Imaging of growth factors on a human tooth root canal by surface-enhanced Raman spectroscopy
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
16-02938S
Grantová Agentura České Republiky
NPU LO1305
Ministry of Education, Youth and Sports of the Czech Republic
PubMed
30112649
DOI
10.1007/s00216-018-1311-4
PII: 10.1007/s00216-018-1311-4
Knihovny.cz E-resources
- Keywords
- Growth factors, Imaging, Nanocomposites, SERS,
- MeSH
- Dentin chemistry MeSH
- Fibroblast Growth Factor 2 analysis MeSH
- Dental Pulp Cavity chemistry MeSH
- Bone Morphogenetic Protein 2 analysis MeSH
- Humans MeSH
- Nanocomposites chemistry MeSH
- Ferrosoferric Oxide chemistry MeSH
- Spectrum Analysis, Raman methods MeSH
- Silver chemistry MeSH
- Transforming Growth Factor beta analysis MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- BMP2 protein, human MeSH Browser
- Fibroblast Growth Factor 2 MeSH
- Bone Morphogenetic Protein 2 MeSH
- Ferrosoferric Oxide MeSH
- Silver MeSH
- Transforming Growth Factor beta MeSH
Endodontic treatment of immature permanent teeth with necrotic pulp poses several clinical challenges and is one of the most demanding interventions in endodontics. Recently, with new discoveries in the field of tissue engineering, novel treatment protocols have been established. The most promising treatment modality is revascularization, whose integral part is the exposure of collagen matrix and embedded growth factors. However, optimization of the treatment protocol requires a development of analytical procedures able to analyze growth factors directly on the sample surface. In this work, method based on surface-enhanced Raman spectroscopy (SERS) was developed to investigate the influence of the time of the medical treatment using EDTA on exposure and accessibility of the growth factors, namely TGF-ß1, BMP-2, and bFGF on the dentine surface. The nanotags, which consist of magnetic Fe3O4@Ag nanocomposite covalently functionalized by tagged antibodies (anti-TGF-ß1-Cy3, anti-BMP-2-Cy5, and anti-bFGF-Cy7), were employed as a SERS substrate. Each antibody was coupled with a unique label allowing us to perform a parallel analysis of all three growth factors within one analytical run. Developed methodology presents an interesting alternative to a fluorescence microscopy and in contrary allows evaluating a chemical composition and thus minimizing possible false-positive results. Graphical abstract.
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