FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF LISINOPRIL

  • Raghavendra Kumar Gunda Narasaraopeta Institute of Pharmaceutical Sciences
  • Dr J.N. Suresh Kumar

Abstract

Objective: The current study's objective is to develop and evaluate Fast dissolving tablets (FDT) of Lisinopril. Lisinopril, an Angiotensin Converting Enzyme Inhibitor (ACEI), preventing the conversion of angiotensin I to angiotensin II. To improve patient compliance making convenience is crucial. hence an effort was made by formulating it as the fast dissolving tablet to reduce the water intake for chronic kidney patients suffered from hypertension.  


Methods: Using various quantities of Vivasol & Explotab as Superdisintegrants, FDT formulations of Lisinopril were preared utilising the Direct Compression technique. Nine trials were developed and assessed for Pharmaceutical Product Performance.


Results: Findings indicate that all formulations meet the acceptance criteria, and kinetic modelling was applied to the in-vitro dissolution profiles.


Conclusion: The best formulation (F1) contained 5 mg of Vivasol and 5 mg of Explotab showed promising results for obtain quicker disintegration and may produce patient compliance by means of rapid onset of action and preventing first pas effect too. Formulation (F1) follow first order (r= 0.934), whereas release mechanism found to be fickian type (n= 0.267).

Keywords: Lisinopril, superdisintegrants, Explotab, fickian, Vivasol

Downloads

Download data is not yet available.

Author Biography

Dr J.N. Suresh Kumar

Dr. J.N.Suresh Kumar M.Pharm., PhD.,  FAGE.,

Professor Cum , Department of Pharmaceutics,

Narasaraopeta Institute of Pharmaceutical Sciences (Autonomous), Narasaraopet,

Palnadu (Dt), Andhra Pradesh, India - 522601.

 

Statistics
5 Views | 4 Downloads
How to Cite
Gunda, R., and D. Kumar. “FORMULATION AND EVALUATION OF FAST DISSOLVING TABLETS OF LISINOPRIL”. Journal of Applied Pharmaceutical Sciences and Research, Vol. 9, no. 1, Apr. 2026, pp. 57-61, doi:10.31069/japsr.v9i1.09.
Section
Research Articles