Formulation and evaluation of sustained release tablets of propranolol hydrochloride

https://doi.org/10.53730/ijhs.v6nS1.6287

Authors

  • Debashis Purohit Research Scholar, Career Point School of Pharmacy, Career Point University, Kota, Rajasthan, India
  • M. K. Gupta Dean, Career Point School of Pharmacy, Career Point University, Kota, Rajasthan, India

Keywords:

Sustained release, in vitro, Propranolol Hydrochloride, F9, Natural Polymers

Abstract

The main objective of sustained release drug delivery system is to provide a steady state blood plasma level concentration which is non-toxic and therapeutically active for a longer period of time. Owing its increased patient compliance and prolonged release of action in delivering drugs several benefits can be contemplated in delivering of sustained release dosage form[1]. Among various route of drug delivery Sustained release drug delivery is most widely preferred as it’s less frequency of dosing and controls the release of drugs. Natural polymers are biodegradable and nontoxic in nature with reduced side effects. It is also eco-friendly and safe to be administered as compared to synthetic polymers. The current work was based on preparation of sustained release tablets of Propranolol Hydrochloride using natural polymers like Gum Acacia, Hibiscus Rosasinesis and Microcrystalline cellulose. Presently much attention is being paid for formulation of sustained release tablets that contains matrix system. Direct compression method was used for formulation of sustained release tablets of Propranolol Hydrochloride. The prepared tablets were evaluated for different pre-formulation studies and in vitro dissolution studies were performed using USP-III dissolution apparatus. Dissolution studies of different formulations were evaluated for 24 hours at 370C.

Downloads

Download data is not yet available.

References

Pradhan, R., Kim, Y. I., Chang, S. W., & Kim, J. O. (2014). Preparation and evaluation of once-daily sustained-release coated tablets of tolterodine-L-tartrate. International Journal of Pharmaceutics, 460(1-2), 205-211.

Fu, Q., Su, X., Hou, Y., Li, M., Li, J., Sun, J., & He, Z. (2016). Once-daily amoxicillin immediate-and extended-release bilayer tablets. Powder Technology, 301, 405-411.

Alkrad, J. A., Shmeis, R. A., Alshwabkeh, I., Abazid, H., & Mohammad, M. A. (2017). Investigation of the potential application of sodium bentonite as an excipient in formulation of sustained release tablets. asian journal of pharmaceutical sciences, 12(3), 259-265.

Dabbagh, M. A., Ford, J. L., Rubinstein, M. H., Hogan, J. E., & Rajabi-Siahboomi, A. R. (1999). Release of propranolol hydrochloride from matrix tablets containing sodium carboxymethylcellulose and hydroxypropylmethylcellulose. Pharmaceutical development and technology, 4(3), 313-324.

Lee, B. J., Ryu, S. G., & Cui, J. H. (1999). Formulation and release characteristics of hydroxypropyl methylcellulose matrix tablet containing melatonin. Drug development and industrial pharmacy, 25(4), 493-501.

Balan, G., Timmins, P., Greene, D. S., & Marathe, P. H. (2001). In vitro–in vivo correlation (IVIVC) models for metformin after administration of modified‐release (MR) oral dosage forms to healthy human volunteers. Journal of pharmaceutical sciences, 90(8), 1176-1185.

Varia, U., Prajapati, B., & Katariya, H. (2018). Formulation and development of bosentan loaded once a daily tablet for pulmonary artery hypertension using lipid matrices by 3 (2) full factorial design. International journal of pharmaceutical sciences and research, 9(11), 4729-4740.

Hasan, A. A., Madkor, H., & Wageh, S. (2013). Formulation and evaluation of metformin hydrochloride-loaded niosomes as controlled release drug delivery system. Drug delivery, 20(3-4), 120-126.

Roy, H., Brahma, C. K., Nandi, S., & Parida, K. R. (2013). Formulation and design of sustained release matrix tablets of metformin hydrochloride: Influence of hypromellose and polyacrylate polymers. International Journal of Applied and Basic Medical Research, 3(1), 55.

Tahara, K., Yamamoto, K., & Nishihata, T. (1995). Overall mechanism behind matrix sustained release (SR) tablets prepared with hydroxypropyl methylcellulose 2910. Journal of controlled release, 35(1), 59-66.

Wadher, K. J., Kakde, R. B., & Umekar, M. J. (2011). Formulation of sustained release metformin hydrochloride matrix tablets: Influence of hydrophilic polymers on the release rate and in vitro evaluation. International Journal of Research in Controlled Release, 1(1), 9-16.

PATEL, M. R., PATEL, A. A., PRAJAPATI, L. M., & PATEL, N. M. (2012). Intragastric floating drug delivery system of metformin hydrochloride as sustained release component and glimepiride as immidiate release component: formulation and evaluation.

Dsilva, L. C., Palmer, J. O. N. A. T. H. A. N., Sudershan, V. I. S. H. W. A. N. A. T. H., & GHORPADE, S. A. (2013). Effect of food on the absorption of metformin from sustained release metformin hydrochloride formulations in healthy Indian volunteers. Asian J Pharm Clin Res, 6, 95-9.

Published

26-04-2022

How to Cite

Purohit, D., & Gupta, M. K. (2022). Formulation and evaluation of sustained release tablets of propranolol hydrochloride. International Journal of Health Sciences, 6(S1), 6233–6240. https://doi.org/10.53730/ijhs.v6nS1.6287

Issue

Section

Peer Review Articles

Most read articles by the same author(s)