Authors :
Prashant Wake; Dr. Rajesh Mujariya
Volume/Issue :
Volume 11 - 2026, Issue 4 - April
Google Scholar :
https://tinyurl.com/y2yr7aa3
Scribd :
https://tinyurl.com/2t83sjr5
DOI :
https://doi.org/10.38124/ijisrt/26apr624
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Abstract :
Almotriptan, a potent 5-HT1B/1D receptor agonist used in migraine therapy, faces clinical challenges due to its
inherently bitter taste, which can hinder patient compliance during acute attacks. This study aimed to develop taste-masked,
rapid-melt tablets (RMTs) of Almotriptan with enhanced dissolution profiles using a combined solid dispersion (SD) strategy.
Ternary solid dispersions were prepared using various polymeric carriers, including Soluplus and Eudragit EPO, via solvent
evaporation. The formulations were characterized using Differential Scanning Calorimetry (DSC), Powder X-ray
Diffraction (PXRD), and Fourier Transform Infrared Spectroscopy (FTIR) to assess drug-polymer interactions and
crystallinity. The optimized SDs were then compressed into RMTs and evaluated for disintegration time, wetting time, and
in vitro drug release. Taste masking was assessed through dissolution in simulated salivary fluid. Physicochemical
characterization confirmed the transformation of Almotriptan from a crystalline to an amorphous state within the polymer
matrix, significantly increasing the saturation solubility compared to the pure drug. The optimized RMT formulation
exhibited a rapid disintegration time of less than 30 seconds. Furthermore, the solid dispersion effectively sequestered the
drug, significantly reducing the perceived bitterness. Stability studies conducted at 40°C/75% RH for six months indicated
that the formulations remained stable with no significant changes in drug content or release kinetics.
Keywords :
Almotriptan Malate, Solid Dispersion, Rapid-Melt Tablets, Orally Disintegrating Tablets - ODTs, Taste masking, Ternary Systems, Soluplus / Eudragit EPO.
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Almotriptan, a potent 5-HT1B/1D receptor agonist used in migraine therapy, faces clinical challenges due to its
inherently bitter taste, which can hinder patient compliance during acute attacks. This study aimed to develop taste-masked,
rapid-melt tablets (RMTs) of Almotriptan with enhanced dissolution profiles using a combined solid dispersion (SD) strategy.
Ternary solid dispersions were prepared using various polymeric carriers, including Soluplus and Eudragit EPO, via solvent
evaporation. The formulations were characterized using Differential Scanning Calorimetry (DSC), Powder X-ray
Diffraction (PXRD), and Fourier Transform Infrared Spectroscopy (FTIR) to assess drug-polymer interactions and
crystallinity. The optimized SDs were then compressed into RMTs and evaluated for disintegration time, wetting time, and
in vitro drug release. Taste masking was assessed through dissolution in simulated salivary fluid. Physicochemical
characterization confirmed the transformation of Almotriptan from a crystalline to an amorphous state within the polymer
matrix, significantly increasing the saturation solubility compared to the pure drug. The optimized RMT formulation
exhibited a rapid disintegration time of less than 30 seconds. Furthermore, the solid dispersion effectively sequestered the
drug, significantly reducing the perceived bitterness. Stability studies conducted at 40°C/75% RH for six months indicated
that the formulations remained stable with no significant changes in drug content or release kinetics.
Keywords :
Almotriptan Malate, Solid Dispersion, Rapid-Melt Tablets, Orally Disintegrating Tablets - ODTs, Taste masking, Ternary Systems, Soluplus / Eudragit EPO.