Nanocomposite chitosan hydrogels based on PLGA nanoparticles as potential biomedical materials

被引:49
作者
Caldas dos Santos, Talitha [1 ,2 ,3 ,4 ]
Hernandez, Rebeca [1 ]
Rescignano, Nicoletta [1 ]
Boff, Laurita [4 ]
Reginatto, Flavio Henrique [3 ]
Oliveira Simoes, Claudia Maria [3 ,4 ]
de Campos, Angela Machado [2 ]
Mijangos, Carmen [1 ]
机构
[1] CSIC, Inst Polymer Sci & Technol, ICTP, Madrid 28006, Spain
[2] Univ Fed Santa Catarina, Ctr Ciencias Saude, Dept Ciencias Farmaceut, Lab Farmacotecn, BR-88040900 Florianopolis, SC, Brazil
[3] Univ Fed Santa Catarina, Ctr Ciencias Saude, Dept Ciencias Farmaceut, Lab Farmacognosia, BR-88040900 Florianopolis, SC, Brazil
[4] Univ Fed Santa Catarina, Dept Ciencias Farmaceut, Lab Virol Aplicada, BR-88040900 Florianopolis, SC, Brazil
关键词
Nanocomposite; Cecropia glaziovii Snethl; Chitosan; PLGA nanoparticles; Thermosensitive hydrogel; Rheology; RHEOLOGICAL PROPERTIES; MECHANICAL-PROPERTIES; CONTROLLED-RELEASE; CROSS-LINKING; GELATION; ALGINATE; GELS;
D O I
10.1016/j.eurpolymj.2017.12.039
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report on the preparation and characterization of nanocomposite chitosan hydrogels with embedded poly (lactic-co-glycolic acid) (PLGA) nanoparticles employed for encapsulation of an enriched flavonoid fraction of Cecropia glaziovii Snethl. As a first step, the experimental conditions to obtain homogeneous chitosan hydrogels at 37 degrees C through gelation with NaHCO3 were optimized. Then, nanocomposite chitosan hydrogels were prepared through direct incorporation of nanoparticlesat different concentrations ranging from 1 to 10% w/w to gelling aqueous chitosan solutions. The resulting hydrogels were characterized through Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), oscillatory rheological experiments and cytotoxicity tests. FT-IR spectra confirmed the PLGA nanoparticles presence within the chitosan matrix through the absorption peak located at 1750 cm(-1). The presence of the PLGA nanoparticles decreased the thermal stability of the nanocomposite chitosan hydrogels compared to the pure chitosan hydrogel. SEM images allowed observing porous matrixes where nanoparticles appeared to be homogeneously dispersed. The elastic moduli found for nanocomposite chitosan hydrogels varied with the PLGA nanoparticles concentration with a maximum at 3% nanoparticles concentration. Cytotoxicity tests revealed that after 48 h, neither thepure hydrogel nor the nanocomposite chitosan hydrogels with 10% nanoparticles concentration showed toxicity on VERO cells.
引用
收藏
页码:456 / 463
页数:8
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