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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

A new medium-throughput screening design approach for the development of hydroxymethylnitrofurazone (NFOH) nanostructured lipid carrier for treating leishmaniasis

Texto completo
Autor(es):
de Souza, Aline [1] ; Yukuyama, Megumi Nishitani [1] ; Barbosa, Eduardo Jose [1] ; Monteiro, Lis Marie [1] ; Breithaupt Faloppa, Ana Cristina [2] ; Calixto, Leandro Augusto [3] ; de Barros Araujo, Gabriel Lima [1] ; Fotaki, Nikoletta [4] ; Lobenberg, Raimar [5] ; Bou-Chacra, Nadia Araci [1]
Número total de Autores: 10
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Fac Pharmaceut Sci, Sao Paulo, SP - Brazil
[2] Univ Sao Paulo, Med Sch, Heart Inst InCor, LIM 11, Sao Paulo, SP - Brazil
[3] Univ Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, Dept Exact & Earth Sci, Diadema, SP - Brazil
[4] Univ Bath, Dept Pharm & Pharmacol, Bath, Avon - England
[5] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB - Canada
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: COLLOIDS AND SURFACES B-BIOINTERFACES; v. 193, SEP 2020.
Citações Web of Science: 0
Resumo

Hydroxymethilnitrofurazone (NFOH) is a nitrofurazone derivative and has potential use in treating leishmaniasis. However, due to low water solubility and bioavailability, NFOH has failed in in vivo tests. Nanostructured lipid carrier (NLC) is an alternative to overcome these limitations by improving pharmacokinetics and modifying drug delivery. This work is focused on developing a novel NFOH-loaded NLC (NLC-NFOH) using a D-optimal mixture statistical design and high-pressure homogenization, for oral administration to treat leishmaniasis. The optimized NLC-NFOH consisted of Mygliol (R) 840, Gelucire (R) 50/13, and Precirol (R) ATO 5 as lipids. These lipids were selected using a rapid methodology Technobis Crystal 16 T M, microscopy, and DSC. Different tools for selecting lipids provided relevant scientific knowledge for the development of the NLC. NLC-NFOH presented a z-average of 198.6 +/- 5.4 nm, PDI of 0.11 +/- 0.01, and zeta potential of -13.7 +/- 0.7 mV. A preliminary in vivo assay was performed by oral administration of NLC-NFOH (2.8 mg/kg) in one healthy male Wistar rat (341 g) by gavage. Blood from the carotid vein was collected, and the sample was analyzed by HPLC. The plasma concentration of NFOH after 5 h of oral administration was 0.22 mu g/mL. This same concentration was previously found using free NFOH in the DMSO solution (200 mg/kg), which is an almost 100-fold higher dose. This study allowed a design space development approach of the first NLC-NFOH with the potential to treat leishmaniasis orally. (AU)

Processo FAPESP: 17/08332-3 - Sistemas nanoestruturados com potencial aplicação no tratamento de doenças negligenciadas
Beneficiário:Nádia Araci Bou-Chacra
Modalidade de apoio: Auxílio à Pesquisa - Regular