Development of a novel drug delivery system: chitosan nanoparticles entrapped in alginate microparticles

被引:24
作者
Garrait, Ghislain [1 ,2 ]
Beyssac, Eric [1 ]
Subirade, Muriel [2 ]
机构
[1] Univ Auvergne, UFR Pharm, Equipe Accueil Concept Ingn & Dev Aliment & Med, F-63001 Clermont Ferrand, France
[2] Univ Laval, Fac Sci Agr & Alimentat, INAF STELA, Quebec City, PQ G1K 7P4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Alginate microparticle; chitosan nanoparticle; gastro-resistant; novel drug delivery system; CONTROLLED-RELEASE; MICROSPHERES; MUCOADHESIVE; FORMULATION; BIOADHESIVE; RATS;
D O I
10.3109/02652048.2013.858792
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel carrier using chitosan nanoparticles entrapped into alginate microparticles is proposed for protecting molecules of interest from degradation in the digestive tract. The effects of polymer concentration, sonication, stirring, pH, and processing conditions on the physical characteristics of the carrier were studied. FITC and RBITC were used to localise the polymers within particles using CLSM. Diffusion of amaranth red (AR) from nanoparticles was quantified during dissolution under gastric and intestinal conditions. Under optimal preparation conditions, the size distribution of nanoparticles loaded with AR was uniform (690 nm) with an encapsulation efficacy of 21.9%. Alginate microparticles (285 mu m) containing a homogenous distribution of nanoparticles and polymers were obtained. At gastric pH, the carrier released less than 5% of the loaded AR and, at intestinal pH, the release was rapid and complete. The drug carriers developed shows a promising use as a vehicle suitable to protect molecules of interest after oral administration.
引用
收藏
页码:363 / 372
页数:10
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