Ir Cluster-Anchored MOFs as Peroxidase-Mimetic Nanoreactors for Diagnosing Hydrogen Peroxide-Related Biomarkers.
Shengdong MuYuting DengZhenyu XingXiao RongChao HeSujiao CaoTian MaChong ChengYinghan WangPublished in: ACS applied materials & interfaces (2022)
Exploring multifaceted and highly sensitive biosensors is a major challenge in biotechnology and medical diagnosis. Here, we create a new iridium (Ir) cluster-anchored metal-organic framework (MOF, namely, Ir NCs @Ti-MOF via a coordination-assisted strategy) as a peroxidase (POD)-mimetic nanoreactor for colorimetrically diagnosing hydrogen peroxide-related biomarkers. Owing to the Ir NCs -N/O coordination of Ti-MOF and unique enzymatic properties of Ir clusters, the Ir NCs @Ti-MOF exhibits exceptional and exclusive POD-mimetic activities ( K m = 3.94 mM, V max = 1.70 μM s -1 , and turnover number = 39.64 × 10 -3 s -1 for H 2 O 2 ), thus demonstrating excellent POD-mimetic detecting activity and also super substrate selectivity, which is considerably more efficient than recently reported POD mimetics. Colorimetric studies disclose that this Ir NCs @Ti-MOF-based nanoreactor shows multifaceted and efficient diagnosing activities and substrate selectivity, such as a limit of detection (LOD): 14.12 μM for H 2 O 2 at a range of 0-900 μM, LOD: 3.41 μM for l-cysteine at a range of 0-50 μM, and LOD: 20.0 μM for glucose at a range of 0-600 μM, which enables an ultrasensitive and visual determination of abundant H 2 O 2 -related biomarkers. The proposed design will not only provide highly sensitive and cheap colorimetric biosensors in medical resource-limited areas but also offer a new path to engineering customizable enzyme-mimetic nanoreactors as a powerful tool for accurate and rapid diagnosis.
Keyphrases
- hydrogen peroxide
- metal organic framework
- nitric oxide
- label free
- healthcare
- gold nanoparticles
- molecularly imprinted
- fluorescent probe
- blood pressure
- high resolution
- living cells
- mass spectrometry
- solid phase extraction
- structural basis
- metabolic syndrome
- liquid chromatography
- skeletal muscle
- single molecule
- drug induced