Rapid identification and detection of aristolochic acids in the herbal extracts by Raman spectroscopy.


Journal

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
ISSN: 1873-3557
Titre abrégé: Spectrochim Acta A Mol Biomol Spectrosc
Pays: England
ID NLM: 9602533

Informations de publication

Date de publication:
05 Nov 2023
Historique:
received: 06 04 2023
revised: 16 05 2023
accepted: 24 05 2023
medline: 19 6 2023
pubmed: 4 6 2023
entrez: 3 6 2023
Statut: ppublish

Résumé

Herbs containing aristolochic acids (AAs) have already been proven to be highly carcinogenic and nephrotoxic. In this study, a novel surface-enhanced Raman scattering (SERS) identification method was developed. Ag-APS nanoparticles with a particle size of 3.53 ± 0.92 nm were produced by combining silver nitrate and 3-aminopropylsilatrane. The reaction between the carboxylic acid group of aristolochic acid I (AAI) and amine group of Ag-APS NPs was used to form amide bonds, and thus, concentrate AAI, rendering it easy to detect via SERS and amplified to obtain the best SERS enhancement effect. Detection limit was calculated to be approximately 40 nM. Using the SERS method, AAI was successfully detected in the samples of four Chinese herbal medicines containing AAI. Therefore, this method has a high potential to be applied in the future development of AAI analysis and rapid qualitative and quantitative analysis of AAI in dietary supplements and edible herbs.

Identifiants

pubmed: 37269653
pii: S1386-1425(23)00603-0
doi: 10.1016/j.saa.2023.122918
pii:
doi:

Substances chimiques

aristolochic acid I 94218WFP5T
Aristolochic Acids 0
Drugs, Chinese Herbal 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122918

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Chin-Chung Lin (CC)

Department of Emergency Medicine, Kaohsiung Armed Forces General Hospital, Kaohsiung 80284, Taiwan.

Pei-Ying Lin (PY)

Department of Chemistry, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.

Zhenyuan Han (Z)

Department of Chemistry, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.

Chen-Yu Tsai (CY)

Department of Chemistry, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.

David E Beck (DE)

Oxford Instruments Asylum Research, Inc., 7416 Hollister Ave., Santa Barbara, CA 93117, USA.

Shuchen Hsieh (S)

Department of Chemistry, National Sun Yat-sen University, Kaohsiung 80424, Taiwan; Regenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan; School of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan. Electronic address: shsieh@faculty.nsysu.edu.tw.

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Classifications MeSH