Comparative evaluation of anti-anemic effect of Sucrosomial iron in experimental model of iron deficiency anemia in Wistar rats
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Keywords

iron deficiency anemia
bloodletting
conventional oral iron
sucrosomial iron
iron store indices

Abstract

Anemia is a grave public health issue that affects 25% of the global population. Conventional iron formulations used in treatment have drawbacks such as poor bioavailability and gastric intolerability. The current study aimed to evaluate the anti-anemic effects of different iron salts in Wistar rats with iron deficiency anemia (IDA).
IDA was induced by the validated pre-clinical model by retro-orbital bloodletting (1 ml) for 21 days along with an iron-deficient diet in Wistar rats. The rats (n=48) were assigned into 8 groups: Control group, IDA rats, IDA rats receiving either vehicle or different iron salts (ferrous sulfate, ferrous ascorbate, ferrous fumarate, and Sucrosomial iron) for 21 days at a dose of 30 mg/kg p.o. Hematological parameters and iron store indices were assessed at each visit.
Anemia induction markedly reduced hemoglobin levels in all IDA groups on day 21. In contrast, iron supplements showed significant improvement in hematological profile after 21 days of treatment. Interestingly, the Sucrosomial iron-supplemented group (group 8) showed significantly higher improvement in hemoglobin levels and hematocrit than did conventional iron supplements such as ferrous sulfate (group 5), ferrous ascorbate (group 6) and ferrous fumarate (group 7) (p <0.05 for each group, respectively). Sucrosomial iron also showed slightly better improvement in iron store indices (serum iron & ferritin levels, total iron binding capacity and transferrin saturation [%]) when compared with other iron supplements (non-significant difference).
Authors concluded that Sucrosomial iron has a significant potential to improve IDA in Wistar rats compared to conventional iron salts. Sucrosomial iron can be useful for the management of IDA either prophylactically or therapeutically.

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References

1. Li Q, Liang F, Liang W, Shi W, Han Y. Prevalence of anemia and its associated risk factors among 6-months-old infants in Beijing. Front Pediatr. 2019;7:286.

2. Ortiz E, Pasquini JM, Thompson K, Felt B, Butkus G, Beard J, et al. Effect of manipulation of iron storage, transport, or availability on myelin composition and brain iron content in three different animal models. J Neurosci Res. 2004;77:681-9.

3. Lozoff B. Iron deficiency and child development. Food Nutr Bull. 2007;28:S560-71.

4. Sheikh NA, Desai TR, Tirgar PR. Investigation into iron chelating and antioxidant potential of melilotus officinalis in iron dextran induced iron overloaded sprague dawley rat model. Drug Res (Stuttg). 2016;66(12):618-27.

5. Desai TR, Tirgar PR. Investigation into iron chelating activity of Triticum aestivum (wheat grass) in iron-dextran induce iron overload model of thalassemia. J Pharm Res. 2011;4(9):1-4.

6. Hassan TH, Badr MA, Karam NA, Zkaria M, El Saadany HF, Rahman DM, et al. Impact of iron deficiency anemia on the function of the immune system in children. Medicine. 2016;95:e5395.

7. Zakaurrab Z, Adnan M, Ahmad SM, Islam N. Effect of oral iron on markers of oxidative stress and antioxidant status in children with iron deficiency anaemia. J. Clin Diagn Res. 2016;10:SC13-SC19.

8. Gupta PM, Perrine CG, Mei Z, Scanlon KS. Iron, anemia, and iron deficiency anemia among young children in the United States. Nutrients. 2016;8:1-4.

9. Jougleux JL, Rioux FM, Church MW, Fiset S, Suretteet ME. Mild maternal iron deficiency anemia during pregnancy and lactation in guinea pigs causes abnormal auditory function in the offspring. J. Nutr. 2011;141:1390-5.

10. Gómez-Ramírez S, Brilli E, Tarantino G, Muñoz M. Sucrosomial® Iron: A new generation iron for improving oral supplementation. Pharmaceuticals (Basel). 2018;11(4):97.

11. Bovellbenjamin AC, Viteri FE, Allen LH. Iron absorption from ferrous bis-glycinate and ferric trisglycinate in whole maize is regulated by iron status. Am J Clin Nutr. 2000;71:1563-9.

12. Kis L, Szuts A, Otomo N, Szabó-Révész P, Deli MA. The Potential of sucrose esters to be used as oral absorption enhancers. Sci Pharm. 2010;78:716.

13. Kiss L, Hellinger E, Pilbat AM, Kittel Á, Török Z, Füredi A, et al. Sucrose esters increase drug penetration, but do not inhibit p-glycoprotein in Caco-2 intestinal epithelial cells. J Pharm Sci. 2014;103:3107-19.

14. Fabiano A, Brilli E, Fogli S, Beconcini D, Carpi S, Tarantino G, et al. Sucrosomial® iron absorption studied by in vitro and ex-vivo models. Eur J Pharm Sci. 2018;111:425-31.

15. Gawde SR, Patel TC, Rege NN, Gajbhiye S, Uchil D. Evaluation of effects of Mandurabhasma on structural and functional integrity of small intestine in comparison with ferrous sulfate using an experimental model of iron deficiency anemia. Ancient Sci Life. 2015;34:134-41.

16. Goldberg L, Martin E. Iron containing hematinics. In: Laurence DR, Bacharach AL, (ed). Pharmacometrics, evaluation of drug activities. London: Academic Press; 1964:535-83.

17. Markandeywar NR. Evaluation of efficacy and safety of an ayurvedic hematinic formulation in an experimental model of iron deficiency anaemia. University of Mumbai; 2011.

18. Suva MA, Tirgar PR. Comparative assessment of anti-anemic effect of Sucrosomial iron in haloperidol-induced iron deficiency anemia in Wistar rats. J Integr Sci Technol. 2022;10(3):204-8.

19. Baqa K, Waris N, Butt A, Nazim U, Abbasi SR, Naz A. Comparative liver function assessment of natural and available drug (Ferrous sulfate) for iron-deficiency anemia in rat model. Pak J Pharm Sci. 2019;32(3):973-9.

20. Moazedi AA, Shooshtari MK, Ali G. Dose-dependent effects of iron supplementation on short-term and long-term memory in adult male wistar rats. J Biol Sci. 2010;10(7):648-52.

21. He H, Huang Q, Liu C, Jia S, Wang Y, An F, et al. Effectiveness of AOS–iron on iron deficiency anemia in rats. RSC Adv. 2019;9: 5053-63.

22. Trivedi A, Mishra S. Evaluation of hematinic potential of a herbomineral Formulation (HMF-TE) in Haloperidol-induced anemic rats. Pharmacognosy Res. 2009;1(4):192-6.

23. Lazarte CE, Soto A, Alvarez L, Bergenståhl B, Medrano N, Granfeldt Y, et al. Nutritional status of children with intestinal parasites from a tropical area of bolivia, emphasis on zinc and iron status. Food Nutr Sci. 2015;6:399-411.

24. Srivastava V, Sarkar S, Pattanayak C, Mishra M, Jena J. Comparative analysis of hematinic effect of Dhatryarista with standard Ferrous sulfate in Tannic acid-induced iron deficiency anemia in albino Wistar rats. Indian J Public Health Res Dev. 2020;11(6):1047-53.

25. Medappa N. Iron absorption and its implications on strategies to control iron deficiency anemia. ICMR Bulletin. 2000;30(2):1-6.

26. Fabiano A, Brilli E, Mattii L, Testai L, Moscato S, Citi V, et al. Ex vivo and in vivo study of sucrosomial iron intestinal absorption and bioavailability. Int J Mol Sci. 2018;19:2722.

27. Rishi G, Subramaniam VN. The liver in regulation of iron homeostasis. Am J Physiol. Gastrointest Liver Physiol. 2017;313: G157-G165.

28. Brilli E, Lipinski P, Barnadas R, Camacho M, Giordano G, Tarantino G. Sucrosomial® iron absorption involves m cells interaction. Blood. 2017;130(1):2217.

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