Development and Validation of UV-visible Spectrophotometry Method for Simultaneous Estimation of Rutin and Curcumin in Bulk Pharmaceuticals

Rutin is a flavanol that is widely distributed in plants, including apples, buckwheat, tea and passion flowers. Its chemical name is 3,3’,4’,5,7-pentahydroxyflavone-3-rhamnoglucoside, illustrated in Figure 1, possesses a molecular formula of C₂₇H₃₀O₁₆ and a molecular mass of 610.5 g/mol. It’s a glycoside made up of the flavonoid aglycone quercetin and the disaccharide rutinose, which has pharmacological activities such as anticancer, antidiabetic, antimicrobial, etc.¹ The effectiveness of Rutin in treating chronic venous insufficiency has been studied in patients in combination with other herbal active moieties. Rutin, classified as a bioflavonoid, enhances collagen synthesis, leading to decreased vascular permeability and enhancement of vascular endothelial barrier function. Prolonged administration of high doses of flavonoid glycosides such as rutoside and rutin found in citrus fruits has led to clinical improvements and, in certain instances, resolution of symptoms.² Curcumin, a hydrophobic aromatic phytoextract, was initially extracted from the aromatic rhizome of the Indian plant turmeric (Curcuma longa L.), which is a member of the ginger family (Zingiberaceae). Chemically identified as (1E, 6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)- 1,6-heptadiene-3,5-dione, as depicted in Figure 2, it possesses a molecular formula of C₂₁H₂₀O₆ and a molecular weight of 368.4 g/mol. Its pharmacological activities include antioxidant, anti-inflammatory, anti-cancer, anti-diabetic and antiviral properties.³ The healing process in stasis dermatitis is impacted by the overexpression of Matrix Metalloproteinases (MMPs), which are involved in tissue repair and cause hyperpigmentation.^4,5 Curcumin inhibits MMP expression and downregulates NF-kappa B, which speeds up healing and prevents hyperpigmentation.⁶ The skin conditions brought on by stasis dermatitis are not currently treatable. This necessitates the creation of a suitable formulation containing rutin and curcumin for the topical treatment of stasis dermatitis.

Figure 1:
Molecular structure of Rutin.⁶

Figure 2:
Molecular structure of Curcumin.⁷

Currently, there is limited available data on the simultaneous estimation of Rutin and Curcumin using the UV method development and validation parameters. Therefore, this study aimed to establish and validate a straightforward, accurate and highly sensitive UV-spectroscopy technique for the simultaneous estimation of Rutin and Curcumin in bulk and pharamaceutical formulations.

Rutin was procured from Fine-Chem Ltd., located in Uran Islampur, Maharashtra, while Curcumin was acquired from the storage facility of KLE College of Pharmacy in Belagavi.

The analytical quality chemicals and reagents used in the experiment were procured from the storehouse of KLE College of Pharmacy, Belagavi. HPLC-grade methanol was employed.

The UV-Spectrophotometers Shimadzu UV-1900 with Lab Solutions software and Shimadzu UV-1800 with UV probe were utilized for simultaneous estimation of Rutin and Curcumin.

Different solvents were tested for the solubility of both samples, like methanol, water, acetonitrile, 0.1N HCl and 1N NaOH, out of which methanol showed better solubility and was selected as the solvent. Both samples were scanned with a UV spectrophotometer in the range of 800-200 nm, with methanol serving as the solvent. Rutin exhibited maximum absorption at 257 nm, while Curcumin showed its peak absorption at 422 nm.

Rutin (10 mg) was carefully weighed and then added to a volumetric flask (10 mL). In a similar way, a separate 10 mL volumetric flask was filled with 10 mg of Curcumin, which was precisely weighed. Methanol was used to adjust the volume in both flasks to the appropriate level, resulting in a concentration of 1000 μg/mL for each, which formed the primary stock solutions. 1 mL of Rutin and 1 mL of Curcumin were individually drawn into 10 mL volumetric flasks from the above-mentioned primary stock solution and adjusted to the mark with methanol. This process resulted in the formation of a secondary stock solution with a concentration of 100 μg/mL for each drug.

The UV-Spectrophotometric method for Rutin and Curcumin was developed and validated following the ICH guidelines to evaluate parameters such as linearity, specificity and selectivity, precision, ruggedness, stability, LOD and LOQ.^7,8

The UV spectra of the rutin and curcumin solution and the blank methanol solvent were scanned from 800 nm to 200 nm in wavelength. This was done to check for solvent-induced interference at the wavelength at which each analyte has its greatest absorbance.

Linearity ranges of 4-20 μg/mL for Rutin and 1-5 μg/mL for Curcumin were tested in triplicate using the stock solution and measuring absorbance at 257 nm and 422 nm. Using absorbance versus concentration, the calibration curve was plotted and a linear regression equation was generated.

Precision was performed:

From the above-mentioned stock solution, six replicates of concentrations of 12 μg/mL and 3 μg/mL of rutin and curcumin, respectively, were prepared, analyzed and the percentage RSD was computed.

On the same day, the concentrations of 1, 3 and 5 μg/mL of Curcumin and 4, 12 and 20 μg/mL of Rutin in triplicate were made from the above-mentioned stock solutions, analyzed and the percentage RSD was computed at various intervals.

On three consecutive days, the concentrations of 1, 3 and 5 μg/ mL of Curcumin and 4, 12 and 20 μg/mL of Rutin in triplicate were made from the above-mentioned stock solutions, analyzed and the percentage RSD was computed.

Ruggedness was achieved by altering both the instrument and the analyst. The concentrations of 4, 12 and 20 μg/mL of Rutin and 1, 3 and 5 μg/mL of Curcumin in triplicate of each were prepared from the above stock solutions and measured absorption at 257 nm and 422 nm, respectively and measured by different analysts and with a different instrument (UV Spectrophotometer: UV-1800), the same concentration as previously mentioned was measured, examined and the percentage RSD was computed.

Robustness parameter was achieved by a change in the wavelength. The concentrations of 4, 12 and 20 μg/mL of Rutin and 1, 3 and 5 μg/mL of Curcumin in triplicate of each were prepared from the above stock solutions and measured absorption at 255 nm, 259 nm of Rutin and 420 nm, 424 nm of Curcumin and analyzed and %RSD was computed.

The stability of the solvent and standard stock solution was demonstrated by making a fresh stock solution. Analyses were carried out on dilutions of 2, 6 and 10 μg/mL containing both analytes after a fresh stock solution was prepared. The absorbance was computed as a percentage of RSD and compared to that of the old stock dilutions.

The linear curve was used to calculate the Limit of Detection (LOD) and Limit of Quantification (LOQ) by statistical methods utilizing the following formulas.^9–12

The maximum absorption of Rutin and Curcumin showed λ_max at 257 nm and 422 nm and the spectra of both drugs are illustrated in Figures 3 and 4 and overlay spectra of different linearity ranges are shown in Figure 5.

Figure 3:
UV-spectrum of Rutin.

Figure 4:
UV-spectrum of Curcumin.

Figure 5:
Overlay Spectra.

In order to carry out simultaneous estimation, a single solvent must dissolve both analytes. For this approach, analytical-grade methanol was chosen as the solvent since both of the analytes, Rutin and Curcumin, are fully soluble in it. Method development parameters are illustrated in Table 1.

The solvent methanol was scanned and the UV spectra showed the absence of any solvent interference, as shown in Figure 6.

Figure 6:
UV-spectrum of solvent (Methanol).

Linearity response for Rutin and Curcumin solutions were obtained by analyzing 4-20 μg/mL and 1-5 μg/mL in triplicate and a graph was plotted of drug concentration against absorbance, which resulted in a regression coefficient of 0.9991 for both drugs. The linearity data are shown in Table 2. The standard calibration curves of Rutin and Curcumin are displayed in Figures 7 and 8, respectively.

Figure 7:
Standard calibration curve of Rutin.

Figure 8:
Standard calibration curve of Curcumin.

Rutin has a Limit of Detection (LOD) of 0.59 μg/mL and a Limit of Quantification (LOQ) of 1.81 μg/mL. Similarly, the LOD and LOQ of Curcumin were computed and found to be 0.15 μg/mL and 0.45 μg/mL.

The approach resulted to be precise as the %RSD for both the analytes was calculated for each level, namely system precision, intraday precision and interday precision and % RSD was calculated from the absorbance and found to be less than 2%. The precision data are illustrated in Tables 3, 4 and 5.

The ruggedness parameter was carried on both the analytes by changing the analyst and the instrument and %RSD was found to be less than 2%. Table 6 illustrates the ruggedness statistics.

The robustness parameter was carried out by a change in the wavelength for both analytes and %RSD was calculated and found to be less than 2%, hence the method was found to be robust. The robustness data is illustrated in Table 7.

After analyses of the fresh stock solution and the old standard stock solution for ten days, the %RSD for both analytes were determined to be less than 2%, indicating that the solvent and the standard stock solution were stable. The solution stability data are illustrated in Tables 8 and 9.

The development and validation of a UV method for the simultaneous estimation of Rutin and Curcumin present a significant advancement in analytical chemistry. UV spectroscopy offers a cost-effective and widely accessible technique for quantifying compounds with distinct absorbance profiles, such as rutin and curcumin. The selection of appropriate wavelengths, 257 nm for rutin and 422 nm for curcumin, reflects careful consideration of their absorption maxima, ensuring optimal sensitivity and specificity for their quantification. The linearity assessment across the concentration ranges of 4-20 μg/mL for rutin and 1-5 μg/mL for curcumin demonstrates the method’s capability to accurately measure a wide range of analyte concentrations. The resulting linear regression equations indicate a strong correlation between concentration and absorbance, highlighting the method’s reliability. Furthermore, the evaluation of precision through %RSD calculations underscores the method’s reproducibility, essential for robust analytical procedures. This UV method’s sensitivity, reflected in low detection and quantification limits, signifies its potential for detecting trace levels of rutin and curcumin in complex matrices. Overall, the developed UV method stands as a valuable industry for pharmaceutica industries, facilitating quality control and formulation studies with enhanced efficiency.

In the context of simultaneous estimation of Rutin and Curcumin, UV spectroscopy might be preferred for its quantitative accuracy and sensitivity, especially if the compounds have distinct UV absorbance spectra. However, Raman spectroscopy could offer advantages in terms of chemical specificity and non-destructive analysis, which might be beneficial if there are potential interferences or if detailed structural information is required. It is worth noting that fluorescence spectroscopy also offers its own set of advantages, such as high sensitivity to trace amounts of analytes and the ability to provide additional structural and dynamic information about molecules. Ultimately, the choice between these techniques would depend on factors such as the specific requirements of the analysis, the nature of the samples and the instrumentation available.¹³

An approach for simultaneously determining Rutin and Curcumin was developed and validated in accordance with the ICH guidelines. The statistical analysis results showed the current method for simultaneous quantification of Rutin and Curcumin in bulk and pharmaceutical formation to be simple, specific, selective, linear, precise, robust and reproducible.

The authors thank Principal Dr. S. S. Jalalpure and Vice Principal Dr. M. B. Patil for their support and guidance. We appreciate Mr. Sarvesh Patil, M. Pharm, KLE College of Pharmacy, Belagavi, for assisting us with the simultaneous estimation and technique development. We are also appreciative to the KLE College of Pharmacy in Belagavi for providing the essential facilities to conduct the research.