用于转移性乳腺癌靶向成像的具有金属增强荧光的脂质聚合物混合纳米系统。

Q1 Pharmacology, Toxicology and Pharmaceutics
Nanotheranostics Pub Date : 2024-02-17 eCollection Date: 2024-01-01 DOI:10.7150/ntno.92410
Tejaswini Appidi, Rajalakshmi P Sivasankaran, Shubham A Chinchulkar, Paloma Patra, Kavipriya Murugaiyan, Bantal Veeresh, Aravind Kumar Rengan
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引用次数: 0

摘要

癌症转移是导致癌症治疗失败的主要原因。由于转移,近 70-80% 的 IV 期乳腺癌患者失去了生命。近来,纳米给药系统在转移性癌症的治疗中发挥着至关重要的作用。本文报道了使用新型纳米脂聚系统(PIR-Au NPs)对转移性乳腺癌进行基于增强渗透和保留(EPR)的靶向治疗。PIR-Au NPs 的荧光增加是由于表面涂覆了金,这与我们早先报道的金属增强荧光现象有关。与游离 IR780 或负载 IR780 的纳米系统(P-IR NPs)相比,在相同浓度、相同时间的培养下,PIR-Au NPs 在小鼠乳腺癌细胞系(4T1)中的荧光增强,这表明它具有成像和增强 IR780 生物利用度的应用潜力。光热介导的体外细胞毒性使乳腺癌细胞(MCF-7 和 4T1)显著死亡。用 PIR-Au NPs 培养的斑马鱼胚胎的荧光增强。PIR-Au NPs 在体内具有增强渗透和保留(EPR)效应。小鼠注射 PIR-Au NPs 后记录到强烈的荧光信号。72 小时后收集的肿瘤组织与其他组相比明显显示出更强的荧光,这表明等离子体增强了荧光。我们还通过光热效应证明了基于 EPR 的 PIR-Au NPs 在体内的靶向性。因此,这种脂质聚合物混合纳米系统可以成功地应用于图像引导的被动靶向,以实现最大的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A lipo-polymeric hybrid nanosystem with metal enhanced fluorescence for targeted imaging of metastatic breast cancer.

Cancer metastasis plays a major role in failure of therapeutic avenues against cancer. Owing to metastasis, nearly 70-80% of stage IV breast cancer patients lose their lives. Nanodrug delivery systems are playing a critical role in the therapy of metastatic cancer in the recent times. This paper reports the enhanced permeation and retention (EPR) based targeting of metastatic breast cancer using a novel nano lipo-polymeric system (PIR-Au NPs). The PIR-Au NPs demonstrated an increase in fluorescence by virtue of surface coating with gold, owing to the metal enhanced fluorescence phenomenon as reported in our earlier reports. Enhanced fluorescence of PIR-Au NPs was observed in murine mammary carcinoma cell line (4T1), as compared to free IR780 or IR780 loaded nanosystems (P-IR NPs), when incubated for same time at same concentrations, indicating its potential application for imaging and an enhanced bioavailability of IR780. Significant cell death was noted with photothermal mediated cytotoxicity in-vitro against breast cancer cells (MCF-7 and 4T1). An enhanced fluorescence was observed in the zebra fish embryos incubated with PIR-Au NPs. The enhanced permeation and retention (EPR) effect was seen with PIR-Au NPs in-vivo. A strong fluorescent signal was recorded in mice injected with PIR-Au NPs. The tumor tissue collected after 72 h, clearly showed a greater fluorescence as compared to other groups, indicating the plasmon enhanced fluorescence. We also demonstrated the EPR-based targeting of the PIR-Au NPs in-vivo by means of photothermal heat. This lipo-polymeric hybrid nanosystem could therefore be successfully applied for image-guided, passive-targeting to achieve maximum therapeutic benefits.

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来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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