Tracing the Photoaddition of Pharmaceutical Psoralens to DNA.

Molecules

Institut für Physikalische Chemie, Heinrich-Heine-Universität Düsseldorf, Universitätsstr. 1, 40225 Düsseldorf, Germany.

Published: November 2020

The psoralens 8-methoxypsoralen (8-MOP), 4,5',8-trimethylpsoralen (TMP) and 5-methoxypsoralen (5-MOP) find clinical application in PUVA (psoralen + UVA) therapy. PUVA treats skin diseases like psoriasis and atopic eczema. Psoralens target the DNA of cells. Upon photo-excitation psoralens bind to the DNA base thymine. This photo-binding was studied using steady-state UV/Vis and IR spectroscopy as well as nanosecond transient UV/Vis absorption. The experiments show that the photo-addition of 8-MOP and TMP involve the psoralen triplet state and a biradical intermediate. 5-MOP forms a structurally different photo-product. Its formation could not be traced by the present spectroscopic technique.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696755PMC
http://dx.doi.org/10.3390/molecules25225242DOI Listing

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Tracing the Photoaddition of Pharmaceutical Psoralens to DNA.

Molecules

November 2020

Institut für Physikalische Chemie, Heinrich-Heine-Universität Düsseldorf, Universitätsstr. 1, 40225 Düsseldorf, Germany.

The psoralens 8-methoxypsoralen (8-MOP), 4,5',8-trimethylpsoralen (TMP) and 5-methoxypsoralen (5-MOP) find clinical application in PUVA (psoralen + UVA) therapy. PUVA treats skin diseases like psoriasis and atopic eczema. Psoralens target the DNA of cells.

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It is well known that furocumarins produce a photoaddition compound with DNA, RNA, and certain kinds of amino acids upon exposure to long-wave ultraviolet light (UVA). It is also well known that both psoralens and psoralen photoconjugated compounds are fluorescent. After 8-methoxypsoralen was administered systemically and subsequently activated by UVA exposure, the hair and the epidermis were taken and observed under a fluorescent light microscope.

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