4.7 Article

Antibacterial mechanism for inactivation of E. Coli by AgNPs@polydoamine/titania nanotubes via speciation analysis of silver ions and silver nanoparticles by cation exchange reaction

期刊

MICROCHEMICAL JOURNAL
卷 160, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.microc.2020.105636

关键词

Cation exchange recation; Speciation analysis; Ag+ and AgNPs; E. Coli; Antibacterial mechanisms

资金

  1. National Natural Science Foundation of China [21605108]
  2. National Key Research and Development Program of China [2017YFB0702602]

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A method was developed for speciation analysis and accurate detection of silver ions and silver nanoparticles at trace levels. The results indicate that silver nanoparticles anchored on polydopamine/titania nanotubes play a crucial role in bactericidal action, while released silver ions synergistically enhance the antibacterial activity.
In this method, silver nanoparticles (AgNPs) were anchored on titania nanotubes (TNT) surface by chelation of polydopamine (PD) to generate an AgNPs@polydopamine/titania nanotubes (TPAS). To reveal the antibacterial mechanism of TPAS, a speciation analysis of silver ion (Ag+) and AgNPs was developed based on cation exchange reaction (CER). Owing to only the Ag+ can exchange the Cd2+ in the CdTe quantum dots (QDs), the speciation of Ag+ and AgNPs was realized via detecting the Cd2+ for the indirect but ultrasensitive detection of Ag+ by hydride generation (HG)-atomic fluorescence spectrometer (AFS). The limit of detections (LODs) of Ag+ and AgNPs were 0.0001 ng mL(-1). Relative standard deviations (n = 7) are better than 2.2% at a concentration of 0.02 ng mL(-1) Ag+. Due to this strategy, the trace AgNPs and Ag+ in antibacterial assay were accurately detected. The results show AgNPs anchored on TPAS predominantly contributed to bactericidal action by contact-killing. Ag+, released from TPAS, synergistically increased the antibacterial activity by release-killing. The proposed method has been successfully utilized for inactivation of E. Coli to explore the antibacterial mechanisms of AgNPs.

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