FORMULATION AND EVALUATION OF IBUPROFEN AND CHLORZOXAZONE SUSPENSION USING NATURAL AND SYNTHETIC SUSPENDING AGENTS
Abstract
The present study was undertaken to formulate and evaluate an oral suspension of Ibuprofen and Chlorzoxazone using natural and synthetic suspending agents, with the objective of comparing their influence on physicochemical properties and suspension stability. Ibuprofen, a non-steroidal anti-inflammatory drug, and Chlorzoxazone, a centrally acting muscle relaxant, are widely prescribed in musculoskeletal disorders but exhibit poor aqueous solubility, making suspension formulation a suitable approach for improving patient compliance. Four formulations (F1–F4) were prepared by the trituration method using methylcellulose as a synthetic suspending agent and fenugreek (Trigonella foenum-graecum) seed powder as a natural suspending agent at different concentrations. Preformulation studies, including melting point determination and FTIR spectroscopy, confirmed the identity and purity of both drugs. The prepared suspensions were evaluated for particle size, sedimentation volume, viscosity, flow rate, pH, swelling index, and phytochemical characteristics. Among the formulations, F2 exhibited the highest viscosity and sedimentation volume with the lowest flow rate, indicating superior physical stability, while F4 demonstrated acceptable stability with improved homogeneity using a natural suspending agent. All formulations showed pH values within an acceptable range for oral administration. The swelling index and phytochemical screening confirmed the presence of mucilage and other bioactive constituents in fenugreek seed powder, supporting its role as an effective natural suspending agent. The study demonstrates that natural suspending agents can serve as promising alternatives to synthetic polymers in suspension formulations.
Keywords:
Ibuprofen, Chlorzoxazone, Oral suspension, Fenugreek seed powder, Methylcellulose, Natural suspending agentDOI
https://doi.org/10.37022/wjcmpr.v8i1.381References
1. Ponnada VNL. Formulation and evaluation of ibuprofen suspension using natural and synthetic suspending agents. 2017.
2. Subramanyam CVS. Textbook of Physical Pharmaceutics. 2nd ed. New Delhi: Vallabh Prakashan; 2002. p. 374–387.
3. Kumar RS, Yagnesh TNS. Pharmaceutical suspensions: patient compliance oral dosage forms. World J Pharm Pharm Sci. 2016;5(12):1471–1537.
4. Jahnavi P., Kumar A. K., Prema S., Ramana Singamaneni V., Vidiyala N., Sunkishala P., Rani S., Shankar Gupta P. Recent Progress in Heterogeneous Catalysis for Sustainable Chemical Processes. J. Chem. Rev., 2026; 8(2): 154-179. doi: 10.48309/jcr.2026.535464.1482
5. Vodeti R, Rejili M, Singamaneni VR, Hani U, Fatima F, Kumar Gupta J, et al. Gamma irradiation crosslinked fluorescent nanocarbon based biodegradable hydrogel for controlled release of antibiotics. Singha NR, editor. PLOS One. 2026 Jan 16;21(1):e0340351.
6. Ansel HC, Popovich NG, Allen LV Jr. Pharmaceutical Dosage Forms and Drug Delivery Systems. 10th ed. Philadelphia: Lippincott Williams & Wilkins; 2020.
7. Martin A, Swarbrick J, Cammarata A, editors. Physical Pharmacy. 3rd ed. Philadelphia: Lea and Febiger; 1983. p. 544.
8. Nutan MT, Reddy IK. General principles of suspensions. In: Pharmaceutical Suspensions. New York: Springer; 2010. p. 39–65.
9. Cooper J, Gunn C. Tutorial Pharmacy. 6th ed. New Delhi: CBS Publishers; 1987. p. 75–78.
10. Sushma G, Kumar KM, Ajay B, Ruchi T. Advancements and patents in pharmaceutical suspension technologies. J Biol Sci Opin. 2013;1(4):1–9.
11. Patel RM. Parenteral suspension: an overview. Int J Curr Pharm Res. 2010;2:4–13.
12. Doye PAKP, Mena T, Das N. Formulation and bioavailability parameters of pharmaceutical suspension. Int J Curr Pharm Res. 2017;9(3):8–14.
13. Chukka S, Puligilla S, Yamsani MR. New formulation and evaluation of domperidone suspension. World J Pharm Pharm Sci. 2014;3:1867–1884.
14. Aulton ME. Pharmaceutics: The Science of Dosage Form Design. 2nd ed. Edinburgh: Churchill Livingstone; 2002. p. 84–86, 273.
15. Martin A. Physical Pharmacy. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2001. p. 479–481.
16. Matalqah SM, Singamaneni VR, Jahnavi P, Hani U, Fatima F, Vodeti R, et al. Bio-waste derived fluorescent carbon dots based biodegradable mechanically strong hydrogel for stimuli-responsive nonsteroidal anti-inflammatory drug (NSAID) delivery. Singha NR, editor. PLOS One. 2026 Jan 23;21(1):e0340974.
17. Dhole RS; Singamaneni VR; Chhabra GS; Taru PP; Pathare SS; Pathare YS; Ram BLGPR; Sakat SS, Formulation and Evaluation of Xanthan Gum-Based Naproxen Matrix Tablets for Controlled Drug Release. Int J Drug Deliv Technol. 2025;15(4): 1794-1804, DOI: 10.25258/ijddt.15.4.32
18. Kulshreshtha AK, Singh ON, Wall GM, editors. Pharmaceutical Suspensions: From Formulation Development to Manufacturing. New York: Springer; 2009.
19. Kellaway IW, Najib NM. Hydrophilic polymers as stabilizers and flocculants of sulphadimidine suspensions. Int J Pharm. 1981;9:59–66.
20. Irvine J, Afrose A, Islam N. Formulation and delivery strategies of ibuprofen: challenges and opportunities. Drug Dev Ind Pharm. 2018;44(2):173–183.
21. Parojčić J, Corrigan OI. Rationale for ibuprofen co-administration with antacids: potential interaction mechanisms affecting drug absorption. Eur J Pharm Biopharm. 2008;69(2):640–647.
22. Moore RA, Derry S, Straube S, Ireson-Paine J, Wiffen PJ. Faster, higher, stronger? Evidence for formulation and efficacy for ibuprofen in acute pain. Pain. 2014;155(1):14–21.
23. Barbagallo M, Sacerdote P. Ibuprofen in the treatment of children’s inflammatory pain: a clinical and pharmacological overview. Minerva Pediatr. 2019;71(1):82–99.
24. Yang Z, Hu Y, Tang G, Dong M, Liu Q, Lin X. Development of ibuprofen dry suspensions by hot melt extrusion: characterization, physical stability and pharmacokinetic studies. J Drug Deliv Sci Technol. 2019;54:101313.
25. Kocbek P, Baumgartner S, Kristl J. Preparation and evaluation of nanosuspensions for enhancing the dissolution of poorly soluble drugs. Int J Pharm. 2006;312(1–2):179–186.
26. Helin-Tanninen M, Autio K, Keski-Rahkonen P, Naaranlahti T, Järvinen K. Comparison of six different suspension vehicles in compounding of oral extemporaneous nifedipine suspension for paediatric patients. Eur J Hosp Pharm Sci Pract. 2012;19(5):432–437.
27. Moqbel HA, ElMeshad AN, El-Nabarawi MA. A pharmaceutical study on chlorzoxazone orodispersible tablets: formulation, in-vitro and in-vivo evaluation. Drug Deliv. 2016;23(8):2998–3007.
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