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pubmed-article:3287708pubmed:abstractTextA modified procedure for measuring cyclosporin in whole blood by high-performance liquid chromatography is described and evaluated for clinical use. Sample preparation uses solid-phase extraction cartridges that can be reused. Life of the reverse-phase analytical column exceeds 1,000 injections at 70 degrees C. Cyclosporins A and D (internal standard) elute after 5.6 and 7.6 min, respectively. Calibration plots are linear from 50 ng/ml to at least 2,000 ng/ml. Within-day and between-day imprecision is less than 9% (coefficient of variation). Minimum measurable concentration is 50 ng/ml.lld:pubmed
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pubmed-article:3287708pubmed:authorpubmed-author:RavenscroftP...lld:pubmed
pubmed-article:3287708pubmed:authorpubmed-author:CharlesB GBGlld:pubmed
pubmed-article:3287708pubmed:authorpubmed-author:NorrisR LRLlld:pubmed
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pubmed-article:3287708pubmed:pagination97-100lld:pubmed
pubmed-article:3287708pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:3287708pubmed:year1988lld:pubmed
pubmed-article:3287708pubmed:articleTitleA modified assay for cyclosporin in blood using solid-phase extraction with high-performance liquid chromatography.lld:pubmed
pubmed-article:3287708pubmed:affiliationDepartment of Clinical Pharmacology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.lld:pubmed
pubmed-article:3287708pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3287708pubmed:publicationTypeClinical Triallld:pubmed