Maria Eduarda Araujo

Prof. Maria Eduarda Araujo

Chemistry and Biochemistry Department, Faculty of Sciences, University of Lisbon, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal
orcid

Research Focus & Metrics

Academic Career Length

44Years (1983-Present)

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

Representative Publications

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1 November 2006 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
AFA. Ferreira
A. Ferreira
CPC. Proença
C. Proença
MSMaria Luísa M. Serralheiro
Maria Luísa M. Serralheiro
MAMaria Eduarda Araujo
Maria Eduarda Araujo

1 January 2007 in Food Chemistry
Verified
Journal Article
Closed access
AMA.T. Mata
A.T. Mata
CPC. Proença
C. Proença
AFA.R. Ferreira
A.R. Ferreira
MSMaria Luísa M. Serralheiro
Maria Luísa M. Serralheiro
JNJosé Nogueira
José Nogueira
MAMaria Eduarda Araujo
Maria Eduarda Araujo

1 June 2014 in Chemosphere
Verified
Journal Article
Closed access
WGW. Gouveia
W. Gouveia
TJT.F. Jorge
T.F. Jorge
SMS. Martins
S. Martins
MMM. Meireles
M. Meireles
MCM. Carolino
M. Carolino
MAMaria Eduarda Araujo
Maria Eduarda Araujo


3 May 2018 in Molecules
Verified
Journal Article
Open access
PDF file
LFLina Falcão
Lina Falcão
MAMaria Eduarda Araujo
Maria Eduarda Araujo
In this review, a brief description of how animal skins were transformed in leathers in Europe using different vegetable tannins will be presented. Special attention will be dedicated to the description of the type of tannins and the characteristics of the most important type of historic leathers thus obtained. The text will also focus on the description of the techniques used in the identification of these tannins in historic objects: colorimetric tests and spectroscopic analysis.

4 February 2020 in Biomolecules
Verified
Journal Article
Open access
PDF file
RCRita Caparica
Rita Caparica
Ana JúlioAna Júlio
Ana Júlio
MAMaria Eduarda Araujo
Maria Eduarda Araujo
André BabyAndré Baby
André Baby
Pedro FontePedro Fonte
Pedro Fonte
Tânia Santos de AlmeidaTânia Santos de Almeida
Tânia Santos de Almeida
The renal cell carcinoma (RCC) is the most common type of kidney cancer. Identifying novel and more effective therapies, while minimizing toxicity, continues to be fundamental in curtailing RCC. Rutin, a bioflavonoid widely found in nature, has shown promising anticancer properties, but with limited applicability due to its poor water solubility and pharmacokinetics. Thus, the potential anticancer effects of rutin toward a human renal cancer cell line (786-O), while considering its safety in Vero kidney cells, was assessed, as well as the applicability of ionic liquids (ILs) to improve drug delivery. Rutin (up to 50 µM) did not show relevant cytotoxic effects in Vero cells. However, in 786-O cells, a significant decrease in cell viability was already observed at 50 µM. Moreover, exposure to rutin caused a significant increase in the sub-G1 population of 786-O cells, reinforcing the possible anticancer activity of this biomolecule. Two choline-amino acid ILs, at non-toxic concentrations, enhanced rutin’s solubility/loading while allowing the maintenance of rutin’s anticancer effects. Globally, our findings suggest that rutin may have a beneficial impact against RCC and that its combination with ILs ensures that this poorly soluble drug is successfully incorporated into ILs–nanoparticles hybrid systems, allowing controlled drug delivery.