Department of Urology, Xiangya Hospital, Central South University, Changsha 410008, China.
Nanoscale. 2021 Aug 21;13(31):13473-13486. doi: 10.1039/d1nr02880d. Epub 2021 Jul 30.
Currently, limited tumor drug permeation, poor oxygen perfusion and immunosuppressive microenvironments are the most important bottlenecks that significantly reduce the efficacy of photodynamic therapy (PDT). The main cause of these major bottlenecks is the platelet activation maintained abnormal tumor vessel barriers. Thus, platelet inhibition may present a new way to most effectively enhance the efficacy of PDT. However, to the best of our knowledge, few studies have validated the effectiveness of such a way in enhancing the efficacy of PDT both in vivo and in vitro. In this study, perfluoro-N-(4-methylcyclohexyl) piperidine-loaded albumin (PMP@Alb) nanoparticles were discovered, which possess excellent platelet inhibition ability. After PMP@Alb treatment, remarkably enhanced intra-tumoral drug accumulation, oxygen perfusion and T cell infiltration could be observed owing to the disrupted tumor vessel barriers. Besides, the effect of ICG@Lip mediated PDT was significantly amplified by PMP@Alb nanoparticles. It was demonstrated that PMP@Alb could be used as a useful tool to improve the efficacy of existing PDT by disrupting tumor vessel barriers through effective platelet inhibition.
目前,肿瘤药物渗透受限、氧灌注不良和免疫抑制的微环境是显著降低光动力疗法(PDT)疗效的最重要瓶颈。这些主要瓶颈的主要原因是血小板激活维持的异常肿瘤血管屏障。因此,血小板抑制可能为最有效地增强 PDT 疗效提供一种新方法。然而,据我们所知,很少有研究在体内和体外验证这种方法增强 PDT 疗效的有效性。在这项研究中,发现了负载全氟-N-(4-甲基环己基)哌啶的白蛋白(PMP@Alb)纳米粒子,它具有优异的血小板抑制能力。经 PMP@Alb 处理后,由于肿瘤血管屏障被破坏,可观察到明显增强的肿瘤内药物蓄积、氧灌注和 T 细胞浸润。此外,PMP@Alb 纳米粒子显著放大了 ICG@Lip 介导的 PDT 作用。研究表明,PMP@Alb 可通过有效抑制血小板来破坏肿瘤血管屏障,作为一种提高现有 PDT 疗效的有用工具。