Synthesis, Characteristics and Potential Application of Poly(β-Amino Ester Urethane)-Based Multiblock Co-Polymers as an Injectable, Biodegradable and pH/Temperature-Sensitive Hydrogel System

被引:26
作者
Cong Truc Huynh [1 ]
Minh Khanh Nguyen [1 ]
Jeong, In Ki [1 ]
Kim, Sung Wan [2 ,3 ]
Lee, Doo Sung [1 ]
机构
[1] Sungkyunkwan Univ, Dept Polymer Sci & Engn, Theranost Macromol Res Ctr, Suwon 440746, Gyeonggi Do, South Korea
[2] Univ Utah, Ctr Controlled Chem Delivery, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
[3] Hanyang Univ, Coll Engn, Dept Bioengn, Seoul 133791, South Korea
基金
新加坡国家研究基金会;
关键词
pH sensitivity; temperature sensitivity; hydrogel; poly(beta-amino ester urethane); biodegradability; doxorubicin; controlled release; DRUG-DELIVERY; BLOCK-COPOLYMERS; TRIBLOCK COPOLYMER; THERMOSENSITIVE HYDROGEL; POLY(ETHYLENE GLYCOL); SUSTAINED-RELEASE; PH; DESIGN; BIOCOMPATIBILITY; DEGRADATION;
D O I
10.1163/092050611X575423
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Physical polymeric hydrogels have significant potential for use as injectable depot drug/protein-delivery systems. In this study, a series of novel injectable, biodegradable and pH/temperature-sensitive multiblock co-polymer physical hydrogels composed of poly(ethylene glycol) (PEG) and poly(beta-amino ester urethane) (PEU) was synthesized by the polyaddition between the isocyanate groups of 1,6-diisocyanato hexamethylene and the hydroxyl groups of PEG and a synthesized monomer BTB (or ETE) in chloroform in the presence of dibutyltin dilaurate as a catalyst. The synthesized co-polymers were characterized by nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy and gel-permeation chromatography. Aqueous solutions of the co-polymers showed a sol-to-gel phase transition with increasing pH and a gel-to-sol phase transition with increasing temperature. The gel regions covered the physiological conditions (37 degrees C, pH 7.4) and could be controlled by changing the molecular weight of PEG, PEG/PEU ratio and co-polymer solution concentration. A gel formed rapidly in situ after injecting the co-polymer solution subcutaneously into SD rats and remained for more than 2 weeks in the body. The cytotoxicity tests confirmed the non-cytotoxicity of this co-polymer hydrogel. The controlled in vitro release of the model anticancer drug, doxorubicin, from this hydrogel occurred over a 7-day period. This hydrogel is a potential candidate for biomedical applications and drug/protein-delivery systems. (C) Koninklijke Brill NV, Leiden, 2012
引用
收藏
页码:1091 / 1106
页数:16
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