Complex formation of flavonoids fisetin and geraldol with β-cyclodextrins-Reference-Cited by-同舟云学术

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Complex formation of flavonoids fisetin and geraldol with β-cyclodextrins

Published:2018-02 Issue: Volume:194 Page:82-90
ISSN:0022-2313
Container-title:Journal of Luminescence
language:en
Short-container-title:Journal of Luminescence

Author:

Sali Nikolett,Csepregi Rita,Kőszegi Tamás,Kunsági-Máté Sándor,Szente Lajos,Poór Miklós

Funder

University of Pécs, Medical School

Publisher

Elsevier BV

Subject

Condensed Matter Physics,Biochemistry,General Chemistry,Atomic and Molecular Physics, and Optics,Biophysics

Reference36 articles.

1. Polyphenols: foodsources and bioavailability;Manach;Am. J. Clin. Nutr.,2004

2. Dietary intakes of flavonols, flavones and isoflavones by Japanese women and the inverse correlation between quercetin intake and plasma LDL cholesterol concentration;Arai;J. Nutr.,2000

3. Neuroprotective effects of fisetin in Alzheimer's and Parkinson's diseases: from chemistry to medicine;Nabavi;Curr. Top. Med. Chem.,2016

4. How fisetin reduces the impact of age and disease on CNS function;Maher;Front. Biosci. (Schol Ed),2015

5. Dietary flavonoid fisetin for cancer prevention and treatment;Lall;Mol. Nutr. Food Res.,2016

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Fisetin—In Search of Better Bioavailability—From Macro to Nano Modifications: A Review;International Journal of Molecular Sciences;2023-09-15

2. Simultaneous qualitative and quantitative analysis of flavonols in Kaempferia galangal L. and honey by machine learning-based fluorescence sensor array;Sensors and Actuators B: Chemical;2023-03

3. Unveiling the flavone-solubilizing effects of α-glucosyl rutin and hesperidin: probing structural differences through NMR and SAXS analyses;Food & Function;2023

4. Cyclodextrins and Cyclodextrin-Based Nanosponges for Anti-Cancer Drug and Nutraceutical Delivery;Targeted Cancer Therapy in Biomedical Engineering;2023

5. Mechanocomposites based on 1(10)β-epoxy-5,7α(Н),6β(Н)-guai-3(4),11(13)-diene-6,12-olide;International Journal of Biology and Chemistry;2022-12

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