Zr‐MOF Carrier‐Enhanced Dual‐Mode Biosensing Platforms for Rapid and Sensitive Diagnosis of Mpox

Author:

Yang Huiyi1,Zheng Judun1,Wang Wei2,Lin Jingyan3,Wang Jingru2,Liu Lunjing4,Wu Wenjie2,Zhang Chengli1,Zhang Mingxia3,Fu Yu4,Yang Bin1,Liao Yuhui24ORCID

Affiliation:

1. Molecular Diagnosis and Treatment Center for Infectious Diseases Dermatology Hospital Southern Medical University Guangzhou 510000 China

2. Institute for Engineering Medicine Kunming Medical University Kunming 650500 China

3. National Clinical Research Center for Infectious Disease The Second Affiliated Hospital of Southern University of Science and Technology Shenzhen Third People's Hospital Shenzhen 518000 China

4. NHC Key Laboratory of Metabolic Cardiovascular Diseases Research Ningxia Key Laboratory of Vascular Injury and Repair Research Ningxia Medical University Yinchuan 750004 China

Abstract

AbstractDual‐mode readout platforms with colorimetric and electrochemiluminescence (ECL) signal enhancement are proposed for the ultrasensitive and flexible detection of the monkeypox virus (MPXV) in different scenes. A new nanotag, Ru@U6‐Ru/Pt NPs is constructed for dual‐mode platforms by integrating double‐layered ECL luminophores and the nanozyme using Zr‐MOF (UiO‐66‐NH2) as the carrier, which not only generates enhanced ECL and colorimetric signals but also provide greater stability than that of commonly used nanotags. Dual‐mode platforms are used within 15 min from the “sample in” to the “result out” steps, without nucleic acid amplification. The colorimetric mode allows the screening of MPXV with the visual limit of detection (vLOD) of 0.1 pM (6 × 108 copies µL−1) and the ECL mode supports quantitative detection of MPXV with an LOD as low as 10 aM (6 copies·µL−1), resulting in a broad sensing range of 60 to 3 × 1011 copies·µL−1 (10 orders of magnitude). Validation is conducted using 50 clinical samples, which is 100% concordant to those of quantitative polymerase chain reaction (qPCR), indicating that Ru@U6‐Ru/Pt NPs‐based dual‐mode sensing platforms showed great promise as rapid, sensitive, and accurate tools for diagnosis of the nucleic acid of MPXV and other infectious pathogens.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Basic and Applied Basic Research Foundation of Guangdong Province

Science Fund for Distinguished Young Scholars of Guangdong Province

Publisher

Wiley

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