144
Views
1
CrossRef citations to date
0
Altmetric
Chromatography

Optimization of High-Performance Liquid Chromatography (HPLC) Conditions for Isoflavones Using Deep Eutectic Solvents (DESs) as Mobile Phase Additives by the HCI Program

ORCID Icon, &
Pages 118-129 | Received 05 Jan 2023, Accepted 27 Mar 2023, Published online: 06 Apr 2023

References

  • Abbott, A. P., G. Capper, D. L. Davies, R. K. Rasheed, and V. Tambyrajah. 2003. Novel solvent properties of choline chloride/urea mixtures. Chemical Communications :70–1. doi:10.1039/b210714g.
  • An, Y., and K. H. Row. 2021. Evaluation of menthol-based hydrophobic deep eutectic solvents for the extraction of bisphenol A from environment water. Analytical Letters 54:1533–45. doi:10.1080/00032719.2020.1811716.
  • Capello, C., U. Fischer, and K. Hungerbühler. 2007. What is a green solvent? A comprehensive framework for the environmental assessment of solvents. Green Chemistry 9:927–34. doi:10.1039/b617536h.
  • da Costa César, I., F. C. Braga, C. D. V. Soares, E. de Aguiar Nunan, G. A. Pianetti, F. A. Condessa, T. A. F. Barbosa, and L. M. M. Campos. 2006. Development and validation of a RP-HPLC method for quantification of isoflavone aglycones in hydrolyzed soy dry extracts. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences 836 (1–2):74–8. doi:10.1016/j.jchromb.2006.03.030.
  • Docherty, K. M., and C. F. Kulpa. Jr. 2005. Toxicity and antimicrobial activity of imidazolium and pyridinium ionic liquids. Green Chemistry 7:185–9. doi:10.1039/b419172b.
  • Espino, M., M. de los Ángeles Fernández, F. J. Gomez, and M. F. Silva. 2016. Natural designer solvents for greening analytical chemistry. Trends in Analytical Chemistry 76:126–36. doi:10.1016/j.trac.2015.11.006.
  • Fayed, A. 2015. Health benefits of some physiologically active ingredients and their suitability as yoghurt fortifiers. Journal of Food Science and Technology 52 (5):2512–21. doi:10.1007/s13197-014-1393-8.
  • Fu, G., J. Chen, and H. Qiu. 2022. Deep eutectic solvents-derivated carbon dots-decorated silica stationary phase with enhanced separation selectivity in reversed-phase liquid chromatography. Journal of Chromatography A 1681:463425. doi:10.1016/j.chroma.2022.463425.
  • Gacek, M. 2014. Soy and legume seeds as sources of isoflavones: Selected individual determinants of their consumption in a group of perimenopausal women. Przeglad Menopauzalny/Menopause Review 13 (1):27–31. doi:10.5114/pm.2014.41081.
  • Gao, F., L. Liu, W. Tang, K. H. Row, and T. Zhu. 2018. Optimization of the chromatographic behaviors of quercetin using choline chloride-based deep eutectic solvents as HPLC mobile-phase additives. Separation Science and Technology 53:397–403. doi:10.1080/01496395.2017.1388257.
  • Gao, Y., Y. Yao, Y. Zhu, and G. Ren. 2015. Isoflavones in chickpeas inhibit adipocyte differentiation and prevent insulin resistance in 3T3-L1 cells. Journal of Agricultural and Food Chemistry 63 (44):9696–703. doi:10.1021/acs.jafc.5b03957.
  • Gökdemir, B., N. Baylan, and S. Çehreli. 2020. Application of a novel ionic liquid as an alternative green solvent for the extraction of curcumin from turmeric with response surface methodology: Determination and optimization study. Analytical Letters 53:2111–21. doi:10.1080/00032719.2020.1730394.
  • González-Miquel, M., and I. Díaz. 2021. Green solvent screening using modeling and simulation. Current Opinion in Green and Sustainable Chemistry 29:100469. doi:10.1016/j.cogsc.2021.100469.
  • Grau, J., C. Azorín, J. L. Benedé, A. Chisvert, and A. Salvador. 2022. Use of green alternative solvents in dispersive liquid‐liquid microextraction: A review. Journal of Separation Science 45 (1):210–22. doi:10.1002/jssc.202100609.
  • Hansen, B. B., S. Spittle, B. Chen, D. Poe, Y. Zhang, J. M. Klein, A. Horton, L. Adhikari, T. Zelovich, B. W. Doherty, et al. 2021. Deep eutectic solvents: A review of fundamentals and applications. Chemical Reviews 121 (3):1232–85. doi:10.1021/acs.chemrev.0c00385.
  • He, S., D. M. Choi, and K. H. Row. 2022. Utilization of ionic deep eutectic solvent as sustainable mobile phase additive in high‐performance liquid chromatography for improving the separation of biogenic amines. Journal of Separation Science 45 (22):4005–11. doi:10.1002/jssc.202200608.
  • He, S., W. Tang, and K. H. Row. 2022. Determination of thiophanate-methyl and carbendazim from environmental water by liquid-liquid microextraction (LLME) using a terpenoid-based hydrophobic deep eutectic solvent and high-performance liquid chromatography (HPLC). Analytical Letters 55:1235–48. doi:10.1080/00032719.2021.1993237.
  • Islam, M. A., A. Punt, B. Spenkelink, A. J. Murk, F. Rolaf van Leeuwen, and I. M. Rietjens. 2014. Conversion of major soy isoflavone glucosides and aglycones in in vitro intestinal models. Molecular Nutrition & Food Research 58 (3):503–15. doi:10.1002/mnfr.201300390.
  • Jin, C. H., J. W. Lee, and K. H. Row. 2006. Optimum condition of mobile phase composition for purine compounds by HCI program. Applied Chemistry for Engineering 17:317–20.
  • Jin, Y., and K. H. Row. 2006. Optimum separation conditions of catechin compounds by hci program in reversed-phase high performance liquid chromatography. Se pu/Chinese Journal of Chromatography 24:466–70.
  • Kaur, G., H. Kumar, and M. Singla. 2022. Diverse applications of ionic liquids: A comprehensive review. Journal of Molecular Liquids 351:118556. doi:10.1016/j.molliq.2022.118556.
  • Khataei, M. M., S. B. H. Epi, R. Lood, P. Spégel, Y. Yamini, and C. Turner. 2022. A review of green solvent extraction techniques and their use in antibiotic residue analysis. Journal of Pharmaceutical and Biomedical Analysis 209:114487. doi:10.1016/j.jpba.2021.114487.
  • Lee, Y.-W., M. S. So, J. W. Lee, S. T. Chung, and K. H. Row. 1996. Retention models of capacity factor with different compositions of organic modifier in RP-HPLC. Korean Journal of Chemical Engineering 13:578–84. doi:10.1007/BF02706024.
  • Li, G., Y. Dai, X. Wang, and K. Row. 2019. Molecularly imprinted polymers modified by deep eutectic solvents and ionic liquids with two templates for the simultaneous solid-phase extraction of fucoidan and laminarin from marine kelp. Analytical Letters 52:511–25.
  • Li, G., T. Zhu, and Y. Lei. 2015. Choline chloride-based deep eutectic solvents as additives for optimizing chromatographic behavior of caffeic acid. Korean Journal of Chemical Engineering 32:2103–8.
  • Li, S., M. Tian, and K. H. Row. 2012. Optimization of mobile phase condition by using HCI program for extracting luteolin and apigenin from celery. Asia‐Pacific Journal of Chemical Engineering 7:337–42.
  • Liu, Y., X. Wei, J. Chen, Y.-L. Yu, J.-H. Wang, and H. Qiu. 2022. Acetylcholinesterase activity monitoring and natural anti-neurological disease drug screening via rational design of deep eutectic solvents and CeO2-Co(OH)2 nanosheets. Analytical Chemistry 94:5970–9.
  • Messina, M. 2016. Soy and health update: Evaluation of the clinical and epidemiologic literature. Nutrients 8:754.
  • Murphy, P. A., K. Barua, and C. C. Hauck. 2002. Solvent extraction selection in the determination of isoflavones in soy foods. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences 777 (1–2):129–38.
  • Payette, M., M. R. Lima, W. M. Coleman, and M. Ashraf-Khorassani. 2022. Separation optimization and quantitative analysis of phytoestrogens employing reverse-phase high-performance liquid chromatography with UV-VIS detection. Journal of Liquid Chromatography & Related Technologies 44:888–96.
  • Pérez-López, L. A., N. Cavazos-Rocha, C. Delgado-Montemayor, N. Waksman-Minsky, M. Hernández-Salazar, and O. J. Portillo-Castillo. 2022. A simple HPLC-DAD method for analysis of phenolic acids: Addition effect of a hydrophilic deep eutectic solvent to the mobile phase. Acta Chromatographica. doi:10.1556/1326.2022.01055.
  • Santana-Mayor, Á., R. Rodríguez-Ramos, A. V. Herrera-Herrera, B. Socas-Rodríguez, and M. Á. Rodríguez-Delgado. 2021. Deep eutectic solvents. The new generation of green solvents in analytical chemistry. Trends in Analytical Chemistry 134:116108.
  • Shoenmakers, P. J., H. A. Billiet, and L. De Galan. 1979. Influence of organic modifiers on the rentention behaviour in reversed-phase liquid chromatography and its consequences for gradient elution. Journal of Chromatography A 185:179–95.
  • Soares, B., H. Passos, C. S. Freire, J. A. Coutinho, A. J. Silvestre, and M. G. Freire. 2016. Ionic liquids in chromatographic and electrophoretic techniques: Toward additional improvements in the separation of natural compounds. Green Chemistry 18:4582–604.
  • Sun, J.-M., B.-L. Sun, F.-X. Han, S.-R. Yan, Y. Hua, and K. Akio. 2011. Rapid HPLC method for determination of 12 isoflavone components in soybean seeds. Agricultural Sciences in China 10:70–7.
  • Tan, T., M. Zhang, Y. Wan, and H. Qiu. 2016. Utilization of deep eutectic solvents as novel mobile phase additives for improving the separation of bioactive quaternary alkaloids. Talanta 149:85–90.
  • Tang, W., and K. H. Row. 2018. Hydrophobic ionic liquid modified thermoresponsive molecularly imprinted monolith for the selective recognition and separation of tanshinones. Journal of Separation Science 41:3372–81.
  • Tsai, H.-S., L.-J. Huang, Y.-H. Lai, J.-C. Chang, R.-S. Lee, and R. Y.-Y. Chiou. 2007. Solvent effects on extraction and HPLC analysis of soybean isoflavones and variations of isoflavone compositions as affected by crop season. Journal of Agricultural and Food Chemistry 55:7712–5.
  • Wu, Z., L. Song, S. Feng, Y. Liu, G. He, Y. Yioe, S. Q. Liu, and D. Huang. 2012. Germination dramatically increases isoflavonoid content and diversity in chickpea (Cicer arietinum L.) seeds. Journal of Agricultural and Food Chemistry 60 (35):8606–15. doi:10.1021/jf3021514.
  • Xiao, J., B. Li, R. Qiang, H. Qiu, and J. Chen. 2022. Highly selective adsorption of rare earth elements by honeycomb-shaped covalent organic frameworks synthesized in deep eutectic solvents. Environmental Research 214:113977.
  • Yatsu, F. K., L. S. Koester, and V. L. Bassani. 2016. Isoflavone-aglycone fraction from glycine max: A promising raw material for isoflavone-based pharmaceutical or nutraceutical products. Revista Brasileira de Farmacognosia 26:259–67.
  • Zhang, J., S. Li, L. Yao, Y. Yi, L. Shen, Z. Li, and H. Qiu. 2022. Responsive switchable deep eutectic solvents: A review. Chinese Chemical Letters 34:107750.
  • Zheng, J., and R. Kyungho. 2007. Optimum of mobile phase condition for resolving isoflavones in RP-HPLC. Chinese Journal of Chemical Engineering 15:291–5.
  • Zin, M. M., and S. Bánvölgyi. 2022. Thermal emerging technology approach for the extraction of bioactive compounds from cylindra beetroot (peel, flesh, and stalk) with green solvent. Journal of Food Processing and Preservation 46: E 16436.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.