Determination of Dihydroartemisinin In Bulk And Pharmaceutical Formulations By Redox Titrations And UV – Spectrophotometry Using Potassium Permanganate As Oxidimetric Reagent
Main Article Content
Abstract
Two new methods are proposed for the determination of dihydroartemisinin (DHA) in bulk and pharmaceutical formulations. Method A Titrimetry, based on the redox reaction of DHA and potassium permanganate in acid medium. Method B, UV-Spectrophotometry based on the redox reaction of DHA and potassium permanganate in acid medium giving a product which absorbs UV light at 520nm. In both methods the amount of potassium permanganate used is proportional to the amount of DHA. Experimental conditions for good linearity, sensitivity, specificity accuracy and precision were optimized. In method A (titrimetry) the calculations are based on a 2:5 (DHA: KMnO4) reaction stoichiometry) and this method is applicable over the practical range of 5.0 – 20mgml-1. Method B obeys Beer’s law. The calibration curve generated is linear with correlation
coefficient of (r) of 0.9998 (n = 10). The molar absoptivity is 2.27 x103 Lmol cm-1 and sandell sensitivity of 0.126?gcm-2 The limit of detection (LOD) and limit of quantification (LOQ) were determined as per the current ICH guidelines and found to be 0.88 and 2.66?gml-1 respectively. Accuracy and precision of both method were determined using intra and inter day variations at three different concentration level of DHA the relative standard deviation (RSD %) were <2.00 and <2.5 respectively. The two methods were used to assay DHA in 4 brands of tablets formulation procured locally in Uyo. South-South, Nigeria at three different concentration level, t and F value of <2.40 and <3.0 at 95% confidence level and 5 degree of freedom. These values are lower than tabulated t and F values. The methods were statistically compared with an official method with congruent results. There was no interference from common pharmaceutical excipients. Recovery study was also performed
via standard addition procedure with excellent recoveries.
Downloads
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
References
McMichael, A. J; Woodruff, R. E., Hales, S., Climate Change and human Health. Present and future Risks. Lancet 2006 367 (9513),
-869.
a. Flassa, S., Muller, O. Possible effects of climatic changes on speed of malaria Tropica. Results of a Strategical Simulation.
Gesundaeitswesen 2005, 67, 492-497.
b. Khasous, A. A., Nettleman, M. D. Global warming and infections Disease. Arch. Med. Res 2005, 36, 689-696.
World Health Organization. The World Malaria Report, World Health Organization: Geneva Switzerland, 2008.
O’Niel, P. M., Barton, V. E. and Ward S. A. (2010). The molecular mechanism of Action of Artemisinin – The Debate Continues. J.
Molecules. J. Molecules 2010, 15, 1705 – 1721.
Meshnick S. R., Taylor T. E., and Kamchonwong Paisan (1996). Artemisinin and the Artimalarial Endopeoxides, from Herbal Remedy to Targeted Chemotherapy. Microbiological Reviews. Journals of American Society of Microbiology pg. 301-315.
Srivastara, M., Singh, H., and Naik P (2010) Molecular modeling Evaluation of the Antimalarial Activity of Artemisinin Analogue:
Molecular Docking and Rescoring using Prime/MM-GBSA Approach. Current Research J of Biological Sciences 2(2):83 – 102.
Dorndorp A. M., Nosten F, Y; Pm Das D, Plyo A. P., et al Artemisinin resistance in plasmodium flaciparum malaria (2009) N. Engl J. Med. 2009, 361: 455-467.
Noedl H., Se Y, Schaecher K, Smith B. L., Socheat D., Fulcuda M. M. (2008) Artmisinin resistance in Western Cambodia. N. Engle J. Med. 2008, 359 -2619-2620
WHO-GMP. Update on artemisinin resistance September 2011 http://www.who.int/malaria/update092011.ref
Atemnkeng, M. A., Decock K. U., and Plaizier – vercammen (2007) Tropical medicine and international health. Vol 12, No.1, pp 68-74. Jan 2007.
Newton P. N., Doudorp et al (2003) Counterfeit artesinate antimalarials in South East Asia. Lancet 362 (9378): 169
Agarawal S. P, Ali A. Yashomati D. Ahuja S. (2009) Indian Journal of Pharmaceutical Research. Vol. 1, 71 , Pg 98 – 100.
Teja – Isavadharm P., Siriyanouda D., Siripokasupkul R., Apinan R., et al (2010) Journal molecules 2010 15, 8747 – 8768; doi: 10.3390/Molécules 15 128747.
Dhust A. Augustijins P. Arens S., Van L., et al (1996) Journal of Chromatographic Science, Vol 34 1996
Gabriels M., Plaizer – Vercammen J. (2004) Development or a reverse T. Chromatograph Phase thin layer chromatographic method
for arteminisinin and it derivatives. Science 2004 Aug, 42 (7): 341-7.
Newton P. N.,Dondorp et al (2003) Counterfeit Artesunate Antimalarials in South East.Lancet 362(9378):169.
Green M. D., Mount D. L., et al (2001). Authentication of artemether, artesunate and dihydroartemisinin antimalarial tablets using
a simple colorimeter method. Tropical medicine and international health, TM & IH 6(12): 980 – 982.
Cornors, K. A. (1982) A textbook of Pharmaceutical analysis. 3rd Edition. Wiley – International Publication, New York.
Mendham, J., Denny, B C., Thomas, M (2000).Redox Titrations. Textbook of Quantitative Analysis. 6th Edition pp 328 – 380. Pearson Education Pvt. India.
Olaniyi A. and Ogunbamila F. O. (1991) Experimental Pharmaceutical Chemistry. Shaneson C. I. Limited, Eleyele, Ibadan,
Nigeria.
Basavaiah K. Rajendraprasad N., Tharpa K. et al (2009) J. Mex. Chem Soc. 2009, 53 (1) 34 – 40. Sociedad Quimica de Mexico.
Gouda A., A., El-sheikh R., El Shafey et al Spectrophotometric determination of Pipazetharte HCl and Dextromethorphan
HBr using potassium permanganate International Journal of Biomedical Science Dec 2008 Vol4 No.4.
Abdulatef, H. E. (2002). Journal of Pharm. Biomed. Analysis. 29,8:35.
Reddy,M.N., Vijaya, V.P.N., Reddy,P,J.C., Murthy, T.k., Srinvasa, Y,(2002) The Antiseptic:99:88.