Microbiological identification by surface-enhanced Raman spectroscopy

被引:18
|
作者
Chauvet, Romain [1 ,2 ]
Lagarde, Fabienne [1 ]
Charrier, Thomas [2 ]
Assaf, Ali [3 ]
Thouand, Gerald [3 ]
Daniel, Philippe [1 ]
机构
[1] Univ Maine, Inst Mol & Mat Mans, IMMM UMR CNRS 6283, F-72085 Le Mans, France
[2] EUROFINS, ELMO, Nantes, France
[3] Univ Nantes, Genie Proc Environm & Agrolimentaire, GEPEA UMR CNRS 6144, La Roche Sur Yon, France
关键词
Raman spectroscopy; bacteria; SERS; SINGLE LIVING CELLS; SCATTERING SERS; SILVER NANOPARTICLES; AG NANOPARTICLES; BACTERIAL-CELLS; PLASMONIC NANOPARTICLES; RELEVANT MICROORGANISMS; RAPID IDENTIFICATION; CARBON CONTAMINATION; GOLD NANOPARTICLES;
D O I
10.1080/05704928.2016.1209760
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
New methods for pathogens identification are of growing interest in clinical and food sectors. The challenge remains to develop rapid methods that are more simple, reliable, and specific. Surface-enhanced Raman spectroscopy (SERS) appears to be a promising tool to compete with current untargeted identification methods. This article presents the intensive research devoted to the use of SERS for bacterial identification, from the first to the very recent published results. Compared to normal Raman spectroscopy, the introduction of nanoparticles for SERS acquisition introduces a new degree of complexity. Bacterial Raman fingerprints, which are already subject to high spectral variability for a given strain, become then very dependent on numerous experimental parameters. To overcome these limitations, several approaches have been proposed to prepare the sample, from the microbiological culture conditions to the analysis of the spectrum including the coupling of nanoparticles on the bacterial membrane. Main strategies proposed over the last 20years are examined here and discussed in the perspective of a protocol transfer towards industry.
引用
收藏
页码:123 / 144
页数:22
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