Publication | Closed Access
Loading and Release of Drugs from Oxygen‐rich Plasma Polymer Coatings
35
Citations
41
References
2012
Year
EngineeringPlasma MedicinePolymersPharmaceutical TechnologyDrug Delivery SystemAntimicrobial ResistancePolymer ChemistryVancomycin PenetrationAntibacterial AgentAntimicrobial CompoundPharmacologyRelease MechanismAntimicrobial PackagingAntimicrobial SusceptibilityAntibioticsOxygen GroupsPolymer ScienceDrug Delivery SystemsEthylene Film CoatingsAntimicrobial PharmacodynamicsMedicine
Abstract Low‐pressure plasma‐polymerized ethylene film coatings rich in bonded oxygen groups (L‐PPE:O) were deposited on poly(ethylene terephthalate; PET) in order to act as hosts for antimicrobial drugs. Increasing O 2 content in the ethylene (C 2 H 4 )/Ar–diluted oxygen (O 2 ) gas mixture reduced the deposition rate, but increased the concentration of bonded oxygen, [O], including that of carboxylic acid groups, [COOH], as determined by X‐ray photoelectron‐ (XPS) and Fourier transform infrared (FTIR) spectroscopies, and by toluidine blue O (TBO) assays. L‐PPE:O coatings took up and sustained the release of ciprofloxacin for several hours. Steric hindrance impeded vancomycin penetration into the cross‐linked L‐PPE:O coatings. Ciprofloxacin‐loaded L‐PPE:O coatings inhibited in vitro the growth of Staphylococcus aureus . Deposition of L‐PPE:O on medical devices may endow them with ability to prevent nosocomial infections. magnified image
| Year | Citations | |
|---|---|---|
Page 1
Page 1