Development of Simple High Performance Liquid Chromatographic Method for the Determination of Astaxanthin in Human Plasma
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概要
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A fast and simple high-performance liquid chromatographic UV-Vis method for the determination of astaxanthin in human plasma was developed and validated. The method involved direct injection of plasma sample after deproteinization using a 1:9 mixture of ethanol-tetrahydrofuran. The mobile phase comprised methanol:water:ethyl acetate (82:8:10% (v/v)) with a total run time of 5 min. Analysis was run at a flow rate of 1.5 mL/min with the detector set at 474nm. This method is specific and sensitive, with a quantification limit of approximately 0.25 µg/mL. The calibration curve was linear over a concentration range of 0.39 - 50.0 µg/mL. The method had a mean absolute recovery of 99%, while the within-day and between day coefficients of variation and percentage errors were all less than 3%. The speed, specificity, sensitivity, reproducibility and stability of this method make it suitable for the determination of human plasma astaxanthin in routine analysis.
- 2012-01-01
著者
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Abdullah A.
Department Of Pharmaceutics Faculty Of Pharmacy Universiti Teknologi Mara Malaysia
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MEOR MOHD
Department of Pharmaceutics, Faculty of Pharmacy, Universiti Teknologi MARA Malaysia
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JULIANTO T.
Department of Pharmaceutics, Faculty of Pharmacy, Universiti Teknologi MARA Malaysia
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MAJEED A.
Research Management Institute, Universiti Teknologi MARA Malaysia
関連論文
- Development of Simple High Performance Liquid Chromatographic Method for the Determination of Astaxanthin in Human Plasma
- Enhanced Oral Bioavailability of Astaxanthin with Droplet Size Reduction