Formulation and Evaluation of Almotriptan Hydrobromide Pellets
DOI:
https://doi.org/10.26452/ijebr.v1i3.384Keywords:
Almotriptan, Controlled Release, Dissolution Profile, In-vitro Drug Release, Stability StudiesAbstract
An objective of the present research was to establish as well as analyze Almotriptan hydrobromide pellets. Almotriptan hydrobromide rapid onset but also controlled drug release pellets have been able to prepare through solution’s/suspension layer-based technique through using croscarmellose but also povidone through former case as well as 3 different polymeric materials hydroxypropyl methylcellulose k 100, Ethyl cellulose and Eudragit RS 100 just like price trying to control polymer through 4 distinct assists ratio such as 1:0.5, 1:1, 1:1.5 as well as 1:2 to accomplish preferred discharge through later case. Evaluation has been conducted according to the pharmacopoeia norms along with opioid components suitability, percent yield, distribution of particle size, drug content evaluation as well as in-vitro release survey. One of the best results have been obtained to use the Almotriptan as well as Eudragit RS 100 through 1:2 ratios. One wide selections like release of drug pattern might be attained through variability like polymeric materials ratio analysis which has been optimized to suit a target release profile. In comparison of in-vitro release studies for various controlled drug release preparations, F12 liberates 98.54% like opioid just at end like 12th hour and also was regarded as greatest preparation.
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