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.
J Magn Reson Imaging. 2024 Jun;59(6):2204-2214. doi: 10.1002/jmri.28949. Epub 2023 Aug 12.
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.
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.
Prospective.
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.
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.
One-way ANOVA followed by Tukey's multiple comparison test, Paired-samples T-test, P < 0.05 was considered significant.
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.
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.
1 TECHNICAL EFFICACY: Stage 1.
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。
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。
前瞻性。
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。
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。
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。
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。
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)。
1 技术功效:阶段 1。