Measurement of Rapamycin in Whole Blood Using Reverse-Phase High-Performance Liquid Chromatography
- 1 April 1992
- journal article
- Published by Wolters Kluwer Health in Therapeutic Drug Monitoring
- Vol. 14 (2) , 138-141
- https://doi.org/10.1097/00007691-199204000-00011
Abstract
Rapamycin (RAPA) is an immunosuppressant with a potency similar to FK 506 and up to 100-fold greater than cyclosporine. To date, no data have been reported on the pharmacokinetics and disposition of the drug, primarily due to a lack of suitable methods for its analysis. We describe here an evaluation of a reverse-phase high-performance liquid chromatographic (HPLC) method for analysis of the drug in whole blood. The method showed excellent analytical recovery of the drug, close to 100%. The sensitivity method was found to be 1.0 μg/L with between-run coefficients of variation of 14.4% and 9.8% at 10 and 50 mg/L. The stability of RAPA was investigated with this method in whole-blood specimens. It was found that the drug was stable for 30 days at 4°C and for 55 days at – 40°C.Keywords
This publication has 0 references indexed in Scilit: