A novel PEG–haloperidol conjugate with a non-degradable linker shows the feasibility of using polymer–drug conjugates in a non-prodrug fashion
Literature Information
Felicity Heath, Amy Newman, Chiara Clementi, Gianfranco Pasut, Hong Lin, Gary J. Stephens, Benjamin J. Whalley, Helen M. I. Osborn, Francesca Greco
A PEG–haloperidol conjugate containing a non-biodegradable linker was synthesised. Incubation with rat plasma demonstrated excellent linker stability, and competition radioligand binding assays demonstrated retained binding to the D2-receptor. In silico studies predicted that the conjugate will not cross the blood–brain barrier (BBB), thus potentially restricting haloperidol action to one side of the BBB.
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