Micellar Electrokinetic Capillary Chromatography Method Research Articles

Analysis of doxorubicin and fullerenol in rat serum by micellar electrokinetic capillary chromatography.

A new micellar electrokinetic capillary chromatographic (MEKC) method has been developed and optimized for simultaneous quantitation of doxorubicin (Dox) and fullerenol (Frl) in rat serum. The separation was carried out in a capillary (48.5-40 cm to the detector - 50 µm id fused-silica capillary with bubble cell, 150 µm) at an applied voltage of 25 kV and temperature of 25 °C. For the background electrolyte 10 mmol L- 1 borate buffer pH 9.3 plus 15 mmol L-1 phosphate buffer pH 7.0 (with the final pH of the mixture adjusted to 7.0 with HCl), with added 10 % (V/V) methanol, and 15 mmol L-1 sodium dodecyl sulfate as a surfactant, were used. The hydrodynamic injection was carried out at 5.0 kPa during the period of 100 s. Linear calibration curves were established over the concentration range 0.5-500.0 mg L- 1 for Dox and 10.0-500.0 mg L- 1 for Frl (at 234 nm). The proposed MEKC procedure was fully validated and applied for the deter mination of Dox and Frl in Wistar rats after intra pe ritoneal administration of both molecules.

Development of a sustainable multianalyte MEKC method for quantitation of the antihyperlipidemic drugs ezetimibe together with three statins. Greenness and whiteness appraisal studies

Implementing powerful and sustainable research that complies with green analytical chemistry (GAC) and white analytical chemistry (WAC) fundamentals can downsize the environmental compliance costs and fruitfully affects practical and economic issues. Within this framework, rapid and white analytical micellar electrokinetic capillary chromatography (MEKC) methodology was developed for the synchronized estimation of the antihyperlipidemic drugs Ezetimibe (EZE), Atorvastatin (ATO), Rosuvastatin (ROS) and Simvastatin (SIM). The technique was established using fused silica capillary (50 cm, 50 µm id) and the background electrolyte was 0.025 M borate buffer pH 9.2 containing 0.025 M sodium dodecyl sulfate (SDS) and 10% v/v acetonitrile as the organic modifier. Diode array detector was adjusted at 243 nm for ATO and ROS and 237 nm for EZE and SIM. Separation was accomplished within 10 min with migration times of 4.12, 5.42, 8.23 and 8.74 min for ROS, ATO, EZE and SIM respectively. The 4 drugs were quantitated in the concentration range of 10–100 μg/mL and the correlation coefficients were not less than 0.9993. The high sensitivity was illustrated by values of the detection and quantitation limits. The limits of detection for ROS, ATO, EZE and SIM were 0.52, 0.75, 0.42 and 0.64 μg/mL, respectively, whereas, the limits of quantitation values were 1.73, 2.50, 1.40 and 2.13 μg/mL for the studied drugs, respectively. In addition to validation, as reported by the ICH guidelines, greenness and whiteness assessment using the novel AGREE calculator and the holistic functionality model RGB12 were performed. The results proved the efficiency and whiteness of the suggested technique to be routinely implemented in quality control laboratories for the assay of the four drugs and the binary mixtures of EZE with either ATO, ROS or SIM in fixed-dose combined tablets.

Validated green micellar electrokinetic capillary chromatography for simultaneous determination of simvastatin and sitagliptin phosphate binary mixture in pharmaceutical formulation

AbstractDiabetics are liable to fatal atherosclerotic cardiovascular diseases. It is clinically attributed to their imbalanced plasma lipoproteins. Fixed‐dose combination “polypill” of simvastatin (10 mg) and sitagliptin phosphate (100 mg) is mainly indicated for the treatment of diabetic dyslipidemia. Novel green micellar electrokinetic capillary chromatographic method has been developed for simultaneous determination of simvastatin and sitagliptin phosphate in binary synthetic mixtures and their pharmaceutical formulation. Separation was achieved using a deactivated fused silica capillary (50 cm effective length × 50 μm id) through a background running electrolyte of 100 mM borate buffer (pH 9.1) and 100 mM sodium dodecyl sulfate. Diode array detection was set at 238 and 210 nm for simvastatin and sitagliptin phosphate, respectively. All experimental parameters were closely varied and optimized. Both drugs declared good linearities over the range of 10–100 μg/mL. Proposed study was validated according to International Council for Harmonization guidelines. It was applied to the assay of laboratory‐made binary mixtures and marketed tablets. Electrophoretic assay was compared with a reported spectrophotometric one. Satisfactory t‐test and F‐ratio indicated insignificant differences between both methods. Moreover, it is the first capillary electrophoretic simultaneous assay for simvastatin and sitagliptin phosphate, and fits a linear correlation with the green analytical attributes.

Development and comprehensive greenness assessment for MEKC and HPTLC methods for simultaneous estimation of sertaconazole with two co-formulated preservatives in pharmaceutical dosage forms

Four greenness assessment tools: National Environmental Methods Index (NEMI), Ecoscale Assessment (ESA), Green Analytical Procedure Index (GAPI) and the most recent Analytical GREEness metric (AGREE) were tested to evaluate two proposed MEKC and HPTLC methods for the simultaneous determination of the antifungal drug sertaconazole (SER) and two co-formulated preservatives methyl paraben (MEP) and sorbic acid (SOR). Method I was micellar electrokinetic capillary chromatography (MEKC). Electrophoretic conditions were optimized to improve separation, sensitivity, and rapidity. The proposed method used a fused silica capillary (50 cm × 50 μm id), and the background electrolyte was 50 mM acetate buffer pH 4.6 containing 15 mM SDS with 17 s injection time. The applied voltage was 30 kV. The diode array detector (DAD) was set at 210 nm for measurement of SER and 254 nm for both MEP and SOR. The Three compounds were resolved in less than 6 min with migration times 3.07, 4.29, and 5.97 min for SER, MEP, and SOR respectively. The described method was linear over the range of 5–100 μg/mL for SER, MEP and SOR with correlation coefficients >0.9995. For method II: high-performance thin-layer chromatography (HPTLC) analysis was carried out on aluminum-backed sheet of silica gel using chloroform-ethyl acetate (3:7) as mobile phase. Retardation factors were 0.20, 0.71, and 0.88 for SER, MEP, and SOR respectively. Quantification was achieved with UV densitometry at 210 nm for SER and 254 nm for MEP and SOR. The linearity ranges were 0.1–1 μg/spot for the three drugs with correlation coefficients >0.9998. The analytical performance of both methods was thoroughly validated according to International Conference on Harmonization (ICH) guidelines with respect to system suitability, linearity, ranges, precision, accuracy, specificity, robustness, detection and quantification limits. The proposed MEKC and HPTLC methods were successfully applied for estimation of the studied drugs in laboratory prepared mixtures and in the cream and spray dosage forms.

Antioxidant activity of a polysaccharide from Dictyophora indusiata volva and MECC analysis of its monosaccharide composition

In this paper, a crude polysaccharide (PDI) was extracted from D. indusiata volva. The antioxidant activities of PDI were examined by 1,1-diphenyl-2-picryl-hydrazyl (DPPH) radical, hydroxyl radical and ABTS radicals scavenge assay. The results showed that PDI had antioxidant activities in all these assays, indicating that it could be used as an antioxidant. Then a rapid and highly efficient micellar electrokinetic capillary chromatography (MECC) method coupled with diode array detector was developed to determine the monosaccharides composition of the polysaccharide sample. The optimum conditions were as follows: 20 ​mM borate (pH ​= ​9.3) and 15 ​mM SDS as the electrophoresis medium, the separation temperature was 20 ​°C. Under these conditions, monosaccharides could be separated within 8 ​min. The polysaccharide of the volva was mainly composed of glucose, mannose, galactose and arabinose.

Simultaneous separation and determination of three huperzine alkaloids in Huperzia serrata and its preparations by cyclodextrin-modified mixed micellar electrokinetic capillary chromatography

In this study, a simple and sensitive cyclodextrin-modified mixed micellar electrokinetic capillary chromatography (CD-MEKC) method has been developed for the simultaneous separation and determination of Huperzine A (HupA), Huperzine B (HupB) and Huperzine C (HupC) in Huperzia serrata (H. serrata). The optimal conditions (pH 9.3) were composed of 10 mM sodium tetraborate solution, 40 mM sodium dodecyl sulfate (SDS), 50 mM sodium cholate (SC) and 3.0 mM mono-(6-ethylenediamine-6-deoxy)-β-cyclodextrin (ED-β-CD). The separation and determination process were performed on a P/ACE MDQ capillary electrophoresis system, the separation voltage was 15 kV, the temperature was 25 °C and the detection wavelength was 308 nm. Under the optimum conditions, the migration time was less than 9 min. The LOD and LOQ were between 0.38 and 0.80 μg/mL and 1.2–2.3 μg/mL, respectively. The developed method, with excellent precision and accuracy, was applied for the determination of three alkaloids in H. serrata and its formulations.

Simple and Rapid Micellar Electrokinetic Chromatography Method for Simultaneous Determination of Febuxostat and its Related Impurities

A micellar electrokinetic capillary chromatography (MEKC) method has been developed and validated for simultaneous analysis of febuxostat and its related substances in active pharmaceutical ingredients and pharmaceutical formulations. Analysis was performed in an uncoated fused silica capillary (34 cm effective length, 50 µm diameter). Method sensitivity was enhanced using an extended light path capillary, with an optical path 150 µm and the choice of 320 nm detector operating wavelength due to lower background noise and higher selectivity. BGE consisted of 20 mM borate buffer pH 9.3 and 50 mM SDS and 2% acetonitrile. Analysis was performed at 30 kV separation voltage and 32 °C capillary temperature. The method was linear over the range 1.0–10.0 µg mL−1 for each impurity corresponding to reporting limits regarding the ICH Q3A guidelines. The method has proven to be selective, precise, accurate and robust. Proposed MEKC method has been successfully applied for the quantitative determination of febuxostat and purity assay of active pharmaceutical ingredient and tablet dosage forms.

Application of spectroscopic and separation techniques to the examination of the chemical composition stability of lipsticks exposed to various factors and storage conditions

In this study, the stability of the chemical composition of lipsticks after exposure to various factors (substrate, time, individual variability, the impact of smoking, the effect of consuming beverages) and storage conditions (laboratory, insolation, without access to light) was examined. The following three analytical methods were used in the study: Attenuated Total Reflection technique (ATR), Gas Chromatography coupled to Mass Spectrometry (GC–MS) and Micellar Electrokinetic Capillary Chromatography (MEKC). Seven red lipsticks characterized by different chemical composition were analyzed. The analysis of variance (ANOVA) was used to estimate the impact of a given factor.It was noticed the lack of influence of individual variability, cigarette smoking and consumed beverages on the stability of the chemical composition of lipsticks. On the other hand, the changes in the chemical composition in lipstick traces depending on the time and storage conditions can be observed – especially when using the GC–MS method. In most cases, the results also indicated the possibility of identifying the lipstick left as a trace, using the ATR and MEKC method even after exposure to various factors and storage conditions. However, the main problem in the case of the ATR analysis is the occurrence of interference originating from the surface on which the trace of lipstick was applied. Ultimately, the conducted research provided evidence for the effectiveness of the MEKC method to the application in forensic science investigation.

Micellar electrokinetic capillary chromatographic determination of pirfenidone and 5-carboxy-pirfenidone by direct injection of plasma from patients receiving treatment for idiopathic pulmonary fibrosis (IPF)

A micellar electrokinetic capillary chromatographic method, a variant of capillary electrophoresis, was developed for the detection and measurement of pirfenidone and 5-carboxy-pirfenidone by direct injection of plasma from patients under treatment for idiopathic pulmonary fibrosis. To achieve the best separation a 35 mmol/L N-lauroylsarcosine sodium salt surfactant added with a 16 mmol/L sodium 1-heptanesulfonate solution was used as a running buffer. Analytes were eluted in a fairly short time, 7.35 and 9.40 min for pirfenidone and 5-carboxy-pirfenidone, respectively, at 15 °C and with an applied voltage of 30 kV in an 80 cm, 75 µm i.d. uncoated fused-silica capillary. In the range of 6.25–200 µmol/L, calibration curves exhibited acceptable linearity with the coefficient of determination higher than 0.999. The recovery of analytes spiked in samples of plasma was found to be 95–109% and 93–106% for pirfenidone and 5-carboxy-pirfenidone, respectively. Intra- and inter-day precisions were around 5%. LOD and LOQ for pirfenidone and 5-carboxy-pirfenidone were, respectively, 1.0 and 4.0 µmol/L. The method, applied to measure analytes in six idiopathic pulmonary fibrosis male patients, provided mean concentrations of 68.91 ± 26.31 and 36.21 ± 26.39 µmol/L for pirfenidone and 5-carboxy-pirfenidone, respectively.

DETERMINATION OF DOXORUBICIN HYDROCHLORIDE IN PHARMACEUTICA DOSAGE FORMS BY A SIMPLE STABILITY-INDICATING MICELLAR ELECTROKINETIC CAPILLARY CHROMATOGRAPHY METHOD

A stability-indicating micellar electrokinetic capillary chromatography (MEKC) method was developed and validated for the analysis of doxorubicin hydrochloride in injectable pharmaceutical dosage forms, using methotrexate as internal standard. A fused-silica capillary (50 µm i.d.; effective length, 40 cm) and a running electrolyte solution consisting of 10 mM borate buffer and 20 mM anionic surfactant SDS, at pH 9.3, were set as the best experimental conditions. Moreover, the capillary temperature was maintained at 26 ºC, while the applied voltage was +26 kV. Hydrodynamic sample injection (6 s at 50 mbar) was used, and the detection was set at 260 nm using a photodiode array detector. The method was validated for the requirements specificity, linearity, precision, accuracy, and robustness, following the International Conference on Harmonisation (ICH) guidelines. The method linearity was proven in the range of 25-125 µg/mL (r = 0.9995). Forced degradation studies were successfully conducted, evidencing the specificity and stability-indicating capability of the method. In addition, no interference of the excipients from the formulation was detected. The values of accuracy and precision were within the acceptable limits, and robustness studies were performed by a two-level full factorial design. The proposed method fulfilled all validation parameters and was shown to be suitable for quantitative analyses of doxorubicin, contributing, thus, to the establishment of new alternatives with advantages for the quality control of pharmaceutical formulations.

Validated micellar electrokinetic capillary chromatography (MECC) method for determination of 5-hydroxymethylfurfural in honey and comparison with HPLC

A simple and validated micellar electrokinetic chromatographic method is described for the determination of 5-hydroxymethylfurfural (HMF). The method was applied to fresh and processed (heated at 65 °C, 85 °C and 105 °C for 5 h and 20 h) multifloral and honeydew honeys. Optimum conditions were: 10 mmol L−1 Tris buffer consisting 110 mmol L−1 SDS and 10% (v/v) MeOH at pH 9.10, 20 kV of applied potential, 3 s of injection time at 5 × 103 N m−2, 280 nm of wavelength and 25 °C of fixed temperature. Mean electrophoretic mobility (m2 s−1 V−1) of HMF and methyl paraben (IS) were − 5.28 × 10−5 (RSD of 0.745%) and − 2.52 × 10−4 (RSD of 0.944%), respectively. The calibration curve was linear in the range of 0.68 µg mL−1 (5.40 × 10−6 mol L−1) and 4.05 µg mL−1 (3.21 × 10−5 mol L−1) with R = 0.9990 for inter-day precision. LOD and LOQ values were 0.007 µg mL−1 (5.48 × 10−8 mol L−1) and 0.023 µg mL−1 (1.83 × 10−7 mol L−1), respectively, as inter-day precision. The accuracy was very high with recovery values between 94.07 and 97.16%. The developed method was fully validated according to ICH guidelines. The results were compared with those of HPLC method adapted from AOAC method no: 980.23.

Eco-friendly micellar electrokinetic capillary chromatographic method for the simultaneous determination of newly developed antiviral agents in pharmaceutical formulations

A novel micellar electrokinetic capillary chromatographic (MEKC) method was developed for the simultaneous determination of ombitasvir (OMB), paritaprevir (PAR), ritonavir (RIT) and dasabuvir (DAS). The technique was based on the separation of all of the selected drugs in a deactivated fused silica capillary with a background electrolyte solution (BGE) composed of 25 mM phosphate buffer with 30 mM sodium dodecyl sulphate (SDS) (the pH of the aqueous phase was adjusted to 8) mixed with ethanol in a ratio of 65:35 (v/v). The capillary and sample temperature was maintained at 24 °C, and the detection was performed at 239 nm. The electrophoresis was performed by applying high voltage (30 kV) to the capillary. The strategy was completely approved according to ICH rules over the concentration range of 2.5 to 100 µg/mL for all of the drugs. The limits of detection were 0.16 µg/mL (PAR, DAS, and OMB) and 0.625 μg/mL (RIT), while the quantitation limits were 0.31 μg/mL (PAR, DAS, and OMB) and 1.250 μg/mL (RIT). The proposed MEKC method was successfully applied for the quantitation of the four drugs in tablets with high precision and accuracy. For the first time, these drugs were simultaneously determined by capillary electrophoresis.

The increase of detection sensitivity of micellar electrokinetic capillary chromatography method of stamp pad inks components by applying a sample stacking mode for the purpose of questioned document examination

The study focused on comparison of on-line sample concentration techniques, i.e. sample stacking modes, applied in capillary electrophoresis in order to improve the detection of components of stamp pad inks so that destruction of analysed document could be minimized. In particular, such techniques were taken into consideration as: normal stacking mode/field amplified sample stacking (NSM/FASS), high-salt concentration, sweeping, electrokinetic injection + FASS, and field enhanced sample injection (FESI). At first, two mixtures of 4 red dyes and 4 violet/blue dyes were examined. As a result, in case of red dyes two environments: ACN/1 mg mL−1 aqueous NaCl (95:5, v/v) and 10-fold water dilution of BGE preceded by water plug (6 s, 0.7 psi) injection, were chosen as the most promising for further examination. Regarding the blue/violet dyes, the 100-fold water dilution of BGE was selected as giving the best increase of height of peaks. Ultimately, nine stamp pad inks in three colours (red, blue and violet) produced by different manufacturers were examined under the optimal conditions. Only 5 dots cut-out from inked paper were sampled. Almost all examined samples were possible to be differentiated basing on the obtained electrophoretic profiles. In conclusion, the developed sample stacking mode of MECC–based method was found as a useful tool in the differentiation of stamp pad inks for the purposes of forensic questioned document analysis.

Determination of strobilurin fungicide residues in fruits and vegetables by nonaqueous micellar electrokinetic capillary chromatography with indirect laser-induced fluorescence.

A nonaqueous micellar electrokinetic capillary chromatography method with indirect LIF was developed for the determination of strobilurin fungicide residues in fruits and vegetables. Hydrophobic CdTe quantum dots (QDs) synthesized in aqueous phase were used as background fluorescent substance. The BGE solution, QD concentration, and separation voltage were optimized to obtain the best separation efficiency and the highest signal intensity. The optimal BGE solution consists of 40mM phosphate, 120mM sodium dodecyl sulfate, 15% v/v water and 15% v/v hydrophobic CdTe QDs in formamide, of which apparent pH is 9.5. The optimized separation voltage is controlled as 25kV. The resultant detection limits of azoxystrobin, kresoxim-methyl, and pyraclostrobin are all 0.001mg/kg, their linear dynamic ranges are 0.005-2.5mg/kg, and the recoveries of the spiked samples are 81.7-96.1%, 86.5-95.7%, and 87.3-97.4%, respectively. This method has been proved to be sensitive enough to detect the aforementioned fungicides in fruits and vegetables at the maximum residue limits.

Simultaneous determination of atorvastatin and ezetimibe from combined pharmaceutical products by micellar electrokinetic capillary chromatography

A rapid and sensitive micellar electrokinetic capillary chromatography method with UV photodiode-array detection was developed for the simultaneous determination of atorvastatin and ezetimibe in fixed dose drug combination. Experimental conditions such as buffer concentration and pH, surfactant concentration, system temperature, applied voltage, injection parameters were optimized in order to improve the efficiency of the separation. The best results were obtained when using fused silica capillary (48 cm length X 50 µm ID) and 25 mM borate buffer electrolyte at pH 9.3 containing 25 mM SDS, + 30 kV applied voltage, 20 oC system temperature. The separation was achieved in approximately 2 minutes, with a resolution of 7.02, the order of migration being atorvastatin followed by ezetimibe. The analytical performance of the method was verified with regard to linearity, precision, robustness and the limit of detection and quantification were calculated.

Analysis of protamine peptides in insulin pharmaceutical formulations by capillary electrophoresis.

Protamines are a group of highly basic peptides that are sometimes added to insulin formulations to prolong the pharmacological action. In this study, different methods were investigated to identify protamine in insulin formulations. Capillary electrophoresis in aqueous and non-aqueous media was tested to separate these peptides with very close amino acid sequences. Different buffers (phosphate or formate, both acidified) and various additives (principally negatively charged and neutral surfactants) were investigated to optimize peptide separation. Finally, a micellar electrokinetic capillary chromatography method using a capillary of 120 cm effective length and an aqueous background electrolyte made up of 100 mM phosphate buffer (pH 2) and 50 mM Thesit® gave the best results, providing the separation of the four major protamine peptides within 25 min.

Development and validation of a micellar electrokinetic capillary chromatography method for the determination of goserelin and related substances.

An MEKC method for the analysis of goserelin and related substances has been developed using a combination of additives including CTAB, β-CD, and sodium hexanesulfonate. For this assay, the running buffer (pH and additives) and separation conditions (voltage and temperature) were optimized. The optimized system was the following: 200 mM 6-aminocaproic acid buffer (pH 4.2) supplemented with 175 mM CTAB, 3.0% w/v β-CD, and 20 mM sodium hexanesulfonate; the voltage was 10 kV in reverse polarity mode, the temperature was 20°C, and UV detection was measured at 220 nm. The method was qualified by evaluating the specificity, precision, linearity, accuracy, LOD, and LOQ. According to validation experiments, the optimized method was specific, accurate, and repeatable and satisfied the requirements for the analysis of goserelin and related substances. Compared with the RP-HPLC method, the MEKC method better solved the problem of overlapping impurity signals, and the migration time required was shorter. This method can be used for quality control and for the analysis of goserelin and its related substances.

Simultaneous determination of ten preservatives in ten kinds of foods by micellar electrokinetic chromatography

An improved micellar electrokinetic capillary chromatography method (MEKC) for the simultaneous determination of ten preservatives in ten different kinds of food samples was reported. An uncoated fused-silica capillary with 50μm i.d. and 70cm total length was used. Under the optimized conditions, the linear response was observed in the range of 1.2–200mg/L for the analytes. The limits of detection (LOD, S/N=3) and limits of quantitation (LOQ, S/N=10) ranging from 0.4 to 0.5mg/L and 1.2 to 1.5mg/L, respectively were obtained. The method was used for the determination of sorbic and benzoic acids in two FAPAS® (Food Analysis Performance Assessment Scheme) proficiency test samples (jam and chocolate cake). The results showed that the current method with simple sample pretreatment and small reagent consumption could meet the needs for routine analysis of the ten preservatives in ten types of food products.

Uniform and orthogonal designs on experimental design and optimization of micellar electrokinetic capillary chromatographic method for the simultaneous analysis of three nucleoside antivirus drugs in disinfectant and anti/bacteriostatic products

To prevent the abuse of nucleoside-based antiviral drugs in disinfectant and anti/bacteriostatic products, a new micellar electrokinetic chromatographic (MEKC) method for the simultaneous determination of three nucleoside antiviral drugs (ganciclovir, acyclovir and penciclovir) was established. Three factors and seven levels uniform design and four factors and four levels orthogonal design were used to optimize the concentration of sodium dodecyl sulfate (SDS), sodium dihydrogen phosphate (NaH2PO4) and sodium borate (Na2B4O7) in the running buffer. The three nucleoside antiviral drugs were separated from each other in the shortest time to obtain effective separation through uniform and orthogonal designs on experimental design and optimization. The separation was performed on an uncoated fused-silica capillary with 50 μ m i. d. and a total length of 30.2 cm (effective length:20 cm). An optimized buffer solution consisting of 25 mmol/L NaH2PO4, 10 mmol/L Na2B4O7 (pH 7.41) and 140 mmol/L dodecyl sulfate sodium was used for separation. The applied voltage was 10 kV, the injected pressure and time was at 0.003 Pa for 4 s. The wavelength of the detection was 250 nm. Under the optimum conditions, the corrected area and the concentration had good linearity. The correlation coefficients (r) were not less than 0.9995. The limits of detection were all 2.0 mg/kg. The limits of quantitation were all 7.0 mg/kg. The relative recoveries ranging from 85.4% to 104.1% with RSDs all lower than 8.0%. It showed that the method was suitable for the detection of ganciclovir, acyclovir and penciclovir in disinfectant and anti/bacteriostat products with simplicity and rapidity.

Validation of a stability-indicating micellar electrokinetic capillary method for the assessment of febuxostat and its correlation with the reversed-phase LC method

A stability-indicating micellar electrokinetic capillary chromatography (MEKC) method was validated for the analysis of febuxostat in pharmaceutical formulations.