Spray-dried Eudragit® L100 microparticles containing ferulic acid: Formulation, in vitro cytoprotection and in vivo anti-platelet effect

被引:24
作者
Nadal, Jessica Mendes [1 ]
Simionatto Gomes, Mona Lisa [1 ]
Borsato, Debora Maria [2 ]
Almeida, Martinha Antunes [3 ]
Barboza, Fernanda Malaquias [2 ]
Zawadzki, Sonia Faria [3 ]
Kanunfre, Carla Cristine [4 ]
Farago, Paulo Vitor [2 ]
Warumby Zanin, Sandra Maria [1 ]
机构
[1] Univ Fed Parana, Dept Pharm, Postgrad Program Pharmaceut Sci, BR-80060000 Curitiba, Parana, Brazil
[2] Univ Estadual Ponta Grossa, Dept Pharmaceut Sci, Postgrad Program Pharmaceut Sci, BR-84030900 Ponta Grossa, Parana, Brazil
[3] Univ Fed Parana, Dept Chem, Postgrad Program Chem, BR-80060000 Curitiba, Parana, Brazil
[4] Univ Estadual Ponta Grossa, Dept Gen Biol, Postgrad Program Biomed Sci, BR-84030900 Ponta Grossa, Parana, Brazil
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2016年 / 64卷
关键词
Anti-inflammatory; Antioxidant; Methacrylic polymer; Phytoalexin; Platelet aggregation; ANTIOXIDANT; RELEASE; INCLUSION; OXIDATION; PROPERTY; DELIVERY; DAMAGE; BETA;
D O I
10.1016/j.msec.2016.03.086
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
This paper aimed to obtain new spray-dried microparticles containing ferulic acid (FA) prepared by using a tnethacrylic polymer (Eudragit (R) L100). Microparticles were intended for oral use in order to provide a controlled release, and improved in vitro and in vivo biological effects. FA-loaded Eudragit (R) L100 microparticles were obtained by spray-drying. Physicochemical properties, in vitro cell-based effects, and in vivo platelet aggregation were investigated. FA-loaded Eudragit (R) L100 microparticles were successfully prepared by spray-drying. Formulations showed suitable encapsulation efficiency, i.e. close to 100%. Microparticles were of spherical and almost-spherical shape with a smooth surface and a mean diameter between 2 and 3 mu m. Fourier-transformed infrared spectra demonstrated no chemical bond between FA and polymer. X-ray diffraction and differential scanning calorimetry analyses indicated that microencapsulation led to drug amorphization. FA-loaded microparticles showed a slower dissolution rate than pure drug. The chosen formulation demonstrated higher in vitro cytoprotection, anti-inflammatory and immunomodulatory potential and also improved in vivo anti-platelet effect These results support an experimental basis for the use of FA spray-dried microparticles as a feasible oral drug delivery carrier for the controlled release of FA and improved cytoprotective and anti-platelet effects. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:318 / 328
页数:11
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