Chitosan-Sodium Lauryl Sulfate Nanoparticles as a Carrier System for the In Vivo Delivery of Oral Insulin

被引:52
|
作者
Elsayed, Amani [2 ,3 ]
Al-Remawi, Mayyas [3 ]
Qinna, Nidal [4 ]
Farouk, Asim [2 ]
Al-Sou'od, Khaldoun A. [5 ]
Badwan, Adnan A. [1 ]
机构
[1] Subsidiary Jordanian Pharmaceut Mfg Co, Suwagh Co Drug Delivery Syst, Naur, Jordan
[2] Gezira Univ, Dept Pharmaceut, Fac Pharm, Medani, Sudan
[3] Taif Univ, Dept Pharmaceut, Fac Pharm, At Taif, Saudi Arabia
[4] Petra Univ, Dept Pharmacol & Med Sci, Fac Pharm, Amman, Jordan
[5] Al Al Bayt Univ, Dept Chem, Fac Sci, Mafraq, Jordan
来源
AAPS PHARMSCITECH | 2011年 / 12卷 / 03期
关键词
chitosan; insulin; nanoparticles; oral delivery system; sodium lauryl sulfate; POLYELECTROLYTE COMPLEXATION; MICROSPHERES; EFFICIENCY; PARTICLES; GELATION; THERAPY; RELEASE; VACCINE; VITRO;
D O I
10.1208/s12249-011-9647-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present work explores the possibility of formulating an oral insulin delivery system using nanoparticulate complexes made from the interaction between biodegradable, natural polymer called chitosan and anionic surfactant called sodium lauryl sulfate (SLS). The interaction between chitosan and SLS was confirmed by Fourier transform infrared spectroscopy. The nanoparticles were prepared by simple gelation method under aqueous-based conditions. The nanoparticles were stable in simulated gastric fluids and could protect the encapsulated insulin from the GIT enzymes. Additionally, the in vivo results clearly indicated that the insulin-loaded nanoparticles could effectively reduce the blood glucose level in a diabetic rat model. However, additional formulation modifications are required to improve insulin oral bioavailability.
引用
收藏
页码:958 / 964
页数:7
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