Original ArticleInternational Journal of Pharmaceutical InvestigationVol. 15 | Issue 2 | 2025 | pp. 664–674Open access
Method Development and Validation of Gramicidin, Neomycin and Triamcinolone Acetonide Related Substances and their Impurities Quantification through UPLC
- 1,
- 2*
- 1 Department of Science and Humanities, Eswar College of Engineering, Kesanupalli Village, Narasaraopet, Palnadu, Andra Pradesh, INDIA.
- 2 PG Department of Chemistry, Jagarlamudi Kuppuswamy Chowdary College, Guntur, Andhra Pradesh, INDIA.
Published in International Journal of Pharmaceutical Investigation
Correspondence: Madhavi Nannapaneni
PG Department of Chemistry, Jagarlamudi Kuppuswamy Chowdary College, Guntur, Andhra Pradesh, INDIA.
Email: madhavijkcchempg@gmail.com
Copyright: © 2025 Manuscript Technomedia. This is an open access article.
- Published:
- Jan 1, 2025
- Received:
- Mar 15, 2024
- Accepted:
- Jul 27, 2024
- DOI:
- 10.5530/ijpi.20251515
How to cite
Syed, I. B., & Nannapaneni, M. (2025). Method Development and Validation of Gramicidin, Neomycin and Triamcinolone Acetonide Related Substances and their Impurities Quantification through UPLC. International Journal of Pharmaceutical Investigation, 15(2), 664–674. https://doi.org/10.5530/ijpi.20251515
Abstract
Aim/Background
To develop and validate a sensitive, accurate, simple, precise and cost-effective receptive and understandable method for concurrent evaluation of Gramicidin, Neomycin and Triamcinolone acetonide and their related contaminants via UPLC.
Materials and Methods
This method includes the separation using a chromatographic Phenyl column (50 mmx2.1 mm, 1.7 µm). A portable stage of 0.1% TEA (Tri-Ethylamine) and acetonitrile in gradient elution mode with 0.5mL/Temperature and minimum flow rate were employed. At 230 nm, UV observations were made. The limitations for Linearity, quantification and recoveries were discovered being within the allowable range. With UPLC, this method was successfully tested and ICH Q2 (R1) recommendations.
Results
Gramicidin, Neomycin and Triamcinolone acetonide retention times were observed at 9.315 min,3.979 min and 1.697 min respectively. A gradient elution of Triamcinolone acetonide, Neomycin and Gramicidin involves phenyl column that flows from 0.5 mL/min and the column internal temperature were held constant. Mobile phase % TEA likewise acetonitrile was utilised. UV monitoring was brought at 230 nm.
Conclusion
This study created an entirely new, straightforward, quick, affordable, sensitive and easily accessible UPLC method for the coincident determination of Triamcinolone acetonide, Neomycin and Gramicidin bulky and ointment dose form. This method has the benefits of being less expensive, assessible, reliable, sensitive and reproducible. Under conditions of oxidation, (Neutral, basic and acidic) hydrolysis, photolysis, thermal stress and medicines degradative activities were investigated. The medications were discovered to be solid underheat, unstable, hydrolysis under acid, alkaline and oxidative circumstances. The Final application of the UPLC method to the commercial formulations followed the ICH recommendations.
Keywords
Subject
Article metadata
| Title | Method Development and Validation of Gramicidin, Neomycin and Triamcinolone Acetonide Related Substances and their Impurities Quantification through UPLC |
|---|---|
| Authors | Ibrahim Baje Syed; Madhavi Nannapaneni |
| Affiliations | Department of Science and Humanities, Eswar College of Engineering, Kesanupalli Village, Narasaraopet, Palnadu, Andra Pradesh, INDIA.; PG Department of Chemistry, Jagarlamudi Kuppuswamy Chowdary College, Guntur, Andhra Pradesh, INDIA. |
| Corresponding author | madhavijkcchempg@gmail.com |
| Journal | International Journal of Pharmaceutical Investigation |
| Volume / Issue | Vol. 15, Issue 2 (2025) |
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