PEGylated Anti-MUC1 Aptamer-Doxorubicin Complex for Targeted Drug Delivery to MCF7 Breast Cancer Cells

被引:70
|
作者
Tan, Lihan [1 ]
Neoh, Koon Gee [1 ]
Kang, En-Tang [1 ]
Choe, Woo Seok [2 ]
Su, Xiaodi [3 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 119260, Singapore
[2] Sungkyunkwan Univ, Sch Chem Engn, Suwon 440746, South Korea
[3] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
基金
英国医学研究理事会;
关键词
aptamers; biological applications of polymers; breast cancer; doxorubicin; drug delivery systems; MAGNETIC NANOPARTICLES; TUMOR-MARKER; RECEPTOR; BINDING; MUC1;
D O I
10.1002/mabi.201100173
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
Targeted drug delivery is especially important in cancer treatment as many anti-cancer drugs are non-specific and highly toxic to both cancer and normal cells. The targeted drug delivery of DOX to the MUC1-expressing breast cancer cell line (MCF7) was obtained using APT as a carrier. Modification of the APT-DOX complex by PEG increases the survivability of the macrophage control (RAW 264.7) by about six-fold as compared to free DOX treatment without significantly affecting the cytotoxicity toward the target cell line. Thus, PEG-APT-DOX is potentially a new therapeutic agent for targeted drug delivery to MUC1-expressing cell lines.
引用
收藏
页码:1331 / 1335
页数:5
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