Efficacy of Mucoadhesive Hydrogel Microparticles of Whey Protein and Alginate for Oral Insulin Delivery

被引:61
作者
Deat-Laine, Emmanuelle [1 ]
Hoffart, Valerie [1 ]
Garrait, Ghislain [1 ]
Jarrige, Jean-Francois [1 ]
Cardot, Jean-Michel [1 ]
Subirade, Muriel [2 ]
Beyssac, Eric [1 ]
机构
[1] Univ Clermont 1, UFR Pharm, ERT 18, Lab Biopharm, F-63001 Clermont Ferrand, France
[2] Univ Laval, Inst Nutraceut & Funct Foods INAF, Milk & Dairy Prod STELA Ctr, Ste Foy, PQ G1K 7P4, Canada
关键词
alginate; insulin; microspheres; oral administration; whey protein; SUPERPOROUS HYDROGEL; GEL BEADS; ABSORPTION; RELEASE; MICROSPHERES; PROTECTION; TRANSPORT; POLYMERS; CHITOSAN; SYSTEMS;
D O I
10.1007/s11095-012-0913-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To evaluate the efficacy of mucoadhesive insulin-loaded whey protein (WP) /alginate (ALG) microparticles (MP) for oral insulin administration. Insulin-loaded microparticles (ins-MP) made of whey protein and alginate were prepared by a cold gelation technique and an adsorption method, without adjunction of organic solvent in order to develop a biocompatible vehicle for oral administration of insulin. In vitro characterization, evaluations of ins-MP in excised intestinal tissues and hypoglycaemic effects after intestinal administration in healthy rats were performed The release properties and swelling behaviors, investigated in different pH buffers, demonstrated a release based on diffusion mechanism following matrix swelling. Mucoadhesion studies in rabbits and insulin transport experiments with excised intestinal rat tissues revealed that encapsulation in microparticles with mucoadhesive properties promotes insulin absorption across duodenal membranes and bioactivity protection. In vivo experiments reinforced the interest of encapsulation in whey protein/alginate combination. Confocal microscopic observations associated with blood glucose levels bring to light duodenal absorption of insulin biologically active following in vivo administration. Insulin-loaded WP/ALG MP with high quantities of drug entrapped, in vitro matrix swelling and protective effect as well as excellent mucohadesive properties was developped. Improvement of intestinal delivery of insulin and increased in bioavailability were recorded.
引用
收藏
页码:721 / 734
页数:14
相关论文
共 39 条
[1]   Elaboration and characterization of whey protein beads by an emulsification/cold gelation process: Application for the protection of retinol [J].
Beaulieu, L ;
Savoie, L ;
Paquin, P ;
Subirade, M .
BIOMACROMOLECULES, 2002, 3 (02) :239-248
[2]   Chemically modified chitosans as enzyme inhibitors [J].
Bernkop-Schnürch, A ;
Kast, CE .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 52 (02) :127-137
[3]  
Beyssac E, 1998, BIOPHARM DRUG DISPOS, V19, P401, DOI 10.1002/(SICI)1099-081X(199809)19:6<401::AID-BDD116>3.0.CO
[4]  
2-U
[5]   Preparation and evaluation of mucinated sodium alginate microparticles for oral delivery of insulin [J].
Builders, Philip F. ;
Kunle, Olobayo O. ;
Okpaku, Larry C. ;
Builders, Modupe O. ;
Attama, Anthony A. ;
Adikwu, Michael U. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 70 (03) :777-783
[6]   The study of drug release from microspheres adhered on pig vesical mucosa [J].
Burjak, M ;
Bogataj, M ;
Velnar, M ;
Grabnar, I ;
Mrhar, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 224 (1-2) :123-130
[7]   Alginate-whey protein granular microspheres as oral delivery vehicles for bioactive compounds [J].
Chen, Lingyun ;
Subirade, Muriel .
BIOMATERIALS, 2006, 27 (26) :4646-4654
[8]   A lecithin-based microemulsion of rh-insulin with aprotinin for oral administration:: Investigation of hypoglycemic effects in non-diabetic and STZ-induced diabetic rats [J].
Çilek, A ;
Çelebi, N ;
Tirnaksiz, F ;
Tay, A .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 298 (01) :176-185
[9]   Nutritional and functional characteristics of whey proteins in food products [J].
de Wit, JN .
JOURNAL OF DAIRY SCIENCE, 1998, 81 (03) :597-608
[10]   Comparative mucoretention of sucralfate suspensions in an everted rat esophagus model [J].
Dobrozsi, DJ ;
Smith, RL ;
Sakr, AA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 189 (01) :81-89