Youchao Qi

Youchao Qi


Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

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

Representative Publications

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20 March 2025 in Advanced Fiber Materials
Verified
Journal Article
Open access
PDF file
JJJinxing Jiang
Jinxing Jiang
XSXian Song
Xian Song
YQYouchao Qi
Youchao Qi
XTXiaoming Tao
Xiaoming Tao
ZZZijian ZHENG
Zijian ZHENG
QHQiyao Huang
Qiyao Huang
Rehabilitation devices that integrate pressure sensors can measure vital metrics such as muscle activities and body posture, allowing patients to perform rehabilitation exercises independently without the need for constant professional oversight. However, traditional devices are commonly constructed based on thin-film plastics and rely on external power sources that are housed in bulky encapsulation cases, compromising user inconvenience and discomfort when worn for rehabilitation activities. While textile-based sensors with self-powering capabilities offer comfort and mobility without external power sources, their sensitivity and sensing range for pressure changes fall short compared to those counterparts. To address this challenge, we herein introduce a skin-inspired, permeable, structure-gradient fiber mat (SGFM) for triboelectric pressure-sensing textiles. Permeable SGFM, created through template-assisted layer-by-layer electrospinning, mimics human skin's rigidity-to-softness mechanical transition. Such a structural design can effectively enhance the dielectric and compressive properties of SGFM, thereby significantly enhancing the sensitivity of the SGFM-based triboelectric pressure sensing textiles over a broad sensing range (0.068 kPa−1 in 0–53 kPa, 0.013 kPa−1 in 53–660 kPa). Notably, the electrospun fibrous structure of SGFM provides pressure sensing textiles with promising moisture permeability, ensuring a comfortable wearing experience. As a proof-of-concept demonstration of applications, SGFM was incorporated into a wearable rehabilitation monitoring system to detect quadriceps, pulse, and plantar pressures for posture tracking and correction, displaying substantial potential for enhancing the efficiency of rehabilitation assistance. Graphical Abstract A permeable, multilayered structure-gradient fiber mat (SGFM) for triboelectric pressure-sensing textiles is proposed. Permeable SGFM, created through template-assisted layer-by-layer electrospinning, mimics human skin's rigidity-to-softness mechanical transition. Such a structural design can effectively enhance the sensitivity of the SGFM-based triboelectric pressure sensing textiles over a broad sensing range. As a proof-of-concept demonstration of applications, SGFM was incorporated into a wearable rehabilitation monitoring system to detect quadriceps, pulse, and plantar pressures for posture tracking and correction, displaying substantial potential for enhancing the efficiency of rehabilitation assistance.

23 November 2021 in Molecules
Verified
Journal Article
Open access
PDF file
YQYouchao Qi
Youchao Qi
GFGuanghui Fan
Guanghui Fan
GDGuozhen Duan
Guozhen Duan
YMYonggui Ma
Yonggui Ma
PLPeifeng Li
Peifeng Li
Taurochenodeoxycholic acid (TCDCA) is one of the main components of bile acids (BAs). TCDCA has been reported as a signaling molecule, exerting anti-inflammatory and immunomodulatory functions. However, it is not well known whether those effects are mediated by TGR5. This study aimed to elucidate the interaction between TCDCA and TGR5. To achieve this aim, first, the TGR5 eukaryotic vector was constructed. The expression level of TGR5 in 293T cells was determined by immunofluorescence, real-time quantitative PCR (RT-PCR, qPCR), and Western blot. The luciferase assay, fluorescence microscopy, and enzyme-linked immunosorbent assay (ELISA) were recruited to check the interaction of TCDCA with TGR5. TCDCA treatment in 293T cells resulted in TGR5 internalization coupled with a significant increase in cAMP luciferase expression. Our results demonstrated that TCDCA was able to bind to the TGR5 receptor and activate it. These results provide an excellent potential therapeutic target for TCDCA research. Moreover, these findings also provide theoretical evidence for further TCDCA research.