Author(s):
Shakeel Memon, Aney Joice, Dilnawaz Pathan, Aasia Patel
Email(s):
memon.shakeel@gmail.com
DOI:
10.52711/0974-360X.2025.00513
Address:
Shakeel Memon1, Aney Joice1, Dilnawaz Pathan2, Aasia Patel1*
1Department of Pharmaceutics, M.C.E. Society’s Allana College of Pharmacy, Azam Campus, Camp, Pune.
2HOD, Department of Pharmaceutics, Trinity College of Pharmacy, Pune.
*Corresponding Author
Published In:
Volume - 18,
Issue - 8,
Year - 2025
ABSTRACT:
The aim of this research was to formulate extended-release Furosemide tablets using Polylacticcoglycolic acid (PLGA) and Hydroxy Propyl Methyl Cellulose (HPMC) polymers. The wet granulation method was employed in the preparation, and a 32 Response Surface Methodology (RSM) factorial design was utilized, yielding a total of nine formulations (F1 to F9). The formulations were then subjected to thorough evaluation, which included assessing their physical parameters such as weight variation, hardness, friability, and thickness, as well as drug content and in vitro release profiles. All formulations conformed to the standards set forth by the Pharmacopoeia. The in-vitro dissolution experiments were performed utilizing the USP dissolution apparatus type-II (paddle method). Analyzing the dissolution profiles, formulation F1 emerged as the most optimal, showing the best extended-release profile.
Cite this article:
Shakeel Memon, Aney Joice, Dilnawaz Pathan, Aasia Patel. Formulation Development for ER Tablets of Furosemide with Statistical Optimization and Characterization by RSM Factorial approach. Research Journal Pharmacy and Technology. 2025;18(8):3565-1. doi: 10.52711/0974-360X.2025.00513
Cite(Electronic):
Shakeel Memon, Aney Joice, Dilnawaz Pathan, Aasia Patel. Formulation Development for ER Tablets of Furosemide with Statistical Optimization and Characterization by RSM Factorial approach. Research Journal Pharmacy and Technology. 2025;18(8):3565-1. doi: 10.52711/0974-360X.2025.00513 Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2025-18-8-16
8. REFRENCES:
1. Fukui S, et al. Design and evaluation of an extended-release matrix tablet formulation; the combination of hypromellose acetate succinate and hydroxypropylcellulose. Asian Journal of Pharmaceutical Sciences. 2017; 12(2): 149–56.doi:10.1016/j.ajps.2016.11.002
2. Aboelwafa AA, Basalious EB. Optimization and In vivo Pharmacokinetic Study of a Novel Controlled Release Venlafaxine Hydrochloride Three-Layer Tablet. AAPS PharmSciTech. 2010; 11(3): 1026–1037. doi:10.1208/s12249-010-9467-z
3. G. Nalini, V. Sai Kishore. Formulation and Evaluation of Extended Release Tablets of Alfuzosin Hydrochloride. Research J. Pharma. Dosage Forms and Tech. 2010; 2(6): 384-387.
4. Praveen KU, Madhusha RY. Formulation and Evaluation of Extended Release Tablets of Alfuzosin HCl. Res. J. Pharm. Dosage Form. And Tech. 2014; 6(2): 91-98.
5. Bawankar DL et al. Design and Characterization of Extended Release Ranolazine Matrix Tablet. Research J. Pharm. and Tech. 2009; 2(4); 756-761.
6. Barzeh H, Sogali BS, Shadvar S. A Review on Extended Release Matrix Tablet. Journal of Pharmaceutical Research. 2016; 15(4): 147-152. doi: 10.18579/jpcrkc/2016/15/4/108823
7. Samir S et al. A review on extended release drug delivery system and multiparticulate system. World Journal of Pharmaceutical Research. 2015; 4 (8): 724-747.
8. Hamed ES. A. Application of multiple response optimization technique to extended release formulations design. Journal of Controlled Release. 2001; 73(2): 329–338.doi.10.1016/S0168-3659(01)00356-X
9. Anas TN et al. Development and in-vitro /in-vivo evaluation of floating in-situ gelling oral liquid extended release formulation of Furosemide. Pharmaceutical and Bioscience Journal. 2014; 2 (5); 1–11. doi.10.20510/ukjpb/2/i5/91114
10. Karkhile Vet al. Formulation and evaluation of floating tablets of Furosemide. International Journal of Pharma Research and Development. 2009; 1 (12): 1–9.
11. Saravanakumar M et al.. Extended release matrix tablets of Stavudine: Formulation and in vitro evaluation. Asian J Pharm. 2014; 4 (3): doi.10.22377/ajp.v4i3.222
12. Ganesh C et al.. Preparation and characterization of solid dispersion tablet of Furosemide with crospovidone. Research J. Pharm. and Tech. 2008; 1(4): 386-389.
13. Rekhi GS et al. Identification of critical formulation and processing variables for metoprolol tartrate extended-release (ER) matrix tablets. Journal of Controlled Release. 1999; 59(3); 327-342.doi.10.1016/S0168-3659(99)00004-8
14. Wakelkamp, M et al. The influence of frusemide formulation on diuretic effect and efficiency. British Journal of Clinical Phazrmacology. 1999; 48(3): 361-366. doi:10.1046/j.1365-2125.1999.00015.x.
15. Vaidyanathan S et al. Pharmacokinetic interaction of the direct renin inhibitor aliskiren with Furosemide and extended‐release Isosorbide ‐5‐Mononitrate in healthy subjects. Cardiovascular Therapeutics. 2008; 26(4): 238–246. doi.10.1111/j.1755-5922.2008.00058.x
16. Vlachou M, Geraniou E, Siamidi A. Modified release of furosemide from Eudragits® and poly(ethylene oxide)-based matrices and dry-coated tablets. Acta Pharm. 2020; 70 (1): 49-61. doi: 10.2478/acph-2020-0010
17. Agyralides GG, Dallas PP, Rekkas DM. Development and in-vitro evaluation of furosemide transdermal formulations using experimental design techniques. International Journal of Pharmaceutics. 2004; 281(1–2): 35–43. doi: 10.1016/j.ijpharm.2004.05.011.
18. Klausner EA et al. Furosemide pharmacokinetics and pharmacodynamics following gastroretentive dosage form administration to healthy volunteers. The Journal of Clinical Pharma. 2003; 43(7): 711–720. doi.10.1177/0091270003254575
19. Darandale SS, Vavia PR. Design of a gastroretentive mucoadhesive dosage form of furosemide for controlled release. Acta Pharmaceutica Sinica B. 2012; 2(5): 509–517.doi.10.1016/j.apsb.2012.05.004
20. Akbug̃a J. Preparation and evaluation of controlled release furosemide microspheres by spherical crystallization. International Journal of Pharmaceutics. 1989; 53(2): 99–105.doi.10.1016/0378-5173(89)90233-0
21. Youm I, Murowchick JB, Youan BC. Entrapment and release kinetics of furosemide from pegylated nanocarriers. Colloids and Surfaces B Biointerfaces. 2012; 94: 133–142. doi.10.1016/j.colsurfb.2012.01.027
22. Perioli L, Alba G, Pagano C. New oral solid dosage form for furosemide oral administration. European Journal of Pharmaceutics and Biopharmaceutics. 2012; 80 (3): 621–629. doi.10.1016/j.ejpb.2011.12.011
23. Nagendrakumar D, Keshavshetti G, Shardor SA. Sustained release matrix tablets of Furosemide. Rajiv Gandhi University of Health Sciences Journal of Pharmaceutical Sciences. 2015; 5(3): 105–112. doi.10.5530/rjps.2015.3.4
24. Cruz R, Hernandez E, Aceves Hernandez JM. Preparation and characterization of Furosemide-eudragit controlled release systems. International Journal of Pharmaceutics, Volume 195, Issues 1–2, 15 February 2000; 45-53. doi.10.1016/s0378-5173(99)00303-8
25. Hasselgren B et al. Pharmacokinetics and hemodynamic and diuretic/natriuretic effects of felodipine administered as an extended-release tablet. Cardiovascular Drugs and Therapy. 1990; 4 (6): 1495–1500. doi.10.1007/bf02026497
26. Shakeel Memon, Kiran SB. Microwave irradiation technique: a green chemistry approach for dissolution enhancement of Ritonavir. Research Journal of Pharmacy and Technology. 2023; 16(6): 2643-2648. doi.10.52711/0974-360X.2023.00434
27. Gajanan D et al. Development and optimization of Dorzolamide Hydrochloride and Timolol Maleate in Situ gel for glaucoma Treatment. Asian J. Pharm. Analysis. 2011; 1(4): 93-97.
28. Lakshmi PJ, Deepthi B, Rama RN. TSP Based Matrix Tablets: studying the effect of formulation variables employing response surface methodology. Asian J. Pharmaceutical Research. 2012; 2(3): 120-126.
29. Indrajeet S et al. Development and Evaluation of Telmisartan pulsatile drug delivery by using response surface methodology. Asian J. Pharmacetical Research 2018; 8(4): 205-214. doi.10.5958/2231-5691.2018.00035.7
30. Shaghayegh R, Farzaaneh Z, Hamid AJ. Optimization of drug loading in modified Nano-zeolites using response surface methodology by Box–Behnken design. Asian J. Pharmaceutical Research. 2020; 10(2): 55-61. doi.10.5958/2231-5691.2020.00011.8
31. Bouaziz BA. Optimization of Extraction conditions of the Polyphenols, Flavonoids and the Antioxidant activity of the plant Ammosperma- cinereum (Brassicaceae) through the response surface methodology (RSM). Asian J.Research Chemistry. 2020; 13(1): 01-06. doi.10.5958/0974-4150.2020.00001.2
32. Lachman L, Lieberman HA, Kanig J. The Theory and Practice of Industrial Pharmacy. 3rd edition. Varghese publishing house, Bombay; 1987: 333-338.