Henrique Rodrigues Marcelino

Prof. Dr. Henrique Rodrigues Marcelino

Federal University of Bahia, Salvador, Bahia, Brazil
orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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1 April 2016 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
AMAndreza Rochelle Do Vale Morais
Andreza Rochelle Do Vale Morais
ÉAÉverton do Nascimento Alencar
Éverton do Nascimento Alencar
FXFrancisco Humberto Xavier-Júnior
Francisco Humberto Xavier-Júnior
COChristian Melo de Oliveira
Christian Melo de Oliveira
HMHenrique Rodrigues Marcelino
Henrique Rodrigues Marcelino
Abdelhamid ElaissariAbdelhamid Elaissari
Abdelhamid Elaissari

1 July 2010 in Bioresource Technology
Verified
Journal Article
Closed access
EOElquio Eleamen OLIVEIRA
Elquio Eleamen OLIVEIRA
ASAcarília Eduardo Silva
Acarília Eduardo Silva
TJToshiyuki Nagashima Júnior
Toshiyuki Nagashima Júnior
MGMonique Christine Salgado Gomes
Monique Christine Salgado Gomes
LALarissa Muratori Aguiar
Larissa Muratori Aguiar
EEEryvaldo Sócrates Tabosa Egito
Eryvaldo Sócrates Tabosa Egito

1 August 2021 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
PLPaulo Vitor França Lemos
Paulo Vitor França Lemos
HMHenrique Rodrigues Marcelino
Henrique Rodrigues Marcelino
LCLucas Guimarães Cardoso
Lucas Guimarães Cardoso
CSCarolina Oliveira de Souza
Carolina Oliveira de Souza
JDJanice Izabel Druzian
Janice Izabel Druzian

13 June 2017 in Materials
Verified
Journal Article
Open access
PDF file
MFMarjorie Freire
Marjorie Freire
FAFrancisco Alexandrino-Junior
Francisco Alexandrino-Junior
HMHenrique Rodrigues Marcelino
Henrique Rodrigues Marcelino
PPPaulo Henrique de Souza Picciani
Paulo Henrique de Souza Picciani
PPPaulo H. S. Picciani
Paulo H. S. Picciani
EEEryvaldo Socrates Egito
Eryvaldo Socrates Egito
Understanding the factors that can modify the drug release profile of a drug from a Drug-Delivery-System (DDS) is a mandatory step to determine the effectiveness of new therapies. The aim of this study was to assess the Amphotericin-B (AmB) kinetic release profiles from polymeric systems with different compositions and geometries and to correlate these profiles with the thermodynamic parameters through mathematical modeling. Film casting and electrospinning techniques were used to compare behavior of films and fibers, respectively. Release profiles from the DDSs were performed, and the mathematical modeling of the data was carried out. Activation energy, enthalpy, entropy and Gibbs free energy of the drug release process were determined. AmB release profiles showed that the relationship to overcome the enthalpic barrier was PVA-fiber > PVA-film > PLA-fiber > PLA-film. Drug release kinetics from the fibers and the films were better fitted on the Peppas–Sahlin and Higuchi models, respectively. The thermodynamic parameters corroborate these findings, revealing that the AmB release from the evaluated systems was an endothermic and non-spontaneous process. Thermodynamic parameters can be used to explain the drug kinetic release profiles. Such an approach is of utmost importance for DDS containing insoluble compounds, such as AmB, which is associated with an erratic bioavailability.

8 December 2022 in Antioxidants
Verified
Journal Article
Open access
PDF file
MVMax Denisson Maurício Viana
Max Denisson Maurício Viana
PLPedro Santana Sales Lauria
Pedro Santana Sales Lauria
ALAlyne Almeida de Lima
Alyne Almeida de Lima
LOLuiza Carolina França Opretzka
Luiza Carolina França Opretzka
HMHenrique Rodrigues Marcelino
Henrique Rodrigues Marcelino
Cristiane Flora VillarrealCristiane Flora Villarreal
Cristiane Flora Villarreal
Neuropathic pain (NP) is the most prevalent and debilitating form of chronic pain, caused by injuries or diseases of the somatosensory system. Since current first-line treatments only provide poor symptomatic relief, the search for new therapeutic strategies for managing NP is an active field of investigation. Multiple mechanisms contribute to the genesis and maintenance of NP, including damage caused by oxidative stress. The naturally occurring antioxidant alpha-lipoic acid (ALA) is a promising therapeutic agent for the management of NP. Several pre-clinical in vitro and in vivo studies as well as clinical trials demonstrate the analgesic potential of ALA in the management of NP. The beneficial biological activities of ALA are reflected in the various patents for the development of ALA-based innovative products. This review demonstrates the therapeutic potential of ALA in the management of NP by discussing its analgesic effects by multiple antioxidant mechanisms as well as the use of patented ALA-based products and how technological approaches have been applied to enhance ALA’s pharmacological properties.

1 June 2020 in European Journal of Pharmaceutics and Biopharmaceutics
Verified
Journal Article
Closed access
SUSilvana Cartaxo da Costa Urtiga
Silvana Cartaxo da Costa Urtiga
HMHenrique Rodrigues Marcelino
Henrique Rodrigues Marcelino
EEEryvaldo Sócrates Tabosa Do Egito
Eryvaldo Sócrates Tabosa Do Egito
EOElquio Eleamen OLIVEIRA
Elquio Eleamen OLIVEIRA