|Year : 2021 | Volume
| Issue : 4 | Page : 378-383
Quantitative determination of dexamethasone sodium phosphate in bulk and pharmaceuticals at suitable pH values using the spectrophotometric method
Mohammed Fanokh Al-Owaidi, Sura L Alkhafaji, Abdulbari Mahdi Mahood
Department of Pharmaceutical Chemistry, College of Pharmacy, University of Kerbala, Kerbala, Iraq
|Date of Submission||06-Mar-2021|
|Date of Decision||30-Jun-2021|
|Date of Acceptance||19-Jul-2021|
|Date of Web Publication||20-Oct-2021|
Dr. Sura L Alkhafaji
Department of Pharmaceutical Chemistry, College of Pharmacy, University of Kerbala, Hai Al-Muadhafeen Campus, 56001 Kerbala
Source of Support: None, Conflict of Interest: None
Dexamethasone sodium phosphate (DSP) is an ester of dexamethasone with anti-inflammatory action. This study provides new insights to develop a simple, precise, and accurate spectrophotometric method for the quantitative determination of DSP in bulk and pharmaceuticals. The method was validated before being applied to determine the DSP in six pharmaceutical injection forms from different companies. DSP is soluble in phosphate buffer, so it was used as a solvent, and a pH of 6 was found to be suitable for determination purposes. The DSP solution was scanned in the ultraviolet range (200–400 nm) using a double-beam spectrophotometer with a 1-cm quartz cell. The wavelength (λ max) of DSP was set at 242.5 nm, following the Beer–Lambert law for concentrations from 2 to 50 μg/ml. Dexa AIWA (Germany) showed the best results, being very close to the bulk value with no significant variation. Similarly, Dexamed (Cyprus) and HEMAZON (Syria) showed no significant differences from the bulk; however, the three remaining injections, DEXAKAL (India), DEXABRU (India), and DEXARON (China), showed significant variations from the bulk. Estimated limit of detection and limit of quantitation values for DSP were 0.83 and 2.5 μg/ml, respectively, with a regression coefficient of 0.999. Recovery studies were then used to determine the accuracy of the suggested method. The percentage of recovery was found to be 98.58%–102.52%. All results are suggesting a pivotal method for the routine analysis of DSP both in pure form and the commercially pharmaceutical forms.
Keywords: Dexamethasone sodium phosphate, phosphate buffer, ultraviolet spectrophotometry, validation
|How to cite this article:|
Al-Owaidi MF, Alkhafaji SL, Mahood AM. Quantitative determination of dexamethasone sodium phosphate in bulk and pharmaceuticals at suitable pH values using the spectrophotometric method. J Adv Pharm Technol Res 2021;12:378-83
|How to cite this URL:|
Al-Owaidi MF, Alkhafaji SL, Mahood AM. Quantitative determination of dexamethasone sodium phosphate in bulk and pharmaceuticals at suitable pH values using the spectrophotometric method. J Adv Pharm Technol Res [serial online] 2021 [cited 2021 Dec 9];12:378-83. Available from: https://www.japtr.org/text.asp?2021/12/4/378/328632
| Introduction|| |
Dexamethasone sodium phosphate (DSP) is an inorganic ester of dexamethasone that is used to treat inflammatory, allergy, endocrine, rheumatic, dermatologic, and others. It is also used in a majority of chemotherapy patients.
Chemically, DSP is a pregna-1,4-diene-3,20-dione, 9-fluoro-11,17-dihydroxy-16-methyl-21-(phosphonoooxy)-, disodium salt, (11 β, 16 α) with the chemical formula of C22H28FO8PNa2 [Figure 1]. DSP generally appears as a white-to-creamy white powder with a molecular weight of 516.41 g/mol. It is excessively hygroscopic, with a water solubility of 1.52 mg/ml, and its solutions have pH values between 7 and 8.5 with pKa of 1.89.
DSP penetrates the central nervous system and is metabolized in the liver, being mainly eliminated in the urine. Unbound dexamethasone crosses cell membranes and binds with a great affinity to specific cytoplasmic glucocorticoid receptors. The forming complex crosses the nuclear membrane and modulates the gene-mediated protein production. Dexamethasone's anti-inflammatory effects are assumed to be due to phospholipase A2 inhibitory proteins called lipocortins, which regulate the manufacture of potent inflammatory mediators such prostaglandins and leukotrienes.
Literature shows various methods have been developed to estimate DSP. These methods include spectrophotometry,, kinetic spectrophotometry, liquid chromatography,,, high-performance liquid chromatography (HPLC),, HPLC with mass spectrometry (HPLC/MS),, reversed-phase HPLC in combination with other drugs,, and electrochemical methods.
This study used a mixed-methods approach based on ICH guidelines for assessing DSP in the injection dosages and then to be checked afterward. The approach proposes a new methodology for assessing DSP uses well-known generic products to develop a cheap, sensitive, and effective method for the quantitative determination of DSP in pure and pharmaceutical in a suitable buffer as a solvent.
| Materials and Methods|| |
An ultraviolet (UV)-visible double-beam spectrophotometer UV-1800, with two 1-cm quartz cells (Shimadzu UV spectrophotometer, Japan), a pH meter (Hanna, Romania), pipettes of various volumes, and a digital electronic balance (Denver, Germany) were used in this study.
DSP (100% purity) was obtained from Samarra Drug Industry; this was used as a reference standard. Monosodium phosphate (NaH2PO4.2H2O) (99% purity) was provided by the Gainland Chemical Company, UK, while HiMedia Laboratories, India, provided disodium phosphate (Na2HPO4) and sodium hydroxide (NaOH) (each of 99% purity). The commercial dosage forms of DSP from six different companies were all injections of 8 mg/2 mL. These dosages were bought from the local market after checking both manufacturing and expire dates, and took the form Dexa AIWA® (T and D Pharma GmbH, Germany), DEXABRU (Brawn Laboratories Limited, India), DEXAKAL (Khandelwal Laboratories Pvt. Ltd., India), Dexamed (Medochemie Ltd., Limassol, Cyprus), DEXARON® (Shanghai Pharm. Co., Ltd., China), and HEMAZON (Ibn Hayyan Pharm., Syria).
Preparation of stock solutions
Dexamethasone sodium phosphate solution (100 μg/mL)
The working solution was prepared by taking 0.01 g of DSP and dissolving it in 10 ml of distilled water (DW); then, the solution was diluted with DW to 100 mL.
Sodium dihydrogen phosphate and disodium hydrogen phosphate solutions
A 7.8 g of sodium dihydrogen phosphate (NaH2PO4) and 7.10 g of Na2HPO4 were accurately weighed and transferred into a 250-ml separate graduated volumetric flask and solubilized in 50 and 100 ml of DW, respectively. The solutions were then made up with DW to achieve a solution of 0.2 M each of NaH2PO4 and Na2HPO4.
Preparation of buffer solutions
Buffers with various pH values (2, 3, 4, 6, 6.4, 7, and 8) were prepared using NaH2PO4 solution and Na2HPO4 solution in different proportions, as shown in [Table 1]; then, 0.1 M HCl and 0.1 M NaOH solution were used to adjust the pH of solutions and measured using the pH meter device.
Determination of dexamethasone spectrum
After dilution of standard drug solutions with different buffers, the solutions containing 40 μg/ml of DSP were scanned from 200 to 400 nm to select the maximum wavelength (λ max). The solution shows maximum absorption at 242.5 nm.
Selection of suitable pH
A 10 μg/ml standard solution of DSP was prepared using 1 mL of 100 μg/ml stock solution; this was then transferred into a series of 10-ml graduated volumetric flasks. Then, the volume was made up to 10 ml with one of the buffers; for each buffer value, two samples were prepared along with a control flask. The samples were scanned using the spectrophotometer to measure the absorbance of DSP at the λ max (242.5 nm). The highest absorbance appeared at pH 6, and this pH was selected for the preparation of the calibration curve. The data are summarized in [Table 2].
|Table 2: Absorbance of 10 μg/ml dexamethasone sodium phosphate at various pH levels|
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Procedure for sample preparation
Each injection solution (8mg/ mL) was transferred to 100 mL volumetric flask and diluted using a previously prepared buffer of pH 6; in each case, the flask was standardized by adding the buffer first. After that, for each product, three different concentrations of the drug (5, 10, and 15 μg/ml) were prepared to estimate absorbance accurately, with a control sample consisting of just the buffer solution at pH 6.
| Results and Discussion|| |
Selection of suitable pH
The highest and lowest levels of pH were determined based on their pKa values (1.8 and 6.4). Consequently, at lower pH (<3), DSP becomes uncharged, while when the pH increases, it takes on anionic forms as monoanionic and dianionic dexamethasone phosphate (DSP−, DSP − 2). This means the reaction is dependent on pH value. In terms of spectroscopy, this is reflected in the transfer of electrons between different energy levels, such as the move from the nonbonding orbital sigma (σ) to the sigma (σ*) antibonding orbital, which reverses higher pH values. This could explain the higher absorbance value at pH = 6 [Table 2].,
Selection of wavelength
With the reference solution, a UV spectroscopic scanning run between 200 and 400 nm that was performed to determine the optimal UV wavelength (maximum) for detection of DSP. Therefore, 242.5 nm was selected as the working wavelength for DSP, as shown in [Figure 2].
|Figure 2: Spectrum of dexamethasone sodium phosphate (40 μg/ml) at pH = 6|
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Linearity and calibration curve
The stock solution was diluted with a buffer (pH = 6) to make a series of DSP standard solution concentrations ranging from 2 to 50 μg/ml. Absorbances were determined. By plotting the absorbance versus concentrations, the calibration curve was constructed and regression equation was intended. Regarding the curve shown in [Figure 3], the linear equation was y = 0.025x + 0.0132 and the correlation coefficient (r2) was 0.9999 which is indicated a good linearity. The calibration data are shown in [Table 3].
Accuracy and precision
The accuracy of the method was represented by percent relative error (RE%) while the precision was represented by the relative standard deviation (RSD%). The accuracy (recovery) and the precision were thus estimated for a series of four replicates of three concentration levels of the standard solution (15, 30, and 45 μg/ml). The percentage of recovery, RE%, and RSD% were estimated for each sample. The mean RE% and the mean recovery were found to be 1.15% and 101.0%, respectively, while the mean RSD% was 1.024%. The results summarized in [Table 4] confirmed that the method used was accurate and precise.
Detection limit and quantification limit
Following ICH guidelines, limit of quantitation (LOQ) and limit of detection (LOD) were estimated as 3 SD/slope and 10 SD/slope, respectively, where SD is the standard deviation of the intercept. The LOD was 0.6371 μg/ml and the LOQ was 1.930 μg/ml in DSP for five replicate determinations. A summary of the validation parameters is shown in [Table 5].
|Table 5: Validation parameters for dexamethasone sodium phosphate using the proposed method|
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Determination of active dexamethasone sodium phosphate in injection dosage forms in the Iraqi market
The summarized analysis results, shown in [Table 6], indicated a high percentage of recovery with low RSD%, and indicated that the method is applicable for routine analysis of pharmaceutical forms.
|Table 6: Accuracy and precision of dexamethasone sodium phosphate determination in injections|
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Statistical analysis of the results of dexamethasone sodium phosphate commercial dosages
Statistical analysis using a t-test showed a set of significant differences between the products. Dexa AIWA offered the best results, being very close to the bulk with no significant variations. This was followed by Dexamed and HEMAZON, which also showed no significant differences in comparison with the bulk.
However, DEXA KAL and DEXABRU showed significant differences from the bulk. Thus, these forms showed a significant variation at the two-star level (**), which represents P < 0.01, suggesting that the drug content of these Indian brands was lower than that of the bulk, while DEXARON showed a very significant variation at the three-star (***) level, which represents P < 0.001, resulting in the injection's drug content differing from that of the bulk chemical.
Comparing the company products with each of the others shows that DEXA KAL and DEXARON are closely matched, with no significant differences between them. In the similar manner, there are no significant differences and approximately equivalent drug content among the following products: DEXAKAL and HEMAZON; DEXAKAL and DEXABRU; DEXARON and Dexamed; DEXARON and; Dexa AIWA and Dexamed; Dexa AIWA and; Dexamed and HEMAZON; and HEMAZON and DEXABRU. However, significant differences could observe between other companies products' such as between DEXA KAL and Dexa AIWA, where a comparison generates a one star (*) significant, representing P < 0.05, which indicates the differences in the drug content of the injections produced by these companies. Similar differences can also be seen between DEXA KAL and Dexamed; DEXARON and DEXA; DEXARON and DEXABRU; Dexa AIWA and DEXABRU; and Dexamed and DEXABRU (India). All result data are reported in [Table 7] and [Figure 4].
|Figure 4: Relative content of dexamethasone sodium phosphate in comparison to the bulk|
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| Conclusion|| |
The findings of this study show that the UV approach can be utilized for routine analysis of DSP in bulk formulations, as well as for the analysis of marketing injections. It is ideal for the intended application, especially in forensic science laboratories and other pharmaceutical analysis laboratories. By comparing a series of the pharmaceutical preparations from different companies with the bulk, Dexa AIWA® (Germany), Dexamed (Cyprus), and HEMAZON (Syria) were found to be close to the bulk, offering reliable drug content levels. However, DEXAKAL (India), DEXABRU (India), and DEXARON® (China) were found to have significant differences in terms of variation in drug content as compared with the bulk.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7]