The Glucose-Responsive Nanogel Based on Phenylboronic Acid

Article Preview

Abstract:

Diabetes mellitus, following cancer and cardiovascular disease, become one of the most serious diseases that threat to human health. The treatment of diabetes is imminent for the health of people. Thus, the developments of efficient insulin administration exhibit great practical significance. The glucose-responsive insulin delivery system (GRIDS) is developing rapidly which is expected to be a promising therapy approach to replace the frequent insulin injection administration. A novel glucose-responsive nanogel was conveniently prepared through one-pot copolymerization of pentaerythritol tetra (3-mercaptopropionate), poly (ethylene glycol) diacrylate, methoxyl poly (ethylene glycol) acrylate and N-acryloyl-3-aminophenylboronic acid. The successful incorporation of phenylboronic acid (PBA) in the nanogel endowed the nanogel high glucose sensitivity in phosphate buffer saline (PBS). Therefore, the PBA incorporated nanogel with high glucose-responsiveness and good biocompatibility may have great potential for self-regulated drug release

You might also be interested in these eBooks

Info:

Periodical:

Pages:

42-45

Citation:

Online since:

October 2014

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2014 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] A.S. Wadajkar, Z., Bhavsar C.Y. Ko, B. Koppolu, W. Cui, L. Tang, et al. Multifunctional particles for melanoma-targeted drug delivery. Acta biomaterialia 8 (2012) 2996-3004.

DOI: 10.1016/j.actbio.2012.04.042

Google Scholar

[2] J. Ding, X. Zhuang, C. Xiao, Y. Cheng, L. Zhao, C. He, et al. Preparation of photo-cross-linked pH-responsive polypeptide nanogels as potential carriers for controlled drug delivery. Journal of Materials Chemistry 21 (2011)11383-11391.

DOI: 10.1039/c1jm10391a

Google Scholar

[3] Y. Yan, D. Wei, J. Li, J. Zheng, G. Shi, W. Luo, et al. A poly(L-lysine)-based hydrophilic star block co-polymer as a protein nanocarrier with facile encapsulation and pH-responsive release. Acta biomaterialia 8 (2012) 2113-2120.

DOI: 10.1016/j.actbio.2012.02.016

Google Scholar

[4] K.C. Hribar, M.H. Lee, D. Lee, J.A. Burdick. Enhanced Release of Small Molecules from Near-Infrared Light Responsive Polymer−Nanorod Composites. ACS Nano 5 (2011) 2948-2956.

DOI: 10.1021/nn103575a

Google Scholar

[5] A. Baeza, E. Guisasola, E. Ruiz-Hernández, M. Vallet-Regí. Magnetically Triggered Multidrug Release by Hybrid Mesoporous Silica Nanoparticles. Chemistry of Materials 24 (2012) 517-524.

DOI: 10.1021/cm203000u

Google Scholar

[6] F. Shi, J. Ding, C. Xiao, X. Zhuang, C. He, L. Chen, et al. Intracellular microenvironment responsive PEGylated polypeptide nanogels with ionizable cores for efficient doxorubicin loading and triggered release. Journal of Materials Chemistry 22 (2012).

DOI: 10.1039/c2jm32033a

Google Scholar

[7] J.X. Ding, C.S. Xiao, C.L. He, M.Q. Li, D. Li, Zhuang XL, et al. Facile preparation of a cationic poly(amino acid) vesicle for potential drug and gene co-delivery. Nanotechnology 22 (2011) 494012-494020.

DOI: 10.1088/0957-4484/22/49/494012

Google Scholar

[8] M. Oishi, Y. Nagasaki. Stimuli-responsive smart nanogels for cancer diagnostics and therapy. Nanomedicine 5 (2010); 451-468.

DOI: 10.2217/nnm.10.18

Google Scholar

[9] Q. Wu, L. Wang, H. Yu, J. Wang, Z. Chen. Organization of Glucose-Responsive Systems and Their Properties. Chemical reviews 111 (2011) 7855-7875.

DOI: 10.1021/cr200027j

Google Scholar

[10] P. Díez, A. Sánchez, M. Gamella, P. Martínez-Ruíz, E. Aznar, C. de la Torre, et al. Toward the Design of Smart Delivery Systems Controlled by Integrated Enzyme-Based Biocomputing Ensembles. Journal of the American Chemical Society 136 (2014).

DOI: 10.1021/ja503578b

Google Scholar

[11] 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) 369-376.

DOI: 10.1016/j.carbpol.2013.12.067

Google Scholar

[12] 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

[13] 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

[14] R. Yin, Z. Tong, D. Yang, J. Nie. Glucose-responsive insulin delivery microhydrogels from methacrylated dextran/concanavalin A: Preparation and in vitro release study. Carbohydrate Polymers 89 (2012) 117-123.

DOI: 10.1016/j.carbpol.2012.02.059

Google Scholar

[15] W. Wu, S. Zhou. Responsive Materials for Self-Regulated Insulin Delivery. Macromolecular Bioscience 13 (2013) 1464-1477.

DOI: 10.1002/mabi.201300120

Google Scholar

[16] M. Samoszuk, D. Ehrlich, E. Ramzi. Preclinical Safety Studies of Glucose-Oxidase. J Pharmacol Exp Ther 266 (1993) 1643-1648.

Google Scholar

[17] 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