Abstract |
Thalidomide is now widely used to treat chronic graft-versus-host disease, but its use is associated with non-teratogenic side effects such as peripheral neuropathy. To examine the value of monitoring plasma concentrations of the drug in such patients, we have developed a high-performance liquid chromatographic (HPLC) assay. The method uses 0.5 mL plasma, is linear to 10 mg/L and had a detection limit of 0.2 mg/L. Thalidomide in plasma specimens was unstable at physiological pH but could be stabilized for several weeks by simple acidification. We describe a protocol for monitoring patients treated with thalidomide which permits convenient transportation and storage of specimens and report, provisionally, that plasma concentrations in the range 1-7 mg/L are therapeutically effective in chronic graft-versus-host disease without adverse side effects.
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Authors | B J Boughton, T M Sheehan, J Wood, D O'Brien, M Butler, A Simpson, K A Hale |
Journal | Annals of clinical biochemistry
(Ann Clin Biochem)
Vol. 32 ( Pt 1)
Pg. 79-83
(Jan 1995)
ISSN: 0004-5632 [Print] England |
PMID | 7762955
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Chromatography, High Pressure Liquid
- Chronic Disease
- Dose-Response Relationship, Drug
- Drug Stability
- Graft vs Host Disease
(drug therapy)
- Humans
- Linear Models
- Male
- Monitoring, Physiologic
(methods)
- Specimen Handling
(methods)
- Thalidomide
(blood)
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