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Acta Chromatographica
Authors: É. Szőke, G. Petroianu, K. Tekes, B. Benkő, P. Szegi, R. Laufer, and G. Veress

Summary

Reversed-phase HPLC has been used to monitor the concentration of the two major Chamomile components rutin and quercetin during rat liver microsomal treatment. The possibility of microsomal oxidative metabolism or stability of these two components was examined using a guard-column without any clean-up. The concentration of quercetin decreased when exposed to rat liver microsomal media whereas the rutin concentration did not change significantly over one hour of treatment.

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Summary

An ultrasensitive and rapid method for the determination of epicatechin, rutin, and quercetin was developed using capillary zone electrophoresis with on-line chemiluminescence detection. Under the optimal conditions, the analytes were baseline separated within 12 min. The limits of detection in turn were 0.60 pg mL−1 for epicatechin, 0.50 pg mL−1 for rutin, and 1.0 pg mL−1 for quercetin. The developed method was an easy and reliable method of determining these analytes concentrations in tea, extract Ginkgo biloba, and rutin tablet, demonstrating the feasibility and reliability of the proposed method.

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as antihypertensive system, which should be superior in activity, tolerability, or both. Additionally, herbal flavonoid component, i.e., Rutin (Ru, quercetin disaccharide conjugate) is used as bioenhancing agent. The specific goals of the research

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, characterize, and optimize isradipine (ISR; 15%–24% oral bioavailability and poor solubility) with enhancing agent (rutin) loaded nano-colloidal carrier via polymer (Eudragit L100)-coated, i.e., SLNbp using central composite design. Basically in this study

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Acta Chromatographica
Authors: Y.T. Kamal, Sayeed Ahmad, Nanjaian Mahadevan, Prawez Alam, Shahana Salam, Yahya I Asiri, Abdullatif Bin Muhsinah, and Abdulrhman Alsayari

free flavonoids like rutin and quercetin forms the basis of bioactivity of these Itrifal formulations [ 5 ]. The anthraquinone glycosides like sennoside A and B were selected as a specific marker for C. angustifolia , which is present in a significant

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Acta Chromatographica
Authors: Milica Atanacković Krstonošić, Jelena Cvejić Hogervorst, Mira Mikulić, and Ljiljana Gojković-Bukarica

. Experimental 2.1. Standards and Reagents Phenolic standards, namely, rutin, naringenin, chlorogenic acid, trans -cinnamic acid, quercetin, p -coumaric acid, caffeic acid, p -hydroxybenzoic acid, syringic acid, vanillic

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from Sigma-Aldrich, St. Louis (Missouri, USA). Precoated TLC (silica gel 60 F254) and quercetin were purchased from Merck (Darmstadt, Germany). Rutin and β-sitosterol were purchased from Sigma-Aldrich (St. Louis, Missouri, USA). The solvents used for

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.095 Gallic acid 10–1000 0.9965 4.50 9.50 Rutin 1–500 0.9925 0

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Acta Chromatographica
Authors: Yuping Shen, Minhui Xu, Peipei Deng, Qinying Gu, Huawu Yin, Guohua Xia, Xiaobin Jia, Huan Yang, and James Tam

quality of bioactive chemical constituents in natural products [ 15 ]. Accordingly, in our previous studies, gallic acid, methyl gallate, and a few non-specific flavonoids such as rutin, kaempferol 3- O - β - d -glucopyranoside, and quercitrin, in Red Toon

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Acta Chromatographica
Authors: Omar M. Khalaf, Mosad A. Ghareeb, Amal M. Saad, Hassan M. F. Madkour, Ahmed K. El-Ziaty, and Mohamed S. Abdel-Aziz

:9, v/v), followed by PTLC eluted with (ethyl acetate: MeOH; 2.1:2.9; v/v) to give quercetin 3- O -α- l -rhamnopyranosyl-(1→6)-β- d -glucopyranoside (rutin) ( 5 ), while fraction (V) was purified on silica gel sub-column eluted with (EtOAc–MeOH; 17: 3, v

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