Controlled release study for captopril by using polymer carboxymethyl cellulose

Main Article Content

Reem Ibrahim Mahdi
R.R. AL-Samarrai
Ahmed A.Ahmed

Abstract

The present study was done to prepare tablet for captopril (CAP) which used in the treatment of hypertension and heart failure. CAP is mainly absorbed from the proximal intestine and to a lesser extent from the stomach. The tablets of CAP were prepared by using the polymer carboxymethyl cellulose (CMC) a captopril drug release system. The buffer solutions were use at (pH=12,7.4,8.5) as a media to release the drug similitude of the acidity index in stomach, in testiness, and blood plasma respective. It was accounted the concentrations of the drug that release in the above–mentioned solutions at the different temperature (25,30,37,40,45,) C°. The study was extended to the effect of the temperature and the acidity function on releasing the drug. The drug release from the polymers increased with  the temperature and the degree of the solution acidity. It was also studied the value of stability constant that increased with the temperature.

Article Details

How to Cite
Reem Ibrahim Mahdi, R.R. AL-Samarrai, & Ahmed A.Ahmed. (2023). Controlled release study for captopril by using polymer carboxymethyl cellulose. Tikrit Journal of Pure Science, 22(4), 87–98. https://doi.org/10.25130/tjps.v22i4.738
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References

1. Bodor, N.; Murakami, T. and Wu, W. M. Soft drugs 18. Oral and rectal delivery of loteprednol etabonate, a novel soft corticosteroid, in rats—for safer treatment of gastrointestinal inflammation. Pharm. Research. 1995; 12(6): 869-874.

2. Gilchrist, F. M. Ph.D thesis, Aston University, Birmingham, September 2002.

3. Pillai, O.; Dhanikula, A. B. and Panchagnula, R. Drug delivery: an odyssey of 100 years. Current Opinion in Chemical Biology 2001; 5: 439-446.

4. Kydonieus, A. F. Controlled release technologies: methods, theory, and applications. CRC Press: Cleveland, Ohio. 1980; Vol. 1.

5. Juliano, R.L. Drug delivery system. ch. Bio. Applications, Oxford University Press, USA 1997.

6. Firyal, M. A.; Rahi, F. A.; Assel, Q. M. and I. alshather, A. Polycondensation of Acid anhydrides with Asparaginyl Imide Diamine and Curing with Styrene as Smart Polymers for Sustained Release Drug Delivery System. Tikrit Journal of Pharmaceutical Sciences 2013; 9(1): 162.

7. Chaudhari, D. controlled Drug Delivery System. University of Alabama, Tuscaloosa 2004.

8. Filipovic-Gric, J.; Maysinger, D. and Jalsenjak, I. Microparticles with neuroactive agents. J. Micmencapsulation 1995; 12(4): 343-362.

9. Kshirsagar, N. A. Drug Delivery System. Indian J. of Pharmacology 2000; 32(4): 554-561.

10. Fung, L. K. and Saltzman, W. M. Polymeric implants for cancer chemotherapy. Adv. Drug Delivery Rev.1997; 26(2): 209-230.

11. Saputra, A.H.; Qadhayna, L. and Pitaloka, A.B. Synthesis and Characterization of Carboxymethyl Cellulose (CMC) from Water Hyacinth Using Ethanol-Isobutyl Alcohol Mixture as the Solvents. International Journal of Chemical Engineering and Applications- 2014; 5(1): P.36.

12. Mahewicz T.G. and Kirk T.J., Othmer Concise of Chemical Technology, 4 ed., Wiley, New York 1999: pp. 368.

13. Anjali, T. Modification of carboxymethyl cellulose through oxidation. Carbohydr. Polym. 2011; 87(1): 457-460.

14. Heinze, T. and Liebert, T. Unconventional methods in cellulose functionalization. Prog. Polym. Sci. 2001; 26(9): 1689-1762.

15. Jones, M. M.; Basinger, M. A. and Holscher, M. A. Control of the nephrotoxicity of cisplatin by clinically used sulfur-containing compounds. Toxicol. Sci. 1992; 18(2): 181-188.

16. Al-Youzbaki, W. B. and Al-Taee, Y. T. Serum uric acid level and renal function tests in hypertensive patients treated by captopril. Iraq J Pharm-2013; 13 (2): 1.

17. Habior, A. Effect of captopril on glutathione level in the liver and paracetamol-induced liver damage in rats. Pol. Arch. Med. Wewn. 1992; 87(6): 332-340.

18. Lindberg, H.; Nielsen, D.; Jensen, B. V.; Eriksen, J. and Skovsgaard, T. Angiotensin converting enzyme inhibitors for cancer treatment?. Acta Oncol. 2004; 43(2):142-152.

19. Romankiewicz, J. A.; Brogden, R. N.; Heel, R. C.; Speight, T. M. and Avery, G. S. Captopril: an update review of its pharmacological properties and therapeutic efficacy in congestive heart failure. Drugs 1983; 25(1): 6-40.

20. Rangaraj, G.; Narra K.; Dhanalekshmi U. M.; Raja M. D.; Senthil kumar C. and Neelakanta Reddy P., Design and study of formulation variables affecting drug loading and its release from Alginate beads J. Pharm. Sci. & Res. 2010; 2(2): 77-81.

21. Gessner, G. H. The Condensed Chemical Dictionary. 8th. Ed., Reinhold, Van Nostrand 1971; pp. 25.

22. Raju, K. N.; Kumar, R. A.; Deepika, B.; Eswaraiah, M. C. and Rao, A. S. Formulation and in vitro evaluation of buccal tablets of Captopril. Int. Res. J. Pharm. App. Sci. 2012; 2(2): 21-43.

23. Biswal, D. R. and Singh, R. P. Characterisation of carboxymethyl cellulose and polyacrylamide graft copolymer. Carbohydr. Polym. 2004; 57(4): 379-387.

24. Silverstein, R. M.; Webster, F. X.; Kiemle, D. and Bryce, D. L. Spectrometric identification of organic compounds. 6th. Ed., John Wiley & Sons 1998.

25. Ikada, Y. and Tsuji, H. Biodegradable polyesters for medical and ecological applications. Macromol. Rapid Commun. 2000; 21(3): 117-132.

26. Korsmeyer, R.W.; Gurny, R.; Doelker, E.; Buri, P. and Peppas, N. A. Mechanisms of solute release from porous hydrophilic polymers. Int. J. Pharm. 1983; 15(1): 25.

27. Siepmann, J. and Peppas, N.A., Modeling of drug release from delivery system based on hydroxypropyl methylcellulose (HPMC). Adv. Drug Delivery Rev. 2012, 64; 163–174.

28. Tadros M. I. Controlled-release effervescent floating matrix tablets of ciprofloxacin hydrochloride: Development, optimization and in vitro–in vivo evaluation in healthy human volunteers. Eur. J. Pharm. Biopharm. 2010; 74(2): 332-9

29. Mutar, M. A. Chloramphenicol controlled release from Poly(acrylic acid-co-methyl methacrylate) hydrogels. Basrah Journal of Researches Sciences 2012; 38(4): 63.

30. Al-Jeboori, F. H. A.; Al-Shimiesawi, T. A. M. and Jassim, O. M. N. Synthesis and characterization of some essential amino acid metal complexes having biological activity. J. chem. pharm. res. (2013); 5(10): 172-176.

31. Apostoli, P. and Catalani, S. Metal ions affecting reproduction and development. Met. Ions Life Sci. 2011; 8: 263-303.

32. Chowdary, K. P. R.; Sambasiva Rao, K. R. S. and Koteswara Rao, N. Design of EVA Microcapsules of Glipizide for controlled release: Influence of solvents used. Int. J. Chem. Sci. 2006; 4(1): 23-30.