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HomeSmall Molecules Analysis & QCDetermination of Baicalin, Chlorogenic acid and Forsythin

Determination of Baicalin, Chlorogenic acid and Forsythin in Shuanghuanglian Oral Liquid acc. to Chinese Pharmacopeia

Dean Duan, Merck R&D
APAC Lab Shanghai, China

Abstract

In this application, Shuanghuang Lian oral liquid, a well-known traditional Chinese medicine (TCM), was prepared following Chinese Pharmacopoeia 2020 and analyzed on a Discovery® HS C18 HPLC column for the content of three key compounds, baicalin, chlorogenic acid, and forsythin (phillyrin). For baicalin the linear range was 0.5 – 200 µg/mL. LOD and LOQ of baicalin is 0.07 µg/mL and 0.23 µg/mL separately. For chlorogenic acid the linear range is 0.1 – 50 µg/mL. LOD and LOQ of baicalin was 0.11 µg/mL and 0.33 µg/mL separately. For forsythin the linear range was 0.2 – 60 µg/mL. LOD and LOQ of baicalin was 0.02 µg/mL and 0.07 µg/mL separately. The SPE cleanup for the forsythin sample showed good recoveries of 88%. The method met the requirements of the Chinese Pharmacopeia 2020. The Discovery® HS C18 HPLC column can be used to determine the baicalin, chlorogenic acid, and forsythin content of Shuanghuang Lian oral liquid.

Section Overview

Introduction

Shuang-Huang Lian oral liquid is a Chinese patent medicine. It is composed of honeysuckle, scutellaria, and forsythia. The determination of baicalin, chlorogenic acid, and forsythin (phillyrin) as key compounds in the oral liquid by HPLC is listed in the Chinese Pharmacopeia 2020.1 Here we describe three dedicated analytical methods using a Discovery® HS C18 HPLC column according to the pharmacopeia monograph.

The image displays the chemical structures of three compounds: Baicalin, Chlorogenic Acid, and Forsythin. Baicalin, on the left, features a multi-ring system with several hydroxyl (OH) groups and a carboxyl (COOH) group. In the center, Chlorogenic Acid's structure includes a central hexane ring, multiple hydroxyl groups, and a carboxyl group. On the right, Forsythin's structure is the most complex, showcasing multiple rings, hydroxyl groups, and methoxy groups (OCH3). Each structure is labeled with its respective compound name below it, and they are depicted in skeletal formula format, illustrating the arrangement of atoms and bonds.

Experimental

HPLC conditions and sample preparation applied for the three analytes of interest are shown in Tables 1–3. For baicalin and chlorogenic acid, a dilution and filtration were applied, for forsythin, a clean-up by SPE  (interference removal, chemical filtration) using a neutral alumina as adsorbent was used.

HPLC Parameters & Samples- Baicalin

Column:

Discovery® HS C18 250x4.6 mm, 5 µm (568523-U)

Mobile phase:

[A] water; [B] methanol; [C] glacial acetic acid

A:B:C = 50:50:1

Gradient:

isocratic

Flow rate:

1.0 mL/min

Pressure drop:

2700 psi

Colum temp.:

25°C

Detector:

UV at 274 nm

Injection Volume:

5 µL

Samples

Standard for System Suitability:

Dissolve appropriate amount of baicalin in 50% aqueous methanol solution to obtain 1 mg/mL stock solution, then dilute with 50% aqueous methanol solution to obtain 50 µg/mL standard solution

Sample preparation:

Accurately measure 1 mL of Shuanghuang Lian oral liquid in a 50 mL volumetric flask with a stopper, add appropriate amount of 50% aqueous methanol, sonicate for 20 minutes, place it at room temperature, add 50% aqueous methanol solution to the tick mark of volumetric flask, mix well, filter (0.45 µm), stand for HPLC analysis.

Table 1.HPLC conditions and sample preparation for baicalin determination

HPLC Parameters & Samples- Chlorogenic acid

Column:

Discovery® HS C18 250x4.6 mm, 5 µm (568523-U)

Mobile phase:

[A] Water; [B] methanol; [C] glacial acetic acid.
A:B:C = 80:20:1

Gradient:

isocratic

Flow rate:

1.0 mL/min

Pressure drop:

2210 psi

Colum temp.:

25°C

Detector:

UV, 324nm

Injection:

10 µL

Samples

Standard for System Suitability:

Dissolve an appropriate amount of chlorogenic acid in water to obtain 1 mg/mL of chlorogenic acid stock solution, then dilute with water to obtain 20 µg/mL standard solution

Sample preparation:

Accurately transfer 2 mL of Shuanghuang Lian oral liquid into a 50-mL brown volumetric flask, add water to required level, mix well, filter (0.45 µm), stand for HPLC analysis.

Table 2.HPLC conditions and sample preparation for chlorogenic acid determination

HPLC Parameters & Samples - Forsythin

Column:

Discovery® HS C18 250x4.6 mm, 5 µm (568523-U)

Mobile phase:

[A] Water; [B] acetonitrile.
A:B = 75:25

Gradient:

isocratic

Flow rate:

1.0 mL/min

Pressure drop:

1660 psi

Colum temp.:

25°C

Detector:

UV at 278nm

Injection Volume:

10 µL

Samples

Standard for System Suitability:

Dissolve an appropriate amount of forsythin (phillyrin) to 50% aqueous methanol solution to obtain 1 mg/mL of forsythin stock solution, then dilute with 50% aqueous methanol solution to obtain 30 µg/mL standard solution.

Sample preparation:

SPE cleanup (Table 4): Accurately transfer 1 mL of Shuanghuang Lian oral liquid onto a neutral alumina SPE tube. Elute with 40 mL of 70% ethanol, collect the eluent, dry down under nitrogen at 45 ℃, add 5 mL of 50% methanol aqueous solution to dissolve the residue, filter with 0.45 µm filter membrane, stand for HPLC analysis.

Table 3.HPLC conditions and sample preparation for forsythin determination

Sample Preparation by SPE for Forsythin Determination in Oral Liquid

For the determination of forsythin, an additional cleanup by SPE was applied.

SPE Sample Preparation

SPE tube/cartridge:

Supelclean LC-Alumina-N SPE Tube, 2 g / 6 mL (57087)

Conditioning:

5 mL of 70% aqueous ethanol solution

Sample addition:

1 mL Shuanghuang Lian oral liquid

Washing:

none

Elution:

40 mL of 70% ethanol aqueous solution

Elution post-treatment:

Evaporate to dryness under nitrogen flow at 45 ℃, add 5 mL of 50% methanol aqueous solution to dissolve the residue, and filter with 0.45 µm filter membrane

Table 4.SPE procedure for determination of Forsythin

Standards Preparation for Calibration

The calibration standards were prepared according to these procedures:

Diluent:  Add 50 mL of methanol and 50 mL of water into a measuring cylinder. Mix well to prepare 50% aqueous methanol solution as diluent.

For Baicalin:

  • Weigh ~10 mg of baicalin reference material into a 10 mL volumetric flask.
  • Add ~8 mL of diluent and sonicate for 5 mins.
  • Top-up to mark with diluent and mix well to prepare 1 mg/mL of baicalin stock solution.
  • Dilute to 0.1, 0.2, 0.5, 1. 2, 5, 10, 50, 100 and 200 µg/mL with diluent.

For Chlorogenic acid:

  • Weigh ~10 mg of chlorogenic acid reference material into a 10 mL volumetric flask.
  • Add ~8 mL of diluent and sonicate for 5 mins.
  • Top-up to mark with diluent and mix well to prepare 1 mg/mL of chlorogenic acid stock solution.
  • Dilute to 0.1, 0.2, 0.5, 1. 2, 5, 10, 20, 40 and 50 µg/mL with diluent.

For Forsythin:

  • Weigh ~10 mg of forsythin reference material into a 10 mL volumetric flask.
  • Add ~8 mL of diluent and sonicate for 5 mins.
  • Top-up to mark with diluent and mix well to prepare 1 mg/mL of forsythin stock solution.
  • Dilute to 0.2, 0.5, 1. 2, 5, 10, 30, 40 and 60 µg/mL with diluent.

Method Suitability / System Suitability Criteria

Acceptance Criteria for Standard Solutions:

  • Theoretical plate number calculated for baicalin peak: NLT 1500
  • Theoretical plate number calculated for chlorogenic acid peak: NLT 6000
  • Theoretical plate number calculated for forsythin peak: NLT 6000

Results & Discussion

The chromatographic results for the three compounds under investigation are displayed in Figures 1–5. The chromatographic data of the separately injected standard solutions is summarized in Table 5.

As an example of the calibration curves, the one for baicalin is displayed in Figure 6.

The methods displayed good reproducibility with RSDs of 0.98%, 0.27%, and 0.98% (Table 6), as well as good linearity and sensitivity (Table 7). In summary, the results for the three analytes determined are:

Baicalin:

  • The theoretical plates is 10377 (>1500). It meets the requirements of the Chinese Pharmacopeia 2020.
  • The Limit of Detection (LOD) for baicalin in Shuanghuang Lian oral liquid is 3.72 µg/mL, and the Limit of Quantification (LOQ) is 11.27 µg/mL. The range from 0.5 to 200 µg/mL is linear with an R2 of 0.9999.

Chlorogenic acid:

  • The theoretical plates is 13128 (>6000). It meets the requirements of the Chinese Pharmacopeia 2020.
  • The LOD for chlorogenic acid in Shuanghuang Lian oral liquid is 2.72 µg/mL, and the LOQ is 8.24 µg/mL. The range from 0.1 to 50 µg/mL is linear, with the R2 being 0.9982.

Forsythin:

  • The theoretical plates is 8258 (>6000). It meets the requirements of the Chinese Pharmacopeia 2020.
  • The LOD for forsythin in Shuanghuang Lian oral liquid is 0.11 µg/mL, and the LOQ is 0.33 µg/mL. The range from 0.2 to 60 µg/mL is linear, with the R2 being 0.9939. 
  • The average SPE recovery (n = 3) for forsythin was assessed using an oral liquid sample spiked at 75 µg/mL and was determined to be 88% (Table 8).
  • The used oral liquid showed a forsythin content below LOD (Figure 4). The chromatogram for a sample spiked at 75 µg/mL is shown in Figure 5.
HPLC-UV chromatogram of a treated Shuanghuang Lian oral liquid sample obtained at 274 nm. Intensity (mAU) on the y-axis and retention time (minutes) on the x-axis. Major ticks on x-axis at 5, 10, and 15 minutes, and on y-axis at 20, 40, 60, 80, 100, 120, and 140 mAU. The green curve starts at 10 mAU, shows 5 small peaks between 3-4 minutes, and a major peak for baicalin at 8.5 minutes labeled as 1.

Figure 1.Sample Solution- Sample treated following procedure in baicalin (1) sample preparation part (Table 1).

HPLC-UV chromatogram of a treated Shuanghuang Lian oral liquid sample obtained at 324 nm. Intensity (mAU) on the y-axis and retention time (minutes) on the x-axis. Major ticks on x-axis at 5, 10, 15, 20, and 25 minutes, and on y-axis at 20, 40, 60, 80, 100, 120, 140, 160, 180, and 200 mAU. The green curve starts at 10 mAU, shows a large peak between 6-7 minutes at 160 mAU, a peak for chlorogenic acid at 12 minutes labeled as 1 at 90 mAU, a peak at 14 minutes at 70 mAU, and a smaller peak at 18 minutes at 30 mAU.

Figure 2.Sample Solution- Sample treated following procedure in chlorogenic acid (1) sample preparation part (Table 2).

HPLC-UV chromatogram of forsythin standard solution at a concentration of 30 µg/mL obtained at 278 nm. Intensity (mAU) on the y-axis and retention time (minutes) on the x-axis. Major ticks on x-axis at 5, 10, 15, 20, and 25 minutes, and on y-axis at 5, 10, 15, 20, 25, 30, 35, and 40 mAU. The green curve starts at 5 mAU, runs parallel to the x-axis, then shows a large peak at 13 minutes reaching 23 mAU labeled as 1 for forsythin, and then runs parallel again.

Figure 3.Chromatogram of forsythin (1) standard solution 30 µg/mL.

HPLC-UV chromatogram of treated Shuanghuang Lian oral liquid sample obtained at 278 nm. Intensity (mAU) on the y-axis and retention time (minutes) on the x-axis. Major ticks on x-axis at 5, 10, 15, 20, and 25 minutes, and on y-axis at 20, 40, 60, 80, and 100 mAU. The green curve starts at 10 mAU, runs parallel to the x-axis, and then from 2-6 minutes shows many peaks of different heights. There is another large peak corresponding to 60 mAU at 8 minutes, followed a small peak at 9.5 minutes. Then there is barely visible peak at 13 minutes, labeled as 1 for forsythin, after which there is another peak at 23 minutes.

Figure 4.Sample Solution - Sample treated following the procedure in forsythin sample preparation part (Table 3). The used oral liquid showed forsythin content below LOD.

HPLC-UV chromatogram of a treated Shuanghuang Lian oral liquid sample, spiked at 75 µg/mL and obtained at 278 nm. Intensity (mAU) on the y-axis and retention time (minutes) on the x-axis. Major ticks on x-axis at 5, 10, 15, 20, and 25 minutes, and on y-axis at 5, 10, 15, 20, 25, 30, 35, and 40 mAU. The green curve starts at 5 mAU, runs parallel to the x-axis, and then from 2-6 minutes shows many peaks of different heights. There is another large peak corresponding to 8 minutes, followed another one at 10 minutes. Then there is a peak at 13 minutes, labeled as 1 for forsythin, corresponding to 10 mAU, after which there is another peak at 23 minutes.

Figure 5.Oral liquid sample spiked with forsythin (1) at 75 µg/mL - Sample treated following the procedure in forsythin sample preparation part (Table 3).

Compound

Retention Time (min)

Theoretical Plates (Determined)

Theoretical Plates (Acceptance Criteria Ch P)

Tailing Factor

Baicalin

8.53

10377

1500

1.07

Chlorogenic acid

11.79

13128

6000

1.04

Forsythin

12.96

8258

6000

1.00

Table 5.The chromatographic data of separate injections of standard solutions and acceptance criteria of the Chinese Pharmacopoeia
Intensity v/s concentration measured in µg/mL plot representing calibration curve obtained for baicalin at concentrations of 0.1, 0.2, 0.5, 1. 2, 5, 10, 50, 100 and 200 µg/mL. Major ticks on x-axis at 50, 100, 150, and 200 µg/mL, and on y-axis at 5, 10, 15, 20, 25, 30, and 35 * sec × 100000 mAU. The linear equation obtained is y = 15,524.4564x - 6,352.1452 with R² = 0.9999.

Figure 6.Calibration curve for baicalin.

Injection number

Baicalin,

50 µg/mL

Chlorogenic acid,

20 µg/mL

Forsythin,

30 µg/mL

Injection 1

752679

470941

752679

Injection 2

758358

469506

758358

Injection 3

769377

472235

769377

Injection 4

770246

472652

770246

Injection 5

764743

471883

764743

Mean

763081

471443

763081

Standard Deviation

7487

1254

7487

RSD (%)

0.98

0.27

0.98

Table 6.Repeatability of standard solution injections (n=5)

Compound

Standards Calibration Range (µg/mL)

No. of Calibrators

R2

Sample Preparation Dilution Factor

Oral Liquid

LOD (µg/mL)

Oral Liquid

LOQ (µg/mL)

Baicalin

0.5 -200

9

0.9999

1:50

3.72

11.27

Chlorogenic acid

0.1 -50

10

0.9982

1:25

2.72

8.24

Forsythin

0.2 -60

9

0.9939

1:5

0.11

0.33

Table 7.Linearity and repeatability data summary for baicalin, chlorogenic acid and forsythin standard injections, the resulting dilution factors during sample prep and derived LODs & LOQs for an oral liquid sample

Sample No.

Recovery (%)

sample 1

90.1

sample 2

85.7

sample 3

88.1

Mean

88.0

Standard Deviation

2.0

RSD (%)

2.5

Table 8.SPE recovery for forsythin spiked at 75 µg/mL in oral liquid

Conclusion

The three HPLC methods using the Discovery® HS C18 column met the system suitability criteria listed in the Chinese Pharmacopeia monograph. The column is therefore suitable for the determination of baicalin, chlorogenic acid and forsythin in Shuanghuang Lian oral liquid. For the determination of forsythin, the used SupelcleanLC-Alumina-N SPE Tube for clean-up of the oral liquid sample provided an average recovery (n=3) of 88%, which is suitable for the method.

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References

1.
Chinese Pharmacopeia 2020 monograph, volume 1, pages 773-774. [Internet]. Available from: http://down.foodmate.net/standard/index
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