Spectrophotometric Determination of Thioridazine Hydrochloride in Tablets and Biological Fluids by Ion-Pair and Oxidation Reactions

El-Didamony, Akram; Hafeez, Sameh

doi:https://doi.org/10.1155/2012/840232

Journal of Spectroscopy

On this page

Abstract Introduction Results and Discussion Conclusions References Copyright Related Articles

Open Access

Volume 27 | Article ID 840232 | https://doi.org/10.1155/2012/840232

Spectrophotometric Determination of Thioridazine Hydrochloride in Tablets and Biological Fluids by Ion-Pair and Oxidation Reactions

Akram El-Didamony¹and Sameh Hafeez²

Published03 Jun 2012

Abstract

Two simple, sensitive and selective spectrophotometric methods have been described for the determination of the psychoactive drug, thioridazine HCl in tablets and in biological fluids. The first method is based on the oxidation of thioridazine HCl with measured excess of KMnO₄ under acidic conditions followed by the determination of unreacted oxidant using indigo carmine and methyl orange. The second method is based on the formation of ion-pair complexes with the acidic sulphophthalein dyes such as bromocresol green and bromocresol purple at pH 1.8 of KCl-HCl buffer. The formed complexes were extracted into methylene chloride and their absorbance was measured at 412 nm. Optimizations of the different experimental conditions are described for both methods. The proposed methods were successfully applied for determination of the drug in tablets and biological fluids with good accuracy and precision. Statistical comparison of the results with those obtained by an official method showed good agreement and indicated no significant difference in accuracy and precision.

1. Introduction

Thioridazine hydrochloride (THZ), the hydrochloride of 10-[2-(lmethyl-2-piper-idyl)ethyl]-2-methylthiophenothiazine, is a phenothiazine neuroleptic drug used for the treatment of schizophrenia and other psychiatric disorders [1]. Phenothiazines also possess antiemetic, sedative, antipruritic, antidyskinetic, analgesic, and antihistaminic properties [2]. Thioridazine has been known as one of the most potent phenothiazines which inhibit trypanothione reductase irreversibly and is commonly used as an antipsychotic and antimuscarinic drug to treat behavioral symptoms [3, 4]. Additionally, thioridazine was effective in the treatment of sweating as an antidepressant and sedative drug [5, 6].

Due to the clinical importance of thioridazine hydrochloride, it is significant to establish a simple and sensitive method for its determination in biological fluids. Different pharmacopoeias recommend the determination of thioridazine base or the hydrochloride by titrating the drug in glacial acetic acid and acetic anhydride against perchloric acid. The BP recommends the titration of the drug in acetone solution containing about 7% mercury(II) acetate solution and using methyl orange as indicator [7]. Several analytical methods have been described for determination of thioridazine hydrochloride. Among the methods, UV spectrophotometry and conventional high performance liquid chromatography are most often used [8–11]. Voltammetry [12–14], spectrophotometry [15–19], and chemiluminescence methods have been reported for the determination of thioridazine hydrochloride [20]. Supercritical fluid chromatography [21] and LC combined with other techniques were also reported for determination of thioridazine hydrochloride [22, 23] and their main metabolites or derivatives. Some of these methods lack adequate sensitivity, and some are expensive and time consuming. Therefore, it is important to develop two new simple and sensitive methods for the spectrophotometric determination of THZ. The first method is based on the oxidation of THZ with slight excess of potassium permanganate in acidic medium. The unconsumed of oxidant is then estimated with the decrease in the color intensity of two dyes. The second method is based on the formation of ion-pair complexes of drug with dyestuffs such as bromocresol green (BCG) and bromocresol purple (BCP) and subsequent extraction into methylene chloride. The proposed methods have been successfully applied for the determination of THZ in pharmaceutical formulations and biological fluids.

2. Experimental Section

2.1. Instruments

A spectroscan 80 D double-beam UV/visible spectrophotometer (Biotech Engineering Ltd., UK), with wavelength range 190–1100 nm, spectral bandwidth 2.0 nm with matched 10 mm quartz cells were used for all the absorbance spectral measurements.

2.2. Reagents and Materials

All chemicals used were of an analytical reagent grade and solutions were made in distilled water.(i)Indigo carmine (IC). A 5 × 10⁻³M of indigo carmine (Aldrich) was prepared by dissolving of an accurate weight dye (99% purity) in water and diluting to 100 mL in a calibrated flask.(ii)Methyl orange (MO). A 5 × 10⁻⁴M of methyl orange was prepared by dissolving an accurate weight of dye in least amount of water and completed to the mark in a 100 mL calibrated flask.(iii)Potassium permanganate. A stock solution of 1.0 × 10⁻³M KMnO₄ (Aldrich) was prepared by dissolving an accurate weight in 10 mL of warm distilled water, then completed to the mark in a 100 mL calibrated flask, and standardized using sodium oxalate. A 2.0 M H₂SO₄ was prepared.(iv)Sulfophthalein dyes. Solutions of 5 × 10⁻⁴M bromocresol green and bromocresol purple (Aldrich product) were prepared by dissolving an accurately weight of the acid dyes in a few drops of acetone and then diluted to the mark with distilled water in a 100 mL calibrated flasks separately.(v)Thioridazine hydrochloride (THZ). Pharmaceutical grade thioridazine hydrochloride was received as a gift from Delta Pharm Company, 10th of Ramadan, Egypt; it was reported to be 99.8% pure and was used as received. A stock standard solution equivalent to 10 mg of THZ was prepared by dissolving an accurately weighed amount of pure drug in distilled water. The solution of THZ was diluted stepwise to obtain working concentration of 100 μg/mL. The standard solutions were kept in amber-colored bottles and stored in a refrigerator when not in use.

2.3. Recommended Procedures and Calibration Curves

2.3.1. Oxidation Reaction

Varying aliquots (0.1–0.7 mL) of the standard 100 μg/mL THZ solution were transferred into a series of 25 mL calibrated flasks by means of a microburette. To each flask, 2.0 mL of 2.0 M H₂SO₄ and 1.2 mL of 1.0 × 10⁻³M KMnO₄ solution were added. The content was mixed well and the flasks were kept aside for 20 min, at room temperature with intermittent shaking. Finally, 1.1 mL of 5 × 10⁻³M of IC and 1.4 mL of 5.0 × 10⁻⁴M of MO solution were added to each flask and the volume was diluted to the mark with water and mixed well. The absorbance was measured against a reagent blank at 610 nm and 508 nm, respectively. In both methods, a standard graph was prepared by plotting the absorbance versus the concentration of THZ. The unknown concentration was read from the calibration graph or computed from the regression equation derived using Beer’s law data.

2.3.2. Ion-Pair Reaction

Suitable aliquots of the stock solution of THZ (4–24 μg) for both BCG and BCP methods were transferred into separate glass-stopper tubes. Then, 2.0 mL KCl + HCl buffer of pH 1.8 and 2.0 mL of 5 × 10⁻⁴M BCG or BCP were added and mixed. The contents were extracted with 10 mL methylene chloride by shaking for 2.0 min and the organic layer was dried over anhydrous sodium sulphate. The absorbance of the yellow-colored complexes was measured at 412 nm for both BCG and BCP, against a methylene chloride. In both methods, a standard graph was prepared by plotting the absorbance versus the concentration of THZ.

2.4. Procedure for Pharmaceutical Preparations

At least twenty of THZ tablets (Thiozine tablets, Delta Pharm Company, Cairo, Egypt, are labeled to contain 25 mg of thioridazine HCl per tablet) were weighed to obtain the mean tablet weight and then ground to a homogenized powder. A quantity of the powdered tablets equivalent to 30 mg was transferred into a 100 mL calibrated flask and dissolved in distilled water and filtered. A suitable amount of filtrate was taken and analyzed as described under recommended procedures. For the proposed methods, the content of a tablet was calculated using the corresponding regression equation of the appropriate calibration graph.

2.5. Procedure for Spiked Urine and Serum

The proposed methods were applied to the determination of THZ in spiked urine and serum provided from several healthy volunteers. Spiked urine was 50-fold diluted with distilled water. A 10 mL of serum sample was deproteinized by adding 5 mL of acetonitrile in a centrifuge for 5 min at 1000 rpm. The supernatant was used to investigate recovery. Add an aliquot of standard aqueous solution of THZ to 1.0 mL of diluted urine or serum. The analysis was completed as in the recommended procedures. A blank value was determined by treating THZ-free urine and THZ-free serum in the same way. The absolute recovery was determined for THZ by comparing the representative absorbance of the treated urine or serum samples with the absorbance of the standard drug at the same concentration.

3. Results and Discussion

Optimization of Variables
The optimum conditions for the assay procedures have been established by studying the reactions as a function of reaction time, concentration of reagents, and stability of the colored species, buffer and pH. Such variables were changed individually while the others were kept constant.

3.1. Oxidation Reaction

In the present method, two dyes indigo carmine and methyl orange have been used for the determination of THZ (Figure 1). The determinations of THZ are indirect and are based on the determination of surplus KMnO₄ after the oxidation reaction of THZ by KMnO₄, [24, 25]. The drug undergoes oxidation according to the reaction scheme given in Scheme 1.

3.1.1. Effects of Temperature and Reaction Time

Keeping other conditions constant, the effect of temperature on the oxidation product was studied. The reaction between THZ and KMnO₄ was found to be instantaneous. However, the reaction is complete within 15 min at room temperature (25 ± 2°C), but 20 min was sufficient to get maximum intensity. Therefore, 20 min at room temperature have been selected for further experiments.

3.1.2. Effect of Acid Concentration

Preliminary investigation showed that sulphuric acid was the medium of choice for the oxidation of THZ by KMnO₄. Two milliliters of 2.0 M H₂SO₄ were ideal for the oxidation step in both methods and the same quantity of acid was employed for the estimation of the dye. It was found that the maximum color was developed within 20 min and remained almost stable for about 24 h.

3.1.3. Effect of Oxidant Concentration

The effect of oxidant concentration was studied by adding different volumes of 1 × 10⁻³M of KMnO₄ solution to a constant amount of THZ (2.4 μg/mL). It was observed that the maximum color intensity was obtained with 1.2 mL of KMnO₄, after which further increase in volume resulted in a decrease of absorbance. Thus, 1.2 mL of KMnO₄ was sufficient to reach with the maximum drug concentration in the Beer’s range.

3.1.4. Effect of Dye Concentration

The effect of the dyeconcentration on the intensity of the color developed at the selected wavelengths was studied separately by measuring the absorbance’s of final solutions resulting from reaction mixtures containing a fixed concentration of THZ (2.4 μg/mL) and various amounts of dyes (0.5–5 mL). The use of 1.1 mL of 5 × 10⁻³M IC and 2.8 mL 5 × 10⁻⁴M of MO was found to be necessary to produce constant absorbance values. The use of excess of reagent produced no further increase in absorbance.

3.2. Ion-Pair Reaction

Extractive spectrophotometric procedures due to their sensitivity are widely used in the assay of drugs and, hence, ion-pair extractive spectrophotometry has received a considerable attention for the quantitative determination of many pharmaceutical compounds [26–31]. THZ reacts with BCG and BCP in an acidic buffer to give methylene chloride soluble ion-pair complexes, which exhibit absorption maxima at 412 nm for BCG and BCP, (Figure 1). Under the experimental conditions, the reagents blank showed negligible absorbance thereby permitting good analytical conditions for the quantitative determination of THZ.

3.2.1. Effect of Buffer and pH

Optimum reaction conditions for the quantitative determination of ion-pair complexes were established via a number of preliminary experiments. It was observed that the effective extraction of the complex depended on the type of buffer used and its pH. The effect of pH was studied by extracting the colored complexes in presence of various buffers namely, KCl-HCl (pH = 1.0–2.2), potassium hydrogen phthalate-HCl (pH = 2.2–3.6), NaOAc-HCl (pH = 1.99–4.92), and NaOAc-AcOH (pH = 3.72–5.57). It was noticed that the maximum color intensity and constant absorbances were observed in KCl-HCl buffer (Clark and Lubs) of pH 1.8 for both dyes. Hence, Clark and Lubs buffer of pH 1.8 was used for all subsequent measurements in both methods. Further, 2.0 mL of KCl-HCl buffer of pH 1.8 for both BCG and BCP gave maximum absorbances and reproducible results.

3.2.2. Choice of Organic Solvent

A number of organic solvents such as chloroform, dichloromethane, carbon tetrachloride, benzene, and toluene were examined for extraction of the ion-pair complexes in order to provide an applicable extraction procedure. Although dichloromethane is not an ecologically friendly solvent, it was preferred for its selective extraction for ion-pair complexes due to the greater stability of the extracted ion pair and considerably lower extraction abilities of the reagent blank. The study reveals that a volume ratio of 1 : 1 (aqueous : organic) was the most suitable for ion-pair extraction.

3.2.3. Effect of Time and Temperature

The effect of temperature on the colored ion associates was studied at different temperatures. It was found that the colored ion associates were stable up to 30°C. Higher temperatures were not suitable due to the volatile nature of methylene chloride. The resulting ion associates were found to be stable up to 24 h at room temperature. Complete color intensity was attained after 2.0 min of mixing for all complexes.

3.2.4. Effect of Dyes Concentration

The effect of dyes’ concentrations were studied separately by measuring the absorbance’s of final solutions resulting from reaction mixtures containing a fixed concentration of THZ and various amounts of the dyestuff. Maximum color intensity of the complex was achieved with 2.0 mL of 5 × 10⁻⁴M of BCG or BCP. Although a larger volume of the reagent had no pronounced effect on the complex formation, the absorbance’s increased slightly due to background of the colored reagent.

3.2.5. Effect of Sequence and Time of Shaking

The most favorable sequence was drug-buffer-dye-solvent for the production of the highest color intensity and the shortest time for developing maximum absorbance, while the other sequences require longer time and produce lower absorbance values. The time of shaking for extraction of ion-pair complexes was studied and found that the absorbance of the extract remains constant between 0.5–5.0 min. Thus, 2.0 min shaking time was utilized as an optimum value throughout the experiment. The ion-pair complexes were quantitatively recovered in one extraction only.

3.2.6. Stoichiometric Relationship

The stoichiometric ratio of the formed products was investigated by Job’s continuous variation method [31]. A 1 × 10^{− 4}M solution of THZ was used with comparable solutions of the reagent (BCG or BCP). For each method, a series of solutions was prepared in which the total volume of the drug and reagents was kept at 2.0 mL, and the procedure was completed as described under general procedures. The application of Job’s continuous variation method indicated 1 : 1 ratio for the drug with each reagent.

3.3. Analytical Data

The calibration graphs were constructed for the two methods under the optimum conditions described above. The molar absorptivity, concentration range, regression equation, and correlation coefficient are tabulated in Table 1. A linear relationship was found between the absorbance at λ_max and the concentration of the drug in the range 0.4–3.2 μg/mL for oxidation method and 4–32 μg/mL for ion-pair method. Regression analysis of the Beer’s law plotted at λ_max reveals a good correlation ( = 0.9972–0.9993). The graphs showed a negligible intercept, which was calculated by the least squares method’s regression equation. The relative sensitivities of the reagents can be determined by comparing the molar absorptivities of the complexes.

3.4. Accuracy and Precision

The interday repeatability of the proposed methods was studied by performing five independent analyses of THZ in pure form at three different concentration levels on six consecutive days (Table 2). The intraday reproducibility of the proposed method was determined by measuring the drug at three concentration levels within one day five times (Table 2). The reagent solutions were prepared freshly and analyzed as described under recommended procedures and calibration graphs. Data of Table 2 show that within day the relative standard deviations are less than 1.8% and interday relative standard deviations are not exceeding 2.17%, which indicates that the proposed methods are highly reproducible.

3.5. Analytical Applications

3.5.1. Analysis of Tablets

The proposed methods were successfully applied to the determination of THZ in representative tablets and the results are summarized in Table 3. For the brands/doses examined, the methods gave results which were in agreement with the declared content. The performance of the proposed methods was judged by calculating the student t- and F-values. At 95% confidence level, the calculated t- and F-values did not exceed the theoretical values as evident from Table 3. Hence, it was concluded that there is no significant difference between the proposed and official methods [7] with respect to accuracy and precision. Moreover, to check the validity of the proposed methods, we applied the standard addition method by adding THZ to the previously analyzed tablets. The recovery of THZ was calculated by comparing the concentration obtained from the spiked mixtures with those of the pure drug and the recoveries of added quantity were found to be more than 96.29%. This indicates that there is no interference from any excipients, which are present in tablets. These results are given in Table 4.

3.5.2. Analysis of Human Samples

Phenothiazines are used as antipsychotic drugs and as reagents to determine the Hb in biological fluids and tissues, but over dosage can cause death, so the quantitative assessment of added thioridazine in serum and urine of healthy human beings is also determined as shown in Table 5. High accuracy and good recovery are obtained, which indicate that the proposed methods can be successfully applied to recover thioridazine in human samples.

3.6. Interference Study

The commonly used excipients and additives which often accompany THZ in its dosage forms, such as (starch, lactose, glucose, sugar, talc, sodium chloride, and magnesium stearate) was studied. The results indicated that there is no interference from the degradation, indicating a high selectivity for determining the studied THZ in its dosage forms.

3.7. Robustness

The robustness of the proposed method was evaluated by using the different instruments by two different analysts under the same optimized conditions. The obtained results were found to be reproducible, since there was no significant difference between the results obtained by the two analysts. Thus, the proposed methods could be considered robust.

4. Conclusions

The data given above reveal that the proposed methods are simple, selective, accurate, and sensitive (oxidation method > ion-pair method) with good preciseness and accuracy. Thus, the proposed methods can be used as alternative methods to reported ones for the routine determination of THZ in pharmaceutical preparations and in biological fluids depending upon the availability of chemicals and the nature of other ingredients present in the sample.

References

E. Z. Abdel-Moety, K. A. Al-Rashood, and k. Florey, Analytical Profiles of Drug Substances, vol. 18, Academic Press, New York, NY, USA, 1988.
M. Gordon, Psychopharmacological Agents, Academic Press, New York, NY, USA, 1964.
J. Gutierrez-Correa, A. H. Fairlamb, and A. O. Stoppani, “Trypanosoma cruzi trypanothione reductase is inactivated by peroxidase-generated phenothiazine cationic radicals,” Free Radical Research, vol. 34, no. 4, pp. 363–378, 2001.
View at: Google Scholar
R. M. Condren and C. Cooney, “Use of drugs by old age psychiatrists in the treatment of psychotic and behavioural symptoms in patients with dementia,” Aging and Mental Health, vol. 5, no. 3, pp. 235–241, 2001.
View at: Publisher Site | Google Scholar
J. Cowap and J. Hardy, “Thioridazine in the management of cancer-related sweating,” Journal of Pain and Symptom Management, vol. 15, no. 5, p. 266, 1998.
View at: Google Scholar
S. Q. Abbas, “Use of thioridazine in palliative care patients with troublesome sweating,” Journal of Pain and Symptom Management, vol. 27, no. 3, pp. 194–195, 2004.
View at: Google Scholar
Stationery Office, British Pharmacopoeia, The Pharmceutical Press, London, UK, 1993.
J. Karpińska, B. Starczewska, and H. Puzanowska-Tarasiewicz, “Analytical properties of 2- and 10-disubstituted phenothiazine derivatives,” Analytical Sciences, vol. 12, no. 2, pp. 161–170, 1996.
View at: Google Scholar
C. B. Eap, L. Koeb, K. Powell, and P. Baumann, “Determination of the enantiomers of thioridazine, thioridazine 2-sulfone, and of the isomeric pairs of thioridazine 2-sulfoxide and thioridazine 5-sulfoxide in human plasma,” Journal of Chromatography B, vol. 669, no. 2, pp. 271–279, 1995.
View at: Publisher Site | Google Scholar
W. J. Allender, “High-preβure liquid chromatographic determination of thioridazine and its major metabolites in biological tiβues and fluids,” Journal of Chromatography, vol. 23, p. 541, 1985.
View at: Google Scholar
A. C. Mehta, “High-performance liquid chromatographic determination of chlorpromazine and thioridazine hydrochlorides in pharmaceutical formulations,” The Analyst, vol. 106, no. 1267, pp. 1119–1122, 1981.
View at: Google Scholar
S. Shahrokhian, M. Ghalkhani, M. Adeli, and M. K. Amini, “Multi-walled carbon nanotubes with immobilised cobalt nanoparticle for modification of glassy carbon electrode: application to sensitive voltammetric determination of thioridazine,” Biosensors and Bioelectronics, vol. 24, no. 11, pp. 3235–3241, 2009.
View at: Publisher Site | Google Scholar
I. Biryol and S. Dermiş, “Voltammetric determination of Thioridazine hydrochloride,” Turkish Journal of Chemistry, vol. 22, no. 4, pp. 325–333, 1998.
View at: Google Scholar
N. Zimova, I. Nemec, and J. Zima, “Determination of chlorpromazine and thioridazine by differential pulse voltammetry in acetonitrile medium,” Talanta, vol. 33, pp. 467–470, 1986.
View at: Google Scholar
K. Basavaiah and G. Krishnamurthy, “Spectrophotometric determination of some phenothiazine drugs acting on the central nervous system using hexacyanoferrate(III),” Annali di Chimica, vol. 89, no. 7-8, pp. 623–629, 1999.
View at: Google Scholar
J. Karpinska, W. Misiuk, and H. Puzanowska-Tarasiewicz, “Flow injection spectrophotometric detérmination of promazine hydrochloride and thoridazine hydrochloride,” Indian Journal of Chemistry, vol. 37, no. 12, pp. 1135–1139, 1998.
View at: Google Scholar
M. Tarasiewicz, E. Wołyniec, and H. Puzanowska-Tarasiewicz, “Analytical application of the reactions of 2,10-disubstituted phenothiazines with organic substances,” Pharmazie, vol. 53, no. 3, pp. 151–155, 1998.
View at: Google Scholar
M. Tarasiewicz and L. KuŸmicka, “Extractive spectrophotometric determinations of some phenothiazines with picric and flavianic acids,” Analytical Letters, vol. 29, no. 6, pp. 929–936, 1996.
View at: Google Scholar
J. B. Raj and H. S. Gowda, “Thioridazine hydrochloride as a new reagent for the spectrophotometric determination of chromium,” The Analyst, vol. 120, no. 6, pp. 1815–1817, 1995.
View at: Google Scholar
A. Kojlo, J. Michalowski, and E. Wolyniec, “Chemiluminescence determination of thioridazine hydrochloride by flow- injection analysis,” Journal of Pharmaceutical and Biomedical Analysis, vol. 22, no. 1, pp. 85–91, 2000.
View at: Publisher Site | Google Scholar
F. Geiser, M. Schultz, L. Betz, M. Shaimi, J. Lee, and W. Champion, “Direct, preparative enantioselective chromatography of propranolol hydrochloride and thioridazine hydrochloride using carbon dioxide-based mobile phases,” Journal of Chromatography A, vol. 865, no. 1-2, pp. 227–233, 1999.
View at: Publisher Site | Google Scholar
T. N. Decaestecker, S. R. V. Casteele, P. E. Wallemacq, C. H. Van Peteghem, D. L. Defore, and J. F. Van Bocxlaer, “Information-dependent acquisition-mediated LC-MS/MS screening procedure with semiquantitative potential,” Analytical Chemistry, vol. 76, no. 21, pp. 6365–6373, 2004.
View at: Publisher Site | Google Scholar
H. Hayen and U. Karst, “Analysis of phenothiazine and its derivatives using LC/electrochemistry/MS and LC/electrochemistry/fluorescence,” Analytical Chemistry, vol. 75, no. 18, pp. 4833–4840, 2003.
View at: Publisher Site | Google Scholar
J. Karpinska and B. Starczewska, “Simultaneous LC determination of some antidepressants combined with neuroleptics,” Journal of Pharmaceutical and Biomedical Analysis, vol. 29, no. 3, pp. 519–525, 2002.
View at: Publisher Site | Google Scholar
A. R. Katritzky and A. J. Boulton, Advances in Heterocyclic Chemistry, vol. 9, Academic Press, New York, NY, USA, 1968.
A. M. El-Didamony, “Extractive spectrophotometric methods for the determination of oxomemazine hydrochloride in bulk and pharmaceutical formulations using bromocresol green, bromocresol purple and bromophenol blue,” Archiv der Pharmazie, vol. 338, no. 4, pp. 190–197, 2005.
View at: Publisher Site | Google Scholar
Z. A. El Sherif, A. O. Mohamed, M. I. Walash, and F. M. Tarras, “Spectrophotometric determination of loperamide hydrochloride by acid-dye and charge-transfer complexation methods in the presence of its degradation products,” Journal of Pharmaceutical and Biomedical Analysis, vol. 22, no. 1, pp. 13–23, 2000.
View at: Publisher Site | Google Scholar
S. Çağlar and A. Önal, “Two simple and rapid spectrophotometric methods for the determination of a new antihypertensive drug olmesartan in tablets,” Journal of Analytical Chemistry, vol. 65, no. 3, pp. 239–243, 2010.
View at: Publisher Site | Google Scholar
A. S. Amin, H. A. Dessouki, M. M. Moustafa, and M. S. Ghoname, “Spectrophotometric methods for sertraline hydrochloride and/or clidinium bromide determination in bulk and pharmaceutical preparations,” Chemical Papers, vol. 63, no. 6, pp. 716–722, 2009.
View at: Publisher Site | Google Scholar
A. M. El-Didamony and M. A. Moustafa, “Spectrophotometric determination of diphenhydramine hydrochloride in pharmaceutical preparations and biological fluids via ion-pair formation,” Arabian Journal of Chemistry, vol. 3, no. 4, pp. 265–270, 2010.
View at: Publisher Site | Google Scholar
P. Job, “Formation and stability of inorganic complexes in solution,” Annali di Chimica, vol. 9, pp. 113–203, 1928.
View at: Google Scholar

Copyright

Copyright © 2012 Akram El-Didamony and Sameh Hafeez. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

2995

Downloads

1922

Citations