Enhanced pH-responsive carrier system based on alginate and chemically modified carboxymethyl chitosan for oral delivery of protein drugs: Preparation and in-vitro assessment

被引:136
作者
El-Sherbiny, Ibrahim M. [1 ]
机构
[1] Mansoura Univ, Fac Sci, Dept Chem, Polymer Lab, ET-35516 Mansoura, Egypt
关键词
Alginate; Chitosan; PEG; Hydrogel; Protein drugs; Microspheres; BOVINE SERUM-ALBUMIN; INTESTINAL DELIVERY; HYDROGEL BEADS; RELEASE; CALCIUM; MUCOADHESIVE; BEHAVIOR; MICROPARTICLES; MICROCAPSULES;
D O I
10.1016/j.carbpol.2010.01.034
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
In this investigation a new series of biodegradable pH-responsive hydrogel microspheres were prepared, characterized and in-vitro evaluated as potential carriers for oral delivery of protein drugs. The microspheres are based on ionotropically-crosslinked mixture of sodium alginate and chemically modified carboxymethyl chitosan and coated through polyelectrolyte complexation with chitosan grafted with poly(ethylene glycol). The main objective of the developed microspheres is to survive the harsh acidity of stomach and preferably release peptide and protein drugs in intestine. Both ionotropic gelation and coating process were carried out under mild aqueous conditions, which should be appropriate for retention of biological activity of protein drugs. Swelling studies were carried out for the microspheres at 37 degrees C in simulated gastric and intestinal fluids. Morphology, size and in-vitro biodegradation of the microspheres were also investigated. A model protein drug was entrapped and the in-vitro drug release profiles were established. The preliminary investigation of the microspheres developed in this study showed a consistent swelling pattern, high entrapment efficiency and promising sustained release profiles of the model protein drug. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1125 / 1136
页数:12
相关论文
共 29 条
[1]
Trypsin inhibition, calcium and zinc ion binding of starch-g-poly(acrylic acid) copolymers and starch/poly (acrylic acid) mixtures for peroral peptide drug delivery [J].
Ameye, D ;
Voorspoels, J ;
Foreman, P ;
Tsai, J ;
Richardson, P ;
Geresh, S ;
Remon, JP .
JOURNAL OF CONTROLLED RELEASE, 2001, 75 (03) :357-364
[2]
Chitosan-alginate multilayer beads for gastric passage and controlled intestinal release of protein [J].
Anal, AK ;
Bhopatkar, D ;
Tokura, S ;
Tamura, H ;
Stevens, WF .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2003, 29 (06) :713-724
[3]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]
Imaging an alginate polymer gel matrix using atomic force microscopy [J].
Decho, AW .
CARBOHYDRATE RESEARCH, 1999, 315 (3-4) :330-333
[5]
Dolatabadi-Farahani T, 2006, IRAN POLYM J, V15, P405
[6]
Preparation and In Vitro Evaluation of New pH-Sensitive Hydrogel Beads for Oral Delivery of Protein Drugs [J].
El-Sherbiny, I. M. ;
Abdel-Bary, E. M. ;
Harding, D. R. K. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2010, 115 (05) :2828-2837
[7]
Synthesis, characterization and metal uptake capacity of a new carboxymethyl chitosan derivative [J].
El-Sherbiny, I. M. .
EUROPEAN POLYMER JOURNAL, 2009, 45 (01) :199-210
[8]
ELSHERBINY IM, J APPL POLY IN PRESS
[9]
Preparation of carboxymethyl chitosan in aqueous solution under microwave irradiation [J].
Ge, HC ;
Luo, DK .
CARBOHYDRATE RESEARCH, 2005, 340 (07) :1351-1356
[10]
Chitosan/calcium alginate microcapsules for intestinal delivery of nitrofurantoin [J].
Hari, PR ;
Chandy, T ;
Sharma, CP .
JOURNAL OF MICROENCAPSULATION, 1996, 13 (03) :319-329