Insulin-loaded alginate microspheres for oral delivery - Effect of polysaccharide reinforcement on physicochemical properties and release profile

被引:114
作者
Martins, Susana [1 ]
Sarmento, Bruno [1 ]
Souto, Eliana B. [1 ]
Ferreira, Domingos C. [1 ]
机构
[1] Univ Porto, Fac Pharm, Dept Pharmaceut Technol, P-4100 Oporto, Portugal
关键词
alginate; chitosan; dextran sulphate; insulin; microspheres; gastric retention;
D O I
10.1016/j.carbpol.2007.02.012
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Oral administration of insulin requires protein protection from degradation in the gastric environment and its absorption improvement in the intestinal tract. To achieve this objective several types of microspheres composed of alginate, chitosan and dextran sulphate have been prepared by ionotropic gelation. Parameters such as the mean particle size, swelling behaviour, insulin encapsulation efficiency, loading capacity and release profiles in simulated gastric and intestinal fluids have been compared for the systems developed. In this study, attempts have been made to increase insulin protection and to improve its release from microspheres by reinforcing the alginate matrix with chitosan and/or dextran sulphate. Dextran sulphate was able to avoid insulin release at pH 1.2, protecting the protein from the acidic environment and reducing the total insulin released at pH 6.8. This effect was explained by an interaction between the permanent negatively charged groups of dextran sulphate and insulin molecules. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:725 / 731
页数:7
相关论文
共 22 条
[1]  
[Anonymous], CHEM IND CHEM ENG Q
[2]  
Arbit Ehud, 2004, Diabetes Technol Ther, V6, P510, DOI 10.1089/1520915041705929
[3]   Dynamics of controlled release of potassium nitrate from a highly swelling binary biopolymeric blend of alginate and pectin [J].
Bajpai, J ;
Bajpai, AK ;
Mishra, S .
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, 2006, A43 (01) :165-186
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   Toward understanding insulin fibrillation [J].
Brange, J ;
Andersen, L ;
Laursen, ED ;
Meyn, G ;
Rasmussen, E .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (05) :517-525
[6]  
Brange J, 1987, GALENICS INSULIN PHY
[7]   Inclusion and release of proteins from polysaccharide-based polyion complexes [J].
Dumitriu, S ;
Chornet, E .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 31 (03) :223-246
[8]   Alginate-diltiazem hydrochloride beads: optimization of formulation factors, in vitro and in vivo availability [J].
El-Kamel, AH ;
Al-Gohary, OMN ;
Hosny, EA .
JOURNAL OF MICROENCAPSULATION, 2003, 20 (02) :211-225
[9]   Reversible and strong immobilization of proteins by ionic exchange on supports coated with sulfate-dextran [J].
Fuentes, M ;
Pessela, BCC ;
Maquiese, JV ;
Ortiz, C ;
Segura, RL ;
Palomo, JM ;
Torres, OAR ;
Mateo, C ;
Fernández-Lafuente, R ;
Guisán, JM .
BIOTECHNOLOGY PROGRESS, 2004, 20 (04) :1134-1139
[10]   Protein release from alginate matrices [J].
Gombotz, WR ;
Wee, SF .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 31 (03) :267-285