Application of Surface Modified Electrodes as a Nano-detection Tool in the Qualitative and Quantitative Assesment of Hydroquinone in a Cosmetic Cream

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Published: 2022-01-25

Page: 66-74


Duke Omondi Orata *

Department of Chemistry, University of Nairobi, P.O.Box 30197-00100, Nairobi, Kenya.

Dorcas Gathoni Ngigi

Department of Chemistry, University of Nairobi, P.O.Box 30197-00100, Nairobi, Kenya.

Vincent Ochieng

Department of Biochemistry, University of Nairobi, P.O.Box 30197-00100, Nairobi, Kenya.

*Author to whom correspondence should be addressed.


Abstract

The results presented confirm that when the surface of the carbon graphite working electrode is modified using the beauty crème the modified electrode displays the electrochemical properties of the immobilized cream.

The oxidation/reduction peak potentials for the hydroquinone in the cosmetic cream occurred at 0.61V/0.21V.

Electrochemical calculation from the oxidative charge for the hydroquinone redox process gave a surface coverage of 1.1 x10-10 mol/cm2 corresponding to an electro-gravimetric weight of 3.57 x10-5 g for hydroquinone in the beauty cream, which corresponds to 0.121 x 10-9 g for hydroquinone in the 12g of the beauty cream.

It was also observed that, the hydroquinone in the beauty cream inhibits the polyaniline electro-degradation process at far positive potentials.

The results also indicate that modification of the carbon-graphite working electrode with bentonite; affect significantly the redox processes associated with hydroquinone in the beauty cream, the oxidation/ reduction peaks occur at 0.58V/0.28V. The effect of the bentonite host matrix is attributed to pre-concentration of electroactive species in the montmorillonite matrix.

The observed changes in the redox profile of the hydroquinone in the beauty cream in sodium chloride supporting electrolyte can be attributed to cationic and anionic effects associated with the sodium cation and the high charge density of the chloride anion.

Keywords: Nano-detection tool, cosmetic cream, top-lemon cream, hydroquinone


How to Cite

Orata, Duke Omondi, Dorcas Gathoni Ngigi, and Vincent Ochieng. 2022. “Application of Surface Modified Electrodes As a Nano-Detection Tool in the Qualitative and Quantitative Assesment of Hydroquinone in a Cosmetic Cream”. Asian Basic and Applied Research Journal 4 (1):66-74. https://www.jofresearch.com/index.php/ABAARJ/article/view/108.

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References

Li Q, Geiselhart L, Mittler JN, Mudzinski SP, Lawrence DA, Freed BM. Inhibition of human T lymphoblast proliferation by hydroquinone. Toxicol Appl Pharmacol. 1996;139(2):317–323.

Rochelle MBN, Kishore B, Bhat R, Sukumar D, Martis J, Ganesh H. A comparative study of the efficacy of 4% hydroquinone vs 0.75% kojic acid cream in the treatment of facial melasma. Indian J Dermatol. 2013;58(2):157–161.

DOI:10.4103/0019-5154.108070

Yetunde MA. Complications of Chronic use of Skin Lightening Cosmetics. Int J Dermatol. 2008; 7:344–353.

Sheehan DC, Hrapchak BB. Theory and Practice of Histotechnology. 2nd ed. St. Louis: Mosby. United States Government has Certain Rights. 1980:55–61.

Masson LE. Verhoeff; 2009. Stain.vetmed.vt.edu.

Available: http://education.vetmed.vt.edu/Curriculum/VM8054/Labs/.

DOI:10.1016/j.soncn.2016.05.005

Sheehan JM, Potten CS, Young AR. Tanning in human skin type’s ii and iii offers modest photo-protection against erythema. Photochem Photobiol. 1998; 68(4):588–592.

DOI:10.1111/j.1751-1097.1998.tb02518.x

Bos D, Meinardi MM. The 500 Dalton rule for the skin penetration of chemical compounds and drugs. Exp Dermatol. 2000;9(3):165–169.

DOI:10.1034/j.1600-0625.2000.009003165.x

Saeedi M, Eslamifar M, Khezri K. Kojic acid applications in cosmetic and pharmaceutical preparations. Biomed Pharmacother. 2019;110:582–593.

DOI:10.1016/j.biopha.2018.12.006

Kooyers TJ, Westerhof W. Toxicology and health risks of hydroquinone in skin lightening formulations. J Eur Acad Dermatol Venereology. 2006;20(7):777–780.

DOI:10.1111/j.1468-3083.2005.01218.x

Westerhof W, Kooyers TJ. Hydroquinone and its analogues in dermatology - a potential health risk. J Cosmet Dermatol. 2005;4(2):55–59.

DOI:10.1111/j.1473-2165.2005.40202.x

Tse TW. Hydroquinone for skin lightening: safety profile, duration of use and when should we stop? J Dermatol Treat. 2010;21(5):272–275.

DOI:10.3109/09546630903341945

Al-Saleh I, Elkhatib R, Al-Rouqi R, Al-Enazi S, Shinwari N. The dangers of skin-lightening creams. Toxicol Environ Chem. 2012;94(1):195–219.

DOI:10.1080/02772248.2011.631925

Bard AJ, Rudzinski WE. Clay modified electrodes, Part VI: aluminum and silicon pillared clay modified electrodes. J. Electroanal. Chem. 1986;199:323-340

Bard AJ, Villemure G. Part 9: Electrochemical studies of the electroactive fraction of adsorbed species in reduced and preadsorbed clay films, J. Electroanal. Chem. 1990;282:107-121.

Gosh PK, Bard AJ. Clay Modified Electrodes part II, J. Electroanal. Chem. Soc. 1983;105:5691-5693.

Orata DO, Buttry DA. Determination of ion population and solvent content as a function of redox state and pH in polyaniline, J.Am.Chem. Soc. 1987;109:357.

Orata DO, Okongo E. Allen- Hickling equation applied to the quasi-reversible polyaniline redox, Reactive and Functional Polymers. 2000;45(3):211-216.

Orata DO. electrochemical characteristics of polyaniline electro polymerized on a phenol modified carbon electrode. Bull. Chem. Soc. Ethiop. 1992;6:1.

Orata DO. Effects of pyridine on porosity and redox properties of poly-thiophene. Bull. Chem. Soc. Ethiop. 1989;3 (1).