Analytical Method Development and Validation: Calcium Butyrate
This study was designed for the analytical method development and validation for Calcium butyrate (CAB) using High-Performance Liquid Chromatography (HPLC). 1H and 13C Nuclear Magnetic Resonance (NMR) and Fourier Transform Infrared (FTIR) spectroscopy analysis were carried out to examine the molecular structure. For HPLC analysis, a blend of acetonitrile and phosphoric acid solution (0.1%) (20:80) (v/v) was used as a mobile phase. A C18 column (5 µm, 250 × 4.6 mm) was used as a stationary phase. The eluent of CAB was monitored with a UV detector at a wavelength of 206 nm and a flow rate of 1 mL/min. According to the results, FTIR and NMR spectra were consistent with the structural characteristics of CAB, and the expected proton and carbon signals were observed. During the HPLC analysis, due to the ionization of CAB, three distinct retention times were observed in the chromatograms at 3.4, 4.5, and 7.4 min. The validation was performed according to ICH guidelines. The obtained results demonstrated that the analytical method was successfully validated, with LOD values of 1.211, 0.606, and 1.816 µg/mL, and LOQ values of 3.670, 1.835, and 3.676 µg/mL. The assay displayed a linear range of 5–1000 µg/L concentration and was found suitable for further formulation content analysis.
Authors
- Neslihan Üstündağ Okur (ORCID: https://orcid.org/0000-0002-3210-3747)
- Ayşe Pınar Yağcılar (ORCID: https://orcid.org/0000-0001-5546-4601)
- Emre Şefik Çağlar (ORCID: https://orcid.org/0000-0003-2010-4918)
Institutions
- Sağlık Bilimleri Üniversitesi (TR)
- University of Health Sciences Antigua (AG)
Publication Details
- Journal
- Analytica—A Journal of Analytical Chemistry and Chemical Analysis
- Published
- 2025-10-23
- DOI
- https://doi.org/10.3390/analytica6040042
- Primary Topic
- Analytical Methods in Pharmaceuticals
- Type
- article
- Field-Weighted Citation Impact
- 0.00