Spectrofluorimetric determination of sertraline in dosage forms and human plasma through derivatization with 9-fluorenylmethyl chloroformate
© El-Enany et al 2011
Received: 26 June 2011
Accepted: 6 October 2011
Published: 6 October 2011
Sertraline is primarily used to treat major depression in adult outpatients as well as obsessive-compulsive, panic and social anxiety disorders in both adults and children. A survey of the literature reveals that most of the reported methods are either insufficiently sensitive or tedious and require highly sophisticated and dedicated instrumentation. The proposed method is considered to be specific for determination of SER in presence of its metabolite (deaminated form).
A sensitive, simple and specific spectrofluorimetric method was developed for the determination of sertraline (SER) in pharmaceutical formulations and biological fluids. The method is based on its reaction with 9-fluorenylmethyl chloroformate (FMOC-Cl) in borate buffer of pH 8.0 to yield a highly fluorescent derivative peaking at 315 nm after excitation at 265 nm. The different experimental parameters affecting the development and stability of the reaction product were carefully studied and optimized. The fluorescence concentration plot was rectilinear over the range of 0.05-1.0 μg mL-1 with a lower detection limit of 5.34 × 10-3 μg mL-1 and limit of quantitation of 0.016 μg mL-1.
The proposed method was successfully applied to the analysis of commercial tablets and the results obtained were in good agreement with those obtained using the reference method. Furthermore, the method was applied for the determination of SER in spiked and real human plasma. The mean % recovery (n = 3) was 94.33 ± 1.53 and 92.00 ± 2.65, respectively. A proposal of the reaction pathway was postulated.
Several methods have been reported for the determination of SER either per se or in pharmaceutical preparations and biological fluids. These methods include: spectrophotometry [2–4], voltammetry , HPLC [6–11] gas chromatography [12, 13]. A literature review up to 2008 has been described by Espinosa et al . The review described the different analytical methodologies for the determination of SER chromatography and liquid mass spectrometry [15, 16].
Most of these methods are either insufficiently sensitive [2–4] or tedious and require highly sophisticated and dedicated instrumentation [6–16]. This led us to study the reaction of sertraline with 9-fluorenylmethyl chloroformate (FMOC-Cl) in an attempt to develop a simple and sensitive spectrofluorimetric method for its determination in pharmaceutical preparations and biological fluids.
9-Fluorenylmethyl chloroformate is a useful derivatizing agent used for the determination of amino acids, primary amines and secondary amines. Several pharmaceutical compounds have been determined through this approach [16–21].
To the best of our knowledge, up till now nothing has been reported concerning the spectrofluorimetric determination of sertraline. This encouraged us to develop a simple and sensitive method for its determination in tablets and human plasma. The results obtained were promising.
The fluorescence spectra and measurements were recorded using a Perkin-Elmer UK model LS 45 luminescence spectrometer, equipped with a 150 Watt Xenon arc lamp, grating excitation and emission monochromators for all measurements and a Perkin-Elmer recorder. Slit widths for both monochromators were set at 10 nm. A 1 cm quartz cell was used. Derivative spectra were evaluated using Fluorescence Data Manager (FLDM) software. Sofware used is FL WINLAB, Version 4.00.02, copyright 2001, Perkin Elmer, Inc., UK.
Reagents and materials
All reagents and solvents used were of Analytical Reagent grade.
(a) Setraline pure sample was kindly provided by Pfizer (Sandwich, UK).
(b) Tablets containing sertraline HCl equivalent to 50 mg of sertraline base each (Lustral® tablets), batch # 7201 were obtained from commercial sources in the local market.
(c) 9-fluorenylmethyl chloroformate (FMOC-Cl), was purchased from Sigma (St. Louis USA). A stock solution containing 20 mg % of FMOC-Cl was freshly prepared in acetonitril and was further diluted with the same solvent to obtain 0.01 mg % solution.
(d) Borate buffer 0.2 M solutions of pH 8.0. and pH 12.
(e) Acetonitrile, acetone and diethylether (Merck, Darmstadt, Germany).
(f) Human plasma samples were kindly provided by Mansoura University Hospital, Mansoura, Egypt and was kept frozen at -2°C until assay after gentle thawing.
A stock solution was prepared by dissolving 20.0 mg of SER in 100 mL of acetonitrile in a volumetric flask. This solution was further diluted with the same solvent as appropriate. The standard solutions were stable for seven days when kept in the refrigerator.
General recommended procedures
Procedure for calibration graph
Aliquots of SER standard solutions were transferred into a series of 10 mL volumetric flasks. Borate buffer, pH 8.0 (2.5 mL) was added, followed by FMOC-Cl (0.01 mg %) (2 mL) and mixed well. Acetonitril (3 mL) were added. The reaction mixture was left at room temperature for 15 min., and then completed to the mark with distilled water. The fluorescence intensity of the reaction product was measured at 315 nm after excitation at 265 nm. A blank experiment was carried out simultaneously. The corrected fluorescence intensity was plotted vs the final drug concentration (μg mL-1) to get the calibration graph. Alternatively, the corresponding regression equation was derived.
Assay procedure for Tablets
Twenty tablets were weighed and pulverized well. A weighed quantity of the "powder, equivalent" to 20.0 mg of SER was transferred into a small conical flask, and extracted with 3 × 30 mL of actonitril. The extract was filtered into 100 mL volumetric flask. The conical flask was washed with few milliliters of acetonitril. The washings were passed into the same volumetric flask and made up the mark with the same solvent. Aliquots covering the working concentration range was transferred into 10 mL volumetric flasks. The procedure described under " General recommended procedures" "was then applied. The nominal content of the tablets was determined either from the calibration curve or by using the corresponding regression equation.
Assay procedure for spiked human plasma
A stock solution containing 20.0 μg mL-1 of SER was prepared in acetonitrile. Control samples of plasma were spiked with different quantities of SER. Acetone (2 mL) was added, then the mixture was vortexed and centrifuged at 3500 xg for 10 min. 3 mL of the clear supernatant was separated, and borate buffer, pH 12 (1 mL)was added. The solution was extracted with 3 × 5 mL of diethylether for 2 min, then centrifuged at 3500 xg for 5 min. The resulting supernatant was evaporated to dryness under nitrogen at ambient temperature. The residue was dissolved in 2 mL of acetonitrile. The general recommended procedures applied for pure sample were then performed. The nominal content of the drug was determined using the corresponding regression equation.
Assay procedure for real human plasma samples
Results and Discussion
FMOC-Cl was chosen as a fluoregnic derivatizing agent for SER because of its superior properties, as compared to other reagents. It reacts under mild conditions with primary and secondary amines in alkaline medium and the resulting derivatives are stable.
It has been utilized for the determination of amino acids and primary amines . Recently FMOC-Cl was further used for the analysis of some pharmaceutical compounds containing primary or secondary amino groups viz; trimetazine  roxithromycin  clarithromycin  alendronate  and topiramate .
Study of Experimental Parameters
The spectrofluorimetric properties of the reaction product as well as the different experimental parameters affecting its development and its stability were carefully studied and optimized. Such factors were changed individually while the others were kept constant. The factors included pH, type of buffer, volume of buffer, concentration of the reagent, reaction time and volume of acetonitrile.
i. Effect of pH
ii. Effect of volume of buffer
It was found that increasing the volume of 0.2 M borate buffer of pH 8.0 up to 2 mL resulted in a gradual increase in the fluorescence intensity of the reaction product and after which it remained constant till 3 mL, therefore 2.5 mL of the buffer was chosen as the optimal volume throughout the study.
iii. Effect of concentration of FMOC-Cl
The influence of the concentration of FMOC-Cl was studied using different volumes of 0. 01 mg % of the reagent solution. It was found that the reaction of FMOC-Cl with SER started upon using 0.25 mL of the reagent in the presence of borate buffer (pH 8.0). Increasing the volume of the reagent produces a proportional increase in the fluorescence intensity of the reaction product up to 1.8 mL and remains constant up to 2.2 mL. Therefore, 2 mL of 0.01 mg % of FMOC-Cl solution was chosen as the optimal volume of the reagent.
iv. Effect of temperature
Increasing the reaction temperature higher than the room temperature up to boiling for 20 minutes. resulted in a subsequent decrease in the fluorescence intensity of the reaction product.
v. Effect of reaction time
vi. Effect of volume of acetonitril
It was found that, 3 mL of acetonitril was sufficient to produce maximum and constant fluorescence intensity of the reaction product. The reaction between FMOC-Cl and SER takes place in an aqueous -organic phase system due to insolubility of FMOC-Cl and reaction product in water. It was necessary to perform the reaction with high content of acetonitril (final concentration, 60%)
Validation of the proposed method
The validity of the method was tested regarding; linearity, specificity, accuracy, repeatability and precision according to ICH Q2B recommendations .
Performance data of the proposed method
-concentration range (μg mL-1).
-Minimum detection limit, LOD (μg mL-1 ).
5.34 × 10-3
-Limit of Quantification, LOQ(μg mL-1).
-Correlation coefficient (r).
where F is the fluorescence intensity, C is the concentration of the drug in μg/ml and r is the correlation coefficient.
The limit of quantification (LOQ) was determined by establishing the lowest concentration that can be measured according to ICH Q2B . The results are shown in Table 1. The limit of detection (LOD) was determined by establishing the minimum level at which the analyte can be reliably detected, and the results are also abridged in Table 1.
Where σ: is the standard deviation of the intercept of regression line.
S: is the slope of the calibration curve.
Application of the proposed and reference methods to the determination of sertraline in pure form
2-Mean found (%)
5-Variance ratio F-test.
To test the validity of the proposed method, it was applied to the determination of an authentic sample of SER over the working concentration range. The results obtained were in good agreement with those obtained using a reference method.11). Using Student's t-test and variance ratio F-test  revealed no significant difference between the performance of the two methods regarding the accuracy and precision, respectively (Table 2).
The validity of the methods was proved by statistical evaluation of the regression lines, using the standard deviation of the residuals (Sy/x), the standard deviation of the intercept (Sa) and standard deviation of the slope (Sb). The results are abridged in Table 1. The small values of the figures point out to the low scattering of the points around the calibration line and high precision.
Validation of the proposed method for the determination of sertraline in pure form and tablets
(μg mL -1 )
98.75 ± 0.65
100.41 ± 1.07
98.66 ± 0.5
99.98 ± 0.82
100.63 ± 0.85
100.74 ± 1.17
(50 mg SER/tablet)
98.00 ± 1.29
100.41 ± 0.92
100.47 ± 1.35
100.19 ± 1.07
99.67 ± 1.56
100.80 ± 0.80
ii. Intermediate precision
It was performed through repeated analysis of SER either in pure form or in tablets, using the concentrations showed in Table 3 for a period of 3 successive days. The results are summarized in Table 3.
The proposed methods were then applied to the determination of SER in its tablets. The methods were tested for linearity, specificity, accuracy, repeatability and precision according to ICH Q2B recommendations.
The selectivity of the method was investigated by observing any interference encountered from the common tablet excepients, such as talc, lactose, starch, avisil, gelatine, and magnesium stearate. These excepients did not interfere with the proposed method
Application of the proposed methods to the determination of sertraline in tablets
Reference method (11)
(50 mg sertraline /tablet)
-Mean found (%) ± SD.
99.69 ± 1.05
99.72 ± 1.06
t - value
The reference is based on an HPLC determination of sertraline HCl either inpure form or in its tablets using a mobile phase consists of methanol: phosphate buffer (20: 80 v/v) of pH 4.5 with UV detection at 270 nm.
Analysis of biological fluid
This investigation conforms to the Egyptian Community guidelines for the use of human in experiments. The human Ethics Committee of Faculty of Pharmacy, Mansoura University, approved the study.
The high sensitivity of the proposed method allowed the determination of SER in spiked and real human plasma. Following oral administration of a single 50 mg sertraline dose after an over night fast, the mean plasma level of 0.05-0.2 μg/mL was achieved after 6.9 hour (25). This values lie within the working concentration range. Sertraline is extensively metabolized via N-desmethylation, oxidative deamination and subsequent reduction, hydroxylation and glucuronide conjugation. About 40-45% of an administered dose is excreted in urine as unchanged drug .
Application of the proposed methods to the determination of sertraline in spiked and real human plasma samples
2- Real Human plasma
% Error Mean
The extraction procedure described by Kim et al  was adopted here. The results are satisfactorily accurate and precise.
The within-day precision was evaluated through replicate analysis of blank human plasma samples spiked with different concentrations of the drug. The percentage recoveries based on the average of three separate determinations were 94.40 ± 1.14, thus indicating the high precision of the method (Table 5).
The inter-day precision was also evaluated through replicate analysis of plasma samples spiked with 0.1 μg mL-1 of drug on four successive days. The percentage recoveries based on the average of four separate determinations were 92.80 ± 2.27. The results are shown in Table 5. On the other hand, for real human plasma, the percentage recoveries based on the average of three separate determinations were 92.23 ± 2.89.
Molar ratio and mechanism of the reaction
The proposed method has the advantage of being simple, sensitive and suitable for routine analysis in quality control laboratories. Also, it is suitable for the determination of sertraline in human plasma with minimum detection limit lower than the reported value. In addition, it could be applied to the determination of sertraline in its pharmaceutical preparation. The proposed method is considered to be specific for determination of SER in presence of its metabolite (deaminated form)
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