Synthesis, characterization and properties of chitosan modified with poly(ethylene glycol)-polydimethylsiloxane amphiphilic block copolymers

被引:61
作者
Rutnakornpituk, M [1 ]
Ngamdee, P
Phinyocheep, P
机构
[1] Naresuan Univ, Fac Sci, Dept Chem, Phitsanulok 65000, Thailand
[2] Mahidol Univ, Fac Sci, Dept Chem, Bangkok 10400, Thailand
关键词
chitosan; polydimethylsiloxane; poly(ethylene glycol);
D O I
10.1016/j.polymer.2005.08.051
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Synthesis of poly(ethylene glycol)-polydimethylsiloxane amphiphilic block copolymers is discussed herein. Siloxane prepolymer was first prepared via acid-catalyzed ring-opening polymerization of octamethylcyclotetrasiloxane (D-4) to form polydimethylsiloxane (PDMS) prepolymers. It was subsequently functionalized with hydroxy functional groups at both terminals. The hydroxy-terminated PDMS can readily react with acid-terminated poly(ethylene glycol) (PEG diacid) to give PEG-PDMS block copolymers without using any solvent. The PEG diacid was prepared from hydroxy-terminated PEG through the ring-opening reaction of succinic anhydride. Their chemical structures and molecular weights were characterized using H-1 NMR, FTIR and GPC, and thermal properties were determined by DSC. The PEG-PDMS copolymer was incorporated into chitosan in order that PDMS provided surface modification and PEG provided good water swelling properties to chitosan. Critical surface energy and swelling behavior of the modified chitosan as a function of the copolymer compositions and contents were investigated. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9742 / 9752
页数:11
相关论文
共 32 条
[1]   Polymeric percutaneous drug penetration enhancer - Synthesis and enhancing property of PEG/PDMS block copolymer with a cationic end group [J].
Akimoto, T ;
Aoyagi, T ;
Minoshima, J ;
Nagase, Y .
JOURNAL OF CONTROLLED RELEASE, 1997, 49 (2-3) :229-241
[2]   A new route for organic-inorganic hybrid material synthesis through reactive processing without solvent [J].
Bounor-Legaré, V ;
Angelloz, C ;
Blanc, P ;
Cassagnau, P ;
Michel, A .
POLYMER, 2004, 45 (05) :1485-1493
[3]   Synthesis of novel poly(ethylene glycol) based amphiphilic polymers [J].
Danprasert, K ;
Kumar, R ;
H-Cheng, M ;
Gupta, P ;
Shakil, NA ;
Prasad, AK ;
Parmar, VS ;
Kumar, J ;
Samuelson, LA ;
Watterson, AC .
EUROPEAN POLYMER JOURNAL, 2003, 39 (10) :1983-1990
[4]   pH dependent hydrolysis and drug release behavior of chitosan/poly(ethylene glycol) polymer network microspheres [J].
Gupta, KC ;
Kumar, MNV .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2001, 12 (09) :753-759
[5]   BLOOD-CONTACTING PROPERTIES OF POLYDIMETHYLSILOXANE POLYUREA-URETHANES [J].
HERGENROTHER, RW ;
YU, XH ;
COOPER, SL .
BIOMATERIALS, 1994, 15 (08) :635-640
[6]   Synthesis and characterization of chitosan-poly(acrylic acid) nanoparticles [J].
Hu, Y ;
Jiang, XQ ;
Ding, Y ;
Ge, HX ;
Yuan, YY ;
Yang, CZ .
BIOMATERIALS, 2002, 23 (15) :3193-3201
[7]  
Jasper J.J., 1972, J PHYS CHEM REF DATA, V1, P841, DOI [10.1063/1.3253106, DOI 10.1063/1.3253106]
[8]  
Khan TA, 2000, J PHARM PHARM SCI, V3, P303
[9]   Implantable applications of chitin and chitosan [J].
Khor, E ;
Lim, LY .
BIOMATERIALS, 2003, 24 (13) :2339-2349
[10]   Spontaneous vesicle formation of short-chain amphiphilic polysiloxane-b-poly(ethylene oxide) block copolymers [J].
Kickelbick, G ;
Bauer, J ;
Hüsing, N ;
Andersson, M ;
Palmqvist, A .
LANGMUIR, 2003, 19 (08) :3198-3201