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Published on: July 11, 2014
Determination of MLN0128, an investigational antineoplastic agent, in human plasma by LC-MS/MS
Sandeep R Kunati1, Yan Xu1,2
1Department of Chemistry, Cleveland State University, Cleveland, OH, USA.
Abstract:
MLN0128, an mTOR kinase inhibitor, is currently undergoing clinical investigation for treatment of a variety of cancers. To support this work, an LC-MS/MS method has been developed for the determination of MLN0128 in human plasma. A structural analog STK040263 was used as the internal standard. Both MLN0128 and the IS were first extracted from plasma using methyl tert-butyl ether; then separated on a Waters XTerra® MS C18 column using a mobile phase consisting of methanol-acetonitrile-10.0 mm ammonium formate (34:6:60, v/v/v) at a flow rate of 0.300 mL min-1 . Quantitation of MLN0128 was done by positive electrospray ionization tandem mass spectrometry in multiple-reaction-monitoring mode. This method has a total run time of <4 min with the retention times of 1.95 and 2.94 min for the IS and MLN0128, respectively. The method has been validated per the US Food and Drug Administration guidance for bioanalytical method validation. It has a calibration range of 0.100-50.0 ng mL-1 in human plasma with a correlation coefficient > 0.999. The overall assay accuracy and precision were ≤ ± 4 and ≤8%, respectively. The IS normalized recovery of MLN0128 was 98-100%. The stability studies showed that MLN0128 was stable under all tested conditions. The method developed may be useful for clinical studies of MLN0128.
Insights
A new LC-MS/MS method quantifies MLN0128, an mTOR kinase inhibitor, in human plasma. This validated assay supports clinical trials for cancer treatment, demonstrating high accuracy and stability.
Area of Science:
- Pharmacology
- Analytical Chemistry
- Biochemistry
Background:
- MLN0128 is an mTOR kinase inhibitor investigated for various cancers.
- Accurate quantification in biological matrices is crucial for clinical trials.
Purpose of the Study:
- To develop and validate a sensitive LC-MS/MS method for determining MLN0128 concentrations in human plasma.
- To support ongoing and future clinical investigations of MLN0128.
Main Methods:
- Liquid chromatography-tandem mass spectrometry (LC-MS/MS) with positive electrospray ionization.
- Methyl tert-butyl ether for plasma extraction; Waters XTerra® MS C18 column for separation.
- Quantification using multiple-reaction-monitoring (MRM) mode with STK040263 as internal standard.
Main Results:
- The validated method achieved a rapid run time of <4 minutes.
- Linear calibration range of 0.100-50.0 ng/mL with R² > 0.999.
- High accuracy (≤±4%) and precision (≤8%), with 98-100% recovery and demonstrated MLN0128 stability.
Conclusions:
- A robust and validated LC-MS/MS assay for MLN0128 in human plasma has been successfully developed.
- This method is suitable for supporting clinical studies evaluating MLN0128 in cancer patients.

