4.7 Article

SERS-active Au@Ag core-shell nanorod (Au@AgNR) tags for ultrasensitive bacteria detection and antibiotic-susceptibility testing

期刊

TALANTA
卷 220, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2020.121397

关键词

Au@AgNR; SERS nanotag; Antibiotic susceptibility testing; Minimum inhibitory concentration; Principal component analysis

资金

  1. National Natural Science Foundation of China [21605005, 81530030, 81873697, 21976209]
  2. National Research Foundation of Korea [2019R1A2C3004375, 2018M3A7B4071203]
  3. Research Initiation Fund of Binzhou Medical University [BY2019KYQD39]
  4. Taishan Scholar Project Special Funding [ts20190962]

向作者/读者索取更多资源

There is a challenge to obtain an ultrasensitive and rapid approach to detect bacteria and identify resistance. As a powerful bioanalytical tool, surface-enhanced Raman scattering (SERS) in bacterial detection have attracted increasing attentions. Herein, we developed a SERS-active Au@Ag core-shell nanorod (Au@AgNR) tag platform for ultrasensitive bacteria detection and antibiotic-susceptibility testing (AST). The platform established that surface enhanced Raman scattered Rhodamine 6G (R6G) absorption at 1517 cm(-1) had a good linearity (RI = 3865 + 193logC; R-2 = 0.97) with logarithm of E. coli concentration over a range of 10(7)-10(2) CFU (colony forming unit)/mL with limit of detection as low 10(2) CFU/mL. When E. coli was exposed to ampicillin at minimum inhibitory concentration (MIC, 4 mu g/mL), Raman spectroscopy showed the obvious variation between ampicillin-susceptible E. coli (Amp(-)-E. coli) and the ampicillin-resistant E. coli (Amp(+)-E. coli). Combined with principal component analysis (PCA) statistical analysis, the Raman intensity variation mentioned above allows to obtain rapid antibiotic resistance testing (<3.5 h). In addition, E.coli spiked into blood from C57BL/6 mice can be identified clearly, indicating the potential for point-of-care diagnostics.

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