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Monte Carlo simulations for optimal light delivery in photodynamic therapy of non-melanoma skin cancer

机译:蒙特卡洛模拟在非黑素瘤皮肤癌光动力治疗中优化光传输

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The choice of light source is important for the efficacy of photodynamic therapy (PDT) of non-melanoma skin cancer. We simulated the photodynamic dose (PDD) delivered to a tumour during PDT using theoretical radiation transfer simulations performed via our 3D Monte Carlo radiation transfer (MCRT) model for a range of light sources with light doses up to 75 J cm 2. The PDD delivered following superficial irradiation from (A) non-laser light sources, (B) monochromatic light, (C) alternate beam diameters and (D) re-positioning of the tumour within the tissue was computed. (A) The final PDD deposited to the tumour at a depth of 2mm by the Paterson light source was 2.75, 2.50 and 1.04× greater than the Waldmann 1200, Photocure and Aktilite, respectively. (B) Tumour necrosis occurred at a depth of 2.23mm and increased to 3.81mm for wavelengths 405 and 630nm, respectively. (C) Increasing the beam diameter from 10 to 50mm had very little effect on depth of necrosis. (D) As expected, necrosis depths were reduced when the tumour was re-positioned deeper into the tissue. These MCRT simulations show clearly the importance of choosing the correct light source to ensure optimal light delivery to achieve tumour necrosis.
机译:光源的选择对于非黑素瘤皮肤癌的光动力疗法(PDT)的疗效很重要。我们使用3D蒙特卡洛辐射传输(MCRT)模型对理论上的辐射传输模拟,对PDT在PDT期间传递给肿瘤的光动力剂量(PDD)进行了研究,该模型对光剂量高达75 J cm 2的一系列光源进行了测量。在从(A)非激光光源,(B)单色光,(C)交替光束直径和(D)组织内肿瘤重新定位后,进行了表面照射。 (A)由Paterson光源在2mm深度处沉积到肿瘤上的最终PDD分别比Waldmann 1200,Photocure和Aktilite大2.75、2.50和1.04倍。 (B)肿瘤坏死发生在2.23mm的深度处,并且对于波长405和630nm分别增加到3.81mm。 (C)将光束直径从10mm增加到50mm对坏死深度的影响很小。 (D)如预期的那样,当将肿瘤重新定位到更深的组织中时,坏死深度减小了。这些MCRT模拟清楚地表明了选择正确光源的重要性,以确保最佳的光传输以实现肿瘤坏死。

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