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. 2017 Feb;87:478–486. doi: 10.1016/j.eurpolymj.2016.08.023

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© 2016 The Authors

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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Fig. 7 — (A) Representative agar plates used to evaluate antimicrobial activity of Pol-B containing PIC particles. Lane 1: No dilution, lane 2: 10²-fold dilution, lane 3: 10⁴-fold dilution, lane 4: 10⁶-fold dilution, and lane 5: 10⁸-fold dilution. (B) CFU/mL of P. aeruginosa in the absence (media, ) and presence of PSS () or PIC particles prepared at different [N:SO₃Na] ratios (dots, each colour represents a different particle formulation). Experiments were done in triplicate in 1:1 LB:HEPES media.

Inline graphic — (A) Representative agar plates used to evaluate antimicrobial activity of Pol-B containing PIC particles. Lane 1: No dilution, lane 2: 10²-fold dilution, lane 3: 10⁴-fold dilution, lane 4: 10⁶-fold dilution, and lane 5: 10⁸-fold dilution. (B) CFU/mL of P. aeruginosa in the absence (media, ) and presence of PSS () or PIC particles prepared at different [N:SO₃Na] ratios (dots, each colour represents a different particle formulation). Experiments were done in triplicate in 1:1 LB:HEPES media.

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