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Aptamer-functionalized pH-responsive polymer-modified magnetic nanoparticles for specific enrichment and sensitive determination of lactoferrin.

Authors :
Ma, Yao
Zhao, Liping
Li, Linsen
Zhu, Chao
Qu, Feng
Source :
Microchimica Acta; Jan2023, Vol. 190 Issue 1, p1-9, 9p
Publication Year :
2023

Abstract

A new type of aptamer-functionalized pH-responsive polymer-modified magnetic nanoparticles (ApMNPs) is introduced for specific enrichment and sensitive determination of lactoferrin (Lf) in complex matrixes. In the construction, Fe<subscript>3</subscript>O<subscript>4</subscript>@3-(Triethoxysilyl)propylmethacrylate@poly(4-Vinyl-1, 3-dioxolan-2-one-acrylic acid) (Fe<subscript>3</subscript>O<subscript>4</subscript>@MPS@p(VEC-AA)) were synthesized as pH-responsive polymer-modified magnetic nanoparticles (pMNPs) through free radical polymerization to increase the tunable interaction. Lf-binding aptamers were conjugated onto pMNPs through the reaction of amino-group in aptamer and epoxide-group in VEC, innovatively applied to prepare Lf-ApMNPs. On the basis of the synergistic effect of specific affinity of aptamer on Lf and tunable hydrophobic/hydrophilic property of pH-responsive polymer, Lf-ApMNPs presented good selectivity toward Lf, excellent adsorption capacity (as high as 233.9 mg g<superscript>−1</superscript>), as well as good recoveries in the range 93.6–99.6% in Lf-related nutrition samples. Significantly, the introduction of pH-responsive monomer (AA) effectively regulated the adsorption–desorption process of Lf, with the function similar to a switch. Moreover, the good performances of Ct-ApMNPs toward α-Chymotrypsin showed that ApMNPs exhibited universality to other proteins through easily changing the binding aptamer, thereby offering a facile and efficient approach for specific enrichment and sensitive determination of targets in real biological samples. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00263672
Volume :
190
Issue :
1
Database :
Complementary Index
Journal :
Microchimica Acta
Publication Type :
Academic Journal
Accession number :
161300711
Full Text :
https://doi.org/10.1007/s00604-022-05589-8