PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
The continued examination of injury sites and mechanisms of cytotoxicity associated with photodynamic therapy (PDT) can take advantage of current molecular and/or biochemical techniques. The increased expression of oxidative stress proteins can be studied as a function of photosensitizer type, treatment conditions and cell type. However, while in-vitro studies can address questions regarding subcellular PDT targets there is growing evidence that in-vivo effects of PDT are mediated by both vascular and direct tumor cell injury. Preclinical PDT studies using mono-l-aspartyl chlorin e6 (NPe6) confirm that the efficacy of this photosensitizer is correlated with plasma levels of this compound and not tumor cell levels.
Charles J. Gomer
"Basic mechanisms and subcellular targets related to PDT", Proc. SPIE 10306, Future Directions and Applications in Photodynamic Therapy, 103060B (21 January 1990); https://doi.org/10.1117/12.2283673
ACCESS THE FULL ARTICLE
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
The alert did not successfully save. Please try again later.
Charles J. Gomer, "Basic mechanisms and subcellular targets related to PDT," Proc. SPIE 10306, Future Directions and Applications in Photodynamic Therapy, 103060B (21 January 1990); https://doi.org/10.1117/12.2283673