TY - JOUR
T1 - Temperature-Controlled Antimicrobial Release from Poly(diethylene glycol methylether methacrylate)-Functionalized Bottleneck-Structured Porous Silicon for the Inhibition of Bacterial Growth
AU - Müller, Stephanie
AU - Cavallaro, Alex
AU - Vasilev, Krasimir
AU - Voelcker, Nicolas H.
AU - Schönherr, Holger
PY - 2016/10
Y1 - 2016/10
N2 - Bacterial infections in wounds slow down the healing process and lead to increased morbidity in affected patients. Polymer coatings on porous membranes were investigated, which facilitate the in situ detection and treatment of, e.g., Escherichia coli and Staphylococcus aureus infections. The theranostic approach relies on the thermoresponsive polymer poly(diethylene glycol methylether methacrylate) (PDEGMA). The increase of the wound temperature due to infection is targeted in this proof of concept study for triggering the release of the fluorescent antibiotic levofloxacin from bottle-shaped porous silicon (pSi) membranes capped with PDEGMA brushes. Below their lower critical solution temperature (LCST) the PDEGMA brushes are expanded and the levofloxacin release is significantly retarded. By contrast, above the LCST the PDEGMA brushes collapse and levofloxacin is released rapidly, which is detectable in solution owing to its fluorescence properties. The concomitant inhibition of bacterial growth agrees favorably with the drug release determined by fluorescence spectroscopy. (Figure presented.).
AB - Bacterial infections in wounds slow down the healing process and lead to increased morbidity in affected patients. Polymer coatings on porous membranes were investigated, which facilitate the in situ detection and treatment of, e.g., Escherichia coli and Staphylococcus aureus infections. The theranostic approach relies on the thermoresponsive polymer poly(diethylene glycol methylether methacrylate) (PDEGMA). The increase of the wound temperature due to infection is targeted in this proof of concept study for triggering the release of the fluorescent antibiotic levofloxacin from bottle-shaped porous silicon (pSi) membranes capped with PDEGMA brushes. Below their lower critical solution temperature (LCST) the PDEGMA brushes are expanded and the levofloxacin release is significantly retarded. By contrast, above the LCST the PDEGMA brushes collapse and levofloxacin is released rapidly, which is detectable in solution owing to its fluorescence properties. The concomitant inhibition of bacterial growth agrees favorably with the drug release determined by fluorescence spectroscopy. (Figure presented.).
KW - atom transfer radical polymerization (ATRP)
KW - bacterial detection
KW - porous membrane
KW - release kinetics
KW - stimuli-sensitive polymers
UR - http://www.scopus.com/inward/record.url?scp=84970021085&partnerID=8YFLogxK
U2 - 10.1002/macp.201600099
DO - 10.1002/macp.201600099
M3 - Article
AN - SCOPUS:84970021085
SN - 1022-1352
VL - 217
SP - 2243
EP - 2251
JO - Macromolecular Chemistry and Physics
JF - Macromolecular Chemistry and Physics
IS - 20
ER -