Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In Vitro

The naringin extraction process was optimised using response surface methodology (RSM). A central component design was adopted, which included four parameters: extraction temperature (X<sub>1</sub>), material–liquid ratio (X<sub>2</sub>), extraction time (X<sub>3</su...

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Main Authors: Xiao-Lei Yu, Xin Meng, Yi-Di Yan, Jin-Cheng Han, Jia-Shan Li, Hui Wang, Lei Zhang
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/28/4/1788
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author Xiao-Lei Yu
Xin Meng
Yi-Di Yan
Jin-Cheng Han
Jia-Shan Li
Hui Wang
Lei Zhang
author_facet Xiao-Lei Yu
Xin Meng
Yi-Di Yan
Jin-Cheng Han
Jia-Shan Li
Hui Wang
Lei Zhang
author_sort Xiao-Lei Yu
collection DOAJ
description The naringin extraction process was optimised using response surface methodology (RSM). A central component design was adopted, which included four parameters: extraction temperature (X<sub>1</sub>), material–liquid ratio (X<sub>2</sub>), extraction time (X<sub>3</sub>), and ultrasonic frequency (X<sub>4</sub>) of 74.79 °C, 1.58 h, 1:56.51 g/mL, and 28.05 KHz, respectively. Based on these optimal extraction conditions, naringin was tested to verify the model’s accuracy. Naringin yield was 36.2502 mg/g, which was equivalent to the predicted yield of 36.0124 mg/g. DM101 macroporous adsorption resin was used to purify naringin. The effects of loading concentration, loading flow rate, and sample pH on the adsorption rate of naringin and the effect of ethanol concentration on the desorption rate of naringin were investigated. The optimum conditions for naringin purification using macroporous resins were determined. The optimal loading concentration, sample solution pH, and loading flow rate were 0.075 mg/mL, 3.5, and 1.5 mL/min, respectively. Three parallel tests were conducted under these conditions, and the average naringin yield was 77.5643%. Naringin’s structure was identified using infrared spectroscopy and nuclear magnetic resonance. In vitro determination of the lipid-lowering activity of naringin was also conducted. These results showed that naringin has potential applications as a functional food for lowering blood lipid levels.
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spelling doaj.art-012b015163da4d6aa2b3b8a8a01f3b942023-11-16T22:23:22ZengMDPI AGMolecules1420-30492023-02-01284178810.3390/molecules28041788Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In VitroXiao-Lei Yu0Xin Meng1Yi-Di Yan2Jin-Cheng Han3Jia-Shan Li4Hui Wang5Lei Zhang6MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, School of Physics, Xi’an Jiaotong University, Xi’an 710049, ChinaMeat Processing and Safety Control Professional Technology Innovation Center, Jinzhou Medical University, Jinzhou 121000, ChinaMeat Processing and Safety Control Professional Technology Innovation Center, Jinzhou Medical University, Jinzhou 121000, ChinaMeat Processing and Safety Control Professional Technology Innovation Center, Jinzhou Medical University, Jinzhou 121000, ChinaMeat Processing and Safety Control Professional Technology Innovation Center, Jinzhou Medical University, Jinzhou 121000, ChinaMeat Processing and Safety Control Professional Technology Innovation Center, Jinzhou Medical University, Jinzhou 121000, ChinaMOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, School of Physics, Xi’an Jiaotong University, Xi’an 710049, ChinaThe naringin extraction process was optimised using response surface methodology (RSM). A central component design was adopted, which included four parameters: extraction temperature (X<sub>1</sub>), material–liquid ratio (X<sub>2</sub>), extraction time (X<sub>3</sub>), and ultrasonic frequency (X<sub>4</sub>) of 74.79 °C, 1.58 h, 1:56.51 g/mL, and 28.05 KHz, respectively. Based on these optimal extraction conditions, naringin was tested to verify the model’s accuracy. Naringin yield was 36.2502 mg/g, which was equivalent to the predicted yield of 36.0124 mg/g. DM101 macroporous adsorption resin was used to purify naringin. The effects of loading concentration, loading flow rate, and sample pH on the adsorption rate of naringin and the effect of ethanol concentration on the desorption rate of naringin were investigated. The optimum conditions for naringin purification using macroporous resins were determined. The optimal loading concentration, sample solution pH, and loading flow rate were 0.075 mg/mL, 3.5, and 1.5 mL/min, respectively. Three parallel tests were conducted under these conditions, and the average naringin yield was 77.5643%. Naringin’s structure was identified using infrared spectroscopy and nuclear magnetic resonance. In vitro determination of the lipid-lowering activity of naringin was also conducted. These results showed that naringin has potential applications as a functional food for lowering blood lipid levels.https://www.mdpi.com/1420-3049/28/4/1788naringinextraction optimisationstructurepurificationin vitrohypolipidemic
spellingShingle Xiao-Lei Yu
Xin Meng
Yi-Di Yan
Jin-Cheng Han
Jia-Shan Li
Hui Wang
Lei Zhang
Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In Vitro
Molecules
naringin
extraction optimisation
structure
purification
in vitro
hypolipidemic
title Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In Vitro
title_full Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In Vitro
title_fullStr Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In Vitro
title_full_unstemmed Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In Vitro
title_short Optimisation of the Extraction Process of Naringin and Its Effect on Reducing Blood Lipid Levels In Vitro
title_sort optimisation of the extraction process of naringin and its effect on reducing blood lipid levels in vitro
topic naringin
extraction optimisation
structure
purification
in vitro
hypolipidemic
url https://www.mdpi.com/1420-3049/28/4/1788
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