Fabrication and optimization of floating tablets of antihypertensive drug losartan

This study developed, optimized, and evaluated floating tablets containing Losartan potassium intended to provide prolonged gastric retention for hypertensive patients. HPMC K15M was found to effectively extend drug release in a gastric pH environment. Formulations were evaluated for drug-excipient compatibility, thickness, hardness, tablet density, floating lag time, total floating time, weight variation, friability, drug content, swelling index, and stability under accelerated conditions. Preliminary findings identified HPMC K15M (X1) and MCC (X2) as independent variables in a 3² full factorial design, with friability (%F) and cumulative drug release at 12 hours (Q12) as dependent variables. Multiple linear regression, ANOVA, and contour plots generated using Design Expert were employed to analyze factor effects. In vitro release data were fitted to kinetic models, with the optimized batch exhibiting a Higuchi release profile (r² = 0.993). A checkpoint batch validated the model. Batch F7 was identified as the optimized formulation, demonstrating friability below 1 (0.80) and 95.94% cumulative drug release at 12 hours. Accelerated stability testing confirmed the stability of the optimized formulation.

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Publication Details

Journal
Journal of Contemporary Pharmacy
Published
2025-12-31
DOI
https://doi.org/10.56770/jcp2025922
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
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article

Fabrication and optimization of floating tablets of antihypertensive drug losartan

Sehrish Rana Rajpoot, Rabia Munir
Journal of Contemporary Pharmacy
Drug Solubulity and Delivery Systems
article

Fabrication and optimization of floating tablets of antihypertensive drug losartan

Sehrish Rana Rajpoot, Rabia Munir
article en

Abstract

This study developed, optimized, and evaluated floating tablets containing Losartan potassium intended to provide prolonged gastric retention for hypertensive patients. HPMC K15M was found to effectively extend drug release in a gastric pH environment. Formulations were evaluated for drug-excipient compatibility, thickness, hardness, tablet density, floating lag time, total floating time, weight variation, friability, drug content, swelling index, and stability under accelerated conditions. Preliminary findings identified HPMC K15M (X1) and MCC (X2) as independent variables in a 3² full factorial design, with friability (%F) and cumulative drug release at 12 hours (Q12) as dependent variables. Multiple linear regression, ANOVA, and contour plots generated using Design Expert were employed to analyze factor effects. In vitro release data were fitted to kinetic models, with the optimized batch exhibiting a Higuchi release profile (r² = 0.993). A checkpoint batch validated the model. Batch F7 was identified as the optimized formulation, demonstrating friability below 1 (0.80) and 95.94% cumulative drug release at 12 hours. Accelerated stability testing confirmed the stability of the optimized formulation.

Journal of Contemporary PharmacyVol. 9(2)
Government College University, Faisalabad (PK), Shandong Normal University (CN)
Good health and well-being
Openalex Percentile: Top 36%
Drug Solubulity and Delivery Systems
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Fabrication and optimization of floating tablets of antihypertensive drug losartan — Sehrish Rana Rajpoot, Rabia Munir · Journal of Contemporary Pharmacy (2025) | TGRS Research Map | TGRS