Please use this identifier to cite or link to this item: https://ri.ufs.br/jspui/handle/riufs/25642
Document Type: Artigo
Title: Phase transitions of isotropic to anisotropic biocompatible lipid-based drug delivery systems overcoming insoluble benznidazole loading
Authors: Streck, Letícia
Sarmento, Victor Hugo Vitorino
Machado, Paula Renata Lima
Farias, Kleber Juvenal Silva
Pedrosa, Matheus de Freitas Fernandes
Silva Junior, Arnobio Antonio da
Issue Date: 2016
Resumo : Previous studies reported low benznidazole (BNZ) loading in conventional emulsions due to the weak interaction of the drug with the most common oils used to produce foods or pharmaceuticals. In this study, we focused on how the type of surfactant, surfactant-to-oil ratio w/w (SOR) and oil-to-water ratio w/w (OWR) change the phase behavior of different lipid-based drug delivery systems (LBDDS) produced by emulsion phase inversion. The surfactant mixture composed of soy phosphatidylcholine and sodium oleate (1:7, w/w, hydrophilic lipophilic balance = 16) stabilized medium chain triglyceride in water. Ten formulations with the clear aspect or less turbid dispersions (five with the SOR ranging from 0.5 to 2.5 and five with the OWR from 0.06 to 0.4) were selected from the phase behavior diagram to assess structural features and drug-loading capacity. The rise in the SOR induced the formation of distinct lipid-based drug delivery systems (nanoemulsions and liquid crystal lamellar type) that were identified using rheological measurements and cross-polarized light microscopy images. Clear dispersions of small and narrow droplet-sized liquid-like nanoemulsions, Newtonian flow-type, were produced at SOR from 0.5 to 1.5 and OWR from 0.12 to 0.4, while clear liquid or gel-like liquid crystals were produced at SOR from 1.5 to 2.5. The BNZ loading was improved according to the composition and type of LBDDS produced, suggesting possible drug location among surfactant layers. The cell viability assays proved the biocompatibility for all of the prepared nanoemulsions at SOR less than 1.5 and liquid crystals at SOR less than 2.5, demonstrating their promising features for the oral or parenteral colloidal delivery systems containing benznidazole for Chagas disease treatment.
Keywords: Nanoemulsions
Liquid crystals
Biocompatible colloidal carriers
Rheology
Lipid-based drug delivery systems
Benznidazole
ISSN: 1422-0067
Is part of: International Journal of Molecular Sciences
Language: eng
Publisher / Institution : MDPI Center
Citation: STRECK, L. et al. Phase transitions of isotropic to anisotropic biocompatible lipid-based drug delivery systems overcoming insoluble benznidazole loading. International Journal of Molecular Sciences, Basel, v. 17, n. 7, 2016. Disponível em: https://www.mdpi.com/1422-0067/17/7/981. Acesso em: 23 jul. 2026.
License: Creative Commons Atribuição 4.0 Internacional (CC BY 4.0)
Identifier: https://doi.org/10.3390/ijms17070981
URI: https://ri.ufs.br/jspui/handle/riufs/25642
Appears in Collections:DQCI - Artigos de periódicos

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