| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1394776 | European Journal of Medicinal Chemistry | 2010 | 6 Pages |
Two-, three-, four and six-arm, star-shaped poly(ɛ-caprolactone) and polylactide homopolymers were synthesized via ring-opening polymerization of cyclic esters in the presence of glycerol, penthaerythritol, dipentaerythritol and poly(ethylene glycol) as initiators and stannous octoate as a catalyst. Thus obtained oligomers were successfully used in the synthesis of novel polyester conjugates of ciprofloxacin. The structures of the polymers and conjugates were determined by means of GPC, MALDI-TOF MS, NMR and IR studies. The in vitro release of ciprofloxacin from obtained conjugates was investigated.
Graphical abstractThe ciprofloxacin was covalently connected to the chain end of the two-, three-, four- and six-arm, star-shaped PCL and PLA via an ester linkage. The CIP release could be effectively controlled by altering the pH values of the environment. Figure optionsDownload full-size imageDownload as PowerPoint slide
