Yusuke Kanno

Dr. Yusuke Kanno

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Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 August 2012 in Analytical Chemistry
Verified
Journal Article
Closed access
Kosuke InoKosuke Ino
Kosuke Ino
YKYusuke Kanno
Yusuke Kanno
TAToshiharu Arai
Toshiharu Arai
KIKumi Y. Inoue
Kumi Y. Inoue
YTYasufumi Takahashi
Yasufumi Takahashi
TMTomokazu Matsue
Tomokazu Matsue

14 May 2015 in Analytical Chemistry
Verified
Journal Article
Closed access
HAHiroya Abe
Hiroya Abe
Kosuke InoKosuke Ino
Kosuke Ino
CLChen-Zhong Li
Chen-Zhong Li
YKYusuke Kanno
Yusuke Kanno
KIKumi Y. Inoue
Kumi Y. Inoue
TMTomokazu Matsue
Tomokazu Matsue

25 May 2012 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
PDF file
Kosuke InoKosuke Ino
Kosuke Ino
TNTaku Nishijo
Taku Nishijo
TAToshiharu Arai
Toshiharu Arai
YKYusuke Kanno
Yusuke Kanno
YTYasufumi Takahashi
Yasufumi Takahashi
TMTomokazu Matsue
Tomokazu Matsue

14 November 2017 in Analytical Chemistry
Verified
Journal Article
Open access
YKYusuke Kanno
Yusuke Kanno
Kosuke InoKosuke Ino
Kosuke Ino
HAHiroya Abe
Hiroya Abe
CSChika Sakamoto
Chika Sakamoto
TOTakehiro Onodera
Takehiro Onodera
TMTomokazu Matsue
Tomokazu Matsue
Multiplexed bioimaging systems have triggered the development of effective assays, contributing new biological information. Although electrochemical imaging is beneficial for quantitative analysis in real time, monitoring multiple cell functions is difficult. We have developed a novel electrochemical imaging system, herein, using a large-scale integration (LSI)-based amperometric device for detecting multiple biomolecules simultaneously. This system is designated as an electrochemicolor imaging system in which the current signals from two different types of biomolecules are depicted as a multicolor electrochemical image. The mode-selectable function of the 400-electrode device enables the imaging system and two different potentials can be independently applied to the selected electrodes. The imaging system is successfully applied for detecting multiple cell functions of the embryonic stem (ES) cell and the rat pheochromocytoma (PC12) cell aggregates. To the best of our knowledge, this is the first time that a real-time electrochemical mapping technique for multiple electroactive species, simultaneously, has been reported. The imaging system is a promising bioanalytical method for exploring complex biological phenomena.

6 October 2015 in Lab on a Chip
Verified
Journal Article
Open access
PDF file
YKYusuke Kanno
Yusuke Kanno
Kosuke InoKosuke Ino
Kosuke Ino
HSHitoshi Shiku
Hitoshi Shiku
TMTomokazu Matsue
Tomokazu Matsue
An electrochemical device, which consists of electrode arrays, nanocavities, and microwells, was developed for multi-electrochemical detection with high sensitivity. A local redox cycling-based electrochemical (LRC-EC) system was used for multi-electrochemical detection and signal amplification. The LRC-EC system consists of n2 sensors with only 2n bonding pads for external connection. The nanocavities fabricated in the sensor microwells enable significant improvement of the signal amplification compared with the previous devices we have developed. The present device was successfully applied for evaluation of embryoid bodies (EBs) from embryonic stem (ES) cells via electrochemical measurements of alkaline phosphatase (ALP) activity in the EBs. In addition, the EBs were successfully trapped in the sensor microwells of the device using dielectrophoresis (DEP) manipulation, which led to high-throughput cell analysis. This device is considered to be useful for multi-electrochemical detection and imaging for bioassays including cell analysis.

12 March 2014 in Analytical Chemistry
Verified
Journal Article
Closed access
Kosuke InoKosuke Ino
Kosuke Ino
YKYusuke Kanno
Yusuke Kanno
TNTaku Nishijo
Taku Nishijo
HKHirokazu Komaki
Hirokazu Komaki
YYYuta Yamada
Yuta Yamada
TMTomokazu Matsue
Tomokazu Matsue