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Fluorescence and absorption assessment of a lipid mTHPC formulation following topical application in a non-melanotic skin tumor model

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dc.contributor.author Johansson, A en
dc.contributor.author Svensson, J en
dc.contributor.author Bendsoe, N en
dc.contributor.author Svanberg, K en
dc.contributor.author Alexandratou, E en
dc.contributor.author Kyriazi, M en
dc.contributor.author Yova, D en
dc.contributor.author Grafe, S en
dc.contributor.author Trebst, T en
dc.contributor.author Andersson-Engels, S en
dc.date.accessioned 2014-03-01T01:26:22Z
dc.date.available 2014-03-01T01:26:22Z
dc.date.issued 2007 en
dc.identifier.issn 1083-3668 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/18039
dc.subject Absorption spectroscopy en
dc.subject Fluorescence imaging en
dc.subject mTHPC en
dc.subject Pharmacokinetics en
dc.subject Photodynamic therapy en
dc.subject.classification Biochemical Research Methods en
dc.subject.classification Optics en
dc.subject.classification Radiology, Nuclear Medicine & Medical Imaging en
dc.subject.other antineoplastic agent en
dc.subject.other drug carrier en
dc.subject.other lipid en
dc.subject.other liposome en
dc.subject.other mesoporphyrin en
dc.subject.other photosensitizing agent en
dc.subject.other temoporfin en
dc.subject.other animal en
dc.subject.other article en
dc.subject.other chemistry en
dc.subject.other disease model en
dc.subject.other fluorescence microscopy en
dc.subject.other hairless mouse en
dc.subject.other male en
dc.subject.other melanoma en
dc.subject.other metabolism en
dc.subject.other methodology en
dc.subject.other mouse en
dc.subject.other pathology en
dc.subject.other photochemotherapy en
dc.subject.other skin absorption en
dc.subject.other skin tumor en
dc.subject.other topical drug administration en
dc.subject.other treatment outcome en
dc.subject.other Administration, Topical en
dc.subject.other Animals en
dc.subject.other Antineoplastic Agents en
dc.subject.other Disease Models, Animal en
dc.subject.other Drug Carriers en
dc.subject.other Lipids en
dc.subject.other Liposomes en
dc.subject.other Male en
dc.subject.other Melanoma en
dc.subject.other Mesoporphyrins en
dc.subject.other Mice en
dc.subject.other Mice, Inbred HRS en
dc.subject.other Microscopy, Fluorescence en
dc.subject.other Photochemotherapy en
dc.subject.other Photosensitizing Agents en
dc.subject.other Skin Absorption en
dc.subject.other Skin Neoplasms en
dc.subject.other Treatment Outcome en
dc.subject.other Absorption spectroscopy en
dc.subject.other Fluorescence en
dc.subject.other Liposomes en
dc.subject.other Pharmacokinetics en
dc.subject.other Photosensitivity en
dc.subject.other Photosensitizers en
dc.subject.other Porphyrins en
dc.subject.other Skin en
dc.subject.other Tumors en
dc.subject.other Meso-tetra(hydroxyphenyl)chlorin en
dc.subject.other Non-melanotic skin tumor model en
dc.subject.other Photodynamic therapy en
dc.subject.other Murinae en
dc.subject.other Tetra en
dc.title Fluorescence and absorption assessment of a lipid mTHPC formulation following topical application in a non-melanotic skin tumor model en
heal.type journalArticle en
heal.identifier.primary 10.1117/1.2743080 en
heal.identifier.secondary http://dx.doi.org/10.1117/1.2743080 en
heal.identifier.secondary 034026 en
heal.language English en
heal.publicationDate 2007 en
heal.abstract Although the benefits of topical sensitizer administration have been confirmed for photodynamic therapy (PDT) ALA-induced, protoporphyrin IX is the only sensitizer clinically used with this administration route. Unfortunately, ALA-PDT results in poor treatment response for thicker lesions. Here, selectivity and depth distribution of the highly potent sensitizer meso-tetra(hydroxyphenyl)chlorin (mTHPC), supplied in a novel liposome formulation was investigated following topical administration for 4 and 6 h in a murine skin tumor model. Extraction data indicated an average [standard deviation (SD)] mTHPC concentration within lesions of 6.0(+/- 3.1) ng/mg tissue with no significant difference (p<0.05) between 4- and 6-h application times and undetectable levels of generalized photosensitivity. Absorption spectroscopy and chemical extraction both indicated a significant selectivity between lesion and normal surrounding skin at 4 and 6 h, whereas the more sensitive fluorescence imaging setup revealed significant selectivity only for the 4-h application time. Absorption data showed a significant correlation with extraction, whereas the results from the fluorescence imaging setup did not correlate with the other methods. Our results indicate that this sensitizer formulation and administration path could be interesting for topical mTHPC-PDT, decreasing the effects of extended skin photosensitivity associated with systemic mTHPC administration. (C) 2007 Society of Photo-Optical instrumentation Engineers. en
heal.publisher SPIE-SOC PHOTOPTICAL INSTRUMENTATION ENGINEERS en
heal.journalName Journal of Biomedical Optics en
dc.identifier.doi 10.1117/1.2743080 en
dc.identifier.isi ISI:000248504500030 en
dc.identifier.volume 12 en
dc.identifier.issue 3 en


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