Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2022 | 43 | 96-107

Article title

Polymerization of Sickle Cell Disease and Methaeglobin in the Presence of Paracetamol

Content

Title variants

Languages of publication

EN

Abstracts

EN
This study was designed to examine the Level of Polymerization of Sickle Cell Disease and Methaeglobin in the Presence of Paracetamol, the research was carried out using standard procedures. The present study has shown the level of polymerization of sickle cell disease and methaemoglobin in the presence of paracetamol. Within the experimental time of 30-180 seconds, the relative polymerizations range between the following; 70.43 ± 0.87 to 72.10 ± 0.37 at the control (0 mg/dl), at 50 mg/dl, there was an increase from 65.78 ± 0.89 to 69.47±1.00, at 100 mg/dl there was an increase in the polymerization from 68.96 ± 0.99 to 72.33 ±1.02, at 200 mg/dl there was an increase in the polymerization from 65.96 ± 69.26 ± 1.00 and at 500 mg/dl, there was an increase in the polymerization form 66.05 ± 0.98 to 69.42 ± 0.92. This increase in polymerization can be said to be due to the increase in the absorbance of paracetamol. However, the absorbance of the polymerization mixture in the presence of the malarial drug was not significantly different (p < 0.05) from the control sample at the 30 second. The present study showed that the level of polymerization of Hemoglobin S (HbS) molecules was attenuated upon the introduction of the anti-malarial drugs in the polymerizing mixture. The percentage of methaemoglobin increases with the increase in concentration of paracetamol from 2.77 ± 0.05 to 3.30 ± 0.03 starting from 0 mg/dl to 500 mg/dl concentration.

Year

Volume

43

Pages

96-107

Physical description

Contributors

  • Department of Chemistry, Imo State University Owerri, Owerri, Nigeria
author
  • Department of Chemistry, Imo State University Owerri, Owerri, Nigeria
  • Quality Assurance, Europharmaceutical Laboratories Jos, Plateau State, Nigeria
  • Department of Biotechnology, Federal University of Technology Owerri, Imo State, Nigeria
  • Department of Chemistry, Imo State University Owerri, Owerri, Nigeria

References

  • [1] Ibegbulem, C. O., Eyong, E. U. and Essien, E. U. (2011). Polymerization inhibition activity of Raphiahookeripalmsap and its effect on osmotic fragility of sickle cellred blood cells. Journal of Medicinal Plants Research 5(17), 4212-4217
  • [2] Hochhauser, D. (2014). Sickle cell disease and its Management. John Wiley & Sons, p. 119
  • [3] Okpuzor, J., Adebesin, O., Ogbunugafor, H. and Amadi, I. (2008). The potential of medicinal plants in sickle cell disease control: A review. Inter J Biomed Health Sci. 4: 47–55
  • [4] Frenette, P. S. and Atweh, G. F. (2007). Sickle cell disease: old discoveries, new concepts, and future promise. Journal of Clinical Investigation.117, 850–858
  • [5] Mangus, B. C. and Miller, M. G. (2005). Pharmacology application in sickle cell patients. Philadelphia, Pennsylvania: F.A. Davis. p. 39.
  • [6] Chikezie, P.C., Akuwudikeand A.R. and C.M. Chikezie (2013). Polymerization Studies of Sickle Cell Hemoglobin Incubated in Aqueous Leaf Extract of Nicotiana tabacum Product. J. Biol. Chem. Research. Vol. 30, No. 1: 158-168
  • [7] Veselina, V., Uzunova, W. P., Oleg, G.,and Peter, G. V. (2010). Free Heme and the Polymerization of Sickle Cell Hemoglobin. Biophys J. 99(6): 1976–1985
  • [8] Walters, M. C., Storband, R. and Patience, M. (2000). Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Blood. 95, 1918-1924.
  • [9] Russell, F. M., Shann, F., Curtis, N. and Mulholland, K. (2003). Evidence on the use of paracetamol in febrile children. Bulletin of the World Health Organization 81 (5): 367–72
  • [10] Oyewole, O. I., Malomo, S. O. and Adebayo, J. O. (2008). Comparative studies on antisickling properties of thiocyanate, tellurite and hydroxyurea. Pakistan Journal of Medical Science 24, 18-22
  • [11] Lewis, J. H. and Stine, J. G. (2013). Prescribing medications in patients with cirrhosis a practical guide. Alimentary Pharmacology & Therapeutics 37 (12): 1132–56
  • [12] Fosdal, M. B. and Alexandrov, A. W. (2007). Events of hospitalization among children with sickle cell disease. J Pediatr Nurs. 22: 342–346
  • [13] Ibegbulem, C. O. and Chikezie, P. C. (2012). Serum lipid profile of rats (Rattusnorvegicus) fed with palm oil and palm kernel oil-containing diets. Asian Journal of Biochemistry 7(1), 46-53
  • [14] Adams, V., Marley, J. and McCarroll, C. (2007). Prilocaine induced methaemoglobinaemia in a medically compromised patient. Was this an inevitable consequence of the dose administered. Br Dent J. 203 (10): 585–587
  • [15] Ataga, K. I. and Stocker, J. (2015). The trials and hopes for drug development in sickle cell disease. Br J Haematol. 170(6): 768-780
  • [16] Ribeil, J. A., Hacein-Bey-Abina, S. and Payen, E. (2017). Gene therapy in a patient with sickle cell disease. N Engl J Med. 376(9): 848-855
  • [17] Bauer, D. E., Kamran, S. C. and Orkin, S. H. (2018). Reawakening fetal hemoglobin: prospects for new therapies for the β-globin disorders. Blood 120(15): 2945-2953
  • [18] Sankaran, V. G., Menne, T. F. and Xu, J. (2008). Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A. Science 322 (5909): 1839-1842
  • [19] Meremikwu, M. and Oyo-Ita, A. (2002). Paracetamol for treating fever in children. Cochrane Database Syst Rev. 3 (2), 122-136
  • [20] Yubisui, T., Takeshita, M. and Yoneyama, Y. (2004). Reduction of methemoglobin through flavin at the physiological concentration by NADPH-flavin reductase of human erythrocytes. Journal of Biochemistry 87(6): 1715-20
  • [21] Galbraith, D. A. and Watts, D. C. (2009). Changes in some cytoplasmic enzymes from red cells fractionated into age groups by centrifugation in Ficoll™/Triosil™ gradients: Comparison of normal human and patients with Duchenne muscular dystrophy. Biochemistry Journal 191, 63-70
  • [22] McKay, G. A., Walters K. and Matthew, R. (2013). Non-Opioid Analgesics. Lecture Notes Clinical Pharmacology and Therapeutics (9th ed.). Hoboken: Wiley. Pp. 54
  • [23] M. Muthulingam, C. Prabhahar, S. Senthilmurugan, K. Pugazhendy, P. Vijayan, M. Baranitharan, Nephroprotective role of Potentilla reptans L. aqueous extract on paracetamol – induced kidney nephrotoxicity in male mice. World News of Natural Sciences 39 (2021) 76-85
  • [24] Hafsat O. Alabere, Efe I. Lucky, A. O. Ogundare, Abeeb I. Akinwunmi, Titilope Y. Abimbola, Comparative Test of Physicochemical Parameters and Microbiological Quality of Different Brands of Paracetamol Tablets Sold in Nigeria. World Scientific News 141 (2020) 12-23

Document Type

article

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.psjd-861cd7a0-0477-4658-9166-530485b91191
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.