原位合成超顺磁性铁纳米颗粒磁热疗治疗乳腺癌和前列腺癌的体外评价。

Mariam Elabbasi, Ahmed A El-Gendy
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引用次数: 0

摘要

在追求有效的癌症治疗中,热疗已经成为一种很有前途的方法;然而,它的成功在很大程度上依赖于先进纳米材料的发展。本研究提出了一种突破性的方法,即利用超顺磁性铁纳米粒子(spin)在乳腺和前列腺肿瘤中特异性地进行细胞内磁热疗,为热疗癌症治疗的发展奠定了重要的基础。与传统的抗癌治疗相比,我们的方法利用了纳米颗粒优越的肿瘤保留能力,因为它们在细胞内的摄取允许有效的诱导局部加热功率。我们开发了一种高度可控的铁碳纳米颗粒合成方法,这种纳米颗粒表现出特殊的自旋产热,磁饱和度超过150 emu/g,突出了它们在热疗方面的潜力。通过扫描电镜(SEM)、x射线衍射(XRD)和振动样品磁强计(VSM)的表征,证实了纳米颗粒具有纯铁相和高磁化强度。这些分散的纳米颗粒表现出显著的加热能力,通过比吸收率(SAR)来量化。体外分析显示了不同的大小分布,而使用Du145前列腺和MCF7乳腺癌细胞系进行的细胞内摄取研究显示了有效的纳米颗粒肿瘤细胞摄取。热疗前后的细胞活力评估显示大量肿瘤细胞死亡,磁场应用后减少近50%。这些发现强调了这些先进的纳米颗粒在细胞内靶向癌症治疗,特别是实体肿瘤治疗方面的巨大潜力,并为进一步的医学研究和应用提供了重要的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-vitroevaluation ofin-situsynthesized superparamagnetic iron nanoparticles (SPINs) for magnetic hyperthermia treatment of breast and prostate cancer.

Magnetic hyperthermia has emerged as a promising approach in the pursuit of effective cancer therapies; however, its success relies heavily on the development of advanced magnetic nanomaterials. This study introduces a groundbreaking approach of intracellular magnetic hyperthermia using superparamagnetic iron nanoparticles (SPINs) specifically within breast and prostate tumors, laying a crucial foundation for the development of hyperthermia cancer therapy. In contrast to traditional anticancer treatments, our approach leverages the superior tumor retention capabilities of nanoparticles due to their intracellular cell uptake allowing efficient induced localized heating power. We developed a highly controllable synthesis method for iron nanoparticles in carbon matrix, which exhibit efficient localized heat generation by SPINs under applied magnetic field within the clinical limit, with magnetic saturation exceeding 150 emu g-1, highlighting their potential for hyperthermia therapy. Characterization through scanning electron microscopy, x-ray diffraction, and vibrating sample magnetometry confirms the spherical-like shape, pure iron phase and high magnetization of the formed nanoparticles. These dispersed nanoparticles demonstrate feasibility for hyperthermia, quantified by the specific absorption rate.In vitrointracellular uptake studies using Du145 prostate and MCF7 breast cancer cell lines indicate efficient nanoparticle tumor cell-uptake. Pre- and post-hyperthermia cell viability assessments show substantial tumor cell death, with nearly 50% reduction post-magnetic field application. These findings highlight the promising potential of these advanced nanoparticles for intracellular targeted cancer therapy, particularly in solid tumors, and suggest significant avenues for further medical research and application.

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