纳米粒子增强放疗使用氧化钛纳米颗粒

G. Wakefield, M. Gardener, M. Stock, M. Adair
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引用次数: 4

摘要

氧化钛是一种光活性物质,通过水分裂产生羟基自由基。当掺杂稀土离子时,氧化钛纳米粒子被x射线和x射线产生的电子激活,并用于增强实体肿瘤的放射治疗。由于纳米粒子通过水分裂产生自由基,分子氧的存在是不需要的,侵袭性缺氧肿瘤可能是目标。放射耐药胰腺癌(PANC- 1)细胞的克隆测定显示,在临床相关的纳米颗粒负载下,放疗剂量增强因子为1.9。快速生长的口咽癌(FaDu)异种移植物表明,通过肿瘤内注射递送的稀土掺杂氧化钛纳米颗粒分散在整个肿瘤中,被癌细胞吸收并在高尔基体中进行被动积累。放射治疗激活纳米颗粒产生羟基自由基,破坏高尔基体,诱导肿瘤细胞凋亡。这导致增殖癌细胞的减少,从而使肿瘤再生速率降低3.8倍。在放射治疗之外使用纳米粒子不会增加全身毒性。因此,稀土掺杂氧化钛纳米颗粒代表了一种通过在放射治疗期间破坏细胞高尔基体来治疗肿瘤的新方法。
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Nanoparticle Augmented Radiotherapy using Titanium Oxide Nanoparticles
Titanium oxide is a photoactive material that generates hydroxyl free radicals via water splitting. When doped with rare earth ions titanium oxide nanoparticles are activated by X-rays and X-ray generated electrons and are used to enhance radiotherapy treatment of solid tumours. As the nanoparticles generate free radicals by water splitting the presence of molecular oxygen is not required and aggressive hypoxic tumours may be targeted. A clonogenic assay of radio resistant pancreatic cancer (PANC- 1) cells shows a radiotherapy dose enhancement factor of 1.9 at clinically relevant nanoparticle loadings. A fast growing oropharyngeal cancer (FaDu) xenograft demonstrates that rare earth doped titanium oxide nanoparticles delivered by intratumoural injection disperse throughout the tumour, being taken up by cancer cells and undergoing passive accumulation in the Golgi apparatus. Incident radiotherapy activates the nanoparticles to produce hydroxyl free radicals, destroying the Golgi apparatus, and inducing tumour cell apoptosis. This results in a reduction in proliferating cancer cells and a consequent reduction in tumour regrowth rate by a factor of 3.8. There is no increase in systemic toxicity when using nanoparticles in addition to radiotherapy. Rare earth doped titanium oxide nanoparticles therefore represent a novel approach to tumour treatment via destruction of the cells Golgi apparatus during radiotherapy.
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