Chitosan/lecithin liposomal nanovesicles as an oral insulin delivery system

被引:48
|
作者
Al-Remawi, Mayyas [1 ]
Elsayed, Amani [2 ]
Maghrabi, Ibrahim [3 ]
Hamaidi, Mohammad [2 ]
Jaber, Nisrein [4 ]
机构
[1] Petra Univ, Fac Pharm & Med Sci, Dept Pharmaceut & Pharmaceut Technol, Amman, Jordan
[2] Taif Univ, Coll Pharm, Dept Pharmaceut & Pharmaceut Technol, POB 888, At Taif 21944, Saudi Arabia
[3] Taif Univ, Coll Pharm, Dept Clin Pharm, At Taif, Saudi Arabia
[4] Jordan Food & Drug Adm, Dept Drug Registrat, Amman, Jordan
关键词
Chitosan; insulin; lecithin; nanovesicles; liposomes; MOLECULAR-WEIGHT CHITOSAN; COATED LIPOSOMES; DRUG-DELIVERY; DIABETIC-RATS; NANOPARTICLES; PH; STABILIZATION; ENCAPSULATION; STABILITY; PROTEINS;
D O I
10.1080/10837450.2016.1213745
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present work, insulin-chitosan polyelectrolyte complexes associated to lecithin liposomes were investigated as a new carrier for oral delivery of insulin. The preparation was characterized in terms of particle size, zeta potential and encapsulation efficiency. Surface tension measurements revealed that insulin-chitosan polyelectrolyte complexes have some degree of hydrophobicity and should be added to lecithin liposomal dispersion and not the vice versa to prevent their adsorption on the surface. Stability of insulin was enhanced when it was associated to liposomes. Significant reduction of blood glucose levels was noticed after oral administration of liposomal preparation to streptozotocin diabetic rats compared to control. The hypoglycemic activity was more prolonged compared to subcutaneously administered insulin.
引用
收藏
页码:390 / 398
页数:9
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