Wei Shih-Chung

Dr. Wei Shih-Chung

Illumina Singapore Pte Ltd, Singapore, Central Singapore, Singapore
orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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14 June 2012 in Sensors
Verified
Journal Article
Open access
PDF file
Chia-Chen ChangChia-Chen Chang
Chia-Chen Chang
CCChien-Cheng Chen
Chien-Cheng Chen
Wei Shih-ChungWei Shih-Chung
Wei Shih-Chung
HLHui-Hsin Lu
Hui-Hsin Lu
YLYang-Hung Liang
Yang-Hung Liang
CLChii-Wann Lin
Chii-Wann Lin
Since the development of the polymerase chain reaction (PCR) technique, genomic information has been retrievable from lesser amounts of DNA than previously possible. PCR-based amplifications require high-precision instruments to perform temperature cycling reactions; further, they are cumbersome for routine clinical use. However, the use of isothermal approaches can eliminate many complications associated with thermocycling. The application of diagnostic devices for isothermal DNA amplification has recently been studied extensively. In this paper, we describe the basic concepts of several isothermal amplification approaches and review recent progress in diagnostic device development.

1 April 2013 in Biosensors and Bioelectronics
Verified
Journal Article
Closed access
Chia-Chen ChangChia-Chen Chang
Chia-Chen Chang
Wei Shih-ChungWei Shih-Chung
Wei Shih-Chung
TWTzu-Heng Wu
Tzu-Heng Wu
CLChung-Han Lee
Chung-Han Lee
CLChii-Wann Lin
Chii-Wann Lin

1 February 2012 in Biosensors and Bioelectronics
Verified
Journal Article
Closed access
TCTsung-Liang Chuang
Tsung-Liang Chuang
Wei Shih-ChungWei Shih-Chung
Wei Shih-Chung
SLSzu-Yuan Lee
Szu-Yuan Lee
CLChii-Wann Lin
Chii-Wann Lin

17 October 2018 in Small
Verified
Journal Article
Closed access
PDF file
MHMyat Noe Hsu
Myat Noe Hsu
Wei Shih-ChungWei Shih-Chung
Wei Shih-Chung
SGSong Guo
Song Guo
DPDinh-Tuan Phan
Dinh-Tuan Phan
YZYong Zhang
Yong Zhang
CCChia-Hung Chen
Chia-Hung Chen

22 September 2011 in Biosensors and Bioelectronics
Verified
Journal Article
Closed access
Chia-Chen ChangChia-Chen Chang
Chia-Chen Chang
SLShenhsiung Lin
Shenhsiung Lin
Wei Shih-ChungWei Shih-Chung
Wei Shih-Chung
CCChen-Yu Chen
Chen-Yu Chen
CLChii-Wann Lin
Chii-Wann Lin

16 June 2014 in Lab on a Chip
Verified
Journal Article
Closed access
PDF file
TCTsung-Liang Chuang
Tsung-Liang Chuang
Chia-Chen ChangChia-Chen Chang
Chia-Chen Chang
YCYu Chu-Su
Yu Chu-Su
Wei Shih-ChungWei Shih-Chung
Wei Shih-Chung
XZXi-Hong Zhao
Xi-Hong Zhao
CLChii-Wann Lin
Chii-Wann Lin
ELISA and ELISPOT methods are utilized for interferon-gamma (IFN-γ) release assays (IGRAs) to detect the IFN-γ secreted by T lymphocytes. However, the multi-step protocols of the assays are still performed with laboratory instruments and operated by well-trained people. Here, we report a membrane-based microfluidic device integrated with a surface plasmon resonance (SPR) sensor to realize an easy-to-use and cost effective multi-step quantitative analysis. To conduct the SPR measurements, we utilized a membrane-based SPR sensing device in which a rayon membrane was located 300 μm under the absorbent pad. The basic equation covering this type of transport is based on Darcy's law. Furthermore, the concentration of streptavidin delivered from a sucrose-treated glass pad placed alongside the rayon membrane was controlled in a narrow range (0.81 μM ± 6%). Finally, the unbound molecules were removed by a washing buffer that was pre-packed in the reservoir of the chip. Using a bi-functional, hairpin-shaped aptamer as the sensing probe, we specifically detected the IFN-γ and amplified the signal by binding the streptavidin. A high correlation coefficient (R2 = 0.995) was obtained, in the range from 0.01 to 100 nM. A detection limit of 10 pM was achieved within 30 min. Thus, the SPR assay protocols for IFN-γ detection could be performed using this simple device without an additional pumping system.