A key bottleneck in the LC/MS workflow for quantitative analysis of drug analytes has been sample preparation and the need to remove endogenous components of the sample matrix, such as proteins and lipids, which can interfere with MS detection and cause ion suppression.
Guifeng Jiang, Ph.D., applications manager, chromatography and mass spectrometry division at Thermo Fisher Scientific, describes an online sample-preparation method designed to be simpler and faster than traditional off-line techniques.
The sample-prep procedure requires only 1–2 minutes per sample and can be applied to a 10 µL plasma sample without the need for dilution or protein precipitation. The method is designed for laboratories performing routine bioanalysis using a single quadrupole mass spectrometer. It incorporates turbulent flow chromatography at a high flow rate to remove high molecular weight matrix components through the combined dynamics of diffusion and column chemistry.
Dr. Jiang demonstrates the use of this method with rat and human plasma matrices spiked with six drug standards at various concentrations. Plasma samples are loaded onto the turbulent flow chromatography column, with subsequent transfer of the cleaned-up sample directly onto the LC separation system, and automated elution of the fractions onto the mass spectrometer.
Mass detection on a single quadrupole MS system was performed in selected ion monitoring mode with constant positive/negative polarity switching. The entire process of online sample extraction, LC separation, and MS detection of the six drug compounds required about 10 minutes per sample.
Dr. Jiang presents chromatograms showing comparable results—in terms of peak size, shape, and position, and the absence of confounding peaks—when comparing samples in which the analytes were spiked into water or rat or human plasma. She reports no evidence of matrix-related ion suppression after sample prep, and presents calibration curves showing high linearity in detector response over analyte levels ranging from 12.5 to 12,500 ng/mL.
To minimize interference from endogenous matrix components and their effects on analyte ionization in MS analysis, Sigma-Aldrich developed a one-step sample-prep procedure that simultaneously removes proteins and phospholipids from biological matrices. The technology combines solid-phase extraction (SPE) for protein precipitation with a separation medium that is selective for phospholipids.
Craig Aurand, senior application chemist, describes a study designed to demonstrate the detrimental effect of phospholipid-induced matrix ionization suppression on LC/MS analysis of plasma samples. The study focused on analytical discrimination between propanolol and the 4-hydroxy-propanolol metabolite, and the comparative effects of a sample-prep method using either standard protein precipitation or a hybrid phospholipid extraction method.
For standard SPE, 100 µL plasma samples were combined with 1% formic acid acetonitrile in 96-well vacuum manifold plates that contained a zirconia-coated silica bed (for trapping the phospholipids) above a hydrophobic graded filter. Each well is topped with a Teflon frit. Application of a vacuum pulls the samples through the packed bed, achieving greater than 99% removal of phospholipids, according to Aurand.
Following the hybrid phospholipid extraction sample-prep technique, no phospholipids were observed in the matrix, resulting in a fourfold increased sensitivity for propanolol detection compared to standard protein precipitation. This improved sensitivity is “directly related to the phospholipid-induced ionization effect,” says Aurand.
Mike Chang, application development scientist at Agilent Technologies, points to lipids as being the major component of biological matrices that causes the greatest interference and ionization suppression in MS analysis. A common sample-prep strategy employed upstream of LC/MS is SPE, which mainly removes large proteins.
Chang describes the use of a hydroxylated SPE sorbent in an automated 96-well plate format that is intended to filter out the large proteins and minimize the interactions between the endogenous materials such as lipid and protein molecules in the matrix and the sorbent, thereby removing them from the sample and resulting in reduced ion suppression downstream.
Coating the SPE adsorbent with hydroxide residues instead of commonly used amides makes it less likely that the lipids in the matrix will react with the sorbent surface. Chang presents data showing reduced lipid content in samples treated with hydroxylated SPE and an associated decrease in ion suppression on MS analysis, with good accuracy and linearity in the calibration curves.