Recent patents on light based therapies: photodynamic therapy, photothermal therapy and photoimmunotherapy.

Emilio J Sanchez-Barcelo, Maria D Mediavilla
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引用次数: 20

Abstract

This article reviews the more recent patents in three kinds of therapeutic strategies using the application of visible light to irradiate photosensible substances (PSs) of different natures. The light-activation of these PSs is directly responsible for the desired therapeutic effects. This group of light therapies includes photodynamic therapy (PDT), photothermal therapy (PTT) and photoimmunotherapy (PIT). Therapeutic mechanisms triggered by the activation of the PSs depend basically (though not exclusively) on the release of reactive oxygen species (ROS) and the activation of immune responses (PDT and PIT) or the local generation of heat (PTT). The main difference between PIT and PDT is that in PIT, monoclonal antibodies (MABs) are associated to PSs to improve the selective binding of the PSs to the target tissues. All these therapeutic strategies offer the possibility of destroying tumor tissue without damaging the surrounding healthy tissue, which is not achievable with chemotherapy or radiotherapy. PDT is also used as an alternative or adjuvant antimicrobial therapy together with the traditional antibiotic therapy since these organisms are unlikely to develop resistance to the ROS induced by PDT. Furthermore, PDT also induces an immune response against bacterial pathogens. The current challenge in PDT, PIT and PTT is to obtain the highest level of selectivity to act on targeted sick tissues with the minimum effects on the surrounding healthy tissue. The development of new PSs with high affinity for specific tissues, new PSs- MABs conjugates to bind to specific kinds of tumors, and new light-sensible nanoparticles with low toxicity, will increase the clinical utility of these therapies.

光疗法的最新专利:光动力疗法、光热疗法和光免疫疗法。
本文综述了利用可见光照射不同性质光敏物质的三种治疗策略的最新专利。这些PSs的光激活直接导致了预期的治疗效果。这组光疗法包括光动力疗法(PDT)、光热疗法(PTT)和光免疫疗法(PIT)。由PSs激活触发的治疗机制基本上(尽管不是完全)依赖于活性氧(ROS)的释放和免疫反应(PDT和PIT)的激活或局部热的产生(PTT)。PIT和PDT的主要区别在于,在PIT中,单克隆抗体(mab)与PSs相关,以提高PSs与靶组织的选择性结合。所有这些治疗策略都提供了在不损害周围健康组织的情况下破坏肿瘤组织的可能性,这是化疗或放疗无法实现的。PDT也被用作传统抗生素治疗的替代或辅助抗菌治疗,因为这些生物不太可能对PDT诱导的ROS产生耐药性。此外,PDT还能诱导对细菌病原体的免疫反应。PDT、PIT和PTT目前面临的挑战是在对周围健康组织的影响最小的情况下,获得最高水平的选择性作用于目标病变组织。对特定组织具有高亲和力的新型ps,新型ps - mab结合特异性肿瘤,新型低毒性光敏感纳米颗粒的开发,将增加这些治疗的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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