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1.
Figure 1

Figure 1. From: Evaluation of the Antimicrobial Activity of Cationic Polymers against Mycobacteria: Toward Antitubercular Macromolecules.

SEC analysis of polymers used in this study, as shown in .

Daniel J. Phillips, et al. Biomacromolecules. 2017 May 8;18(5):1592-1599.
3.
Figure 2

Figure 2. From: Evaluation of the Antimicrobial Activity of Cationic Polymers against Mycobacteria: Toward Antitubercular Macromolecules.

Time-kill assay of P3 against M. smegmatis. Errors bars represent the standard deviation from n = 3.

Daniel J. Phillips, et al. Biomacromolecules. 2017 May 8;18(5):1592-1599.
4.
Figure 5

Figure 5. From: Evaluation of the Antimicrobial Activity of Cationic Polymers against Mycobacteria: Toward Antitubercular Macromolecules.

TEM analysis of M. smegmatis with and without P1. P1 applied at 10 μg·mL–1 (0.3× MIC99). Top three panels, scale bar = 1 μm. Bottom three panels, scale bar = 100 nm.

Daniel J. Phillips, et al. Biomacromolecules. 2017 May 8;18(5):1592-1599.
5.
Figure 3

Figure 3. From: Evaluation of the Antimicrobial Activity of Cationic Polymers against Mycobacteria: Toward Antitubercular Macromolecules.

Assessment of hemolytic activity of polymers P24 after 1 h of exposure against ovine red blood cells. Error bars represent the standard deviation n = 3.

Daniel J. Phillips, et al. Biomacromolecules. 2017 May 8;18(5):1592-1599.
6.
Figure 4

Figure 4. From: Evaluation of the Antimicrobial Activity of Cationic Polymers against Mycobacteria: Toward Antitubercular Macromolecules.

Fluorescence microscopy of M. smegmatis upon exposure to varying concentrations of P3 and P4. Green channel is SYTO-9 (nucleic acid stain), and red is propidium iodide (damage membrane stain). Each image is 85 × 85 μm2.

Daniel J. Phillips, et al. Biomacromolecules. 2017 May 8;18(5):1592-1599.

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