Drug Development and Industrial Pharmacy · 1993 · 18 citations · 4 references
PharmacyPharmaceutical AnalysisAnalytical ChemistryChromatographic AnalysisFood AnalysisChromatographic Analysis Of PharmaceuticalsChromatographyDegradation Product AnalysisLiquid ChromatographyPharmaceutical StabilityChromatographic Peak PurityChromatographic Separation Of DegradantsDegradation Product AssessmentQuality Control Applications
An HPLC method for the assay and chromatographic purity assessment of dipyridamole raw material and capsule product was developed. A mobile phase composing of methanol: aq 200 mM pentane sulphonic acid, sodium salt, [70:30 v/v], had triethylamine added [2ml/L] and was then adjusted to pH 3.0 with phosphoric acid. The mobile phase was pumped through an octadecylsilated-silica column, being held at 60° C, at a flow rate of 1.5ml/min. Detection was made at 288nm.The resolution of degradation products, along with precision and accuracy were investigated for the system.
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Practical HPLC Method Development
Analytical Chemistry · 1993 · 1.4K citations
Business, Pharmaceutical Analysis, Norm-referenced Assessment +5
Henderson Ve · PubMed · 1926 · 348 citations · Full text