2019
CdS quantum dots-based immunoassay combined with particle imprinted polymer technology and laser ablation ICP-MS as a versatile tool for protein detection
VANECKOVA, T.; J. BEZDEKOVA; Michaela TVRDOŇOVÁ; M. VLCNOVSKA; V. NOVOTNA et. al.Základní údaje
Originální název
CdS quantum dots-based immunoassay combined with particle imprinted polymer technology and laser ablation ICP-MS as a versatile tool for protein detection
Autoři
VANECKOVA, T.; J. BEZDEKOVA; Michaela TVRDOŇOVÁ; M. VLCNOVSKA; V. NOVOTNA; J. NEUMAN; Aneta ŠTOSSOVÁ; Viktor KANICKÝ; V. ADAM; M. VACULOVICOVA a Tomáš VACULOVIČ
Vydání
Scientific reports, LONDON, NATURE PUBLISHING GROUP, 2019, 2045-2322
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10406 Analytical chemistry
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.998
Kód RIV
RIV/00216224:14310/19:00113292
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000480678100039
EID Scopus
2-s2.0-85070782595
Klíčová slova anglicky
MAGNETIC NANOPARTICLES; SENSITIVE DETECTION; SURFACE-CHEMISTRY; RECOGNITION; SENSOR; EXTRACTION; SEPARATION; DNA
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 17. 3. 2020 19:50, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
For the first time, the combination of molecularly imprinted polymer (MIP) technology with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is presented with focus on an optimization of the LA-ICP-MS parameters such as laser beam diameter, laser beam fluence, and scan speed using CdS quantum dots (QDs) as a template and dopamine as a functional monomer. A non-covalent imprinting approach was employed in this study due to the simplicity of preparation. Simple oxidative polymerization of the dopamine that creates the self-assembly monolayer seems to be an ideal choice. The QDs prepared by UV light irradiation synthesis were stabilized by using mercaptosuccinic acid. Formation of a complex of QD-anti body and QD-antibody-antigen was verified by using capillary electrophoresis with laser-induced fluorescence detection. QDs and antibody were connected together via an affinity peptide linker. LA-ICP-MS was employed as a proof-of-concept for detection method of two types of immunoassay: 1) antigen extracted from the sample by MIP and subsequently overlaid/immunoreacted by QD-labelled antibodies, 2) complex of antigen, antibody, and QD formed in the sample and subsequently extracted by MIP. The first approach provided higher sensitivity (MIP/NIP), however, the second demonstrated higher selectivity. A mixture of proteins with size in range 10-250 kDa was used as a model sample to demonstrate the capability of both approaches for detection of IgG in a complex sample.
Návaznosti
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