Abstract |
A high-performance liquid chromatographic (HPLC) assay has been developed for the determination of the anticancer drug doxorubicin and the metabolites doxorubicinol, doxorubicinone, 7-deoxydoxorubicinone, doxorubicinolone and 7-deoxydoxorubicinolone in plasma of AIDS patients. Samples can be heated at 60 degrees C for 30 min to inactivate the human immunodeficiency virus. The sample pre-treatment involves a liquid-liquid extraction of the buffered plasma sample (pH 9) with a chloroform-1-propanol (4:1, v/v) mixture. The chromatographic analysis is performed on a Lichrosorb RP-8 (5 microns) column and by isocratic elution with a mobile phase of acetonitriletetrahydrofuran- phosphate buffer (pH 2.2) (800:5:200, w/w/w) with fluorescence detection (excitation wavelength: 460 nm; emission wavelength: 550 nm). The proposed method has been validated and, subsequently, implemented in a pharmacokinetic study of doxorubicin in AIDS patients with Kaposi's sarcoma who are treated with the combination regimen doxorubicin, vincristine and bleomycin.
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Authors | J H Beijnen, P L Meenhorst, R van Gijn, M Fromme, H Rosing, W J Underberg |
Journal | Journal of pharmaceutical and biomedical analysis
(J Pharm Biomed Anal)
Vol. 9
Issue 10-12
Pg. 995-1002
( 1991)
ISSN: 0731-7085 [Print] England |
PMID | 1822225
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
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Topics |
- Acquired Immunodeficiency Syndrome
(blood)
- Calibration
- Chromatography, High Pressure Liquid
- Doxorubicin
(analogs & derivatives, blood, pharmacokinetics)
- Humans
- Molecular Structure
- Reproducibility of Results
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