首页> 外文会议>Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic Therapy XIV; Progress in Biomedical Optics and Imaging; vol.6 no.4 >Basic study on therapeutic effect distribution formation along depth using high-intensity pulsed photodynamic therapy
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Basic study on therapeutic effect distribution formation along depth using high-intensity pulsed photodynamic therapy

机译:高强度脉冲光动力疗法沿深度形成治疗效果分布的基础研究

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Photodynamic therapy (PDT) against murine macrophage like cells with the second-generation hydrophilic photosensitizer ME2906 (mono-L-aspartyl chlorin e_6: NPe6) was performed in vitro to study therapeutic effect distribution formation along depth with high-in tensity pulsed irradiation. The photocytotoxicity of macrophage like cell with ME2906 under various fluence rates was measured. We found photocytotoxicity suppression from 64 % to 16% in the cell lethality ranging the fluence rate of a pulsed laser from 20 to 400mW/cm~2 (corresponding pulse peak power: from 0.07 to 1.4 MW/cm~2). The cell lethality of about 80 % was obtained with continues wave (cw) laser irradiation under the fluence of 10 J/cm~2. Photobleaching and oxygen consumption of the photosensitizer solution, were measured to know photoreaction of the photosensitizer solution under the high fluence rate pulsed irradiation. Type-Ⅱ photochemical reaction suppression was indicated with the high fluence rate pulsed irradiation. The transient absorption of the photosensitizer solution during pulse irradiation was measured by the pump-and-probe technique with pulse peak power density up to 1.2 MW/cm~2 to investigate absorption saturation. In the case of the pump beam peak power of 1.2MW/cm~2, the transmittance of the probe beam increased approximately 7% from that of without the pump beam, so that huge absorption saturation did not occur in this case. We think the main cause of the photocytotoxicity suppression in this study may not to be attributed to the absorption saturation. This photocytotoxicity suppression induced by the high-intensity irradiation may be available to control treatment depth of PDT to preserve healthy internal wall of a hollow organ.
机译:在体外进行了第二代亲水性光敏剂ME2906(单L-天冬氨酰二氢卟酚e_6:NPe6)对鼠巨噬细胞样细胞的光动力疗法(PDT),以研究高强度脉冲辐射沿深度的治疗效果分布。测量了ME2906在不同通量率下对巨噬细胞样细胞的光细胞毒性。我们发现,在细胞致死率范围从20%到400mW / cm〜2的脉冲激光(相应的脉冲峰值功率:从0.07到1.4 MW / cm〜2)的细胞致死率中,光致细胞毒性的抑制范围从64%到16%。在10 J / cm〜2的注量下,连续波(cw)激光照射可获得约80%的细胞杀伤力。测量光敏剂溶液的光漂白和氧气消耗,以了解光敏剂溶液在高通量率脉冲辐射下的光反应。高能量通量脉冲辐照表明Ⅱ型光化学反应的抑制。用脉冲探测技术测量脉冲辐照过程中光敏剂溶液的瞬态吸收,其脉冲峰值功率密度最高为1.2 MW / cm〜2,以研究吸收饱和度。在泵浦光束峰值功率为1.2MW / cm〜2的情况下,探测光束的透射率比没有泵浦光束的情况下提高了约7%,因此在这种情况下不会出现巨大的吸收饱和。我们认为本研究中抑制光细胞毒性的主要原因可能不是由于吸收饱和所致。由高强度照射引起的这种光细胞毒性抑制作用可用于控制PDT的治疗深度,以保持中空器官的健康内壁。

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