CV Lattes
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ORCID
Universidade Estadual Paulista (UNESP). Campus de Araraquara. Faculdade de Ciências Farmacêuticas (FCFAR) (Institutional affiliation from the last research proposal) Birthplace: Brazil
Graduation in biomedical sciences at São Paulo State University (UNESP) "Júlio de Mesquita Filho", Botucatu-São Paulo.Current PhD at Faculty of Pharmaceutical Sciences (UNESP), Araraquara-São Paulo. Working with nanotecnology focused on neurodegenerative diseases. One year experience in research (2021-2022) financed by FAPESP (São Paulo Research Foundation) on brazilian red propolis and its effects on skin wound healing. The project is named "Characterization of fibroblasts and endothelial cells activity on wound healing in rats treated topically with red brazilian propolis", process number 2021/01258-8, oriented by professor Cláudia Helena Pellizzon at UNESP - Botucatu. One year experience in research (2017-2018) in the Medicine Faculty at UNESP in Botucatu - São Paulo with emphasis in studies about the effects of oxidative stress in rats metabolism. Scholarship financed by the nacional council of cientific and tecnological development (CNPq) during the years of 2017 and 2018.ORCID: 0000-0003-4398-1817 (Source: Lattes Curriculum)
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Alzheimer's disease (AD), the neurodegenerative disorder with the highest prevalence among cases of dementia in the world, is characterized by functional and cognitive decline, with emphasis on memory loss. The current treatment involves acetylcholinesterase inhibitors that causes significant adverse effects such as nausea, vomiting and liver toxicity. Thus, alternatives to the treatment …
The wound healing process depends on many biochemical and physiological factors that trigger mediators to cellular activation and tissue reorganization. Depending on metabolic changes, wounds may take years to complete closure, and this results from the fact that there is no gold standard for effective skin wound healing. Thus, the search for a new product is necessary and red propolis ha…
Neurodegenerative diseases such as Alzheimer's, Parkinson's, Huntington's, and Amyotrophic lateral sclerosis share the common feature of pathological protein aggregation that become toxic to brain tissue leading to cell death. While in Alzheimer's beta-amyloid (²A) and Tau proteins aggregate in insoluble amyloid plaques and neurofibrillary tangles, in Parkinson's disease (PD) alfa-synucle…
| 2 / 2 | Completed scholarships in Brazil |
| 1 / 1 | Ongoing scholarships abroad |
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