International Journal For Multidisciplinary Research
E-ISSN: 2582-2160
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Volume 8 Issue 1
January-February 2026
Indexing Partners
Revolutionizing Topical Drug Evaluation: A Discriminative and Validated In-Vitro Release Testing Paradigm for Mupirocin Cream 2%
| Author(s) | Mr. PRADIP SHANKAR PATIL, Dr. MAHESH M SAVANT, Pankajkumar Nariya, Ganesh S. Kamble, Jegan Jayabalan |
|---|---|
| Country | India |
| Abstract | The development of a robust and discriminative in-vitro release testing (IVRT) method for Mupirocin Cream 2% w/w was undertaken to support regulatory expectations for Q1/Q2 sameness and Q3 similarity in topical semisolid formulations. The method was designed using a vertical Franz diffusion cell system with a synthetic nylon membrane and optimized for sensitivity, specificity, and reproducibility. A comprehensive screening of receptor media identified USP buffer (pH 6.8): ethanol (70:30 v/v) as the most suitable medium, offering high solubility (675.88 µg/mL) and stability for Mupirocin. Membrane binding studies confirmed minimal drug retention, and pretreatment was deemed unnecessary. The method was validated using HPLC-UV detection at 222 nm, with a linearity range of 2.70–205.24 µg/mL (R² ≥ 0.999). Accuracy ranged from 95.56% to 101.48%, and precision (%RSD) was consistently below 3%. The method demonstrated excellent specificity, with no interference from placebo or blank matrices. Discriminatory power was established by evaluating release profiles of 50%, 100%, and 150% strength formulations. Confidence interval analysis confirmed equivalence for Test-02 and Test-03 with the reference product, while Test-01 was non-equivalent. Mass balance studies showed recovery between 91.1% and 99.4%, with drug depletion ranging from 11.5% to 13.3%. This validated IVRT method is suitable for routine quality control, formulation development, and regulatory submissions. It provides a sensitive and reliable tool for assessing the release characteristics of Mupirocin from semisolid matrices and supports the demonstration of bioequivalence in generic product development. |
| Field | Medical / Pharmacy |
| Published In | Volume 8, Issue 1, January-February 2026 |
| Published On | 2026-01-02 |
| DOI | https://doi.org/10.36948/ijfmr.2026.v08i01.65127 |
| Short DOI | https://doi.org/hbhrcz |
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E-ISSN 2582-2160
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IJFMR DOI prefix is
10.36948/ijfmr
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