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A liposome encapsulated methylene blue-mediated electrochemical and UV-visible dual mode split-type immunoassay for the detection of 17β-estradiol.

Authors :
Xia Y
Liu Y
Tang Y
Chen Y
Li T
Zhao F
Zeng B
Source :
Talanta [Talanta] 2024 Aug 15; Vol. 276, pp. 126243. Date of Electronic Publication: 2024 May 10.
Publication Year :
2024

Abstract

Herein, we fabricated an electrochemical (EC) and UV-visible absorption (UV-vis) dual mode split-type immunoassay for the detection of 17β-estradiol (E2), which was mediated by liposome encapsulated methylene blue (MB@lip). MB molecule acted as the probe in the EC and UV-vis absorption dual mode detections, and its release was controlled by liposome. The competitive immune recognition was conducted between the E2 in the sample and E2 conjugated bovine serum protein (E2-BSA) adsorbed on the 96-wells plate in combining with E2 antibody labeled with MB@lip (E2-Ab/MB@lip). MB molecule could be released from the resulting immune composite of E2-BSA/E2-Ab/MB@lip in the presence of Triton X-100, and quantified by UV-vis and EC methods. The three-dimensional cross-linked reduced graphene oxide/Ti <subscript>3</subscript> C <subscript>2</subscript> (3D-rGO/Ti <subscript>3</subscript> C <subscript>2</subscript> ) aerogel was prepared through hydrothermal method, then complexed with the electroactive anthraquinone (AQ) and used as the electrode modified material. The AQ/3D-rGO/Ti <subscript>3</subscript> C <subscript>2</subscript> composite had high surface area and provided abundant adsorption sites for MB, and the displacement/competitive behavior between AQ and MB could dexterously achieve the ratiometric EC detection of E2. In addition, the inherent blue color of MB allowed it to be analyzed by UV-vis absorption method. The proposed dual mode detection method exhibited broad linear ranges of 0.1 pg mL <superscript>-1</superscript> to 50 ng mL <superscript>-1</superscript>  (by UV-vis) and 0.03 pg mL <superscript>-1</superscript> to 50 ng mL <superscript>-1</superscript>  (by EC) for E2 detection, and the detection limits were 0.023 pg mL <superscript>-1</superscript> (S/N = 3) and 8.0 fg mL <superscript>-1</superscript>  (S/N = 3), respectively. Moreover, the proposed immunoassay exhibited good practicability and was applied to monitor E2 in milk and serum successfully.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-3573
Volume :
276
Database :
MEDLINE
Journal :
Talanta
Publication Type :
Academic Journal
Accession number :
38749160
Full Text :
https://doi.org/10.1016/j.talanta.2024.126243