Chitosan-g-MPEG-modified alginate/chitosan hydrogel microcapsules : a quantitative study of the effect of polymer architecture on the resistance to protein adsorption

The chemical modification of the alginate/chitosan/alginate (ACA) hydrogel microcapsule with methoxy poly(ethylene glycol) (MPEG) was investigated to reduce nonspecific protein adsorption and improve biocompatibility in vivo. The graft copolymer chitosan-g-MPEG (CS-g-MPEG) was synthesized, and then...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 26(2010), 22 vom: 16. Nov., Seite 17156-64
1. Verfasser: Zheng, Jia N (VerfasserIn)
Weitere Verfasser: Xie, Hong G, Yu, Wei T, Liu, Xiu D, Xie, Wei Y, Zhu, Jing, Ma, Xiao J
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Aldehydes Alginates Capsules Hexuronic Acids Hydrogels Immunoglobulin G methoxy poly(ethylene glycol)-grafted chitosan Polyethylene Glycols mehr... 3WJQ0SDW1A Glucuronic Acid 8A5D83Q4RW Chitosan 9012-76-4
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245 1 0 |a Chitosan-g-MPEG-modified alginate/chitosan hydrogel microcapsules  |b a quantitative study of the effect of polymer architecture on the resistance to protein adsorption 
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520 |a The chemical modification of the alginate/chitosan/alginate (ACA) hydrogel microcapsule with methoxy poly(ethylene glycol) (MPEG) was investigated to reduce nonspecific protein adsorption and improve biocompatibility in vivo. The graft copolymer chitosan-g-MPEG (CS-g-MPEG) was synthesized, and then alginate/chitosan/alginate/CS-g-MPEG (ACAC(PEG)) multilayer hydrogel microcapsules were fabricated by the layer-by-layer (LBL) polyelectrolyte self-assembly method. A quantitative study of the modification was carried out by the gel permeation chromatography (GPC) technique, and protein adsorption on the modified microcapsules was also investigated. The results showed that the apparent graft density of the MPEG side chain on the microcapsules decreased with increases in the degree of substitution (DS) and the MPEG chain length. During the binding process, the apparent graft density of CS-g-MPEG showed rapid growth-plateau-rapid growth behavior. CS-g-MPEG was not only bound to the surface but also penetrated a certain depth into the microcapsule membranes. The copolymers that penetrated the microcapsules made a smaller contribution to protein repulsion than did the copolymers on the surfaces of the microcapsules. The protein repulsion ability decreased with the increase in DS from 7 to 29% with the same chain length of MPEG 2K. CS-g-MPEG with MPEG 2K was more effective at protein repulsion than CS-g-MPEG with MPEG 550, having a similar DS below 20%. In this study, the microcapsules modified with CS-g-MPEG2K-DS7% had the lowest IgG adsorption of 3.0 ± 0.6 μg/cm(2), a reduction of 61% compared to that on the chitosan surface 
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650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Alginates  |2 NLM 
650 7 |a Capsules  |2 NLM 
650 7 |a Hexuronic Acids  |2 NLM 
650 7 |a Hydrogels  |2 NLM 
650 7 |a Immunoglobulin G  |2 NLM 
650 7 |a methoxy poly(ethylene glycol)-grafted chitosan  |2 NLM 
650 7 |a Polyethylene Glycols  |2 NLM 
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650 7 |a Glucuronic Acid  |2 NLM 
650 7 |a 8A5D83Q4RW  |2 NLM 
650 7 |a Chitosan  |2 NLM 
650 7 |a 9012-76-4  |2 NLM 
700 1 |a Xie, Hong G  |e verfasserin  |4 aut 
700 1 |a Yu, Wei T  |e verfasserin  |4 aut 
700 1 |a Liu, Xiu D  |e verfasserin  |4 aut 
700 1 |a Xie, Wei Y  |e verfasserin  |4 aut 
700 1 |a Zhu, Jing  |e verfasserin  |4 aut 
700 1 |a Ma, Xiao J  |e verfasserin  |4 aut 
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