Volume : 10, Issue : 04, April – 2023

Title:

05.FORMULATION AND IN VITRO CHARACTERIZATION OF IBRUTINIB EXTENDED RELEASE TABLETS

Authors :

M. Gnana Sowmya,* K. Jyothi Rama Devi , B. Mounika,K.S.V.L Prasanna,G. Bhavani , A. Venkata Rajesh, D. Aakash

Abstract :

The aim of the present study was to develop extended release formulation of Ibrutinib to maintain constant therapeutic levels of the drug for over 12 hrs. HPMC K100M, HPMC (K4M) and Carbopol 71 G were employed as polymers. All the formulations were passed various physicochemical evaluation parameters and they were found to be within limits. Whereas from the dissolution studies it was evident that the formulation (F6) showed better and desired drug release pattern i.e., 98.85% in 12 hours. It contains the HPMC (K4M) as Extended release material. It followed peppas release kinetics mechanism.
Keywords: Ibrutinib, Extended release system.

Cite This Article:

Please cite this article in press M. Gnana Sowmya et al, Formulation And In Vitro Characterization Of Ibrutinib Extended Release Tablets., Indo Am. J. P. Sci, 2023; 10 (04).

Number of Downloads : 10

References:

1. Mr. Samir J. Shah , Dr. Paresh B. Shah Dr. Mukesh S. Patel , Dr. Mukesh R. Patel. A review on extended release drug delivery system And multiparticulate system. Vol 4, Issue 08, 2015.
2. Gupta PK and Robinson JR. Oral controlled release delivery. Treatise on controlled drug delivery., 1992; 93(2): 545-555.
3. Jantzen GM and Robinson JR. Sustained and Controlled-Release Drug Delivery systems. Modern Pharmaceutics., 1995; 121(4): 501-502.
4. Khyati patel , dr. Upendra patel , bhavin bhimani , ghanshyam patel, dhiren daslaniya. Extended Release Oral Drug Delivery System. IJPRBS, 2012: Volume1(3): 1-26.
5. Wani MS. Controlled Release System A Review; Pharmaceutical Reviews., 2008; 6(1): 41-46.
6. Hayashi T. Formulation, study and drug release mechanism of a new Theophylline sustained release preparation, Int. J Pharm., 2005; 304: 91-101.
7. Venkatraman S, Davar N and Chester A. An overview of controlled release systems: Edited by Donald L Wise, New York, Marcel Dekker Inc. Handbook of Pharmaceutical controlled release Technology., 2000; 431- 465.
8. Patel P., Pellets: A General Overview, International Journal of Pharma World Research; 2010; 1(2): 1-15.
9. Hamed Barzeh , Bharani S Sogali, Sepideh Shadvar. A Review On Extended Release Matrix Tablet. Journal of Pharmaceutical Research Vol.15. No.4, Oct. – Dec. 2016 : 148.
10. Brahmankar H A, Jaiswal S B. Bio pharmaceutics and pharmacokinetics. Treatise: Vallabh Prakashan; 2000.
11. Bhargava A, Rathore R P S, Tanwar Y S,Gupta S, Bhaduka G. oral sustained release dosage form an opportunity to prolong the release of drug. Int J Adv Res Pharm Bio Sci. 2013;3(1):7-14.
12. Chauhan M J, Patel S A. Aconcise review on sustained drug delivery system and its opportunities. Am J Pharm Tech Res. 2012;2(2): 227-238.
13. Venkatraman S, Davar N, Chester A. An overview of controlled release systems. Donald L Wise, Marcel Dekker Inc; 2000.p.431- 465.
14. Jantzen GM and Robinson JR. Sustained and controlled release drug delivery systems, in Banker GS, Rhodes CT(Eds.) Modern pharmaceutics. 3rd Ed. Revised and expanded, drugs and the pharmaceutical sciences. Marcel Dekker Inc:New York; 1995.p. 575-609.
15. Brahmankar H A, Jaiswal S B. Bio pharmaceutics and pharmacokinetics.Treatise: Vallabh Prakashan; 2000.p. 337,348-357.
16. Patel KK, Patel MS, Bhatt NM, Patel LD, Pathak NL, Patel KJ. An overview: extendedrelease matrix technology. Int J Pharm Chem Sci 2012;1(2):828.
17. Patel Kundan K , Patel Mehul S , Bhatt Nayana M, Patel Laxmanbhai D , PathakNimish L and Patel Kanu J. An Overview: Extended Release Matrix Technology. Vol. 1 (2) Apr – Jun 2012.
18. Venkatraman S, Davar N and Chester A. An overview of controlled release systems: Edited by Donald L Wise, New York, Marcel Dekker Inc. Handbook of Pharmaceutical controlled release Technology, 2000; 431- 465.
19. Jantzen GM., Robinson JR, Sustained and controlled-release drug delivery systems, in Banker GS, Rhodes CT (Eds.) Modern Pharmaceutics, Third Edition, Revised and Expanded, Drugs and the Pharmaceutical Sciences, Marcel Dekker, Inc., New York., 1995; 72: 575-609.
20. Brahmankar HA ., Jaiswal SB. Biopharmaceutics and Pharmacokinetics A Treatise, Vallabh Prakashan., 2000; 337: 348-357.
21. Cox PJ., Khan KA., Munday DL, Development and evaluation of a multiple-unit oral sustained release dosage form for S (+)-ibuprofen: preparation and release kinetics. Int. J. Pharm.; 1999; 193: 73 – 84.
22. Kincl M., Meleh M., Veber M., Vrecer F. Study of physiochemical parameters affecting the release of diclofenac sodium from lipophillic matrix tablets, Acta Chim Slov; 2004; 51: 409-425.
23. Schwartz JB., Simonelli AP., Higuchi WI. Drugs release from wax matrices I : Analysis of data with first order kinetics and with the diffusion controlled model. J Pharm Sci.; 1968; 57: 274-277.