Patterson M S, Wilson B C, Graff R
Hamilton Regional Cancer Centre, Ontario, Canada.
Photochem Photobiol. 1990 Mar;51(3):343-9. doi: 10.1111/j.1751-1097.1990.tb01720.x.
In its simplest form, the photodynamic therapy (PDT) threshold dose model states that tissue necrosis due to PDT will occur if the number of photons absorbed by the photosensitizer per unit volume of tissue exceeds a critical value. This threshold is given by the product of photon fluence, photosensitizer concentration and specific absorption coefficient. To test the validity of this concept for PDT of normal rat liver sensitized with aluminum chlorosulphonated phthalocyanine (AISPC), all three of these parameters were varied by changing the injected AISPC dose, the wavelength of excitation and the irradiation geometry. The extent of necrosis caused by the treatment was consistent with the threshold model, except when the concentration of AISPC in the liver exceeded 20 micrograms g-1. For this animal model, we estimate the threshold to be (3.8 +/- 0.2) x 10(19) photons cm-3.
光动力疗法(PDT)阈值剂量模型的最简形式表明,如果组织单位体积内被光敏剂吸收的光子数超过临界值,PDT就会导致组织坏死。该阈值由光子注量、光敏剂浓度和比吸收系数的乘积给出。为了检验用氯磺化铝酞菁(AISPC)敏化的正常大鼠肝脏PDT这一概念的有效性,通过改变注射的AISPC剂量、激发波长和照射几何形状来改变所有这三个参数。除了肝脏中AISPC浓度超过20微克/克时,治疗引起的坏死程度与阈值模型一致。对于这个动物模型,我们估计阈值为(3.8±0.2)×10¹⁹光子/立方厘米。