Open Access

Chemical fingerprinting and quantitative constituent analysis of Siwu decoction categorized formulae by UPLC-QTOF/MS/MS and HPLC-DAD

  • Shulan Su1,
  • Wenxia Cui2, 1,
  • Wei Zhou1,
  • Jin-ao Duan1Email author,
  • Erxin Shang1 and
  • Yuping Tang1
Chinese Medicine20138:5

https://doi.org/10.1186/1749-8546-8-5

Received: 29 October 2012

Accepted: 14 February 2013

Published: 1 March 2013

Abstract

Background

Siwu decoction categorized formulae (SWDCF) are widely used for treating gynecological diseases. This study aims to elucidate the differences of bioactive constituents in SWDCF by ultra-high performance liquid chromatography coupled with time-of-flight mass spectrometry (UPLC - QTOF - MS /MS) and HPLC-DAD.

Methods

An efficient method based on UPLC - QTOF - MS /MS was developed for identifying the chemical profiles of SWDCF. HPLC-DAD method was used for quantifying seven chemical markers in SWDCF.

Results

Eighty four components were identified or characterized, including ten organic acids, thirty glycosides (monoterpene or iridoid or phenylpropanoids glycosides), fourteen lactones, eighteen flavonoids, and eleven alkaloids in the complex system. The datasets of tR-m/z pairs, ion intensities and sample codes were processed with supervised orthogonal partial least squared discriminant analysis to compare these decoction samples. After a clear classification was established, OPLS-DA was performed and 16 common components with relative quantity in SWDCF samples were determined. Gallic acid, protocatechuic acid, vanillic acid, caffeic acid, paeoniflorin, ferulic acid, and senkyunolide I were selected as the chemical markers to identify SWDCF by HPLC-DAD.

Conclusion

The chemical profiles with 84 components in SWDCF, including monoterpene glycosides, acetophenones, galloyl glucoses, even some isomers in the complex system were characterized by UPLC–QTOF–MS/MS.

Background

Chinese medicine (CM) is holistically formulated for treating complicated CM syndromes (“ZHENG” in Chinese) [1]. The researches on categorized formulae (CF) based on a basic formula composition may help understand the rules of formulation and Fang-Zheng consistency in CM [2].

Siwu decoction (SWD) is a classical prescription that is widely used for the treatment of women’s diseases in CM, such as relief of emmeniopathy, climacteric syndrome, dysmenorrhea and other estrogen-related diseases [3]. A recent study demonstrated that the SWD can be synergistically used with Western medicine [4]. SWD consists of four herbs, i.e., Angelicae sinensis Radix, Chuanxiong Rhizoma, Paeoniae Radix Alba, and Rehmanniae Radix[5]. A series of SWD-based formulae used to treat women’s diseases especially for primary dysmenorrheal (PD) are considered as Siwu decoction categorized formulae (SWDCF), including Taohong Siwu decoction (THSWD), Xiangfu Siwu decoction (XFSWD), Shaofu Zhuyu decoction (SFZYD), and Qinlian Siwu decoction (QLSWD). The compositions and applications of SWDCF were described in Table 1. These formulae are usually adopted to treat different symptoms of different kinds of PD.
Table 1

The composition and application of SWDCF

Prescriptions

Composition

Application

Siwu decoction (SWD)

(Angelica sinensis) Angelicae sinensis Radix 9 g, (Ligustium chuanxiong) Chuanxiong Rhizoma 9 g, (Paeonia lactiflora) Paeoniae Radix Alba 9 g, and (Rehmannia glutinosa) Rehmanniae Radix 9 g

Cure women’ diseases, such as dysmenorrhea and other estrogen related diseases

Taohong-Siwu decoction (THSWD)

(Angelica sinensis) Angelicae sinensis Radix 9 g, (Ligustium chuanxiong) Chuanxiong Rhizoma 9 g, (Paeonia lactiflora) Paeoniae Radix Alba 9 g, (Rehmannia glutinosa) Rehmanniae Radix 9 g, (Prunus persica) Persicae Semen 9 g, and (Carthamus tinctorius) Carthami Flos 6 g

Cure PD with syndrome of deficiency of blood.

Xiangfu-Siwu decoction (XFSWD)

(Angelica sinensis) Angelicae sinensis Radix 9 g, (Ligustium chuanxiong) Chuanxiong Rhizoma 4.5 g, (Paeonia lactiflora) Paeoniae Radix Alba 4.5 g, (Rehmannia glutinosa) Rehmanniae Radix 12 g, (Cyperus rotundus) Cyperi Rhizoma, 4.5 g, (Corydalis yanhusuo) Corydalis Rhizoma 4.5 g, and (Aucklandia lappa) Aucklandiae Radix 3 g

Cure PD induced by stagnation of the circulation of vital energy

Shaofu-Zhuyu decoction (SFZYD)

(Angelica sinensis) Angelicae sinensis Radix 9 g, (Ligustium chuanxiong) Chuanxiong Rhizoma 3 g, (Corydalis yanhusuo)Corydalis Rhizoma 3 g, (Paeonia veitchii) Paeoniae Radix Rubra 6 g, (Cinnamomum cassia) Cinnamomi Cortex 3 g, (Foeniculum vulgare) Foeniculi Fructus 1.5 g, (Zingiber officinale) Zingiberis Rhizoma 3 g, (Commiphora myrrha) Myrrha 3 g, (Trogopterprus xanthipes) Trogopterpri Faeces 6 g, and (Typha angustifolia) Typhae Pollen 9 g

Cure PD with syndrome of cold coagulation and blood stasis

Qinlian-Siwu decoction (QLSWD)

(Angelica sinensis) Angelicae sinensis Radix 9 g, (Ligustium chuanxiong) Chuanxiong Rhizoma 9 g, (Paeonia lactiflora) Paeoniae Radix Alba 9 g, and (Rehmannia glutinosa) Rehmanniae Radix 9 g, (Scutellaria baicalensis) Scutellariae Radix 4.5 g and (Coptis chinensis) Coptidis Rhizoma 4.5 g

Cure PD resulted from pathogenic heat or inflammation

Our recent studies [6, 7] showed that SWDCF inhibited uterine contraction and had analgesic effects on primary dysmenorrhea model mice. Their anti-inflammatory activities, hemorheological improvement and ovarian regulation in rats with blood stasis were elucidated [8, 9]. Moreover, SWDCF inhibited COX-2 enzyme and platelet aggregation in vitro[9, 10]. The main constituents of SWDCF belong to several natural product groups, such as phenolic acids, phthalides, alkaloids, terpene glycosides, iridoid glycosides, flavones, and etc.[1013]. However, no report on the constituent profiles of SWDCF is available.

The investigations of the components of SWDCF are important to reveal their effects and action mechanisms. However, the complicated chemical profiles of SWDCF components demand a rapid and efficient method for chemical profiling of SWDCF.

This study aims to profile the constituents of SWDCF by UPLC-QTOF-MS/MS with MarkerLynx analysis and identify SWDCF with several chemical markers.

Methods

Chemicals, reagents and materials

Gallic acid, protocatechuic acid, vanillic acid, caffeic acid, paeoniflorin, ferulic acid, and senkyunolide I (Figure 1) were purchased from National Institute for the Control of Pharmaceutical and Biological products (China).
Figure 1

Chemical structures of the quantitative compounds in the Siwu decoction categorized formulae.

Acetonitrile was HPLC-grade from Merck (Darmstadt, Germany) and deionized water was purified by a Millipore water purification system (Millipore, Milford, MA, USA) and filtered with 0.22 μm membranes. Other reagent solutions were of analytical grade (Sinopharm Chemical Reagent Co., Ltd., Shanghai, China).

Herbal medicines of Angelicae sinensis Radix, Chuanxiong Rhizoma, Paeoniae Radix Alba, Rehmanniae Radix, Persicae Semen, Carthami Flos, Cyperi Rhizoma, Aucklandiae Radix, Corydalis Rhizoma, Paeoniae Radix Rubra, Cinnamomi Cortex, Foeniculi Fructus, Zingiberis Rhizoma, Myrrha, Trogopterpri Faeces, Typhae Pollen, Scutellariae Radix and Coptidis Rhizoma, were purchased from the following towns (provinces): Minxian (Gansu), Pengzhou (Sichuan), Tongling (Anhui), Huaiqing (Hehan), Anguo (Hebei), Tacheng (Xinjiang), Linyi (Shandong), Lijiang (Yunnan), Songyang (Zhejiang), Chifeng (Neimeng), Yulin (Guangsi), Wuwei (Gansu), Yulin (Guangsi), Guangdong, Changzhi (Shanxi), Yixing (Jiangsu), Chengde (Hebei), and Mianyang (Sichuan), respectively. All crude herbs were identified by the Prof. Jin-ao Duan in accordance with the Pharmacopoeia of People’s Republic of China [14]. The voucher specimens (no. NJUTCM-20101112-20101129) were deposited in Jiangsu Key Laboratory for TCM Formulae Research, Nanjing University of Chinese Medicine.

Apparatus and chromatographic conditions

UPLC-QTOF-MS/MS qualitative analysis

Chromatography was performed on an AcQuity™ UPLC system with a conditioned autosampler (Waters Corp., Milford, MA, USA) at 4°C. The separation was carried out on an AcQuity UPLCTM BEH C18 column (100 mm × 2.1 mm i.d., 1.7 μm; Waters Corp., Milford, MA, USA) maintained at 35°C. The mobile phase consisted of 0.1% formic acid (HCOOH) in water as solvent A and acetonitrile (ACN) as solvent B. The gradient conditions of the mobile phase were: 0 min 95% A, 9.0 min 56% A, 12.0 min 26% A, 20.0 min 10% A, 22.0 min 10% A, 25.0 min 95% A. The flow rate was 0.40 mL/min. The sample injection volume was 5 μL.

Mass spectrometric detection was carried out on an AcQuity Synapt Mass Spectrometer equipped with an electrospray ionization (ESI) interface (Waters, Milford, MA, USA). High purity nitrogen was used as the nebulizer and auxiliary gas; argon was utilized as the collision gas. The ESI source was operated in positive and negative ionization mode with a capillary voltage of 3 kV, sampling cone voltage of 10 V, cone gas flow of 50 L/h, desolvation gas flow of 700 L/h, desolvation temperature of 350°C, source temperature of 120°C, collision energy of 45 V, and the full scan spectra from 100 to 1000 Da. Leucine-enkephalin was used as the lock mass generating an [M + H]+ ion (m/z 556.2771) and [M-H]- ion (m/z 554.2615) at a concentration of 200 pg/mL and flow rate of 100 μL/min. Data acquisition and processing were performed by MassLynx 4.1 and MarkerLynx 4.1 (Waters Corp., Milford, MA, USA) for peak detection.

HPLC-PDA quantificative analysis

The quantification analysis was performed on a Waters-2695 Alliance HPLC (Waters Corporation, Milford, MA, USA) equipped with an on-line degasser, an auto-sampler and a 2996 photodiode array detector. UV detection was achieved at 210–400 nm. A Waters Sun Fire™ C18 column (4.6 × 250 mm, 5 μm, serial no. 186002560 Waters Corporation, USA) was used. A linear gradient elution of A CH3OH and B (CH3COOH: H2O = 0.1: 100) was used. The gradient program is 85% B in 0–8 min, 85-80% B in 8–10 min, 80-74% B in 10–30 min, 74-66% B in 30–40 min, 66-34% B in 40–60 min, 34-10% B in 60–85 min. The solvent flow rate was 1 mL/min and the column temperature was set at 30°C. Re-equilibration duration was 15 min between individual runs. A Waters 2996 photo diode array was connected to the liquid chromatography for detection of the raw data.

Preparation of standard solutions

A mixed standard stock solution containing gallic acid (1), protocatechuic acid (2), vanillic acid (3), caffeic acid (4), paeoniflorin (5), ferulic acid (6), and senkyunolide I (7) was prepared in methanol. The working standard solutions were prepared by diluting the mixed standard solution with methanol to a series of proper concentrations within the ranges: 1, 148–1480.0 μg/mL; 2, 38.40–384.00 μg/mL; 3, 32.0-320.0 μg/mL; 4, 35.6-356.0 μg/mL; 5, 476.0-4760.0 μg/mL; 6, 136.0-1360.0 μg/mL; 7, 46.0-460.0 μg/mL. The standard stock and working solutions were all stored at 4°C and filtered through a 0.22 μm membrane prior to injection.

Preparation of sample solutions

The mixtures of SWDCF (Table 1) were crushed into small pieces and refluxed with 10 times water for 2 h twice. The filtrates from each decoction were combined and concentrated to 1.0 mg/mL at 70°C. The filtrates were added 95% ethanol until the concentration of ethanol was adjusted to 50%. After centrifugation at 3000 × g for 10 min, the supernatant was stored at 4°C and filtered through a 0.22 μm membrane filter before the UPLC-QTOF-MS analysis and the HPLC-DAD analysis.

Validation of the HPLC method

Calibration curves, limits of detection and quantification

The working standard solutions with at least six different concentrations (1, 148–1480.0 μg/mL; 2, 38.40-384.00 μg/mL; 3, 32.0-320.0 μg/mL; 4, 35.6-356.0 μg/mL; 5, 476.0-4760.0 μg/mL; 6, 136.0-1360.0 μg/mL; 7, 46.0-460.0 μg/mL) were analyzed, and the calibration curves were calculated by linear regression of the double logarithmic plots of the peak area versus the concentration of the reference solution injected. The limits of detection and quantification (LODs and LOQs) under the present chromatographic conditions in this study were determined by diluting the standard solution when the signal-to-noise ratios (S/N) of analytes were about 3 and 10, respectively. The S/N was calculated as the peak height divided by the background noise value.

Precision, repeatability and accuracy

The intra-day and inter-day variations, which were chosen to determine the precision of the developed method, were investigated by determining the seven analytes in six replicates during a single day and by duplicating the experiments on three consecutive days. Variations of the peak area were taken as the measures of precision and expressed as relative standard deviations (R.S.D.).

Repeatability was confirmed with six independent analytical sample solutions prepared according to the methods describing before and expressed by R.S.D. These SWTCF sample solutions was stored at 4°C, and injected into the HPLC apparatus at 0, 2, 4, 8, and 12 hr, respectively, to evaluate the stability of the solution.

Recovery test was performed by adding accurate amounts of the seven standards into a certain amounts separately to evaluate the accuracy of this method. The spiked samples were then extracted, processed, and quantified in accordance with the methods mentioned above. Six replicates were performed for the test. The average recovery percentage was calculated by the formula: recovery (%) = (observed amount − original amount)/spiked amount × 100%.

MarkerLynx™ analysis

The data obtained from positive and negative ion mode of all determined samples were analyzed by MarkerLynx v4.1 software (Waters, Manchester, UK) with the help of multivariate statistical analysis, to reveal any potential changed components in SWDCF. The original data were processed using the following parameters: initial retention time of 0 min, final retention time of 25 min, and mass in the range 100–1000 Da, with a mass tolerance of 0.02 Da, mass window of 0.02 Da, retention time window of 0.1 min, noise elimination level 6. For peak integration, peak width at 5% of the height was 1 s, peak-to-peak baseline noise was automatically calculated, and peak intensity threshold was 10. No specific mass or adduct was excluded. Isotopic peaks were excluded for analysis. For data analysis, a list of the intensities of the peaks detected was generated using tR and mass data (m/z) pairs as the identifier of each peak. An ID was assigned to each of these tR-m/z pairs in the order of their UPLC elution for data alignment [15]. The process was repeated for each run. After completion, the correct peak intensity data for each tR-m/z pair of the entire batch of samples were aligned in the final data table. The ions that showed the same tR (with a tolerance of 0.1 min) and m/z value (with a tolerance of 0.05 Da) in different samples were considered as the same ion. For those peaks hard to be detected in the sample, the ion intensities were documented as zero in the final data table. Before submitted for multivariate analyses, the ion intensities for each detected peak were normalized against the sum of the peak intensities. The resulting three-dimensional data comprising of peak number (tR-m/z pair), sample name and ion intensity were analyzed by OPLS-DA with the MarkerLynx software.

Results and discussion

Identification of SWDCF constituents by UPLC-QTOF-MS/MS

The multiple chemical components in the SWDCF samples were identified and characterized by both negative and positive ESI modes. The total current chromatograms at the two modes were shown in Additional file 1: Figures S1-1 and 1-2. Diagnostic fragmentations were then checked by MS/MS to confirm the results. Eighty-four constituents were identified by comparing the tR, UVλmax, and MS fragments characteristics of the compounds. The analyzed and identified compounds were listed in Table 2. Among these 84 compounds, there were ten organic acids, thirty glycosides (monoterpene or iridoid glycosides or phenylpropanoids), fourteen lactones, eighteen flavonoids, and eleven alkaloids.
Table 2

Characterization of compounds in Siwu decoction categorized formulae by UPLC-QTOF-MS/MS

Peak no.

TR(min)

Positive ions ( m/z)

Negative ions ( m/z)

λmax(nm)

Identification

Origins

1

1.42

171 [M + H]+

169 [M-H]-, 125 [M-HCOO]-, 97 [M-H-CO2-CO]-

216, 270

Gallic acid

A, B, C, D, E

2

3.07

355 [M + H]+, 377 [M + Na]+

353 [M-H]-, 191[M-C9H7O3]-, 179[M-C7H11O5]-, 173 [M-C9H7O3-H2O]-

326

Chlorogenic acid

A, B, C, D, E

3

4.10

181 [M + H]+

179 [M-H]-, 135 [M-HCOO]-

320, 240

Caffeic acid

A, B, C, D, E

4

3.52

169 [M + H]+

167 [M-H]-, 153 [M-CH3]-, 137 [M-OCH3]-, 123 [M-HCOO]-

290

Vanillic acid

A, B, C, D, E

5

4.90

195 [M + H]+

193 [M-H]-, 178 [M-H-CH3]-, 149 [M-H-CO2]-, 134 [M-HCOO]-

320

Ferulic acid

A, B, C, D, E

6

8.90

195 [M + H]+

193 [M-H]-, 237 [M-H + HCOO]-, 179 [M-CH3]-

310

Isoferulic acid

A, B, C, D, E

7

4.68

-

153 [M-H]-, 141 [M-H-CH3]-, 109 [M-H-CO2]-

310

Protocatechuic acid

A, B, C, D, E

8

9.44

-

163 [M-H]-, 117 [M-H-HCOO]-

 

Coumaric acid

A, B

9

2.98

139 [M + H]+, 161 [M + Na]+

137 [M-H]-, 119 [M-H-H2O]-

 

p-hydroxy benzoic acid

A, B

10

7.02

-

121 [M-H]-

238, 272

Benzoic acid

A, B

11

1.47

361 [M + H]+

359 [M-H]-, 493 [M-H + HCOO]-, 405 [M + HCOO]-, 197 [M-H-glu]-, 179 [M-H-glu-H2O]-

210, 270

1-O-β-D- glucopyranosyl -paeonisuffrone

A, B

12

1.51

517 [M + Na]+

493 [M-H]-, 457 [M-H-2H2O]-, 443 [M-H-2H2O- CH3]-, 331 [M-2H-glu]-, 169 [M-sucrose]-

220, 270

1-O-galloylsucrose

A

13

2.89

562 [M + Na]+, 383 [M + H-glu]+, 261[M + H-glu-benzoyl]+, 197[M + H-glu-benzoyl-SO2]+

543[M-H]-, 495[M-CH2OH-H2O]-, 461[M-SO2-H2O-H]-, 341[M-SO2-C7H5O-2OH]-, 243[M-glu-benzoyl-H2O-CH3]-

232

Paeoniflorin sulfonate

A, B

14

3.85

481 [M + H]+, 319 [M + H - glu]+, 197 [M + H -glu-benzoyl]+, 161 [M + H -glu-benzoyl-2H2O]+, 133 [M + H -glu-benzoyl-2H2O-CO]+

479 [M-H]-, 525 [M + HCOO]-, 416 [M-CH2OH-CH3-H2O]-, 283[M- glu-H2O-OH]-, 177[M-glu-benzoyl-2H2O]-

233

Albiflorin

A, B, C, D, E

15

4.29

-

695[M-H]-, 631[M-SO2-H]-, 525[M-galloyl-H2O]-, 519[M-benzoyl-4H2O]-, 479[M-galloyl-SO2]-, 449[M-galloyl-SO2-CO-H]-

275

Galloylpaeoniflorin sulfonate

A, B

16

5.84

481 [M + H]+, 503 [M + Na]+, 397, 319, 197

479[M-H]-, 525[M + HCOO]-, 449[M-CH2OH]-, 416[M-CH2OH-CH3-H2O]-, 327[M-benzoyl-CH2OH-CH3-2H]-, 176[M-benzoyl-glu-2H2O-H]-,121[benzoyl]-

230

Paeoniflorin

A, B, C, D, E

17

4.36

497 [M + H]+, 519 [M + Na]+, 381 [M + Na–pOHBA]+, 357 [M + Na–Glc]+, 323 [M + Na–aglycone]+, 271 [M + Na–C13H12O5]+

495[M-H]-, 449[M-CH3-CH2OH-H]-, 479[M-OH]-, 327[M-p-hydroxybenzoyl-CH2OH-OH]-

235, 322

Oxypaeoniflorin

A

18

3.91

481 [M + H]+, 503 [M + Na]+

479 [M-H]-, 525[M + HCOO]-, 449[M-CH2OH]-, 327[M-benzoyl-CH2OH-OH]-

220, 275

Isopaeoniflorin / albiflorin R1

A

19

4.97

633 [M + H]+, 655 [M + Na]+, 153[galloyl + H-H2O]+

631[M-H]-, 525[M-benzoyl-2H]-, 449[M-galloy-HCHO]-

275

Galloylpaeoniflorin

A, B

20

4.87

-

939 [M-H]-, 631 [M-2galloyl-3H]-, 469 [M- 2galloyl -3H-glu]-

220, 280

Pentagalloylglucose

A, B,C

21

5.20

-

623[M-H]-, 515[M-C6H5O2]-

 

Acteoside/isoacteoside / forsythoside A

A, B

22

5.78

481[M + H]+, 319[M + H-glu]+, 197[aglycone + H]+, 179[aglycone + H-H2O]+, 161[aglycone + H-2H2O]+, 133[aglycone + H-2H2O-CO]+

479[M-H]-, 463[M-OH]-, 341[M-benzoyl-2OH]-

 

Mudanpioside I

A, B

23

6.67

 

647[M-H]-, 513[M-benzoyl-HCHO]-, 507[M-benzoyl-2H2O]-, 391[M-2benzoyl-HCHO-OH]-

 

Benzoypaeoniflorin sulfonate

A, B

24

9.29

585[M + H]+, 607 [M + Na]+, 602[M + H2O], 463[M + H-benzoyl]+, 301[M + H-glu]+, 179[M + H-benzoyl-glu]+, 151[M + H-benzoyl-glu-CO]+

583[M-H]-, 629[M + HCOO]-

220, 270

Benzoylpaeoniflorin

A, C

25

8.09

 

583[M-H]-, 629[M + HCOO]-

220, 270

Isobenzoylpaeoniflorin

A, B

26

4.20

-

799[M-H]-, 637[M-caffeoyl]-, 525, 479, 449

 

cistanoside A or jionoside A1/A2

A

27

3.66

660[M + H2O], 625[M + H-H2O]+, 341[M + H-H2O-glu-benzoyl]+, 301[M + H-H2O-2glu]+

641[M-H]-, 687[M + HCOO]-, 611[M-CH2OH]-, 593[M-CH2OH-H2O]-, 341[maltosyl]-, 497[M-benzoyl-2H2O-4H]-

212, 277

Isomaltopaeoniflorin/6-O-β-D-glucopyranosylalbiflorin

A

28

2.75

729[M + Na]+

705[M-H]-, 495, 443, 341, 271, 193

215

Isomaltopaeoniflorin sulfonate

A

29

4.14

463[M + H]+, 484[M + Na]+, 498, 301, 179

461[M-H]-, 525, 479, 449, 327

232

decaffeoyl-verbascoside

A

30

5.68

363[M + H]+, 385[M + Na]+, 340, 319, 197

361[M-H]-, 407[M + HCOO]-, 311, 287

232

6-O-β-D-glucopyranosyl lactinolide

A

31

1.40

687 [M + H]+

685[M-H]-, 731 [M-H + HCOO]-, 493 [M-H-glu- HCOO]-

215, 273

Rehmannioside D

A, B

32

7.18

525 [M + H]+, 207

523[M-H]-, 569 [M + HCOO]-, 407, 341, 183

 

Melittoside

A, B

33

3.71

-

785[M-H]-, 687[M-98]-

236, 279

Echinacoside

A

34

4.55

 

435[M + HCOO]-, 389[M-H]-, 327[M-3CH3-H2O]-, 178[M-C13H24O2]-

-

Rehmaionoside A/B

A, B

35

4.94

-

813[M-H]-, 515[M-C6H12O4-C9H10O2-H]-, 469[M-glu-feruloyl]-

 

Jionoside B1/B2

A, B

36

6.51

653[M + H]+

651[M-H]-, 505[M-rhamnosyl-H]-

276

Martynoside isomer

A

37

4.98

653[M + H]+

651[M-H]-, 445[M-ferulic acid-2CH3]-, 389[M-feruloyl-HCHO-3H2O-2H]-

235, 322

Martynoside

A

38

5.52

347[M + H]+

345[M-H]-, 391[M + HCOO]-, 183[M-gku]-, 179[M-C10H15O2]-

-

Rehmapicroside

A,E

39

7.21

207[M + Na]+

183[M-H]-, 165[M-H2O-H]-, 139[M-HCOO]-

-

Rehmapicrogenin

A,E

40

3.20

459[M + H]+, 325, 163

457[M-H]-, 323

215,237

Amygdalin

B

41

6.09

249[M + Na]+, 227[M + H]+, 209[M-H2O + H]+, 191[M-2H2O + H]+, 181[M-H2O-CO + H]+

225[M-H]-, 195, 125

277

Senkyunolide J

A, B, C, D,E

42

6.26

225[M + H]+, 247[M + Na]+, 207.1014[M-H2O + H]+, 189.0889[M + H-2H2O]+, 165.0890 [M + H-H2O-C3H6]+

223[M-H]-, 205, 177

270

Senkyunolide I

A, B, C, D, E

43

6.61

225[M + H]+, 247[M + Na]+, 207[M-H2O + H]+, 189[M + H-2H2O]+, 165[M + H-H2O-C3H6]+

223[M-H]-

270

Senkyunolide H

A, B, C, D, E

44

10.82

191[M + H]+, 173, 149, 135

189[M-H]-, 207[M-H + H2O]-

295, 325

E-ligustilide

A, B, C, D, E

45

13.74

191[M + H]+, 173, 149, 135

-

295, 325

Z-ligustilide

A, B, C, D, E

46

9.44

381[M + H]+, 426[M + 2Na]+, 191[C12H15O2]+

-

280

Z-ligustilide dimmer E-232

A, B, C, D, E

47

13.62

381[M + H]+, 426[M + 2Na]+, 191[C12H15O2]+

-

296

Z,Z-3,3,8,8-Diligustilide

A, B, C, D

48

10.33

203[M + H]+, 225[M + Na]+

-

-

3-butylidene-7-hydroxyphthalide

A, B, C, D, E

49

8.04

189[M + H]+, 171[M-H2O + H]+, 153[M-2H2O + H]+, 117[M + 3H-H2O-CO-C2H4]+

187[M-H]-

260, 310

E-Butylideniphthalide

A, B, C, D, E

50

9.31

189[M + H]+, 161[M-CO + H]+, 133[M + H-CO-C2H4]+

187[M-H]-, 205[M-H + H2O]-

260, 310

Z-Butylidenephthalide

A, B, C, D, E

51

12.90

381[M + H]+, 426[M + H + HCOO]+, 236, 191

379[M-H]-, 424[M-H + HCOO]-, 397[M-H + H2O]-

282

Angelicide

A

52

13.65

381[M + H]+, 403[M + Na]+, 426[M + 2Na]+, 191[C12H15O2]+

379[M-H]-, 411

284

Riligustilide

A

53

14.70

381[M + H]+, 403[M + Na]+, 191[C12H15O2]+

-

280

Tokinolide B

A

54

12.60

381[M + H]+, 399[M + H2O + H]+, 191[C12H15O2]+

379[M-H]-, 397[M-H + H2O]-

230, 276

Levistolide A

A, B, C, D, E

55

3.01

613[M + H]+, 635[M + Na]+, 451, 433, 163, 144

611[M-H]-, 543, 353, 191

227

Hydroxysafflor yellow A

B

56

4.01

625[M + H]+, 593, 481, 433, 319, 301, 197

623[M-H]-, 611, 525, 479, 395

232

Isorhamnetin-3-O-nehesperridin

B

57

2.56

803[M + H]+, 789, 627, 325

801[M-H]-, 787, 593, 515, 236

230, 269, 328

6-hydroxy-keampferol −3, 6-O-7-O-glucuronide

B

58

3.85

627[M + H]+, 481, 319, 197

625[M-H]-, 525, 479, 449

232

6- hydroxy-keampferol −3, 6 – O – glucoside

B

59

5.13

595[M + H]+, 617[M + Na]+, 449, 287

593[M-H]-, 515, 449, 341, 193

241,265,330

Safflor yellow A

B

60

7.29

303[M + H]+

301[M-H]-

275

Queretin

D

61

4.81

625[M + H]+, 317, 479

623[M-H]-, 525, 315

253, 351

Isohammetin-3-O-neohesperidoside

D

62

5.25

625[M + H]+, 370, 356, 325, 317

623[M-H]-, 515, 315, 309, 279, 181

244, 332

Isohammetin-3-O-rutinoside

D

63

4.40

771[M + H]+, 793[M + Na]+, 625[M + H-rha]+, 479[M + H-2rha]+, 317[M + H-3rha]+

769[M-H]-, 525, 449, 327

253, 353

Typhaneoside

D

64

12.10

287[M + H]+

285[M-H]-

279

Keampferol

D

65

5.64

317[M + H]+

315[M-H]-

230, 273

Isohamnetin

D

66

4.90

463[M + H]+, 352, 322

461[M-H]-, 285, 193

235, 323

Scutellarin

E

67

6.33

447[M + H]+, 336, 352, 271

445[M-H]-, 891, 269

216, 277, 316

Baicalin

E

68

7.48

461[M + H]+, 285

459[M-H]-, 919, 283

220, 273

Wogonoside

E

69

8.83

271[M + H]+

269[M-H]-

275, 322

Baicalein

E

70

10.46

285[M + H]+

283[M-H]-, 268[M-H-CH3]-

274

Wogonin

E

71

7.19

461[M + H]+, 285

459[M-H]-, 283, 175

271, 310

Oroxylin-A-glucuroside

E

72

10.66

315, 373, 283

313[M-H]-, 375, 285

271

6-dimethoxy-wogonin

E

73

0.64

136[M + H]+

134[M-H]-

 

Tetramethylpyrazine

A, B, C, D, E

74

5.36

356[M + H]+, 338[M + H-H2O]+, 312[M + H-CO2]+

354[M-H]-

239, 297

Tetrahydropalmatin

C, D, E

75

4.56

342[M + H]+, 311, 193, 179

-

237, 278

Tetrahydrocolumbamine

C, D

76

5.71

354[M + H]+, 376[M + Na]+, 340, 320

352[M-H]-

238, 285

Protopine

C, D

77

5.26

370[M + H]+, 356[M + H-CH2]+, 327[M + H-CH3-CO]+, 326[M + H-CO2]+

368[M-H]-

245, 330

Allocryptopine

C, D, E

78

5.40

324[M + H]+, 338, 356

322[M-H]-

-

Tetrahydrocoptisine

C, D, E

79

6.29

356[M + H]+, 207

354[M-H]-

-

Glaucine

C, D, E

80

6.22

336[M + H]+, 207

354[M-H]-

277

Berberine

C, D, E

81

6.48

366[M + H]+, 308

-

262, 332

Dehydrocorydaline

C, D, E

82

5.78

368[M + H]+, 352[M + H-H2O]+

366[M-H]-

239, 277, 331

Corydaline

C, D, E

83

6.52

339[M + H]+, 357[M + H + H2O]+, 320[M-H2O]

337[M-H]-

237, 285

Jatrorrhizine

C, E

84

1.44

127[M + H]+, 149[M + Na]+

125[M-H]-, 169[M-H + HCOO]-

215, 272

5-hydroxymethyl-2-furfural (5-HMF)

A

Identification of phenolic acids

In this study, 10 phenolic acids were identified from SWDCF samples according to the tR, UVλmax, and MS fragment characteristics compared with reference compounds and the literature [16, 17]. They are gallic acid (1), chlorogenic acid (2), caffeic acid (3), vanillic acid (4), ferulic acid (5), isoferulic acid (6), protocatechuic acid (7), coumaric acid (8), p-hydroxy benzoic acid (9), and benzoic acid (10), respectively. The MS characteristics (Table 2) were m/z 169 [M - H]-, m/z 353 [M - H]-, m/z 179 [M - H]-, m/z 167 [M - H]-, m/z 193 [M - H]-, m/z 193 [M - H]-, m/z 153 [M - H]-, m/z 163 [M-H]-, m/z 137 [M - H]-, and m/z 121 [M - H]-, respectively.

Identification of monoterpene, iridoid and phenylpropanoid glycosides

In the positive and negative MS experiments, there were 16 monoterpenes compounds with a pinane skeleton were analyzed and identified (Table 2). These constituents come from herbs of Paeoniae Radix Alba (in SWD, THSWD, XFSWD, and QLSWD) and Paeoniae Radix Rubra (in SFZYD). According to the MS/MS analysis of authentic compounds, the major fragmentation mechanisms of monoterpene glycosides were concluded. In the positive MS experiments, all monoterpene glycosides were ionized as sodiated molecules. The diagnostic ions of this type of compounds were the loss of glucosyl group, aglycone group, benzoyl group, which lead to the occurrence of ions at m/z 185, 219 or 121. Based on fragmentation patterns, the compounds 14, 16, and 18 were identified albiflorin, paeoniflorin, and isopaeoniflorin with MS characteristics of m/z 481 [M + H]+, m/z 503 [M + Na]+, and m/z 481 [M + H]+ by comparing to reference compounds. And compound 18 had a typical ion of m/z 525 [M + HCOO]- at ES- mode.

Structures of compounds 17, 19, 22, 24 and 25 were deduced from their characteristic UV and MS spectra and fragmentation patterns. According to the literature [1820], compounds 17, 19 and 22 were tentatively identified as oxypaeoniflorin, galloylpaeoniflorin and mudanpioside I, respectively. The fragmentation patterns of compounds 24 and 25 were similar with those of monoterpene glycosides. In the ESI-MS/MS experiment, the diagnostic ions of m/z 585 [M + H]+, m/z 463 [M + H - benzoyl]+, m/z 179 [M + H – benzoyl - glu]+, m/z 151 [M + H - benzoyl – glu -CO] + at, and m/z 629 [M + HCOO]- at ES- mode. According to the literature [17], the compound 24 (tR = 7.90 min), 25 (tR = 8.09 min) were tentatively identified as benzoylalbiflorin, and isobenzoylpaeoniflorin, respectively.

Compounds 13, 15, 23, and 28 were identified as sulfonates of monoterpene glycosides. Compound 13 was C23H28O13S and had ions of m/z 495 [M-CH2OH-H2O]-, 461 [M-SO2-H2O-H]-, 341 [M-SO2-C7H5O- 2OH]- and 243 [M-glu- benzoyl-H2O-CH3]-. Compound 13 was plausibly identified as paeoniflorin sulfonate [21]. With the similar MS characteristics, compounds 15, 23, 28 were tentatively identified as galloylpaeoniflorin sulfonate, benzoypaeoniflorin sulfonate, isomaltopaeoniflorin sulfonate [1820].

Compounds 11, 12, 20, 27 and 30 all exhibited glucosyl group. According to the MS fragments and UVλmax documented in the literature [22], compounds 11, 12, 20, 27 and 30 were tentatively identified as 1-O-β-D- glucopyranosyl –paeonisuffrone, 1 -O -galloylsucrose, pentagalloylglucose, isomaltopaeoniflorin or 6-O-β-D- glucopyranosylalbiflorin, and 6-O-β-D-glucopyranosyl lactinolide, respectively.

Three phenylpropanoid glycosides were detected and tentatively assigned as acteoside/isoacteoside / forsythoside A (21), cistanoside A or jionoside A1/A2 (26), decaffeoyl-verbascoside (29) according to the literatures [21, 2325]. The MS spectrums were listed in Table 2.

The Rehmanniae Radix is rich sources of iridoid glycosides [21, 2325]. At the positive and negative MS experiments, 9 iridoid compounds were analyzed and identified in SWDCF expcept SFZYD (Table 2). By comparing the tR, UVλmax and MS characteristics with reference compounds and literature [23, 26], they were identified as rehmannioside D (31), melittoside (32), echinacoside (33), rehmaionoside A/B (34), jionoside B1/B2 (35), martynoside isomer (36), martynoside (37), rehmapicroside (38), and rehmapicrogenin (39), respectively. And amygdalin (40) was detected and identified in THSWD.

Identification of lactones

Angelicae sinensis Radix and Chuanxiong Rhizoma are rich sources of lactones or phthalide compounds [16, 2628]. In the positive ion mode, 14 lactones were analyzed and identified by comparing with reference compounds and literature data [27, 29]. Compounds 41, 42, and 43 were tentatively identified as senkyunolide J (41), senkyunolide I (42), and senkyunolide H (43), respectively.

Compounds 44, 45, 49 and 50 were isomers of ligustilide and butylideniphthalide. The Z-Ligustilide and Z-Butylidenephthalide were adopted as references, the compounds 44 and 45 were isomers and identified as E-ligustilide and Z- ligustilide with MS ion m/z 191 [M + H]+; the compounds 49 and 50 were isomers and identified as E-Butylideniphthalide and Z-Butylidenephthalide with MS ion of m/z 189[M + H]+, respectively [22].

Six dimmer compounds were identified from SWDCF possessing the same MS fragments ion m/z 381 [M + H]+. According to the literature data [21, 28, 30], these compounds were tentatively identified as Z-ligustilide dimmer E-232 (46), Z, Z-3,3,8,8-Diligustilide (47), angelicide (51), riligustilide (52), tokinolide B (53), and levistolide A (54), respectively.

Identification of flavonoids

Among 18 flavonoids identified from SWDCF, there were eight flavonoid aglycones including quercetin (60), isorhamnetin (65), keampferol (64), scutellarin (66), baicalein (69), wogonin (70), 6-dimethoxy-wogonin (72), and oroxylinA (71). The flavonoid glycosides were identified by comparing the tR, UVλmax, and the MS fragments characteristics to the standard substances.

Compounds 61, 62, and 63 contained fragment ion m/z 317 (Table 2). The MS/MS of m/z showed fragments including m/z 287, 273, 153, and 123. These data were consistent with those in the literatures [31, 32]. The aglucone was identified as isohamnetin. The three flavonoid glycosides were identified as isohamnetin-3-O-neohesperidoside (61), isohamnetin-3-O-rutinoside (62), and typhaneoside (63), respectively.

Hydroxysafflor yellow A (55) and safflor yellow A (59) were detected in THSWD from Carthami Flos. Compound 59 possessed MS ions characteristics of m/z 595[M + H]+ and m/z 617[M + Na]+ at ES+ mode and m/z 593[M-H]- at ES- mode. Compound 55 had diagnostic ions of m/z 613[M + H]+, and m/z 635[M + Na]+ at ES+ mode and m/z 611[M-H]- at ES- mode. Baicalin (67) and wogonoside (68) were identified from QLSWD [33, 34].

Identification of alkaloids

The alkaloids compounds derived mainly from Chuanxiong Rhizoma, Corydalis Rhizoma, and Coptidis Rhizoma. At the positive ion mode, 11 alkaloids constituents were analyzed and identified from SWDCF by comparing with reference compounds and literature data [35]. Compound 74 with MS characteristics of m/z 356 [M + H]+, 338 [M + H-H2O]+, and 312 [M + H-CO2]+ was identified as tetrahydropalmatine compared with the reference standard. Compounds 73, 76, 78, 80, 81, 82, and 83 were detected and identified from XFSWD, SFZYD, and QLSWD as tetramethylpyrazine (73), protopine (76), tetrahydrocoptisine (78), berberine (80), dehydrocorydaline (81), corydaline (82), and jatrorrhizine (83) by comparing with the reference standards, respectively. The MS characteristics were m/z 136 [M + H]+, m/z 354 [M + H]+, m/z 324 [M + H]+, m/z 336 [M + H]+, m/z 366 [M + H]+, m/z 368 [M + H]+, and m/z 339 [M + H]+, respectively. According to the literature [35], compounds 75, 77, and 79 were tentatively identified as tetrahydrocolumbamine, allocryptopine, and glaucine, respectively. The MS characteristics ions were m/z 342 [M + H]+, m/z 370 [M + H]+, and m/z 356 [M + H]+, respectively. In addition, 5-hydroxymethyl-2-furfural (5-HMF) (84) was identified from SWD only.

UPLC-Q-TOF-MS method was employed to identify the constituents from SWDCF. In ESI-TOF-MS experiment, accurate molecular mass of the components can be obtained. As ESI was a soft ionization technique, the interface produces little fragmentation of analytes and generally forms protonated molecular ions [M + H]+ for positive ionization mode or [M-H]- for negative ionization mode. Comparing the mass spectra of the compounds with the standards and those in the literature, the common and different components were unequivocally identified from every formula of SWDCF. These data would be provided the bioactive components for activities of different formulae.

The markers obtained by MarkerLynx™

The principal components analysis (PCA) was done by the Waters MarkerLynx™ software. In this study, SWD, THSWD, XFSWD, SFZYD and QLSWD were injected six times each in two ESI modes. Unsupervised PCA was performed to globally evaluate the chemical consistency among these five SWDCF decoctions. The data from both positive and negative ion modes were displayed as scores plots (Additional file 1: Figures S2-1 and 2-2). The scores plots demonstrated a clear classification trend among SWDCF samples, with all the observations falling within the Hotelling T2 (0.95) ellipse, which confirmed the fact that chemical difference exists among SWDCF. The results showed that the SFZYD and QLSWD were significantly different to SWD, THSWD, and XFSWD, while SWD, THSWD, and XFSWD were close to each other. These data indicated that the chemical composition and quantity of components changed after combining SWD with different herbs.

Chemical markers were analyzed to find out the changed common components contributing most to the SWDCF. Figures 2 showed the representative mass spectra of sixteen common and the greatest change compounds. According to the intensity trends of fragment ions from five decoctions samples, the intensity of the common chemical markers (paeoniflorin 16, albiflorin 14, ferulic acid 5, isoferulic acid 6, senkyunolide I 42, 3-butylidene-7-hydroxyphthalide 48, levistolide A 54, tetramethylpyrazine 73, E-Butylideniphthalide 49, Z-Butylidenephthalide 50, Z-ligustilide 45, E-ligustilide 44, Z-ligustilide dimmer 46, gallic acid 1, chlorogenic acid 2, benzoylpaeoniflorin 24) were different in every formula of SWDCF.
Figure 2

The intensity trend plots of sixteen representative changed common components in SWDCF samples. X axis represent for SWDCF samples (XF: XFSWD; TH: THSWD; SW: SWD; QL: QLSWD; SF: SFZYD). Y axis represent for relative quantity of target compounds.

The peak areas of components 16 (tR 5.80 min, m/z 481.1750), 14 (tR 3.90 min, m/z 481.1710), 42 (tR 6.26 min, m/z 225.1144), 54 (tR 12.60 min, m/z 399.2193), 73 (tR 0.64 min, m/z 136.0622), 49 (tR 8.08 min, m/z 189.0919), 50 (tR 9.27 min, m/z 189.0919), 46 (tR 13.80 min, m/z 191.1049), 45 (tR 10.82 min, m/z 191.1079), 44 (tR 9.44 min, m/z 191.1073) were higher in SWD than other formulae. XFSWD possessed greater peak area of compound 2 and 5, while SFZYD possessed high content of compound 6.

Optimization of the HPLC conditions

A small amount of acid was added into the mobile phase which could inhibit the ionization of these components to improve the peak shape and restrain the peak tailing due to the existence of acidic ingredients in SWDCF samples. 0%, 0.1% and 0.2% aqueous formic acid and acetic acid solutions were compared. The results showed that 7 compounds could be baseline separated when 0.1% aqueous formic acid solution was selected.

DAD detection was set at the wavelength range of 190–400 nm. For the satisfactory sensitivity, resolution and lower noise, four wavelengths at 230 nm, 260 nm, 277 nm, and 320 nm were selected for determining the different compounds in SWDCF. According to absorption curve of the tested analytes, the paeoniflorin had optimal sensitivity for detection at 230 nm, 320 nm for ferulic acid, 260 nm for gallic acid, vanillic acid, and caffeic acid, and 277 nm for senkyunolide I. Thus, a switching UV wavelength method was established by a variable-wavelength spectrophotometric detector. Under the optimized HPLC-UV conditions, the investigated analytes were well separated and detected in 85 min (Figure 3).
Figure 3

Typical HPLC-DAD chromatograms of mixed standards and samples. A: mixed standards; B: SWD; C: THSWD; D: XFSWD; E: SFZYD; F: QLSWD (1. gallic acid, 2. protocatechuic acid,3. vanillic acid, 4. caffeic acid, 5. paeoniflorin, 6. ferulic acid, 7. senkyunolide I).

Prior to sample analysis the optimal process of extraction had to be investigated. According to the applied form of decoction, the SWDCF were extracted by refluxing with water for twice. Ethanol (95%) was added to the filtrates until the concentration of ethanol was adjusted to 50% and seven compounds were almost completely extracted.

Validation of the quantitative analysis

The HPLC–DAD method for quantitation analysis was validated to determine the linearity, LOD, and LOQ. Good linear correlation and high sensitivity at these chromatographic conditions were confirmed by the correlation coefficients r2 > 0.9990 and P = 3.7501 × 10-9, 1.3503 × 10-7, 3.7553 × 10-8, 0, 3.7513 × 10-7, 3.7553 × 10-8, 3.7501 × 10-9 for gallic acid, protocatechuic acid, vanillic acid, caffeic acid, paeoniflorin, ferulic acid, senkyunolide I, respectively, within the test ranges, and the overall LODs and LOQs were in the range of 5.0–24.8 and 10.0–59.6 μg/mL, respectively (Table 3).
Table 3

Calibration curves, LOD and LOQ data of investigated compounds by HPLC-DAD

Analytes

Calibration curvesa

r 2

Linear range (μg/mL)

LOD (μg/mL)

LOQ (μg/mL)

Gallic acid

Y = 2.4 × 106X-8022.9

0.9999

148.0-1480.0

7.5

14.1

Protocatechuic acid

Y = 8.0 × 106X-36350

0.9994

38.4-384.0

8.6

19.2

Vanillic acid

Y = 2.6 × 106X-18490

0.9997

32.0-320.0

5.0

10.0

Caffeic acid

Y = 3.5 × 106X-25506

1.0000

35.6-356.0

6.5

13.6

Paeoniflorin

Y = 1.1 × 106X + 160000

0.9990

476.0-4760.0

24.8

59.6

Ferulic acid

Y = 1.1 × 107X-1.2 × 105

0.9997

136.0-1360.0

6.2

12.4

Senkyunolide I

Y = 6.5 × 106X-9533.5

0.9999

46.0-460.0

6.3

12.6

a y is the logarithmic value of peak area and x is the logarithmic value of the reference compound’s concentration (μg/ml).

As shown in Table 4, the intra- and inter-day precisions, repeatability and stability of the seven analytes were less than 3%. The overall recoveries lay between 92.20% and 104.60% with RSD less than 3.54% for seven components in all samples. These results indicated that the HPLC fingerprint chromatograms had a good repeatability, precision, accuracy, and recovery (Tables 4 and 5) and the developed HPLC-DAD method was a reliable and useful method for assessment of SWDCF.
Table 4

Precision, repeatability of seven analytes

Analytes

Precision (RSD,%)

Repeatability (RSD,%; n = 6)

Intraday (n = 6)

Interday (n = 6)

SWD

SFZYD

XFSWD

THSWD

QLSWD

Gallic acid

1.75

1.78

1.81

1.26

2.84

3.32

1.31

Protocatechuic acid

0.76

1.21

3.16

1.90

2.72

4.18

3.19

Vanillic acid

1.31

1.55

1.79

1.05

2.26

3.97

2.80

Caffeic acid

0.98

0.97

2.27

2.47

1.60

4.52

3.04

Paeoniflorin

1.06

2.01

2.72

3.58

2.38

3.96

2.19

Ferulic acid

0.88

1.05

2.19

3.01

1.26

2.95

2.22

Senkyunolide I

1.16

1.12

2.22

3.97

1.43

1.82

3.75

Table 5

Stability and recovery of seven analytes

Analytes

Stability (RSD,%; n = 6)

Recovery (%; n = 6)

A

B

C

D

E

SWD

THSWD

XFSWD

SFZYD

QLSWD

Mean

RSD (%)

Mean

RSD (%)

Mean

RSD (%)

Mean

RSD (%)

Mean

RSD (%)

Gallic acid

6.36

3.34

7.13

5.16

1.03

98.1

2.71

98.9

1.32

97.8

2.32

101.2

3.12

99.7

1.44

Protocatechuic acid

5.79

5.46

6.18

4.0

4.62

101.2

3.32

99.8

1.43

97.6

1.18

103.7

3.54

102.7

1.98

Vanillic acid

3.14

3.68

6.25

8.80

2.19

96.2

1.39

97.3

1.79

102.3

1.25

92.2

2.81

103.1

2.32

Caffeic acid

6.61

5.10

8.50

2.47

7.87

103.8

1.48

95.8

3.24

98.3

2.50

98.6

2.44

98.2

3.16

Paeoniflorin

6.13

3.79

7.37

8.36

4.07

97.1

3.25

98.2

2.77

95.4

1.15

94.0

1.36

95.8

2.17

Ferulic acid

4.54

3.74

1.31

7.65

2.10

99.7

1.22

103.2

1.94

99.3

1.43

97.5

2.65

104.6

1.89

Senkyunolide I

6.87

2.82

2.47

8.91

4.07

96.9

2.31

98.1

2.13

98.1

2.86

94.0

1.91

98.1

2.34

Sample analysis

The HPLC-DAD method was then subsequently applied to simultaneously determine the chemical markers including gallic acid, protocatechuic acid, vanillic acid, caffeic acid, paeoniflorin, ferulic acid, senkyunolide I in SWDCF samples. The results (Table 6) showed there were remarkable differences among the contents of the chemical markers analyzed in different samples. Paeoniflorin (5) was found to be a predominant constituent in both of QLSWD and SFZYD, while the lowest contents in SWD except XFSWD, suggesting that the active compounds of paeoniflorin was dissolved increasedly after the SWD combined with other herbs. The contents of senkyunolide I in SWDCF were decreased except SFZYD varing from 31.30 to 84.70 mg/g. The phenolic acids including gallic acid, caffeic acid, ferulic acid, vanillic acid, and protocatechuic acid were increased significantly except in XFSWD.
Table 6

Contents of seven investigated compounds in SWDCF

Analytes

Contents of analyst (mean ± SD; n = 3; μg/g)

SWD

THSWD

XFSWD

SFZYD

QLSWD

Gallic acid

316.00

421.20

143.50

436.00

729.80

Protocatechuic acid

6.50

11.60

5.40

2.46

4.05

Vanillic acid

18.40

33.90

13.80

90.70

44.00

Caffeic acid

58.20

69.70

31.30

67.30

84.70

Paeoniflorin

2050.00

3430.00

790.00

3840.00

5140.00

Ferulic acid

120.00

166.70

81.30

225.70

310.70

Senkyunolide I

180.00

30.00

70.00

210.00

80.00

Conclusion

The chemical profiles with 84 components in SWDCF, including monoterpene glycosides, acetophenones, galloyl glucoses, even some isomers in the complex system were characterized by UPLC–QTOF–MS/MS.

Abbreviations

SWDCF: 

Siwu decoction categorized formulae

UPLC - QTOF - MS /MS: 

Ultra-high performance liquid chromatography coupled with time-of-flight mass spectrometry

CM: 

Chinese medicine

CF: 

Categorized formulae

SWD: 

Siwu decoction

THSWD: 

Taohong Siwu decoction

PD: 

Primary dysmenorrheal

XFSWD: 

Xiangfu Siwu decoction

SFZYD: 

Shaofu Zhuyu decoction

QLSWD: 

Qinlian Siwu decoction

ESI: 

Electrospray ionization

Declarations

Acknowledgements

This work was supported by Key Research Project in Basic Science of Jiangsu College and University (No. 11KJA360002; 06KJA36022), National Natural Science Foundation of China (No. 30973885), and 2006 Training Program of Scientific and Technological Innovation Team for “Qinglan Project” of Jiangsu College and University. And this work was supported by Construction Project for Jiangsu Key Laboratory for High Technology Research of TCM Formulae (BM2010576), Construction Project for Jiangsu Engineering Center of Innovative Drug from Blood-conditioning TCM Formulae and a Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (ysxk-2010).

Authors’ Affiliations

(1)
Jiangsu Key Laboratory for TCM Formulae Research, Nanjing University of Chinese Medicine
(2)
College of Pharmacy, Jiangsu University

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