Development and validation of stability-indicating high performance liquid chromatography method to analyze gatifloxacin in bulk drug and pharmaceutical preparations

Quantitative determination of gatifloxacin in tablets, solid lipid nanoparticles (SLNs) and eye-drops using a very simple and rapid chromatographic technique was validated and developed. Formulations were analyzed using a reverse phase SUPELCO® 516 C-18-DB, 50306-U, HPLC column (250 mm × 4.6 mm, 5 μ...

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Bibliographische Detailangaben
Veröffentlicht in:Saudi Pharm J
Hauptverfasser: Aljuffali, Ibrahim A., Kalam, Mohd. Abul, Sultana, Yasmin, Imran, Ahamad, Alshamsan, Aws
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2014
Schlagworte:
Original Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4310989/
https://ncbi.nlm.nih.gov/pubmed/25685047
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jsps.2014.06.005
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