Volume 217, Issue 20 pp. 2243-2251
Full Paper

Temperature-Controlled Antimicrobial Release from Poly(diethylene glycol methylether methacrylate)-Functionalized Bottleneck-Structured Porous Silicon for the Inhibition of Bacterial Growth

Stephanie Müller

Stephanie Müller

Physical Chemistry I, Department of Chemistry and Biology & Research Center of Micro and Nanochemistry and Engineering (Cμ), University of Siegen, Adolf-Reichwein-Str. 2, 57076 Siegen, Germany

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Alex Cavallaro

Alex Cavallaro

School of Engineering, University of South Australia, Mawson Lakes, SA, 5095 Australia

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Krasimir Vasilev

Krasimir Vasilev

School of Engineering, University of South Australia, Mawson Lakes, SA, 5095 Australia

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Nicolas H. Voelcker

Corresponding Author

Nicolas H. Voelcker

Future Industries Institute, University of South Australia, Mawson Lakes Boulevard, 5095 Adelaide, Australia

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Holger Schönherr

Corresponding Author

Holger Schönherr

Physical Chemistry I, Department of Chemistry and Biology & Research Center of Micro and Nanochemistry and Engineering (Cμ), University of Siegen, Adolf-Reichwein-Str. 2, 57076 Siegen, Germany

E-mail: [email protected], [email protected]Search for more papers by this author
First published: 17 May 2016
Citations: 26

Abstract

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.

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