NANOTECHNOLOGY AS A PROMISING STRATEGY FOR ALTERNATIVE ROUTES OF INSULIN DELIVERY

被引:31
作者
Reis, Catarina Pinto [1 ,2 ]
Damge, Christiane [3 ]
机构
[1] Lusophone Univ Humanities & Technol, CBIOS LNBN Lab Nanosci & Biomed Nanotechnol, Lisbon, Portugal
[2] Lusophone Univ Humanities & Technol, Fac Sci & Hlth Technol, Lisbon, Portugal
[3] Univ Henri Poincare, EA 3452, Fac Pharm, Nancy, France
来源
NANOMEDICINE: CANCER, DIABETES, AND CARDIOVASCULAR, CENTRAL NERVOUS SYSTEM, PULMONARY AND INFLAMMATORY DISEASES | 2012年 / 508卷
关键词
SOLID LIPID NANOPARTICLES; ORAL INSULIN; POLYALKYLCYANOACRYLATE NANOCAPSULES; POLYMERIC NANOPARTICLES; DRUG-DELIVERY; IN-VIVO; CHITOSAN NANOPARTICLES; TRANSMUCOSAL DELIVERY; ABSORPTION ENHANCERS; TRANSDERMAL DELIVERY;
D O I
10.1016/B978-0-12-391860-4.00014-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Since its discovery, insulin has been used as highly specific and effective therapeutic protein to treat type 1 diabetes and later was associated to oral antidiabetic agents in the treatment of type 2 diabetes. Generally, insulin is administered parenterally. Although this route is successful, it still has several limitations, such as discomfort, pain, lipodystrophy at the injection sites and peripheral hyperinsulinemia, which may be the cause of side effects and some complications. Thus, alternative routes of administration have been developed, namely, those based on nanotechnologies. Nanoparticles, made of synthetic or natural materials, have been shown to successfully overcome the inherent barriers for insulin stability, degradation, and uptake across the gastrointestinal tract and other mucosal membranes. This review describes some of the many attempts made to develop alternative and more convenient routes for insulin delivery.
引用
收藏
页码:271 / 294
页数:24
相关论文
共 76 条
[1]  
Aboubakar M, 1999, J BIOMED MATER RES, V47, P568, DOI 10.1002/(SICI)1097-4636(19991215)47:4<568::AID-JBM14>3.3.CO
[2]  
2-O
[3]   TRANSMUCOSAL PASSAGE OF POLYALKYLCYANOACRYLATE NANOCAPSULES AS A NEW DRUG CARRIER IN THE SMALL-INTESTINE [J].
APRAHAMIAN, M ;
MICHEL, C ;
HUMBERT, W ;
DEVISSAGUET, JP ;
DAMGE, C .
BIOLOGY OF THE CELL, 1987, 61 (1-2) :69-76
[4]   SITE DEPENDENCE OF ABSORPTION-PROMOTING ACTIONS OF LAURETH-9, NA SALICYLATE, NA2EDTA, AND APROTININ ON RECTAL, NASAL, AND BUCCAL INSULIN DELIVERY [J].
AUNGST, BJ ;
ROGERS, NJ .
PHARMACEUTICAL RESEARCH, 1988, 5 (05) :305-308
[5]   MORPHO-CYTOCHEMICAL AND BIOCHEMICAL-EVIDENCE FOR INSULIN ABSORPTION BY THE RAT ILEAL EPITHELIUM [J].
BENDAYAN, M ;
ZIV, E ;
BENSASSON, R ;
BARON, H ;
KIDRON, M .
DIABETOLOGIA, 1990, 33 (04) :197-204
[6]   Chitosan reduced gold nanoparticles as novel carriers for transmucosal delivery of insulin [J].
Bhumkar, Devika R. ;
Joshi, Hrushikesh M. ;
Sastry, Murali ;
Pokharkar, Varsha B. .
PHARMACEUTICAL RESEARCH, 2007, 24 (08) :1415-1426
[7]   Solid Lipid Nanoparticles as Insulin Inhalation Carriers for Enhanced Pulmonary Delivery [J].
Bi, Ru ;
Shao, Wei ;
Wang, Qun ;
Zhang, Na .
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2009, 5 (01) :84-92
[8]  
Brange J, 1997, Pharm Biotechnol, V10, P343
[9]   Nanosphere based oral insulin delivery [J].
Carino, GP ;
Jacob, JS ;
Mathiowitz, E .
JOURNAL OF CONTROLLED RELEASE, 2000, 65 (1-2) :261-269
[10]   Concept, strategies, and feasibility of noninvasive insulin delivery [J].
Cefalu, WT .
DIABETES CARE, 2004, 27 (01) :239-246