将主动靶向光动力疗法和光激活化疗相结合,加强癌症治疗。

Nkune Williams Nkune, Heidi Abrahamse
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引用次数: 0

摘要

科学家们一直在积极研究新的治疗方法,这些方法可以在单独使用或联合使用时有效地根除正常组织中的癌细胞,而副作用可以忽略不计。光动力疗法已经成为一种很有前途的非侵入性疗法,它将光敏剂、氧气和特定波长的光结合在一起,用于治疗癌症。尽管PDT取得了令人鼓舞的成果,但传统的ps面临着长期存在的挑战,如水溶性差、半衰期短和脱靶毒性。纳米疗法的发展在克服这一问题方面显示出巨大的潜力。肿瘤微环境本身是缺氧的,这促进了肿瘤对PDT的抵抗,因为它是氧依赖的。光激活化疗是一种不依赖氧的基于光的治疗方法,利用化疗方案在暴露于光下之前保持惰性,允许目标特异性激活,同时最大限度地减少脱靶毒性。这些技术的整合可以提高选择性和产生协同细胞毒效应,可以改善癌症治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Combination of Active-Targeted Photodynamic Therapy and Photoactivated Chemotherapy for Enhanced Cancer Treatment.

Scientists have been actively investigating novel therapies that can effectively eradicate cancer cells with negligible side effects in normal tissues when used alone or in a combinatorial approach. Photodynamic therapy has emerged as a promising non-invasive therapy that integrates photosensitizer, oxygen, and a specific wavelength of light for the treatment of cancer. Despite encouraging outcomes yielded by PDT, conventional PSs are faced with longstanding challenges such as poor water solubility, a short half-life, and off-target toxicity. Development of nanotherapeutics has shown great potential in overcoming this issue. The tumor microenvironment is inherently hypoxic, and this promotes tumor resistance to PDT, as it is oxygen-dependent. Photoactivated chemotherapy, an oxygen-independent light-based therapy, utilizes chemotherapeutic regimens that remain inert until exposed to light, allowing target-specific activation while minimizing off-target toxicity. Integration of these techniques can improve selectivity and yield synergistic cytotoxic effects that could improve cancer treatment.

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