利用多谐低频 EPR 高灵敏度检测黑色素瘤中的黑色素

IF 3 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Molecular Imaging and Biology Pub Date : 2024-06-01 Epub Date: 2024-03-22 DOI:10.1007/s11307-024-01911-3
Mohammad Wehbi, Lionel Mignion, Nicolas Joudiou, Evelyne Harkemanne, Bernard Gallez
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引用次数: 0

摘要

目的:低频 EPR 可以无创检测黑色素细胞皮肤病变中的内源性黑色素自由基,并有可能区分良性非典型痣和恶性黑色素瘤病变。我们最近成功证明了临床 EPR 无创检测患者皮肤病变中内源性黑色素自由基的能力。然而,该方法的信噪比(SNR)极低,需要进一步研究以提高检测灵敏度。在本研究中,我们评估了具有多谐波(MH)分析能力的临床 EPR 系统在检测黑色素方面的性能:程序:在体外黑色素模型、体内黑色素瘤模型(细胞植入皮肤、淋巴结和肺部定植)以及置于人体皮肤表面的模型中,将 MH-EPR 的灵敏度与经典的连续波 (CW) -EPR(1 次谐波)检测进行了比较:在体外,我们观察到在黑色素平面模型中使用 MH 分析法时,信噪比比使用 CW 分析法时提高了 10 倍,同时调制幅度也增加了。在无毛小鼠皮肤中生长的 B16 黑色素瘤中,我们观察到体内灵敏度的提高与体外观察到的类似,能够在黑色素瘤的早期发展阶段检测到黑色素瘤细胞。MH-EPR 还能非侵入性地检测来自淋巴结和肺部黑色素瘤细胞的黑色素信号。我们还观察到,利用放置在人体皮肤表面的黑色素模型提高了灵敏度:总之,我们的研究结果为新的临床试验铺平了道路,这些试验将使用 MH 临床 EPR 对色素性皮肤病变进行定性。
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Highly Sensitive Detection of Melanin in Melanomas Using Multi-harmonic Low Frequency EPR.

Purpose: Low frequency EPR can noninvasively detect endogenous free radical melanin in melanocytic skin lesions and could potentially discriminate between benign atypical nevi and malignant melanoma lesions. We recently succeeded in demonstrating the ability of clinical EPR to noninvasively detect the endogenous melanin free radical in skin lesions of patients. However, the signal-to-noise ratio (SNR) was extremely low warranting further research to boost the sensitivity of detection. In the present study, we assessed the performance of a clinical EPR system with the capability to perform multi-harmonic (MH) analysis for the detection of melanin.

Procedures: The sensitivity of MH-EPR was compared with a classical continuous wave (CW)-EPR (1st harmonic) detection in vitro in melanin phantoms, in vivo in melanoma models with cells implanted in the skin, in lymph nodes and having colonized the lungs, and finally on phantoms placed at the surface of human skin.

Results: In vitro, we observed an increase in SNR by a factor of 10 in flat melanin phantoms when using MH analysis compared to CW combined with an increase in modulation amplitude. In B16 melanomas having grown in the skin of hairless mice, we observed a boost in sensitivity in vivo similar to that observed in vitro with the capability to detect melanoma cells at an earlier stage of development. MH-EPR was also able to detect non-invasively the melanin signal coming from melanoma cells present in lymph nodes as well as in lungs. We also observed a boost of sensitivity using phantoms of melanin placed at the surface of human skin.

Conclusions: Overall, our results are paving the way for new clinical trials that will use MH clinical EPR for the characterization of pigmented skin lesions.

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来源期刊
CiteScore
6.90
自引率
3.20%
发文量
95
审稿时长
3 months
期刊介绍: Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures. Some areas that are covered are: Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes. The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets. Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display. Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging. Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics. Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations. Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.
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