A sandwich-type of electrochemical immunoassay is described for the determination of insulin. It is based on the use of a glassy carbon electrode that was modified with MoS nanosheets decorated with gold nanoparticles (AuNPs) to immobilize a large amount of first antibody (Ab). Following exposure to insulin, secondary antibody (Ab) that was cross-linked to a DNA initiator strand (T) to form an Ab@T conjugate was added to undergo a sandwich immunoreaction. Subsequently, the long dsDNA concatemer was formed by a hybridization chain reaction between Ab@T and auxiliary probes (H, H). Finally, the electrochemical probe ruthenium(II) hexaammine was intercalated into the dsHCR products via electrostatic interaction between the anionic DNA phosphate backbones and the cationic probe. The electrochemical response, best measured at a potential of around -0.21 V (vs Ag/AgCl) has a dynamic range that extends from 0.1 pmol L to 1 nmol L insulin, and the detection limit is as low as 50 fmol L. The assay was acceptably specific, reproducible and stable. In our perception, it represents a viable new tool for determination of this important clinical parameter. Graphical abstract Schematic of a sandwich-type of electrochemical immunoassay for the determination of insulin based on the use of MoS nanosheets modified with gold nanoparticles (AuNP@MoS) and hybridization chain reaction (HCR).
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http://dx.doi.org/10.1007/s00604-018-3124-8 | DOI Listing |
Adv Sci (Weinh)
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Department of Laboratory Medicine, Guangdong Provincial Key Laboratory of Precision Medical Diagnostics, Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Guangdong Provincial Key Laboratory of Single Cell Technology and Application, School of Laboratory Medicine and Biotechnology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, P. R. China.
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Instituto de Biología, Universidad Nacional Autónoma de México (UNAM), México City, México.
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January 2025
Division of Endocrinology, Mayo Clinic, Rochester, Minnesota, USA.
There is an increasing need for biomarkers of senescent cell burden to facilitate the selection of participants for clinical trials. p16 is encoded by the CDKN2A locus, which produces five variant transcripts in humans, two of which encode homologous p16 proteins: p16, encoded by p16_variant 1, and p16ɣ, encoded by p16_variant 5. While distinct quantitative polymerase chain reaction primers can be designed for p16_variant 5, primers for p16_variant 1 also measure p16_variant 5 (p16_variant 1 + 5).
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Center for Advanced Biomolecular Recognition, Biomedical Research Division, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
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Department of Gynecology, Hangzhou Children's Hospital, Hangzhou, China.
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