Prostate-Specific Membrane Antigen Targeted Gold Nanoparticles for Theranostics of Prostate Cancer

被引:131
|
作者
Mangadlao, Joey Dacula [1 ]
Wang, Xinning [1 ,2 ]
McCleese, Christopher [3 ]
Escamilla, Maria [3 ]
Ramamurthy, Gopalakrishnan [1 ]
Wang, Ziying [1 ]
Govande, Mukul [1 ]
Basilion, James P. [1 ,2 ]
Burda, Clemens [3 ]
机构
[1] Case Western Reserve Univ, Dept Radiol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Chem, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
prostate cancer; PSMA; gold nanoparticles; photodynamic therapy; theranostics; PHOTODYNAMIC THERAPY; DRUG-DELIVERY; POLY(ETHYLENE GLYCOL); IN-VIVO; SENSITIVITY; STATISTICS; OUTCOMES; AGENTS;
D O I
10.1021/acsnano.8b00940
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Prostate cancer is one of the most common cancers and among the leading causes of cancer deaths in the United States. Men diagnosed with the disease typically undergo radical prostatectomy, which often results in incontinence and impotence. Recurrence of the disease is often experienced by most patients with incomplete prostatectomy during surgery. Hence, the development of a technique that will enable surgeons to achieve a more precise prostatectomy remains an open challenge. In this contribution, we report a theranostic agent (AuNP-SkPEG-PSMA-1-Pc4) based on prostate-specific membrane antigen (PSMA-1)-targeted gold nanoparticles (AuNPs) loaded with a fluorescent photodynamic therapy (PDT) drug, Pc4. The fabricated nanoparticles are well-characterized by spectroscopic and imaging techniques and are found to be stable over a wide range of solvents, buffers, and media. In vitro cellular uptake experiments demonstrated significantly higher nanoparticle uptake in PSMA-positive PC3pip cells than in PSMA-negative PC3flu cells. Further, more complete cell killing was observed in Pc3pip than in PC3flu cells upon exposure to light at different doses, demonstrating active targeting followed by Pc4 delivery. Likewise, in vivo studies showed remission on PSMA-expressing tumors 14 days post-PDT. Atomic absorption spectroscopy revealed that targeted AuNPs accumulate 4-fold higher in PC3pip than in PC3flu tumors. The nanoparticle system described herein is envisioned to provide surgical guidance for prostate tumor resection and therapeutic intervention when surgery is insufficient.
引用
收藏
页码:3714 / 3725
页数:12
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