In vitro antiherpes effect of C-glycosyl flavonoid enriched fraction of Cecropia glaziovii encapsulated in PLGA nanoparticles

被引:15
作者
Caldas dos Santos, Talitha [1 ,2 ]
Rescignano, Nicoletta [1 ]
Boff, Laurita [2 ]
Reginatto, Flavio Henrique [2 ]
Oliveira Simoes, Claudia Maria [2 ]
de Campos, Angela Machado [2 ]
Mijangos, Carmen [1 ]
机构
[1] CSIC, ICTP, Inst Polymer Sci & Technol, E-28006 Madrid, Spain
[2] Univ Fed Santa Catarina, Dept Pharmaceut Sci, BR-88040900 Florianopolis, SC, Brazil
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 75卷
关键词
PLGA nanoparticles; Surfactant; Drug release; C-glycosylflavonoid enriched fraction; Antiherpetic effect; Cytotoxicity assay; STANDARDIZED AQUEOUS EXTRACT; SNETH; VIVO; DEGRADATION; STABILIZERS; INHIBITION; TOXICITY; DESIGN;
D O I
10.1016/j.msec.2017.02.135
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In this work is reported a novel and promising approach for the preparation of C-glycosylflavonoid enriched fraction of Cecropia glaziovii (EFF-Cg) loaded PLGA nanoparticles (NP) with antiherpes properties. The purpose of this study was to evaluate and to compare the effect of two nonionic surfactants (poloxamer 188 (PLU) and polyvinyl alcohol (PVA)), and also an emulsion stabilized by solid particles of cellulose nanocrystal (CNC) in place of surfactants. The characterization of these nanoparticles was in terms of size, polydispersity index, zeta potential, morphology, thermogravimetric analysis (TGA), loading capacity and percent yield. Since TGA analysis revealed thermo stability especially for NP-PLU, this formulation was selected for the evaluation of drug release profile, cytotoxicity and antiherpes activity. The drug delivery profile demonstrated a sustained release through the polymer structure and a significant reduction of the polymer molecular weight at 21-day period. The cytotoxicity of these nanoparticles was determined on Vero cells, and the selected formulation did not exhibit cytotoxicity even at the highest tested concentration. The results demonstrated a potential antiherpetic effect of the EFF-Cg loaded NP at 48 h of testing. In summary, EFF-Cg loaded NP exhibited a promising system for the effective drug delivery in the treatment of herpes infections. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1214 / 1220
页数:7
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