OSMOTIC DRUG DELIVERY SYSTEM OF NICORANDIL: DESIGN AND EVALUATION

Authors

  • SRILATHA CHOUDHARY Department of Pharmaceutics, Gokaraju Rangaraju College of Pharmacy, Osmania University, Hyderabad-50090, Telangana, India https://orcid.org/0000-0002-8284-7437
  • CVS SUBRAHMANYAM Department of Pharmaceutics, Gokaraju Rangaraju College of Pharmacy, Osmania university, Hyderabad-50090, Telangana, India
  • K. PRIYANKA Department of Pharmaceutics, Gokaraju Rangaraju College of Pharmacy, Osmania University, Hyderabad-50090, Telangana, India

DOI:

https://doi.org/10.22159/ijap.2024v16i3.50298

Keywords:

Elementary osmotic pump tablet, Osmogens, Zero-order release, 24 factorial design, Controlled drug delivery

Abstract

Objective: The purpose of the current research was to design a nicorandil formulation with controlled drug release using the principles of osmotic pump technology. Nicorandil is a biopharmaceutical classification system (BCS) class 3 drug, having a shorter plasma elimination half-life and bioavailability of 75 to 80%.

Methods: The elementary osmotic pump (EOP) was prepared by coating a cellulose acetate polymer on the prepared core tablet. A 24-factorial design was applied to optimize the parameters for the osmotic tablet. A surface orifice was drilled.

Results: Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and powder X-ray diffraction (PXRD) results showed that there was no interaction between drugs and excipients. A 24-factorial design was applied to optimize the parameters for the elementary osmotic pump. The optimized batch was characterized for in vitro drug release studies, and the effects of pH, osmotic pressure, and agitation intensity were analyzed. All the batches showed a drug release ranging from 90.48% to 98.78% after 12 hours. There was no change in the drug release pattern at different pHs and agitation intensities. The drug release was found to decrease with the increasing osmotic pressure of the dissolution medium. The results showed that the amounts of sodium chloride and mannitol were positively affecting the drug release, while the plasticizers PEG400 and DBP were not critical. Scanning electron microscopic studies (SEM) showed the integrity and surface morphology of the coating membrane before and after dissolution. The prepared EOP was found to deliver nicorandil at zero-order for up to 12 hours.

Conclusion: Nicorandil was developed successfully as a controlled drug delivery during a 12-hour period, with variables optimized by the use of a 24-factorial design.

Downloads

Download data is not yet available.

References

Adepu S, Ramakrishna S. Controlled drug delivery systems: current status and future directions.Molecules.2021Sep29;26(19):5905.doi:10.3390/molecules26195905, PMID: 34641447

Arafat M. Approaches to achieve an oral controlled release drug delivery system using polymers. A recent review. Int J Pharm Pharm Sci. 2015Jul1;7(7):16-21.

Kunal NP, Tejal AM. A review on oral osmotically driven systems. Int J Pharm Pharm Sci. 2013 May 20; 5(3):1005-13.

Shireen F, Ajitha M, Roshan S. Development of nateglinide modified release dosage form using elementary osmotic pump and push-pull osmotic pump methods. Int J Pharm Sci Res. 2022 Feb1; 13(2): 891-01. doi: 10.13040/IJPSR.0975-8232.

Mehta TA, Kunal P. Development and optimization of an elementary osmotic pump tablet of nicardipine hydrochloride using a central composite experimental design. Int J Drug Dev Res. 2013 Jul 9; 5(3):382-395.

Theeuwes F. Elementary osmotic pump. J Pharm Sci. 1975 Dec;64(12):1987-91. PMID: 1510; doi: 10.1002/jps.2600641218.

Abdelbary GA,Tadros MI. Design and in vitro/in vivo evaluation of novel nicorandil extended-release matrix tablets based on hydrophilic inter polymer complexes and a hydrophobic waxy polymer. Eur J Pharm Biopharm. 2008 Aug; 69(3):1019- 1018. doi: 10.1016/j.ejpb.2008.01.011

Rabti H, Mohammed Salmani J, Elamin E, Lammari N, Zhang J, Ping Q. Carbamazepine solubility enhancement in tandem with a swellable polymer osmotic pump tablet, a promising approach for extended delivery of poorly water-soluble drugs. Asian J Pharm Sci. 2014 Jun; 9(3):146-154. doi: 10.1016/j.ajps.2014.04.001

Salve PS. Development and evaluation of oral osmotic tablets for metoprolol succinate. Research J Pharm Tech. 2011 Dec; 4(12):1797-1804. doi: 10.5958/0974-360X

Ahmed LA. Nicorandil: A drug with ongoing benefits and different mechanisms in various diseased conditions. Indian J Pharmacol. 2019 Oct;51(5):296-301. doi: 10.4103/ ijp.IJP_298_19. PMID 31831918.

Pahade A, Jadhavand VM, Kadam VJ. Formulation and development of sustained release matrix tablet of nicorandil. Int J Pharm Sci Rev Res. 2010 Oct; 4(1):107-111.

Hadke AV, Pethe AM, Kesalkar MA. Nicorandil mucoadhesive microspheres: formulation development, physico-chemical and functional characterization. Int J App Pharm. 2023 Mar 7;15(2):123-30.

Patel SS, Patel MR, Patel MJ. Formulation and evaluation of microsponge-based nicorandil sustained released tablet. J Sci Res. 2017Sep;9(3):285-96. doi: 10.3329/jsr.v9i3.31193.

Frydman A, ChapelleP, Diekmann H, Bruno R, Thebault J, Bouthier J. Pharmacokinetics of nicorandil. Am J Cardiol.1989Jun20;63(21):25J-33J.doi: 10.1016/0002-9149(89)90201-4.

Hiremath JG, Valluru R, Narhare J, Katta SA, Matad P. Pharmaceutical aspects of nicorandil. Int J Pharm Pharm Sci. 2010 Jun 25;2(4):24-9.

Dave Rutwij A, Morris Marilyn E. Novel high or low solubility classification methods for new molecular entities. Int J Pharm. 2016 Sep10; 511(1): 111-126. doi: 10.1016/j.ijpharm.2016.06.060

Anthony C Moffat, M david Osselton, Brain Widdop. Clarkes analysis of drugs and poisons. 3rd ed. London:Pharmaceutical Press; 2004.

Pharmacopoeia of India. 9th ed. New Delhi: Ministry of Health and Family Welfare, Government of India, Controller of Publications; 2022.

Reddy KR, Mutalik S, Reddy S. Once-daily sustained-release matrix tablets of nicorandil formulation and in vitro evaluation. AAPS PharmSciTech. 2003 Dec; 4(4):480–488. doi: 10.1208/pt040461.

Khandagale PM, Bhairav B, Saudagar R. Osmotically controlled drug delivery system:A novel approach. Asian J Res Pharm Sci. 2017Sep17;7(2):68–76. doi: 10.5958/2231-5659.2017.00010.8.

Kishan Pavani J, Pavani S, Shravan Kumar Y, Venkatesh A, Madhusudhan Rao Y. Formulation and evaluation of oral elementary osmotic pump tablets of sumatriptan succinate. BrJPharmRes.2014Apr28;4(10):1163-1173. doi: 10.9734/BJPR/2014/8666

Ahmed AB, Nath LK. Design and development of controlled release floating matrix tablet of nicorandil using hydrophilic cellulose and pH independent acrylic polymer: in vitro and in vivo evaluations. Expert Opin Drug Deliv. 2016 Feb 1; 13(1):315-324. doi: 10.1517/17425247.2016.1118047.

Sahoo CK, Rao SRM, Sudhakar M, Formulation and evaluation of controlled porosity osmotic pump tablets for Zidovudine and Lamivudine combination using fructose as osmogen. J Drug Deliv Ther. 2017Aug; 7(4):41-50.

doi https://doi.org/10.22270/jddt.v7i4.1465

Dasankoppa FS, Ningangowdar M, Sholapur H. Formulation and evaluation of controlled porosity osmotic pump for oral delivery of ketorolac. J Basic Clin Pharm. 2012 Dec;4(1):2-9. doi: 10.4103/0976-0105.109398. PMID: 24808662;

Madgulkar AR, Bhalekar MR, Kolhe VJ, Kenjale YD. Formulation and optimization of sustained release tablets of venlafaxine resinates using response surface methodology. Indian J Pharm Sci. 2009 Jul;71(4):387-94. doi: 10.4103/0250-474X.57287. PMID: 20502544.

Thakkar HP, Pancholi N, Patel CV. Development and evaluation of a once-daily controlled porosity osmotic pump of tapentadol hydrochloride. AAPS Pharm Sci Tech. 2016 Dec 17; 17(1):1248–1260. doi: 10.1208/s12249-015-0463-1

Published

20-02-2024

How to Cite

CHOUDHARY, S., SUBRAHMANYAM, C., & PRIYANKA, K. (2024). OSMOTIC DRUG DELIVERY SYSTEM OF NICORANDIL: DESIGN AND EVALUATION. International Journal of Applied Pharmaceutics, 16(3). https://doi.org/10.22159/ijap.2024v16i3.50298

Issue

Section

Original Article(s)