“…This can be achieved using different non-covalent binding modes, including intercalation, [12][13][14] groove-binding, [15][16][17] or simple electrostatic binding. [18][19][20] Depending on the drug molecule in question, these rather straightforward drug loading approaches unfortunately often suffer from complications such as a competition of several different binding modes, 15,21,22 limited accessibility of binding sites, 15,23 and difficulties in the unambiguous detection of drug-DNA binding events. The latter is usually attempted by analyzing binding-specific UV-vis or fluorescence spectroscopic signatures, which may, however, be obscured by or sometimes even originate in other processes such as drug aggregation.…”