Volume : 10, Issue : 09, September – 2023

Title:

21.PREPARATION AND IN-VITRO EVALUATION OF IMMEDIATE RELEASE TABLETS OF CHLORPROPAMIDE

Authors :

EMMADI SATHISH KUMAR*, MRS.KABITA BANIK

Abstract :

The aim of the present study is to develop and evaluate the immediate release tablet of Chlorpropamide by direct compression method. The Superdisintegrant Primojel, Ac-Di-Sol and Polyplasdone XL10 were used for immediate release of drug from tablet. The prepared tablets were evaluated for all pre-compression parameters and post-compression parameters. The drug excipients interaction was investigated by FTIR. All formulation showed compliances with Pharmacopoeial standards. The study reveals that formulations prepared by direct compression F3 exhibit highest dissolution using Crospovidone showed faster drug release 98.01% over the period of 45min while disintegration time of the tablet was showed 25sec comparison to other formulations of Chlorpropamide.
Key words: Chlorpropamide, superdisintegrant and Immediate release tablet.

Cite This Article:

Please cite this article in press Emmadi Sathish Kumar et al, Preparation And In-Vitro Evaluation Of Immediate Release Tablets Of Chlorpropamide, Indo Am. J. P. Sci, 2023; 10 (09).

Number of Downloads : 10

References:

1. Manish Jaimini, Sonam Ranga, Amit Kumar, Sanjay Kumar Sharma, Bhupendra Singh Chauhan. A Review On Immediate Release Drug Delivery System By Using Design Of Experiment, Journal of Drug Discovery and Therapeutics 2013, 1 (12), 21-27.
2. Pande V, Karale P, Goje P and Mahanavar S. An Overview on Emerging Trends in Immediate Release Tablet Technologies. 2016, Austin Therapeutics – Volume 3 Issue 1.
3. Ghosh R, Bhuiyan MA, Dewan I, Ghosh DR, Islam A. Immediate Release Drug Delivery System (Tablets): An overview, International Research Journal of Pharmaceutical and Applied Sciences; 2012, 2: 88-94.
4. Velivela S, Mayasa V, Guptha RM, Pati NB, Ramadevi C. Formulation, Development and Evaluation of Rosuvastatin Calcium Immediate Release Tablets. European Journal of Pharmaceutical and Medical Research. 2016; 3: 351-358.
5. Gabrielsson J, Lindberg N, Lundstedt T. Multivariate Methods in Pharmaceutical Applications. Journal of Chemomatrics. 2002; 16: 141-160.
6. Dedhiya MG, Rastogi SK, Chhettry A. Lercanidipine Immediate Release Compositions. United States Patient Application. 2006; 134-212.
7. Patrik E, Barbro J. New Oral Immediate Release Dosage Form. United States Patient Application. 2006.
8. Kaur V, Mehara N. A Review on: Importance of Superdisintegrant on Immediate Release Tablets. International Journal of Research and Scientific Innovation. 2016; 3: 39-43.
9. Nyol Sandeep , Dr. M.M. Gupta. Immediate Drug Release Dosage Form: A Review. Journal of Drug Delivery & Therapeutics; 2013, 3(2), 155-161.
10. GS Banker, NR Anderson, Tablets in: The theory and practice of industrial pharmacy, Varghese publishing house, 3 rd edition, Mumbai 1987, 314-324.
11. Ansel`S Pharmaceutical Dosage Forms & Drug Delivery Systems, Eighth Edition, 227-260
12. Aulton`S Pharmaceutics, The Design & Manufacture of Medicines,Biopharmaceutics And Pharmacokinetics: A Treatise, Vallabh Prakashan, Second Edition, 315-384. 13. EL Parrot, Compression in pharmaceutical dosage form, Marcel Dekker Inc.New York,1990,2:153-182.
13. L Lachman, HA Liberman, LJ Kanig, Theory and practice of industrial pharmacy,Vargese publication house, 3rd Edition, Mumbai 1990, 293-294; 329-335.
14. J Swarbrick, JC Boylan, L Augsburger, Tablet formulation, Encyclopedia of pharmaceutical technologyx, Marcel Dekker, 3rd Edition, New York 2002, 2711.
15. Susijit Sahoo, Biswal, Omprakash Panda, Satosh Kumar Mahapatra and Goutam Kumar Jana, Fast Disslving Tablet: As A Potential Drug Delivery System, Drug Invention Today , 2010; (2): 130-133.