Document Type

Article

Publication Date

1-1-2011

Abstract

This paper reports a new and simple flow injection analysis with chemiluminescence (CL) system for determination of quercetin through the reverse flow injection technique. The method was based on the inhibition of the CL of H 2O 2-luminal-permanganate with quercetin. The reverse flow was used to avoid continuous monitors of CL which leads to unstable baseline. Various parameters associated with this flow system were studied and essential optimizations were carried out. Two calibration graphs were constructed for determination of quercetin in the range (6.0-12 μg/ml) with correlation coefficient (0.9994) for low concentration level and (20-190 μg/ml) with correlation coefficient (0.9962) for high concentration and a sampling frequency 80 samples/h. Possible interferences were studied and the results showed that the interferences caused less than 5 error. The method was applied successfully for the determination of quercetin in various natural products.

Keywords

Chemiluminescence, Flavonoids, Flow injection analysis, Natural products, Quercetin, hydrogen peroxide, permanganate potassium, analytic method, calibration, chemoluminescence, cherry, concentration process, controlled study, drug determination, drug structure, measurement error, onion, process monitoring, quantitative analysis, reaction optimization, reverse flow injection analysis with chemoluminescence method, review, tea.

Divisions

fac_eng

Publication Title

Der Pharma Chemica

Volume

3

Issue

2

Publisher

Der Pharma Chemica

Additional Information

Export Date: 5 March 2013 Source: Scopus Language of Original Document: English Correspondence Address: Hussain, M.A.; Salahaddin University, Science College, Chemistry DepartmentIraq Chemicals/CAS: hydrogen peroxide, 7722-84-1; permanganate potassium, 7722-64-7; quercetin, 117-39-5 References: Hetrog, M.L.G., Hollman, P.C.H., Katan, M.B., (1992) J. Agric. Food Chem, 40, pp. 2379-2383; Cook, N.C., Samman, S., (1996) J. Nutr. Biochem, 7, pp. 66-76; Ross, J.A., Kasum, C.M., (2002) Annu. Rev. Nutr., 22, pp. 19-34; Leite, J.P.V., Rastrelli, L., Romussi, G., Oliveira, A.B., Vilegas, J.H.Y., Pizza, C., (2001) J. Agric. Food Chem., 49 (8), pp. 3796-3801; Li, W.K., Fitzloff, J.F., (2001) J. Chromatogr. B: Biomed. Appl., 765 (1), pp. 99-105; Sun, L., Meng, L., Chen, J., Hu, R., Jia, D.Z., (2001) Sepu., 19 (5), pp. 395-397; Baranowska, I., Rarog, D., (2001) Talanta, 55 (1), pp. 209-212; Kuntic, V., Blagojevic, S., Malesev, D., Radovic, Z., Bogavac, M., (1998) Monatsh. Chem., 129, pp. 41-48; Pejic, N., Kuntic, V., Malesev, D., (2001) Pharmazie, 56 (3), pp. 216-217; Cui, H., He, C., Zhao, G., (1999) J. Chromatogr., 855 (1), p. 3; Agnes, D., Blum, L.J., (2000) J. Medicin and Biochemistry, 4 (1), p. 32; Vogel, A., (1979) Text book of macro and semimicro qualitative inorganic analysis, p. 365. , 5th edition, London; Harborne, J.B., (1973) Phytochemical Methods, p. 59. , first edition, London

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