Generation of free radicals by the effect of vitamin C on a ferrous sulfate antianemic syrup

Authors

DOI:

https://doi.org/10.24265/horizmed.2018.v18n4.05

Keywords:

Ferrous sulfate, Vitamin C, Anemia, Free radicals

Abstract

Objective: To determine the effect of vitamin C on ferrous sulfate, the active ingredient of an antianemic syrup. Materials and methods: The reaction between the ferrous sulfate contained in an antianemic syrup and vitamin C was determined using the decomposition technique of deoxyribose, which evaluates the formation of malondialdehyde by the action of free radicals. Results: In an assay medium consisting of 50 mM phosphate buffer (pH 7.4), the ferrous sulfate antianemic syrup at a concentration of 1.080 mM reacted with vitamin C at concentrations between 5.0 x 10-6 mM and 0.5 mM, generating levels of free radicals that decrease when vitamin C is used at a concentration of 5.0 x 10-2 mM, and increase at a concentration of 0.5 mM. When ferrous sulfate is used under similar conditions, an increase in the generation of free radicals is observed, which reaches a maximum value with vitamin C at a concentration of 5.0 x 10-6 mM, remains unchanged at concentrations of two orders of magnitude higher, and subsequently decreases at higher concentrations. Vitamin C at a concentration of 1.0 mM reacts with ferrous sulfate used at concentrations between 0.270 and 2.160 mM, describing a hyperbolic curve. In contrast, ferrous sulfate syrup used at the same concentrations showed a high increase at low non-linear concentrations, but a linear response from the 0.540 mM concentration of the syrup, a response that was higher than that reached by the ferrous sulfate dissolved in distilled water. Conclusions: Vitamin C reacts with ferrous sulfate syrup generating free radicals. This response depends on the relative concentrations of ferrous sulfate, vitamin C and syrup excipients.

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References

Instituto Nacional de Estadística e Informática Perú (INEI). Ficha técnica: Encuesta demográfica y de salud familiar- ENDES. 2016. Lima: INEI;2017

Knutson DM. Iron transport proteins: Gateways of cellular and systemic iron homeostasis. J Biol Chem. 2017;293(31):12735- 12743.

Lane DJR, Richardson DR. The active role of vitamin C in mammalian iron metabolism: Much more than just enhanced iron absorption!. Free Rad Biol Med. 2014;75:69-83

Fisher AEO, Naughton DP. Vitamin C contributes to inflammation via radical generating mechanisms: A cautionary note. Medical Hypotheses. 2003;61(5–6):657–660.

Guija E. Troncoso L. Radicales libres y envejecimiento. Bol Soc Quim Perú. 2000;LXVI:33-51.

Prousek J. Fenton chemistry in biology and medicine. Pure Appl. Chem. 2007;79(12):2325–2338.

Andrisica L, Dudzika D, Barbasa C, Milkovicb L, Grunec T, Zarkovicb N. Short overview on metabolomics approach to study pathophysiology of oxidative stress in cancer. Redox Biology. 2018;14:47-58.

Szeto YT, Chu WK, Benzie IFF. Antioxidants in fruits and vegetables: a study of cellular availability and direct effects on human DNA. Biosci Biotechnol Biochem. 2006;70(10): 2551-2555.

Buettner GR, Jurkiewicz BA. Catalytic Metals, Ascorbate and Free Radicals: Combinations to Avoid. Radiation Research. 1996;145:532-541.

Gutteridge JMC. Ferrous-salt-promoted damage to deoxyribose and benzoate. Biochem J. 1987;243:709-714.

Buege JA, Aust SD. Microsomal lipid, Peroxidation. En: Flesicher S, Packer L. (Eds.), Methods in Enzymology Vol. 52. (Academic Press, New-York, 1978) pag. 302–310.

Gomberg M. An incidence of trivalent carbon trimetilfenil. J Am Chem Soc. 1900;22:757-771.

Gerschman R, Gilbert DL, Nye SW, Dwyer P, Fenn WO. Oxygen poisoning and X-radiation. A mechanism in common. Science. 1954;119:623-626.

Harman D. Aging: a theory based on free radical and radiation chemistry. J Gerontol. 1956; 11(3): 298–300.

Mc Cord JM, Fridovich I. Superoxide dismutase an enzymatic function for erythrocuprein (chemocuprein). J Biol Chem. 1969;244(22):6049-6055.

Lane DJR, Merlot AM, Huang ML, Bae D, Jansson PJ, Sahni S, et al. Cellular iron uptake, trafficking and metabolism: Key molecules and mechanisms and their roles in desease. Biochim Biophs Acta. 2015;1853(5):1130-1144.

Herbert V, Shaw S, Jayatillekee E. Vitamin C-Driven Free Radical Generation from Iron. J Nutr. 1996;126(4S):1213S- 1220S.

Fujimoto Y, Matsui M, Fujita T. The accumulation of ascorbic acid and iron in rat liver mitochondria after lipid peroxidation. Japan J Pharmacol. 1982;32(2):397-399.

Lachili B, Hininger I, Faure H, Arnaud J, Richard MJ, Favier A, et al. Increased lipid peroxidation in pregnant women after iron and vitamin C supplementation. Biol Trace Elem Res. 2001;83(2):103–110.

Published

2018-12-09

How to Cite

1.
Guija-Guerra H, Guija-Poma E, Ponce-Pardo J, Inocente-Camones M, Camarena-Chaviguri L. Generation of free radicals by the effect of vitamin C on a ferrous sulfate antianemic syrup. Horiz Med [Internet]. 2018Dec.9 [cited 2025May1];18(4):35-41. Available from: https://www.horizontemedico.usmp.edu.pe/index.php/horizontemed/article/view/782

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