Veenhuizen R B, Ruevekamp M C, Oppelaar H, Ransdorp B, van de Vijver M, Helmerhorst T J, Kenemans P, Stewart F A
Division of Experimental Therapy, Netherlands Cancer Institute/Antoni van Leeuwenhoek Huis, Amsterdam, The Netherlands.
Photochem Photobiol. 1997 Sep;66(3):389-95. doi: 10.1111/j.1751-1097.1997.tb03163.x.
The aim of this study was to compare red (652 nm) and green (514 nm) light for photodynamic therapy (PDT) of the peritoneal cavity with emphasis on light distribution and toxicity. Red-light PDT was limited by intestinal toxicity and it was hypothesized that less penetrating green light would allow higher light doses to be used in the peritoneal cavity. Female non-tumor-bearing rats were photosensitized with mTHPC (meta-tetrahydroxyphenylchlorin, Foscan) intravenously or intraperitoneally and the peritoneum was illuminated using a minimally invasive technique. For both red and green light, the time of illumination was varied to give the required dose. Light fluence rate was measured in situ at multiple sites within the abdominal cavity. The toxicity experiments were carried out with a total of 160 J incident red or 640 J incident green light and a drug dose of 0.15 mg/kg Foscan. For red light a mean fluence rate of 55.2 +/- 38.5 mW cm-2 was measured, with a peak fluence rate of 128 mW cm-2 on the intestines. For green light the mean and peak fluence rates were 8.2 +/- 9.0 (i.e. including zero fluence rate measurements) and 28 mW cm-2, respectively. Intestines were most vulnerable to red light illumination. The intravenous injection route resulted in increased toxicity for red light, but for green light there were no major differences between intravenous and intraperitoneal routes. The 4 h interval between drug and illumination resulted in very little toxicity for both wavelengths. We conclude that for intraperitoneal PDT green light allows higher light doses than red light, but the light distribution over the peritoneum is much less favorable and may not be suitable for whole peritoneal illumination using a minimal-access technique.
本研究旨在比较红色(652纳米)和绿色(514纳米)光用于腹腔光动力疗法(PDT)的效果,重点关注光分布和毒性。红光PDT受肠道毒性限制,据推测穿透性较弱的绿光可使腹腔内使用更高的光剂量。对雌性无瘤大鼠静脉或腹腔注射mTHPC(间四羟基苯基氯卟啉,Foscan)进行光敏化,然后采用微创技术照射腹膜。对于红光和绿光,均改变照射时间以给予所需剂量。在腹腔内多个部位原位测量光通量率。毒性实验采用160焦耳入射红光或640焦耳入射绿光,药物剂量为0.15毫克/千克Foscan。对于红光,测得的平均光通量率为55.2±38.5毫瓦/平方厘米,肠道上的峰值光通量率为128毫瓦/平方厘米。对于绿光,平均和峰值光通量率分别为8.2±9.0(即包括零光通量率测量值)和28毫瓦/平方厘米。肠道对红光照射最为敏感。静脉注射途径导致红光毒性增加,但对于绿光,静脉和腹腔注射途径之间无显著差异。药物与照射之间间隔4小时,两种波长的毒性都很小。我们得出结论,对于腹腔内PDT,绿光比红光允许更高的光剂量,但腹膜上的光分布不太理想,可能不适合使用微创技术进行全腹膜照射。