Lihui Yin

Lihui Yin


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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10 October 2013 in Analytical Sciences
Verified
Journal Article
Open access
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YZYan Zhang
Yan Zhang
XHXiaoyan Huang
Xiaoyan Huang
WLWenfang Liu
Wenfang Liu
ZCZeneng Cheng
Zeneng Cheng
Chuanpin ChenChuanpin Chen
Chuanpin Chen
LYLihui Yin
Lihui Yin
Illegal chemicals, which could cause unpredictable side effects, may be added into traditional Chinese medicine (TCM) for a rapid healing effect. In this report, a surface-enhanced Raman scattering (SERS) analysis method for five kinds of illegally added drugs (rosiglitazone maleate, phenformin hydrochloride, metformin hydrochloride, pioglitazone hydrochloride and sibutramine hydrochloride) in Chinese traditional patent medicine (CTPM) has been demonstrated, including simultaneous detections of drug mixtures with CTPM. Silver colloidal, prepared by a sodium citrate reaction, was used as a SERS substrate. The optimum pH condition for each drug has also been explored because of its combined effect on protonation, surface charge, repulsion of an analyte and nanoparticles. Furthermore, the simultaneous detection of two or three kinds of these chemicals has been carried out. Characteristic peaks are employed for qualitative analysis. This is the first research using SERS for the analysis of drug mixtures in CTPM without any separation process.

24 February 2021 in The Analyst
Verified
Journal Article
Closed access
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LZLi Zhu
Li Zhu
YZYu Zhao
Yu Zhao
SYShangchen Yao
Shangchen Yao
MXMingzhe Xu
Mingzhe Xu
LYLihui Yin
Lihui Yin
XTXu Teng
Xu Teng
In this study, a novel colorimetric aptasensor was developed for the rapid detection and visual screening of HPV16 L1 proteins using gold nanoparticles (AuNPs) and an RNA aptamer against HPV16 L1 protein (APTHPV16 L1). The AuNP-APTHPV16 L1 conjugates could be aggregated by the addition of a salt in the presence of HPV16 L1 proteins at the ppb level. At the same time, the surface plasma resonance absorption peaks of AuNPs shifted to a short wavelength, and an observable change in color from red to blue occurred. The relative absorbance (Ablank − Asample/Ablank) at 520 nm exhibited a stable response to HPV16 L1 proteins over a concentration range from 9.6 to 201.6 ng mL−1. The visual detection limit of HPV16 L1 proteins was found to be 9.6 ng mL−1. Finally, the proposed colorimetric aptasensor was successfully applied for the rapid and effective detection of HPV16 L1 proteins in clinical samples and vaccine samples. The validity and reliability of the proposed colorimetric aptasensor were verified by the enzyme-linked immunosorbent assay method. The proposed colorimetric aptasensor provided a promising indicator for screening and quantitative detection of HPV16 L1 proteins in clinical samples.

16 January 2015 in AAPS PharmSciTech
Verified
Journal Article
Closed access
PDF file
YZYu Zhao
Yu Zhao
NJNan Ji
Nan Ji
LYLihui Yin
Lihui Yin
JWJun Wang
Jun Wang

20 January 2023 in The Analyst
Verified
Journal Article
Closed access
PDF file
LZLi Zhu
Li Zhu
YTYun Teng
Yun Teng
WHWeidan Han
Weidan Han
LYLihui Yin
Lihui Yin
XTXu Teng
Xu Teng

In this study, a rapid screening method for elemental impurities in pharmaceutical products has been established by portable energy dispersive X-ray fluorescence (EDXRF) spectroscopy combined with the efficient fundamental parameter method. The proposed method has been used for the screening of 22 elemental impurities (i.e., Cd, Pb, As, Hg, Co, V, Ni, Tl, Au, Pd, Ir, Os, Rh, Ru, Se, Ag, Pt, Sb, Mo, Cu, Sn, and Cr) in the International Conference on Harmonization (ICH) Q3D guideline. The verification of results could meet the acceptance criteria for accuracy, precision and linearity in the United States Pharmacopoeia 〈233〉. On the other hand, the limit of quantitation of the proposed EDXRF method for the screening of 22 elemental impurities in pharmaceutical products could meet the concentration limits of each element at 10 g maximum daily intake based on the established permitted daily exposure to oral drugs in the ICH Q3D guideline. Our findings open up new possibilities in the rapid screening of pharmaceutical products for the detection of elemental impurities by EDXRF, which can be expected to provide a novel, nondestructive, high-throughput, portable, and sensitive platform for the process control of elemental impurities to ensure the quality and safety of drugs.


20 January 2026 in Life
Verified
Journal Article
Open access
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YQYao Qiao
Yao Qiao
JYJie Yin
Jie Yin
SLShuyu Lu
Shuyu Lu
LYLihui Yin
Lihui Yin
Mass spectrometry imaging (MSI) is an innovative analytical technique that integrates chemical analysis with spatial localization, enabling label-free, in situ detection and visualization of diverse biomolecules within tissue sections. This review summarizes the recent advances in the application of MSI to neurological disorders, with a focus on Parkinson’s disease, Alzheimer’s disease, schizophrenia, and traumatic brain injury. Studies have demonstrated that MSI can delineate the spatial heterogeneity of disease-related molecules—such as neurotransmitters, lipids, and metabolites—thereby providing new perspectives for understanding the pathological mechanisms of neurodegenerative and psychiatric diseases. Platforms including MALDI-MSI and DESI-MSI have been effectively employed for visualizing drug distribution, characterizing lipid metabolic pathways, and identifying spatial biomarkers. Although challenges remain in quantitative accuracy, spatial resolution, and the detection of low-abundance molecules, advances in high-resolution mass spectrometry, single-cell-level imaging, and multi-omics integration are expected to further enhance the utility of MSI in the investigation of brain diseases.

18 July 2021 in Phytochemical Analysis
Verified
Journal Article
Closed access
PDF file
LZLi Zhu
Li Zhu
YZYu Zhao
Yu Zhao
CHChangqin Hu
Changqin Hu
MXMingzhe Xu
Mingzhe Xu
LYLihui Yin
Lihui Yin