- *Corresponding Author:
- T. K. Pal
Bioequivalence Study Centre, Department of Pharmaceutical Technology, Jadavpur University, Kolkata-700 032, India.
|Date of Submission||08 August 2005|
|Date of Revision||11 November 2005|
|Date of Acceptance||25 July 2006|
|Indian J Pharm Sci,2006, 68 (4): 485-489|
A simple high-performance liquid chromatographic method for the determination of etoricoxib in human plasma has been developed. An aliquot quantity of 1 ml plasma sample was taken and 10 ml internal standard was added and mixed. Saturated borate solution of 0.3 ml was added to it and mixed for 1 minute followed by liquid-liquid extraction with ethyl acetate. Organic layer was separated and evaporated to dryness under nitrogen atmosphere at low temperature (below 50°). Residue was reconstituted with 150 µl of mobile phase. During the whole procedure the samples were protected from light. The assay was performed on Hypersil BDS, C18 (150×4.6 mm, 5 m particle size) column, using 10 milimol ammonium acetate buffer:acetonitrile = 65:35 v/v as mobile phase with ultra violet detection at 235 nm. Lower limit of detection was 10 ng/ml and lower limit of quantitation was 20 ng/ml. Maximum between-run precision was 7.94%. Mean extraction recovery was found to be 79.53 to 85.70%. Stability study showed that after three freeze-thaw cycles the loss of three quality control samples were less than 10%. Samples were stable at room temperature for 12 h and at -20° for 3 months. Before injecting onto HPLC system, the processed samples were stable for at least 8 h. The method was used to perform bioequivalence study in human.
Non-steroid antiinflammatory drugs (NSAID) are widely used in clinical practice for the treatment of pain, inflammation and fever. The pharmacological effects of these drugs are due to their ability to block prostaglandin synthesis by inhibiting the enzyme cyclooxygenase (COX) [1-4]. COX exists in two isoforms in man, COX-1 and COX-2. COX-1 is required for many physiologic housekeeping functions, such as protection of the gastric mucosa, maintenance of renal homeostatic and platelet aggregation. Conversely, COX-2 is responsible for the synthesis of prostaglandins, which mediate responses to pathologic processes such as pain, fever and inflammation. Etoricoxib is a selective inhibitor of COX-2 that is used for the treatment of osteoarthritis, rheumatoid arthritis and pain . Etoricoxib is 5-chloro-6'-methyl-3-[4-(methyl -sulfonyl) phenyl]-2, 3' -bipyridine.s
Etoricoxib administered as a tablet is rapidly and completely absorbed and available; the absolute bioavailability is estimated to be 100%. It is metabolized extensively via oxidation 6' -methyl hydroxylation and 1'- N-oxidation. These metabolites are excreted largely in the urine . A high-fat meal decreased the rate of absorption without affecting the extent of absorption of etoricoxib; therefore, Etoricoxib can be dosed irrespective of food .
The numbers of published method for analyzing etoricoxib in plasma are very few. Matthews et al.  described a solid phase extraction of etoricoxib from plasma using a 96 well plate format followed by reverse- phase HPLC in a system equipped with a post column photochemical reactor and a fluorescence detector. So there is still the need of simple, sensitive method for analyzing the same in plasma. This paper describes a method of analyzing etoricoxib in plasma, which is very simple as well as sensitive using UV detector. The method was validated according to procedures and acceptance criteria based on FDA guidelines and recommendations of ICH [9-10].
Materials and Methods
Etoricoxib was obtained from Glenmark Pharmaceutical Ltd., Mumbai and valdecoxib from Virdev Intermediate, Surat. Acetonitrile and water for the mobile phase were of chromatographic grade (Make-Qualigens Fine Chemicals, Mumbai). All other reagents were of analytical grade (Merck, Mumbai).
The HPLC apparatus consisted of a Knauer (Germany) Model, K-1001 HPLC pump, K-2501 variable wave length UV detector and Eurochrom 2000 software. RP-HPLC analysis was performed using a BDS Hypersil C18 (average particle size 5 μ) column (150 mm, 4.6 mm). The mobile phase consisting of 65 volume of 10 milimol ammonium acetate buffer and 35 volume of acetonitrile. The mobile phase was filtered through 0.45 μm membrane filter. The eluent was monitored with a UV detector set at 235 nm with a flow rate of 1 ml/min and sample size of 20 μl was carried out at room temperature all over the study.
An aliquot quantity of 1 ml of plasma spiked with etoricoxib raw drug was taken in a stoppered test tube. To this 10 μl of 150 μg/ml of internal standard (valdecoxib in acetonitrile) was added and mixed well. Saturated borate solution of 0.3 ml was added to this and mixed for 1 min. This mixture was extracted with 6 ml of ethyl acetate by shaking for 10 min followed by centrifugation for three minutes at 3000 rpm. The organic layer was removed in a separate centrifuge tube with cap. The resulting organic layer was evaporated to dryness in water bath in presence of nitrogen atmosphere at low temperature (below 50°). The residue was reconstituted with 150 μl of mobile phase and the same was injected onto HPLC for chromatographic analysis. During the whole procedure the samples were protected from light.
Stock solutions of etoricoxib and internal standard were prepared in acetonitrile as 1 mg/ml for both and kept at -20°. Working solutions were prepared by diluting the stock solutions with mobile phase. For calibration curve eight different concentrations (20, 50, 100, 200, 500, 1000, 1500 and 2500 ng/ml) in plasma were prepared by adding required volume of working solution of analyte to blank plasma. For internal standard the final concentration in plasma was 1500 ng/ml. The plasma samples were subjected to the sample preparation procedure and injected onto HPLC. Plasma calibration curve was prepared by taking area ratio of analyte to internal standard as Y-axis and concentration of analyte (ng/ml) as X-axis. Six replicates of calibration curve were prepared taking each concentration for six times.
The limit of quantitation (LOQ) and limit of detection (LOD)
The limit of quantitation (LOQ) and Limit of detection (LOD) were determined from the peak signal and noise level (S/N) as ten and three times the baseline noise, respectively.
The extraction recovery of analyte was determined by measuring the peak areas of the drug from the prepared plasma quality control samples. 30 ng/ml, 1200 ng/ml and 2000 ng/ml plasma samples were taken as LQC (low quality control), MQC (medium quality control) and HQC (high quality control) samples respectively. The peak areas of extracted LQC, MQC and HQC were compared to the absolute peak area of the unextracted samples containing the same concentration of the drug as 100%. To obtain good extraction efficiency the extraction recovery of etoricoxib was determined using five replicates of each QC samples.
Accuracy and precision
Precision and accuracy were also determined from LQC (30 ng/ml), MQC (1200 ng/ml) and HQC (2000 ng/ml). Five replicates of each concentration were analysed on the same day to determine the within-run accuracy and precision of the method. To confirm the between-run accuracy and precision five replicates of each concentration on the first day and four replicates of each concentration on second day and third day were analysed.
The stability of etoricoxib in plasma was evaluated with four studies; a short-term stability study, a long-term stability study, a freeze thaw study and stability in processed sample. Plasma blank samples were spiked with etoricoxib at concentration of 30 ng/ml (LQC), 1200 ng/ml (MQC) and 2000 ng/ml (HQC) and each concentration was carried out for five times. Plasma samples were extracted and subsequent HPLC analysis was carried out as described previously.
Short-term stability test was performed at room temperature. Plasma samples spiked with etoricoxib were kept at room temperature for 12 h, extracted and then analysed. The long term stability study was carried out with plasma blank samples spiked with etoricoxib, which were stored -20° and they were analysed periodically 2 months against a standard curve prepared on the analysis day. For freeze thaw stability spiked samples were analysed immediately after preparation and on a daily basis after repeated freeze thaw cycles at -20° on three consecutive days. Finally the stability in the processed sample ready for injection was determined at three levels of concentration, 30 ng/ml (LQC), 1200 ng/ml (MQC) and 2000 ng/ml (HQC). The processed QC samples ready for injection were kept for 8 h before HPLC analysis.
The above mentioned bioanalytical method was used in bioequivalence study of etoricoxib. The study was approved by the ethics committee of Jadavpur University, Kolkata, India. It was an open, randomized crossover study to asses relative bioavailability of etoricoxib in twelve healthy male volunteers following single dose administration of etoricoxib 120 mg tablet.Test preparation was etoricoxib 120 mg tablet manufactured by Vivek Pharmachem (India) Ltd., Jaypur. Tablet Ebov containing 120 mg of etoricoxib, manufactured by Glenmark Pharmaceutical Ltd., Mumbai, was used as Reference preparation. The pharmacokinetic parameters like area under the plasma-concentration–time curve from time zero to the last measurable etoricoxib sample time and to infinity (AUC0-t and AUC0-inf), maximum concentration (Cmax), time to maximum concentration (Tmax), elimination rate constant (Kel) and elimination half-life(t1/2) were determined for the period of 0 to 120 h by non compartmental method.
Results and Discussion
Representative chromatogram of blank plasma and plasma spiked with etoricoxib and internal standard are shown in figs. 1 and 2, respectively. Retention time for the etoricoxib and internal standard were 5.975 min and 11.015 min, respectively. No interfering peaks at these times were found in the chromatogram obtained from blank plasma. Good separation and baselines with low background noise were observed. The chromatographic run time was 15 minutes for plasma sample analysis. The linearity of the calibration curve was evaluated by calculating the r2 (regression coefficient) value. The standard curves of etoricoxib in human plasma were linear over the ranges of 20 to 2500 ng/ml and the regression coefficients (r2) were over 0.998 from each standard curve of six separate runs.
The limit of detection defined as three times the base noise was 10 ng/ml for this analytical method and the limit of quantitation defined as ten times the base noise was 20 ng/ml (n=13, SD=1.08)
Within- and between-run precision and accuracy of the method was assed by analyzing the QC samples spiked with known amount of etoricoxib according to the procedure described in the previous section. Results are shown in Table 1 and 2. The accuracy of this bioanalytical method for within- and between-run was from 99.86 to 101.93% and from 100.15 to 107.92%, respectively. The within- and between-run precision ranged from 0.38 to 1.38% and from 0.34 to 7.94%, respectively.
|Q. C. Samples||LQC||MQC||HQC|
|Concentration spiked (ng/ml)||30||1200||2000|
|LQC, MQC, HQC are low quality control, medium quality control, high quality control samples of 30, 1200 and 2000 ng/ml. Data obtained are average of five observations (n= 5) where SD means Standard Deviation, CV% (precision) means coefficient of variation calculated as (SD/Mean concentration found)×100 and% nominal means accuracy which is calculated as (Concentration found/ Concentration spiked)×00.|
Table 1: Within-Run Accuracy And Precision Of The Analytical Method For Etoricoxib
|Q. C. Samples||LQC||MQC||HQC|
|Concentration spiked (ng/ml)||30||1200||2000|
|LQC, MQC, HQC are low quality control, medium quality control, high quality control samples of 30, 1200 and 2000 ng/ml. Data obtained are average of thirteen observations (n= 13) where SD means Standard Deviation, CV% (precision) means Coefficient of Variation calculated as (SD/Mean concentration found) ×100 and % nominal means accuracy which is calculated as (Concentration found/ Concentration spiked) ×100.|
Table 2: Between-Run Accuracy And Precision Of The Analytical Method For Etoricoxib
The recovery of etoricoxib from plasma was determined in accordance with the method described in the previous section. The recoveries (mean) of etoricoxib from plasma were found to be 79.53% at 30 ng/ml, 83.56% at 1200 ng/ ml and 85.70% at 2000 ng/ml.
The stability of etoricoxib in plasma was determined under various conditions according to the procedure described in the earlier section. Short-term stability test performed at room temperature showed that three QC samples were stable for 12 h (mean recoveries were 93.46%, 98.69% and 95.23% at LQC, MQC and HQC, respectively).
The long- term stability results indicated that etoricoxib samples were stable during 2 months, with an average recovery of 94.08%. No significant decrease of etoricoxib concentration in plasma was detected after exposing samples to three freeze/thaw cycles and mean recovery was found to be 94.57%. Finally, the stability in the processed sample ready for injection was also determined. Result showed that three QC samples were stable at least for 8 h with loss not higher than 10%.
The above mentioned bioanalytical method was used in the plasma analysis of a bioequivalence study of etoricoxib as described in the earlier section. Fig. 3 shows the mean plasma level of etoricoxib for test and reference preparation after the oral administration of a single dose 120 mg of etoricoxib in 12 healthy human volunteers. Maximum plasma concentration (Cmax) ranged from 1946.39 to 2393.99 ng/ml at 1.042 to 1.250 h (tmax).
The half life (t1/2) ranged from 29.26 to 33.91 h. Also the mean value of area under the concentration time curve (AUC0-t) obtained was 31342.32±5790.03 ng×h/ml and AUC0-inf was found to be 33672.37±7412.74 ngxh/ml. Relative bioavailability of test preparation was 98.03% to that of reference preparation and both the products were bioequivalent.
From the above discussion it is found that the analytical method for analysis of etoricoxib in plasma is simple, rapid and sensitive. The main advantage of this method is the use of liquid-liquid extraction procedure for sample preparation, which is easy and fast. It also uses UV detection, which is less costly than LC-MS (Liquid chromatography coupled with mass spectrometry). It can be used as a reliable assay method in the study of Pharmacokinetics of etoricoxib as well as bioavailability / bioequivalence study.
The authors would like to acknowledge the financial support by All India Council For Technical Education (AICTE), India to carry out this project through their Grant No. 1-10/NDF (PG)/JU (02)/2004-05.
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