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Brazilian Journal of Pharmaceutical Sciences

On-line version ISSN 2175-9790

Braz. J. Pharm. Sci. vol.53 no.1 São Paulo  2017  Epub Apr 20, 2017

http://dx.doi.org/10.1590/s2175-97902017000115181 

Article

Development and validation of alternative methods by non-aqueous acid-base titration and derivative ultraviolet spectrophotometry for quantification of sildenafil in raw material and tablets

Taízia Dutra Silva*  1 

Cibele Rodrigues Toledo1 

Cristina Duarte Vianna-Soares1 

1Department of Pharmaceutical Products, Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil

ABSTRACT

Sildenafil citrate (SILC) is a potent phosphodiesterase-5 inhibitor used for erectile dysfunction and pulmonary hypertension. This study shows two simple, fast and alternative analytical methods for SILC determination by non-aqueous titration and by derivative ultraviolet spectrophotometry (DUS) in active pharmaceutical ingredient and/or dosage forms. The quantitation method of SILC active pharmaceutical ingredient by non-aqueous acid-base titration was developed using methanol as solvent and 0.1 mol/L of perchloric acid in acetic acid as titrant. The endpoint was potentiometrically detected. The non-aqueous titration method shows satisfactory repeatability and intermediate precision (RSD 0.70-1.09%). The neutralization reaction occurred in the stoichiometric ratio 1:1 in methanol. The determination of SILC active pharmaceutical ingredient or dosage forms by DUS was developed in the linear range from 10 to 40 µg/mL, in 0.01 mol/L HCl, using the first order zero-peak method at λ 256 nm. The DUS method shows selectivity toward tablets excipients, appropriate linearity (R2 0.9996), trueness (recovery range 98.86-99.30%), repeatability and intermediate precision in three concentration levels (RSD 1.17-1.28%; 1.29-1.71%, respectively). Therefore, the methods developed are excellent alternatives to sophisticated instrumental methods and can be easily applied in any pharmaceutical laboratory routine due to simple and fast executions.

Uniterms: Sildenafil citrate; Vasodilator; Derivative ultraviolet spectrophotometry; Non-aqueous acid-base titrimetry; Sildenafil citrate/quality control.

INTRODUCTION

Sildenafil citrate (SILC, Figure 1) is a potent 5-fosfodiesterase (PDE-5) inhibitor with a pharmacological effect through an increase in intracellular concentration of cyclic guanosine monophosphate (cGMP), a potent vasodilator. SILC is a compound of the pyrazolo-pyrimidinyl-methyl piperazine class used not only for erectile dysfunction treatment but also for pulmonary arterial hypertension (Escribano, Jimínez, Calzada, 2005; American College of Cardiology Foundation; American Heart Association, 2009; Galiè et al., 2010, Sawatdee, Phetmung, Srichana, 2013).

FIGURE 1 Chemical structure of vasodilator sildenafil citrate, MM 666.70 g/mol.*Correspondence: T. D. Silva.  

Since the patent of the reference medicine Viagra(r) (Pfizer Laboratories Ltd.) expired in 2010, many generic drug companies were able to bring out to the market similar dosage forms with lower prices. Moreover, the trend of the number of pharmaceutical companies around the world, that will produce drugs containing SILC, is to increase. Compounding pharmacies also aim the production in a smaller scale of the different formula containing SILC, as their dispensation is commonly high due to the PDE-5 inhibitor popularity. Therefore, in order to assure the manufacturing uniformity for the treatment of erectile dysfunction or pulmonary hypertension, as well as for quality control purposes, it is important to establish alternative validated methods that can be performed as a simple and fast drug quantitation in either the active pharmaceutical ingredient (API) or the pharmaceutical dosage forms. Furthermore, with a simple and fast development of standard analytical methods for SILC it is possible to support the pharmacovigilance, once SILC tablets have frequently been a target of contraband and counterfeit (Ortiz, Antunes, Linden, 2010; Ames, Souza, 2012).

There are several methods described in the literature for SILC API determination or dosage forms by various techniques. Most of these methods are based on the high-performance liquid chromatography (HPLC) or ultra-performance liquid chromatography (UPLC) using UV-Vis or mass detectors, however, they require several pieces of expensive reagents/equipments (Gratz, Flurer, Wolnik, 2004; De Orsi et al., 2009; Song, El-Demerdash, Lee, 2012; Damiano et al., 2014; Fejos et al., 2014).

Methods based on the formation of colored complexes for the determination of SILC in tablets have also been described by visible spectrophotometry (Amin, El-Beshbeshy, 2001; Dinesh et al., 2002; Salem, 2006; Weinert, Pezza, Pezza, 2008; Issa et al., 2010; Frag, Mohamed, Alelaiwe, 2011a). Spectrofluorimetry and electroanalytical methods such as voltammetry using different electrodes were exploited by several researchers (Othman, Rizk, El-Shahawi, 2004; Hassan et al., 2006; Tyszczuk, Korolczuk, 2010; Wang et al., 2010; Balasoiu et al., 2011; Frag, Mohamed, Alelaiwe, 2011b; Wang, Gómez, Fernandez, 2013). However, these methods are laborious to be performed since they demand several types of reagents or sample treatment or involve many reactions steps and/or extraction processes for a quality control routine.

The titrimetry of several API based on chemical reactions of neutralization, oxi-reduction, precipitation or complexation can be found in the pharmacopeias. They show many advantages such as the ease of execution, a small consumption and simplicity/availability of reagents, the low cost, with precise and reliable results. Such features make the titration an excellent alternative to instrumental sophisticated analytical methods for the SILC raw material's determination because it can be easily applied by any pharmaceutical company or compounding pharmacy in the drugs' routine quality control.

The non-aqueous acid-base titrimetry is used more to quantify weak acids or bases, which do not provide a well-defined endpoint in the aqueous solvent. Moreover, this technique allows working with many water-insoluble substances when dissolved in appropriate organic solvents (USP, 2013a; BRITISH Pharmacopoeia, 2014). Pure substances can be titrated directly; however it is often necessary to isolate the API in pharmaceutical preparations from any interfering excipients. The environmental contamination and operator exposure to the organic solvents are reduced with the use of a small volume burette (such as 5.00 or 10.00 mL), or better, with the utilization of an automatic titrator, under the hood.

The derivative ultraviolet spectrophotometry (DUS) is widely used as an analytical tool in the medicines quality control for drug determination in multicomponent systems. This technique is simple and fast and allows the interference elimination of placebo, impurities or degradation products, improving the selectivity without a need of sample pre-treatment or drug extraction (Rojas, Ojeda, 2009; Donato et al., 2010).

A non-aqueous acid-base titrimetry and a DUS were chosen for the SILC analysis due to its simplicity and fastness. In addition, these analysis methods bear a lower cost, compared to methods such as liquid chromatography, and have a greater chance of application in compounding pharmacies and the majority of laboratory providers of routine quality control certificates.

Therefore, the aim of this work is to develop simple and alternative methods for the SILC API quantitation and dosage forms by titration in non-aqueous media and by DUS.

MATERIAL AND METHODS

Material and reagents

SILC working standard (99.69% purity; batch UT2100403; Ultratech India Limited, New Mumbai, India) and SILC 25 mg and 100 mg tablets (Sollevare(r)) were kindly donated by Vita Nova Institute (Hortolândia, SP, Brazil). Placebo was prepared using excipients: anhydrous calcium hydrogenated phosphate; hypromellose; magnesium stearate; lactose (Ipiranga Química, Santos, SP); blue aluminum lake color; croscarmellose sodium (Blanver, Taboão da Serra, SP); microcrystalline cellulose Microcel(r) MC102 (Colorcon do Brasil, São Paulo, SP); polyethylene glycol (PEG) 4000 (LabSynth, Diadema, SP); titanium dioxide (JB Química Indústria e Comércio Ltda, Suzano, SP, Brazil). Methanol (Tedia Company, Fairfield, IO, USA); hydrochloric acid; perchloric acid; glacial acetic acid (Merck, Darmstadt, Germany). All chemicals and reagents were of analytical grade.

Instrumental

An ultrasonic cleaner (1400, Unique; Indaiatuba, SP, Brazil), a centrifuge (Jouan B4i, Thermo Scientific; Waltham, MA, USA), a dry oven (306/1, Fanem; São Paulo, SP, Brazil) were used. For the non-aqueous acid-base titrimetry of SILC raw material was used an automatic titrator (DL53, Mettler Toledo; Columbus, OH, USA) equipped with a burette (resolution 0.002 mL) and a proper combined glass electrode.

DUS method for the quantitation of SILC in bulk drug and tablets was performed in a Shimadzu 1800 UV-Visible spectrophotometer (Shimadzu, Tokyo, Japan) with photodiode array detector. UV probe software version 2.33 was used for data acquisition. The absorption spectra were scanned using 1 cm quartz cells.

SILC active pharmaceutical ingredient determination by non-aqueous acid-base titrimetry

For the non-aqueous acid-base titrimetry of the API about 200 mg of SILC, previously dried (105 °C, 5 h, dry heat), were accurately weighed and dissolved in 40 mL of solvent previously neutralized. The solvents tested were glacial acetic acid and methanol. The samples were sonicated for 10 min. A volumetric solution (VS) of 0.1 mol/L HClO4 in acetic acid, previously standardized with potassium biphthalate, was used as titrant. The titration was preceded by 90 s of mechanical agitation in the automatic titrator for drug dissolution. The endpoint was indicated potentiometrically.

The repeatability and intermediate precision were evaluated by means of analysis of average content of six SILC replicates dissolved in methanol, in two days.

SILC active pharmaceutical ingredient determination and dosage form by DUS

All SILC or placebo's solutions were dissolved and diluted in 0.01 mol/L HCl. Parameters for the optimization were selected in the range from λ 200 to 400 nm. The absorption measurement in the first order of derivative (D1) using the zero-peak method was at λ 256 nm; the differential wavelength selected was λ 2 nm for a medium scan speed.

Validation

The parameters studied in the DUS method validation were selectivity, linearity, matrix effect, recovery, precision, detection limit, quantitation limit and robustness. These parameters were considered in order to verify the fitness for the purpose of the method (International Conference on Harmonization, 1996; Thompson, Ellison, Wood, 2002). The significance levels in hypothesis tests were α = 0.05.

The DUS method selectivity was evaluated using a placebo containing excipients commonly used in the SILC tablets manufacturing: anhydrous calcium hydrogenated phosphate (diluent, 36%); microcrystalline cellulose (diluent, 36%); croscarmellose sodium (disintegrant, 5.0%); magnesium stearate (lubricant, 5.0%) and coating constituents as blue aluminum lake color (0.6%); hypromellose (0.5%); lactose (4.0%); PEG 4000 (0.1%) and titanium dioxide (0.4%).

To verify the selectivity in D1, SILC solutions of 25 µg/mL and placebo were prepared in triplicate. The placebo solutions containing proportional amounts of excipients compared to a 25 µg/mL SILC from a dosage form solution were also prepared in the same solvent, 0.01 mol/L HCl, in triplicate. SILC and placebo solutions were separately scanned and overlapped in the D1 in the range λ 200-400 nm, and evaluated for any potential interference at λ 256 nm.

The DUS linearity method was evaluated using SILC standard solutions in the concentration range from 10 to 40 µg/mL in 0.01 mol/L HCl. The calibration curve was prepared at five concentration levels, in three independent replicates. The ordinary least squares method (OLSM) was applied to the experimental data to estimate the regression parameters. This method assumes that the residuals are normally distributed, homoscedastic, independent of each other and that the model is linear (Draper, Smith, 1998). Violations of assumptions underlying OLSM residuals were evaluated by the following tests: residual normality by Ryan-Joiner, homoscedasticity by Brown-Forsythe and independence by Durbin-Watson; F tests were applied to check the regression significance and linearity deviation (Durbin, Watson, 1951; Souza, Junqueira, 2005).

The matrix effect in the measurement of analyte concentration was investigated by the comparison of the slopes obtained for the solvent curve with that achieved for the matrix-matched curve by t test.

The DUS method validation for repeatability and intermediate precision was performed using SILC 25 mg tablets. SILC solutions at three levels of concentration, 10, 25 and 40 µg/mL, correspondent to 40%, 100% and 160% of the working concentration (25 µg/mL) were prepared in 0.01 mol/L HCl, in triplicate.

For the repeatability evaluation of DUS method, twenty units of SILC 25 mg tablets were crushed, and an accurately weighed portion of the powder, equivalent to one average weight, was transferred to a 100 mL volumetric flask followed by the addition of 60 mL of 0.01 mol/L HCl. The dispersions were sonicated for 10 min and the volume was completed with the same solvent to obtain the concentration 250 μg/mL. After centrifugation (10 min, 4,000 rpm) aliquots removed from the supernatant of each stock solution were diluted to final concentrations 10, 25 and 40 µg/mL, in 0.01 mol/L HCl (each in triplicate). The precision, under repeatability and intermediate precision conditions, was estimated by ANOVA and expressed in terms of relative standard deviation (RSD) for the replicates of tablets samples at each level and in three different days (International Organization for Standardization, 1994).

The method accuracy was reported as recovery percentage of known amount of SILC standard added to the placebo. An amount of 25 mg SILC standard was added to an equivalent mass of placebo, transferred to 100 mL volumetric flasks containing 60 mL of 0.01 mol/L HCl. The flasks were sonicated for 10 minutes and filled up to the mark with the respective solvents. The dispersions prepared in triplicate, were centrifuged (10 min, 4,000 rpm) and aliquots removed from the supernatant were diluted to final concentrations as described for the precision. The evaluated analytical method accuracy by recovery was calculated according to the equation %R=[CP/CS]×100, where CP is the concentration in a spiked dispersion of placebo, and CS is the standard solution concentration.

Limits of quantitation (LOQ), the lowest SILC concentration that can accurately be determined, was calculated by the equation LOQ = 10 sa/b, where sa is the standard deviation of the calibration curve intercept, a; b is the slope of the calibration curve (International Conference on Harmonization, 1996; FDA, 1994).

The DUS method robustness was evaluated by assay of sextuplicate 25 µg/mL solutions of SILC tablets and their reference solution in the working concentration 25 µg/mL using different instrumentation: a HP8453 UV-visible (Agilent Technologies, Inc., Santa Clara, CA, USA) with photodiode array detector and HP ChemStation software; and a Shimadzu 1800 UV-Visible with UV probe software version 2.33. The results obtained with the two spectrophotometers were compared by ANOVA and Tukey tests (α = 0.05).

RESULTS AND DISCUSSION

SILC active pharmaceutical ingredient determination by non-aqueous acid-base titrimetry

Due to the presence of the functional groups piperazine, pyrimidinone and pyrazole in the sildenafil molecule, as shown in Figure 2, four ionization sites are expected: three of which are basic centers (A, B, C) and one acid center (D).

FIGURE 2 Potential ionization sites of sildenafil (666.70 g/mol) in basic functional groups (A) piperazine, (B) pyrimidinone, (C) pyrazole and (D) weak amide acid group. (Adapted from Gobry et al., 2000). 

Gobry et al. (2000) have shown the determination of the ionization constant (pKa), in water/methanol, of the most basic nitrogen (A, piperazine, pKa 6.78) which shows sp3 hybridization and the pKa of a weak amide acid group (D, pyrimidinone, sp3, pKa 9.12). Hence, sildenafil is an amphoteric compound with a moderate basicity and a weak acidity for the ionization sites A and D, respectively. The authors mention that the ionization constants for the B and C groups were not determined due to uncertain basicity (Gobry et al., 2000; Wang, Chow, Zuo, 2008). On the other hand, the pKa of the salt molecule, SILC, for the tertiary protonated nitrogen of the piperazine ring, is found to be 8.7 as stated, for instance, in the drug's reference book Clarke's Analysis of Drugs and Poisons (Moffat, Osselton, Widdap, 2004).

The presence of such groups in the molecule leads to a partial ionization in aqueous solution and a low inflexion endpoint, therefore, requiring a non-aqueous medium for the acid-base titration. Thus, SILC basicity or acidity can be leveled at the hydroxilate or oxonium ions strength, if dissolved in a proper organic leveling solvent capable of evidencing their inflexion point.

In the present SILC acid-base titration in non-aqueous solvent, acidic amphiprotic glacial acetic acid was initially tested as the drug solvent because it is more commonly used in the determination of weak organic bases. The titration curve for the accurately weighed mass 200 mg of SILC in this solvent showed two inflection points, as shown in Figure 3a and b in zero and first orders, respectively. The volumes of titrant consumed due to the presence of two equivalence points were detected in 2.89 mL and 6.36 mL, as evidenced in Figure 3a and b. Therefore, the stoichiometric ratio of the reaction was found to be 1 SILC to 2 HClO4. The volumetric factor found for the mass of the analyte reacted with the volume of titrant is equivalent to 33.336 mg of SILC per milliliter of 0.1 mol/L perchloric acid VS, i.e., each mL of titrant is equivalent to 33.336 mg of SILC.

FIGURE 3 Graphical representation of the non-aqueous titration curves in (a) zero and (b) first order using potentiometric endpoint detection for 200 mg of SILC in glacial acetic acid with volumetric solution of 0.1 mol/L of perchloric acid in acetic acid, as titrant. Volumes of titrant consumed in the two equivalence points detected were 2.89 mL and 6.36 mL. 

The first endpoint was attributed to the citrate ion titration formed by SILC dissociation in the medium as long as the strongest basic group, A (Figure 2), present in the piperazine ring has already been protonated in the SILC molecule. Thus, the drug is titrated indirectly through its counterion, citrate and a displacement of the citrate ion of SILC takes place by the perchlorate ion. The second endpoint was attributed to the weak basic nitrogen titration (B, Figure 2) in the SILC pyrimidinone ring. In acetic acid, the titration of this group was possible because its strength was evidenced due to the solvent leveling effect for weak basic compounds.

Similarly, methanol, a neutral amphyprotic organic solvent, was used as a medium free of water for the SILC titration. Unlike observed using glacial acetic acid as solvent, the presence of only one inflection, hence, only one equivalence point was detected by the consumption of 2.70 mL of titrant for the same mass of SILC, due to titration of the citrate ion (Figure 4).

Figure 4 Graphical representation of the non-aqueous titration curves in (a) zero and (b) first order using potentiometric endpoint detection for 200 mg of SILC in methanol with volumetric solution of 0.1 mol/L perchloric acid in acetic acid, as titrant. Volumes of titrant consumed in the equivalence point was 2.70 mL. 

The explanation for the observation of only one equivalence point in methanol is that this solvent presents a differentiation effect, so that the weak basic nitrogens are not titrated in SILC salt molecule. The stoichiometric ratio of titration reaction in this case is 1 SILC to 1 HClO4. The titre found for the mass of the analyte reacting with the volume of titrant is equivalent to 66.671 mg of SILC per milliliter of 0.1 mol/L perchloric acid VS.

The partial and global reactions of the SILC titration in acetic acid or methanol with 0.1 mol/L perchloric acid in acetic acid are shown in Figure 5.

Figure 5 General chemical reaction for the first endpoint of the non-aqueous SILC titration in acetic acid (following the titration takes up another drug to titrant stoichiometric ratio 1:2), as well as for the single endpoint of SILC titration in methanol (stoichiometric ratio 1:1) using 0.1 mol/L perchloric acid VS as titrant and potentiometric endpoint detection. 

The chemical equation (Figure 5) shows that when the titrant is a strong acid such as perchloric acid dissolved in acetic acid, the latter can act as a base and accept protons donated by perchloric acid, forming acetic acid oxonium (CH3COOH2 +) and a very weak base, the perchlorate. The first endpoint of the non-aqueous SILC titration ([RN+H]RCOO - ), dissociated in protonated sildenafil (R3N+H) and citrate ion (RCOO-) in either acetic acid or methanol, is attributed to the reaction of strong acetic acid oxonium. The species (CH3COOH2 +) easily donates protons to the strong base citrate and, a rapid reaction to regenerate acetic acid and citric acid occurs in the medium. Following the titrant addition, SILC takes up another mole of 0.1 mol/L of perchloric acid so that the stoichiometric ratio is 1:2 (drug to titrant), in acetic acid solvent (reaction of the second endpoint not shown). On the other hand, when SILC is dissolved in the differentiating solvent methanol there is no subsequent reaction and the stoichiometric ratio is 1:1. The global reaction shows the displacement of citrate counterion by perchlorate to produce sildenafil perchlorate.

Hence, either solvent acetic acid or methanol can be used for the SILC titration of. The use of methanol as the organic solvent was selected due to a less irritant odor than acetic acid and the lower titrant consumption for the same mass of SILC. Therefore, the method using methanol contributes to a lower chemical residue production for the environment; however, it is up to the analyst to choose what is more convenient to their reality.

Six replicates of raw material dissolved in methanol were analyzed in two days for determination of repeatability (n=6) and intermediate (n=12) precision. The results for SILC precision and quantitation by non-aqueous acid-base titrimetry are described in Table I.

TABLE I Precision results for SILC raw material (circa 200 mg) determination by non-aqueous acid-base titrimetry using methanol as the drug solvent, 0.1 mol/L HClO4 VS in acetic acid (concentration correction factor 0.9878) as titrant and potentiometric endpoint detection 

Precision results Day 1 Day 2
Average volume (mL) of titrant ± SDa 3.04 ± 0.03 3.05 ± 0.02
Average content (%) ± SDa 100.51 ± 0.79 100.45 ± 0.57
Repeatability (%RSDa) 0.79 0.57
Intermediate precision (%RSDb) 0.66

a: SD, standard deviation, n = 6; RSD, relative standard deviation; b: n = 12.

The average content results for SILC determination comply with the established range of purity (98.0-102.0%) for the active ingredient, as described in the monograph for SILC raw material in United States Pharmacopeia (USP, 2013b). The RSD found values were satisfactory (<1.0%) because they did not exceed 2% for repeatability, or 5% for intermediate precision in two days, what demonstrates that the method is adequately precise (Green, 1996, International Conference on Harmonization, 1996).

The goal of this work was to determine SILC API only, by non-aqueous titration as commonly seen in the general compendia for the weak bases assay (USP, 2013a). In case of solid dosage forms, it is noteworthy that the presence of certain excipients in solid dosage forms such as other basic compounds, calcium hydrogenated phosphate or magnesium stearate, can be a potential interference. Therefore, the drug must previously be extracted, as it is also the case for liquid pharmaceutical dosage forms, recommended by Beckett and Stenlake (1988).

SILC active pharmaceutical ingredient determination and dosage form by DUS

The DUS method has been used to determine pharmaceutical analytes in dosage forms due to the ease of interference elimination due to excipients and sometimes from degradation products. It is used for the simultaneous determination of drugs in associations, as well. This technique allows to extract qualitative and quantitative information from spectra composed of analytes overlapping bands and interfering with the advantages of being simple, fast, inexpensive and accessible to most analytical quality control laboratories (O'Haver et al. 1982; Rojas, Ojeda, 2009; Donato et al., 2010).

In order to apply the DUS method not only for the drug quantitation, but also for the dissolution profile study, a 0.01 mol/L HCl solution was selected as the diluent solvent because the drug solubility is enhanced in acidic medium. In addition, this solvent is the one recommended as the medium for the SILC tablets' dissolution profile study by the United States Food and Drugs Administration (Wang, Chow, Zuo, 2008; FDA, 2014; Badwan et al, 2001).

During the method development, the spectra of standard SILC solutions (100% working concentration 25 µg/mL) and placebo solutions (equivalent to the amount of excipients in the 25 µg/mL SILC solution) in the UV region were plotted in zero order and then overlapped in order to assess interferences from excipients present in proportions normally found in solid dosage forms containing SILC.

In the zero order spectrum, the placebo absorbs throughout the wavelength range that SILC absorbs, resulting in interference, as shown in Figure 6a. The percentage average of interference from placebo solution on SILC solution in the maximum absorption wavelengths λ 211 nm, 224 nm and 292 nm were 4.4; 4.1 and 7.2%, respectively. These values are well above the maximum acceptable for spectrophotometric methods, a value of 2.0%, according to recommendations of the United States Pharmacopeia (USP, 2013c). Therefore, it is not suitable to quantify SILC colored tablets by UV absorption spectrophotometry in the conventional mode.

Figure 6 (a) UV absorption spectra overlay in zero order for SILC reference standard (SILC, 25 µg/mL) and a mixture of excipients (placebo, equivalent to the amount of excipients in the 25 µg/mL SILC solution) in 0.01 mol/L HCl; (b) in first order (Δλ=2 nm; scaling factor x1) and third order (Δλ=4 nm; scaling factor x10) and (c) second (Δλ=4 nm; scaling factor x1) and fourth order of derivative (Δλ=8 nm; scaling factor x1); medium scan speed for SILC reference standard (SILC, 25 µg/mL). 

The zero-peak derivative quantitation method was sought to reduce the systematic error in the SILC determination compared to the zero order, conventional method (Donato et al., 2010). Thus, the absorption spectra of zero (Figure 6a), first (Figure 6b), second (Figure 6c), third (Figure 6b) and fourth (Figure 6c) derivative of SILC and placebos were recorded and overlapped to determine the most appropriate wavelength, as well as the order of the derivative for quantitative SILC determination in tablets.

The UV absorption spectra for SILC in second, third and fourth orders of derivative represented in Figure 6 shows that the UV spectra complexity increases as the order increases, nevertheless, the absorptivity significantly reduces as a consequence of impaired sensitivity. Thus, the first order derivative curves were chosen for the quantitation of the drug because it provides a greater sensitivity and a better signal-noise ratio compared to other orders of derivative, as shown in Figure 6 b, c.

Figure 7 shows the first order UV spectra of SILC with maximum or minimum absorption in λ 208 nm, 221 nm, 238 nm, 256 nm, 272 nm and 313 nm. The peak with the highest amplitude is in λ 238 nm, where there is a small interference from placebo. The λ of greater amplitude, which coincides with the point of zero crossing absorption of placebo corresponds to the valley in λ 256 nm. Therefore, the absorption at λ 256 nm in the first derivative was selected to quantify SILC in dosage form because at this λ elimination of excipients interference occurs.

Figure 7 Overlay of first order UV spectra for SILC reference standard (SILC, 25 µg/mL) and placebo (equivalent to 25 µg/mL SILC) in 0.01 mol/L HCl (wavelength range λ 200-400 nm; Δλ=2 nm; average scan speed). 

The DUS parameters established after optimization of the SILC spectra at first order of derivative ultraviolet spectrophotometry were the average scan speed with a selected wavelength interval Δλ 2 nm. These conditions provided well-resolved spectra and precise first order absorbance results. The scan speed and the wavelength interval are critical and essential features in the method optimization since they influence the shape and the signal to noise ratio of the spectrum, as well as the method sensitivity (O'Haver, Begley, 1981; Morelli, 2003).

Validation

The method selectivity to the excipients was attested by the superposed spectra of the placebo and SILC reference standard solutions in the first order of derivative, in the described conditions. In the scanned spectrum for the placebo, a decreasing absorption is noticed from λ 200 to approximately λ 253 nm, as shown in Figure 7. From λ 256 nm until λ 400 nm, it was possible to observe the elimination of such interference by using the zero-peak method towards a mixture of excipients, commonly found in colored SILC tablets. Therefore, the absorbance measurement at λ 256 nm was selected.

For the linearity assessment the normality assumptions (Ryan-Joiner test), homoscedasticity (Brown-Forsythe test) and independence (Durbin-Watson test) of the regression residues were confirmed, as shown in Table II. The assumptions relative to residues were investigated by means of the hypotheses tests. For the normality assessment, the null hypothesis (Ho) tested was that the residues follow a normal distribution. If the value of the test statistic, the correlation coefficient (R) of the normal probability graph is greater than or equal to the critical R (tabulated), there is no evidence to reject Ho. For the homoscedasticity assessment, Ho was tested as if the residues variability were constant along the X-axis. For Ho confirmation, the test statistic, Levene t, t L, must be less than or equal to the critical t L. Finally, for the residual autocorrelation evaluation, Ho was tested as if the residues were independent. For Ho to be confirmed, the calculated value of the test statistic, Durbin-Watson d, must be between the two critical values, a lower limit, dL and an upper limit, dU (Durbin, Watson, 1951; Brown, Forsythe, 1974; Ryan, Joiner, 1976; Draper, Smith, 1998; Souza, Junqueira, 2005).

TABLE II Results and statistics for assumptions tests for linearity evaluation of the DUS method (Conditions: first order of derivative; zero-peak method, λ 256 nm; Δλ=2 nm; in 0.01 mol/L HCl; medium scan speed) 

Assumption Statisticsd Critical Value Calculated Value
Normalitya R 0.9383 0.9683
Homoscedasticityb t L 2.160 0.562
Independencea dL; dU 1.07; 2.93 2.851
Regression significancec F 4.67 29,415.52
Lack of fitb F 3.71 0.067

a: p>0.10; b: p>0.05; c: p<0.001; d: R, correlation coefficient of the normal probability graph; t L, Levene t; dL, lower limit; dU, upper limit of Durbin-Watson; F, Fisher statistic.

These results indicate the adequate estimation of the regression parameters by OLSM. The Fisher test, F, for the regression was significant (F>>critical F; p< 0.001) while the lack of fit from linear model was not significant (F<critical F; p>0.05), indicating linearity in the studied concentration range from 10 to 40 µg/mL (Table II). The determination coefficient, R2 was 0.9996 for the analytical curve equation y = (0.00111±0.00001)x + (0.00018±0.0002).

No matrix effects were detected, because no significant differences were observed between the slopes achieved for the solvent and matrix-matched curves (p>0.05).

The method precision was expressed by the %RSD values of a series of measurements in three non-consecutive days by different analysts. In Table III, the summarized results are shown for repeatability and intermediate precision for three levels of concentration (triplicate). The %RSD values obtained for repeatability and intermediate precision were satisfactory, not exceeding the maximum acceptable value of 2% or 5%, respectively (Green, 1996; International Conference on Harmonization, 1996).

TABLE III Precision and trueness results for SILC determination by DUS (first order of derivative; zero-peak method; λ 256 nm; Δλ=2 nm; in 0.01 mol/L HCl; medium scan speed) 

Concentration (µg/mL) %RSDa
Repeatability (n = 3) Intermediate precision, (n = 9) %Recovery (%RSDa; n = 3)
10 1.17 1.71 98.86 (0.98)
25 1.28 1.29 99.79 (1.61)
40 1.25 1.60 99.30 (1.61)

a: RSD, relative standard deviation.

The results for the trueness, evaluated by the standard addition method to the placebo and expressed as the percentage of recovery are shown in Table III. They indicate no lack of trueness, since the average recovery obtained for the replicates was within the range (98.0-102.0%), as recommended by Green (1996) at each concentration level.

The estimated LOD and LOQ of the method, calculated by the equations using standard deviation of the curve intercept and the slope of the calibration curve were 0.48 and 1.58 µg/mL, respectively.

The DUS method robustness was evaluated by the parameter that has the greatest potential to interfere in the assay results generated by a DUS method, the differentiation program. The assay of sextuplicate sample solutions of SILC tablets (25 µg/mL, 0.01 mol/L HCl) using two different spectrophotometers was performed for comparison of the obtained results by means of t test (α = 0.05). The equipments used to assess the method robustness have internal differentiation programs that operate in different modes. In the Agilent HP8453 software, it is not allowed to change important derivatization parameters such as Δλ and scanning speed, which are automatically selected and optimized. On the other hand, in the Shimadzu UV1800 software the user is able to select such parameters in order to assess the method optimization.

The results for the DUS method robustness are shown in Table IV.

TABLE IV Robustness results for SILC determination by DUS (first order of derivative; zero-peak method; λ 256 nm; Δλ=2 nm; in 0.01 mol/L HCl; medium scan speed) 

Sample Content (%)
Condition
HP8453 Shimadzu UV1800
1 98.82 99.10
2 99.25 99.33
3 98.17 98.38
4 99.30 99.79
5 99.57 100.03
6 96.50 97.01
Average; RSDa 98.60; 1.16 98.94; 1.12

a: RSD, relative standard deviation.

The calculated value for t statistic test (t=0.522) was lower than the critical value (t=2.228; α=0.05). Thus, there was no significant difference between the assay results for the SILC tablets pool analyzed in different spectrophotometers, what proves the method robustness.

In a study performed by El-Gindy et al. (2010), SILC was quantified by DUS in the concentration range from 4 to 36 µg/mL in the presence of four separate impurities by first, second or third derivative order. Different wavelengths were chosen for the selective SILC determination in methanol:water (30:70) for each derivative order and for each impurity, by zero-peak methods or ratio spectra derivative (El-Gindy et al., 2010). Noteworthy, that method is not able to quantify the SILC in the presence of all four impurities simultaneously. Moreover, the interference towards excipients commonly found in SILC tablets was not appropriately evaluated. The authors ran only a recovery assay by means of standard addition to the tablets. A study of the matrix effect should have been conducted, as well as a careful evaluation of the spectral interference of excipients, the proper selection of λ, and the derivative order in which the interferences were null or minimal, in light of what was done in the present work.

Doubtless, the method developed by El-Gindy et al. (2010) is effective towards the SILC determination in the presence of its impurities, when evaluated separately. Therefore, the method shows limited applicability and the validation protocol is incomplete, since it is necessary to evaluate the stability indication of the method for a formulation in the presence of its placebo.

The method developed to quantify SILC API or tablets in the described conditions was satisfactorily validated. The interference regarding the placebo including the blue dye present in SILC tablets was eliminated and carefully evaluated in the first derivative order by zero-peak method, λ 256 nm. Moreover, the use of aqueous 0.01 mol/L HCl as the drug diluent, hence, a chemical residue, is easy to neutralize or discharge and is less aggressive to the environment.

CONCLUSION

The SILC determination, such as API or as blue dyed tablets, by first derivative ultraviolet spectrophotometry showed no placebo interference and was successfully validated and achieved. The simple, fast and low cost developed methods, by non-aqueous titration and DUS, are excellent alternatives to sophisticated instrumental methods and can be easily applied in the quality control routine of such a popular drug, as SILC.

ACKNOWLEDGMENTS

The authors are grateful to FAPEMIG, CNPq (Brazil) for the research financial support and Instituto Vita Nova (Hortolândia, SP, Brazil) for the kind donation of citrate of sildenafil raw materials.

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Received: October 14, 2015; Accepted: November 21, 2016

Departamento de Farmácia. Faculdade de Ciências Biológicas e da Saúde. Universidade Federal dos Vales do Jequitinhonha e Mucuri, Campus JK. Rodovia MGT 367, Km 583, n° 5000, 39100-000, Diamantina, MG, Brasil. E-mail: taizia.dutra@ufvjm.edu.br

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