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Improvement of Photodynamic Activity by a Stable System Consisting of a C 60 Derivative and Photoantenna in Liposomes
A dyad system comprising a lipid membrane-incorporated fullerene derivative with an , -dimethylpyrrodinium group (C - ) and a photoantenna molecule (DiD) did not exhibit the high photodynamic activity expected based on its singlet oxygen generation ability. Comparison with a fullerene derivative wit...
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Published in: | ACS medicinal chemistry letters 2022-04, Vol.13 (4), p.641-647 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A dyad system comprising a lipid membrane-incorporated fullerene derivative with an
,
-dimethylpyrrodinium group (C
-
) and a photoantenna molecule (DiD) did not exhibit the high photodynamic activity expected based on its singlet oxygen generation ability. Comparison with a fullerene derivative with an amide substituent (C
-
) suggested the cause to be that some of the fullerene derivative had been released from the liposomes, partly disrupting the dyad system. The dyad system of C
-
and DiD exhibited about twice the photodynamic activity toward HeLa cells as that of C
-
and DiD, due to the suppression of the release of the fullerene derivative from the liposomes. The hydrophobicity/hydrophilicity balance of the substituent in fullerene derivatives was shown to be very important to obtain a dyad system in liposomes characterized by high photodynamic activity. |
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ISSN: | 1948-5875 1948-5875 |
DOI: | 10.1021/acsmedchemlett.1c00691 |