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. Author manuscript; available in PMC: 2015 Jul 1.
Published in final edited form as: Adv Healthc Mater. 2014 Feb 4;3(7):1020–1025. doi: 10.1002/adhm.201300518

Figure 1.

Figure 1

(a) Chemical structures of monomers. (b–c) Confocal images of SYTO17 stained UPEC on (b) PPGdA 70 :30 TMPEMEdA or (c) BACOEA 70:30 MEEMA at 37 °C (left) and 4 °C (right). Each image is 160 × 160 µm. Images from controls are shown in Figure SI1. (d) Coverage of UPEC on polymer coupons or a glass coverslip grown at 37 °C (graphic file with name nihms566546ig1.jpg) and grown at 37 °C then incubated at 4 °C (graphic file with name nihms566546ig2.jpg) for 4 h. Error bar equals ± one standard deviation, n = 3. The coverage of bacteria on homopolymers of the 4 monomers after 72 h incubation is also shown. (e) By analysis of the supernatant and sonication of the substrates the –total number of bacterial cells on the substrate(graphic file with name nihms566546ig1.jpg) and in the supernatant (graphic file with name nihms566546ig2.jpg) on glass or PPGdA 70 :30 TMPEMEdA respectively was determined when either maintaining the temperature at 37 °C or reducing it to 4 °C.