Can natural polymers assist in delivering insulin orally?

被引:46
作者
Nur, Mokhamad [1 ,2 ]
Vasiljevic, Todor [1 ]
机构
[1] Victoria Univ, Coll Hlth & Biomed, Adv Food Syst Res Unit, POB 14428, Melbourne, Vic 8001, Australia
[2] Brawijaya Univ, Fac Agr Technol, Dept Agr Prod Technol, Jl Vet, Malang 65145, Indonesia
关键词
Oral insulin delivery; Natural polymers; Insulin release; IN-VITRO CHARACTERIZATION; CHITOSAN NANOPARTICLES; ALGINATE-CHITOSAN; POLYELECTROLYTE COMPLEXES; INTESTINAL DELIVERY; CONTROLLED-RELEASE; MICROSPHERES; SYSTEMS; CARRIER; ALGINATE/CHITOSAN;
D O I
10.1016/j.ijbiomac.2017.05.138
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetes mellitus is one of the most grave and lethal non communicable diseases. Insulin is normally used to medicate diabetes. Due to bioavailability issues, the most regular route of administration is through injection, which may pose compliance problems to treatment. The oral administration thus appears as a suitable alternative, but with several important problems. Low stability of insulin in the gastrointestinal tract and low intestinal permeation are some of the issues. Encapsulation of insulin into polymer-based particles emerges as a plausible strategy. Different encapsulation approaches and polymers have been used in this regard. Polymers with different characteristics from natural or synthetic origin have been assessed to attain this goal, with natural polymers being preferable. Natural polymers studied so far include chitosan, alginate, carrageenan, starch, pectin, casein, tragacanth, dextran, carrageenan, gelatine and cyclodextrin. While some promising knowledge and results have been gained, a polymeric-based particle system to deliver insulin orally has not been introduced onto the market yet. In this review, effectiveness of different natural polymer materials developed so far along with fabrication techniques are evaluated. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:889 / 901
页数:13
相关论文
共 85 条
[21]   Global estimates of diabetes prevalence for 2013 and projections for 2035 [J].
Guariguata, L. ;
Whiting, D. R. ;
Hambleton, I. ;
Beagley, J. ;
Linnenkamp, U. ;
Shaw, J. E. .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2014, 103 (02) :137-149
[22]   Chitosan Based Polyelectrolyte Complexes as Potential Carrier Materials in Drug Delivery Systems [J].
Hamman, Josias H. .
MARINE DRUGS, 2010, 8 (04) :1305-1322
[23]   Insulin-Loaded pH-Sensitive Hyaluronic Acid Nanoparticles Enhance Transcellular Delivery [J].
Han, Lina ;
Zhao, Yuefang ;
Yin, Lifang ;
Li, Ruiming ;
Liang, Yang ;
Huang, Huan ;
Pan, Shirong ;
Wu, Chuanbin ;
Feng, Min .
AAPS PHARMSCITECH, 2012, 13 (03) :836-845
[24]   Novel alginate gel microspheres produced by impinging aerosols for oral delivery of proteins [J].
Hariyadi, Dewi Melani ;
Wang, Yiwei ;
Lin, Sharon Chien-Yu ;
Bostrom, Thor ;
Bhandari, Bhesh ;
Coombes, Allan G. A. .
JOURNAL OF MICROENCAPSULATION, 2012, 29 (03) :250-261
[25]   Synthesis of new thermo/pH sensitive drug delivery systems based on tragacanth gum polysaccharide [J].
Hemmati, Khadijeh ;
Ghaemy, Mousa .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2016, 87 :415-425
[26]   RETRACTED: Synthesis, Characterization, and In vitro Studies of PLGA-PEG Nanoparticles for Oral Insulin Delivery (Retracted article. See vol. 94, pg. 1422, 2019) [J].
Hosseininasab, Sara ;
Pashaei-Asl, Roghiyeh ;
Khandaghi, Amir Ahmad ;
Nasrabadi, Hamid Tayefi ;
Nejati-Koshki, Kazem ;
Akbarzadeh, Abolfazl ;
Joo, Sang Woo ;
Hanifehpour, Younes ;
Davaran, Soodabeh .
CHEMICAL BIOLOGY & DRUG DESIGN, 2014, 84 (03) :307-315
[27]   Stability of insulin during the erosion of poly(lactic acid) and poly(lactic-co-glycolic acid) microspheres [J].
Ibrahim, MA ;
Ismail, A ;
Fetouh, MI ;
Göpferich, A .
JOURNAL OF CONTROLLED RELEASE, 2005, 106 (03) :241-252
[28]   Cyclodextrins in peptide and protein delivery [J].
Irie, T ;
Uekama, K .
ADVANCED DRUG DELIVERY REVIEWS, 1999, 36 (01) :101-123
[29]   Novel strategies in the oral delivery of antidiabetic peptide drugs - Insulin, GLP 1 and its analogs [J].
Ismail, Ruba ;
Csoka, Ildiko .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2017, 115 :257-267
[30]   Double emulsion-templated nanoparticle colloidosomes with selective permeability [J].
Lee, Daeyeon ;
Weitz, David A. .
ADVANCED MATERIALS, 2008, 20 (18) :3498-+