Abstract

To explore a green and efficient extraction technology for the extraction of active ingredients of Asarum, the deep eutectic solvent combined with ultrasonic was applied to compare the extraction efficiency of 10 kinds of deep eutectic solvents, taking the extraction rate of methyl eugenol and asarinin as indices. Single-factor experiments were adopted to investigate the influence of molar ratio, liquid-to-solid ratio, eddy time, ultrasonic time, and temperature of the deep eutectic solvent on the extraction rate of methyl eugenol and asarinin. Based on single-factor experiments, the surface response methodology was used to optimize the extraction process conditions. The results showed that the optimum extracting process conditions of methyl eugenol and asarinin in Asarum consisted of a ratio of choline chloride to glycerol of 1 : 3, a DES volume of 2 mL, an ultrasonic temperature of 60°C, an ultrasonic time of 30 min, and a vortex oscillation of 7 min. Under the optimum extracting process conditions, the contents of methyl eugenol and asarinin were 1.9428 mg/g and 0.9989 mg/g, respectively, and the comprehensive index was 2.3280 (RSD of 1.91%). The results were close to the predicted values of the response surface model, demonstrating the applicability of the model. The extraction rate of methyl eugenol and asarinin in Asarum by this method was higher than that of water extraction and alcohol extraction, which fully indicated the high efficiency of ultrasonic-assisted green deep eutectic solvent extraction technology. The results provide data support for further development and utilization of Asarum.

1. Introduction

Asarums are the dry roots and rhizomes of Aristolochiaceae plants such as Asarum heterotropoides Fr. Schmidt var. mandshuricum (Maxim.) Kitag., Asarum sieboldii Miq. Var. seoulense Nakai, or Asarum sieboldii Miq. [1]. Asarum is pungent, warm in nature, and enters the heart, lung, and kidney meridians, with slight toxicity [2]. It has the effect of reliving the exterior syndrome and dispersing cold, dispelling wind and relieving pain and opening into five organs, and warming the lung and resolving fluid [3]. Asarum contains a variety of components, including volatile oil, lignans, flavonoids, steroids, polysaccharides [47], asarinin, methyl eugenol, safrole, and so on [8]. Asarum is commonly used in the clinical treatment of common cold due to wind cold, headache, toothache, stuffy and runny nose, allergic rhinitis, nasosinusitis, rheumatism and pain syndrome, and phlegm and retained fluid, dyspnea with cough [9].

In 2003, Abbott et al. [10] first found a solvent composed of hydrogen bond acceptors and donors with certain molar ratio and called it deep eutectic solvent (DES). As it has good physical and chemical properties, such as green, low melting point, easy to synthesis, low cost, strong solubility, and can be repeatedly used [11, 12], DESs currently have gradually replaced organic solvents and ionic liquids and showed great potential in the extraction and separation of natural plants [1315]. In recent years, water-soluble DESs based on choline chloride have been widely applied in various fields, from physical, material, and chemical to the efficient extraction and separation of alkaloids, flavonoids, polysaccharides, and acids from medicinal plants [16, 17].

In the study, 10 kinds of DESs were first used in the extraction of the active ingredients of Asarum. With the index of the extraction rate of methyl eugenol and asarinin, the response surface methodology was applied to analyze the optimal conditions of the extraction of methyl eugenol and asarinin from Asarum, which was subsequently compared with the traditional extraction method, so as to provide a more green, efficient, and economical novel extraction method, promote the deep development of Asarum, and provide a theoretical basis for the comprehensive development and utilization of Asarum.

2. Materials and Methods

2.1. Reagents

Asarum used in this experiment was from Sichuan Province in China and purchased from Jilin Pharmacy (Changchun), and all of them met the requirements of Chinese Pharmacopoeia (2020 edition). Chromatography-grade methanol (batch no. 20200601) and acetonitrile (batch no. 20200601) were purchased from Fisher Company, USA; analytical grade phosphoric acid (batch no. 20170408) was obtained from Tianjin Guangfu Science and Technology Development Co., Ltd.; ultrapure water was acquired from Hangzhou Wahaha Co., Ltd.; methyl eugenol (batch no. 111642–200301) and asarinin (batch no. 111889–201705) were acquired from the National Institute of Food and Drug Control; choline chloride (batch no. 150120) was obtained from Shanghai Zhanyun Chemical Co., Ltd.; maltose (batch no. 117101), malic acid (batch no. 117101), lactic acid (batch no. 117101), fructose (batch no. 117001), xylitol (batch no. 117101), and citric acid (batch no. 117101) were acquired from Zhengzhou Kangyuan Chemical Products Co., Ltd.; phenol (batch no. 170902) and acetic acid (batch no. 117101) were purchased from Xilong Scientific Co., Ltd.; glycerin (batch no. 20180406) was purchased from Guangzhou Yaya Cosmetics Co., Ltd.; propylene glycol (batch no. 20180309) was obtained from Tianjin Zhonghe Shengtai Chemical Co., Ltd.; and urea (batch no. 20170109) was purchased from Tianjin Ruijinte Chemical Co., Ltd.

2.2. Instrumentation

The chromatographic analysis was performed with the use of Huapu S3000 high performance liquid chromatography system (including four-element low-pressure stirring pump, automatic sampler, column box, 1100 diode array detector, and chemical workstation). Jp-300 G ultrasonic extractor was purchased from Wuhan Jiapeng Electronics Co., Ltd. AB135-S electronic balances were purchased from Mettler Toledo International Ltd. Ql-901 vortex instrument was purchased from Haimen Qilin Beier instrument Manufacturing Co., Ltd. TGL-16 refrigerated centrifuge was purchased from Hunan Xiangyi Laboratory Instrument Development Co., Ltd.

2.3. HPLC Method for the Determination of Asarum

The chromatographic column was Diamonsil®C18 (4.6 × 250 mm, 5 μm). The mobile phase included acetonitrile-0.1% phosphoric acid aqueous solution. The selected wavelength was 287 nm, the injection volume was 10 μL, and the column temperature was 40°C. The detailed gradient elution conditions are displayed in Table 1. HPLC chromatogram of Asarum is given in Figure 1.

2.4. Preparation of DESs

In this paper, choline chloride was selected as the hydrogen bond acceptor (HBA) and the 10 materials in Table 2 were selected as the hydrogen bond donors (HBD) to prepare DESs considering their nature, safety, and low cost. HBA and HBD were accurately weighed and mixed at a certain molar ratio, heated, and stirred at 80–100°C until a clear and uniform liquid was formed.

2.5. Extraction of Methyl Eugenol and Asarinin from Asarum

The process of preparation of the test product is shown in Figure 2. 50 mg of Asarum powder was weighed and subsequently added to the DES at a solid-liquid ratio of 1 : 30 (g/mL), warm bath for 5 min, eddy oscillation for 5 min, ultrasonic extraction at 60°C for 30 min, ultrasonic power of 200 W [18], eddy oscillation for 1 min, and centrifugation at 3000 r/min for 5 min at obtain the Asarum extract.

2.6. Box–Behnken Response Surface Experimental Design

According to the experimental design principles of Box–Behnken and the results of the previous single-factor pretest, the most influencing factors of the extraction of Asarum (molar ratio, DES volume, ultrasonic temperature (°C), and ultrasonic time (min)) were selected and numbered −1, 0, and 1, respectively. The extraction rate of methyl eugenol and asarinin was averaged to obtain the comprehensive index (CI) as the investigation index. 29 test sites were designed for the response surface test, and then the optimal process conditions were verified. The test factors and level design are shown in Table 3.

3. Results and Discussion

3.1. Method Validation
3.1.1. Linear Range and Detection Limit

Prepared standard series solutions were injected under the established chromatographic conditions to obtain HPLC peak areas at different concentrations. There was a linear relationship between peak area and the concentrations of methyl eugenol and asarinin in the range of 0.005–0.495 mg/mL and 0.002–0.230 mg/mL, respectively. The results are shown in Table 4.

3.1.2. Precision and Accuracy

The precision and accuracy of the analysis method were verified by the precision test, repeatability test, and sampling recovery test. The same Asarum extract was continuously injected 6 times according to the above HPLC analysis conditions, and the RSDs of methyl eugenol and asarinin peak area were 0.54% and 0.78%, respectively. 6 Asarum extracts were prepared and analyzed by HPLC using the above method. The average contents of methyl eugenol and asarinin were 1.528 mg/g and 0.802 mg/g, and the RSDs were 1.06% and 1.72%, respectively.

Six pieces of Asarum with known content were taken, each of which was about 25 mg. 0.2 mL of methyl eugenol (at a concentration of 0.468 mg/mL) and 0.1 mL of asarinin (at a concentration of 0.453 mg/mL) were accurately transferred to a centrifugal tube. After the solvent was dried in a water bath, the measured Asarum powder was added. Asarum extract was extracted according to the method in Section 2.3 and analyzed by HPLC. The average recovery percentages of methyl eugenol and asarinin were 99.07% and 98.89%, respectively, with RSDs of 1.90% and 1.19%. It means that this method was of high precision and accuracy.

3.2. Effect of DES Types

In this paper, choline chloride is used as the HBA, which can combine with hydrogen bond donors to form hydrogen bond, and it has the advantages of low cost, low toxicity, and biodegradation [19]. The extraction of methyl eugenol and asarinin is the most important factor that should be considered in the optimization of the HBD component. In this study, the effects of 10 kinds of DESs (see Table 1) on the extraction amount of methyl eugenol and asarinin were investigated. The results are shown in Figure 3. DES-5, the combination of choline chloride with glycerol, had the highest efficiency in the extraction of methyl eugenol and asarinin from Asarum.

3.3. Effect of Molar Ratio

Because the recoveries of different molar ratios about DES may have different extraction properties, several DESs with different molar ratios were synthesized for the extraction of methyl eugenol and asarinin, as it is a standard to evaluate the extracting abilities of different DESs. In this paper, the effects of DES at the molar ratios of choline chloride to glycerol of 1 : 1, 1 : 2, 1 : 3, and 1 : 4 on the extraction rates of methyl eugenol and asarinin from Asarum were investigated. As shown in Figure 4, when the molar ratio of choline chloride to glycerol is 1 : 3, the extraction efficiency is the highest, so this molar ratio is selected for subsequent experiments.

3.4. Effect of DES Volume

As the only extraction solvent, the amount of DES directly affects the extraction efficiency of methyl eugenol and asarinin. The main reason is that if the amount of extraction solvent is insufficient, the target components cannot be completely extracted, while excessive DES will lead to a waste. Therefore, this paper focuses on the DES volume in the range of 0.5–2.0 mL. As shown in Figure 5, when the DES volume was 1.5 mL, the extraction rates of methyl eugenol and asarinin were the highest. Finally, 1.5 ml of DES was chosen as the optimum amount of extraction solvent in this study.

3.5. Effect of Ultrasonic Temperature

In the whole extraction process, temperature has a significant effect on the extraction efficiency of the target compounds. Generally, an increased temperature will accelerate the movement and transfer of the materials [20]. In this paper, the effect of temperature in the range of 40–70°C on the extraction rate of methyl eugenol and asarinin was investigated. As can be seen from Figure 6, at the temperature of 40–60 C, the extraction rate of methyl eugenol and asarinin increased, but when the temperature is higher than 60°C, the extraction rate of both of them decreased, which may be caused by the destruction of the original structure of some substances at excessively high temperature. Therefore, 60°C was set as the optimal condition in the following study.

3.6. Effect of Ultrasonic Time

Ultrasonic time is also one of the important factors affecting the extraction effect. As can be seen from Figure 7, the ultrasonic time in the range of 10–30 min was positively correlated with the extraction rate of methyl eugenol and asarinin, but after 30 min, the ultrasonic time was negatively correlated with the extraction rate. This may be because the longer the time, the greater the energy generated by the ultrasonic wave, the stronger the cavitation effect formed in the solution, the stronger the damage to the cell wall of Asarum, and the higher the extraction yield. However, as the extraction time increases, the temperature also increases gradually, and the system is under the action of ultrasonic radiation and thermal effect at the same time, which may lead to double degradation [21, 22].

3.7. Effect of Vortex Time

In the extraction of sample, the vortex oscillation is mainly to ensure that the sample and the extraction solvent can be fully mixed to form a uniform solvent system so that the target components can be completely extracted. Therefore, in the study, the changes of extraction rate during the eddy time in the range of 3–9 min were investigated. As shown in Figure 8, with the longer vortex time, the extraction rates of methyl eugenol and asarinin increased slightly, but after more than 7 min, almost no change was observed in the extraction rates, indicating that the optimal extraction rate could be achieved when the vortex time was 7 min. Therefore, the time of the first eddy oscillation was finally determined to be 7 min.

3.8. Optimization of Box–Behnken Response Surface Experiment
3.8.1. Results of Response Surface Experiment

The response surface test design and results are shown in Table 5.

3.8.2. Model Establishment and Analysis

The analysis of experimental data was performed by Design-Expert 8.0.6 software. The results were fitted by multiple regression, and the regression equation Y = 2.25 + 0.16 A + 0.051 B + 0.029 C + 0.024D + 0.17 AB − 0.027AC − 0.029AD  + 0.033BC − 0.033BD − 0.031CD − 0.52 A2 − 0.032 B2− 0.015 C2 − 0.045D2 was obtained, with R2 = 0.9429, indicating that the model can be used for analysis and prediction due to its good fitting and few experimental errors. Further analysis of variance was performed on the equation, and the results are shown in Table 6.

According to the results in Table 3, for the comprehensive evaluation value CI, A and A2 factors all reached extremely significant levels (). The influence of the interaction term AB was statistically significant (). There was no statistically significant difference found in the influence of misfitting terms, suggesting that the regression equation presented a good fitting. The overall regression model developed reaches the extremely significant level (). The order of the influence of each factor on CI value is A > B > C > D.

3.8.3. Interaction of Various Factors

The response surface diagram of the quadratic regression equation was obtained by Design-Expert 8.0.6 software, and the shape of the response surface diagram was investigated. The effects of molar ratio, DES volume, ultrasonic temperature, and ultrasonic time on the extraction rate of methyl eugenol and asarinin were analyzed. The response surface diagram and contour line can well reflect the interaction between the independent variables. By observing the slope of the response surface diagram, the influence of two factors on the response value can be determined. The steeper the response surface diagram is, the more obvious the interaction between the two factors is. As shown in Figure 9, the surface slope of AB’s interaction is relative steep, indicating that the combination of molar ratio and DES volume has a great influence on the extraction rate of methyl eugenol and asarinin in Asarum.

3.8.4. Optimization of Extraction Conditions and Model Verification Results

The optimum extraction conditions of methyl eugenol and asarinin in Asarum obtained by the response surface method were as follows: molar ratio of 1 : 3.3, DES volume of 2 mL, ultrasonic temperature of 70 C, ultrasonic time of 24.61 min, and the theoretical comprehensive index (CI) was 2.3736. Combined with the actual needs, the optimum process conditions are modified: molar ratio was 1 : 3, DES volume was 2 mL, ultrasonic temperature was 70°C, and ultrasonic time was 25 min. Under these conditions, by conducting parallel experiment 3 times, the contents of methyl eugenol and asarinin was 1.9428 mg/g and 0.9989 mg/g, respectively, and the CI was 2.3280 (RSD of 1.91%). It was 0.046 lower than the model’s CI, which was related to the actual correction molar ratio, and the ultrasound time because both had a significant impact on the results, which shows that the prediction of the model established by Design-Expert 8.0.6 has a good accuracy. As a consequence, the technological conditions of methyl eugenol and asarinin in Asarum DES extraction can be well optimized.

3.9. Comparison with Other Extraction Solvents

The results of the DES extraction were compared with those of common solvent extraction, such as water extraction, methanol extraction, and ethanol extraction. In terms of the experimental process, the DES extraction is simple and stable and does not require a large number of reagents. Furthermore, the extraction time is significantly shortened and the process of solvent concentration is removed [23, 24]. As can be seen from Figure 10, the extraction effect of the DES is better than that of conventional solvent extraction.

4. Conclusion

In this paper, a green, efficient, and economical novel extraction method was put forward [25, 26]. The effects of 13 solvents including water, ethanol, methanol, and 10 kinds of DESs on the extraction rates of asarinin and methyl eugenol were compared. Through single-factor experiments and response surface test, the optimal extraction process conditions of asarinin and methyl eugenol in Asarum were obtained: choline chloride and glycerol as the extraction solvent, with a molar ratio of 1 : 3, a DES volume of 2 ml, an ultrasonic temperature of 60°C, a ultrasonic time of 30 min, and a vortex oscillation of 7 min. Under the optimal extraction conditions, the extraction rates of methyl eugenol and asarinin were 1.9428 mg/g and 0.9989 mg/g. The extraction conditions of this method were mild and did not require high temperature and high pressure and with higher extraction rate and lower loss rates from hydrolysis and biodecomposition. On top of that, the DES is green, natural, nontoxic, and nonpolluting [27, 28], and thus, the extract can be applied to food, medicine, and other fields.

Data Availability

The main table and figure data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was supported by a grant from the National Key Research and Development Program of China: “Demonstration research on the standardized cultivation of high-quality genuine herbs such as Radix Saposhnikoviae, Schisandra chinensis and Asarum” (2019YFC1710700).