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Combination of Photodynamic Therapy and Nanotechnology: Non-Invasive Weapon Against Cancer

机译:光动力疗法与纳米技术的结合:抗癌的无创武器

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摘要

Cancer has been reported as the second leading cause of death in the United States. Photodynamic therapy (PDT) has been introduced for clinical approaches as a non-invasive treatment and effective modality to selectively destroy cancers. It was more than 100 years ago when scientists noticed about the toxicity of combined light and some specific drugs which may result in cell death. In PDT, cancer destruction relies on applying a photosensitizing (PS) drug followed by light. Absorbed light can activate PS to transfer energy to existing molecules and substrates or oxygen to generate reactive oxygen species (ROS) and singlet oxygen. These products are highly toxic to cells and are able to damage or kill cancer cells. It is believed that singlet oxygen cannot damage cells far from the exposed area by light due to its high reactivity, short half-life (<0.04 /as), and short distance diffusion (<0.02 μm). High tumor selectivity, low systemic toxicity, low possibility of secondary effects, possibility of inducing the repeatable cycles of treatments as well as the possibility for combination with other therapies such as radiotherapy and chemotherapy are the advantages of PDT over other treatments. All of the adverse effects of PDT have been limited to photosensitivity reaction and swelling in the treated area which may cause pain or trouble swallowing or breathing. Here we review the history, mechanisms, potential challenges and alternative solutions for practical applications of PDT on cancer treatment.
机译:据报道,癌症是美国第二大死亡原因。光动力疗法(PDT)已作为一种非侵入性治疗手段和选择性摧毁癌症的有效方法被引入临床方法。距今已有100多年的历史了,科学家们注意到混合光和某些特定药物的毒性可能会导致细胞死亡。在PDT中,癌症的消除依赖于先使用光敏(PS)药物,再使用光。吸收的光可以激活PS,将能量转移到现有的分子和底物或氧气上,以产生活性氧(ROS)和单线态氧。这些产品对细胞有剧毒,能够破坏或杀死癌细胞。据信单线态氧由于其高反应性,短半衰期(<0.04 / as)和短距离扩散(<0.02μm)而不能通过光破坏远离暴露区域的细胞。 PDT相对于其他疗法的优势在于,肿瘤选择性高,全身毒性低,二次效应的可能性低,诱导治疗可重复周期的可能性以及与放射线和化学疗法等其他疗法相结合的可能性。 PDT的所有不利影响都仅限于光敏反应和治疗区域的肿胀,这可能会引起疼痛或吞咽或呼吸困难。在这里,我们回顾了PDT在癌症治疗中的实际应用的历史,机制,潜在挑战和替代解决方案。

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