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Technical Briefs |
1
Dept. of Clin. Pharmacol., First Floor Lions Clin. Res. Bldg.,
2
Univ. of Queensland Dept. of Med., and
3
Univ. of Queensland Dept. of Surgery, Princess Alexandra Hosp., Ipswich Rd., Brisbane, QLD, Australia, 4102;
a author for correspondence: fax 61-7-3240-5031;
e-mail Ptaylor@gpo.pa.uq.edu.au
The immunosuppressant drug tacrolimus (FK506), which exhibits 50100 times the potency of cyclosporin A, is proving to be highly effective in preventing rejection in solid-organ transplantation (1). However, because of a narrow therapeutic range, variable pharmacokinetics, and potential drug interactions, continual therapeutic drug monitoring (TDM) of tacrolimus is essential (2). Recently, we published a report that detailed the development of a specific, sensitive method for quantification of tacrolimus concentrations in blood (3). This methodology, which utilizes HPLC in combination with tandem mass spectrometry (LC-MS2), was found to have greater specificity, lower detection limits, and a more rapid turnaround time than existing immunoassays. These attributes make this methodology ideal for TDM of tacrolimus.
Since our initial report, several modifications that have further
improved the assay for TDM have been implemented. The use of a 100
x 2 mm C8 column (rather than a 30 x 2 mm
C4
Acknowledgments
References
The following articles in journals at HighWire Press have cited this article:
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B. L. KASISKE, M. A. VAZQUEZ, W. E. HARMON, R. S. BROWN, G. M. DANOVITCH, R. S. GASTON, D. ROTH, J. D. SCANDLING JR., and G. G. SINGER Recommendations for the Outpatient Surveillance of Renal Transplant Recipients J. Am. Soc. Nephrol., October 1, 2000; 11 (90001): S1 - S86. [Abstract] [Full Text] [PDF] |
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J. L. Cogill, P. J. Taylor, I. S. Westley, R. G. Morris, S. V. Lynch, and A. G. Johnson Evaluation of the tacrolimus II microparticle enzyme immunoassay (MEIA II) in liver and renal transplant recipients Clin. Chem., September 1, 1998; 44(9): 1942 - 1946. [Abstract] [Full Text] [PDF] |
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