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Dilek Kul, Burcu Doğan-Topal, Sibel A. Özkan, Bengi Uslu, "Differential Pulse Voltammetric Determination of Fulvestrant in Pharmaceutical Dosage Forms and Serum Samples", International Journal of Electrochemistry, vol. 2011, Article ID 941583, 7 pages, 2011. https://doi.org/10.4061/2011/941583
Differential Pulse Voltammetric Determination of Fulvestrant in Pharmaceutical Dosage Forms and Serum Samples
The electrooxidation behavior and determination of fulvestrant at a glassy carbon electrode were investigated. The voltammetric study of the model compounds allowed elucidating the possible oxidation mechanism of fulvestrant. The dependence of the peak current and peak potentials on pH, concentration, nature of the buffer, and scan rate was determined. The oxidation of fulvestrant showed a single and irreversible peak at glassy carbon electrode, and the process was found diffusion controlled. Linear responses were obtained for the concentrations between M and M in standard samples and between M and M in serum samples. The repeatability of the method was found 0.93 RSD%. The repeatability, reproducibility, precision, and accuracy of proposed method were investigated.
Fulvestrant is a member of a group of drugs called estrogen receptor downregulators. Most breast cancer cells have estrogen receptors on their cell surface. Estrogen stimulates these cells with estrogen receptors to divide without regard to the body’s estrogen needs. This is referred to as “estrogen-receptor-positive breast cancer.” Fulvestrant works by blocking and destroying the estrogen receptor in the cell so that estrogen cannot bind to it. The action effectively lowers (downregulates) the estrogen receptor activity in the cell so that it acts more like a normal cell [1, 2].
Fulvestrant has a steroidal structure 7-alpha-(9-((4,4,5,5,5-pentafluoropentyl) sulfinyl) nonyl) estra-1,3,5(10)-triene, 3,7 beta-diol) (Scheme 1), which when complexed with oestrogen receptors prevents its dimerisation and renders the receptor transcriptionally inactive [3–6].
There has been no study published on quantitative determination of fulvestrant in pharmaceutical formulations. Moreover, no monograph of fulvestrant has been reported in the official pharmacopoeias as of today.
The widespread use of this compound and the need for clinical and pharmacological studies require fast and sensitive analytical techniques to assay the drug in pharmaceutical dosage forms and biological samples. These may also be used for monitoring patient compliance and establishing relationship between blood concentration and the therapeutic effects, which are not always fully understood.
In the last decades, modern-computer-based voltammetric techniques have been used to realize the determination of organic chemicals in diverse types of samples, especially pharmaceutical fields. The advance in experimental electrochemical techniques in the field of drug analysis is because of their straightforwardness, low cost, and relatively short analysis times no need for derivatizations or time-consuming extraction steps when compared with other analytical techniques [7–12]. Cyclic voltammetry (CV) is the most widely used technique for qualitative information about electrochemical reactions. Conventionally, glassy carbon (GC) is widely used for working electrodes especially for analytical applications because of its relatively wide potential window in comparison with metal electrodes such as Au and Pt. GC is composed almost exclusively of sp2-type carbon. The electronic and electrochemical properties of this electrode depend on several factors including surface preparation, microstructure, and presence of carbon-oxygen functional groups.
This work is aimed to study the detailed voltammetric oxidation mechanism of fulvestrant at GC electrode using CV. Also, the proposed method has been applied to the determination of electroactive fulvestrant and quantitation of fulvestrant in pharmaceutical dosage form, and human serum samples using differential pulse voltammetry (DPV).
Voltammetric experiments were performed using a BAS 100 W (Bionalytical System, USA) electrochemical analyzer associated to one-compartment glass electrochemical cell equipped with a three-electrode system consisting of a glassy carbon (GC) electrode (BAS; 3 mm, diameter), working electrode, a platinum wire counter electrode and an Ag/AgCl saturated KCl reference electrode. GC electrode was polished manually with aqueous slurry of alumina powder (0.01 μm, diameter) on a damp smooth polishing cloth (BAS velvet polishing pad) before each experiment.
The pH measurements were completed using a model 538, WTW pH-meter (Austria) with a combined electrode (Glass-reference electrodes) with an accuracy of pH ± 0.05.
The experimental conditions for differential pulse voltammetry (DPV) were as follows: pulse amplitude of 50 mV, pulse width of 50 ms, and scan rate of 20 mV/s.
Fulvestrant and its pharmaceutical dosage form were kindly supplied by Astra Zeneca (Istanbul, Turkey). Model compounds, levodopa, carbidopa, benserazide, epirubicin, and doxorubicin were kindly supplied from different pharmaceutical companies in Turkey. Other chemicals were reagent grade (Merck or Sigma).
Stock solutions of fulvestrant ( M) were prepared in acetonitrile and kept in the dark at 4°C. Fulvestrant working solutions for voltammetric investigations were prepared by dilution of the stock and contained 30% acetonitrile. Four different supporting electrolytes, sulphuric acid solution (0.1 M and 0.5 M), phosphate buffer (0.2 M H3PO4; 0.2 M NaH2PO4·2 H2O; 0.2 M Na2HPO4; pH 2.0–8.0), Britton-Robinson buffer (0.04 M H3BO3; 0.04 M H3PO4, and 0.04 M CH3COOH; pH 2.0–10.0), and acetate buffer (0.2 M CH3COOH; pH 3.5–5.5), were used for electrochemical measurements. All the solutions were protected from light and were used within 24 h to avoid decomposition. All measurements were carried out at the ambient temperature of the laboratory (23–27°C). The calibration curve for DPV analysis was constructed by plotting the peak current versus the fulvestrant concentration.
The ruggedness and precision were checked at different days. The results were given as repeatability (within day) and reproducibility (between days). Relative standard deviations (RSDs) were calculated to check the ruggedness and precision of the method [9, 13–19].
The accuracy and precision of the developed methods are described in a quantitative fashion by the use of relative errors (Bias%). An example of the Bias% is the accuracy which describes the deviation from the expected results.
2.3. Injectable Solution Assay
1.21 mL of Faslodex injectable solution, maintain to contain 250 mg fulvestrant per 5 mL of the solution, was dissolved in 100 mL of acetonitrile. An aliquot of this solution was transferred into a 10.0 mL volumetric flask and diluted to the mark with supporting electrolyte, and the voltammogram was recorded.
The nominal content of the injectable solution was determined from corresponding regression equation.
2.4. Analysis of Serum
Drug-free human blood, obtained from healthy volunteers (after obtaining their signed consent), was centrifuged (5000 rpm) for 30 min at room temperature. The separated serum samples were stored frozen until assay. An aliquot volume of the serum sample was fortified with fulvestrant dissolved in acetonitrile to achieve final concentration of M. This solution contained acetonitrile as serum precipitating agent. Acetonitrile removed serum proteins effectively, by the addition of 1 volume to 1.5 volumes of the serum. The mixture was vortexed for 30 s and centrifuged for 10 min at 5000 rpm to remove serum protein residues, and the supernatant was taken carefully. Appropriate volumes of the supernatant were transferred to the volumetric flask and diluted to the chosen volumes with 0.1 M sulphuric acid solution. The concentration of fulvestrant in the prepared solutions was varied in the range of M– M using DPV technique with GC electrode in human serum samples.
Quantifications were performed by means of the calibration curve method from the related calibration equation.
3. Results and Discussion
The electrochemical behavior of fulvestrant on the glassy carbon electrode was studied by CV, linear sweep voltammetry (LSV), and differential pulse voltammetry (DPV). Various supporting electrolytes were investigated using CV: phosphate buffer, Britton-Robinson buffer, acetate buffer, and sulphuric acid. The best result was obtained with 0.1 M sulphuric acid; peak oxidation potential 0.83 V versus Ag/AgCl (3.0 molL−1 KCl) was obtained for fulvestrant (Figure 1).
Voltammogram obtained for fulvestrant at the GC electrode presented an irreversible chemical behavior in all supporting electrolytes. Cyclic voltammogram of M fulvestrant using GC electrode (sweep rate 100 mV/s) exhibited a single well-defined and irreversible oxidation peak at 0.83 V. No peaks were observed on the reverse scan corresponding to the main anodic peak. This observation confirmed the irreversibility of the oxidation process (Figure 2).
The plot of the peak potential (Ep) versus pH created a straight line (Figure 3(a)) between pH 1.0 and 10.0. The peak potential moved to less positive values by increasing the pH. This can be expressed by the following equation:
The intersection of the curves was located around pH 10.0 for GC electrode. This value was found similar to the value given in the literature which is 10.03 . The peak potential seemed to be pH independent after a pH value of 10.0.
The effect of pH (within the range of 1.8–12.0) on the peak current of fulvestrant was investigated (Figure 3(b)). The plot of Ip versus pH indicated that the peak current reached a maximum for 0.1 M H2SO4. Therefore, 0.1 M H2SO4 was chosen as the supporting electrolyte for the quantitative determination part of the study. This supporting electrolyte showed sharp response and better peak shape for the calibration equation of pharmaceutical dosage forms and biological samples.
The peak potential shifted to more positive potentials (about 66 mV) to the anodic direction when the scan rate was increased for GC electrode which can be expressed by the following equation:
The rate increased to the observed potential until 100 mV/s and levelled off thereafter.
Scan rate studies were then carried out to understand whether the processes on GC electrode were under diffusion or adsorption control. When the scan rate was varied from 5 to 750 mV/s in M fulvestrant, a linear dependence of the peak intensity Ip (A) upon the square root of the scan rate () (mV/s) was found, demonstrating a diffusional behavior.
The equation is for GC electrode in 0.1 M H2SO4 solution
It followed from the variation of the logarithm of the peak current as a function of the logarithm of the sweep rate in the range of 5–750 mV/s that the process was diffusion controlled since the value of the straight line log Ip = f (log ) was equal to 0.58. This demonstrated that the process had a diffusive component.
Tafel plot was obtained with a scan rate of 5 mV/s beginning from a steady-state potential in 0.1 M H2SO4 from the slope of the linear part. The n value was 0.33. The exchange current density (Io) was A cm−2 for this system.
The results showed that oxidation of fulvestrant may be postulated by oxidation of the phenolic hydroxyl group. To investigate this founding, comparative studies on levodopa, carbidopa, benserazide, epirubicin, and doxorubicin related for the hydroxyl group of fulvestrant were carried out by CV on GC electrode as a function of pH in order to identify the other oxidation step of fulvestrant. The cyclic voltammograms of the compounds closely matched the more positive part of the voltammograms of fulvestrant. It was assumed that the oxidation process, via an initial oxidation of two electrons and the conversion of hydroxyl group to quinone, might be occurring on the selected compounds and the hydroxyl group of fulvestrant, which was electroactive in both acidic and basic media.
3.1. Analytical Applications and Validation of the Proposed Method
After the preliminary trials using different percentage of methanol and acetonitrile, 30% of acetonitrile ratio gave the finest response and solubility. The best result with respect to signal enhancement and peak shape accompanied by sharper response was obtained with 0.1 M sulphuric acid with constant amount acetonitrile as 30%. The calibration graph from the standard solution of fulvestrant according to the procedures described above was constructed by DPV. A linear relation in the concentration range between M and M was found, indicating that the response was diffusion controlled in this range. The characteristics of the calibration plot are summarized in Table 1.
The limit of detection (LOD) and the limit of quantification (LOQ) were calculated on the peak current using the following equations: where s is the standard deviation of the peak currents (three runs), and m is the slope of the calibration curve. The LOD and LOQ values were also shown is Table 1.
The low values of SE of slope, the intercept, and a correlation coefficient greater than 0.99 in the supporting electrolyte and human serum samples confirmed the precision of the proposed method.
The stability of the reference substance and sample solutions was checked by analyzing prepared standard solution of fulvestrant in the supporting electrolyte aged at in the dark against freshly prepared sample. The results demonstrated that the working reference solutions were stable at least for 3 days. The fulvestrant response for the assay reference solutions did not change considerably over 3 days.
The developed techniques were validated according to the ICH guidelines . The results are summarized in Table 1. Accuracy, precision, specificity, selectivity, reproducibility, LOD, and LOQ of the proposed techniques were assessed by performing replicate analysis of the standard solutions in the supporting electrolyte and human serum samples within calibration curves. The selected concentrations were prepared in both media, assayed with the related calibration equations to determine repeatability and reproducibility, and were shown as RSD% values in Table 1. The validation results shown in Table 1 demonstrate good precision, accuracy, and reproducibility.
3.2. Determination of Fulvestrant in Injectable Dosage Forms
On the basis of above results, DPV method was applied to the direct determination of fulvestrant in injectable dosage forms, using related calibration straight line without any sample extraction, evaporation, or filtration other than an adequate dilution step. The mean results were found very close to the confirmed value of 250 mg/5 mL. The results showed that the proposed method was successfully applied for the assay of fulvestrant in its dosage forms (Table 2). There is no official method present in any pharmacopoeias (e.g., USP, BP, or EP) related to pharmaceutical dosage forms or bulk drugs of fulvestrant. For checking the accuracy, precision, and selectivity of the proposed methods and in order to know whether the excipients in pharmaceutical dosage forms show any interference with the analysis, the proposed methods were evaluated by recovery tests after addition of known amounts of pure drug to various preanalyzed formulation of fulvestrant.
aEach value means five experiments.|
In order to detect interactions of excipients, the standard addition technique was applied to the same pharmaceutical preparations, which were analyzed by the calibration curve. Recovery experiments using the developed assay procedures further indicated the absence of interference from commonly encountered pharmaceutical excipients used in the selected formulations (Table 2). The results indicated the validity of the proposed techniques for the determination of fulvestrant in injectable dosage form (Table 2).
3.3. Determination of Fulvestrant in Spiked Human Serum
The optimized procedure was successfully applied to the determination of fulvestrant in protein-free spiked human samples. Acetonitrile was used as a serum precipitating agent. The best results were obtained with 5.4 mL of acetonitrile. No extraction or evaporation other than the centrifugal protein separation was required prior to assay for the drug. The measurements of fulvestrant in serum samples were performed as described in Section 2.
The applicability of the proposed method to the human serum samples and the calibration equation were obtained in spiked human serum samples. Calibration equation parameters and essential validation data were shown in Table 1. The recovery results of fulvestrant in serum samples were calculated from the related linear regression equation, which were given in Table 1. Recovery results of spiked human serum samples were given in Table 3.
Analysis of drugs from serum samples usually requires extensive time-consuming sample preparation and use of expensive organic solvents and other chemicals. In this study, the serum proteins and endogenous substances in serum samples were precipitated by the addition of acetonitrile and centrifugation at 5000 rpm. The supernatant was taken and diluted with the supporting electrolyte and directly analyzed. Typical DPV curves of fulvestrant examined in serum samples were shown in Figure 4. There were no oxidation compounds and no extra noise peaks presented in biological material peak occurred in the potential range where the analytical peak appeared.
Stability of serum samples kept in cold () was tested with five consecutive analyses of the sample over a period of approximately 5 h. There were no significant changes in the peak currents and potentials between the first and last measurements.
The electrochemical behavior of fulvestrant was examined for the first time with this study. The voltammetric oxidation steps of fulvestrant in different buffer solutions of pH 0.3–12.0 have been elucidated with glassy carbon electrode. The detailed electrooxidation outcome of fulvestrant at carbon-based electrodes might be used for analytical purposes, particularly as a sensor.
Fully validated, highly selective and sensitive, simple and precise voltammetric procedures were described for determination of fulvestrant in bulk form, pharmaceutical dosage form, and human serum samples without the necessity of sample pretreatment or time-consuming extraction and evaporation steps prior to the analysis.
In this study, possible oxidation pathways were investigated to identify the functional groups responsible from the oxidation. Therefore, the oxidation process of fulvestrant was compared with some model compounds. Comparative studies on levodopa, carbidopa, benserazide, epirubicin, and doxorubicin related for the hydroxyl group of fulvestrant were performed by CV on BDD electrode, as a function of pH, in order to identify the oxidation step of fulvestrant. The oxidation mechanism of fulvestrant found related to the oxidation of the hydroxyl group on the aromatic ring.
Consequently, the above-presented technique is a good analytical alternative for determining fulvestrant in pharmaceutical dosage forms and spiked serum samples. This study only shows the possibility of monitoring this compound that makes the method useful for pharmacokinetic and pharmacodynamic purposes. However, the proposed methods might be alternatives to the HPLC techniques in therapeutic drug monitoring, or the experimental data might be used for the development of HPLC-EC method.
This work is produced from Ph.D. thesis of Pharm. Burcu Dogan-Topal (Ankara University, Health Science Institute). This research was supported by a Grant from Ankara University Scientific Project Foundation (Grant no. 20030803043) for Dr. B. Uslu. The authors would like to thank Asta Zeneca (Istanbul, Turkey) for providing standard fulvestrant and pharmaceutical dosage forms for developing the proposed method.
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