|ORIGINAL RESEARCH ARTICLE
|Year : 2017 | Volume
| Issue : 2 | Page : 94-100
Simultaneous determination of rutin, isoquercetin, and quercetin flavonoids in Nelumbo nucifera by high-performance liquid chromatography method
P Naveen1, HB Lingaraju2, Anitha1, K Shyam Prasad2
1 Analytical Research and Development, Vidya Herbs Pvt. Ltd, Bengaluru, Karnataka, India
2 Phytochemistry Lab, Vidya Herbs Pvt., Ltd., Bengaluru, Karnataka, India
|Date of Web Publication||24-Jul-2017|
Analytical Research and Development, R and D Centre for Excellence, Vidya Herbs Pvt. Ltd., 14 A, 1st Phase, KIADB Industrial Area, Jigani, Anekal Taluk, Bengaluru - 560 105, Karnataka
Source of Support: None, Conflict of Interest: None
Objective: The present study was investigated to provide a documentary evidence for the determination of rutin, isoquercetin, and quercetin flavonoids from the flora of Nelumbo nucifera by reversed-phase high-performance liquid chromatography (RP-HPLC).
Materials and Methods: RP-HPLC analysis was performed by gradient elution with a low-pressure gradient using 0.5% acetic acid: acetonitrile as a mobile phase with a flow rate of 1.0 ml/min. The separation was done at 26°C using a Kinetex XB-C18 column as stationary phase and the detection wavelength at 356 nm. The proposed method was validated as per International Conference on Harmonisation guidelines with respect to specificity, linearity, precision, accuracy, limit of detection (LOD), and limit of quantification (LOQ).
Results: The validated results were within the acceptable limits. In specificity, the retention time of rutin, isoquercetin, and quercetin peak in the sample was matched with the reference standard peak and showed good resolution. An excellent linearity was obtained with correlation coefficient (r) higher than 0.999. In precision, the repeatability and intermediate showed <1.0% of % relative standard deviation of peak area percentage indicating high precision and accurate. The recovery rate for rutin, isoquercetin, and quercetin was between 99.85%–101.37%, 101.90%–103.24%, and 101.74%–106.73%, respectively. The lower LOD and LOQ of rutin, isoquercetin, and quercetin enable the detection and quantitation of these flavonoids in N. nucifera at low concentrations.
Conclusion: The developed analytical method is convenient for the determination of flavonoids content in herbal drugs.
Keywords: International Conference on Harmonisation, linearity, precision, recovery, limit of detection, limit of quantification
|How to cite this article:|
Naveen P, Lingaraju H B, Anitha, Prasad K S. Simultaneous determination of rutin, isoquercetin, and quercetin flavonoids in Nelumbo nucifera by high-performance liquid chromatography method. Int J Pharma Investig 2017;7:94-100
|How to cite this URL:|
Naveen P, Lingaraju H B, Anitha, Prasad K S. Simultaneous determination of rutin, isoquercetin, and quercetin flavonoids in Nelumbo nucifera by high-performance liquid chromatography method. Int J Pharma Investig [serial online] 2017 [cited 2017 Nov 23];7:94-100. Available from: http://www.jpionline.org/text.asp?2017/7/2/94/211473
| Introduction|| |
Herbal drugs have become the main subject of attention and global importance since a decade and are used for exploring botanical materials as medicines, where standardization and quality control with proper integration of modern scientific techniques and traditional knowledge is important. Flavonoids are the secondary metabolites derived from plants having antioxidant and free radical scavenging properties. Flavonoids play an important role in plants for normal growth, development, defense against infection, and injury.
Nelumbo nucifera is a perennial aquatic plant belonging to family Nelumbonaceae. It is commonly known as Indian lotus, which is distributed throughout Asia. Leaves, seeds, flower, and rhizome of N. nucifera are good source of nutritional and medicinal values. The main active phytoconstituents present in the N. nucifera contain flavonoids, alkaloids, steroids, triterpenoids, tannins, glycosides, and polyphenols.
N. nucifera has been reported for antioxidant, anticancer, antiviral, anti-obesity, lipolytic, hepatoprotective, antidiabetic,, antidiarrheal, antifungal, antibacterial, anti-ischemia, anti-inflammatory, and diuretic activities.
| Materials and Methods|| |
Rutin, quercetin, and isoquercetin were used as calibration standards. Rutin (94%) and isoquercetin (90%) were obtained from Sigma-Aldrich (India) and quercetin (99%) was obtained from S.D Fine-Chem Ltd. All reagents and solvents were analytical and high-performance liquid chromatography (HPLC) grade. The powdered floral material of N. nucifera was procured from Ess Kay Herbs, Lucknow, Uttar Pradesh, India.
Preparation of the extract
Lotus flower extract (LFE) of N. nucifera was prepared by Soxhlet extraction of 100 g of powdered floral material using 70% ethanol at 80°C for about 5 h in successive batches. The first batch was extracted by adding 500 ml solvent for about 3 h, and further two successive extractions were done by adding 300 ml/batch for 1 h. After completion of extraction, the cooled liquid was concentrated by evaporating its liquid contents in rotary evaporator to remove the solvent residue to nil, with an approximate yield of 2%. The extract powder was used for further experiments.
Instrumentation and chromatographic conditions
HPLC was performed on a Shimadzu LC-2030 C Prominence-i (Japan) system equipped with a quaternary low-pressure gradient solvent delivery LC-2030 pump with a high-pressure switching valves, online LC-2030 degasser unit, a high-sensitivity LC-2030 ultraviolet (UV) detector, high-speed drive LC-2030 autosampler with a 100 μl loop and it accommodates 216 samples at a time with direct access rack system and large-capacity column oven. The system controlled and data analyzed by laboratory solution system software. A gradient elution was carried out in Kinetex XB-C18 column (100 A°, 100 mm × 4.6 mm, 2.6 μm pore size). The mobile phase consists of two different solutions 0.5% acetic acid and acetonitrile which act as solution A and solution B. All solutions were degassed and filtered through 0.45 μm pore size filter. The gradient elution initial conditions were 18% of eluent B with linear gradient to 18.5% from 0.01 to 7 min, followed by linear gradient to 35% of eluent B at 9 min and this proportion being maintained for 2 min. The mobile phase composition returned to the initial condition at 10 min and allowed to run for another 5 min before the injection of another sample. The total runtime of each sample is 15 min. The flow rate was 1.0 ml/min and the sample injection volume was 5 μl. The column was maintained at 26°C throughout analysis and the UV detector was set at 356 nm. Seventy percentage methanol used as a diluent for assay by HPLC analysis and the total LC runtime was 15 min. The instrument was calibrated and qualified before the analysis. Using these chromatographic conditions, it was possible to confirm the retention time (RT) of rutin, isoquercetin, and quercetin by injection of corresponding standards separately.
Preparation of standard solution
Accurately weighed appropriate amounts of rutin, isoquercetin, and quercetin reference standards were dissolved in 70% methanol in a 25 ml volumetric flask to obtain a stock solution. The concentration of rutin, isoquercetin, and quercetin in the solution was 220, 80, and 220 ppm, respectively. Working standard solutions were obtained by diluting the 2.0 ml standard stock solution to 10 ml volumetric flask and made up with 70% methanol to get a final concentration of 44, 16, and 44 ppm for rutin, isoquercetin, and quercetin.
Preparation of sample solution
The dried LFE was prepared in 70% methanol to achieve the final concentration of 400 ppm. Before analysis, the solutions were filtered through 0.20 μm nylon membrane filters.
Preparation of spiked sample solution
Three different volumes (1, 2, 3 ml) of standard stock solution were added to the sample solution (400 ppm) separately. The standard stock solution was spiked into the samples to determine recovery. Before analysis, the solutions were filtered through 0.20 μm nylon membrane filters.
Validation of the method
The validation of the developed method was done according to the International Conference on Harmonisation (ICH) guidelines. The method is validated for specificity, linearity, repeatability, precision, accuracy, limit of detection (LOD), limit of quantification (LOQ), and robustness.
Specificity is the ability of a method to discriminate between the study analytes and other components in the sample. In this study, the specificity was demonstrated by running a procedure blank, standard, and sample. The chromatographic parameters such as column efficiency and peak symmetry were done according to the ICH guidelines.
Linearity was determined by different known concentrations of rutin, isoquercetin, and quercetin standard solution in triplicate by diluting the standard stock solution. The standard solutions were injected and the peak area was measured. The concentration of 44, 16, and 44 ppm for rutin, isoquercetin, and quercetin standards in the solution was considered to be 100%. Calibration curve of 50%, 75%, 100%, 125%, and 150% was constructed for rutin, isoquercetin, and quercetin by plotting peak areas against concentration and linear regression equations. The correlation coefficient was also computed.
Precision is a measure of the reproducibility of the whole analytical method. Precision was determined by studying the repeatability and intermediate precision. The repeatability was determined at a minimum of three different concentrations (75%, 100%, and 125%) of rutin, isoquercetin, and quercetin standards per six replicates. According to ICH Guidelines the intermediate precision variations have to be studied for different analysts only. The precision was expressed as percentage relative standard deviation (% RSD).
Accuracy is a measure of closeness of test results obtained by a method to the true value. The accuracy of the method was tested by performing the recovery studies at three different levels of standard stock solution added to the samples. The standard stock solution was spiked into the samples to determine recovery. Three different volumes (1, 2, 3 ml) of standard stock solution were added to the sample solution (400 ppm). Triplicate injections were made with all the spiked samples.
% of recovery = (b − a)/c × 100
Where, “a” is the amount of drug found in the sample before addition of standard drug.
“b” is the amount of drug found after addition of standard drug.
“c” is the amount of standard drug added.
Limit of detection and limit of quantification
Detection limit of an individual analytical procedure is the lowest amount of analyte in a sample which can be detected but not necessarily quantitated under the stated experimental conditions. Quantitation limit of an individual analytical procedure is the lowest amount of analyte in a sample which can be quantitatively determined with accuracy. LOD and LOQ were determined based on the signal-to-noise ratio response. For LOD, it should not be not <3. For LOQ, it should not be not <10.
Results were expressed as mean ± SD and % RSD. The data were submitted to statistical analysis using excel software.
| Results|| |
Specificity was determined by comparing the chromatogram obtained from blank, standard, and sample solutions are summarized in [Figure 1]. Good separation between the peaks of rutin, isoquercetin, and quercetin was achieved. The RT of rutin, isoquercetin, and quercetin reference standards and sample (LFE) peak were found to be at 3.748, 4.557, 11.465 and 3.756, 4.562, 11.496, respectively.
|Figure 1: High-performance liquid chromatograms of blank, standard and sample. The retention time of rutin, isoquercetin and quercetin reference standard and sample (LFE) peak were found to be at 3.748, 4.557, 11.465 and 3.756, 4.562, 11.496 respectively|
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Linearity was evaluated by the peak area against concentration of rutin, isoquercetin, and quercetin standards which is summarized in [Figure 2]. The calibration plots were linear in the range 50%, 75%, 100%, 125%, and 150%, and the correlation coefficient (r) of all the three rutin, isoquercetin, and quercetin compounds is 0.999.
|Figure 2: Calibration curve for (a) Rutin, (b) Isoquercetin, and (c) Quercetin, by plotting peak area against concentration and linear regression equation|
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Precision was evaluated on the basis of the % RSD value. The data pertaining to repeatability (intra) and intermediate (inter-day) precision was summarized in the [Table 1]. In repeatability, the % RSD of peak area at three different levels (75%, 100%, and 125%) of rutin was found to be 0.053%, 0.121%, and 0.140%, isoquercetin: 0.048%, 0.084%, and 0.121%, and quercetin: 0.019%, 0.091%, and 0.110%, respectively. In intermediate precision, the % RSD of peak area at three different levels (75%, 100%, and 125%) of rutin was found to be 0.090%, 0.081%, and 0.122%, isoquercetin: 0.098%, 0.176%, and 0.157%, and quercetin: 0.082%, 0.098%, and 0.113%, respectively.
|Table 1: Repeatability (intra) and intermediate (inter-day) precision study for the developed method for rutin, isoquercetin, and quercetin|
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The recovery of the compounds rutin, isoquercetin, and quercetin was determined by spiking the LFE with known amounts of standard stock solution. Recovery of each substance was obtained from the calculated amount found and original amount. The results are presented in [Table 2]. The average percent recoveries at three different levels (50%, 100%, and 150% spiked sample) of rutin were found to be 100.71%, 101.37%, and 99.85%, isoquercetin: 102.91%, 103.24%, and 101.90%, and quercetin: 106.73%, 104.03%, and 101.74%, respectively. The average % RSD at three different levels (50%, 100%, and 150% spiked sample) of rutin was found to be 0.08%, 0.08%, and 0.06%, isoquercetin: 0.15%, 0.01%, and 0.01%, and quercetin: 0.21%, 0.13%, and 0.04%, respectively.
|Table 2: Recovery study for the developed method for rutin, isoquercetin, and quercetin|
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Limit of detection and limit of quantification
LOD at signal-to-noise ratio (3:1) with the smallest concentration of rutin, isoquercetin, and quercetin standard that gives a measurable response was found to be 0.38, 0.97, and 0.21 ppm, respectively. The LOQs at signal-to-noise ratio (10:1) of rutin, isoquercetin, and quercetin were found to be 1.26, 2.94, and 0.60 ppm, respectively.
| Discussion|| |
Standardization of herbal medicines is fraught with many challenges. In the present study, we have developed a simple, optimized, and validated HPLC method for the standardization of N. nucifera. Flavonoids are the active antioxidant components in the flora of N. nucifera. Flavonoids belong to a group of natural substances with variable phenolic structure and are found in the fruits, vegetables, grains, bark roots, stem, flowers, tea, and wine. N. nucifera which contains biologically effective flavonoids including rutin, quercetin, and isoquercetin exhibits pharmacological activities. Rutin is a phenolic compound with glycosidic linkage. Isoquercetin is a flavonoid, a type of chemical compound. It is the 3-O-glucoside of quercetin. It is comparatively much more bioavailable than quercetin aglycone, the commonly available form as a supplement. Quercetin is a major representative of the flavonol subclass. It is an aglycone, meaning that it lacks a glycoside side chain. The rutin, isoquercetin, and quercetin flavonoids were selected for quantification, and these are responsible for physiological action of the plant.
Validation of analytical procedure is the process of demonstrating that analytical procedure is suitable for their intended use and that they support the identity, strength, quality, purity, and potency of the drug substances and drug products. Results obtained from method validation can be used to judge the quality, reliability, and consistently of results.
A novel HPLC method for quantitative determination of three flavonoids: rutin, isoquercetin, and quercetin from floral part of N. nucifera was developed and validated. In HPLC method, the optimization of the mobile phase and stationary phases giving that rutin, isoquercetin, and quercetin peaks simultaneously detected using the gradient elution method. The mobile phase was chosen after several trials with 0.5% acetic acid and acetonitrile in various proportions giving the satisfactory resolution and the shortest analysis time.
Specificity of an analytical method is its ability to measure accurately an analyte in the presence of interference in the sample matrix. The RT of the standard and sample peak was same so that the method was specific. The chromatographic peaks of rutin, isoquercetin, and quercetin were well separated at different RT with the good resolution of 4.47 and 41.64 for rutin-isoquercetin and isoquercetin-quercetin, respectively. The theoretical plates (United States Pharmacopeia) 7571 for rutin, 9233 for isoquercetin, and 104102 for quercetin were observed. The tailing factor was found to be 1.24, 1.22, and 1.39 for rutin, isoquercetin, and quercetin, respectively, which indicated column efficiency is satisfactory.
Linearity of an analytical procedure is the ability for showing the response of the analyte which is proportional to the analytical concentration within a given range. The R2 values for rutin, isoquercetin, and quercetin were >0.990. This indicates that the good fitting of the curve and method is good linearity corresponds to peak area on concentrations. The minimum acceptable correlation coefficient is 0.990.,
The precision of an analytical procedure expresses the closeness of agreement between a series of measurements obtained from multiple sampling of the same homogeneous sample under the prescribed condition. Repeatability expresses the precision under the same operating conditions over a short interval of time. Intermediate precision is the same procedure performed by a second operator within the laboratory. The repeatability and intermediate precisions of the % RSD of peak area at three different levels (75%, 100%, and 125%) of rutin, isoquercetin, and quercetin were found to be <1.0%, which shows high precision of the method.
The accuracy to be assessed using a minimum of nine determinations over a minimum of three concentration levels covering the specified range. The recovery rate for rutin, isoquercetin, and quercetin was between 99.85%–101.37%, 101.90%–103.24%, and 101.74%–106.73%, respectively. The low percentage relative SD value (%RSD <1) shows the high accuracy of the method. Therefore, this HPLC method can be regarded as selective.
Limit of detection and limit of quantification
The low LOD and LOQ values indicate that the method provides adequate sensitivity.
| Conclusion|| |
Here, we have developed and validated the new reversed-phase-HPLC method which is simple, rapid, and reliable and is recommended for routine quality control analysis of rutin, isoquercetin, and quercetin from the flora of N. nucifera. Therefore, the method was proved to be suitable for flavonoids determination in various alcoholic extracts of N. nucifera. Further investigations are required to standardization of individual phytoconstituents of N. nucifera.
The authors are grateful to the all members of analytical research and development at Vidya Herbs Pvt Ltd., Bangalore, for their cooperation and technical help.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]
[Table 1], [Table 2]