Abstract
New macromolecular conjugates of camptothecin were prepared. The polymeric matrixes were obtained by the ring-opening polymerization of ϵ-caprolactone, glycolide, rac-lactide or trimethylene carbonate. The synthesized polymers and camptothecin were coupled via 1,6-diisocyanatohexane. The received macromolecular conjugates of camptothecin were characterized by 1H and 13C-NMR or FT-IR spectroscopy. Toxicity of the received polymeric products were evaluated with bacterial luminescence test and two protozoan assays. Furthermore, the in vitro release of camptothecin from the obtained conjugates was investigated.
Acknowledgments
The authors are indebted to Andrzej Jaklewicz from the Medical University of Warsaw for the AAS analysis.