternatives have been developed and validated epidermis models for human and rat skin are already available. Our goal was to develop a histotypical canine skin analog, suitable for non-animal biocompatibility and biosafety assessment. Canine keratinocytes were seeded in an air-lift culture using an adapted version of the CELLnTEC protocol. Corrosion and irritation protocols were adapted from human EpiSkinTM. For histological analysis, sample biopsies were fixed in neutral-buffered formalin, and paraffin slices were routinely processed and stained with hematoxylin and eosin. A canine multilayer and stratified epidermal-like tissue (cEpiderm), confirmed by histological analysis, was obtained. The cEpiderm tissue exhibited normal morphological and functional characteristics of epidermis, namely impermeability and an adequate response to stressors. The cEpiderm is a promising canine skin model for non-animal safety testing of veterinary pharmaceuticals and/or cosmetics, significantly contributing to reducing undesirable in vivo approaches. cEpiderm is therefore a valid canine skin model and may be made commercially available either as a service or as a product.

28 June 2022 in Chemistry Proceedings
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Conference Paper
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AMAndreea Miron
Andreea Miron
CFCesar Filho
Cesar Filho
Radu Claudiu FierascuRadu Claudiu Fierascu
Radu Claudiu Fierascu
INIulia Elena Neblea
Iulia Elena Neblea
Anita-Laura ChiriacAnita-Laura Chiriac
Anita-Laura Chiriac
TANTA-VERONA IORDACHETANTA-VERONA IORDACHE
TANTA-VERONA IORDACHE
Chitosan is a natural, nontoxic, biocompatible, biodegradable, and water- insoluble polymer, obtained by deacetylation of chitin