纳米革命:利用二氧化硅纳米颗粒进行下一代癌症治疗。

Yashaswi Dutta Gupta, Suman Bhandary
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引用次数: 0

摘要

二氧化硅纳米颗粒(SiNPs)在纳米技术领域是一种很有前途的材料,具有与活体组织的相容性、适应性和易于定制的表面的独特组合,使其成为创新癌症治疗的有吸引力的基础。sinp允许有效装载治疗剂、核酸和显像剂,利用其结构设计增强有效载荷能力。精确调整其尺寸、形态和表面特性的能力允许对药物释放时间和定位进行控制,从而提高治疗精度并减少对健康组织的意外影响。配体、抗体或肽的表面功能化促进了癌细胞的活性靶向,促进了肿瘤特异性药物的积累,降低了全身毒性。除了药物输送,SiNPs在光热和光动力治疗方面表现出色。这些纳米颗粒的光响应特性促进了有效的光子到能量转换,产生局部热疗或细胞毒性反应物质,用于选择性肿瘤消融。此外,它们在MRI和荧光等成像技术中作为对比度增强剂的双重作用使治疗反应和肿瘤动态的实时可视化成为可能。尽管它们前景光明,但诸如持久的生物相容性、免疫系统反应和可扩展生产等挑战需要进一步开发以用于临床应用。正在进行的研究优先考虑优化纳米结构结构、表面功能化和配方方法,以克服现有的挑战。总之,sinp标志着精准肿瘤学的开创性进步,提供量身定制的治疗策略。它们的多功能性使多模式治疗和图像引导治疗成为可能,并最大限度地减少不良反应。跨学科的合作努力和持续的创新对于释放他们的全部能力,推动下一代精确肿瘤学的发展,以改善患者的预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nano-Revolution: Harnessing Silica Nanoparticles for Next-Generation Cancer Therapeutics.

Silica nanoparticles (SiNPs) emerge as a promising material in the realm of nanotechnology, boasting a unique combination of compatibility with living tissues, adaptable characteristics, and easily customizable surfaces, making them an attractive foundation for innovative cancer therapies. SiNPs permit the efficient loading of therapeutic agents, nucleic acids, and imaging agents, leveraging their structural design for enhanced payload capacity. The ability to precisely tune their dimensions, morphology, and surface properties allows controlled regulation of drug release timing and localization, thereby improving therapeutic precision and reducing unintended impacts on healthy tissues. Surface functionalization with ligands, antibodies, or peptides facilitates active targeting of cancer cells, boosting tumor-specific drug accumulation and reducing systemic toxicity. Beyond drug delivery, SiNPs excel in photothermal and photodynamic therapies. The light-responsive nature of these nanoparticles facilitates efficient photon-to-energy conversion, generating localized hyperthermia or cytotoxic reactive species for selective tumor ablation. Additionally, their dual role as contrast enhancers in imaging techniques like MRI and fluorescence enables real-time visualization of therapeutic response and tumor dynamics. Despite their promise, challenges like durable biological compatibility, immune system reactions, and scalable production need further development for clinical use. Ongoing studies prioritize optimizing nanostructure architecture, surface functionalization, and formulation methodologies to overcome existing challenges. In summary, SiNPs signify pioneering advancements in precision oncology, offering tailored therapeutic strategies. Their versatility enables multimodal therapies and image-guided treatments and minimizes adverse effects. Collaborative interdisciplinary efforts and continuous innovation are essential to unlocking their full capabilities, driving the development of next-generation precision oncology tailored to improve patient prognosis.

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