A Comparative Quality Control Study of Commercial and Formulated Ibuprofen Film-Coated Tablets (400mg)

This review paper presents a comparative analysis of the quality control measures applied to commercial ibuprofen tablets versus a formulated version of ibuprofen tablets. The study aims to evaluate the physicochemical properties, dissolution profiles, and overall efficacy of both formulations. By assessing parameters such as hardness, disintegration time, and dissolution rates, we aim to determine the quality and reliability of commercially available ibuprofen compared to a laboratory-formulated Tablet. The findings suggest significant differences in quality control metrics, which could have implications for clinical efficacy and patient safety. This study evaluates the physicochemical properties, disintegration times, dissolution profiles, and overall quality attributes of both formulations. The findings reveal significant differences in quality control parameters, emphasizing the importance of rigorous quality assessments in pharmaceutical manufacturing to ensure therapeutic efficacy and patient safety.

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Publication Details

Journal
Research Journal of Science and Technology
Published
2025-03-21
DOI
https://doi.org/10.52711/2349-2988.2025.00001
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
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article

A Comparative Quality Control Study of Commercial and Formulated Ibuprofen Film-Coated Tablets (400mg)

Harshal D. Kedare, Utkarsha Lasure, Rushikesh D. Kakade, Pallavi Bhingare et al.
Research Journal of Science and Technology
Drug Solubulity and Delivery Systems
article

A Comparative Quality Control Study of Commercial and Formulated Ibuprofen Film-Coated Tablets (400mg)

Harshal D. Kedare, Utkarsha Lasure, Rushikesh D. Kakade, Pallavi Bhingare, Sanket Pokale
article en

Abstract

This review paper presents a comparative analysis of the quality control measures applied to commercial ibuprofen tablets versus a formulated version of ibuprofen tablets. The study aims to evaluate the physicochemical properties, dissolution profiles, and overall efficacy of both formulations. By assessing parameters such as hardness, disintegration time, and dissolution rates, we aim to determine the quality and reliability of commercially available ibuprofen compared to a laboratory-formulated Tablet. The findings suggest significant differences in quality control metrics, which could have implications for clinical efficacy and patient safety. This study evaluates the physicochemical properties, disintegration times, dissolution profiles, and overall quality attributes of both formulations. The findings reveal significant differences in quality control parameters, emphasizing the importance of rigorous quality assessments in pharmaceutical manufacturing to ensure therapeutic efficacy and patient safety.

Research Journal of Science and Technology
Swami Vivekanand College of Pharmacy (IN)
Openalex Percentile: Top 94%
Drug Solubulity and Delivery Systems
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