Chen Ying, Ding Dan, Mao Zhiqing, He Yafeng, Hu Yong, Wu Wei, Jiang Xiqun
Laboratory of Mesoscopic Chemistry and Department of Polymer Science and Engineering, College of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210093, People's Republic of China.
Biomacromolecules. 2008 Oct;9(10):2609-14. doi: 10.1021/bm800484e. Epub 2008 Aug 30.
To develop a novel type of semi-IPN particles using biocompatible materials, hydroxypropylcellulose-poly(acrylic acid) (HPC-PAA) particles with semi-interpenetrating polymer network structure and a porosity-structural surface were prepared by direct polymerization of acrylic acid monomer in the reaction system comprised of HPC and AA monomer and N,N'-methylenebisacrylamide (MBAAm). The properties of HPC-PAA gel particles were characterized by dynamic light scattering, FT-IR, transmission electron microscopy, and atomic force microscope. It is found that the formation of HPC-PAA gel particles is driven by the hydrogen bonding interaction between proton-donating PAA and proton-accepting HPC. These HPC-PAA gel particles exhibit thermo and pH dual-responsive behaviors. Depending on the chemical composition and the degree of cross-linking, the thermo-responsive property of HPC-PAA gel particles can be shifted from the UCST to the LCST property, and particle sizes can be changed from 100 to 1 microm in a controllable way. Successful loading of the gel particles with oxaliplatin, a hydrophilic antitumor drug, was achieved by take advantage of the complex interaction between the platinum atom of oxaliplatin and the carboxylic group of PAA in the gel particles. In vitro cytotoxicity assay indicates that the oxalipatin-loaded HPC-PAA gel particles have high anticancer activity. Considering the good biosafety, simple and mild preparation strategy and tunable size as well as the stimuli-responsive properties, the HPC-PAA gel particles should be a promising candidate for the drug delivery system.
为了使用生物相容性材料开发一种新型的半互穿聚合物网络(semi-IPN)粒子,通过在由羟丙基纤维素(HPC)、丙烯酸(AA)单体和N,N'-亚甲基双丙烯酰胺(MBAAm)组成的反应体系中直接聚合丙烯酸单体,制备了具有半互穿聚合物网络结构和孔隙结构表面的羟丙基纤维素-聚丙烯酸(HPC-PAA)粒子。通过动态光散射、傅里叶变换红外光谱(FT-IR)、透射电子显微镜和原子力显微镜对HPC-PAA凝胶粒子的性能进行了表征。发现HPC-PAA凝胶粒子的形成是由供质子的PAA和质子接受体HPC之间的氢键相互作用驱动的。这些HPC-PAA凝胶粒子表现出热和pH双重响应行为。根据化学组成和交联程度,HPC-PAA凝胶粒子的热响应性质可以从低临界溶液温度(UCST)转变为高临界溶液温度(LCST)性质,并且粒径可以以可控的方式从100微米变化到1微米。通过利用奥沙利铂的铂原子与凝胶粒子中PAA的羧基之间的络合相互作用,成功地将亲水性抗肿瘤药物奥沙利铂负载到凝胶粒子中。体外细胞毒性试验表明,负载奥沙利铂的HPC-PAA凝胶粒子具有高抗癌活性。考虑到良好的生物安全性、简单温和的制备策略、可调节的尺寸以及刺激响应特性,HPC-PAA凝胶粒子应该是药物递送系统的一个有前途的候选者。