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Analysis of prostaglandin E1 and related impurities by mixed aqueous-organic capillary electrophoresis

✍ Scribed by Roberto Gotti; Romeo Pomponio; Vincenza Andrisano; Vanni Cavrini


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
114 KB
Volume
24
Category
Article
ISSN
1615-9306

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✦ Synopsis


Analysis of prostaglandin E 1 and related impurities by mixed aqueous-organic capillary electrophoresis

A capillary electrophoretic method was developed for the separation and quantification of prostaglandin E 1 (PGE 1 , alprostadil) and its major impurities prostaglandin E 2 (PGE 2 , dinoprostone), prostaglandin A 1 (PGA 1 ), and prostaglandin B 1 (PGB 1 ). The documented good stability of the studied analytes in organic solvents led us to try CE separation in non-aqueous media. In mixed solvents (methanol-acetonitrile), good analyte peak shapes were obtained using bile acid salts as buffer electrolytes; in particular, sodium cholate and sodium deoxycholate were found to be suitable additives when used at sub-micellar concentrations. Interestingly, the addition of water to the organic running buffer permitted simultaneous improvement of the separation selectivity and the sample compatibility with the CE system. Optimisation of the experimental conditions was carried out considering the requirements for a method devoted to analysis of impurities: precision, selectivity, and sensitivity (quantitation limits of 0.1%). In a fused-silica "extended path" capillary of 32.5 cm total length, the complete prostaglandin separation was obtained in about 10 min, using 15 mM sodium deoxycholate in a mixed aqueous-organic solvent. The best separation was attained in the presence of 20% water and 80% of methanol-acetonitrile 75 : 25 (v/v). The method was then validated for linearity, LOD and LOQ, precision, selectivity, accuracy, and robustness; finally, it was applied to real samples, demonstrating its ability to quantify prostaglandin-related impurities.


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