A temperature-responsive copolymer hydrogel in controlled drug delivery

被引:170
作者
Dai, Hongjun
Chen, Qiang
Qin, Huaili
Guan, Ying
Shen, Deyan
Hua, Youqing
Tang, Yalin [1 ]
Xu, Jian
机构
[1] Chinese Acad Sci, Inst Chem, State Key Lab Polymer Phys & Chem, Beijing 100080, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100080, Peoples R China
[3] Beijing Univ Chem Technol, Sch Mat Sci & Engn, Beijing 100029, Peoples R China
关键词
D O I
10.1021/ma060486p
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A novel optical transition for a hydrogel of polyacrylamide and poly( acrylic acid) random copolymer was observed. The poly( acrylamide- co- acrylic acid) hydrogel is opaque white at low temperature, while it will become transparent gradually or sharply on a fast or slow increase of temperature. Meanwhile, the hydrogel can swell or collapse with changing temperature. Both optical transition and volume swelling are reversible responding to temperature stimuli. The FT- IR, laser Raman, and 1H NMR spectroscopy demonstrated the driving force of optical and volume transition: formation and dissociation of hydrogen bonds in the hydrogel. The heterogeneity of the network results in these reversible transition responding to temperature stimuli. The effects of monomer, initiator, and cross- linker on the optical transition of the hydrogel were studied in detail. The formation and dissociation of hydrogen bonds in the limited domain of the hydrogel is related to the network structure. Because of the property of swelling or collapse, the P( AAm- co- AAc) hydrogel has potential value of application in drug controlled release.
引用
收藏
页码:6584 / 6589
页数:6
相关论文
共 43 条
[1]   SELECTIVE COMPLEXATION OF MACROMOLECULES [J].
ABE, K ;
KOIDE, M ;
TSUCHIDA, E .
MACROMOLECULES, 1977, 10 (06) :1259-1264
[2]  
Afrassiabi A, 1986, J CONTROL RELEASE, V4, P213
[3]   A SIMPLE MULTI-NUCLEAR NMR THERMOMETER [J].
AMMANN, C ;
MEIER, P ;
MERBACH, AE .
JOURNAL OF MAGNETIC RESONANCE, 1982, 46 (02) :319-321
[4]   TEMPERATURE-RESPONSIVE INTERPENETRATING POLYMER NETWORKS CONSTRUCTED WITH POLY(ACRYLIC ACID) AND POLY(N,N-DIMETHYLACRYLAMIDE) [J].
AOKI, T ;
KAWASHIMA, M ;
KATONO, H ;
SANUI, K ;
OGATA, N ;
OKANO, T ;
SAKURAI, Y .
MACROMOLECULES, 1994, 27 (04) :947-952
[5]   EFFECT OF VARYING CROSSLINKING DENSITY ON POLYACRYLAMIDE GELS [J].
BANSIL, R ;
GUPTA, MK .
FERROELECTRICS, 1980, 30 (1-4) :63-71
[6]   QUANTITATIVE STUDIES OF INTERACTION BETWEEN COMPLEMENTARY POLYMERS AND OLIGOMERS IN SOLUTIONS [J].
BARANOVSKY, VY ;
LITMANOVICH, AA ;
PAPISOV, IM ;
KABANOV, VA .
EUROPEAN POLYMER JOURNAL, 1981, 17 (09) :969-979
[7]  
BEKTUROV EA, 1981, ADV POLYM SCI, V41, P99
[8]   A comparison of the swelling behaviour of copolymer and interpenetrating network microgel particles [J].
Bouillot, P ;
Vincent, B .
COLLOID AND POLYMER SCIENCE, 2000, 278 (01) :74-79
[9]   Temperature-responsive gels and thermogelling polymer matrices for protein and peptide delivery [J].
Bromberg, LE ;
Ron, ES .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 31 (03) :197-221
[10]   Effect of drug physicochemical properties on swelling/deswelling kinetics and pulsatile drug release from thermoresponsive poly(N-isopropylacrylamide) hydrogels [J].
Coughlan, DC ;
Quilty, FP ;
Corrigan, OI .
JOURNAL OF CONTROLLED RELEASE, 2004, 98 (01) :97-114