Strain-induced crack formations in PDMS/DXA drug collars.

Drug-eluting systems are currently used in cardiac leads in order to reduce inflammation and fibrosis at the lead-tissue interface. Drug release from these drug delivery systems can be modulated by the manufacturing processes used to create the drug systems and assemble them onto the cardiac lead. In this study, scanning electron microscopy, atomic force microscopy and Raman microscopy are employed to explore the material characteristics of a polydimethylsiloxane-dexamethasone acetate drug collar used on cardiac leads when varying the strain during collar assembly on the lead.