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Magnetic nanohybrids loaded with bimetal core-shell-shell nanorods for bacteria capture, separation, and near-infrared photothermal treatment.

Identifieur interne : 000772 ( Main/Corpus ); précédent : 000771; suivant : 000773

Magnetic nanohybrids loaded with bimetal core-shell-shell nanorods for bacteria capture, separation, and near-infrared photothermal treatment.

Auteurs : Bo Hu ; Ning Wang ; Lu Han ; Ming-Li Chen ; Jian-Hua Wang

Source :

RBID : pubmed:25754902

English descriptors

Abstract

A novel antimicrobial nanohybrid based on near-infrared (NIR) photothermal conversion is designed for bacteria capture, separation, and sterilization (killing). Positively charged magnetic reduced graphene oxide with modification by polyethylenimine (rGO-Fe3 O4 -PEI) is prepared and then loaded with core-shell-shell Au-Ag-Au nanorods to construct the nanohybrid rGO-Fe3 O4 -Au-Ag-Au. NIR laser irradiation melts the outer Au shell and exposes the inner Ag shell, which facilitates controlled release of the silver shell. The nanohybrids combine physical photothermal sterilization as a result of the outer Au shell with the antibacterial effect of the inner Ag shell. In addition, the nanohybrid exhibits high heat conductivity because of the rGO and rapid magnetic-separation capability that is attributable to Fe3 O4 . The nanohybrid provides a significant improvement of bactericidal efficiency with respect to bare Au-Ag-Au nanorods and facilitates the isolation of bacteria from sample matrixes. A concentration of 25 μg mL(-1) of nanohybrid causes 100 % capture and separation of Escherichia coli O157:H7 (1×10(8) cfu mL(-1) ) from an aqueous medium in 10 min. In addition, it causes a 22 °C temperature rise for the surrounding solution under NIR irradiation (785 nm, 50 mW cm(-2) ) for 10 min. With magnetic separation, 30 μg mL(-1) of nanohybrid results in a 100 % killing rate for E. coli O157:H7 cells. The facile bacteria separation and photothermal sterilization is potentially feasible for environmental and/or clinical treatment.

DOI: 10.1002/chem.201405960
PubMed: 25754902

Links to Exploration step

pubmed:25754902

Le document en format XML

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