Nanostructure-coated diclofenac-loaded microparticles:: Preparation, morphological characterization, in vitro release and in vivo gastrointestinal tolerance

被引:32
作者
Beck, RCR
Pohlmann, AR
Benvenutti, EV
Costa, TD
Guterres, SS
机构
[1] Univ Fed Rio Grande Sul, Fac Farm, Programa Posgrad Ciencias Farmaceut, BR-90610000 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande Sul, Inst Quim, Dept Quim Organ, BR-91501970 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande Sul, Inst Quim, Dept Quim Inorgan, BR-91501970 Porto Alegre, RS, Brazil
关键词
diclofenac; polymer; nanostructure-coating; microparticles; gastrointestinal tolerance;
D O I
10.1590/S0103-50532005000700022
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work reports the preparation and characterization of polymeric nanostructure-coated diclofenac-loaded microparticles. After spray-drying, powders presented 80% of yield and encapsulation efficiency of 83%. SEM analyses showed nanostructures adsorbed onto the surface of microparticles presenting surface area (BET) and pore volumes (BJH) (83 m(2) g(-1), 0.10 cm(3) g(-1)) smaller than the uncoated-core (163 m(2) g(-1), 0.25 cm(3) g(-1)). In vitro drug release experiments at pH 5.0 and 7.4 showed dissolution efficiencies of 34% and 78% (uncoated-core), 74% and 83% (physical mixture of raw materials), and 58% and 85% (nanostructure- coated microparticles), respectively. Mathematical modeling of the dissolution profiles fitted a biexponential model at pH 5.0 and a monoexponential model at pH 7.4. Regarding the digestive tolerance experiments, the total lesional indexes were 156.1 +/- 48.5 for sodium diclofenac aqueous solution, 132.4 +/- 45.7 for uncoated-core, 109.1 +/- 35.8 for physical mixture and 29.9 +/- 12.1 for microparticles showing a protective effect of these microparticles against the mucosal diclofenac damage. This strategy of coating presents a potential use for oral administration of drugs.
引用
收藏
页码:1233 / 1240
页数:8
相关论文
共 42 条