Fabiane Galdino

Dr. Fabiane Galdino

orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

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

Representative Publications

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10 April 2008 in Chemical Communications
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Journal Article
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EHElizabeth Hillard
Elizabeth Hillard
FGFabiane Galdino
Fabiane Galdino
DFDanielle Cristhina Melo Ferreira
Danielle Cristhina Melo Ferreira
GJGérard Jaouen
Gérard Jaouen
Marília O. F. GoulartMarília O. F. Goulart
Marília O. F. Goulart
CAChristian Amatore
Christian Amatore
This review article summarizes recent applications of electrochemical techniques to redox-active drug development and mechanistic studies. It includes a general introduction to the use of electrochemistry in biology, with a focus on how electrochemistry can uniquely provide both kinetic and thermodynamic information. A number of studies are reported from the literature and the authors’ laboratories, including the investigation of reactive oxygen species, biooxidative/bioreductive activation of pro-drugs, and DNA alkylation, with a particular emphasis on quinones and related compounds. Data from techniques ranging from traditional cyclic voltammetry to sophisticated single cell studies are presented. The examples herein presented illustrate how electrochemical, biochemical and medical knowledge can be integrated to develop strategies for the design and development of redox-selective therapeutics.

1 February 2002 in Journal of the Brazilian Chemical Society
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Journal Article
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FGFabiane Galdino
Fabiane Galdino
PFPatrícia A. de L. Ferraz
Patrícia A. de L. Ferraz
Marília O. F. GoulartMarília O. F. Goulart
Marília O. F. Goulart

1 August 1997 in Bioorganic & Medicinal Chemistry Letters
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Journal Article
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Marília O. F. GoulartMarília O. F. Goulart
Marília O. F. Goulart
CZCarlos Leomar Zani
Carlos Leomar Zani
JTJosealdo Tonholo
Josealdo Tonholo
LFLuciano R. Freitas
Luciano R. Freitas
FGFabiane Galdino
Fabiane Galdino
ECEgler Chiari
Egler Chiari

1 July 2001 in Journal of Electroanalytical Chemistry
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Journal Article
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PFPatrı́cia A.L Ferraz
Patrı́cia A.L Ferraz
FGFabiane Galdino
Fabiane Galdino
APAntônio V Pinto
Antônio V Pinto
VGVictor Glezer
Victor Glezer
JTJosealdo Tonholo
Josealdo Tonholo
Marília O. F. GoulartMarília O. F. Goulart
Marília O. F. Goulart

1 June 2012 in Bioorganic & Medicinal Chemistry
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Journal Article
Closed access
FBFrancisco W.A. Barros
Francisco W.A. Barros
TSTeresinha Gonçalves Silva
Teresinha Gonçalves Silva
MPMarina Galdino da Rocha Pitta
Marina Galdino da Rocha Pitta
Daniel P. BezerraDaniel P. Bezerra
Daniel P. Bezerra
LCLetícia V. Costa-Lotufo
Letícia V. Costa-Lotufo
Marília O. F. GoulartMarília O. F. Goulart
Marília O. F. Goulart

13 April 2011 in Analytical Methods
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Journal Article
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WRWilliame Farias Ribeiro
Williame Farias Ribeiro
TSThiago Matheus Guimaraes Selva
Thiago Matheus Guimaraes Selva
ILIlanna Campelo Lopes
Ilanna Campelo Lopes
ECElaine Cristina S. Coelho
Elaine Cristina S. Coelho
Sherlan Guimarães LemosSherlan Guimarães Lemos
Sherlan Guimarães Lemos
MAMário César Ugulino de Araújo
Mário César Ugulino de Araújo
A preconcentrating/voltammetric multiwalled carbon nanotube modified glassy carbon electrode (MWCNT–GCE) has been developed for stripping analysis of carbendazim (Methyl Benzimidazol-2-yl Carbamate—MBC), based on dispersing MWCNT in water. The effect of experimental variables, such as the dispersion and loading of MWCNT, was assessed. A quasi-reversible behavior for MBC in acetic acid/acetate buffer 0.1 mol L−1 (pH 4.7) was verified and its high effective pre-concentration was attributed to the high adsorption capability and enormous surface area of the MWCNT. No evidence of carry-over effect, combined with the easiness of electrode preparation, led to the development of a highly sensitive and reliable method with an experimental work range from 0.256 to 3.11 µmol L−1 with a detection limit of 10.5 ppb for a short (60 s) accumulation period. Measurement of MBC in a river water sample was demonstrated. The accuracy of the method for real sample analysis was assessed by estimating the apparent recovery (93 ± 2.9% and 86 ± 4.1% for 4.3 × 10−7 mol L−1) for a MBC spiked river water sample.