Core-shell "loading-type" nanomaterials enabling glucometer readout for portable and sensitive detection of p-aminophenol in real samples.
Xiang-Ling LiLei ZhaoZi-Heng WangTian-Shun SongTing GuoJing Jing XiePublished in: Mikrochimica acta (2024)
A one-target-many-trigger signal model sensing strategy is proposed for quickly, sensitive and on-site detection of the environmental pollutant p-aminophenol (PAP) by use of a commercial personal glucose meter (PGM) for signal readout with the core-shell "loading-type" nanomaterial MSNs@MnO 2 as amplifiable nanoprobes. In this design, the mesoporous silica nanoparticles (MSNs) nanocontainer with entrapped signal molecule glucose is coated with redoxable manganese dioxide (MnO 2 ) nanosheets to form the amplifiable nanoprobes (Glu-MSNs@MnO 2 ). When encountered with PAP, the redox reaction between the MnO 2 and PAP can induce the degradation of the outer layer of MSNs@MnO 2 , liberating multiple copies of the loaded glucose to light up the PGM signal. Owing to the high loading capability of nanocarriers, a "one-to-many" relationship exists between the target and the signal molecule glucose, which can generate adequate signal outputs to achieve the requirement of on-site determination of environmental pollutants. Taking advantage of this amplification mode, the developed PAP assay owns a dynamic linear range of 10.0-400 μM with a detection limit of 2.78 μM and provides good practical application performance with above 96.7 ± 4.83% recovery in environmental water and soil samples. Therefore, the PGM-based amplifiable sensor for PAP proposed can accommodate these requirements of environment monitoring and has promising potential for evaluating pollutants in real environmental samples.
Keyphrases
- sensitive detection
- human health
- blood glucose
- loop mediated isothermal amplification
- drug delivery
- quantum dots
- life cycle
- heavy metals
- type diabetes
- label free
- skeletal muscle
- fluorescence imaging
- adipose tissue
- gold nanoparticles
- mass spectrometry
- drug release
- real time pcr
- photodynamic therapy
- liquid chromatography
- molecularly imprinted
- single cell