利用掺稀土纳米颗粒通过微针输送的短波红外成像引导放射增敏用于增强黑色素瘤治疗。

Mohd Yaqub Khan, Jen-Kun Chen, Lokesh Agrawal, Garima Joshi, Yu-Ting Chuang, Cheng-An J Lin, Min-Hua Chen
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引用次数: 0

摘要

由于异常皮肤细胞不受控制的生长、对常规治疗的耐药性以及晚期病例预后不良,黑色素瘤仍然是一个主要的全球健康挑战。局部,早期黑色素瘤,定义为局限于皮肤的黑色素瘤,没有区域或远处扩散,提供了一个关键的治疗窗口,因为薄病变通常可以通过手术切除治愈。然而,治疗的延迟会导致淋巴结受累和远处转移,从而恶化预后并限制可用的治疗。尽管手术和放疗仍然是标准的选择,但它们往往存在局限性,如黑色素瘤靶向不完全、对健康组织的损害以及治疗耐药性。为了应对这些挑战,我们探索了一种更精确的放疗方法,旨在提高治疗效果,同时最大限度地减少对周围组织的伤害。在这项研究中,我们通过将稀土掺杂纳米颗粒(RENPs)与微针(MNs)和短波红外(SWIR)成像相结合,研究了其作为放射增敏剂的潜力,以提高局部早期黑色素瘤治疗的放疗精度。采用改进的热分解方法合成了RENPs,并用Tween 20 (Tw)对其进行表面修饰,使其易于过渡到水相中用于生物应用。将RENP-Tw加入到MNs中可以精确和局部地递送到黑色素瘤组织中。同时,SWIR成像具有深入组织和高对比度分辨率,可以实时监测RENP-Tw定位,确保黑色素瘤部位的最佳放射致敏。我们的体内研究表明,RENP-Tw/MNs显著增强了黑色素瘤小鼠辐射诱导的细胞死亡,同时最小化了全身毒性。此外,SWIR成像显示黑色素瘤部位RENP-Tw/MNs持续发光,进一步支持精确放疗和改善治疗效果。这种创新的方法通过提高黑色素瘤特异性、减少脱靶效应和提高放射增敏效率来解决传统放疗的局限性。总的来说,我们的研究结果表明,RENP-Tw/MNs具有通过精确的成像引导放射治疗推进局部早期黑色素瘤治疗的有效策略的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shortwave infrared imaging-guided radiosensitization using rare-earth-doped nanoparticles delivered via microneedles for enhanced melanoma therapy.

Melanoma remains a major global health challenge due to the uncontrolled growth of abnormal skin cells, resistance to conventional therapies, and poor prognosis in advanced cases. Localized, early-stage melanoma, defined as melanoma confined to the skin without regional or distant spread, offers a critical treatment window, as thin lesions are often curable with surgical excision. However, delays in treatment allow progression to lymph node involvement and distant metastasis, which worsen prognosis and limit available therapies. Although surgery and radiotherapy remain standard options, they often struggle with limitations like incomplete melanoma targeting, damage to healthy tissues, and treatment resistance. To address these challenges, we explored a more precise radiotherapy approach aimed at enhancing treatment efficacy while minimizing harm to surrounding tissues. In this study, we investigated the potential of rare-earth-doped nanoparticles (RENPs) as radiosensitizers by integrating them with microneedles (MNs) and shortwave infrared (SWIR) imaging to improve the precision of radiotherapy for localized, early-stage melanoma treatment. RENPs were synthesized using a modified thermal decomposition method and surface-modified them with Tween 20 (Tw) to facilitate their transition into the aqueous phase for biological applications. Incorporating RENP-Tw into MNs enabled precise and localized delivery into melanoma tissue. Meanwhile SWIR imaging, with its deep tissue penetration and high contrast resolution, allowed real-time monitoring of RENP-Tw localization, ensuring optimal radiosensitization at the melanoma site. Ourin vivostudies demonstrated that RENP-Tw/MNs significantly enhanced radiation-induced cell death in melanoma-bearing mice while minimizing systemic toxicity. Moreover, SWIR imaging revealed sustained luminescence of RENP-Tw/MNs at the melanoma site, further supporting precise radiotherapy with improved therapeutic outcomes. This innovative approach addresses the limitations of conventional radiotherapy by improving melanoma specificity, reducing off-target effects, and enhancing radiosensitization efficiency. Overall, our findings suggest that RENP-Tw/MNs hold potential as an effective strategy for advancing localized, early-stage melanoma treatment through precise, imaging-guided radiotherapy.

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