Image-Guided Prostate Cancer Therapy Using Aptamer-Functionalized Thermally Cross-Linked Superparamagnetic Iron Oxide Nanoparticles

被引:175
作者
Yu, Mi Kyung [1 ]
Kim, Dongkyu [2 ]
Lee, In-Hyun [1 ]
So, Jee-Soo [1 ]
Jeong, Yong Yeon [3 ]
Jon, Sangyong [1 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Life Sci, Res Ctr Biomol Nanotechnol, Cell Dynam Res Ctr, Kwangju 500712, South Korea
[2] Korea Basic Sci Insititute, Div Magnet Resonance, Chungbuk 363883, South Korea
[3] Jeonnam Natl Univ Hwasun Hosp, Dept Diagnost Radiol, Jeonnam 519809, South Korea
关键词
DRUG-DELIVERY; MAGNETIC NANOPARTICLES; MEMBRANE ANTIGEN; STATISTICS; DIAGNOSIS;
D O I
10.1002/smll.201100472
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CG-rich duplex containing prostate-specific membrane antigen (PSMA) aptamer-conjugated thermally cross-linked superparamagnetic iron oxide nanoparticles (TCL-SPIONs) is reported as prostate cancer-specific nanotheranostic agents. These agents are capable of prostate tumor detection in vivo by magnetic resonance imaging (MRI) and selective delivery of drugs to the tumor tissue, simultaneously. The prepared PSMA-functionalized TCL-SPION via a hybridization method (Apt-hybr-TCLSPION) exhibited preferential binding towards target prostate-cancer cells (LNCaP, PSMA+) in both in vitro and in vivo when analyzed by T-2-weighted MRI. After Dox molecules were loaded onto the Apt-hybr-TCL-SPION through the intercalation of Dox to the CG-rich duplex containing PSMA aptamer as well as electrostatic interaction between the Dox-and-polymer coating layer of the nanoparticles, the resulting Dox@Apt-hybr-TCL-SPION showed selective drug-delivery efficacy in the LNCaP xenograft mouse model. These results suggest that Dox@Apt-hybr-TCLSPION has potential for use as novel prostate cancer-specific nanotheranostics.
引用
收藏
页码:2241 / 2249
页数:9
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