Rapid SERS-based recognition of cell secretome on the folic acid-functionalized gold gratings
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F19%3A43919490" target="_blank" >RIV/60461373:22310/19:43919490 - isvavai.cz</a>
Result on the web
<a href="https://link.springer.com/article/10.1007%2Fs00216-019-01801-6" target="_blank" >https://link.springer.com/article/10.1007%2Fs00216-019-01801-6</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00216-019-01801-6" target="_blank" >10.1007/s00216-019-01801-6</a>
Alternative languages
Result language
angličtina
Original language name
Rapid SERS-based recognition of cell secretome on the folic acid-functionalized gold gratings
Original language description
Nowadays, functionalization of the plasmon-supported nanostructured surface is considered as a powerful tool for tumour cell recognition. In this study, the SERS on a surface plasmon polariton-supported gold grating functionalized with folic acid was used to demonstrate an unpretentious recognition of melanoma-associated fibroblasts. Using cultivation media conditioned by different cells, we were able to detect reproducible differences in the secretome of melanoma-associated and normal control fibroblasts. The homogeneous distribution of plasmon energy along the grating surface was proved to provide excellent SERS signal reproducibility, while, to increase the affinity of (bio)molecules to SERS substrate, folic acid molecules were covalently grafted to the gold gratings. As proof of concept, fibroblasts were cultured in vitro, and culture media from the normal and tumour-associated lines were collected and analysed with our proposed SERS substrates. Identifying individual peaks of the Raman spectra as well as comparing their relative intensities, we showed that the proposed functional SERS platform can recognise the melanoma-associated cells without the need for further statistical spectral evaluation directly. We also demonstrated that the SERS chip created provided a stable SERS signal over a period of 90 days without loss of sensitivity. [Figure not available: see fulltext.]. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
20501 - Materials engineering
Result continuities
Project
<a href="/en/project/NV15-33459A" target="_blank" >NV15-33459A: Biomedical photonic devices for advanced medicinal diagnostics and therapy</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Analytical and Bioanalytical Chemistry
ISSN
1618-2642
e-ISSN
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Volume of the periodical
411
Issue of the periodical within the volume
15
Country of publishing house
DE - GERMANY
Number of pages
11
Pages from-to
3309-3319
UT code for WoS article
000469757300009
EID of the result in the Scopus database
2-s2.0-85066499217