Target-Induced Horseradish Peroxidase Deactivation for Multicolor Colorimetric Assay of Hydrogen Sulfide in Rat Brain Microdialysis

2018 ◽  
Vol 90 (10) ◽  
pp. 6222-6228 ◽  
Author(s):  
Zhonghui Chen ◽  
Chaoqun Chen ◽  
Huawei Huang ◽  
Fang Luo ◽  
Longhua Guo ◽  
...  
2019 ◽  
Vol 11 (24) ◽  
pp. 3085-3089 ◽  
Author(s):  
Zheng Fang ◽  
Guiyin Yue ◽  
Jian Wang ◽  
Fang Luo ◽  
Longhua Guo ◽  
...  

The detection of hydrogen sulfide (H2S) is important due to its role in the diagnosis of many diseases since H2S is involved in the protection of neurons from oxidative stress and neuronal transmission modulation in the brain.


2019 ◽  
Vol 91 (24) ◽  
pp. 15915-15921 ◽  
Author(s):  
Chaoqun Chen ◽  
Qing Cai ◽  
Fang Luo ◽  
Nuo Dong ◽  
Longhua Guo ◽  
...  

2004 ◽  
Vol 522 (1) ◽  
pp. 99-104 ◽  
Author(s):  
Takeshi Fukushima ◽  
Emi Naka-aki ◽  
Xingjie Guo ◽  
Famei Li ◽  
Tineke Vankeirsbilck ◽  
...  

Chemosensors ◽  
2022 ◽  
Vol 10 (1) ◽  
pp. 27
Author(s):  
Jae-Hyung Kim ◽  
Young-Ju Lee ◽  
Yong-Jin Ahn ◽  
Minyoung Kim ◽  
Gi-Ja Lee

In this study, a paper-integrated analytical device that combined a paper-based colorimetric assay with a paper-based cell culture platform was developed for the in situ detection of hydrogen sulfide (H2S) in three-dimensional (3D)-cultured, live prostate cancer cells. Two kinds of paper substrates were fabricated using a simple wax-printing methodology to form the cell culture and detection zones, respectively. LNCaP cells were seeded directly on the paper substrate and grown in the paper-integrated analytical device. The cell viability and H2S production of LNCaP cells were assessed using a simple water-soluble tetrazolium salt colorimetric assay and H2S-sensing paper, respectively. The H2S-sensing paper showed good sensitivity (sensitivity: 6.12 blue channel intensity/μM H2S, R2 = 0.994) and a limit of quantification of 1.08 μM. As a result, we successfully measured changes in endogenous H2S production in 3D-cultured, live LNCaP cells within the paper-integrated analytical device while varying the duration of incubation and substrate concentration (L-cysteine). This paper-integrated analytical device can provide a simple and effective method to investigate H2S signaling pathways and drug screening in a 3D culture model.


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