Search

Hyperbranched polyglycerols (HPGs) with hydrophobic cores and derivatized with methoxy poly(ethylene glycol) were synthesized and further functionalized with carboxylate groups to bind and deliver cisplatin. Low and high levels of carboxylate were conjugated to HPGs (HPG-C8/10-MePEG6.5-COOH113and HPG-C8/10-MePEG6.5-COOH348) and their structures were confirmed through NMR and FTIR spectroscopy and potentiometric titration. The hydrodynamic diameter of the HPGs ranged from 5−10 nm and the addition of COOH groups decreased the zeta potential of the polymers. HPG-C8/10-MePEG6.5-COOH113bound up to 10% w/w cisplatin, whereas HPG-C8/10-MePEG6.5-COOH348bound up to 20% w/w drug with 100% efficiency. Drug was released from HPG-C8/10-MePEG6.5-COOH113over 7 days at the same rate, regardless of the pH. Cisplatin release from HPG-C8/10-MePEG6.5-COOH348was significantly slower than HPG-C8/10-MePEG6.5-COOH113at pH 6 and 7.4, but similar at pH 4.5. Release of cisplatin into artificial urine was considerably faster than into buffer. Carboxylated HPGs demonstrated good biocompatibility, and drug-loaded HPGs effectively inhibited proliferation of KU-7-luc bladder cancer cells. [ABSTRACT FROM AUTHOR]