Protective effect of quercetin encapsulated in gelatin nanoparticles against induced cellular oxidative stress
https://doi.org/10.29235/1561-8323-2026-70-1-45-53
Abstract
The aim of this study was to evaluate the potential of gelatin nanoparticles as a means of increasing the efficacy and bioavailability of phytocompounds, in particular quercetin. The protective effect of native quercetin and quercetin incorporated into gelatin nanoparticles was studied by initiating oxidative stress in human keratinocytes with tert-butyl hydroperoxide. Cell viability was assessed using the PrestoBlueTM reagent, apoptotic and necrotic cells were detected by double intravital staining using an assay kit including annexin V-FITC. DNA damage was analyzed using the comet assay. The results demonstrated that encapsulation of quercetin into gelatin nanoparticles enables its application in aqueous suspensions without compromising its antioxidant capacity, geneand cytoprotective effects under cellular oxidative stress conditions, indicating a high efficiency of quercetin release from this nanocarrier. Consequently, the utilization of gelatin nanoparticles represents a promising approach for improving the bioavailability and therapeutic efficacy of phytochemicals.
Keywords
About the Authors
A. I. PotapovichBelarus
Potapovich Alla I. – Ph. D. (Biology), Associate Professor, Leading Researcher.
4, Nezavisimosti Ave., 220030, Minsk
T. V. Kostyuk
Belarus
Kostyuk Tatyana V. – Researcher.
4, Nezavisimosti Ave., 220030, Minsk
T. G. Shutova
Belarus
Shutava Tatsiana G. – Ph. D. (Chemistry), Leading Researcher.
36, F. Skorinа Str., 220084, Minsk
V. A. Kostyuk
Russian Federation
Kostyuk Vladimir A. – D. Sc. (Chemistry), Professor, Head of the Laboratory.
4, Nezavisimosti Ave., 220030, Minsk
References
1. Sies H. Oxidative stress: а concept in redox biology and medicine. Redox Biology, 2015, vol. 4, pp. 180–183. https://doi.org/10.1016/j.redox.2015.01.002
2. Birben E., Sahiner U. M., Sackesen C., Erzurum S., Kalayci O. Oxidative stress and antioxidant defense. World Allergy Organization Journal, 2012, vol. 5, no. 1, pp. 9–19. https://doi.org/10.1097/wox.0b013e3182439613
3. Shahidi F., Ambigaipalan P. Phenolics and polyphenolics in foods, beverages and spices: Antioxidant activity and health effects – A review. Journal of Functional Foods, 2015, vol. 18, pp. 820–897. https://doi.org/10.1016/j.jff.2015.06.018
4. Wu L. Y., Zheng X. Q., Lu J. L., Liang Y. R. Protective effect of green tea polyphenols against ultraviolet B-induced damage to HaCaT cells. Human Cell, 2009, vol. 22, pp. 18–24. https://doi.org/10.1111/j.1749-0774.2008.00063.x
5. Korkina L., Kostyuk V., Potapovich A., Mayer W., Talib N., De Luca C. Secondary plant metabolites for sun protective cosmetics: from pre-selection to product formulation. Cosmetics, 2018, vol. 5, no. 2, pp. 32–52. https://doi.org/10.3390/cosmetics5020032
6. Sahu T., Ratre Y. K., Chauhan S., Bhaskar L. V. K. S., Nair M. P., Verma H. K. Nanotechnology based drug delivery system: current strategies and emerging therapeutic potential for medical science. Journal of Drug Delivery Science and Technology, 2021, vol. 63, art. 102487. https://doi.org/10.1016/j.jddst.2021.102487
7. Potapovich A. I., Kostyuk T. V., Ishutina O. V., Shutava T. G., Kostyuk V. A. Effects of native and particulate polyphenols on DNA damage and cell viability after UV-C exposure. Naunyn-Schmiedeberg’s Archives of Pharmacology, 2023, vol. 396, pp. 1923–1930. https://doi.org/10.1007/s00210-023-02443-3
8. Coester C. J., Langer K., Van Briesen H., Kreuter J. Gelatin nanoparticles by two step desolvation – a new preparation method, surface modifications and cell uptake. Journal of Microencapsulation, 2000, vol. 17, no. 2, pp. 187–193. https://doi.org/10.1080/026520400288427
9. Tice R. R., Agurell E., Anderson D., Burlinson B., Hartmann A., Kobayashi H., Miyamae Y., Rojas E., Ryu J.-C., Sasaki Y. F. Single cell gel/comet assay: guidelines for in vitro and in vivo genetic toxicology testing. Environmental and Molecular Mutagenesis, 2000, vol. 35, no. 3, pp. 206–221. https://doi.org/10.1002/(sici)1098-2280(2000)35:3<206::aid-em8>3.0.co;2-j
10. Zhao W., Feng H., Sun W., Liu K., Lu J. J., Chen X. Tert-butyl hydroperoxide (t-BHP) induced apoptosis and necroptosis in endothelial cells: Roles of NOX4 and mitochondrion. Redox Biology, 2017, vol. 11, pp. 524–534. https://doi.org/10.1016/j.redox.2016.12.036
11. Zhanataev A. K., Anisina E. A., Chayka Z. V., Miroshkina I. A., Durnev A. D. The phenomenon of atypical DNA comets. Cell and Tissue Biology, 2017, vol. 11, no. 4, pp. 286–292. https://doi.org/10.1134/s1990519x17040113
12. Muse® Annexin V & Dead Cell Kit, 2019. Available at: https://www.luminexcorp.com/muse-annexin-v-dead-cellkit/ (accessed: 12.05.2025).
13. Elmore S. Apoptosis: a review of programmed cell death. Toxicologic Pathology, 2007, vol. 35, no. 4, pp. 495–516. https://doi.org/10.1080/01926230701320337
14. Filippov E. V. Use of the “DNA comet” method for detection and assessment of the degree of DNA damage to cells of plant, animal and human organisms caused by environmental factors. Nauka i obrazovaniye = Science and Education, 2014, no. 2, pp. 72–78 (in Russian).
15. Sharma K., Sarkar J., Trisal A., Ghosh R., Dixit A., Singh A. K. Targeting mitochondrial dysfunction to salvage cellular senescence for managing neurodegeneration. Advances in Protein Chemistry and Structural Biology, 2023, vol. 136, pp. 309–337. https://doi.org/10.1016/bs.apcsb.2023.02.016
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