Design, Development and Evaluation of Nimesulide-Loaded Nanosponges for Compression into Fast Dissolving Tablets to Enhance Solubility and Dissolution Rate
Abstract
The present study aimed to design, develop, and evaluate Nimesulide-loaded nanosponges incorporated into fast dissolving tablets to enhance solubility and dissolution rate. Nimesulide, a BCS Class II non-steroidal anti-inflammatory drug, suffers from poor aqueous solubility leading to limited dissolution and bioavailability. To overcome this limitation, nanosponges were prepared by the emulsion solvent diffusion method using ethyl cellulose and polyvinyl alcohol. The optimized formulation exhibited a particle size of 180 ± 5.2 nm, PDI of 0.21, and zeta potential of -28.6 ± 1.4 mV, indicating uniformity and stability. SEM analysis confirmed a porous, sponge-like structure suitable for drug entrapment.
The optimized nanosponges were further compressed into fast dissolving tablets using direct compression with suitable excipients. Pre-compression studies indicated good flow properties, while post-compression evaluation showed acceptable weight variation, friability (0.48%), hardness (3.8 ± 0.4 kg/cm²), and high drug content (98.6 ± 1.2%). The tablets exhibited rapid wetting and dispersion times, confirming fast disintegration characteristics. In vitro dissolution studies demonstrated enhanced drug release, with 98% release achieved within 45 minutes.
The results indicate that nanosponge-based fast dissolving tablets significantly improve the solubility, dissolution rate, and potential bioavailability of Nimesulide. This approach provides an effective and patient-friendly strategy for delivering poorly water-soluble drugs with improved therapeutic performance.
Keywords: Nimesulide, Nanosponges, Fast Dissolving Tablets, Solubility Enhancement, Dissolution Rate, BCS Class II Drug.
Keywords:
Nimesulide, Nanosponges, Fast Dissolving Tablets, Dissolution Rate, BCS Class II Drug, Solubility EnhancementDOI
https://doi.org/10.22270/jddt.v16i6.7771References
1. Singla AK, Chawla M, Singh A. Review nimesulide: some pharmaceutical and pharmacological aspects-an update. Journal of pharmacy and pharmacology. 2000 May;52(5):467-86. https://doi.org/10.1211/0022357001774255 PMid:10864134
2. Bernareggi A. Clinical pharmacokinetics of nimesulide. Clinical pharmacokinetics. 1998 Oct;35(4):247-74. https://doi.org/10.2165/00003088-199835040-00001 PMid:9812177
3. Davis R, Brogden RN. Nimesulide: an update of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy. Drugs. 1994 Sep;48(3):431-54. https://doi.org/10.2165/00003495-199448030-00008 PMid:7527762
4. Rainsford KD, Consensus Report Group on Nimesulide. Nimesulide-a multifactorial approach to inflammation and pain: scientific and clinical consensus. Current medical research and opinion. 2006 Jun 1;22(6):1161-70. https://doi.org/10.1185/030079906X104849 PMid:16846549
5. Kress HG, Baltov A, Basiński A, Berghea F, Castellsague J, Codreanu C, Copaciu E, Giamberardino MA, Hakl M, Hrazdira L, Kokavec M. Acute pain: a multifaceted challenge-the role of nimesulide. Current medical research and opinion. 2016 Jan 2;32(1):23-36. https://doi.org/10.1185/03007995.2015.1100986 PMid:26414386
6. Tejashri G, Amrita B, Darshana J. Cyclodextrin based nanosponges for pharmaceutical use: A review. Acta pharmaceutica. 2013 Sep 30;63(3):335-58. https://doi.org/10.2478/acph-2013-0021 PMid:24152895
7. Trotta F, Dianzani C, Caldera F, Mognetti B, Cavalli R. The application of nanosponges to cancer drug delivery. Expert opinion on drug delivery. 2014 Jun 1;11(6):931-41. https://doi.org/10.1517/17425247.2014.911729 PMid:24811423
8. Shringirishi M, Prajapati SK, Mahor A, Alok S, Yadav P, Verma A. Nanosponges: a potential nanocarrier for novel drug delivery-a review. Asian pacific journal of tropical disease. 2014 Sep 1;4:S519-26. https://doi.org/10.1016/S2222-1808(14)60667-8
9. Gowda BJ, Ahmed MG, Almoyad MA, Wahab S, Almalki WH, Kesharwani P. Nanosponges as an emerging platform for cancer treatment and diagnosis. Advanced Functional Materials. 2024 Feb;34(7):2307074. https://doi.org/10.1002/adfm.202307074
10. Siddiqui MN, Garg G, Sharma PK. Fast dissolving tablets: preparation, characterization and evaluation: an overview. International Journal of Pharmaceutical Sciences Review and Research. 2010 Sep;4(2):87-96.
11. Chang RK, Guo X, Burnside BA, Couch RA. Fast-dissolving tablets. Pharmaceutical technology. 2000;24(6):52-.
12. Gupta AK, Mittal A, Jha KK. Fast dissolving tablet-A review. The pharma innovation. 2012 Mar 1;1(1):1-8.
13. Ahmed MM, Fatima F, Anwer MK, Ansari MJ, Das SS, Alshahrani SM. Development and characterization of ethyl cellulose nanosponges for sustained release of brigatinib for the treatment of non-small cell lung cancer. Journal of Polymer Engineering. 2020 Nov 26;40(10):823-32. https://doi.org/10.1515/polyeng-2019-0365
14. Moin A, Roohi NF, Rizvi SM, Ashraf SA, Siddiqui AJ, Patel M, Ahmed SM, Gowda DV, Adnan M. Design and formulation of polymeric nanosponge tablets with enhanced solubility for combination therapy. RSC advances. 2020;10(57):34869-84. https://doi.org/10.1039/D0RA06611G PMid:35514416 PMCid:PMC9056836
15. Altinöz S, Dursun ÖÖ. Determination of nimesulide in pharmaceutical dosage forms by second order derivative UV spectrophotometry. Journal of pharmaceutical and biomedical analysis. 2000 Feb 1;22(1):175-82. https://doi.org/10.1016/S0731-7085(99)00264-2 PMid:10727137
16. Uppar AL, Patil CC, Namannavar S, Deshmane PA. Formulation and evaluation of Caffeine-Loaded Cubosomes hydrogel for topical delivery. Journal of Drug Delivery and Therapeutics. 2026 Apr 15;16(4):39-47. https://doi.org/10.22270/jddt.v16i4.7666
17. Ural N. The significance of scanning electron microscopy (SEM) analysis on the microstructure of improved clay: An overview. Open Geosciences. 2021 Feb 19;13(1):197-218. https://doi.org/10.1515/geo-2020-0145
18. Vreeman G, Sun CC. A strategy to optimize precompression pressure for tablet manufacturing based on in-die elastic recovery. International journal of pharmaceutics. 2024 Apr 10;654:123981. https://doi.org/10.1016/j.ijpharm.2024.123981 PMid:38460772
19. Nayak S, Rakshita AS, Kamath S. Study of post compression parameters of various marketed paracetamol tablets in India. PharmaTutor. 2019 Feb 1;7(2):35-42. https://doi.org/10.29161/PT.v7.i2.2019.35
20. Kim KH, Park JB, Kang JH, Lee KH, Kang CY. Formulation and Evaluation of Sustained Release Preparation of Ibuprofen Fast-Disintegrating Tablet (FDT). Journal of Pharmaceutical Investigation. 2011;41(1):51-7. https://doi.org/10.4333/KPS.2011.41.1.051a
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Copyright (c) 2026 Sahil Ansari , Pradeepa Ganesan , Shruti A Khandke , Vaishnavi Vanasakrithmath , K. Sandhiya, Soham M. Naik Gaonkar , Divya Vivek Donage , C K Anusha , Ganavi Maheshappa Halageri

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