光学学报, 2009, 29 (s1): 305, 网络出版: 2009-06-25   

监测化学发光评估光敏效应对生物分子的氧化伤害

Evaluation of Oxidative Damage to Biologic Molecule by Monitoring Chemiluminescence During the Course of Photosensitization
作者单位
华南师范大学生物光子学研究院激光生命科学研究所暨激光生命科学教育部重点实验室, 广东 广州 510631
摘要
活性氧对生物活性分子如蛋白质、脂类等具有强烈的氧化作用, 从而对生物细胞产生杀伤作用。光敏反应过程会产生大量的活性氧, 利用光子监测判断光敏反应的氧化伤害程度和光敏作用剂量具有重要意义。实验表明, 体外人血清白蛋白在光敏氧化反应后具有长寿命的化学发光过程, 这种氧化损伤的滞后特性可实现暗背景下的低噪声光子监测; 光敏作用后光子检测证明, 不同的光敏剂都存在生物分子的氧化化学发光(CL)。同时, 肿瘤细胞的光敏作用实验中也观测到较强的化学发光信号, 且信号的积累与光敏作用剂量有相关性。因此检测化学发光的实时信号和积累可以评估光敏作用对生物活性分子和细胞造成的损坏程度, 将有望应用到光动力肿瘤治疗等光敏效应的剂量监测上。
Abstract
Reactive oxygen species (ROS) can damage molecules such as lipids and proteins, thus cause oxidative damages to cells. During photosensitization process such as photodynamic therapy (PDT), a large amount of ROS is produced. By monitoring the ROS production, it is possible to evaluate the oxidation caused by ROS and the subsequent biological outcome by a PDT treatment. Results indicate that, there is a long-life delayed chemiluminescence (CL) after the human serum oxidized with photosensitization. This property may be used to monitor CL after turning off the excitation light source, thus achieve a high signal/noise ratio in detection. With the delayed CL detection method, CL was evaluated with various photosensitizes. The technique was also tested in vitro, it was found that the CL signal was readily detectable and showed a linear relationship with the dose of PDT treatment. In conclusion, the detection of real-time CL is tested both in solutions doped with various photosensitizes and in vitro and the cumulated CL can be used as a marker for evaluating the damage to biologic molecule and cell. This method can be used on photosensitization such as photodynamic therapy to monitor the dose.
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魏言春, 邢达, 杨利勇, 陈群. 监测化学发光评估光敏效应对生物分子的氧化伤害[J]. 光学学报, 2009, 29(s1): 305. Wei Yanchun, Xing Da, Yang Liyong, Chen Qun. Evaluation of Oxidative Damage to Biologic Molecule by Monitoring Chemiluminescence During the Course of Photosensitization[J]. Acta Optica Sinica, 2009, 29(s1): 305.

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