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ArticleMikrochimica acta2026

A dual-mode aptasensor based on UiO-66-NH₂@MOF-919 for subtype-specific detection of carbapenem-resistant Klebsiella pneumoniae.

Ruiwen Li, Hao Shen, Dandan Shi, Shaoning Yu, Guoqing Qian

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Article in Mikrochimica acta, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Ruiwen LiDepartment of Infectious Diseases, The First Affiliated Hospital of Ningbo University, Ningbo, 315211, Zhejiang, China.
Hao ShenInstitute of Mass Spectrometry, School of Material Science and Chemical Engineering, Ningbo University, Ningbo, 315211, Zhejiang, China.
Dandan ShiHealth Science Center, Ningbo University, Ningbo, 315211, Zhejiang, China.
Shaoning YuInstitute of Mass Spectrometry, School of Material Science and Chemical Engineering, Ningbo University, Ningbo, 315211, Zhejiang, China.
Guoqing QianDepartment of Infectious Diseases, The First Affiliated Hospital of Ningbo University, Ningbo, 315211, Zhejiang, China. bill.qian@outlook.com.ORCID http://orcid.org/0000-0003-2427-8042

Funding

Ningbo Key Discipline of Medical Sciences 2026-A19Ningbo Municipal Major Project for Medical and Health High-Level Teams 2025021222Ningbo University Biomedical Innovation Institute Project H2025000422the Key Project of Zhejiang Provincial Medical and Health Science and Technology Plan WKJ-ZJ-2552
6 · The paper itself

Abstract

Rapid and reliable detection of multidrug-resistant bacteria is essential for effective clinical management. In this study, we have developed a dual-mode aptasensing platform based on a core-shell MOF-on-MOF structure (UiO-66-NH₂@MOF-919) for the subtype-specific detection of carbapenem-resistant Klebsiella pneumoniae strains carrying NDM-1 and KPC-2. This bifunctional system integrates the peroxidase-like activity of the MOF-919 shell with the fluorescence quenching capability of the UiO-66-NH₂ core, enabling both colorimetric and fluorometric detection within a single platform. Benefiting from this design, the method achieves sensitive and selective detection over a wide linear range from 10 to 10⁸ CFU mL⁻¹, with low detection limits of 7 CFU mL⁻¹ for NDM-1 KP and 4 CFU mL⁻¹ for KPC-2 KP. The proposed platform exhibits good selectivity against non-target bacteria and strong anti-interference capability. Spiked recovery experiments in human serum, urine, and bronchoalveolar lavage fluid yielded recoveries ranging from 93.0% to 110.0% with RSDs below 5.0%, demonstrating good analytical accuracy and applicability in complex biological samples. Compared to conventional aptasensing systems, this approach enables dual-subtype detection within a single platform, improving analytical efficiency and practicality. This work provides a feasible strategy for MOF-on-MOF-based biosensing systems and shows promising potential for rapid clinical detection of drug-resistant bacteria.

Indexed as

Aptamers, NucleotideBiosensing TechniquesKlebsiella pneumoniaeMetal-Organic FrameworksAnti-Bacterial Agentsbeta-LactamasesCarbapenemsColorimetryHumansLimit of DetectionPhthalic AcidsSpectrometry, FluorescenceAnti-Bacterial AgentsAptamers, Nucleotidebeta-lactamase NDM-1beta-LactamasesCarbapenemsMetal-Organic FrameworksPhthalic AcidsUiO-66AptasensorCarbapenem resistanceDual-mode detectionFluorescenceKlebsiella pneumoniaeMOF-on-MOFMultidrug-resistant bacteriaUV-vis spectrometry

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.