Synthesis and characterization of partially biodegradable and thermosensitive hydrogel

被引:31
作者
Zhang, XZ
Sun, GM
Wu, DQ
Chu, CC [1 ]
机构
[1] Cornell Univ, Dept Text & Apparel, Ithaca, NY 14853 USA
[2] Cornell Univ, Biomed Engn Program, Ithaca, NY 14853 USA
关键词
D O I
10.1023/B:JMSM.0000036274.83104.fe
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A partially biodegradable and thermosensitive hybrid hydrogel network (DAN series) based on dextran-allylisocyanate (Dex-Al) and poly(N-isopropylacrylamide) (PNIPAAm) was synthesized via UV photocrosslinking. These hybrid hydrogels were characterized in terms of their chemical structure, thermal, mechanical, morphological and temperature-induced swelling properties. The effect of the composition ratio of Dex-Al to PNIPAAm on such properties were examined. The differential scanning calorimetry data show that this Dex-Al/ PNIPAAm hybrid network has an increased lower critical solution temperature (LCST) and glass transition temperature (T-g) with an increase in the Dex-Al content. The interior morphology of these hybrid hydrogels revealed a decreased porous microstructure with an increase in the Dex-Al content in the hybrid network. Furthermore, if the Dex-Al composition became too high, a distinctive network structure with two different microporous structures appeared. The mechanical properties of these hybrid hydrogels also increased with an increase in the Dex-Al content. The temperature dependence of the swelling ratio, the deswelling kinetics as well as the reswelling kinetics was also characterized by gravimetric method. When comparing with a normal PNIPAAm hydrogel, these Dex-Al/PNIPAAm hybrid networks, due to the presence of Dex-Al moiety, also show improved temperature-induced intelligent properties, such as the faster and controllable response dynamics, which may find promising applications in a wide variety of fields, such as biomedical and bioengineering fields. (C) 2004 Kluwer Academic Publishers.
引用
收藏
页码:865 / 875
页数:11
相关论文
共 48 条
[11]   PHASE-TRANSITION OF N-SUBSTITUTED ACRYLAMIDE GELS [J].
INOMATA, H ;
GOTO, S ;
SAITO, S .
MACROMOLECULES, 1990, 23 (22) :4887-4888
[12]   Thermosensitive sol-gel reversible hydrogels [J].
Jeong, B ;
Kim, SW ;
Bae, YH .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (01) :37-51
[13]   Drug release from biodegradable injectable thermosensitive hydrogel of PEG-PLGA-PEG triblock copolymers [J].
Jeong, B ;
Bae, YH ;
Kim, SW .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (1-2) :155-163
[14]   Biodegradable block copolymers as injectable drug-delivery systems [J].
Jeong, B ;
Bae, YH ;
Lee, DS ;
Kim, SW .
NATURE, 1997, 388 (6645) :860-862
[15]   INFLUENCE OF FREELY MOBILE GRAFTED CHAIN-LENGTH ON DYNAMIC PROPERTIES OF COMB-TYPE GRAFTED POLY(N-ISOPROPYLACRYLAMIDE) HYDROGELS [J].
KANEKO, Y ;
SAKAI, K ;
KIKUCHI, A ;
YOSHIDA, R ;
SAKURAI, Y ;
OKANO, T .
MACROMOLECULES, 1995, 28 (23) :7717-7723
[16]   In vitro release behavior of dextran-methacrylate hydrogels using doxorubicin and other model compounds [J].
Kim, SH ;
Chu, CC .
JOURNAL OF BIOMATERIALS APPLICATIONS, 2000, 15 (01) :23-46
[17]   Polymer chemistry - Swell gels [J].
Kopecek, J .
NATURE, 2002, 417 (6887) :388-+
[18]   Modulatory factors on temperature-synchronized degradation of dextran grafted with thermoresponsive polymers and their hydrogels [J].
Kumashiro, Y ;
Huh, KM ;
Ooya, T ;
Yui, N .
BIOMACROMOLECULES, 2001, 2 (03) :874-879
[19]   Novel systems for controlled delivery of macromolecules [J].
Kuo, PYP ;
Saltzman, WM .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 1996, 6 (01) :59-73
[20]   KINETICS OF DISCONTINUOUS VOLUME PHASE-TRANSITION OF GELS [J].
MATSUO, ES ;
TANAKA, T .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (03) :1695-1703