Journal of Analytical Methods in Chemistry
Volume 2020 (2020), Article ID 8861765, 9 pages
https://doi.org/10.1155/2020/8861765

Research Article

Simultaneous Determination of Phenolic Acids, Anthraquinones, Flavonoids, and Triterpenes of Cynomorii Herba in Different Harvest Times by LC-MS/MS

Hua Jin,¹ Ge Tang,² Jin Li,³ Lin Ma,⁴ Yuhong Li,³ and Yan-xu Chang³

¹College of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China
²Department of Nephrology, The First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China
³Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China
⁴College of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China

Correspondence should be addressed to Yuhong Li; liyuhong@tjutcm.edu.cn and Yan-xu Chang; tcmcyx@126.com

Received 3 May 2020; Revised 6 July 2020; Accepted 5 August 2020; Published 26 August 2020

Academic Editor: Antony C. Calokerinos

Copyright © 2020 Hua Jin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

A sensitive and accurate method was developed for the simultaneous determination of twelve components including phenolic acids (gallic acid, protocatechuic aldehyde, protocatechuic acid, and ferulic acid), flavonoids (catechin, epicatechin, rutin, luteolin, luteolin-7-glucoside, and epicatechin gallate), anthraquinones (emodin), and triterpenes (ursolic acid) in Cynomorii herba in different harvest times by liquid chromatography tandem mass spectrometry (LC-MS/MS). The chromatographic separation was achieved on an Eclipse plus C₁₈ (3.0 mm × 50 mm, 1.8 μm) column at 40°C. The mobile phase consisted of acetonitrile and 0.05% formic acid with a gradient elution at a flow rate of 0.4 mL·min ⁻¹. Under the optimized conditions, there was good linear relation (r ≥ 0.9944) and satisfactory precision (RSD values less than 5.65%). The recoveries of the twelve components were in the range of 93.5–105%. Moreover, the limits of detection (LOD) ranged from 0.003 to 21 ng mL⁻¹ for the twelve analytes. In conclusion, the validated method was successfully applied to analyze the change regularity of the twelve components of Cynomorii herba in different harvest times. It provides a theoretical basis for choosing the suitable harvesting time of Cynomorii herba.

1. Introduction

Cynomorii herba (Suoyang in Chinese, CH), one kind of traditional Chinese medicines, is the dried succulent stem of Cynomorium songaricum Rupr. It is an edible and medicinal plant that is widely distributed in the northwest desert of China, especially in Inner Mongolia, Ningxia, and Gansu province. It is usually used to make medicated wine and also used as food and fodder in the northwest region of China. CH has been widely used to improve sexual function, remedy intestinal ailments, postpone senility, nourish kidney, and treat impotence [1, 2]. Many pharmacological research studies revealed that CH could improve male fertility by enhancing spermatogenesis and glial-cell-derived neurotrophic factor (GDNF) expression. Moreover, the components of CH exhibited phytoestrogenic and phytoandrogenic activities, which were benefited for inhibition of oestrogen/androgen-induced BPH development [3–5]. Only one or several components were stipulated as a quality control marker of traditional Chinese medicine in Chinese Pharmacopoeia 2015. However, hundreds of components were existed in TCM, which may possess so many bioactivities. There was no components as a marker for CH in Chinese Pharmacopoeia 2015 [6]. However, the phytochemical investigation indicated that the main chemistry components of CH incorporate flavonoids, organic acids, polysaccharides, triterpenes, steroidal compounds, volatile oil, phenolic acids, steroids, alkaloids, and condensed tannins [7–9]. These components possessed many bioactivities including antitumor, antioxidant, antiaging, antibacterial activity, and the activities of inhibiting HCV protease and α-glucosidase [10–16]. Thus, it is necessary that multiple components were used for the quality control of CH.

A few analytical methods were established for analyzing chemical constituents of CH, such as thin-layer chromatography, capillary electrophoresis, high-performance liquid chromatography, and ultrahigh-performance liquid chromatography [17–20]. However, these methods suffered from low resolution, low sensitivity, or few analytes (less than five analytes). It was well known that the content of a single or a few compounds might not accurately reflect the quality of the complex herbal products [21]. Therefore, it was necessary to develop a simple and effective method to simultaneously determine multiple components for the quality control of CH.

Moreover, for herbal medicine, the contents of phytochemicals were usually influenced by many factors, such as producing area, harvest time, cultivation techniques, climatic conditions, drying method, and processing method. The constituents and contents of components changed with the harvest time [22, 23]. Therefore, choosing an appropriate harvesting time is the key to ensure the quality and efficiency of medicinal materials. In addition, the major source of CH is wild in traditional Chinese medicine. Due to the excessive collection and nonstandard collection methods, the wild resources of CH have decreased sharply in recent years. The artificial cultivation helped protecting the ecological environment and resource of CH. Thus, comparing the difference of components contents in wild and cultivated CH is necessary for ensuring the quality of medicinal materials.

The aim of this study was to establish a rapid and sensitive LC-MS/MS method for simultaneous determination of phenolic acids (gallic acid, protocatechuic aldehyde, protocatechuic acid, and ferulic acid), flavonoids (catechin, epicatechin, rutin, luteolin, luteolin-7-glucoside, and epicatechin gallate), anthraquinones (emodin), and triterpenes (ursolic acid) in wild and cultivated CH samples in different harvesting seasons (Figure 1). A validated method can be used as a valid analytical method for intrinsic quality control of CH. Moreover, the quantitative analysis results can be helpful for choosing the best harvesting season of CH.

Figure 1: Chemical structures of twelve components and IS.

2. Materials and Methods

2.1. Materials and Reagents

Reference standards of gallic acid, caffeic acid (IS1), protocatechuic aldehyde, protocatechuic acid, ferulic acid, luteolin, luteolin-7-glucoside, catechin, epicatechin, emodin, and ursolic acid were purchased from the Chinese National Institute of Control of Pharmaceutical and Biological Products (Beijing, China). Epicatechin gallate, astragalin (IS2), and rutin were obtained from Chengdu Must Bio-Technology Co., Ltd. (Chengdu, China). The purity of all references is over 98.0%. Acetonitrile and formic acid of HPLC grade were achieved from Merck (Germany). The water with ultrapure grade was obtained from Milli-Q Water System (Millipore, USA). Other reagents were of analytical grade.

2.2. Herbal Plant

The Cynomorii herba, both wild and cultivated, were collected from Inner Mongolia province in China in different harvest times. The Cynomorii herba were identified by Professor Yan-xu Chang (Tianjin University of Traditional Chinese Medicine), and the voucher specimens were deposited at the Tianjin University of Traditional Chinese Medicine. First, the fresh samples were dried natural. Then, they were dried in oven at 105 °C until constant weight was obtained. Finally, these samples were smashed into powder using a pulverizer and passed through a 60-mesh sieve, which were prepared for the following experiment.

2.3. Chromatographic and Mass Spectrometric Conditions

The Agilent series 1200 HPLC system, which equipped with Agilent 6430 triple quadrupole mass spectrometer, was used for chromatographic analysis. All separations were carried out on an Agilent Eclipse plus C₁₈ (3.0  mm × 50  mm i.d., 1.8 μm) column. The mobile phases consisted of (A) aqueous formic acid (0.05%, v/v) and (B) acetonitrile. The gradient elution was as follows: 0–7 min, 10–25% B; 7–10 min, 25–90% B; and 10–15 min, 90–90% B at a flow rate of 0.4 mL·min ⁻¹. The aliquot of 4 μL was injected. In addition, the pressure of MS nebulizer was 35 psi. The flow rate and temperature of dried gas were 10 L min⁻¹ and 325°C, respectively. The mass spectrometric parameters of all analytes were listed in Table 1.

Table 1: Mass spectrometric parameters for all analytes.

Compounds
Precursor ion
Product ion
Fragmentor
CE

Gallic acid
169.0
125.0
90
8

Protocatechuic acid
153.0
108.8
75
9

Catechin
288.9
245.0
140
10

Protocatechuic aldehyde
136.9
107.5
100
19

Epicatechin
289.0
245.0
145
10

Ferulic acid
193.1
133.8
75
10

Rutin
609.0
300.0
235
39

Epicatechin gallate
441.0
288.9
150
10

Luteolin-7-glucoside
447.0
284.9
210
25

Luteolin
285.0
133.0
160
33

Emodin
269.0
225.0
140
21

Ursolic acid
455.2
455.2
115
0

Caffeic acid (IS1)
179.0
135.0
90
10

Astragalin (IS2)
447.0
283.9
180
25

2.4. Preparation of Internal Standard and Quality Control (QC) Samples

Caffeic acid and astragalin were dissolved with methanol to make a mixed internal standard (IS) solution at a concentration of 100 ng mL ⁻¹. Each standard (10 mg) was dissolved by 10 mL methanol for preparing the twelve stock solutions. Quality control (QC) samples of the twelve components were prepared at medium concentration level by dissolving appropriate mixed standard solution in methanol, respectively. Then, a series of working standard solutions was achieved by mixing the twelve stock solution and diluted with methanol before use, including gallic acid, protocatechuic acid, catechin, protocatechuic aldehyde, epicatechin, ferulic acid, rutin, epicatechin gallate, luteolin-7-glucoside, luteolin, emodin, and ursolic acid in the range of 101–5050, 20.2–5050, 204–10200, 44.8–1120, 21.6–1080, 8.16–1020, 20.8–1040, 20.2–5050, 20.2–1010, 20.2–1010, 0.4–20, and 7.92–198 ng mL ⁻¹, respectively. All solutions were stored at 4°C.

2.5. Sample Solution Preparation

The samples were powdered and passed through a 60-mesh sieve. The accurately weighed sample powder (0.100 g) was ultrasonic extracted with 10 mL of 70% (v/v) methanol for 20 min, cooled at room temperature, and subsequently centrifuged for 10 min at 14000 rpm. Then, IS (10 μL) was added to the supernatant (990 μL). The final solutions were vortexed for 30 seconds and centrifuged for 10 min. 4 μL of the supernatant was injected into the HPLC.

2.6. Method Validation

These analytes of standard stock solutions were diluted to a series of appropriate concentrations for plotting the calibration curves. Then, the curves were constructed by plotting the peak areas versus the concentration of each analyte.

The QC samples at three levels of different concentration were applied to evaluate the accuracy and precision in same day (intraday) and between three different days (interday). The assessed index was RSD and the percent ratios of the calculated concentration to nominal concentration. The range of accuracy should be 95.0 to 105%.

Stability study was performed with sample solution in 24 h (the time-point is 0, 2, 4, 6, 8, 12, and 24 h, respectively) at the condition of temperature. The repeatability was investigated by using the developed method parallelly six times.

The recovery was tested by adding mixed reference standard solution to the untreated sample to yield final concentration. The sample was processed by the sample preparation procedure (n = 6).

3. Results

3.1. Internal Standard (IS) Selection

In the study, the four kinds of compounds were simultaneously determined. Caffeic acid and astragalin were chosen as internal standard for phenolic acid, flavonoid, anthraquinone, and triterpene and no interference from endogenous substances.

3.2. Optimization of Extraction Conditions

In order to achieve an optimum extraction of target components in CH, the key factors such as methanol concentration (50, 70 and 90%, v/v) and ultrasonic time (20, 30 and 40 min) were investigated by using combination experiment, while sample-solvent ratio (1 : 100, w/v) was kept constant. Total concentration of the twelve target components in the extract solution was selected as the evaluating indicator (Table 2). It was found that total concentration of the twelve target components in the extract solution was 6323.8 ng/mL when 70% (v/v) methanol was selected to extract the target components for 20 min in ultrasonic extraction process. Finally, the optimum condition was obtained when the sample was extracted by 70% (v/v) methanol for 20 min.

Table 2: The effect of the different extract conditions on the target components (ng/mL).

Extract condition
Gallic acid
Protocatechuic acid
Catechin
Protocatechuic aldehyde
Epicatechin
Ferulic acid
Rutin
Epicatechin gallate
Luteolin-7-glucoside
Luteolin
Emodin
Ursolic acid
Total concentrations

50%–20 min
1346
773
490
51
431
18
121
1052
477
68
5.7
27
4859.7

50%–30 min
1435
852
508
96
446
21
152
906
509
52
1.8
26
5004.8

50%–40 min
1803
949
557
91
487
19
141
1282
499
50
1.0
37
5916.0

70%–20 min
1899
942
641
98
559
18
170
1347
538
51
0.8
60
6323.8

70%–30 min
1683
914
591
122
517
18
159
1086
505
42
0.7
56
5693.7

70%–40 min
1581
938
589
75
515
17
144
1083
504
46
0.5
59
5551.5

90%–20 min
1224
843
533
118
467
15
106
569
355
35
0.5
61
4326.5

90%–30 min
1381
960
595
113
520
20
144
748
452
42
0.5
68
5043.5

90%–40 min
1541
936
603
124
527
21
126
966
444
44
0.4
67
5399.4

Note. The sample powder (0.100 g) was ultrasonic extracted with 10 mL methanol solution at different concentrations.

3.3. Optimization of HPLC-MS/MS Conditions

To obtain good chromatographic separation, various HPLC parameters including mobile phase modifier (0, 0.05, 0.1, and 0.2% formic acid), column temperature (35, 40, and 45°C), and flow rate (0.3, 0.4 and 0.5 mL·min ⁻¹) were also investigated in detail for analyzing the target compounds. Take into consideration the peak response and separation, the optimum HPLC conditions were obtained when mobile phase modifier was 0.05% formic acid, column temperature was 40 °C, and flow rate was 0.4 mL·min ⁻¹.

Twelve components were identified by comparing their retention time and the MS information with those of reference standards, respectively. The results showed that the highest sensitivity was obtained at a certain value of collision energy (CE).

3.4. Method Validation

3.4.1. Specificity

Figure 2 showed the chromatograms of twelve compounds of CH in the MRM mode. The results demonstrated that there was good separation and no interference from endogenous components for all analytes.

(a)

(b)

Figure 2: Representative chromatograms of (a) mixed standard solution and (b) the real sample solution of gallic acid (A), protocatechuic acid (B), catechin (C), protocatechuic aldehyde (D), epicatechin (E), ferulic acid (F), rutin (G), epicatechin gallate (H), luteolin-7-glucoside (I), luteolin (J), emodin (K), ursolic acid (L), caffeic acid (M), and astragalin (N).

3.4.2. Precision and Stability

The accuracy was achieved by evaluating QC samples of twelve components in one day (n = 6). The accuracies of twelve components for intraday and interday within range of 87.2–107.3%. The RSD value was below 5.65% (Table 3). These results demonstrated that the developed method was accurate and reproducible.

Table 3: Precision and stability of twelve components (n = 6).

Components
Concentration (ng·mL⁻¹)
Intraday
Interday
Stability (n = 6)

RSD (%)
Accuracy (%)
RSD (%)
Accuracy (%)
RSD (%)
Accuracy (%)

Gallic acid
505
3.1
103.7
0.1
103.7
3.08
96.6

Protocatechuic acid
505
3.5
103.9
0.6
104
2.38
101.5

Catechin
5100
3.1
103.2
1.8
101.1
3.70
94.6

Protocatechuic aldehyde
560
2.4
103.3
1.7
104.2
5.34
102.8

Epicatechin
540
2.4
104.8
1.6
104.2
3.54
95.3

Ferulic acid
102
2.6
100.5
3.2
98.7
3.43
103.0

Rutin
104
4.2
103.4
2.2
102.6
5.83
96.1

Epicatechin gallate
505
2.6
104.5
2.0
102.9
8.32
82.6

Luteolin-7-glucoside
101
3.2
103.7
1.2
102.9
4.70
104.9

Luteolin
100
3.0
102.7
2.9
101.3
8.98
93.6

Emodin
2
4.4
101.1
1.2
102.0
4.53
110.8

Ursolic acid
99
3.1
103.3
0.5
103.3
5.58
105.9

The stabilities of the twelve components were determined at 0 h, 2 h, 4 h, 6 h, 8 h, 12 h, and 24 h, respectively. As present in Table 3, the RSD values were below 8.98%. The results indicated that there was good stability within 24 h for all analytes.

3.4.3. Calibration Curves, Limit of Detection (LOD), Limit of Quantification (LOQ), Repeatability, and Recovery

Under the optimum chromatographic conditions, all calibration curves of the twelve components were achieved with wide concentration ranges and the correlation coefficients of them were greater than 0.9944. For the twelve components, the LOD ranged from 0.003 to 21 ng mL⁻¹, and the limit of LOQ ranged from 0.01 to 18 ng mL⁻¹. RSD values of the repeatability were less than 9.10%. These results were shown in Table 4.

Table 4: Calibration curves, LOD, LOQ, Repeatability, and Recovery of all analytes (n = 6).

Components
Linear regression
Linear range (ng·mL⁻¹)
r ²
LOD (ng·mL⁻¹)
LOQ (ng·mL⁻¹)
Repeatability RSD (%)
Recovery

Mean (%)
RSD (%)

Gallic acid
Y = 0.2895X + 0.0354
101–5050
0.9994
5
15
5.75
94.0
3.08

Protocatechuic acid
Y = 0.1929X − 0.0040
20.2–5050
0.9994
6
18
4.32
95.5
4.00

Catechin
Y = 0.1018X + 0.0280
204–10200
0.9998
6
18
5.48
101.6
6.43

Protocatechuic aldehyde
Y = 0.0122X + 0.0034
44.8–1120
0.9998
1.5
4
3.71
100.5
5.04

Epicatechin
Y = 0.9618X + 0.0280
21.6–1080
0.9998
7
21
3.11
97.7
5.12

Ferulic acid
Y = 0.1414X − 2.2003e-004
20.2–1020
0.9995
3
10
7.36
99.3
5.53

Rutin
Y = 0.9379X − 0.0038
20.8–1040
0.9996
0.5
1.5
7.86
98.1
5.83

Epicatechin gallate
Y = 0.3410X − 0.0124
20.2–5050
0.9994
1
3
6.93
97.7
6.63

Luteolin-7-glucoside
Y = 1.6412X + 0.0779
20.2–1010
0.9998
0.1
0.3
2.64
105.0
4.28

Luteolin
Y = 21.2695X + 17.0019
20.2–1010
0.9990
0.1
0.3
2.35
102.5
3.71

Emodin
Y = 5.3529X + 0.0097
0.4–20
0.9997
0.003
0.01
0.00
104.3
2.24

Ursolic acid
Y = 0.1071X + 1.1690
7.92–198
0.9944
0.3
1.0
9.10
93.5
1.43

The recovery was performed for evaluating the precision and accuracy of the established method. The recoveries of twelve compounds were in range of 93.5–105.0%, and their RSD values were less than 6.63% (Table 4). The above results indicated that the developed method possessed good accuracy and precision.

3.5. Analysis of Four Kinds of Components (Phenolic Acid, Flavonoid, Anthraquinone, and Triterpene) at Different Harvest Times and from Different Sources

The established method was applied to simultaneously determine the twelve components of CH at four different harvesting times and from two different sources (wild and cultivated). The variation of contents of twelve components in different harvest times and sources were shown in Table 5.

Table 5: Quantitative analytical results (n = 3).

Source
Harvesting times
Mean contents of compounds 1–12 (μg g⁻¹)

Phenolic acids
Flavonoids
Anthraquinones
Triterpenes

1
2
3
6
Total
4
5
7
8
9
10
Total
11
Total
12
Total

Cultivated
Pre-unearth period
25.287
17.815
4.575
0.645
48.322
100.364
10.626
0.480
8.574
6.725
0.473
127.774
0
0
1.873
1.873

Unearth period
12.305
22.674
5.231
0.966
41.176
128.430
13.598
0.495
5.003
1.707
0.099
149.894
0
0
1.890
1.890

Flowering period
12.134
22.455
10.233
0.678
45.500
58.809
6.227
0.585
2.829
0.842
0.090
70.442
0
0
2.031
2.031

Fructicative period
21.095
29.393
10.725
2.608
63.821
48.740
5.161
1.087
3.525
0.886
0.139
59.867
0.0133
0.0133
2.409
2.409

Wild
Pre-unearth period
17.7035
12.7555
6.0535
0.7875
37.3
83.425
8.834
0.322
1.2105
1.572
0.0955
95.966
0
0
1.55
1.55

Unearth period
14.103
23.22
4.9295
0.361
42.6135
81.847
8.666
0.457
1.6785
0.3025
0.0535
93.533
0
0
1.835
1.835

Flowering period
14.462
22.908
3.546
0.229
41.145
7.833
0.829
0.365
0.728
0.266
0.056
10.384
0
0
1.551
1.551

Fructicative period
14.714
14.043
1.897
4.534
35.188
53.972
5.715
0.721
2.745
0.531
0.116
63.979
0.0003
0.0003
1.982
1.982

Note: gallic acid (1), protocatechuic acid (2), catechin (3), protocatechuic aldehyde (4), epicatechin (5), ferulic acid (6), rutin (7), epicatechin gallate (8), luteolin-7-glucoside (9), luteolin (10), emodin (11), and ursolic acid (12).

For different sources, the results revealed that the total contents of the four kinds of components including phenolic acids, flavonoids, anthraquinones, and triterpenes in the cultivated sample were higher than those of the four kinds of components in the wild sample in four harvesting times. Therefore, cultivated CH can be used instead of wild CH. Artificial cultivation has solved the problems such as resource scarcity and destruction of ecological environment for CH.

For different harvest times, the contents of phenolic acids (protocatechuic acid, catechin, and ferulic acid) and the total phenolic acid were the highest in fructicative period. Compared with the other periods, the content of gallic acid was higher in pre-unearth period. Emodin (anthraquinones) was detected only in the sample at fructicative period. Moreover, the content of ursolic acid (triterpenes) was highest during fructicative period. These results indicated that the fructicative period could be the optimum harvest time for anthraquinones and triterpenes. In addition, the contents of flavonoids (epicatechin gallate, luteolin-7-glucoside, luteolin) were highest in pre-unearth period. The contents of protocatechuic aldehyde, epicatechin, and total flavonoids were higher in unearth period.

To sum up, for the three kinds of components (phenolic acid, anthraquinones, and triterpenes), the productive period was the optimum harvest time. However, the unearth period was the appropriate harvest time for flavonoids. Because Cynomorium songaricum is a parasitic plant, its standardized cultivation is difficult. At present, Cynomorium songaricum was only cultivated in one area in Inner Mongolia of China. In the future, more cultivated and wild samples with different harvesting times should be analyzed to support the results and conclusion by the established LC-MS/MS method.

4. Conclusions

A simple and effective method was developed for the simultaneous determination of the twelve components in wild and cultivated Cynomorii herba in different harvest times. The results indicated that the established method possessed excellent sensitivity and selectivity. Moreover, the application of this method could successfully evaluate the quality of wild and cultivated CH. It is crucial for solving the problem of resource scarcity.

In addition, the contents of the four kinds of components varied with the different harvest period. We can choose the optimum harvest time according to the requirements of different types of chemical ingredients. Consequently, the developed HPLC-MS/MS method provided the theoretic basis for quality control and resource protection of CH.

Data Availability

The data used to support the ﬁndings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare no conflicts of interest.

Authors’ Contributions

Conceptualization of the study was done byYuhong Li and Yan-xu Chang. Data curation was by Hua Jin, Ge Tang, Jin Li and Yuhong Li. Formal analysis was performed by Hua Jin, Ge Tang, Jin Li and Yuhong Li. Funding acquisition was carried out by Yan-xu Chang. Investigation and original draft preparation was carried out by Hua Jin, Ge Tang, Lin Ma, Yuhong Li, Jin Li, and Yan-xu Chang. Lin Ma and Yan-xu Chang reviewed and edited the draft. Hua Jin and Ge Tang have contributed equally to this work.

Acknowledgments

This research was supported by the Tianjin Research Program of Application Foundation and Advanced Technology (18JCYBJC95000) and Special Program of Talents Development for Excellent Youth Scholars in Tianjin.

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