Quantification of steroids in human and mouse plasma using online solid phase extraction coupled to liquid chromatography tandem mass spectrometry

doi:10.1038/nprot.2010.22

Method Article

Quantification of steroids in human and mouse plasma using online solid phase extraction coupled to liquid chromatography tandem mass spectrometry

https://doi.org/10.1038/nprot.2010.22

This work is licensed under a CC BY-NC 3.0 License

This protocol has been posted on Protocol Exchange, an open repository of community-contributed protocols sponsored by Nature Portfolio. These protocols are posted directly on the Protocol Exchange by authors and are made freely available to the scientific community for use and comment.

Version 1

posted 16 Feb, 2010

You are reading this latest protocol version

liquid chromatography

tandem mass spectrometry

online solid phase extraction

steroid analysis

Steroids are powerful signalling molecules regulating a variety of physiological processes such as cell proliferation, cell differentiation, and reproduction. Variations in steroid concentrations may hint at hormonal imbalances or metabolic disorders that allow for a diagnosis of human diseases. The measurement of steroid hormone concentrations is relevant to basic research as well as clinical sciences. For example, the systematic generation of mouse mutants has led to a need for comprehensive phenotyping. As these mouse models may bear defects that affect steroid synthesis or homeostasis, knowledge of the mouse steroid metabolome could help to identify these mutants and connect phenotypes to their molecular cause ¹.Metabolic characterisation of a large human cohort recently led to the discovery of associations between phenotype, metabolome, and genotype as shown by us ². To expand our knowledge of the metabolome to other substance classes, a high-throughput, robust, sensitive and specific steroid phenotyping method is required.

For several years, immunoassays have been the standard method for measuring steroid concentrations. Recently, liquid chromatography tandem mass spectrometry methods for steroid analysis have been developed that combine the advantages of immunoassays (i.e. sensitivity) with the specificity of mass spectrometry ³.

This protocol describes a high-throughput method to analyze several different steroids in plasma. By using online-SPE coupled to LC-MS/MS, six different steroids (androstenedione, testosterone, cortisone, cortisol, progesterone, 17OH-progesterone) are readily quantifiable in human plasma, while three steroids (androstenedione, testosterone, corticosterone) can be quantified in mouse plasma. The method requires a minimum of hands-on time by the experimenter while simultaneously providing concentrations of several interesting steroids.

d8-Corticosterone (C/D/N Isotopes)

d4-Cortisol (C/D/N Isotopes)

d9-Progesterone (C/D/N Isotopes)

¹³C₂-Testosterone (Cambridge Isotope Laboratories)

17OH-Progesterone (Sigma)

Androstenedione (Steraloids)

Cortisol (Sigma)

Cortisone (Sigma)

Progesterone (Sigma)

Testosterone (Sigma)

Acetonitrile (HPLC grade, Roth)

Methanol (HPLC grade, Merck)

ZnSO₄ (Merck)

Allure Biphenyl column 3 µm; 50 mm x 2.1 mm (Restek)

Oasis HLB column 15 µm; 20 mm x 2.1 mm (Waters)

4000 Q TRAP triple quadrupole mass spectrometer with a Turbo V source (Applied Biosystems)

Analyst software 1.4.2 (Applied Biosystems)

HPLC system consisting of two HPLC pumps (one of them a binary gradient pump), an autosampler, a column oven with a built-in 6 port switching valve, and matching controlling unit e.g. Shimadzu LC-20AB, LC-20AD, SIL-20AC, CTO-20, and CBM-20A (Shimadzu)

A. Sampling of blood

collect blood from subject (human or mouse)
prepare EDTA plasma
store plasma at -80 °C before use

B. Preparation of precipitation agent containing internal standards

dissolve 50 g/L ZnSO₄ in water
mix ZnSO₄ solution 1:1 with methanol (v/v) to get the precipitation agent
dilute internal standards in precipitation agent: ¹³C₂-Testosterone 1.5 ng/mL (final concentration); d4-Cortisol 7.5 ng/mL (final concentration); d9-Progesterone 1.5 ng/mL (final concentration); d8-Corticosterone 15 ng/mL (final concentration)
place at -20 °C before use

C. Sample preparation

mix 50 µL plasma with 100 µL precipitation agent
vortex mix for 60 s
incubate at 4 °C for 30 min with continuous shaking
centrifuge at 14000 rpm at 4 °C for 10 min
transfer supernatant to deep well plate for measurement

D. Chromatographic separation of samples

prepare solvents for chromatography; methanol:water (5:95) for solid phase extraction; acetonitrile:water:formic acid (10:90:0.1) as solvent A for gradient run; acetonitrile:formic acid (100:0.1) as solvent B for gradient run
equilibrate chromatographic system with solvents (gradient flow rate is 0.5 mL/min; online-SPE flow rate is 3 mL/min
inject 80 µL of supernatant via autosampler
apply gradient and valve switching information (sample is enriched on online-SPE column and eluted in backflush onto the analytical column) from table 1

E. MS/MS analysis

measure samples in positive mode using an ESI source
set ion source parameters to CUR = 20; CAD = 6; IS = 4500; TEM = 600; GS1 = 40; GS2 = 55
use the multiple reaction monitoring (MRM) mass transitions given in table 1
for calibration run standards in the following concentrations: 0.1, 0.19, 0.39, 0.78, 1.56, 3.13, 6.25, 12.5, 25 ng/mL for androstenedione, testosterone, progesterone, and 17OH-progesterone; 0.98, 1.95, 3.91, 7.81, 15.63, 31.25, 62.5, 125, 250 ng/mL for cortisone, cortisol, and corticosterone
also run appropriate blanks (steroid stripped plasma) and quality control samples
evaluate results using Analyst 1.4.2 software (Applied Biosystems)

For preparation of 100 samples: hands-on time 2-3 h

For measurement of 100 samples: about 8.5 h (no hands-on time, performed by autosampler and LC-MS/MS system)

Chromatography solvents and the precipitation agent should be prepared fresh for each run. Pipetting steps before addition of internal standards are critical and should be performed as exactly as possible.

Typical results for human and mouse plasma are shown in Figures 1 and 2, respectively.

V. Gailus-Durner, H. Fuchs, L. Becker et al., Nat Methods 2 (6), 403 (2005).
T. Illig, C. Gieger, G. Zhai et al., Nat Genet (2009).
F. Z. Stanczyk, J. S. Lee, and R. J. Santen, Cancer Epidemiol Biomarkers Prev 16 (9), 1713 (2007).

PDF

Version 1

posted 16 Feb, 2010

You are reading this latest protocol version

Quantification of steroids in human and mouse plasma using online solid phase extraction coupled to liquid chromatography tandem mass spectrometry

Status:

Version 1

Figures

Introduction

Reagents

Equipment

Procedure

Timing

Critical Steps

Anticipated Results

References

Status:

Version 1

Privacy Policy

Terms of Service