Controlling the Particle Size of Interpolymer Complexes through Host-Guest Interaction for Drug Delivery

被引:30
作者
Chen, Yan [1 ]
Pang, Yan [1 ]
Wu, Jieli [4 ]
Su, Yue [1 ]
Liu, Jinyao [1 ]
Wang, Ruibin [4 ]
Zhu, Bangshang [4 ]
Yao, Yefeng [2 ,3 ]
Yan, Deyue [1 ]
Zhu, Xinyuan [1 ,4 ]
Chen, Qun [2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[2] E China Normal Univ, Dept Phys, Shanghai 200062, Peoples R China
[3] E China Normal Univ, Shanghai Key Lab Funct Magnet Resonance Imaging, Shanghai 200062, Peoples R China
[4] Shanghai Jiao Tong Univ, Instrumental Anal Ctr, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
INCLUSION COMPLEXES; POLY(ETHYLENE GLYCOL); POLY(ACRYLIC ACID); ALPHA-CYCLODEXTRIN; POLYROTAXANE; COPOLYMER; MEMBRANES; POLYMERS; PHASE;
D O I
10.1021/la9048133
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new method to adjust the particle size of interpolymer complexes has been developed by introduction of host-guest interaction into the dilute aqueous solution of poly(acrylic acid) (PAA) and poly(ethylene glycol) (PEG). Because of the cooperative hydrogen-bonding interaction, PAA can form the interpolymer complexes with PEG. Putting beta-cyclodextrin (beta-CD) into dilute PAA/PEG aqueous solution, the competition between host-guest and hydrogen-bonding interactions happens. The beta-CD/PAA/PEG ternary systems have been well characterized by ultraviolet-visible absorption spectroscopy (UV-vis), dynamic light scattering (DLS), transmission electron microscopy (TEM), diffusion NMR spectroscopy, attenuated total reflectance-Fourier transform infrared (ATR-FTIR), and solid-state C-13 NM R spectroscopy. The results indicate that the hydrophobic cavity of beta-CD is threaded by linear polymers so that the hydrophilicity of PAA/PEG interpolymer complexes is improved greatly. Adjusting the amounts of beta-CD, the particle size of the interpolymer complexes can be readily controlled. The low cytotoxicity of various beta-CD/PAA/PEG ternary complexes has been confirmed using the MTT assay in COS-7 cell line. Doxorubicin (DOX), an anticancer drug, has been encapsulated into the beta-CD/PAA/PEG ternary complexes. The DOX-loaded beta-CD/PAA/PEG ternary complexes have been analyzed by confocal laser scanning microscopy (CLSM), flow cytometry analysis, and the MTT assay against human cervical carcinoma cell (Hela). The results indicate that beta-CD/PAA/PEG ternary complexes with controlled particle size could be used as safe and promising drug carriers.
引用
收藏
页码:9011 / 9016
页数:6
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