Facial Layer-by-Layer Engineering of Upconversion Nanoparticles for Gene Delivery: Near-Infrared-Initiated Fluorescence Resonance Energy Transfer Tracking and Overcoming Drug Resistance in Ovarian Cancer

被引:64
作者
Lin, Min [1 ,3 ,4 ]
Gao, Yan [1 ]
Diefenbach, Thomas J. [5 ]
Shen, Jacson K. [1 ]
Hornicek, Francis J. [1 ]
Park, Yong Il [2 ,6 ]
Xu, Feng [3 ,4 ]
Lu, Tian Jian [3 ,4 ]
Amiji, Mansoor [7 ]
Duan, Zhenfeng [1 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Sarcoma & Connect Tissue Oncol, Boston, MA 02114 USA
[2] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[3] Xi An Jiao Tong Univ, Key Lab Biomed Informat Engn, Minist Educ, Sch Life Sci & Technol, Xian 710049, Peoples R China
[4] Xi An Jiao Tong Univ, BEBC, Xian 710049, Peoples R China
[5] Ragon Inst MGH Massachusetts Inst Technol MIT & H, Cambridge, MA 02139 USA
[6] Chonnam Natl Univ, Sch Chem Engn, Gwangju 61186, South Korea
[7] Northeastern Univ, Dept Pharmaceut Sci, Sch Pharm, Boston, MA 02115 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
upconversion nanoparticles; gene delivery; FRET; gene knockdown; drug sensitivity; PACLITAXEL RESISTANCE; SIRNA; FRET; RNA; NANOPHOSPHORS; CISPLATIN; REVERSAL; CHITOSAN; SYSTEMS; PROBES;
D O I
10.1021/acsami.6b15321
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Development of multidrug resistance (MDR) contributes to the majority of treatment failures in clinical chemotherapy. We report facial layer-by-layer engineered upconversion nanoparticles (UCNPs) for near-infrared (NIR)-initiated tracking and delivery of small interfering RNA (siRNA) to enhance chemotherapy efficacy by silencing the MDR1 gene and resensitizing resistant ovarian cancer cells to drug. Layer-by-layer engineered UCNPs were loaded with MDR1 gene-silencing siRNA (MDR1-siRNA) by electrostatic interaction. The delivery vehicle enhances MDR1-siRNA cellular uptake, protects MDR1-siRNA from nuclease degradation, and promotes endosomal escape for silencing the MDR gene. The intrinsic photon upconversion of UCNPs provides an unprecedented opportunity for monitoring intracellular attachment and release of MDR1-siRNA by NIR-initiated fluorescence resonance energy transfer occurs between donor UCNPs and acceptor fluorescence dye-labeled MDR1-siRNA. Enhanced chemotherapeutic efficacy in vitro was demonstrated by cell viability assay. The developed delivery vehicle holds great potential in delivery and imaging-guided tracking of therapeutic gene targets for effective treatment of drug-resistant cancers.
引用
收藏
页码:7941 / 7949
页数:9
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