Abstract
Aluminium comprises about 8% of earth's crust so there is possibility that aluminium can contaminate the natural resources, with references to previous researches on determination of aluminium, we developed a simple, rapid, and economic colorimetric method for the detection of aluminium from various sources. Aluminium has an electric charge and a small ionic radius of about 0.51Å, conferring upon it strong polarizing capabilities. Standard reduction potential for reacting Al+3 is -1.67 V. This high electronegativity makes aluminium highly reactive. 8-hydroxyquinoline-5-sulphonic acid has been used for chelation and subsequent determination of aluminium content from samples. It is a light-yellow coloured compound and is a derivative of heterocyclic quinoline substituted with the hydroxyl group on carbon number 8 and sulphonic acid group at carbon number 5. Sulfonic acid improves the solubility of the molecule and of the corresponding fluorescent complexes in polar solvents. Aluminium readily complexes with 8-hydroxyquinoline-5-sulphonic acid in acidic buffer and remains stable for 30 mins. The maximum absorbance of aluminium and 8-hydroxyquinoline-5-sulphonic acid complex was determined using UV spectro-photometry at 359 nm. Concentration of aluminium in the sample was found to be linear within the range of 1.2-2.8 mM with acceptable precision and accuracy, as per guidelines. The developed method was validated according to ICH (Q2R1) guidelines. The developed method was used to assess the aluminium content in a marketed antacid formulation. The recovered aluminium content was within the industrial acceptance limit. The developed method is thus effective for accurate determination of aluminium from marketed samples.
References
Organization, W. H., Aluminium in drinking-water: Background document for development of WHO guidelines for drinking-water quality. 2003
Ogimoto, M.; Suzuki, K.; Haneishi, N.; Kikuchi, Y.; Takanashi, M.; Tomioka, N.; Uematsu, Y.; Monma, K., Aluminium content of foods originating from aluminium-containing food additives. Food Additives & Contaminants: Part B 2016,9 (3), 185-190.
Bache, B., Aluminium mobilization in soils and waters. Journal of the Geological Society 1986,143 (4), 699-706.
Reinke, C. M.; Breitkreutz, J.; Leuenberger, H., Aluminium in over-the-counter drugs. Drug Safety 2003,26 (14), 1011-1025.
Kawahara, M.; Muramoto, K.; Kobayashi, K.; Mori, H.; Kuroda, Y., Aluminium Promotes the Aggregation of Alzheimer? s Amyloid β-Protein in Vitro. Biochemical and biophysical research communications 1994,198 (2), 531-535.
Ogawa, M.; Kayama, F., A study of the association between urinary aluminium concentration and pre-clinical findings among aluminium-handling and non-handling workers. Journal of Occupational Medicine and Toxicology 2015,10 (1), 13.
Zanjanchi, M.; Noei, H.; Moghimi, M., Rapid determination of aluminum by UV-vis diffuse reflectance spectroscopy with application of suitable adsorbents. Talanta2006,70 (5), 933-939.
Zanjanchi, M.; Noei, H.; Moghimi, M., Rapid determination of aluminium by UV-vis diffuse reflectance spectroscopy with application of suitable adsorbents. Talanta2006,70 (5), 933-939.
Kefala, G.; Economou, A.; Sofoniou, M., Determination of trace aluminium by adsorptive stripping voltammetry on a preplated bismuth-film electrode in the presence of cupferron. Talanta2006,68 (3), 1013-1019.
Hejri, O.; Bzorgzadeh, E.; Soleimani, M.; Mazaheri, R., Determination of trace aluminium with eriochrome cyanineafter cloud point extraction. World Applied Sciences Journals 2011,15, 218-222.
Memon, N.; Bhanger, M., Micellar liquid chromatographic determination of aluminium as its complex with 8-hydroxyquinoline-5-sulfonic acid. Acta Chromatographica2004,14, 172-179.
Lian, H.; Huang, Q.; Kang, Y.; Zou, G.; Bi, S.; Tian, L. C., Extraction with Toluene and HPLC Determination of Aluminium in the Form of an 8?Hydroxyquinoline Derivative. Journal of liquid chromatography & related technologies 2003,26 (2), 273-283.
Guideline, I.H.T.,Validation of analytical procedure; text and methodology, Q2 (R1), 2005. 1.
Huber, L., Validation of analytical methods. Agilent Technologies. Germany 2010.
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