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Your search keyword '"Xu, Yongqian"' showing total 473 results
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473 results on '"Xu, Yongqian"'

15. Exploring Virtual Discrete Manufacturing Assembly

Author

Yang, Rui, Hu, Ruihan, Mo, Qinglong, Xu, Yongqian, Zheng, Zheng, Editor-in-Chief, Xi, Zhiyu, Associate Editor, Gong, Siqian, Series Editor, Hong, Wei-Chiang, Series Editor, Mellal, Mohamed Arezki, Series Editor, Narayanan, Ramadas, Series Editor, Nguyen, Quang Ngoc, Series Editor, Ong, Hwai Chyuan, Series Editor, Sun, Zaicheng, Series Editor, Ullah, Sharif, Series Editor, Wu, Junwei, Series Editor, Zhang, Baochang, Series Editor, Zhang, Wei, Series Editor, Zhu, Quanxin, Series Editor, Zheng, Wei, Series Editor, Kandel, Bijay Kumar, editor, Yang, Jun, editor, PRABHU, J. JOSE, editor, and Wang, Xueyuan, editor

Published
2023
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16. China’s Metaverse Serves Traditional Chinese Medicine

Author

Yang, Rui, Mo, Qinglong, Xu, Yongqian, Zhang, Yina, Dou, Runliang, Editor-in-Chief, Liu, Jing, Editor-in-Chief, Khasawneh, Mohammad T., Editor-in-Chief, Balas, Valentina Emilia, Series Editor, Bhowmik, Debashish, Series Editor, Khan, Khalil, Series Editor, Masehian, Ellips, Series Editor, Mohammadi-Ivatloo, Behnam, Series Editor, Nayyar, Anand, Series Editor, Pamucar, Dragan, Series Editor, Shu, Dewu, Series Editor, Akhtar, Nadeem, editor, Draman, Azah Kamilah, editor, and Abdollah, Mohd Faizal, editor

Published
2023
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40. Ratiometric Electrochemical Detection of Interleukin-6 Using Electropolymerized Methylene Blue and a Multi-Walled Carbon-Nanotube-Modified Screen-Printed Carbon Electrode.

Author

Liu, Zhuo, Liu, Fengyu, Wang, Chaofan, Li, Hongjuan, Xu, Yongqian, and Sun, Shiguo

Subjects
MULTIWALLED carbon nanotubes, ELECTROCHEMICAL sensors, METHYLENE blue, SCHIFF bases, SERUM albumin, BIOSENSORS, CARBON electrodes, CARBON nanotubes
Abstract

Herein, we report a ratio-based electrochemical biosensor for the detection of interleukin-6 (IL-6). We electropolymerized methylene blue (MB) on the surface of screen-printed carbon electrodes; introduced an internal reference signal probe; modified the carboxylate multi-walled carbon nanotubes on the electrode surface to increase the electrochemically active area; and finally linked the amino-modified IL-6 aptamer to the electrode surface through the Schiff base reaction, with bovine serum albumin (BSA) added to mask non-specific adsorption. After adding IL-6 to the samples, the signal of IMB remained almost unchanged, while the signal of I[Fe(CN)6]3−/4− decreased with increasing IL-6 concentration. Thus, a novel ratiometric electrochemical sensor with a linear range of 0.001~1000.0 ng/mL and a low detection limit of 0.54 pg/mL was successfully developed. The sensor had high repeatability, stability, sensitivity, and practicability. It provides a new method for constructing proportional electrochemical sensors and detecting IL-6. [ABSTRACT FROM AUTHOR]

Published
2024
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46. Multidimension‐Regulated Dynamic Timing Control Over Multicolor Emission of Host–Guest Assemblies for Information Encryption and Advanced Anti‐Counterfeiting.

Author

Zhang, Qi, Chang, Zhidong, Han, Weiqiang, Wang, Chaofan, Liu, Guoxin, Li, Hongjuan, Sun, Shiguo, and Xu, Yongqian

Subjects
FLUORESCENCE resonance energy transfer, DIARYLETHENE
Abstract

Dynamical control over molecular luminescence, especially in a time‐dependent manner, holds great promise for the development of smart luminescent materials for anti‐counterfeiting and preventing information leakage. Herein, a series of self‐assembled systems are reported using pillar[5]arene (DMP[5]) and spiropyran derivatives (SP‐C4‐Py). The assemblies rely on the time‐encoded locking and unlocking ring‐switching and fluorescence resonance energy transfer (FRET) units for information camouflage and multilevel encryption. DMP[5] with cyan solid fluorescence color acts as the host and energy transfer (EnT) donor, while photochromic SP‐C4‐Py with the ring‐opened and closed isomers acts as guest and EnT acceptor. When irradiated, the assemblies undergo a time‐dependent luminescence color change ranging from cyan to yellow to red through a FRET process. The molar ratio of host and guest in the assembly systems affects the FRET efficiency, and the power of the irradiation source influences the isomerization degree and rate of SP‐C4‐Py, allowing for precise control over the fluorescent color transition time. The combination of molecular composition and external stimuli governs the kinetics of color change, resulting in a difference in the appearance time of a specific fluorescent color pre‐designed as correct authorized information. By combining these diverse assembles in one label, information encryption and dynamic information identification are achieved in the dimensions of time, ratio, and light power. This time‐dependent feature offers the assembly materials with a multilevel security and provides new possibilities for anti‐counterfeiting and blocking information leakage. [ABSTRACT FROM AUTHOR]

Published
2024
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