氮螺旋菌细胞在槲皮素检测中的应用。

IF 3.4 Q2 CHEMISTRY, MEDICINAL ADMET and DMPK Pub Date : 2023-01-01 DOI:10.5599/admet.1661
Matvey V Kanevskiy, Irina S Kosheleva, Vladislav O Menukhov, Elizaveta S Zhdanova, Svetlana V Borisova, Gennady L Burygin, Svetlana A Konnova, Victor D Bunin, Olga I Guliy
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引用次数: 0

摘要

利用槲皮素- baldaniorum偶氮螺旋菌Sp245模型体系,首次证明了利用微生物细胞检测黄酮类化合物的可能性。研究了槲皮素、芦丁和柚皮素三种黄酮类化合物对巴草Sp245的抑菌活性。结果表明,槲皮素浓度在50 ~ 100 μM范围内,细菌细胞数量减少。芦丁和柚皮素对细菌数量没有影响。槲皮素在100 μM时使细菌阻抗增加60%。在槲皮素的作用下,细胞的电光信号强度比没有槲皮素的对照组降低了75%。我们的数据显示了开发基于传感器的系统来检测和测定黄酮类化合物的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Use of Azospirillum baldaniorum cells in quercetin detection.

The possibility of detection and determination of flavonoids by using microbial cells was shown for the first time using the quercetin - Azospirillum baldaniorum Sp245 model system. The activity of the flavonoids quercetin, rutin and naringenin toward A. baldaniorum Sp245 was evaluated. It was found that when the quercetin concentration ranged from 50 to 100 μM, the number of bacterial cells decreased. Rutin and naringenin did not affect bacterial numbers. Quercetin at 100 μM increased bacterial impedance by 60 %. Under the effect of quercetin, the magnitude of the electro-optical signal from cells decreased by 75 %, as compared with the no-quercetin control. Our data show the possibility of developing sensor-based systems for the detection and determination of flavonoids.

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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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