Quantification of phosphatidylserine, phosphatidic acid and free fatty acids in an ultrasound contrast agent by normal-phase high-performance liquid chromatography with evaporative light scattering detection

• Published in: Journal of pharmaceutical and biomedical analysis 2006-10, Vol.42 (4), p.506-512
• Main Authors: Hvattum, Erlend, Uran, Steinar, Sandbæk, Anne Gunvor, Karlsson, Anders Å., Skotland, Tore
• Format: Article
• Language: English
• Subjects: Analysis; Analytical, structural and metabolic biochemistry; Biological and medical sciences; Chromatography, High Pressure Liquid - methods; Contrast Media - chemistry; Evaporative light scattering detector; Fatty Acids, Nonesterified - analysis; Ferric Compounds - chemistry; Free fatty acids; Fundamental and applied biological sciences. Psychology; General pharmacology; HPLC; Iron - chemistry; Light; Medical sciences; Oxides - chemistry; Pharmacology. Drug treatments; Phosphatidic acid; Phosphatidic Acids - analysis; Phosphatidylserine; Phosphatidylserines - analysis; Reproducibility of Results; Scattering, Radiation; Spectrometry, Mass, Electrospray Ionization
• ISSN: 0731-7085; 1873-264X
• DOI: 10.1016/j.jpba.2006.04.027

Sonazoid™ is a new contrast agent for ultrasound imaging. The product is an aqueous suspension of perfluorobutane microbubbles coated with phospholipids obtained from hydrogenated egg phosphatidylserine (H-EPS). A normal-phase high-performance liquid chromatographic (HPLC) method with evaporative light scattering detection was developed for quantification of free fatty acids, phosphatidylserine and phosphatidic acid in H-EPS and Sonazoid™. Separation of the lipids was carried out on an HPLC diol column and a gradient of chloroform and methanol with 0.2% formic acid titrated to pH 7.5 with ammonia. The calibration standards contained stearic acid, distearoyl-phosphatidic acid (DSPA) and distearoyl-phosphatidylserine (DSPS) in the concentration range of 0.016–1.0 mg/ml (0.4–25 μg injected). The method was validated with a limit of quantification of the three lipids set to 0.4 μg (approximately 20–60 μM). The best fit of the three calibration curves were obtained when the logarithmic transformed theoretical lipid concentration was plotted against the logarithmic transformed area under the peak and fitted to a second order polynomial equation. Stearic acid, DSPA and DSPS were analysed with an intermediate precision ranging from 4.4% to 5.3% R.S.D. and they were extracted from an aqueous suspension with a recovery ranging from 103.3% to 113.3%. The sum of total phospholipid concentration determined in H-EPS ranged from 96.4% to 103.2% of the theoretical values. The lipids in the ultrasound product were quantitated with a repeatability ranging from 6.2% to 11.7% R.S.D.