scholarly journals Photosensitizing Agent

2020 ◽  
Author(s):  
Photobiology ◽  
1991 ◽  
pp. 839-845
Author(s):  
G. Jori ◽  
R. Biolo ◽  
C. Milanesi ◽  
E. Reddi ◽  
G. Valduga

1980 ◽  
Vol 11 (40) ◽  
Author(s):  
P. RODIGHIERO ◽  
A. GUIOTTO ◽  
G. PASTORINI ◽  
P. MANZINI ◽  
F. DALL'ACQUA ◽  
...  

1987 ◽  
Vol 73 (1) ◽  
pp. 11-17 ◽  
Author(s):  
Renato Marchesini ◽  
Elsa Melloni ◽  
Giovanni Bottiroli ◽  
Salvatore Andreola ◽  
Giannino Fava ◽  
...  

The main side effect in photodynamic therapy is photosensitization of the patient's skin following systemic administration of the photosensitizing agent. In the case of superficial lesions, this problem can be avoided by topically applying the drug: in this way a local treatment can be performed. We tested the photosensitizing properties of a 2 % solution of TPPS (tetrasodium-tetraphenylporphinesulfonate) in a vehicle containing a penetration enhancer, Azone, on skin of nude mice. An aliquot of 0.1 ml/cm2 of the solution was painted on the skin overlying an s.c. implanted NMU-1 tumor. Subsequently, animals were sacrificed at different times after application. Fluorescence microscopy revealed that TPPS penetration depth was related to time elapsed after application and to painting modalities. Solution penetration was enhanced by wiping with ether immediately before painting. Irradiation at 80 mW/cm2 for 20 min with a dye laser emitting at 640 am, 4 h after TPPS application, produced necrosis of the upper skin layers, up to 0.2 mm in depth. These findings suggest that topical TPPS administration, followed by laser irradiation, may be a suitable treatment modality for skin lesions involving epithelial layers, even though several aspects of this metodology need further investigation.


2004 ◽  
Vol 48 (6) ◽  
pp. 2000-2006 ◽  
Author(s):  
Joseph M. Bliss ◽  
Chad E. Bigelow ◽  
Thomas H. Foster ◽  
Constantine G. Haidaris

ABSTRACT The in vitro susceptibility of pathogenic Candida species to the photodynamic effects of the clinically approved photosensitizing agent Photofrin was examined. Internalization of Photofrin by Candida was confirmed by confocal fluorescence microscopy, and the degree of uptake was dependent on incubation concentration. Uptake of Photofrin by Candida and subsequent sensitivity to irradiation was influenced by culture conditions. Photofrin uptake was poor in C. albicans blastoconidia grown in nutrient broth. However, conversion of blastoconidia to filamentous forms by incubation in defined tissue culture medium resulted in substantial Photofrin uptake. Under conditions where Photofrin was effectively taken up by Candida, irradiated organisms were damaged in a drug dose- and light-dependent manner. Uptake of Photofrin was not inhibited by azide, indicating that the mechanism of uptake was not dependent on energy provided via electron transport. Fungal damage induced by Photofrin-mediated photodynamic therapy (PDT) was determined by evaluation of metabolic activity after irradiation. A strain of C. glabrata took up Photofrin poorly and was resistant to killing after irradiation. In contrast, two different strains of C. albicans displayed comparable levels of sensitivity to PDT. Furthermore, a reference strain of C. krusei that is relatively resistant to fluconazole compared to C. albicans was equally sensitive to C. albicans at Photofrin concentrations of ≥3 μg/ml. The results indicate that photodynamic therapy may be a useful adjunct or alternative to current anti-Candida therapeutic modalities, particularly for superficial infections on surfaces amenable to illumination.


2016 ◽  
Vol 510 (1) ◽  
pp. 240-249 ◽  
Author(s):  
Nathalia Luiza Andreazza ◽  
Christine Vevert-Bizet ◽  
Geneviève Bourg-Heckly ◽  
Franck Sureau ◽  
Marcos José Salvador ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Wei Li ◽  
Qingyong Ma ◽  
Erxi Wu

Photodynamic therapy (PDT) is a noninvasive procedure involving a photosensitizing agent that is activated by light to produce reactive oxygen species (ROS) that selectively destroy tumor cells. In recent years, PDT has been used in the treatment of pancreatic cancer (PC). The antitumor effects of PDT include three main mechanisms: direct tumor cell death (necrosis, apoptosis, and autophagy), vascular destruction, and immune system activation. The present paper systematically summarizes the effects of PDT in the treatment of PC from the experimental studies to the clinical studies and discusses the mechanisms of PDT-induced PC destruction.


2008 ◽  
Vol 139 (11) ◽  
pp. 1387-1390 ◽  
Author(s):  
Joachim Zuschrader ◽  
Wolfgang Schöfberger ◽  
Heinz Falk

1986 ◽  
Vol 65 (3) ◽  
pp. 364-369 ◽  
Author(s):  
John D. Steichen ◽  
Kathleen Dashner ◽  
Robert L. Martuza

✓ Hematoporphyrin derivative (HPD) is a photosensitizing agent that has been used to locate and kill tumors. The distribution of tritiated (3H)-HPD was studied in a transplantable canine glioma model following intraperitoneal or direct intraneoplastic injection. Compared to intraperitoneal adminstration of 3H-HPD, direct injection resulted in levels that were more than 2.5 times higher in tumor tissue and approximately 10 times lower in skin. Dose-corrected analysis of the data indicated that outside the central nervous system (CNS) the distribution of 3H-HPD is dose-related, regardless of route of injection. Within the CNS, direct injection leads to more efficient uptake of 3H-HPD, especially at the tumor periphery. Fluorescence microscopy confirmed the selective biodistribution of HPD fluorescence within the cytoplasm of tumor cells.


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