Tumor-Targeting Co-Delivery of Drug and Gene from Temperature-Triggered Micelles

被引:14
|
作者
Seo, Seog-Jin [1 ,2 ,3 ]
Lee, Seon-Young [1 ,2 ,3 ]
Choi, Seong-Jun [1 ,2 ,3 ]
Kim, Hae-Won [1 ,2 ,3 ,4 ]
机构
[1] Dankook Univ, Inst Tissue Regenerat Engn ITREN, Cheonan 330714, South Korea
[2] Dankook Univ, Dept Nanobiomed Sci, Cheonan 330714, South Korea
[3] Dankook Univ, PLUS Nbm Global Res Ctr Regenerat Med BK21, Cheonan 330714, South Korea
[4] Dankook Univ, Sch Dent, Dept Biomat Sci, Cheonan 330714, South Korea
基金
新加坡国家研究基金会;
关键词
folic acid; pluronic F127; polyethylenimine; temperature trigger; tumor-targeting nanocarrier; PLURONIC COPOLYMER; POLYMERIC MICELLES; RELEASE; DOXORUBICIN; CANCER; RESISTANCE; NANOGELS; THERAPY; SYSTEMS;
D O I
10.1002/mabi.201500137
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Co-delivery strategy using multifunctional nanocarriers is an attractive option for the synergistic and enhanced effects in cancer treatment, but one system integrating multiple functions for controlled release at the target is still challenging. Herein, this study shows the synthesis and characterization of our stimulus-responsive co-delivery system for the controlled release into tumors, which is composed of polyethylenimine (PEI)-linked Pluronic F127 (PF127) and folic acid (FA), called PF127-PEI-FA. PF127-PEI-FA system facilitated drug loading and gene complex formation, and showed controlled release behaviors in response to hitting temperature to hyperthermia. PF127-PEI-FA system was demonstrated to be biocompatible and showed receptor-mediated gene delivery. The results of our multifunctional nanocarrier system that enabled co-delivery suggest a promising potential for controlled drug release at targeted areas. However, further in-depth studies on the use of therapeutic drugs and genes in multiple cell types and the animal response are required.
引用
收藏
页码:1198 / 1204
页数:7
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