A Novel Approach to a Bifunctional Photosensitizer for Tumor Imaging and Phototherapy

Optical imaging has attracted a great attention for studying molecular recognitions because minute fluorescent tracers can be detected in homogeneous and heterogeneous media with existing laboratory instruments. In our preliminary study, a clinically relevant photosensitizer (HPPH, a chlorophyll-a a...

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Published inBioconjugate chemistry Vol. 16; no. 5; pp. 1264 - 1274
Main Authors Chen, Yihui, Gryshuk, Amy, Achilefu, Samuel, Ohulchansky, Tymish, Potter, William, Zhong, Tuoxiu, Morgan, Janet, Chance, Britton, Prasad, Paras N, Henderson, Barbara W, Oseroff, Allan, Pandey, Ravindra K
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 01.09.2005
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Abstract Optical imaging has attracted a great attention for studying molecular recognitions because minute fluorescent tracers can be detected in homogeneous and heterogeneous media with existing laboratory instruments. In our preliminary study, a clinically relevant photosensitizer (HPPH, a chlorophyll-a analog) was linked with a cyanine dye (with required photophysical characteristics but limited tumor selectivity), and the resulting conjugate was found to be an efficient tumor imaging (fluorescence imaging) and photosensitizing agent. Compared to HPPH, the presence of the cyanine dye moiety in the conjugate produced a significantly higher uptake in tumor than skin. At a therapeutic/imaging dose, the conjugate did not show any significant skin phototoxicity, a major drawback associated with most of the porphyrin-based photosensitizers. These results suggest that tumor-avid porphyrin-based compounds can be used as “vehicles” to deliver the desired fluorescent agent(s) to tumor. The development of tumor imaging or improved photodynamic therapy agent(s) by itself represents an important step, but a dual function agent (fluorescence imaging and photodynamic therapy) provides the potential for tumor detection and targeted photodynamic therapy, combining two modalities into a single cost-effective “see and treat” approach.
AbstractList Optical imaging has attracted a great attention for studying molecular recognitions because minute fluorescent tracers can be detected in homogeneous and heterogeneous media with existing laboratory instruments. In our preliminary study, a clinically relevant photosensitizer (HPPH, a chlorophyll-a analog) was linked with a cyanine dye (with required photophysical characteristics but limited tumor selectivity), and the resulting conjugate was found to be an efficient tumor imaging (fluorescence imaging) and photosensitizing agent. Compared to HPPH, the presence of the cyanine dye moiety in the conjugate produced a significantly higher uptake in tumor than skin. At a therapeutic/imaging dose, the conjugate did not show any significant skin phototoxicity, a major drawback associated with most of the porphyrin-based photosensitizers. These results suggest that tumor-avid porphyrin-based compounds can be used as "vehicles" to deliver the desired fluorescent agent(s) to tumor. The development of tumor imaging or improved photodynamic therapy agent(s) by itself represents an important step, but a dual function agent (fluorescence imaging and photodynamic therapy) provides the potential for tumor detection and targeted photodynamic therapy, combining two modalities into a single cost-effective "see and treat" approach.
Optical imaging has attracted a great attention for studying molecular recognitions because minute fluorescent tracers can be detected in homogeneous and heterogeneous media with existing laboratory instruments. In our preliminary study, a clinically relevant photosensitizer (HPPH, a chlorophyll-a analog) was linked with a cyanine dye (with required photophysical characteristics but limited tumor selectivity), and the resulting conjugate was found to be an efficient tumor imaging (fluorescence imaging) and photosensitizing agent. Compared to HPPH, the presence of the cyanine dye moiety in the conjugate produced a significantly higher uptake in tumor than skin. At a therapeutic/imaging dose, the conjugate did not show any significant skin phototoxicity, a major drawback associated with most of the porphyrin-based photosensitizers. These results suggest that tumor-avid porphyrin-based compounds can be used as "vehicles" to deliver the desired fluorescent agent(s) to tumor. The development of tumor imaging or improved photodynamic therapy agent(s) by itself represents an important step, but a dual function agent (fluorescence imaging and photodynamic therapy) provides the potential for tumor detection and targeted photodynamic therapy, combining two modalities into a single cost-effective "see and treat" approach. [PUBLICATION ABSTRACT]
Author Ohulchansky, Tymish
Henderson, Barbara W
Potter, William
Prasad, Paras N
Achilefu, Samuel
Gryshuk, Amy
Chance, Britton
Zhong, Tuoxiu
Chen, Yihui
Pandey, Ravindra K
Morgan, Janet
Oseroff, Allan
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Snippet Optical imaging has attracted a great attention for studying molecular recognitions because minute fluorescent tracers can be detected in homogeneous and...
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SubjectTerms Animals
Cell Line
Dogs
Fluorescence
Medical imaging
Mice
Molecular Structure
Neoplasms - blood supply
Neoplasms - diagnosis
Neoplasms - drug therapy
Photochemotherapy
Photosensitizing Agents - chemistry
Photosensitizing Agents - pharmacology
Photosensitizing Agents - therapeutic use
Skin - drug effects
Spectrum Analysis
Tumors
Xenograft Model Antitumor Assays
Title A Novel Approach to a Bifunctional Photosensitizer for Tumor Imaging and Phototherapy
URI http://dx.doi.org/10.1021/bc050177o
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https://www.proquest.com/docview/216201478/abstract/
https://search.proquest.com/docview/19412628
https://search.proquest.com/docview/68603380
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