Abstract
A supramolecular five-component cascade is presented that enables light-controlled transport of an in situ modified ligand between three host systems based on the different complexation preferences of cyclodextrin, cucurbituril, and double-stranded DNA. The results point out novel approaches for the control of drug-DNA interactions in DNA-targeting therapy.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Cyclodextrins / chemistry*
-
DNA / chemistry*
-
DNA / radiation effects*
-
Drug Carriers
-
Drug Delivery Systems
-
Drug Liberation
-
Ligands
-
Light*
-
Macrocyclic Compounds / chemistry*
-
Macromolecular Substances
Substances
-
Cyclodextrins
-
Drug Carriers
-
Ligands
-
Macrocyclic Compounds
-
Macromolecular Substances
-
cucurbit(n)uril
-
DNA