Selective Imaging and Inactivation of Bacteria over Mammalian Cells by Imidazolium-Substituted Polythiophene

被引:82
作者
Huang, Yun [1 ,3 ]
Pappas, Harry C. [2 ]
Zhang, Liqin [3 ]
Wang, Shanshan [3 ]
Ca, Ren [3 ]
Tan, Weihong [3 ]
Wang, Shu [4 ]
Whitten, David G. [2 ]
Schanze, Kirk S. [1 ]
机构
[1] Univ Texas San Antonio, Dept Chem, One UTSA Circle, San Antonio, TX 78249 USA
[2] Univ New Mexico, Dept Chem & Biol Engn, Albuquerque, NM 87131 USA
[3] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[4] Chinese Acad Sci, Inst Chem, Key Lab Organ Solids, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
关键词
CATIONIC CONJUGATED POLYELECTROLYTES; BIOCIDAL ACTIVITY; PHOTODYNAMIC INACTIVATION; MEMBRANE; LIGHT; PHOTOPHYSICS; ETHYNYLENE); ADHESION; CHARGE; DARK;
D O I
10.1021/acs.chemmater.7b01796
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Antibiotic-resistant bacterial infections have become a serious public health threat. In an effort to address this threat, we develop an imidazolium-functionalized conjugated polyelectrolyte that exhibits profound light-activated biocidal activity. Here we report the synthesis, photophysical properties, and biocidal activity of a regioregular head-to-tail polythiophene substituted with cationic imidazolium units (P3HT-Im) prepared by Grignard metathesis controlled polymerization. In water, P3HT-Im has a broad absorption in the visible region and exhibited a remarkably high biocidal efficiency with both Gram-positive and Gram-negative bacteria at sub-microgram per milliliter concentrations. Moreover, mammalian cell studies suggest that P3HT-Im is nontoxic to mammalian cells at concentrations of <= 20 mu g/mL over a short time scale (<= 1 h) in the dark and light, and the targeting rate-dependent selective mechanism is revealed. This Study demonstrates the capability of P3HT-Im to achieve selective imaging and inactivation of bacteria over mammalian cells, suggesting that the polymer has significant potential for ameliorating antibiotic-resistant bacteria in a clinical setting.
引用
收藏
页码:6389 / 6395
页数:7
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