Analytical and preparative high-performance liquid chromatographic separation of the enantiomers of ifosfamide, cyclophosphamide and trofosfamide and their determination in plasma |
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Authors: | D Masurel I W Wainer |
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Affiliation: | St. Jude Children's Research Hospital, Pharmaceutical Division, Memphis, TN 38101. |
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Abstract: | A high-performance liquid chromatography chiral stationary phase (HPLC-CSP) based upon cellulose-tris(3,5-dimethylphenylcarbamate), the OD-CSP, was used to stereochemically resolve three racemic anticancer drugs: ifosfamide (IFF), cyclophosphamide (CTX) and trofosfamide (TFF). The observed enantioselectivities (alpha) were 1.45 (IFF), 1.21 (CTX) and 1.10 (TFF). The OD-CSP was also used on a preparative scale to isolate the enantiomers of IFF with an optical purity greater than 97%. In addition, an analytical assay was developed for the determination of the enantiomeric composition of IFF and CTX in plasma using achiral-chiral coupled column chromatography. A racemic form of another CSP, the D,L-naphthylalanine-CSP, was used as the achiral pre-column. The sample clean-up prior to HPLC analysis was realized by liquid-liquid extraction with chloroform. The correlation coefficient was 0.987 for both standard curves (20-130 micrograms/ml) and the controls were within 10% of the real value. The analysis time for each serum sample was less than 30 min. |
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