Quantitative determination of total and unbound paclitaxel in human plasma following Abraxane treatment

被引:44
作者
Gardner, Erin R. [2 ]
Dahut, William [1 ]
Figg, William D. [1 ]
机构
[1] NCI, Clin Pharmacol Program, Ctr Canc Res, Med Oncol Div, Bethesda, MD 20892 USA
[2] NCI, SAIC Frederick Inc, Clin Pharmacol Program, Frederick, MD 21702 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2008年 / 862卷 / 1-2期
关键词
albumin; nanoparticle; paclitaxel; taxane; anticancer; formulation; LC-MS/MS; unbound fraction; free fraction;
D O I
10.1016/j.jchromb.2007.12.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple, rapid liquid chromatography/tandem mass spectrometric (LC-MS/MS) assay was developed and validated for the quantification of both unbound and total paclitaxel in plasma following treatment with Abraxane (ABI-007) or Taxol. Accurate and reproducible analysis of ABI-007, an albumin nanoparticle formulation of paclitaxel could not be achieved using previously published methodology designed for Taxol. The final validated method involved protein precipitation followed by vacuum filtration, in a 96-well format for rapid processing. The 4 min run employed gradient elution on a Waters SymmetryShield C8 (2.1 mm x 50 mm, 3.5 mu m) column, followed by tandem mass spectrometric detection, in electrospray positive mode. Calibrator samples were prepared daily with paclitaxel and analyzed with both ABI-007 and paclitaxel quality control samples. To measure unbound drug, sample preparation was preceded by ultrafiltration. The assay was linear over the range of 10-2500 ng/mL, with dilution providing measurement up to 50,000 ng/mL. Within-run and between-run precision for all QC samples was less than 5.0% and 10.4%, respectively. Accuracy was high, with deviation of less than 6.1% for all QCs. Measurement of unbound paclitaxel was precise (BRP and WRP <10%). (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:213 / 218
页数:6
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