A quantitative method using precoated silica gel-60 Lichrosphere high-performance thin-layer chromatography (HPTLC) plates, automated band wise sample application, and n-hexane:acetone:formic acid (2:1:0.025 υ/υ/υ) as mobile phase, has been developed and validated for the analysis of psoralen in marketed formulations and novel solid lipid nanoparticles (SLNs). Densitometric analysis was performed at 250 nm in absorbance mode. Compact bands of psoralen were obtained at Rf 0.32 ± 0.02. The method was validated for linearity, precision, robustness, sensitivity, specificity, and recovery. Linearity (r2 = 0.995), limit of detection (8.0 ng band-1), limit of quantification (18.1 ng band) -1, recovery (98.06–99.64%), and precision (≤0.74) were satisfactory. Statistical analysis established that the developed method for quantification of psoralen in marketed formulation and from solid lipid nanoparticles is reproducible and selective.
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A simple, selective, precise, accurate, and cost-effective thin-layer chromatographic (TLC) method for analysis of psoralen in different brands of babchi (Psoralea corylifolia) oil has been developed and validated. Aluminium TLC plates precoated with silica gel 60F254 were used as the stationary phase and n-hexane-acetone-formic acid 2:1:0.025 (v/v) as mobile phase. A compact, resolved psoralen peak (RFvalue 0.32 š 0.02) was observed by densitometric analysis in absorbance mode at 250 nm. Calibration data revealed a good linear relationship (r2 = 0.9956) between peak area and concentration in the range 20-200 ng per spot. Mean š SD values of slope and intercept were 11.35 š 0.36 and 14.64 š 0.31, respectively. Statistical analysis proved the method to be a repeatable, selective, and accurate means of estimation of psoralen in different brands of babchi oil.
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