The paper describes a new and simple approach for spectrophotometric determination of tricyclic antidepressant drug amitriptyline. Enhancement of the colour intensity of the Fe(III)-SCN? complex on addition of the drug amitriptyline forms the basis of the proposed method. The value of molar absorptivity of the Fe(III)-SCN? amitriptyline ion pair complex in terms of the drug lies in the range of (2.82–3.36) × 103?L·mol?1·cm?1 at the absorption maximum 460?nm. The detection limit of the method was 0.3?μg·mL?1. The slope, intercept, and correlation coefficients for the present method were found to be 0.008, 0.002, and +0.998, respectively. The effect of analytical variables on the determination of the drug and the composition of the complex are discussed in the paper. The method is applicable in the determination of amitriptyline in pharmaceutical preparations. 1. Introduction Amitriptyline [3-(10,11-dihydro-5H-dibenzol[a,d]cyclohept-5-ylidene) propyldimethylamine] constitutes an important class among the neurotherapeutics belonging to first generation of antidepressant drug [1, 2]. Recent studies show proinflammatory cytokine process takes place during clinical depression, mania, and bipolar disorder, and it is possible that symptoms of these conditions are attenuated by the pharmacological effect of antidepressants on the immune system [3–8]. Amitriptyline has a carboxylic structure with an exocyclic double bond at C-5 which is substituted with an N, N-dimethyl-1-propanamino side chain (Figure 1). Figure 1: Amitriptyline. Amitriptyline hydrochloride [AMIYTP]Cl represents a large group of compounds used in treatment of various mental diseases. The chemical structure of this compound is based on the condensed aromatic three-ring system which includes substituents in positions 2 and 10. The difference in chemical structure causes the different pharmaceutical activity of drug. The value of angle of these molecules is important; the more nearly planar the greater the neuroleptic activity. It is believed that drug amitriptyline acts by blocking the receptors of neurotransmitters, noradrenalin, in the synopsis in the central nervous system, which results in an increase of concentration of both molecules with a subsequent enhancement of their antidepressant potency. However, this drug suffers from several drawbacks, such as antiarrhythmic, anticholinergic, cardiovascular, and hyperthermia side effect, which may be reduced if the drugs are suitably vectored to the organism. Various analytical methods have been reported for determination of amitriptyline including
References
[1]
R. J. Baldessarini, “Drugs and the treatment of psychiatric disorders, depression and mania,” in Goodman & Gilman's: The Pharmacological Basis of Therapeutics, J. G. Hardman, L. E. Limbird, P. B. Molinoff, R. W. Ruddon, and A. G. Gilman, Eds., chapter 19, pp. 431–459, McGraw Hill, New York, NY, USA, 9th edition, 1996.
[2]
C. D. Las Cuevas, W. Penate, and E. J. Sanz, “Psychiatric outpatients' self-reported adherence versus psychiatrists' impressions on adherence in affective disorders,” Human Psychopharmacology: Clinical and Experimental, vol. 28, no. 2, pp. 142–150, 2013.
[3]
A. Remlinger-Molenda, P. Wojciak, M. Michalak, and J. Rybakowski, “Activity of selected cytokines in bipolar patients during manic and depressive episodes,” Psychiatria Polska, vol. 46, no. 4, pp. 599–611, 2012.
[4]
S. M. O'Brien, P. Scully, L. V. Scott, and T. G. Dinan, “Cytokine profiles in bipolar affective disorder: focus on acutely ill patients,” Journal of Affective Disorders, vol. 90, no. 2-3, pp. 263–267, 2006.
[5]
E. Obuchowicz, A. Marcinowska, and Z. S. Herman, “Antidepressants and cytokines—Clinical and experimental studies,” Psychiatria Polska, vol. 39, no. 5, pp. 921–936, 2005.
[6]
C.-J. Hong, Y. W.-Y. Yu, T.-J. Chen, and S.-J. Tsai, “Interleukin-6 genetic polymorphism and Chinese major depression,” Neuropsychobiology, vol. 52, no. 4, pp. 202–205, 2005.
[7]
I. J. Elenkov, D. G. Iezzoni, A. Daly, A. G. Harris, and G. P. Chrousos, “Cytokine dysregulation, inflammation and well-being,” NeuroImmunoModulation, vol. 12, no. 5, pp. 255–269, 2005.
[8]
M. Kubera, M. Maes, G. Kenis, Y.-K. Kim, and W. Lasoń, “Effects of serotonin and serotonergic agonists and antagonists on the production of tumor necrosis factor α and interleukin-6,” Psychiatry Research, vol. 134, no. 3, pp. 251–258, 2005.
[9]
F. A. Mohamed, H. A. Mohamed, S. A. Hussein, and S. A. Ahmed, “A validated spectrofluorimetric method for determination of some psychoactive drugs,” Journal of Pharmaceutical and Biomedical Analysis, vol. 39, no. 1-2, pp. 139–146, 2005.
[10]
J. Karpinska and J. Suszynska, “The spectrophotometric simultaneous determination of amitryptyline and chlorpromazine hydrochlorides in their binary mixtures,” Journal of Trace and Microprobe Techniques, vol. 19, no. 3, pp. 355–364, 2001.
[11]
F. A. F. Nour El-Dien, G. G. Mohamed, and N. A. Mohamed, “Spectrophotometric determination of trazodone, amineptine and amitriptyline hydrochlorides through ion-pair formation using methyl orange and bromocresol green reagents,” Spectrochimica Acta Part A, vol. 65, no. 1, pp. 20–26, 2006.
[12]
T. Aman, A. A. Kazi, M. I. Hussain, S. Firdous, and I. U. Khan, “Spectrophotometric determination of amitriptyline-HCl in pure and pharmaceutical preparations,” Analytical Letters, vol. 33, no. 12, pp. 2477–2490, 2000.
[13]
J. O. Onah, “Spectrophotometric determination of amitriptyline by the method of charge-transfer complexation with chloranilic acid,” Global Journal of Pure and Applied Sciences, vol. 11, no. 2, pp. 237–240, 2005.
[14]
D. J. Patel and V. Patel, “Simultaneous estimation of amitriptyline HCl and perphenazine in tablets by UV-Visible spectrophotometric and HPTLC,” International Journal of Pharmaceutical Sciences and Research, vol. 1, no. 2, pp. 20–23, 2010.
[15]
P. Venkatesan, P. V. R. S. Subrahmanyam, and D. Raghu Pratap, “Spectrophotometric determination of pure amitriptyline hydrochloride through ligand exchange on mercuric ion,” International Journal of ChemTech Research, vol. 2, no. 1, pp. 54–56, 2010.
[16]
R. M. El-Nashar, N. T. Abdel Ghani, and A. A. Bioumy, “Flow injection potentiometric determination of amitriptyline hydrochloride,” Microchemical Journal, vol. 78, no. 2, pp. 107–113, 2004.
[17]
D. J. Patel and V. Patel, “simultaneous estimation of amitriptyline hydrochloride and perphenazine by absorption ratio (Q-analysis) UV spectrophotometric method in combined tablet dosage form,” International Journal of Pharmaceutical Sciences and Research, vol. 1, no. 12, pp. 133–137, 2010.
[18]
B. Starczewska and A. Jasińska, “Analytical application of the reactions of amitriptyline with eriochrome cyanine R and pyrocatechol violet,” Acta Poloniae Pharmaceutica, vol. 60, no. 6, pp. 417–423, 2003.
[19]
Y. A. Beltagg, “Colorimetric determination of tricyclic antidepressant and dibenzazepine and dibenz—cycloheptadine with citric acid—acetic anhydride,” Pharmazie, vol. 31, pp. 483–488, 1976.
[20]
W. N. French, F. Matsui, and J. F. Truelove, “Flow-injection spectrophotometric determination of amitriptyline hydrochloride,” Canadian Journal of Pharmaceutical Sciences, vol. 3, no. 3, pp. 33–37, 1968.
[21]
E. Domagalina and L. Przyborowski, “Flow injection extractive spectrophotometric determination of antidepressant amitriptyline hydrochloride,” Chemia Analityczna, vol. 7, pp. 1153–1159, 1962.
[22]
E. M. Elnemma, F. M. El Zawawy, and S. S. M. Hassan, “Determination of amitriptyline, imipramine and orphenadrine in antidepressant drugs by potentiometry, spectrophotometry and atomic absorption spectrometry,” Mikrochimica Acta, vol. 110, no. 1-3, pp. 79–88, 1993.
[23]
B. Dembinski, “Extractive colorimetric determination of amitriptyline and imipramine hydrochloride with bismuth hex iodide,” Acta Poloniae Pharmaceutica, vol. 34, pp. 509–514, 1977.
[24]
H. E. Hamilton, J. E. Wallace, and K. Blumk, “Spectrophotometric and gas-liquid chromatographic determination of amitriptyline,” Analytical Chemistry, vol. 47, no. 7, pp. 1139–1144, 1975.