| Literature DB >> 31487833 |
Le Wang1, Shusheng Fan2, Xiaoping Wang3, Xiuhuan Wang4, Xin Yan5, Dongjie Shan6, Wuqing Xiao7, Jiamu Ma8, Yanran Wang9, Xiao Li10, Xiao Xu11, Gaimei She12.
Abstract
Nü-Er-Cha, produced from the leaves of Rhamnus heterophylla Oliv., is known as an herbal tea and used in the treatment of bleeding, irregular menstruation and dysentery. A method was developed for the quality assessment of herbal tea, Nü-Er-Cha, adopting physical parameters, chemical constituents and sensory profiles as various potential factors. Their inner relationship was mined by multivariate statistical analysis tools, and the three factors were integrated by a technique for order preference by a similarity to ideal solution (TOPSIS) approach to comprehensively analyze the characters of Nü-Er-Cha. Viscosity was also introduced to the physical parameter determination besides conductivity, pH and color. Seven common peaks of eight batches of Nü-Er-Cha were marked by a high performance liquid chromatography (HPLC) fingerprint. They were further identified by HPLC mass spectrometry/mass spectrometry (HPLC-MS/MS) as hydroxybenzoic acids and flavanol glycosides. Fifty trained members participated in the sensory evaluation. Significant correlations between total sensory scores and conductivity, viscosity as well as pH were observed, a relatively innovative result for the quality assessment of herbal teas. The common peaks, belonging to hydroxybenzoic acids and flavanol glycosides, were mainly related to the color of infusions and leaves. The result of the TOPSIS analysis showed that S3 and S4 ranked as the top two in the comprehensive quality assessment. This may be related to rhamnetin triglycoside with a galactose/glucose and two rhamnoses, which had a higher peak response in S3 and S4 than that in the other samples. The present study may contribute to a better understanding of the relationship regarding physical properties, chemical composition and sensory profiles, and it may supply ideas for the comprehensive quality assessment of the herbal tea Nü-Er-Cha.Entities:
Keywords: Nü-Er-Cha; TOPSIS; flavonol glycosides; hydroxybenzoic acids; inner relationship; physical parameters; sensory evaluation
Mesh:
Substances:
Year: 2019 PMID: 31487833 PMCID: PMC6767605 DOI: 10.3390/molecules24183211
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411
Figure 1Histogram for the descriptive sensory analysis of Nü-Er-Cha: (A) The scores plot of five descriptors; (B) the scores plot of twelve indicators.
The physicochemical properties analysis of Nü-Er-Cha A.
| Samples | DpH B | Dcond. C (μs/cm) | Viscosity (m2/s) | Color | |||||
|---|---|---|---|---|---|---|---|---|---|
| Leaves D | Infusions E | ||||||||
| L*1 | a*1 | b*1 | L*2 | a*2 | b*2 | ||||
| S1 | 0.74 ± 0.05 a | 47 ± 12 cd | 1.53 ± 0.19 b | 33.29 ± 0.01 ab | 2.78 ± 0.02 a | 19.02 ± 0.01 c | 98.32 ± 0.00 a | 0.59 ± 0.00 abc | 6.08 ± 0.00 c |
| S2 | 0.65 ± 0.04 b | 40 ± 7 d | 1.53 ± 0.05 b | 34.05 ± 0.01 ab | 2.10 ± 0.02 c | 18.52 ± 0.04 d | 98.08 ± 0.00 ab | 0.69 ± 0.01 abc | 6.28 ± 0.01 bc |
| S3 | 0.61 ± 0.02 bc | 41 ± 6 cd | 1.56 ± 0.09 ab | 43.28 ± 0.02 ab | 1.22 ± 0.00 f | 26.76 ± 0.05 a | 97.51 ± 0.00 abc | −2.69 ± 0.01 bc | 13.19 ± 0.02 abc |
| S4 | 0.57 ± 0.02 c | 56 ± 8 cd | 1.57 ± 0.04 ab | 43.41 ± 0.00 a | −0.58 ± 0.01 h | 24.82 ± 0.02 b | 95.73 ± 0.01 bc | −2.54 ± 0.01 bc | 18.35 ± 0.04 a |
| S5 | 0.59 ± 0.02 bc | 61 ± 7 bc | 1.55 ± 0.06 ab | 33.34 ± 0.01 ab | 1.09 ± 0.02 g | 17.59 ± 0.02 f | 96.07 ± 0.00 abc | 0.32 ± 0.00 abc | 14.95 ± 0.02 abc |
| S6 | 0.60 ± 0.01 bc | 113 ± 6 a | 1.58 ± 0.33 ab | 36.35 ± 0.01 ab | 1.59 ± 0.01 e | 17.61 ± 0.03 f | 95.33 ± 0.00 c | 0.88 ± 0.01 ab | 17.58 ± 0.02 ab |
| S7 | 0.50 ± 0.01 c | 77 ± 5 b | 1.56 ± 0.05 ab | 32.55 ± 0.01 ab | 2.44 ± 0.02 b | 18.08 ± 0.03 e | 97.60 ± 0.00 abc | 0.72 ± 0.00 abc | 7.49 ± 0.00 abc |
| S8 | 0.43 ± 0.02 d | 66 ± 3 bc | 1.60 ± 0.03 a | 28.68 ± 0.42 b | 1.78 ± 0.02 d | 16.04 ± 0.03 g | 96.88 ± 0.00 abc | 2.03 ± 0.00 a | 8.18 ± 0.01 abc |
a–h One-way ANOVA conducted at α = 0.05. Post-hoc test conducted using Tukey’s honestly significant difference test. A Values are expressed in terms of mean ± standard deviation. N = 3 panelists. B The differential values between the conductivity of tap water and infusions. C The differential values between the conductivity of tap water and infusions. D The color parameters of leaves. E The color parameters of infusions.
Figure 2HPLC fingerprint (A) and total ion current (TIC) chromatogram (B) of Nü-Er-Cha.
The relative peak area of common peaks.
| Common Peaks | S1 | S2 | S3 | S4 | S5 | S6 | S7 | S8 |
|---|---|---|---|---|---|---|---|---|
| X1 | 0.5926 | 5.0868 | 0.2053 | 0.3683 | 2.1660 | 3.9654 | 1.5900 | 3.0771 |
| X2 | 0.0290 | 0.1588 | 0.0348 | 0.0314 | 0.0812 | 0.1189 | 0.1600 | 0.2555 |
| X3 | 0.7450 | 1.5302 | 0.1738 | 0.1919 | 1.3710 | 2.3854 | 1.4628 | 2.2161 |
| X4 | 0.6424 | 1.4100 | 0.0536 | 0.0662 | 1.5070 | 2.7684 | 1.6495 | 2.0251 |
| X5 | 0.0650 | 0.0987 | 0.0736 | 0.0651 | 0.0627 | 0.1103 | 0.0867 | 0.1200 |
| X6 | 1.0000 | 1.0000 | 1.0000 | 1.0000 | 1.0000 | 1.0000 | 1.0000 | 1.0000 |
| X7 | 0.2055 | 0.2393 | 0.1535 | 0.1906 | 0.1574 | 0.2434 | 0.1593 | 0.2050 |
Results of similarity analyzes of the HPLC fingerprint of Nü-Er-Cha.
| S1 | S2 | S3 | S4 | S5 | S6 | S7 | S8 | R | |
|---|---|---|---|---|---|---|---|---|---|
| S1 | 1 | 0.696 | 0.801 | 0.829 | 0.893 | 0.810 | 0.910 | 0.849 | 0.888 |
| S2 | 0.696 | 1 | 0.400 | 0.514 | 0.910 | 0.879 | 0.806 | 0.906 | 0.915 |
| S3 | 0.801 | 0.400 | 1 | 0.988 | 0.536 | 0.427 | 0.561 | 0.467 | 0.548 |
| S4 | 0.829 | 0.514 | 0.988 | 1 | 0.618 | 0.518 | 0.627 | 0.556 | 0.634 |
| S5 | 0.893 | 0.910 | 0.536 | 0.618 | 1 | 0.950 | 0.953 | 0.975 | 0.989 |
| S6 | 0.810 | 0.879 | 0.427 | 0.518 | 0.950 | 1 | 0.948 | 0.953 | 0.963 |
| S7 | 0.910 | 0.806 | 0.561 | 0.627 | 0.953 | 0.948 | 1 | 0.964 | 0.971 |
| S8 | 0.849 | 0.906 | 0.467 | 0.556 | 0.975 | 0.953 | 0.964 | 1 | 0.987 |
| R | 0.888 | 0.915 | 0.548 | 0.634 | 0.989 | 0.963 | 0.971 | 0.987 | 1 |
The compounds identified by HPLC-DAD-ESI-MS/MS.
| Compounds | Molecular Formula | Observed Mass ( | Expected Mass ( | Mass Error (ppm) | RT (min) | [M − H]− ( | MS/MS Fragment Ions ( |
|---|---|---|---|---|---|---|---|
|
| |||||||
| 3′,5,7-Trihydroxy-4′-methoxyflavone 7- | C28H32O15 | 608.1738 | 608.1741 | −0.49 | 46.779 | 607.1699 | 461.6880, 299.0577, 152.016, 148.6852 |
| quercetin | C15H10O7 | 302.0429 | 302.0427 | 0.91 | 48.095 | 301.0316 | 152.0082, 153.0085, 121.0286 |
| quercetin 3-methyl ether | C16H12O7 | 316.0588 | 316.0583 | 1.3 | 54.461 | 315.0529 | 300.0259, 272.0315, 152.0128 |
| rhamnezin | C17H14O7 | 330.0738 | 330.074 | −0.41 | 67.703 | 329.0734 | 314.0509, 299.0226, 271.0245, 227.0336 |
| kaempferol | C15H10O6 | 286.0484 | 286.0477 | 1.62 | 54.037 | 285.0414 | 257.0445, 229.0508, 121.026, 93.0356, 65.00333 |
| rhamnocitrin | C16H12O6 | 300.0636 | 300.0634 | 1.01 | 67.449 | 299.0624 | 271.0607, 243.0695, 166.0197 |
| quercetin galactoside(3- | C21H20O12 | 464.0953 | 464.0955 | 0.2 | 32.434 | 463.088 | 301.0325, 273.0334, 245.0515, 136.9104 |
| kaempferol 3- | C21H20O11 | 448.1011 | 448.1006 | 0.51 | 37.484 | 285.0333 | 257.0445, 229.0511, 152.0099 |
| quercetin diglycoside with a rhamnose and a galactose/glucose) | C27H30O16 | 610.1532 | 610.1534 | −0.36 | 31.288 | 609.1523 | 301.0313, 273.0802, 152.8107, 136.9585 |
| quercetin triglycoside with a galactose/glucose and two rhamnoses (X5) | C33H40O20 | 756.2144 | 756.2113 | 0.88 | 30.906 | 755.2144 | 301.0349, 463.0765, 152.4898, 137.3381 |
| quercetin 3-methyl ether 7- | C22H22O12 | 478.1106 | 478.1111 | −0.34 | 51.788 | 477.1018 | 315.0430, 300.0189, 165.0141, 137.5443, 109.0301 |
| kaempferol triglycoside with a galactose/glucose and two rhamnoses (X6) | C33H40O19 | 740.2158 | 740.2164 | 0.07 | 32.901 | 739.2122 | 285.0403, 57.0435, 229.0946, 152.0061, 120.0288 |
| rhamnocitrin diglycoside with a rhamnose and a galactose/glucose) | C28H32O15 | 608.1738 | 608.1741 | −0.83 | 47.012 | 607.1597 | 299.0577, 255.7552, 165.5555, 119.9104 |
| rhamnocitrin triglycoside with a galactose/glucose and two rhamnoses (X7) | C34H42O19 | 754.2335 | 754.232 | 1.01 | 40.015 | 753.2289 | 299.0507, 271.0618, 255.0335, 165.0185 |
| rhamnazin triglycoside with a galactose/glucose and two rhamnoses | C35H44O20 | 784.2431 | 784.2426 | 0.71 | 46.822 | 783.236 | 329.0661, 314.0414, 286.0448, |
| rhamnazin diglycoside with a rhamnose and a galactose/glucose) | C29H34O16 | 638.1852 | 638.1847 | 0.61 | 47.586 | 637.1799 | 329.0737, 314.0414, 299.0407 |
| rhamnetin triglycoside with a galactose/glucose and two rhamnoses | C34H42O20 | 770.2276 | 770.2269 | 0.48 | 34.280 | 769.2203 | 315.0507, 300.0245, 272.0272, 165.5149, 137.721 |
|
| |||||||
| emodin | C15H10O5 | 270.053 | 270.0528 | 0.49 | 64.562 | 269.0462 | 225.0574, 241.0480, |
| emodin-3- | C21H20O9 | 416.1109 | 416.1107 | 0.4 | 64.605 | 415.1148 | 269.0459, 241.0525, 197.0590 |
| emodin glucoside(1- | C21H20O10 | 432.1065 | 432.1056 | 2.01 | 49.708 | 431.094 | 269.0461, 240.0423, 241.0514, 225.0562 |
| emodin 3- | C25H24O11 | 500.1321 | 500.1319 | 0.48 | 58.069 | 499.1353 | 269.0411, 240.0461, 212.0476 |
|
| |||||||
| malic acid (X1) | C4H6O5 | 134.0216 | 134.0215 | 0.76 | 3.701 | 133.0128 | 115.0039, 71.047, |
| gallic acid (X2) | C7H6O5 | 170.0213 | 170.0215 | −1.48 | 5.992 | 169.0127 | 152.0945, 125.0271 |
| protocatechuic acid (X3) | C7H6O4 | 154.0264 | 154.0266 | −1.74 | 10.391 | 153.0181 | 109.0283, 91.0185, 63.0259 |
| salicylic acid (X4) | C7H6O3 | 138.0318 | 138.0317 | −1.02 | 15.435 | 137.0245 | 93.0348, 65.0386,51.0226 |
Figure 3The heat-map based on the Pearson coefficient.
Figure 4The correlation bi-plot for sensory and physical–chemical parameters.
Figure 5The variable importance to projection (VIP) of the partial least squares regression (PLSR) analysis of total sensory evaluation scores and physical–chemical parameters.
The rankings according to different factors used in the technique for order preference by a similarity to ideal (TOPSIS) approach.
| Rankings | Sensory and Physicochemical Parameters | Physical Parameters | Chemical Constituents | Sensory Profiles |
|---|---|---|---|---|
| 1 | S3 | S6 | S3 | S2 |
| 2 | S4 | S4 | S4 | S1 |
| 3 | S1 | S3 | S1 | S3 |
| 4 | S5 | S5 | S5 | S4 |
| 5 | S6 | S7 | S8 | S5 |
| 6 | S8 | S1 | S7 | S6 |
| 7 | S7 | S8 | S6 | S8 |
| 8 | S2 | S2 | S2 | S7 |
Final rankings by the TOPSIS approach.
| Rankings | Samples | D+ | D− | R |
|---|---|---|---|---|
| 1 | S3 | 0.28362 | 0.57927 | 0.67131 |
| 2 | S4 | 0.42034 | 0.33637 | 0.44451 |
| 3 | S1 | 0.47427 | 0.27501 | 0.36703 |
| 4 | S5 | 0.53332 | 0.26859 | 0.33493 |
| 5 | S6 | 0.57201 | 0.27990 | 0.32855 |
| 6 | S8 | 0.57241 | 0.23610 | 0.29202 |
| 7 | S7 | 0.56961 | 0.21190 | 0.27114 |
| 8 | S2 | 0.59041 | 0.21846 | 0.27008 |
The sources of Nü-Er-Cha.
| No. | Location | Batches Number | Date |
|---|---|---|---|
| S1 | Zhennanshan | 6 | 2015.05 |
| S2 | Zhennanshan | 6 | 2015.05 |
| S3 | yangjiaba | 6 | 2015.05 |
| S4 | yangjiaba | 6 | 2015.05 |
| S5 | Sizhuya | 6 | 2015.05 |
| S6 | Sizhuya | 6 | 2015.05 |
| S7 | Matongmiao | 6 | 2015.05 |
| S8 | Matongmiao | 6 | 2015.05 |