Photodynamic therapy using Verteporfin (benzoporphyrin derivative monoacid ring A, BPD-MA) and 630 nm laser light in canine esophagus

Background and Objective Verteporfin is a new photosensitizer with short‐term skin photosensitivity. The objective of this preclinical study was to find the light dose that effectively ablates canine esophageal mucosa when delivered 30 minutes after Verteporfin injection. Study Design/Materials and...

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Published inLasers in surgery and medicine Vol. 30; no. 1; pp. 26 - 30
Main Authors Panjehpour, Masoud, DeNovo, Robert C., Petersen, Mark G., Overholt, Bergein F., Bower, Robert, Rubinchik, Valery, Kelly, Barbara
Format Journal Article
LanguageEnglish
Published New York John Wiley & Sons, Inc 01.01.2002
Wiley-Liss
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Summary:Background and Objective Verteporfin is a new photosensitizer with short‐term skin photosensitivity. The objective of this preclinical study was to find the light dose that effectively ablates canine esophageal mucosa when delivered 30 minutes after Verteporfin injection. Study Design/Materials and Methods Verteporfin was administered intravenously (0.75 mg/kg). 630 nm light from KTP/Dye laser was delivered using an esophageal Photodynamic therapy (PDT) balloon. In Phase I study, animals were treated 30 minutes after drug injection using 40, 60, and 80 J/cm to find the desired light dose. Using results from phase I and application of reciprocity principle (light dose vs. plasma concentration of drug), additional light doses were calculated for delivery at other times. In phase II, animals were treated at 15, 60, and 120 minutes, using the calculated light doses of 60, 145, and 200 J/cm, respectively. Animals were followed for 2 days to 4 weeks. Results In Phase I, 80 J/cm at 30 minutes induced total mucosal ablation. In Phase II, light doses of 60, 145, and 200 J/cm induced similar mucosal injuries when delivered at 15, 60, and 120 minutes, respectively. Conclusions Effective mucosal ablation in canine esophagus was achieved using Verteporfin and 630 nm light doses of 60, 80, 145, and 200 J/cm when delivered at 15, 30, 60, and 120 minutes after the drug injection, respectively. Lasers Surg. Med. 30:26–30, 2002. © 2002 Wiley‐Liss, Inc.
Bibliography:ArticleID:LSM10014
Thompson Cancer Survival Center, (Knoxville, TN)
istex:ECD70DE9AC7A17414DD5386C82B13D3AC0D1F658
QLT, Inc., (Vancouver, British Columbia, Canada)
Robert Bower, Valery Rubinchik, and Barbara Kelly have disclosed a potentical conflict of interest with this study.
ark:/67375/WNG-CPX6VVWQ-4
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:0196-8092
1096-9101
DOI:10.1002/lsm.10014