Polymeric hydrogels for oral insulin delivery

被引:210
作者
Chaturvedi, Kiran [1 ]
Ganguly, Kuntal [1 ]
Nadagouda, Mallikarjuna N. [1 ]
Aminabhavi, Tejraj M. [1 ]
机构
[1] Soniya Educ Trusts Coll Pharm, Dharwad 580002, Karnataka, India
关键词
Hydrogels; Insulin; Oral delivery; Peptides; Chitosan; Bioavailability; POLYMETHACRYLIC ACID-CHITOSAN; PEPTIDE DRUG-DELIVERY; IN-VIVO EVALUATION; COMPLEXATION HYDROGELS; SUPERPOROUS HYDROGEL; INTESTINAL-MEMBRANE; ENTERAL ABSORPTION; ALPHA-CHYMOTRYPSIN; SENSITIVE HYDROGEL; BETA-CYCLODEXTRIN;
D O I
10.1016/j.jconrel.2012.11.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The search for an effective and reliable oral insulin delivery system has been a major challenge facing pharmaceutical scientists for over many decades. Even though innumerable carrier systems that protect insulin from degradation in the GIT with improved membrane permeability and biological activity have been developed, yet a clinically acceptable device is not available for human application. Efforts in this direction are continuing at an accelerated speed. One of the preferred systems widely explored is based on polymeric hydrogels that protect insulin from enzymatic degradation in acidic stomach and delivers effectively in the intestine. Swelling and deswelling mechanisms of the hydrogel under varying pH conditions of the body control the release of insulin. The micro and nanoparticle (NP) hydrogel devices based on biopolymers have been widely explored, but their applications in human insulin therapy are still far from satisfactory. The present review highlights the recent findings on hydrogel-based devices for oral delivery of insulin. Literature data are critically assessed and results from different laboratories are compared. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 138
页数:10
相关论文
共 100 条
  • [1] Recent advances on chitosan-based micro- and nanoparticles in drug delivery
    Agnihotri, SA
    Mallikarjuna, NN
    Aminabhavi, TM
    [J]. JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) : 5 - 28
  • [2] Region-dependent role of the mucous/glycocalyx layers in insulin permeation across rat small intestinal membrane
    Aoki, Y
    Morishita, M
    Asai, K
    Akikusa, B
    Hosoda, S
    Takayama, K
    [J]. PHARMACEUTICAL RESEARCH, 2005, 22 (11) : 1854 - 1862
  • [3] EFFECT OF CHITOSAN ON THE PERMEABILITY OF MONOLAYERS OF INTESTINAL EPITHELIAL-CELLS (CACO-2)
    ARTURSSON, P
    LINDMARK, T
    DAVIS, SS
    ILLUM, L
    [J]. PHARMACEUTICAL RESEARCH, 1994, 11 (09) : 1358 - 1361
  • [4] ABSORPTION CHARACTERISTICS OF CHEMICALLY MODIFIED-INSULIN DERIVATIVES WITH VARIOUS FATTY-ACIDS IN THE SMALL AND LARGE-INTESTINE
    ASADA, H
    DOUEN, T
    WAKI, M
    ADACHI, S
    FUJITA, T
    YAMAMATO, A
    MURANISHI, S
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (06) : 682 - 687
  • [5] Avadi M R, 2011, ISRN Pharm, V2011, P860109, DOI 10.5402/2011/860109
  • [6] Preparation and characterization of insulin nanoparticles using chitosan and Arabic gum with ionic gelation method
    Avadi, Mohammad Reza
    Sadeghi, Assal Mir Mohammad
    Mohammadpour, Nasser
    Abedin, Saideh
    Atyabi, Fatemeh
    Dinarvand, Rassoul
    Rafiee-Tehrani, Morteza
    [J]. NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2010, 6 (01) : 58 - 63
  • [7] Developments in polymeric devices for oral insulin delivery
    Babu, V. Ramesh
    Patel, Pradip
    Mundargi, Raghavendra C.
    Rangaswamy, Vidhya
    Aminabhavi, Tejraj M.
    [J]. EXPERT OPINION ON DRUG DELIVERY, 2008, 5 (04) : 403 - 415
  • [8] Novel thermo- and pH-responsive hydroxypropyl cellulose- and poly (L-glutamic acid)-based microgels for oral insulin controlled release
    Bai, Yunyan
    Zhang, Zhe
    Zhang, Aiping
    Chen, Li
    He, Chaoliang
    Zhuang, Xiuli
    Chen, Xuesi
    [J]. CARBOHYDRATE POLYMERS, 2012, 89 (04) : 1207 - 1214
  • [9] Thermo- and pH-responsive microgels for controlled release of insulin
    Bai, Yunyan
    Zhang, Zhe
    Deng, Mingxiao
    Chen, Li
    He, Chaoliang
    Zhuang, Xiuli
    Chen, Xuesi
    [J]. POLYMER INTERNATIONAL, 2012, 61 (07) : 1151 - 1157
  • [10] Banting FG, 1922, J LAB CLIN MED, V7, P251