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用于前列腺癌治疗诊断的前列腺特异性膜抗原靶向金纳米颗粒。

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

出版信息

ACS Nano. 2018 Apr 24;12(4):3714-3725. doi: 10.1021/acsnano.8b00940. Epub 2018 Apr 16.

Abstract

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-5kPEG-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.

摘要

前列腺癌是美国最常见的癌症之一,也是癌症死亡的主要原因之一。被诊断患有这种疾病的男性通常会接受根治性前列腺切除术,这通常会导致尿失禁和阳痿。大多数接受不完全前列腺切除术的患者在手术中都会复发这种疾病。因此,开发一种能够使外科医生实现更精确前列腺切除术的技术仍然是一个悬而未决的挑战。在本研究中,我们报告了一种基于前列腺特异性膜抗原(PSMA-1)靶向金纳米颗粒(AuNPs)的治疗药物(AuNP-5kPEG-PSMA-1-Pc4),该纳米颗粒负载了荧光光动力治疗(PDT)药物 Pc4。通过光谱和成像技术对制备的纳米颗粒进行了很好的表征,发现它们在广泛的溶剂、缓冲液和介质中都很稳定。体外细胞摄取实验表明,在 PSMA 阳性的 PC3pip 细胞中,纳米颗粒的摄取明显高于 PSMA 阴性的 PC3flu 细胞。此外,在不同剂量的光照射下,Pc3pip 细胞的细胞杀伤更为完全,表明在主动靶向后递送至 Pc4。同样,在体内研究中,在 PDT 后 14 天,PSMA 表达的肿瘤出现消退。原子吸收光谱显示,靶向 AuNPs 在 PC3pip 肿瘤中的积累量比在 PC3flu 肿瘤中高 4 倍。预计本文所述的纳米颗粒系统将为前列腺肿瘤切除术提供手术指导,并在手术不足时提供治疗干预。

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