Author(s):
Gauri Dewangan, Pratikshya Panda, Anju Mishra, Digeshwari Patel, Anish Chandy
Email(s):
anishc@cecbilaspur.ac.in
DOI:
10.52711/0975-4377.2026.00048
Address:
Gauri Dewangan1, Pratikshya Panda1, Anju Mishra2, Digeshwari Patel2, Anish Chandy3
1Students, School of Pharmacy, Chouksey Engineering College, Bilaspur, Chhattisgarh, India.
2Assistant Professor, School of Pharmacy, Chouksey Engineering College, Bilaspur, Chhattisgarh, India.
3Associate Professor, School of Pharmacy, Chouksey Engineering College, Bilaspur, Chhattisgarh, India.
*Corresponding Author
Published In:
Volume - 18,
Issue - 4,
Year - 2026
ABSTRACT:
Levocetirizine dihydrochloride is a potent oral third-generation antihistamine that is not sedative in nature and is prescribed for the treatment of allergic rhinitis, both seasonal and perennial. The objective of the current study was to create immediate-release films of levocetirizine that could produce instant therapeutic effects that are helpful in managing serious allergy attacks, enhancing bioavailability of the drug, and increasing convenience of administration. Films of levocetirizine dihydrochloride were prepared using either single polymer or combination of two polymers that include hydroxypropyl methylcellulose (HPMC) and polyvinyl alcohol (PVA) by means of the solvent casting method, and underwent evaluation of the physical properties that included weight uniformity, thickness, tensile strength, elongation, surface pH, folding endurance, and drug content uniformity, yielding satisfactory results. The formulations underwent tests of disintegration and in vitro drug release and were subjected to in vivo studies on rats. Fast dissolving films of levocetirizine dihydrochloride with HPMC were found to demonstrate a greater rate of dissolution than normal tablets. Levocetirizine dihydrochloride fast dissolving films may be clinically applied in the treatment of allergic rhinitis and other allergic diseases when prompt onset of action of the dosage form is needed and the user-friendliness of the application is wanted.
Cite this article:
Gauri Dewangan, Pratikshya Panda, Anju Mishra, Digeshwari Patel, Anish Chandy. Development and Optimization of Oral Films of Levocetrizine using Natural Polymer. Research Journal of Pharmaceutical Dosage Forms and Technology. 2026; 18(4):345-9. doi: 10.52711/0975-4377.2026.00048
Cite(Electronic):
Gauri Dewangan, Pratikshya Panda, Anju Mishra, Digeshwari Patel, Anish Chandy. Development and Optimization of Oral Films of Levocetrizine using Natural Polymer. Research Journal of Pharmaceutical Dosage Forms and Technology. 2026; 18(4):345-9. doi: 10.52711/0975-4377.2026.00048 Available on: https://rjpdft.com/AbstractView.aspx?PID=2026-18-4-10
REFERENCES:
1. Pacheco MS, Barbieri D, Silva CF, Moraes MA. A review on orally disintegrating films (ODFs) made from natural polymers such as pullulan, maltodextrin, starch, and others. Int J Biol Macromol. 2021; 178: 504-513. doi: 10.1016/j.ijbiomac.2021.02.180.
2. He M, Zhu L, Yang N, Li H, Yang Q. Recent advances of oral film as platform for drug delivery. Int J Pharm. 2021; 604:120759. doi: 10.1016/j.ijpharm.2021.120759.
3. Morath B, Sauer S, Zaradzki M, Wagner AH. Orodispersible films—recent developments and new applications in drug delivery and therapy. Biochem Pharmacol. 2022; 200: 115036. doi: 10.1016/j.bcp.2022.115036.
4. Shinde S, Ghonge M, Kathpalia H. Recent updates on oral and dermal film-based formulations and their applications. Curr Drug Deliv. 2023; 20(4): 335-349. doi:10.2174/1567201819666220307112525.
5. Ferlak J, Guzenda W, Osmałek T. Orodispersible films—current state of the art, limitations, advances and future perspectives. Pharmaceutics. 2023; 15(2): 361. doi:10.3390/pharmaceutics15020361.
6. Gupta MS, Kumar TP, Reddy D, Pathak K, Gowda DV, Babu AVN, et al. Development and characterization of pullulan-based orodispersible films of iron. Pharmaceutics. 2023; 15(3): 1027. doi:10.3390/pharmaceutics15031027.
7. Shruthi BK, Chandrakala V, Srinivasan S. Formulation and evaluation of mouth-dissolving film of an H1 antihistamine drug. Int J Curr Pharm Res. 2022; 14(6): 55-66. doi:10.22159/ijcpr.2022v14i6.2062.
8. Jadach B, Kowalczyk M, Froelich A. Assessment of alginate gel films as the orodispersible dosage form for meloxicam. Gels. 2024; 10(6): 379. doi:10.3390/gels10060379.
9. Helfenstein AA, Dias ER, Reis IMA, Freitas EES, Biondi IB, Branco CRC, et al. Mucoadhesive oral film based on high methoxyl pectin and phosphated cassava starch incorporated with Calendula officinalis extract. J Drug Deliv Sci Technol. 2024; 102(Pt B): 106428. doi: 10.1016/j.jddst.2024.106428.
10. Wargantiwar S, Bhattacharya S. Biocompatible natural polymers and cutting-edge fabrication techniques in the development of next-generation oral thin films for enhanced drug delivery systems. Curr Pharm Des. 2025; 31(5): 331-343. doi:10.2174/0113816128329293241001090601.
11. Li Y, Zhao M, Zhao MY, Li B, Tian JL. Advances in oral dissolving film research in the food field. Food Prod Process Nutr. 2025; 7:9. doi:10.1186/s43014-024-00285-x.
12. Kozakiewicz-Latała M, Dyba AJ, Marciniak D, Szymczyk-Ziółkowska P, Cieszko M, Nartowski KP, et al. PVA-based formulations as a design-technology platform for orally disintegrating film matrices. Int J Pharm. 2024; 665: 124666. doi: 10.1016/j.ijpharm.2024.124666.
13. Saxena A, Singh T. Oral dissolving films: a comprehensive review on recent perspectives and current approach to effective drug delivery. J Drug Deliv Ther. 2022; 12(2): 109-116. doi:10.22270/jddt. v12i2.5244.
14. Prakash D, Arora V, Dewangan HK. A systematic review of the application of natural polymers in the formulation of oro-dispersible tablet. Int J Appl Pharm. 2023; 15(5): 27-36. doi:10.22159/ijap.2023v15i5.48183.
15. Zarekar NS, et al. Orodispersible film (ODF) platform based on maltodextrin for therapeutical applications. Pharmaceutics. 2022; 14. doi:10.3390/pharmaceutics14102087.
16. Nair AB, et al. Multiple roles of chitosan in mucosal drug delivery: an updated review. Mar Drugs. 2022; 20(5): 335. doi:10.3390/md20050335.
17. Pezik E, et al. Development and characterization of pullulan-based orally disintegrating films containing amlodipine besylate. Eur J Pharm Sci. 2021; 158:105639. doi: 10.1016/j.ejps.2020.105639.
18. Patel GJ, Modi AD. Formulation, optimization and evaluation of levocetirizine dihydrochloride oral thin strip. J Pharm Bioallied Sci. 2012; 4(Suppl 1): S35-S36. doi:10.4103/0975-7406.94133.
19. Kathpalia H, Patil A. Formulation and evaluation of orally disintegrating films of levocetirizine dihydrochloride. Indian J Pharm Sci. 2017; 79(2): 204-211. doi:10.4172/pharmaceutical-sciences.1000218.
20. Lakshmi PK, Sreekanth J, Sridharan A. Formulation development of fast releasing oral thin films of levocetirizine dihydrochloride with Eudragit® EPO and optimization through Taguchi orthogonal experimental design. Asian J Pharm. 2014; 5(2). doi:10.22377/ajp. v5i2.89.
21. Shruthi et al., 2022 — directly investigates levocetirizine + sodium alginate + guar gum, making it one of the most directly relevant papers. The sodium-alginate formulation showed 14.28 s disintegration and 98.24% dissolution.
22. Pacheco et al., 2021 — excellent scientific basis for selecting natural polymers such as pullulan, starch, alginate, pectin, gelatin and chitosan.
23. Gupta et al., 2023 — useful experimental precedent for pullulan-based films, including formulation and characterization.
24. Jadach et al., 2024 — particularly useful if you are considering sodium alginate as your primary natural film-forming polymer.
25. Helfenstein et al., 2024 — useful for pectin/starch-based oral films and natural-polymer combinations.
26. Wargantiwar and Bhattacharya, 2025 — very recent review supporting the scientific rationale for natural polymers in oral thin films.
27. Patel and Modi, 2012 and Kathpalia and Patil, 2017 — important levocetirizine-specific formulation precedents, even though they are older.