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基于 PSMA-11 肽的特定氧化铁纳米颗粒的前列腺癌分子磁共振成像:一项临床前研究。

Molecular MR Imaging of Prostate Cancer by Specified Iron Oxide Nanoparticles With PSMA-11 Peptides: A Preclinical Study.

机构信息

Department of Medical Physics and Radiology, Faculty of Medicine, Gonabad University of Medical Sciences, Gonabad, Iran.

Department of Radiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

J Magn Reson Imaging. 2024 Jun;59(6):2204-2214. doi: 10.1002/jmri.28949. Epub 2023 Aug 12.

Abstract

BACKGROUND

Prostate-specific membrane antigen (PSMA) can provide a prostate cancer (PCa) detection approach in positron emission tomography (PET) using Food and Drug Administration (FDA)-approved PSMA-11 peptide. There are some studies evaluated magnetic-nanoprobes for PSMA detection by MRI, using non-FDA-approved ligands including antibodies or peptides, which are not as specific as PSMA-11.

PURPOSE

To assess targeted iron oxide nanoparticles (IONPs) by PSMA-11 peptides as a potential specific nano-molecular probes to investigate a PSMA PCa-xenograft model by MRI.

STUDY TYPE

Prospective.

ANIMAL MODEL

Twenty male C57BL6 nude mice induced subcutaneously PSMA LNCaP cell line tumor.

FIELD STRENGTH/SEQUENCE: 1.5 T, T-W Fast Spin echo and T*-W Gradient echo.

ASSESSMENT

Coated IONPs with Carboxymethylated-dextran (DNPs) and with bovine serum albumin (BNPs), as well as, targeted DNPs with PSMA-11-HYNIC peptide (TDNPs) and targeted BNPs with PSMA-11-HBED peptide (TBNPs) were injected intravenously with dose 2.8 mg Fe/kg. Coronal T-W and the T*-W images were obtained before and 4 hours and 6 hours post-injection. Signal intensity (SI) and relative signal enhancement (RSE) were computed in two- and three-dimensional analyses. Histological analysis of tumors was evaluated, and the Fe distribution within the body based on atomic absorption spectroscopy was calculated.

STATISTICAL TESTS

One-way ANOVA followed by Tukey's multiple comparison test, Paired-samples T-test, P < 0.05 was considered significant.

RESULTS

A reduction in T-W SI was achieved as 22 ± 7%, 59 ± 3%, 65 ± 5%, and 78 ± 3% respectively for BNPs, TBNPs, DNPs, and TDNPs 6 hours post-injection. The most difference between targeted and non-targeted groups was observed at 6 hours for PSMA-11-HBED, and at 4 hours for PSMA-11-HYNIC. RSE indicated 88.6 ± 3.1% and 80.7 ± 3.2% enhanced contrast between tumor and muscle region for TBNPs and TDNPs on T*-W images.

CONCLUSIONS

Both TBNPs and TDNPs are promising novel nano-molecular probes for PSMA PCa tumor detection. The injection dose of non-targeted IONPs can be reduced by using targeted nanoprobes three times for BNPs and two times for DNPs.

EVIDENCE LEVEL

1 TECHNICAL EFFICACY: Stage 1.

摘要

背景

前列腺特异性膜抗原 (PSMA) 可通过美国食品和药物管理局 (FDA) 批准的 PSMA-11 肽在正电子发射断层扫描 (PET) 中提供前列腺癌 (PCa) 的检测方法。有一些研究使用非 FDA 批准的配体(包括抗体或肽)评估了用于 MRI 中 PSMA 检测的磁性纳米探针,这些配体不如 PSMA-11 那样具有特异性。

目的

评估 PSMA-11 肽靶向氧化铁纳米颗粒 (IONPs) 作为一种潜在的特异性纳米分子探针,通过 MRI 研究 PSMA PCa 异种移植模型。

研究类型

前瞻性。

动物模型

20 只雄性 C57BL6 裸鼠皮下诱导 PSMA LNCaP 细胞系肿瘤。

磁场强度/序列:1.5T,T-W 快速自旋回波和 T*-W 梯度回波。

评估

用羧甲基化葡聚糖 (DNPs) 和牛血清白蛋白 (BNPs) 包裹 IONPs,用 PSMA-11-HYNIC 肽靶向 DNPs (TDNPs) 和用 PSMA-11-HBED 肽靶向 BNPs (TBNPs),静脉注射剂量为 2.8mg Fe/kg。在注射前、注射后 4 小时和 6 小时获得冠状 T-W 和 T*-W 图像。在二维和三维分析中计算信号强度 (SI) 和相对信号增强 (RSE)。评估肿瘤的组织学分析,并根据原子吸收光谱计算体内的铁分布。

统计学检验

单因素方差分析,然后进行 Tukey 多重比较检验,配对样本 T 检验,P < 0.05 被认为具有统计学意义。

结果

BNPs、TBNPs、DNPs 和 TDNPs 分别在 6 小时时 T-W SI 降低 22±7%、59±3%、65±5%和 78±3%。PSMA-11-HBED 在 6 小时时和 PSMA-11-HYNIC 在 4 小时时观察到靶向和非靶向组之间的最大差异。T*-W 图像上 TBNPs 和 TDNPs 的 RSE 分别为 88.6±3.1%和 80.7±3.2%,肿瘤与肌肉区域之间的对比度增强。

结论

TBNPs 和 TDNPs 均是 PSMA PCa 肿瘤检测的有前途的新型纳米分子探针。使用靶向纳米探针时,非靶向 IONPs 的注射剂量可减少 3 倍(BNPs)和 2 倍(DNPs)。

证据水平

1 技术功效:阶段 1。

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