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Details

Autor(en) / Beteiligte
Titel
Aptamer based fluorometric β-lactoglobulin assay based on the use of magnetic nanoparticles and carbon dots
Ist Teil von
  • Mikrochimica acta (1966), 2018-01, Vol.185 (1), p.40-8, Article 40
Ort / Verlag
Vienna: Springer Vienna
Erscheinungsjahr
2018
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • The authors describe a fluorometric aptamer based assay for detecting β-lactoglobulin by using carbon dots (C-dots) as a signal indicator. The aptamer was immoblized on magnetite (Fe 3 O 4 ) nanoparticles (MNPs), and the C-dots served as a label for the complementary oligonucleotide (cDNA). The assay is based on the hybridization that takes place between aptamer and cDNA. In the presence of β-lactoglobulin (β-LG), the aptamer preferentially binds to β-LG, and this leads to a partial release of the C-dots-cDNA into the solution. After magnetic separation, the supernatant of the solution contains the released C-dots-cDNA which are quantified by fluorometry, best under excitation/emission wavelengths of 354/447 nm. Under the optimal conditions, the fluorescence intensity is proportional to the logarithm of the β-LG concentration in the 0.25 to 50 ng mL −1 range, with a 37 pg mL −1 detection limit. The method was successfully applied to the determination of β-LG in hypoallergenic formulations, and the results demonstrated that this assay is a promising tool in food quality control. Conceivably, it also provides the opportunity for detection of other analytes. Graphical abstract Schematic of a novel aptamer based fluorometric β-lactoglobulin assay based on the use of magnetite (Fe 3 O 4 ) nanoparticles (MNPs) and carbon dots (C-dots). C-dots were used as a signal indicator and Fe 3 O 4 MNPs acted as a magnetic separator. This assay exhibits high sensitivity and selectivity with a detection limit as low as 37 pg mL −1 .

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