Intestinal mucoadhesive devices for oral delivery of insulin

被引:81
作者
Banerjee, Amrita [1 ]
Lee, JooHee [1 ]
Mitragotri, Samir [1 ,2 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem Engn, Engn 2,Room 3349, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Ctr Bioengn, Santa Barbara, CA 93106 USA
关键词
D O I
10.1002/btm2.10015
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Oral delivery of proteins such as insulin has been a long-lasting challenge owing to gastrointestinal degradation and poor permeability of therapeutic macromolecules across biological membranes. We have developed mucoadhesive intestinal devices for oral delivery of insulin to address this challenge. Here we demonstrate a combination of intestinal devices and a permeation enhancer, dimethyl palmitoyl ammonio propanesulfonate (PPS), for oral delivery of insulin. The devices were delivered from a capsule coated with a pH-responsive enteric coating. The devices adhere to intestinal mucosa, release their protein load unidirectionally, and prevent enzymatic degradation in the gut. Devices were found to completely release their drug load within 3-4 hr and showed excellent strength of mucoadhesion to porcine intestine. Devices loaded with insulin and PPS significantly decreased blood glucose levels by 30 and 33% in diabetic and nondiabetic rats, respectively. These studies demonstrate that intestinal mucoadhesive devices are a promising oral alternative to insulin injections and therefore should be further explored for the treatment of diabetes.
引用
收藏
页码:338 / 346
页数:9
相关论文
共 45 条
[1]
Peptide delivery using phospholipid micelles [J].
Banerjee, Amrita ;
Onyuksel, Hayat .
WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2012, 4 (05) :562-574
[2]
Mucin structure, aggregation, physiological functions and biomedical applications [J].
Bansil, Rama ;
Turner, Bradley S. .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2006, 11 (2-3) :164-170
[3]
Permeation enhancing polymers in oral delivery of hydrophilic macromolecules:: thiomer/GSH systems [J].
Bernkop-Schnürch, A ;
Kast, CE ;
Guggi, D .
JOURNAL OF CONTROLLED RELEASE, 2003, 93 (02) :95-103
[4]
Mucoadhesive drug delivery system: An overview [J].
Boddupalli, Bindu M. ;
Mohammed, Zulkar N. K. ;
Nath, Ravinder A. ;
Banji, David .
JOURNAL OF ADVANCED PHARMACEUTICAL TECHNOLOGY & RESEARCH, 2010, 1 (04) :381-387
[5]
Oral insulin delivery [J].
Carino, GP ;
Mathiowitz, E .
ADVANCED DRUG DELIVERY REVIEWS, 1999, 35 (2-3) :249-257
[6]
Effective oral delivery of insulin in animal models using vitamin B12-coated dextran nanoparticles [J].
Chalasani, Kishore B. ;
Russell-Jones, Gregory J. ;
Jain, Akhlesh K. ;
Diwan, Prakash V. ;
Jain, Sanjay K. .
JOURNAL OF CONTROLLED RELEASE, 2007, 122 (02) :141-150
[7]
A review of the prospects for polymeric nanoparticle platforms in oral insulin delivery [J].
Chen, Mei-Chin ;
Sonaje, Kiran ;
Chen, Ko-Jie ;
Sung, Hsing-Wen .
BIOMATERIALS, 2011, 32 (36) :9826-9838
[8]
Oral delivery of insulin associated to polymeric nanoparticles in diabetic rats [J].
Damge, Christiane ;
Maincent, Philippe ;
Ubrich, Nathalie .
JOURNAL OF CONTROLLED RELEASE, 2007, 117 (02) :163-170
[9]
Poly(ε-Caprolactone)/Eudragit Nanoparticles for Oral Delivery of Aspart-Insulin in the Treatment of Diabetes [J].
Damge, Christiane ;
Socha, Marie ;
Ubrich, Nathalie ;
Maincent, Philippe .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 99 (02) :879-889
[10]
Gastrointestinal mucoadhesive patch system (GI-MAPS) for oral administration of G-CSF, a model protein [J].
Eiamtrakarn, S ;
Itoh, Y ;
Kishimoto, J ;
Yoshikawa, Y ;
Shibata, N ;
Murakami, M ;
Takada, K .
BIOMATERIALS, 2002, 23 (01) :145-152