Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 May 19:2022:9618344.
doi: 10.1155/2022/9618344. eCollection 2022.

Formulation of Ebastine Fast-Disintegrating Tablet Using Coprocessed Superdisintegrants and Evaluation of Quality Control Parameters

Affiliations

Formulation of Ebastine Fast-Disintegrating Tablet Using Coprocessed Superdisintegrants and Evaluation of Quality Control Parameters

Bhawana Dhakal et al. ScientificWorldJournal. .

Abstract

Ebastine is a long-acting, nonsedating, second-generation antihistaminic drug that prevents histamine action, mainly in immediate hypersensitivity. This project was aimed to formulate and characterize orodispersible tablets of ebastine, utilizing different proportions of three disintegrants, namely crospovidone, sodium starch glycolate, and coprocessed superdisintegrant. Initially, fifteen trial batches of ebastine orodispersible tablets were outlined using the central composite design of Minitab software. The tablets were formulated by the direct compression method. The compressed tablets were then evaluated for precompression and postcompression physicochemical parameters, such as angle of repose, Carr's index, Hausner's ratio, hardness, thickness, weight variation, drug content, friability, wetting time, disintegration time, dispersion time, and water absorption ratio. The in vitro dissolution test was conducted according to Indian Pharmacopeia 2018, with the help of the rotating paddle method using 0.5% w/v sodium lauryl sulfate buffer in 0.1 N HCl. For the optimized batch (8th batch), all the physicochemical parameters like angle of repose (33.77°), Carr's index (19.34%), Hausner's ratio (1.24), weight variation (202.5 mg), hardness (4.3 kg/cm2), friability (0.44%), thickness (3.16 mm), dissolution (95.78%), and drug content (101.67%) were within the acceptable limit as per Indian Pharmacopeia 2018. The wetting time, disintegration time, dispersion time, and water absorption ratio were reported to be 25.1 seconds, 16.0 seconds, 38.6 seconds, and 91.92%, respectively. Hence, the results suggested that orodispersible tablets of ebastine can be formulated. Furthermore, the mixing of crospovidone, sodium starch glycolate, and coprocessed super disintegrants can result in excellent desirable properties in the orodispersible tablet.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Standard calibration curve of ebastine.
Figure 2
Figure 2
Bar diagram showing drug content and dissolution behavior of different batches.
Figure 3
Figure 3
Bar diagram for the measurement of wetting time (in seconds) for different batches.
Figure 4
Figure 4
Bar diagram for the measurement of in vitro disintegration time (in seconds) for different batches.
Figure 5
Figure 5
Bar diagram for the measurement of water absorption ratio (in percentage) for different batches.
Figure 6
Figure 6
Bar diagram for the measurement of in vitro dispersion time (in seconds) for different batches.
Figure 7
Figure 7
Chromatogram of FTIR for ebastine (green color: FTIR chromatogram of standard drug ebastine, red color: FTIR chromatogram of the ebastine mixed with all the excipients).

References

    1. Gandhi A. Mouth dissolving tablets: a new venture in modern formulation technology. The Pharma Innovation . 2012;1(8):14–31.
    1. Koirala S., Nepal P., Ghimire G., et al. Formulation and evaluation of mucoadhesive buccal tablets of aceclofenac. Heliyon . 2021;7(3) doi: 10.1016/j.heliyon.2021.e06439.e06439 - DOI - PMC - PubMed
    1. Shravani B., Rao N. G. R. Formulation and evaluation of fast dissolving tablets of montelukast sodium using co-processed superdisintegrants. International Journal of Drug Development & Research . 2014;6(1):125–134.
    1. Ratnaparkhi M. P., Mohanta G. P., Upadhyay L. Review on: fast dissolving tablet. Journal of Pharmacy Research . 2009;2(1):5–12.
    1. Nagendrakumar D., Raju S. A., Shirsand S. B., Para M. S. Design of fast dissolving granisetron HCL tablets using novel coprocessed superdisintegrants. International Journal of Pharmaceutical Sciences Review and Research . 2010;1(1):58–62.

LinkOut - more resources