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Complementary Metal–Oxide–Semiconductor Potentiometric Field-Effect Transistor Array Platform Using Sensor Learning for Multi-ion Imaging
Author(s) -
Nicolas Moser,
Chi Leng Leong,
Yuanqi Hu,
Chiara Cicatiello,
Sally A. N. Gowers,
Martyn G. Boutelle,
Pantelis Georgiou
Publication year - 2020
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.9b05836
Subject(s) - isfet , chemistry , sensor array , analyte , passivation , pixel , potentiometric sensor , analytical chemistry (journal) , ion , transistor , membrane , field effect transistor , potentiometric titration , optoelectronics , artificial intelligence , chromatography , materials science , voltage , layer (electronics) , electrical engineering , computer science , biochemistry , organic chemistry , machine learning , engineering
This work describes an array of 1024 ion-sensitive field-effect transistors (ISFETs) using sensor-learning techniques to perform multi-ion imaging for concurrent detection of potassium, sodium, calcium, and hydrogen. Analyte-specific ionophore membranes are deposited on the surface of the ISFET array chip, yielding pixels with quasi-Nernstian sensitivity to K + , Na + , or Ca 2+ . Uncoated pixels display pH sensitivity from the standard Si 3 N 4 passivation layer. The platform is then trained by inducing a change in single-ion concentration and measuring the responses of all pixels. Sensor learning relies on offline training algorithms including k -means clustering and density-based spatial clustering of applications with noise to yield membrane mapping and sensitivity of each pixel to target electrolytes. We demonstrate multi-ion imaging with an average error of 3.7% (K + ), 4.6% (Na + ), and 1.8% (pH) for each ion, respectively, while Ca 2+ incurs a larger error of 24.2% and hence is included to demonstrate versatility. We validate the platform with a brain dialysate fluid sample and demonstrate reading by comparing with a gold-standard spectrometry technique.

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