Reconstituted spray-dried phenytoin-loaded nanocapsules improve the in vivo phenytoin anticonvulsant effect and the survival time in mice

被引:21
作者
de Oliveira, Edilene Gadelha [1 ]
Cardoso, Aline Marquez [1 ]
Paese, Karina [2 ]
Coradini, Karine [1 ]
de Oliveira, Clarissa Vasconcelos
Pohlmann, Adriana Raffin [3 ]
Oliveira, Mauro Schneider [4 ]
Guterres, Silvia Staniscuaski [1 ]
Ruver Beck, Ruy Carlos [1 ]
机构
[1] Univ Fed Rio Grande do Sul, Programa Posgrad Ciencias Farmaceut, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Dept Prod & Controle Med, Ave Ipiranga 2952, BR-90610000 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Inst Quim, Dept Quim Organ, Porto Alegre, RS, Brazil
[4] Univ Fed Santa Maria, Programa Posgrad Farmacol, Santa Maria, RS, Brazil
关键词
Anticonvulsant; Chitosan; Nanocapsules; Phenytoin; Powder; Spray-drying; LIPID-CORE NANOCAPSULES; POLYMERIC NANOCAPSULES; INDUCED SEIZURES; DELIVERY-SYSTEM; DRYING METHODS; DRUG-DELIVERY; NANOPARTICLES; FORMULATIONS; PILOCARPINE; CHITOSAN;
D O I
10.1016/j.ijpharm.2018.09.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study evaluated the in vivo anticonvulsant effect of a spray-dried powder for reconstitution containing phenytoin-loaded lipid-core nanocapsules. The effect of chitosan coating on redispersibility, gastrointestinal stability, and drug release from nanoparticles was evaluated during the development of the powders. Maltodextrin was used as adjuvant in the spray-drying process. Chitosan coating played an important role in redispersibility, and large particles (> 100 mu m) were obtained using the highest concentration of solids in the feed. However, after aqueous redispersion, volume-based particle size was reduced to about 1 mu m. The release of nanoparticles from the surface of the spherical microagglomerates (roundness index = 0.75) was confirmed by SEM analysis. Powders reconstituted in water recovered partially the nanometric properties of the original suspensions and were stable for 24 h. Phenytoin-loaded chitosan-coated nanocapsules and their redispersed powders have good gastrointestinal stability, and are able to control drug release in simulated gastric and intestinal fluids. Besides that, the reconstituted powder containing chitosan-coated nanocapsules exhibited improved anticonvulsant activity against seizures induced by pilocarpine in mice, compared to the non-encapsulated drug, representing an important approach in anticonvulsant treatments for children and adults.
引用
收藏
页码:121 / 132
页数:12
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