Formulation and Evaluation of Fast Disintegrating Tablet of Eletriptan Hydrobromide

The present study focuses on the formulation and evaluation of fast disintegrating tablets (FDTs) of Eletriptan hydrobromide, an antimigraine agent with poor oral bioavailability due to extensive first-pass metabolism.The aim was to develop a formulation that ensures rapid onset of action by enhancing disintegration time and drug release.Different amounts of superdisintegrants, such as croscarmellose sodium (CCS) and sodium starch glycolate (SSG), were employed.Among the formulations developed, formulation F5, containing SSG and CCS, demonstrated optimal results with a disintegration time of less than 15 seconds, meeting all required physicochemical parameters.In vitro drug release studies showed up to 99.7% release, indicating excellent dissolution characteristics.These findings support the potential of FDTs of Eletriptan hydrobromide as a fast-acting, patient-friendly alternative for the effective management of acute migraine attacks.

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Publication Details

Journal
International Journal of Research Publication and Reviews
Published
2025-05-01
DOI
https://doi.org/10.55248/gengpi.6.0525.1918
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
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article

Formulation and Evaluation of Fast Disintegrating Tablet of Eletriptan Hydrobromide

Vishal B Ambekar, Mr.Babasaheb L Chopade, Dr.Megha T Salve
International Journal of Research Publication and Reviews
Drug Solubulity and Delivery Systems
article

Formulation and Evaluation of Fast Disintegrating Tablet of Eletriptan Hydrobromide

Vishal B Ambekar, Mr.Babasaheb L Chopade, Dr.Megha T Salve
article en

Abstract

The present study focuses on the formulation and evaluation of fast disintegrating tablets (FDTs) of Eletriptan hydrobromide, an antimigraine agent with poor oral bioavailability due to extensive first-pass metabolism.The aim was to develop a formulation that ensures rapid onset of action by enhancing disintegration time and drug release.Different amounts of superdisintegrants, such as croscarmellose sodium (CCS) and sodium starch glycolate (SSG), were employed.Among the formulations developed, formulation F5, containing SSG and CCS, demonstrated optimal results with a disintegration time of less than 15 seconds, meeting all required physicochemical parameters.In vitro drug release studies showed up to 99.7% release, indicating excellent dissolution characteristics.These findings support the potential of FDTs of Eletriptan hydrobromide as a fast-acting, patient-friendly alternative for the effective management of acute migraine attacks.

International Journal of Research Publication and ReviewsVol. 6(5)
American Association of Colleges of Pharmacy (US)
Openalex Percentile: Top 91%
Drug Solubulity and Delivery Systems
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