Packed column supercritical fluid chromatography of a peroxysome proliferator-activating receptor agonist drug - Achiral and chiral purity of substance, formulation assay and its enantiomeric purity

被引:25
作者
Gyllenhaal, O [1 ]
机构
[1] AstraZeneca R&D Molndal, Analyt Dev, S-43183 Molndal, Sweden
关键词
supercritical fluid chromatography; enantiomer separation; pharmaceutical analysis; peroxysome proliferator-activating receptor agonist;
D O I
10.1016/j.chroma.2004.05.035
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes packed column supercritical fluid chromatography (SFC) for the analysis of a peroxysome proliferator-activating gamma-receptor agonist that is a carboxylic acid. Evaluation of conditions for the separation of this candidate drug and related compounds in bulk substance is described. A Chiralcel OD column was used for this purpose due to its high selective retention of related substances and relative inertness, though the enantioselectivity was negligible, with methanol as polar modifier. A high enantioselectivity was obtained on Chiralpak AD and it was possible to determine the enantiometic purity within 10 min on a 5 cm short column. Both the achiral and the chiral systems were run without acid additive in the mobile phase and the level of detection of impurities by area was about 0.1%. For the analysis of samples dissolved in water, without any isolation step, 2-propanol was used as modifier. Due to the column surface activity, evidently generated by injected water, citric acid I mM was included as additive in the 2-propanol in order to maintain symmetric and undistorted peak shape. The detection limit for the assay was 21 mug mL(-1) (50 nmol mL(-1)) for 5 muL injected (R.S.D. 6.4 %, n = 8). A 5 cm short Chiralcel OD column was used. Determination of enantiomeric purity of the drug in aqueous samples required increased sensitivity. The sample was acidified and extracted into a small volume of I-pentanol, out of which 25 mul was analyzed by SFC. The minor enantiomer at the 3% (w/w) level added could be confirmed. Its ratio remained constant during the procedure as measured relative to a reference solution in organic media. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:173 / 180
页数:8
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