Peptide Specific Nanoplastic Detection Based on Sandwich Typed Localized Surface Plasmon Resonance.
Seungju OhHyeyeon HurYoonjae KimSeongcheol ShinHyunjeong WooJonghoon ChoiHyun Ho LeePublished in: Nanomaterials (Basel, Switzerland) (2021)
Recently, various waste microplastics sensors have been introduced in response to environmental and biological hazards posed by waste microplastics. In particular, the detrimental effects of nano-sized plastics or nanoplastics have been reported to be severe. Moreover, there have been many difficulties for sensing microplastics due to the limited methodologies for selectively recognizing nanoplastics. In this study, a customized gold nanoparticles (Au NPs) based localized surface plasmon resonance (LSPR) system having bio-mimicked peptide probes toward the nanoplastics was demonstrated. The specific determination through the oligo-peptide recognition was accomplished by chemical conjugation both on the LSPR chip's 40~50 nm Au NPs and sandwiched 5 nm Au NPs, respectively. The peptide probe could selectively bind to polystyrene (PS) nanoplastics in the forms of fragmented debris by cryo-grinding. A simple UV-Vis spectrophotometer was used to identify the LSPR sensing by primarily measuring the absorbance change and shift of absorption peak. The sandwich-binding could increase the LSPR detection sensitivity up to 60% due to consecutive plasmonic effects. In addition, microwave-boiled DI water inside of a styrofoam container was tested for putative PS nanoplastics resource as a real accessible sample. The LSPR system could be a novel protocol overcoming the limitations from conventional nanoplastic detection.
Keyphrases
- gold nanoparticles
- loop mediated isothermal amplification
- sensitive detection
- label free
- reduced graphene oxide
- human health
- real time pcr
- randomized controlled trial
- photodynamic therapy
- heavy metals
- single molecule
- living cells
- escherichia coli
- small molecule
- high resolution
- risk assessment
- early onset
- oxide nanoparticles
- cystic fibrosis
- staphylococcus aureus
- molecularly imprinted
- climate change
- single cell
- drug induced
- solid phase extraction