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Research Article | Open Access

Optimization of ultrasound-assisted extraction of flavonoids from Emilia prenanthoidea DC. using response surface methodology and exploration of the ecological factors on total flavonoid and antioxidant activity

Dan-Ni Zhao1,Xiao-Mei Zhou1,Xiao-Jian Gong1Wen-Xuan Quan1Geng-Shen Gao2( )Chao Zhao1( )
Key Laboratory for Information System of Mountainous Areas and Protection of Ecological Environment, Guizhou Normal University, Guiyang 550025, China
Guizhou Environmental Scientific Research and Design Institute, Guiyang 550081, China

These authors contributed equally to this work.

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Highlights

(1) An effective method was developed for the extraction of total flavonoids from Emilia prenanthoidea DC. (EP).

(2) The correlation of total flavonoid content and antioxidant capacity of EP with ecological factors was analyzed for the first time.

(3) Total flavonoid content and antioxidant activity of EP in 12 regions were related to ecological factors, especially annual sunshine hours.

Graphical Abstract

In the present study, ultrasound-assisted extraction (UAE) conditions were optimized using response surface methodology (RSM) for the extraction of total flavonoids from Emilia prenanthoidea DC. (EP). The total flavonoid content and antioxidant activity of EP in 12 regions were determined using optimized conditions. Finally, the correlation of ecological factors on total flavonoid content and antioxidant activity was analyzed.

Abstract

Emilia prenanthoidea DC. (EP) is a medicinal plant that belongs to the tribe Emilia Cass in the family Asteraceae. Although it has a long history of medicinal use, there are few research reports on this herb. In this study, for the first time, ultrasound-assisted extraction (UAE) conditions were optimized by response surface methodology (RSM) to extract total flavonoids from EP. An optimized method was used to determine the total flavonoid content (TFC) and antioxidant activity of EP extracts from 12 regions in Guizhou, China. Combining environmental factors in 12 regions, the effects of different growth environments on TFC and antioxidant activity of EP extracts were analyzed. In this work, it is proven that the optimal conditions for extraction are a solvent concentration of 45%, an ultrasonication time of 25 min, and a liquid-solid ratio of 46.25 mL/g. Under this condition, the highest TFC (41.182 mg/g) was found in the EP extract from Daping, while the lowest TFC (28.865 mg/g) was found in the EP extract from Liping. Evaluation of antioxidant activity showed that the highest antioxidant capacity was found in EP extracts from Daping, followed by Tuan Shan, Yaobai and Green Lake. Ecological factors affected both total flavonoids and antioxidant activity in EP. Annual sunshine hours in different regions had a significant effect on TFC in EP (r = −0.841, P < 0.01). In conclusion, this study established an effective method for the extraction of total flavonoids from EP, an effective natural antioxidant. The effects of the growth environment on the TFC and antioxidant capacity were also analyzed. It provides an experimental basis for the extensive utilization of EP.

References

[1]

Scherer, R., Godoy, H. T. Antioxidant activity index (AAI) by the 2,2-diphenyl-1-picrylhydrazyl method. Food Chemistry, 2009, 112: 654–658. https://doi.org/10.1016/j.foodchem.2008.06.026

[2]

Butterfield, D. A., Halliwell, B. Oxidative stress, dysfunctional glucose metabolism and Alzheimer disease. Nature Reviews Neuroscience, 2019, 20: 148–160. https://doi.org/10.1038/s41583-019-0132-6

[3]

Hayes, J. D., Dinkova-Kostova, A. T., Tew, K. D. Oxidative stress in cancer. Cancer Cell, 2020, 38: 167–197. https://doi.org/10.1016/j.ccell.2020.06.001

[4]

Zhao, Y., Han, C., Wu, Y., et al. Extraction, structural characterization, and antioxidant activity of polysaccharides from three microalgae. Science of the Total Environment, 2024, 931: 172567. https://doi.org/10.1016/j.scitotenv.2024.172567

[5]

Namiki, M. Antioxidants/antimutagens in food. Critical Reviews in Food Science and Nutrition, 1990, 29: 273–300. https://doi.org/10.1080/10408399009527528

[6]

Deng, G. F., Lin, X., Xu, X. R., et al. Antioxidant capacities and total phenolic contents of 56 vegetables. Journal of Functional Foods, 2013, 5: 260–266. https://doi.org/10.1016/j.jff.2012.10.015

[7]

Wen, Y., Zeng, X., Dai, H. J., et al. Optimization of ultrasonic assisted extraction and biological activity of total flavonoids from Ligusticum chuanxiong Hort. using response surface methodology. Biomass Conversion and Biorefinery, 2023, 14: 17101–17113. https://doi.org/10.1007/s13399-023-03832-7

[8]

Wufuer, Y., Yang, X., Guo, L. Y., et al. The antitumor effect and mechanism of total flavonoids from Coreopsis tinctoria Nutt (snow chrysanthemum) on lung cancer using network pharmacology and molecular docking. Frontiers in Pharmacology, 2022, 13: 761785. https://doi.org/10.3389/fphar.2022.761785

[9]

Patil, S. S., Pathak, A., Rathod, V. K. Optimization and kinetic study of ultrasound assisted deep eutectic solvent based extraction: a greener route for extraction of curcuminoids from Curcuma longa. Ultrasonics Sonochemistry, 2021, 70: 105267. https://doi.org/10.1016/j.ultsonch.2020.105267

[10]

Ashrafizadeh, M., Rafiei, H., Mohammadinejad, R., et al. Anti-tumor activity of resveratrol against gastric cancer: a review of recent advances with an emphasis on molecular pathways. Cancer Cell International, 2021, 21: 66. https://doi.org/10.1186/s12935-021-01773-7

[11]

Jiang, Z. M., Zhao, C., Gong, X. J., et al. Quantification and efficient discovery of quality control markers for Emilia prenanthoidea DC. by fingerprint-efficacy relationship modelling. Journal of Pharmaceutical and Biomedical Analysis, 2018, 156: 36–44. https://doi.org/10.1016/j.jpba.2018.04.020

[12]

Shylesh, B. S., Padikkala, J. Antioxidant and anti-inflammatory activity of Emilia sonchifolia. Fitoterapia, 1999, 70: 275–278. https://doi.org/10.1016/s0367-326x(99)00037-4

[13]

Couto, V. M., Vilela, F. C., Dias, D. F., et al. Antinociceptive effect of extract of Emilia sonchifolia in mice. Journal of Ethnopharmacology, 2011, 134: 348–353. https://doi.org/10.1016/j.jep.2010.12.028

[14]

Shen, S. M., Shen, L. G., Zhang, J., et al. Emiline, a new alkaloid from the aerial parts of Emilia sonchifolia. Phytochemistry Letters, 2013, 6: 467–470. https://doi.org/10.1016/j.phytol.2013.05.018

[15]

Wang, D., Lv, J., Fu, Y., et al. Optimization of microwave-assisted extraction process of total flavonoids from Salicornia bigelovii Torr. and its hepatoprotective effect on alcoholic liver injury mice. Foods, 2024, 13: 647. https://doi.org/10.3390/foods13050647

[16]

Zhou, J., Zhang, L., Li, Q., et al. Simultaneous optimization for ultrasound-assisted extraction and antioxidant activity of flavonoids from Sophora flavescens using response surface methodology. Molecules, 2018, 24: 112. https://doi.org/10.3390/molecules24010112

[17]

Chen, F., Wang, B., Zhao, G., et al. Optimization extraction of flavonoids from peony pods by response surface methodology, antioxidant activity and bioaccessibility in vitro. Journal of Food Measurement and Characterization, 2022, 17: 460–471. https://doi.org/10.1007/s11694-022-01649-y

[18]

Varinskii, B. A., Khil'ko, N. A., Petrenko, V. V. Express method for the quantitative determination of the total flavonoids in the flowers of Sophora japonica. Chemistry of Natural Compounds (Translation of Khimiya Prirodnykh Soedinenii), 1999, 35: 215–216. https://doi.org/10.1007/bf02234940

[19]

Chen, Z., Bertin, R., Froldi, G. EC50 estimation of antioxidant activity in DPPH assay using several statistical programs. Food Chemistry, 2013, 138: 414–420. https://doi.org/10.1016/j.foodchem.2012.11.001

[20]

Van den Berg, R., Haenen, G. R. M. M., Van den Berg, H., et al. Applicability of an improved Trolox equivalent antioxidant capacity (TEAC) assay for evaluation of antioxidant capacity measurements of mixtures. Food Chemistry, 1999, 66: 511–517. https://doi.org/10.1016/s0308-8146(99)00089-8

[21]

Benzie, I. F. F., Strain, J. J. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Analytical Biochemistry, 1996, 239: 70–76. https://doi.org/10.1006/abio.1996.0292

[22]

Han, H. Q., Cai, G. P., Wu, J., et al. Spatial and temporal variations of absolute humidity in Guizhou Province from 1960 to 2013. Journal of Sichuan Agricultural University, 2016, 34: 348–353. https://doi.org/10.16036/j.issn.1000-2650.2016.03.015

[23]

Wang, X., Cao, J. G., Dai, X. L., et al. Total flavonoid concentrations of bryophytes from Tianmu Mountain, Zhejiang Province (China): phylogeny and ecological factors. PLoS ONE, 2017, 12: e0173003. https://doi.org/10.1371/journal.pone.0173003

[24]

Chua, L. S. A review on plant-based rutin extraction methods and its pharmacological activities. Journal of Ethnopharmacology, 2013, 150: 805–817. https://doi.org/10.1016/j.jep.2013.10.036

[25]

Zhang, Y. L., Yu, X. M., Wang, M. M., et al. Hyperoside from Z. bungeanum leaves restores insulin secretion and mitochondrial function by regulating pancreatic cellular redox status in diabetic mice. Free Radical Biology and Medicine, 2021, 162: 412–422. https://doi.org/10.1016/j.freeradbiomed.2020.10.320

[26]

Wu, W., Xie, Z. L., Zhang, Q., et al. Hyperoside ameliorates diabetic retinopathy via anti-oxidation, inhibiting cell damage and apoptosis induced by high glucose. Frontiers in Pharmacology, 2020, 11: 797. https://doi.org/10.3389/fphar.2020.00797

[27]

Hu, C., Chen, Y., Cao, Y. Y., et al. Metabolomics analysis reveals the protective effect of quercetin-3- O-galactoside (hyperoside) on liver injury in mice induced by acetaminophen. Journal of Food Biochemistry, 2020, 44: e13420. https://doi.org/10.1111/jfbc.13420

[28]

Ham, Y. M., Yoon, W. J., Park, S. Y., et al. Quercitrin protects against oxidative stress-induced injury in lung fibroblast cells via up-regulation of Bcl-XL. Journal of Functional Foods, 2012, 4: 253–262. https://doi.org/10.1016/j.jff.2011.12.001

[29]

Wagner, C., Fachinetto, R., Dalla Corte, C. L., et al. Quercitrin, a glycoside form of quercetin, prevents lipid peroxidation in vitro. Brain Research, 2006, 1107: 192–198. https://doi.org/10.1016/j.brainres.2006.05.084

[30]

Ahmad, R., Ahmad, N., Naqvi, A., et al. Antioxidant and antiglycating constituents from leaves of Ziziphus oxyphylla and Cedrela serrata. Antioxidants, 2016, 5: 9. https://doi.org/10.3390/antiox5010009

[31]
Silva, C. G., Raulino, R. J., Cerqueira, D. M., et al. In vitro and in vivo determination of antioxidant activity and mode of action of isoquercitrin and Hyptis fasciculata. Phytomedicine, 2009 , 16: 761–767. https://doi.org/10.1016/j.phymed.2008.12.019
[32]

Xie, W. Y., Wang, M., Chen, C., et al. Hepatoprotective effect of isoquercitrin against acetaminophen-induced liver injury. Life Sciences, 2016, 152: 180–189. https://doi.org/10.1016/j.lfs.2016.04.002

Food & Medicine Homology
Article number: 9420017
Cite this article:
Zhao D-N, Zhou X-M, Gong X-J, et al. Optimization of ultrasound-assisted extraction of flavonoids from Emilia prenanthoidea DC. using response surface methodology and exploration of the ecological factors on total flavonoid and antioxidant activity. Food & Medicine Homology, 2024, 1(2): 9420017. https://doi.org/10.26599/FMH.2024.9420017

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Received: 15 May 2024
Revised: 25 June 2024
Accepted: 27 June 2024
Published: 12 August 2024
© National R & D Center for Edible Fungus Processing Technology 2024. Published by Tsinghua University Press.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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