The Glucose-Sensitive Nanocarrier Based on Phenylboronic Acid

Article Preview

Abstract:

Recently, diabetes mellitus has become one of the most serious diseases that threat to human health and even life following cancer and cardiovascular disease. Thus, the developments of efficient insulin administration exhibit great practical significance. However, insulin, which could low blood concentration rapidly, cannot be oral delivery due to very low oral bioavailability for the pure absorption through the gastrointestinal epithelium as well as the rapid hydrolytic and enzymatic degradation in contact with the gastrointestinal fluids. While the frequent administration of exogenous insulin by injection everyday is not perfect due to the inevitable pain, which will cause inflammation, lumps and nodules. In recently, the glucose-responsive insulin delivery system (GRIDS) is developing rapidly which not only has high bioavailability of insulin but also extenuates the pain of diabetics caused by frequent insulin injection. GRIDS is expected to be a promising therapy approach to replace the frequent insulin injection administration. Therefore, the exploited intelligent glucose-responsive insulin delivery system has significant practical application for diabetes treatment.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

46-49

Citation:

Online since:

October 2014

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2014 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] S. Wild, G. Roglic, A. Green, R. Sicree, H. King. Global prevalence of diabetes - Estimates for the year 2000 and projections for 2030. Diabetes Care 27 (2004) 1047-1053.

DOI: 10.2337/diacare.27.10.2569-a

Google Scholar

[2] Q. Wu, L. Wang, H. Yu, J. Wang, Z. Chen. Organization of Glucose-Responsive Systems and Their Properties. Chem Review 12 (2011) 7855-7875.

DOI: 10.1021/cr200027j

Google Scholar

[3] M. Chen, C. Huang, C. He, W. Zhu, Y. Xu, Y. Lu. A glucose-responsive controlled release system using glucose oxidase-gated mesoporous silica nanocontainers. Chemical Communications 48 (2012) 9522-9524.

DOI: 10.1039/c2cc34290a

Google Scholar

[4] K. Sato, K. Yoshida, S. Takahashi, J. Anzai. pH- and sugar-sensitive layer-by-layer films and microcapsules for drug delivery. Advanced drug delivery reviews 63 (2011) 809-821.

DOI: 10.1016/j.addr.2011.03.015

Google Scholar

[5] W. Zhao, H. Zhang, Q. He, Y. Li, J. Gu, L. Li, H. Li, J. Shi. A glucose-responsive controlled release of insulin system based on enzyme multilayers-coated mesoporous silica particles. Chemical Communications 47 (2011) 9459-9461.

DOI: 10.1039/c1cc12740c

Google Scholar

[6] M. Samoszuk, D. Ehrlich, E. Ramzi. Preclinical Safety Studies of Glucose-Oxidase. Journal of Pharmacology and Experimental Therapeutics 266 (1993) 1643-1648.

Google Scholar

[7] X. Shao, Q. Liu, C., X. Zheng, J. Chen, Y. Zha and so on. Concanavalin A-conjugated poly(ethylene glycol)–poly(lactic acid) nanoparticles for intranasal drug delivery to the cervical lymph nodes. Journal of Microencapsulation 30 (2013) 780-786.

DOI: 10.3109/02652048.2013.788086

Google Scholar

[8] R. Yin, K. Wang, S. Du, L. Chen, J. Nie, W. Zhang. Design of genipin-crosslinked microgels from concanavalin A and glucosyloxyethyl acrylated chitosan for glucose-responsive insulin delivery. Carbohydrate Polymers 103 (2014) 369-676.

DOI: 10.1016/j.carbpol.2013.12.067

Google Scholar

[9] R. Ballerstadt, C. Evans, R. McNichols, A. Gowda. Concanavalin A for in vivo glucose sensing: a biotoxicity review. Biosensors & bioelectronics 22 (2006) 275-284.

DOI: 10.1016/j.bios.2006.01.008

Google Scholar

[10] R. Nishiyabu, Y. Kubo, T.D. James, J.S. Fossey. Boronic acid building blocks: tools for self assembly. Chem Commun (Camb) 47 (2011) 1124-1150.

DOI: 10.1039/c0cc02921a

Google Scholar

[11] Véronique Lapeyre, Isabelle Gosse, Sylviane Chevreux, Valérie Ravaine. Monodispersed glucose-responsive microgels operating at physiological salinity. Biomacromolecules 7 (2006) 3356-3363.

DOI: 10.1021/bm060588n

Google Scholar

[12] D. James Tony, K.R.A.S. Sandanayake, Shinkai Seiji. Saccharidnachweis mit Rezeptoren auf Boronsäurebasis. Angewandte Chemie 108 (1996) 2038-(2050).

DOI: 10.1002/ange.19961081706

Google Scholar

[13] R. Ma, L. Shi. Phenylboronic acid-based glucose-responsive polymeric nanoparticles: synthesis and applications in drug delivery. Polymer Chemistry 5 (2014) 1503-1518.

DOI: 10.1039/c3py01202f

Google Scholar

[14] S. Lee, J. H. Nam, Y. J. Kim, Y. J. Cho, N. H. Kwon, J. Y. Lee, et al. Synthesis of PEO-based glucose-sensitive block copolymers and their application for preparation of superparamagnetic iron oxide nanoparticles. Macromolecular Research 19 (2011).

DOI: 10.1007/s13233-011-0810-3

Google Scholar

[15] L. Zhao, C. Xiao, J. Ding, P. He, Z. Tang, X. Pang, et al. Facile one-pot synthesis of glucose-sensitive nanogel via thiol-ene click chemistry for self-regulated drug delivery. Acta biomaterialia 9 (2013) 6535-6543.

DOI: 10.1016/j.actbio.2013.01.040

Google Scholar

[16] Springsteen Greg, Wang Binghe. Alizarin Red S. as a general optical reporter for studying the binding of boronic acids with carbohydrates. Chemical Communications 17 (2001) 1608-1609.

DOI: 10.1039/b104895n

Google Scholar

[17] M. Akira, Y. Kazuya, Y. Ryo, K. Kazunori, A. Takao, Y. Miyahara. A totally synthetic glucose responsive gel operating in physiological aqueous conditions. Chem Commun (Camb) 46 (2010) 2203-2205.

DOI: 10.1039/b920319b

Google Scholar