Literature DB >> 10823375

The quantification of sirolimus by high-performance liquid chromatography-tandem mass spectrometry and microparticle enzyme immunoassay in renal transplant recipients.

P Salm1, P J Taylor, P I Pillans.   

Abstract

BACKGROUND: Sirolimus, an immunosuppressive agent, is undergoing clinical trials in the prophylaxis of organ rejection.
OBJECTIVES: The aim of this study was to compare the performance of the semi-automated prototype (mode IA) microparticle enzyme immunoassay (MEIA) against a validated high-performance liquid chromatography-mass spectrometry (HPLC-MS) method for measuring sirolimus concentrations. A secondary objective was to identify potential factors that may influence sirolimus measurement.
METHODS: The comparison was based on predose samples (n = 841) from 74 renal transplant patients receiving sirolimus therapy. Samples were collected up to 12 months after transplantation.
RESULTS: The mean (+/- SD) overestimation by MEIA was 42.5%+/-16.9%. Several variables were investigated to determine potential contributors to the observed overestimation. Stratification of the data based on the mean sirolimus concentrations determined by both assays yielded no statistically significant differences in bias between concentration subgroups within the clinically relevant range. Multiple linear regression analysis identified HPLC-MS sirolimus concentration (P = 0.03), hemoglobin concentration (P < 0.001), and time after transplantation (P < 0.001) as significant variables in the prediction of overestimation by MEIA. Analysis of the effect of time after transplantation on overestimation yielded a statistically significant difference up to 6 months after transplantation (35.6% to 46.4%) compared with 9 (23.9%) and 12 months (24.4%). A relationship between hemoglobin concentration and time after transplantation may explain the reduction in bias observed after 6 months.
CONCLUSION: The MEIA overestimates sirolimus concentrations in renal transplant patients compared with HPLC-MS. The clinical importance of this observed overestimation requires further investigation.

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Year:  2000        PMID: 10823375     DOI: 10.1016/s0149-2918(00)89024-4

Source DB:  PubMed          Journal:  Clin Ther        ISSN: 0149-2918            Impact factor:   3.393


  8 in total

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2.  Switching from HPLC/UV to MEIA for whole blood sirolimus quantitation: comparison of methods.

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Journal:  J Clin Lab Anal       Date:  2006       Impact factor: 2.352

3.  Development and validation of an HPLC method for the analysis of sirolimus in drug products.

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Journal:  Adv Pharm Bull       Date:  2012-05-20

Review 4.  Clinical pharmacokinetics of sirolimus.

Authors:  K Mahalati; B D Kahan
Journal:  Clin Pharmacokinet       Date:  2001       Impact factor: 6.447

Review 5.  Sirolimus: the evidence for clinical pharmacokinetic monitoring.

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6.  Target of rapamycin inhibitors (TOR-I; sirolimus and everolimus) for primary immunosuppression in kidney transplant recipients.

Authors:  Deirdre Hahn; Elisabeth M Hodson; Lorraine A Hamiwka; Vincent Ws Lee; Jeremy R Chapman; Jonathan C Craig; Angela C Webster
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7.  Comparison of LC-MS/MS and EMIT methods for the precise determination of blood sirolimus in children with vascular anomalies.

Authors:  Yue-Tao Zhao; Hao-Ran Dai; Yue Li; Yuan-Yuan Zhang; Hong-Li Guo; Xuan-Sheng Ding; Ya-Hui Hu; Feng Chen
Journal:  Front Pharmacol       Date:  2022-09-06       Impact factor: 5.988

8.  Determination of blood sirolimus concentrations in liver and kidney transplant recipients using the Innofluor fluorescence polarization immunoassay: comparison with the microparticle enzyme immunoassay and high-performance liquid chromatography-ultraviolet method.

Authors:  Lorena Bouzas; Jesús Hermida; J Carlos Tutor
Journal:  Ups J Med Sci       Date:  2009       Impact factor: 2.384

  8 in total

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