| Literature DB >> 32275209 |
Arnab Guha1, Omar Sheej Ahmad2, Antonio Guerreiro3, Kal Karim4, Niklas Sandström5, Victor P Ostanin6, Wouter van der Wijngaart5, Sergey A Piletsky4, Sourav K Ghosh7.
Abstract
Small molecule detection is of wide interest in clinical and industrial applications. However, its accessibility is still limited as miniaturisation and system integration is challenged in reliability, costs and complexity. Here we combined a 14.3 MHz quartz crystal resonator (QCR), actuated and analysed using a fixed frequency drive (FFD) method, with a nanomolecular imprinted polymer for label-free, realtime detection of N-hexanoyl-L-homoserine lactone (199 Da), a gram-negative bacterial infection biomarker. The lowest concentration detected (1 μM) without any optimisation was comparable with that of a BIAcore SPR system, an expensive laboratory gold standard, with significant enhancement in sensitivity and specificity beyond the state-of-the-art QCR. The analytical formula-based FFD method can potentially allow a multiplexed "QCR-on-chip" technology, bringing a paradigm shift in speed, accessibility and affordability of small molecule detection.Entities:
Keywords: Acyl-homoserine lactone (AHL); Fixed frequency drive; Nanomolecular imprinted polymer (nano-MIP); Quartz crystal microbalance (QCM); Quartz crystal resonator (QCR)
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Year: 2020 PMID: 32275209 DOI: 10.1016/j.bios.2020.112176
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618