PSs, photosensitizers

PS,光敏剂
  • 文章类型: Journal Article
    如今,传染病作为全球危机持续存在,对世界各国的公共卫生和经济稳定造成重大破坏。尤其是由于多药耐药性(MDR)的流行和出现以及现有治疗选择的局限性,细菌感染仍然是最严重的问题。抗菌光动力疗法(APDT)是一种潜在的治疗方式,涉及光敏剂(PS)的系统给药,光,和分子氧(O2)用于应对细菌感染。尽管现有的卟啉和非卟啉PS在APDT中有效,溶解性差,对革兰氏阴性细菌的疗效有限,和非特异性分布阻碍了它们的临床应用。因此,为了提高传统PS的效率,各种聚合物驱动的改性和功能化策略已被采用来设计多功能混合光疗。这篇综述评估了为APDT应用开发的聚合物-PSs混合材料的最新进展和最新研究。Further,以下方面的关键研究成果被认为是深入的建设性讨论:i)通过各种分子相互作用的PSs集成/功能化聚合物复合材料;ii)PSs沉积在不同基材和设备上的涂层,以消除与医疗保健相关的感染;iii)PSs嵌入膜,脚手架,和用于再生医学应用的水凝胶。
    Nowadays, infectious diseases persist as a global crisis by causing significant destruction to public health and the economic stability of countries worldwide. Especially bacterial infections remain a most severe concern due to the prevalence and emergence of multi-drug resistance (MDR) and limitations with existing therapeutic options. Antibacterial photodynamic therapy (APDT) is a potential therapeutic modality that involves the systematic administration of photosensitizers (PSs), light, and molecular oxygen (O2) for coping with bacterial infections. Although the existing porphyrin and non-porphyrin PSs were effective in APDT, the poor solubility, limited efficacy against Gram-negative bacteria, and non-specific distribution hinder their clinical applications. Accordingly, to promote the efficiency of conventional PSs, various polymer-driven modification and functionalization strategies have been adopted to engineer multifunctional hybrid phototherapeutics. This review assesses recent advancements and state-of-the-art research in polymer-PSs hybrid materials developed for APDT applications. Further, the key research findings of the following aspects are considered in-depth with constructive discussions: i) PSs-integrated/functionalized polymeric composites through various molecular interactions; ii) PSs-deposited coatings on different substrates and devices to eliminate healthcare-associated infections; and iii) PSs-embedded films, scaffolds, and hydrogels for regenerative medicine applications.
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  • 文章类型: Journal Article
    虽然作为癌症治疗的主要模式,放疗(RT)的临床效果尚不能满足癌症患者的需要。开发肿瘤优先放射增敏剂或将RT与其他治疗结合已被认为是增强RT功效的高度必要的。本研究报道了一种多功能生物活性小分子(称为IR-83),同时表现出肿瘤优先积累,近红外成像和无线电/光动力/光热治疗效果。IR-83是通过将2-硝基咪唑作为放射增敏剂引入具有肿瘤靶向和光敏作用的七甲基花青染料的框架中来设计和合成的。作为结果,IR-83优先积累在肿瘤中,通过整合放射/光动力/光热多模式疗法抑制肿瘤生长和转移。机制研究表明,IR-83在癌细胞线粒体中积累,诱导过量的活性氧(ROS),激光照射后产生高热。一方面,这些现象导致线粒体功能障碍和氧化磷酸化急剧下降,从而减少了组织耗氧量。另一方面,线粒体中过量的ROS通过下调细胞内抗氧化系统来破坏抗氧化剂的平衡和氧化应激平衡,随后敏化电离辐射产生不可逆的DNA双链断裂。因此,这项研究提出了一种有前景的放射增敏剂和一种新的替代策略,通过线粒体靶向多模式协同治疗增强RT疗效.
    Although as a mainstay modal for cancer treatment, the clinical effect of radiotherapy (RT) does not yet meet the need of cancer patients. Developing tumour-preferential radiosensitizers or combining RT with other treatments has been acknowledged highly necessary to enhance the efficacy of RT. The present study reported a multifunctional bioactive small-molecule (designated as IR-83) simultaneously exhibiting tumour-preferential accumulation, near-infrared imaging and radio/photodynamic/photothermal therapeutic effects. IR-83 was designed and synthesized by introducing 2-nitroimidazole as a radiosensitizer into the framework of heptamethine cyanine dyes inherently with tumour-targeting and photosensitizing effects. As results, IR-83 preferentially accumulated in tumours, suppressed tumour growth and metastasis by integrating radio/photodynamic/photothermal multimodal therapies. Mechanism studies showed that IR-83 accumulated in cancer cell mitochondria, induced excessive reactive oxygen species (ROS), and generated high heat after laser irradiation. On one hand, these phenomena led to mitochondrial dysfunction and a sharp decline in oxidative phosphorylation to lessen tissue oxygen consumption. On the other hand, excessive ROS in mitochondria destroyed the balance of antioxidants and oxidative stress balance by down-regulating the intracellular antioxidant system, and subsequently sensitized ionizing radiation-generated irreversible DNA double-strand breaks. Therefore, this study presented a promising radiosensitizer and a new alternative strategy to enhance RT efficacy via mitochondria-targeting multimodal synergistic treatment.
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