Oxygen generating nanoparticles for improved photodynamic therapy of hypoxic tumours

光动力疗法 活性氧 氧气 化学 纳米颗粒 聚合物 缺氧(环境) 生物物理学 药理学 癌症研究 医学 纳米技术 生物化学 材料科学 生物 有机化学
作者
Yingjie Sheng,Heather Nesbitt,Bridgeen Callan,Mark Taylor,Mark Love,A. P. McHale,John F. Callan
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:264: 333-340 被引量:111
标识
DOI:10.1016/j.jconrel.2017.09.004
摘要

Photodynamic therapy (PDT) is a clinically approved anti-cancer treatment that involves the activation of an otherwise inactive sensitiser drug with light, which in the presence of molecular oxygen, generates cytotoxic reactive oxygen species (ROS). As oxygen is a key requirement for the generation of ROS in PDT and given the fact that hypoxia is a characteristic of most solid cancerous tumours, treating hypoxic tumours using PDT can be a challenge. In this manuscript, we have prepared a CaO2 nanoparticle (NP) formulation coated with a pH-sensitive polymer to enable the controlled generation of molecular oxygen as a function of pH. The polymer coat was designed to protect the particles from decomposition while in circulation but enable their activation at lower pH values in hypoxic regions of solid tumours. The oxygen generating capability of the polymer coated NPs was demonstrated in aqueous solution with minimal oxygen produced at pH 7.4, whereas it increased significantly when the pH was reduced to 6.2. The polymer coated CaO2 NPs were also observed to significantly increase tumour pO2 levels (p < 0.05) in mice bearing ectopic human xenograft MIA PaCa-2 pancreatic tumours with an average increase in tumour pO2 of 6.5 mm Hg in the period 10–30 min following administration. A statistically significant improvement in PDT mediated efficacy (p < 0.001) was also observed when the particles were administered to mice bearing the same tumours 20 min prior to PDT treatment. These results suggest that the polymer coated CaO2 NP formulation offers significant potential as an in situ method for oxygen generation to enhance the efficacy of treatments that depend on the presence of oxygen to elicit a cytotoxic effect.
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