Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

is an essential medicinal herb in traditional Chinese medicine, with its pharmacological properties largely attributed to bioactive flavonoids. The types and amounts of these flavonoids act as vital quality markers for both the raw materials and the resultant products. In this work, we introduce a TiO@AgNP nanocomposite designed as a surface-enhanced Raman scattering (SERS) sensor aimed at the preliminary quantification and identification of flavonoids. This is achieved by leveraging the effective molecular adsorption properties of TiO alongside the 'hot spots' generated by AgNPs. By optimizing SERS performance through adjustment of the molar ratio between TiO and Ag, we can quantitatively evaluate four flavonoids-luteolin, kaempferol, quercetin, and rutin-with low detection concentrations of 10 M, 10 M, 5 × 10 M, and 10 M, respectively. Additionally, we observe a nearly linear relationship between the SERS signals and the flavonoid concentrations, allowing for dual or multiplex analysis of these compounds. Furthermore, we successfully differentiated samples from six different geographical regions in China based on the detection of significant flavonoid constituents. This serves as a proof of concept for practical applications that can enhance the identification and distinction of traditional Chinese medicine, as well as assess quality and medicinal efficacy.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12384181PMC
http://dx.doi.org/10.3390/bios15080536DOI Listing

Publication Analysis

Top Keywords

traditional chinese
8
chinese medicine
8
bifunctional tio@agnp
4
tio@agnp superstructures
4
superstructures sers-sensing
4
sers-sensing platform
4
platform identifying
4
flavonoids
4
identifying flavonoids
4
flavonoids chinese
4

Similar Publications

Objective: This study aimed to probe the role of Shenling Baizhu powder (SLBZP) in inhibiting breast cancer (BC) lung metastasis, focusing on epithelial-to-mesenchymal transition (EMT) and ferroptosis.

Methods: BC 4T1 cells were treated with low (3.13 µg/mL) and high (12.

View Article and Find Full Text PDF

Aberrant activation of fibroblast growth factor receptors (FGFRs) plays a critical role in tumorigenesis across multiple cancer types, driving the development of various FGFR inhibitors. Despite clinical advances, therapeutic efficacy remains limited by the emergence of drug resistance, primarily mediated by gatekeeper mutations in FGFRs. To overcome this challenge, we designed and synthesized a novel series of 7-(1-methyl-1-indole-3-yl)-5-pyrrolo[2,3-]pyrazine derivatives as covalent pan-FGFR inhibitors targeting both wild-type and gatekeeper mutants.

View Article and Find Full Text PDF

Background: Sleep duration plays a crucial role in cognitive health and is closely linked to cognitive decline. However, the relationship between sleep duration and cognitive function in the Chinese population remains poorly understood.

Objective: This study aims to evaluate the association between sleep duration and cognitive function among middle-aged and older adults in China.

View Article and Find Full Text PDF

Plant-Derived Anticancer Candidates Targeting mTOR, EGFR, HER2: Insights From Molecular Docking and Dynamics Simulations.

Chem Biodivers

September 2025

School of Traditional Chinese Materia Medica, Key Laboratory of Ethnomedicine Material Basis & Pharmacological Mechanisms, Shenyang, Shenyang Pharmaceutical University, Shenyang, China.

In intracellular signaling, mammalian target of rapamycin (mTOR) as an important mammalian target for breast cancer therapy, plays a key role in receiving upstream signals from growth factor receptors such as epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 2 (HER2). Using 30 compounds from Meehania fargesii var. Radicans, structure-based virtual screening and molecular docking were performed to develop novel and safe breast cancer targeting inhibitors from natural products.

View Article and Find Full Text PDF

Usnic acid, a compound from Usneae Filum, has shown notable antitumor effects. Nevertheless, the mechanism of its anti-NSCLC action remains incompletely elucidated. This study used metabolomics, network pharmacology, molecular docking, and dynamics simulation to investigate usnic acid's potential mechanism on NSCLC utilizing A549 cell samples.

View Article and Find Full Text PDF