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姜黄素包封脂质体纳米粒作为蓝光发光二极管诱导光动力治疗系统用于癌症治疗。

Curcuminoids encapsulated liposome nanoparticles as a blue light emitting diode induced photodynamic therapeutic system for cancer treatment.

机构信息

Department of Nuclear Medicine, Molecular Imaging & Therapeutic Medicine Research Center, Research Institute of Clinical Medicine, Biomedical Research Institute, Jeonbuk National University Hospital, Jeonju 54907, South Korea.

Research Institute for Endocrine Sciences, Department of Physiology, Jeonbuk National University Hospital, Jeonju 54907, South Korea.

出版信息

J Photochem Photobiol B. 2020 Apr;205:111840. doi: 10.1016/j.jphotobiol.2020.111840. Epub 2020 Feb 22.

Abstract

Unlike normal cells, cancer cells mutate to thrive in exaggerated levels of reactive oxygen species (ROS). This potentially makes them more susceptible to small molecule-induced oxidative stress. The intracellular ROS increase in cancer cells is a potential area under investigation for the development of cancer therapeutics targeting cancer cells. Visible photons of 430-490 nm wavelengths from a blue-light emitting diode (BLED) encompass the visible region of the spectrum known to induce ROS in cancer cells. Curcuminoids (CUR) naturally occurring photosensitizers sensitized by the blue wavelength of the visible light, well known for its potent anti-inflammatory and anticancer activity. Poor solubility and bioavailability, of the compound of the small molecule CUR restrict the therapeutic potential and limits CUR to be used as a photosensitizer. Here, our research group reports the use of small molecules CUR, encapsulated in liposome nanocarriers (LIP-CUR) coupled with blue light-emitting diode (BLED) induced photodynamic therapy (BLED-PDT). In A549 cancer cells in vitro, LIP-CUR coupled with BLED initiated BLED-PDT and triggered O, ultimately resulting in caspase-3 activated apoptotic cell death. The combination of a non-cytotoxic dose of small molecule CUR co-treated with BLED to trigger BLED-PDT could be translated and be developed as a novel strategy for the treatment of cancer.

摘要

与正常细胞不同,癌细胞发生突变以在过度水平的活性氧物种 (ROS) 中茁壮成长。这可能使它们更容易受到小分子诱导的氧化应激。癌细胞内 ROS 的增加是开发针对癌细胞的癌症治疗药物的一个潜在研究领域。来自蓝光发射二极管 (BLED) 的 430-490nm 波长可见光包含已知可诱导癌细胞产生 ROS 的光谱可见区域。姜黄素类化合物 (CUR) 是天然存在的光增敏剂,被可见光的蓝光敏化,因其具有强大的抗炎和抗癌活性而闻名。小分子 CUR 的化合物的溶解度和生物利用度差,限制了其治疗潜力,使其只能作为光增敏剂使用。在这里,我们的研究小组报告了使用脂质体纳米载体 (LIP-CUR) 包裹的小分子 CUR 与蓝光发射二极管 (BLED) 联合应用光动力疗法 (BLED-PDT)。在体外 A549 癌细胞中,LIP-CUR 与 BLED 联合引发 BLED-PDT,并触发 O,最终导致 caspase-3 激活的细胞凋亡。将非细胞毒性剂量的小分子 CUR 与 BLED 联合治疗以引发 BLED-PDT 的组合可以转化并开发为治疗癌症的新策略。

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