Synthesis of pH-responsive crosslinked poly[styrene-co-(maleic sodium anhydride)] and cellulose composite hydrogel nanofibers by electrospinning

被引:34
作者
Cao, Shengguang [1 ]
Hu, Binghuan [1 ,2 ]
Liu, Haiqing [1 ,2 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fuzhou 350007, Peoples R China
[2] Fujian Key Lab Polymer Mat, Fuzhou 350007, Peoples R China
基金
中国国家自然科学基金;
关键词
electrospinning; nanofiber; hydrogel; cellulose; biomedical applications; SWELLING BEHAVIOR; DIAMETER FIBERS; MEMBRANES; ACETATE; POLYMER; ACID);
D O I
10.1002/pi.2565
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
BACKGROUND: Stimuli-sensitive materials show enormous potential in the development of drug delivery systems. But the low response rate of most stimuli-sensitive materials limits their wider application. We propose that electrospinning, a technique for the preparation of ultrafine fibrous materials with ultrafine diameters, maybe used to prepare materials with a fast response to stimuli. RESULTS: Poly[styrene-co-(maleic sodium anhydride)] and cellulose (SMA-Na/cellulose) hydrogel nanofibers were prepared through hydrolysis of precursor electrospun poly[styrene-co-(maleic anhydride)]/cellulose acetate (SMA/CA) nanofibers. In the presence of diethylene glycol, the SMA/CA composite nanofibers were crosslinked by esterification at 145 degrees C, and then hydrolyzed to yield crosslinked SMA-Na/cellulose hydrogel nanofibers. These nanofibers showed better mechanical strengths and were pH responsive. Their water swelling ratio showed a characteristic two-step increase at pH = 5.0 and 8.2, with the water swelling ratio reaching a maximum of 27.6 g g(-1) at pH = 9.1. CONCLUSION: The crosslinked SMA-Na hydrogel nanofibers supported on cellulose showed improved dimensional stability upon immersion in aqueous solutions. They were pH responsive. This new type of hydrogel nanofiber is a potential material for biomedical applications. (C) 2009 Society of Chemical Industry
引用
收藏
页码:545 / 551
页数:7
相关论文
共 25 条
[1]   Preparation of fibers with nanoscaled morphologies: Electrospinning of polymer blends [J].
Bognitzki, M ;
Frese, T ;
Steinhart, M ;
Greiner, A ;
Wendorff, JH ;
Schaper, A ;
Hellwig, M .
POLYMER ENGINEERING AND SCIENCE, 2001, 41 (06) :982-989
[2]   Ultrafine hydrogel fibers with dual temperature- and pH-responsive swelling behaviors [J].
Chen, H ;
Hsieh, YL .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2004, 42 (24) :6331-6339
[3]   Beaded nanofibers formed during electrospinning [J].
Fong, H ;
Chun, I ;
Reneker, DH .
POLYMER, 1999, 40 (16) :4585-4592
[4]  
GEHRKE SH, 1993, ADV POLYM SCI, V110, P81
[5]   Electrospinning: A fascinating method for the preparation of ultrathin fibres [J].
Greiner, Andreas ;
Wendorff, Joachim H. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (30) :5670-5703
[6]  
GROSS JR, 1976, Patent No. 3954721
[7]   Electrospinning functional nanoscale fibers: a perspective for the future [J].
Hunley, Matthew T. ;
Long, Timothy E. .
POLYMER INTERNATIONAL, 2008, 57 (03) :385-389
[8]   pH-responsive swelling behavior of poly(vinyl alcohol)/poly(acrylic acid) bi-component fibrous hydrogel membranes [J].
Jin, X ;
Hsieh, YL .
POLYMER, 2005, 46 (14) :5149-5160
[9]   Reactive electrospinning of cross-linked poly(2-hydroxyethyl methacrylate) nanofibers and elastic properties of individual hydrogel nanofibers in aqueous solutions [J].
Kim, SH ;
Nair, S ;
Moore, E .
MACROMOLECULES, 2005, 38 (09) :3719-3723
[10]   DISSOCIATION BEHAVIOR OF POLY(FUMARIC ACID) AND POLY(MALEIC ACID) .1. POTENTIOMETRIC TITRATION AND INTRINSIC-VISCOSITY [J].
KITANO, T ;
KAWAGUCHI, S ;
ITO, K ;
MINAKATA, A .
MACROMOLECULES, 1987, 20 (07) :1598-1606