Synthesis, Characterization and Staining Ability of Novel Azo Dye Based on Curcumin and Its Au(III) Complex

https://doi.org/10.22146/ijc.84388

Wesam Dheyab Kzar(1), Hasan Shamran Mohammed(2*), Fatimah Swadi Zghair(3), Zahia Zizi(4)

(1) College of Science, Al-Qadissiya University, Al-Diwaniyah 58002, Iraq
(2) College of Science, Al-Qadissiya University, Al-Diwaniyah 58002, Iraq
(3) College of Veterinary Medicine, Al-Qadissiya University, Al-Diwaniyah 58001, Iraq
(4) Laboratory of Advanced Materials and Physicochemistry for Environment and Health, Djillali Liabes University of Sidi Bel Abbes, Sidi Bel Abbès 89, Algeria
(*) Corresponding Author

Abstract


Azo dye ligand (HMDA), namely N-(4-((E)-((1E,6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)-3,5-dioxohepta-1,6-dien-4-yl)diazenyl)phenyl)acetamide was prepared by coupling diazonium salt of 4-aminoacetanilide with curcumin in basic conditions. The HMDA ligand and its Au(III) complex were characterized by elemental analysis, mass spectroscopy, 1H-NMR, FTIR, UV-visible spectra, and molar conductivity. The molar ratio method was applied to ascertain the stoichiometric composition of the Au(III) complex in aqueous solution, which was 1:2 (metal ion to ligand). HMDA ligand binding with Au(III) ion used the enolate form moiety of curcumin under alkaline conditions which was observed by infrared spectra and investigated by elemental analysis and 1H-NMR. HMDA and its Au(III) complex have been evaluated as stains for intestine, pancreas and kidney tissues of mice and exhibited important contrast. Both compounds showed the most potent staining activity toward blood cells, collagen, muscle fibers and cytoplasm in the selected tissues of mice. This azo dye and its complex of Au(III) succeeded in dyeing mice tissues, compared with the conventional stains.


Keywords


Curcumin, azo dye, stain, coordination compound

Full Text:

Full Text PDF


References

[1] Rekaby, M.M., Swelam, S.A., Shahin, A.A., and Elhag, F.A., 2018, Evaluation of colouration properties of newly synthesized curcumin derivatives, Egypt. Pharm. J., 17 (3), 155–162.

[2] Mezgebe, K., and Mulugeta, E., 2022, Synthesis and pharmacological activities of azo dye derivatives incorporating heterocyclic scaffolds: A review, RSC Adv., 12 (40), 25932–25946.

[3] Prasad, S., DuBourdieu, D., Srivastava, A., Kumar, P., and Lall, R., 2021, Metal–curcumin complexes in therapeutics: An approach to enhance pharmacological effects of curcumin, Int. J. Mol. Sci., 22 (13), 7094–7107.

[4] Kazakova, O., Lipkovska, N., and Barvinchenko, V., 2022, Keto-enol tautomerism of curcumin in the preparation of nanobiocomposites with fumed silicam, Spectrochim. Acta, Part A, 277, 121287.

[5] Bukhari, S.N.A., Jantan, I., Jasamai, M., Ahmad, W., and Amjad, M.W., 2013, Synthesis and biological evaluation of curcumin analogues, J. Med. Sci., 13 (7), 501–513.

[6] Priya, R.S., Balachandran, S., Daisy, J., and Mohanan, P.V., 2015, Reactive centers of curcumin and the possible role of metal complexes of curcumin as antioxidants, Univers. J. Phys. Appl., 9 (1), 6–16.

[7] Priyadarsini, K.I., 2014, The chemistry of curcumin: From extraction to therapeutic agent, Molecules, 19 (12), 20091–9112.

[8] Devasena, T., Balasubramanian, N., Muninathan, N., Baskaran, K., and John, S.T., 2022, Curcumin is an iconic ligand for detecting environmental pollutants, Bioinorg. Chem. Appl., 2022, 9248988.

[9] Zhang, W., Chen, C., Shi, H., Yang, M., Liu, Y., Ji, P., Chen, H., Tan, R.X., and Li, E., 2016, Curcumin is a biologically active copper chelator with antitumor activity, Phytomedicine, 23 (1), 1–8.

[10] Nakamae, I., Morimoto, T., Shima, H., Shionyu, M., Fujiki, H., Yoneda-Kato, N., Yokoyama, T., Kanaya, S., Kakiuchi, K., Shirai, T., Meiyanto, E., and Kato, J., 2019, Curcumin derivatives verify the essentiality of ROS upregulation in tumor suppression, Molecules, 24 (22), 4067.

[11] Hope-Roberts, M., and Horobin, R.W., 2017, A review of curcumin as a biological stain and as a self-visualizing pharmaceutical agent, Biotech. Histochem., 92 (5), 315–323.

[12] Sarhan, B.M., and Fyyadh, B.M., 2017, Synthesis and characterization of some metal complexes of [4-methoxy-N-(pyrimidine-2-ylcarbamothioyl)benzamide], Baghdad Sci. J., 14 (4), 765–765.

[13] Ali, R.R., and Mohammed, H.S., 2021, Biological activity and latent fingerprints detection by azo quinoline dye and its complexes, Period. Eng. Nat. Sci., 9 (3), 317–329.

[14] Abbas, A.K., and AL-Qaysi, W.W., 2023, Synthesis and characterization of novel nano azo compounds as a new pH sensor, Arabian J. Sci. Eng., 48 (1), 399–415.

[15] Al-Daffay, R.K.H., and Al-Hamdani, A.A.S., 2022, Synthesis and characterization of some metals complexes with new acidicazo ligand 4-[(2-amino-4-phenylazo)-methyl]-cyclohexane carboxylic acid, Iraqi J. Sci., 63 (8), 3264–3275.

[16] Falah, N.S., Abdullah, S.A.H., and Jabir, M.S., 2023, Synthesis, characterization, and mass spectral fragmentation of novel azo derivative and its divalent metal ion complexes, J. Surv. Fish. Sci., 10 (3S), 1436–1444.

[17] Sarhan, B.M., and Neema, B.Z., 2017, Synthesis and spectroscopic studies of some divalent metall ion complexes of 3-(4-hydroxyphenyl)-2-(3-(4-nitrobenzoyl) thioureido) propanoic acid, Baghdad Sci. J., 14 (3), 0588.

[18] Fayyadh, B.M., Abd, N.A.B., and Sarhan, B.M., 2022, Synthesis and characterization of new Mn(II), Co(II), Cd(II) and Hg(II) complexes with ligand [N-(pyrimidin-2-ylcarbamothioyl)benzamide] and their anti-bacterial study, IOP Conf. Ser.: Earth Environ. Sci., 1029, 012030.

[19] Witwit, I.N., Motaweq, Z.Y., and Mubark, H.M., 2018, Synthesis, characterization, and biological efficacy on new mixed ligand complexes based from azo dye of 8-hydroxy quinoline as a primary ligand and imidazole as a secondary ligand with some of transition metal ions, J. Pharm. Sci. Res., 10 (12), 3074–3083.

[20] Mohammed, H.S., Al-Hasan, H.A., Chaieb, Z., Zizi, Z., and Abed, H.N., 2023, Synthesis, characterization, DFT calculations and biological evaluation of azo dye ligand containing 1, 3-dimethylxanthine and its Co(II), Cu(II) and Zn(II) complexes, Bull. Chem. Soc. Ethiop., 37 (2), 347–356.

[21] Mohammed, H.S., 2021, Synthesis and characterization of some complexes of azo-chalcone ligand and assessment of their biological activity, Mater. Plast., 58 (3), 23–31.

[22] Alzamili, S.K., and Shamran, M.H., 2022, Synthesis, characterization and biological activity of azo guanine and its complexes, Res. J. Chem. Environ., 26 (10), 129–141.

[23] Abbas, A., and Kadhim, R.S., 2016, Preparation, spectral and biological studies of azo ligand derived from proline with Cu(II), Ag(I) and Au(III) metal ion, IOSR J. Appl. Chem., 9 (8), 20–31.

[24] Lavanya, A., Sowmya, S.V., Rao, R.S., Augustine, D., and Haragannavar, V.C., 2021, Natural stain (Kumkum) formulated by the extract of Curcuma aromatica and slaked lime in histostaining of oral tissues: An observational study, J. Oral Maxillofac. Pathol., 25 (1), 88–96.

[25] Al-Redah, S.A.A., Zghair, F.S., and Alhacham, E.I.D., 2021, Pancreas in sheep histochemical and immunohistochemical analysis, Ann. Rom. Soc. Cell Biol., 25 (3), 229–240.



DOI: https://doi.org/10.22146/ijc.84388

Article Metrics

Abstract views : 903 | views : 452


Copyright (c) 2023 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.