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dc.contributor.authorHaylett, Ann K
dc.contributor.authorForbes, E
dc.contributor.authorMacLennan, A
dc.contributor.authorTruscott, T G
dc.contributor.authorMoore, James V
dc.date.accessioned2010-04-07T10:48:19Z
dc.date.available2010-04-07T10:48:19Z
dc.date.issued1996-08-02
dc.identifier.citationNovel asymmetric photosensitizers: an in vitro study. 1996, 105 (2):187-93 Cancer Lett.en
dc.identifier.issn0304-3835
dc.identifier.pmid8697443
dc.identifier.doi10.1016/0304-3835(96)04279-6
dc.identifier.urihttp://hdl.handle.net/10541/95847
dc.description.abstractA series of compounds based on an asymmetrical protoporphyrin molecule have been examined. The paired groups of sensitizers differed in terms of the presence or absence of a permanent positive charge, in the alkyl side chain length and in having either a primary or secondary amine substituent. The effects of these variables on drug uptake, partition coefficient and photodynamic cell kill were tested. Drug uptake and partition coefficient were shown to be correlated. Differences in gross uptake were found within paired groups of sensitizers although cell-associated uptake alone did not correlate with clonogenic cell survival. Of the compounds tested it was the sensitizers with alkyl side chains, rather than the permanently positively charged compounds, which resulted in the greatest degree of clonogenic cell kill.
dc.language.isoenen
dc.subjectSkin Canceren
dc.subjectCultured Tumour Cellsen
dc.subject.meshCell Survival
dc.subject.meshHumans
dc.subject.meshLethal Dose 50
dc.subject.meshLight
dc.subject.meshMelanoma
dc.subject.meshPermeability
dc.subject.meshPhotosensitizing Agents
dc.subject.meshSkin Neoplasms
dc.subject.meshTumor Cells, Cultured
dc.titleNovel asymmetric photosensitizers: an in vitro study.en
dc.typeArticleen
dc.contributor.departmentDepartment of Experimental Radiation Oncology, Paterson Institute for Cancer Research, Manchester, UK.en
dc.identifier.journalCancer Lettersen
html.description.abstractA series of compounds based on an asymmetrical protoporphyrin molecule have been examined. The paired groups of sensitizers differed in terms of the presence or absence of a permanent positive charge, in the alkyl side chain length and in having either a primary or secondary amine substituent. The effects of these variables on drug uptake, partition coefficient and photodynamic cell kill were tested. Drug uptake and partition coefficient were shown to be correlated. Differences in gross uptake were found within paired groups of sensitizers although cell-associated uptake alone did not correlate with clonogenic cell survival. Of the compounds tested it was the sensitizers with alkyl side chains, rather than the permanently positively charged compounds, which resulted in the greatest degree of clonogenic cell kill.


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