Authors :
Motiki F. Beleme; Lebohang A. Moetseloa; Letuka J. Sello
Volume/Issue :
Volume 9 - 2024, Issue 8 - August
Google Scholar :
https://tinyurl.com/28b9yed5
Scribd :
https://tinyurl.com/y8a6afd4
DOI :
https://doi.org/10.38124/ijisrt/IJISRT24AUG262
Abstract :
A simple spectrophotometric technique has
been developed and validated for determination of
betamethasone 17-valerate in pharmaceutical
formulations. The method is based on cream dissolution
in absolute ethanol and assaying spectrophotometrically
at 240nm. The amount of betamethasone 17-valerate in
cream was determined as 101.6 ± 0.0037 % w/w. The
method validation demonstrated linearity for
concentration range of 0.006mg/ml to 0.0014mg/ml
(R2=0.9995). The method is simple and accurate and has
successfully been employed in the analysis of some of
Tripharm pharmaceutical formulations.
Keywords :
Betamethasone 17-Valerate, Spectrophotometry, Betamethasone, HPLC.
References :
- Asra, R., Rivai, H. and Astuty, W. (2017) ‘Pengembangan dan Validasi Metode Analisis Betametason Tablet dengan Metode Absorbansi dan Luas Daerah di Bawah Kurva Secara Spektrofotometri Ultraviolet’, Jurnal Farmasi Higea, 9(2), pp. 118–126.
- Awen, B. et al. (2010) ‘2. Development and validation of a new spectrophotometric method for the determination of betamethasone in bulk and pharmaceutical dosage forms’, International Journal of Pharmaceutical and Biomedical Research (IJPBR) [Preprint].
- Deceuninck, Y. et al. (2011) ‘Determination of MRL regulated corticosteroids in liver from various species using ultra high performance liquid chromatography–tandem mass spectrometry (UHPLC)’, Analytica chimica acta, 700(1–2), pp. 137–143.
- Gupta, M.K. et al. (2022) ‘A comparative review on High-Performance Liquid Chromatography (HPLC), Ultra Performance Liquid Chromatography (UPLC) & High-Performance Thin Layer Chromatography (HPTLC) with current updates’, Current Issues in Pharmacy and Medical Sciences [Preprint].
- Nikolin, B. et al. (2004) ‘High perfomance liquid chromatography in pharmaceutical analyses’, Bosnian journal of basic medical sciences, 4(2), p. 5.
- Permata, Y. et al. (2019) ‘Formulation and Quantitative Analysis of Betamethasone Valerate and Neomycin Sulfate Cream by High Performance Liquid Chromatography and Spectrophotometry’, Open Access Macedonian Journal of Medical Sciences, 7, pp. 3841–3846. Available at: https://doi.org/10.3889/oamjms.2019.516.
- da Silva Solon, L.G. et al. (2016) ‘Development and validation of an UHPLC method for the determination of betamethasone valerate in cream, gel, ointment and lotion’, Steroids, 106, pp. 70–77.
- Smith, E.W., Haigh, J.M. and Kanfer, I. (1985) ‘A stability-indicating HPLC assay with on-line clean-up for betamethasone 17-valerate in topical dosage forms’, International journal of pharmaceutics, 27(2–3), pp. 185–192.
- Walfish, S. (2006) ‘Analytical methods: a statistical perspective on the ICH Q2A and Q2B guidelines for validation of analytical methods’, BioPharm International, 19(12), pp. 1–6.
A simple spectrophotometric technique has
been developed and validated for determination of
betamethasone 17-valerate in pharmaceutical
formulations. The method is based on cream dissolution
in absolute ethanol and assaying spectrophotometrically
at 240nm. The amount of betamethasone 17-valerate in
cream was determined as 101.6 ± 0.0037 % w/w. The
method validation demonstrated linearity for
concentration range of 0.006mg/ml to 0.0014mg/ml
(R2=0.9995). The method is simple and accurate and has
successfully been employed in the analysis of some of
Tripharm pharmaceutical formulations.
Keywords :
Betamethasone 17-Valerate, Spectrophotometry, Betamethasone, HPLC.