Chitosan-g-PAA hydrogels for colon-specific drug delivery: Preparation, swelling behavior and in vitro degradability

Shiqiong Gong , Houwei Tu , Hua Zheng , Haixing Xu , Yihua Yin

Journal of Wuhan University of Technology Materials Science Edition ›› 2010, Vol. 25 ›› Issue (2) : 248 -251.

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Journal of Wuhan University of Technology Materials Science Edition ›› 2010, Vol. 25 ›› Issue (2) : 248 -251. DOI: 10.1007/s11595-010-2248-4
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Chitosan-g-PAA hydrogels for colon-specific drug delivery: Preparation, swelling behavior and in vitro degradability

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Abstract

A series of cross-linked hydrogels for colon-specific drug delivery were synthesized by graft copolymerization of Chitosan and acrylic acid using N, N′-methylene-bis-(acrylamide) as a cross-linker. Their swelling behavior in different pH buffer solutions and colonic enzymatic degradability were studied. The obtained results show that these hydrogels have good pH sensitivity which can avoid drug release in stomach, and their swelling kinetics in stimulant intestinal environment follow second-order swelling kinetics equation. The factors influencing the swelling kinetics include the degree of cross-linking and the composition, which may control no release or a little amount release of drug inside the hydrogels in the small intestine by tailoring these factors. The gels are degradable by colonic enzymes and there is a correlativity between the degradation of networks and the swelling degree of the gels, which may trigger the release of drug in the colon. The hydrogels show a great potential for their application in oral colon-specific drug delivery system.

Keywords

hydrogel / pH sensitivity / swelling behavior / colonic enzymatic degradability / colon-specific drug delivery

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Shiqiong Gong, Houwei Tu, Hua Zheng, Haixing Xu, Yihua Yin. Chitosan-g-PAA hydrogels for colon-specific drug delivery: Preparation, swelling behavior and in vitro degradability. Journal of Wuhan University of Technology Materials Science Edition, 2010, 25(2): 248-251 DOI:10.1007/s11595-010-2248-4

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References

[1]

Rubinstein A. Colonic Drug Delivery[J]. Drug Discovery Today: Technologies, 2005, 2(1): 33-37.

[2]

Mastiholimath V. S., Dandagi P. M., Samata Jain S., Gadad A. P., Kulkarni A. R. Time and pH Dependent Colon Specific, Pulsatile Delivery of Theophylline for Nocturnal Asthma[J]. International Journal of Pharmaceutics, 2007, 328: 49-56.

[3]

Yin Y.H., Yang Y.J., Xu H.B. Hydrogels for Colon-specific Drug Delivery: Swelling Kinetics and Mechanism of Degradation in vitro[J]. J. Polym. Sci. Part B: Polymer, Physics, 2001, 39: 3128-3137.

[4]

Emma L., McConnell a., Michael D., Basit S. A. W. An in vivo Comparison of Intestinal pH and Bacteria as Physiological Trigger Mechanisms for Colonic Targeting in Man[J]. Journal of Controlled Release, 2008, 130: 154-160.

[5]

Zhang H., Alsarra I.A., Neau S.H. An in vitro Evaluation of a Chitosan-containing Multiparticulate System for Macro-Molecule Delivery to the Colon[J]. International Journal of Pharmaceutics, 2002, 239: 197-205.

[6]

Friend D. Colonic-specific Drug Delivery[J]. Adv. Drug Deliv. Rev., 1991, 7(1): 149-201.

[7]

Schott H.J. Swelling Kinetics of Polymers[J]. Macromol Sci. Phys., 1992, B31: 1-9.

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