Strategies for effective oral insulin delivery with modified chitosan nanoparticles: A review

被引:175
作者
Mukhopadhyay, Piyasi [1 ,2 ]
Mishra, Roshnara [2 ]
Rana, Dipak [3 ]
Kundu, Patit P. [1 ]
机构
[1] Univ Calcutta, Dept Polymer Sci & Technol, Kolkata 700009, W Bengal, India
[2] Univ Calcutta, Dept Physiol, Kolkata 700009, W Bengal, India
[3] Univ Ottawa, Ind Membrane Res Inst, Dept Chem & Biol Engn, Ottawa, ON K1N 6N5, Canada
关键词
Chitosan; Nanoparticles; Insulin; Oral delivery; Effective bio-availability; IN-VIVO EVALUATION; DRUG-DELIVERY; INTESTINAL-ABSORPTION; BETA-CYCLODEXTRIN; POLYELECTROLYTE NANOCOMPLEXES; BIODEGRADABLE NANOPARTICLES; POLYMERIC NANOPARTICLES; CONTROLLED-RELEASE; GLOBAL PREVALENCE; PERORAL DELIVERY;
D O I
10.1016/j.progpolymsci.2012.04.004
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Over the last few decades, various natural polymers have been applied to the problem of oral insulin delivery using advanced nanotechnology. Parenteral administration of insulin is widely accepted, but administration via the oral route could overcome the poor patient compliance with repeated injection. Polymers from natural as well as synthetic sources have recently been used in the synthesis of insulin delivery vehicles suitable for oral administration. The biopolymer chitosan has been widely studied in oral insulin delivery due to its favorable properties such as biocompatibility, biodegradability, non-immunogenicity and non-toxicity. This review focuses on progress in the synthesis of chitosan and modified chitosan nanoparticles for efficient oral insulin delivery, with an emphasis on the biological efficacy of the nanoparticles. Obstacles to oral delivery and possible remedies are also brought into focus. Modifications to protect insulin from the harsh acidic environment of the gastrointestinal (GI) tract are described. Chemical barriers such as the acidic gastric pH and the presence of proteolytic enzymes in the stomach and intestine limit the effective absorption of external insulin within the GI tract. Absorption of insulin is physically hindered by the absorption barrier consisting of a single layer of columnar epithelial cells joined at the apical surface by a tight junction complex. The presence of negative charges in the junction complex leads to segregation of the apical layer from the basolateral compartment of the epithelial cells, making the intestinal environment selective for particles based on size and charge. Nanoparticles are able to overcome these barriers and deliver insulin. While this technology still has some drawbacks, chitosan and modified chitosan nanoparticles are highly promising agents for oral insulin delivery. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1457 / 1475
页数:19
相关论文
共 122 条
[1]   Formulation and evaluation of novel tableted chitosan microparticles for the controlled release of clozapine [J].
Agnihotri, SA ;
Aminabhavi, TM .
JOURNAL OF MICROENCAPSULATION, 2004, 21 (07) :709-718
[2]   Recent Challenges in Insulin Delivery Systems: A Review [J].
Al-Tabakha, M. M. ;
Arida, A. I. .
INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 70 (03) :278-286
[3]   Polymeric nano- and microparticles for the oral delivery of peptides and peptidomimetics [J].
Allémann, E ;
Leroux, JC ;
Gurny, R .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 34 (2-3) :171-189
[4]  
Aman SF, 2010, PAK J PHARM SCI, V23, P313
[5]   ABSORPTION CHARACTERISTICS OF CHEMICALLY MODIFIED-INSULIN DERIVATIVES WITH VARIOUS FATTY-ACIDS IN THE SMALL AND LARGE-INTESTINE [J].
ASADA, H ;
DOUEN, T ;
WAKI, M ;
ADACHI, S ;
FUJITA, T ;
YAMAMATO, A ;
MURANISHI, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (06) :682-687
[6]   Preparation and characterization of insulin nanoparticles using chitosan and Arabic gum with ionic gelation method [J].
Avadi, Mohammad Reza ;
Sadeghi, Assal Mir Mohammad ;
Mohammadpour, Nasser ;
Abedin, Saideh ;
Atyabi, Fatemeh ;
Dinarvand, Rassoul ;
Rafiee-Tehrani, Morteza .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2010, 6 (01) :58-63
[7]   Diethyl methyl chitosan as an intestinal paracellular enhancer: ex vivo and in vivo studies [J].
Avadi, MR ;
Jalali, A ;
Sadeghi, AMM ;
Shamimi, K ;
Bayati, KH ;
Nahid, E ;
Dehpour, AR ;
Rafiee-Tehrani, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 293 (1-2) :83-89
[8]   Preparation and characterization of insulin nanoparticles using chitosan and its quaternized derivatives [J].
Bayat, Akbar ;
Larijani, Bagher ;
Ahmadian, Shahin ;
Junginger, Hans E. ;
Rafiee-Tehrani, Morteza .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2008, 4 (02) :115-120
[9]   The use of inhibitory agents to overcome the enzymatic barrier to perorally administered therapeutic peptides and proteins [J].
Bernkop-Schnurch, A .
JOURNAL OF CONTROLLED RELEASE, 1998, 52 (1-2) :1-16
[10]   Thiolated chitosans:: development and in vitro evaluation of a mucoadhesive, permeation enhancing oral drug delivery system [J].
Bernkop-Schnürch, A ;
Guggi, D ;
Pinter, Y .
JOURNAL OF CONTROLLED RELEASE, 2004, 94 (01) :177-186