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Photodynamic Therapy

Thomas J. DoughertyPhotodynamic Therapy Center, Roswell Park Cancer Institute, Buffalo, NY, USACharles J. GomerUniversity of Southern California, Los AngelesBarbara W. HendersonPhotodynamic Therapy Center, Roswell Park Cancer Institute, Buffalo, NYG. JoriDepartment of Biology, University of Padova, ItalyDavid KesselDepartment of Pharmacology, Wayne State University, School of Medicine, Detroit, MIMladen KorbelikCancer Imaging, British Columbia Cancer Agency, Vancouver, BC, CanadaJohan MoanDepartment of Biophysics, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, NorwayQian PengDepartments of Pathology and Biophysics, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, Norway
1998en
ABI

Annotatsiya

Photodynamic therapy involves administration of a tumor-localizing photosensitizing agent, which may require metabolic synthesis (i.e., a prodrug), followed by activation of the agent by light of a specific wavelength. This therapy results in a sequence of photochemical and photobiologic processes that cause irreversible photodamage to tumor tissues. Results from preclinical and clinical studies conducted worldwide over a 25-year period have established photodynamic therapy as a useful treatment approach for some cancers. Since 1993, regulatory approval for photodynamic therapy involving use of a partially purified, commercially available hematoporphyrin derivative compound (Photofrin) in patients with early and advanced stage cancer of the lung, digestive tract, and genitourinary tract has been obtained in Canada, The Netherlands, France, Germany, Japan, and the United States. We have attempted to conduct and present a comprehensive review of this rapidly expanding field. Mechanisms of subcellular and tumor localization of photosensitizing agents, as well as of molecular, cellular, and tumor responses associated with photodynamic therapy, are discussed. Technical issues regarding light dosimetry are also considered.

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