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3 protocols using pentadecafluorooctanoyl chloride

1

Antimicrobial Fluorinated Chitosan Synthesis

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Chitosan (degree of deacetylation:
92%, MW: 50–190 kDa), pentafluoropropionic anhydride, pentadecafluorooctanoyl
chloride, 2,3,4,5,6-pentafluorobenzaldehyde, glycidyl trimethylammonium
chloride (GTMAC), and silver nitrate (AgNO3) were purchased
from Sigma-Aldrich. Glacial acetic acid (AcOH), acetone, and all other
chemicals were purchased from reputable local commercial suppliers
and were of analytical reagent grade unless otherwise stated. The
water used in all experiments was double distilled.
Clinical
isolates of methicillin-resistant Staphylococcus aureus (MRSA) were obtained from Lancet Laboratories, Durban, South Africa,
with ethical approval BE394/15 from the Biomedical Research Ethical
Committee of the University of KwaZulu-Natal. Other reference strains
of bacteria, namely Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Streptococcus sanguinis ATCC 10556, Salmonella enterica ATCC
10708, Staphylococcus epidermidis ATCC
12228, Bacillus subtilis ATCC 6051,
and S. aureus ATCC 29213 and 43300
were obtained from the American Type Culture Collection (ATCC).
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2

Fluorinated EDOT Polymer Synthesis

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As described in the Supporting Information, fluorinated 3,4-ethylenedioxythiophene with a
perfluorooctanyl side chain (EDOTF) was custom-synthesized from hydroxymethyl
EDOT (95%) and pentadecafluorooctanoyl chloride (97%) obtained from
Sigma-Aldrich. High-molecular-weight PVC (HMW PVC), bis(2-ethylhexyl)
sebacate (DOS), potassium ionophore I (valinomycin), and tetrahydrofuran
(THF), all Selectophore grade, and anhydrous acetonitrile (ACN; 99.5%)
were purchased from Sigma-Aldrich. KTFAB (97%; Figure S-1) was obtained from Alfa Aesar, and KCl (99.999%,
Suprapur grade) was received from Merck Millipore. All aqueous solutions
were prepared from deionized water (DIW) with a resistivity of 18.2
MΩ cm (ELGA).
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3

Synthesis and Characterization of Fluorinated Chitosan Polymers

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Fluorinated methacrylamide chitosan (MACF) and methacrylamide chitosan were synthesized (Fig. 1) and characterized as previously described.25 (link), 38 (link) Briefly, to prepare MACF first 3 wt% chitosan (ChitoClear 43010, Primex, Siglufjordur, Iceland) was dissolved in 2 vol% acetic acid:water. Fluorinated groups were added to chitosan by adding 0.14 M pentadecafluorooctanoyl chloride (Sigma-Aldrich, Saint Louis, MO, USA). Next, the resulting polymer was modified with methacrylic anhydride (Sigma-Aldrich) to add methacrylate groups to the polymer to create MACF. For purification, MACF or MAC solutions were placed in dialysis membranes (12,000–14,000 Da MW cut-off; Spectra/Por, Spectrum Labs, Rancho Dominguez, CA, USA) and dialyzed against deionized water for 3 d with 3 changes of water each day followed by lyophilizing (Labconco, Kansas City, MO, USA) to yield dry MACF or MAC polymer.38 (link) Finally, small samples of each were dissolved in 2 vol% deuterated acetic acid/D2O and 1H and 19F nuclear magnetic resonance (NMR; Varian 500 MHz, Varian, Inc., Palo Alto, CA, USA) were conducted to find percent methacrylation and percent fluorination respectively as previously described. 25 (link), 38 (link)
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