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Cortisol & Dexamethasone in plasma/serum LC-MS/MS kit Evaporation Method RUO

Cortisol & Dexamethasone in plasma/serum LC-MS/MS kit

SKU: 1320E KIT M CCD / 1320S KIT M CCD

Key benefits

  • Quantitative analysis of cortisol, cortisone and dexamethasone in a single LC-MS/MS run.
  • Focused, cost-effective panel for dexamethasone research in combination with cortisol and cortisone, without implementing a broad general steroid panel.
  • Suitable for human serum, EDTA plasma and lithium-heparin plasma.
  • Available with two sample preparation routes: Evaporation Method (without the need of SPE) and SPE Method.
  • High analytical specificity using LC-MS/MS with MRM detection.
  • Choice between a rapid, cost-effective workflow and a workflow with more extensive sample clean-up.

Product description


The Cortisol, Cortisone & Dexamethasone LC-MS/MS Reagent kit (RUO) has been developed for laboratories that want to quantitatively analyse cortisol, cortisone and dexamethasone in a single LC-MS/MS run in human serum or plasma.

Cortisol and cortisone are endogenous glucocorticoids that are relevant in research into glucocorticoid metabolism and the hypothalamic-pituitary-adrenal axis. Dexamethasone is a synthetic glucocorticoid frequently used in research protocols involving glucocorticoid exposure or suppression models.

By measuring cortisol, cortisone and dexamethasone simultaneously, this reagent kit supports research in which the interpretation of endogenous glucocorticoids in relation to dexamethasone exposure is relevant. The LC-MS/MS method combines chromatographic separation with mass-selective detection, enabling selective measurement of the three analytes within one workflow.

The reagent kit is available in two configurations. The 1320E KIT M CCD is intended for the Evaporation Method. This workflow uses protein precipitation, centrifugation, evaporation of the supernatant under nitrogen and reconstitution prior to LC-MS/MS analysis. This route provides a rapid and cost-effective sample preparation workflow.

The 1320S KIT M CCD is intended for the SPE Method. This workflow uses solid phase extraction for more extensive sample clean-up before LC-MS/MS analysis. The SPE Method may help reduce matrix background and contamination of the LC-MS/MS system and may be preferred when enhanced clean-up, contamination control or analytical sensitivity is required.

Both configurations are developed for use with human serum, EDTA plasma and lithium-heparin plasma. The applicable sample preparation route must be selected before starting the procedure. Components and procedural steps from the Evaporation Method and SPE Method must not be interchanged unless explicitly stated in the instructions for use.

Which sample preparation workflow fits your laboratory?

The Cortisol, Cortisone & Dexamethasone LC-MS/MS Reagent kit is available in two configurations. Both kits support quantitative analysis of cortisol, cortisone and dexamethasone in human serum or plasma, but they differ in sample preparation, workflow and degree of sample clean-up.

1320E KIT M CCD – Evaporation Method


The 1320E KIT M CCD is intended for laboratories looking for a rapid and cost-effective sample preparation workflow. This method uses protein precipitation, centrifugation, evaporation of the supernatant under nitrogen and reconstitution prior to LC-MS/MS analysis.


Advantages

Rapid and practical sample preparation.
Cost-effective workflow.
Limited need for additional consumables.
Suitable for laboratories that want to process larger sample series efficiently.
Liquid handling steps may be semi-automated.

Considerations

Less extensive sample clean-up than SPE.
May result in a higher matrix background.
On LC-MS/MS systems with lower sensitivity, this may affect analytical sensitivity at low analyte concentrations.
The evaporation step may limit full workflow automation, depending on the available equipment.


1320S KIT M CCD – SPE Method


The 1320S KIT M CCD is intended for laboratories that require more extensive sample clean-up. This method uses solid phase extraction prior to LC-MS/MS analysis and is particularly suitable when matrix reduction, contamination control or analytical sensitivity are important.


Advantages

More extensive sample clean-up than the Evaporation Method.
May reduce matrix background.
May reduce contamination of the LC-MS/MS system.
May be preferred when enhanced analytical sensitivity is required.
Can be automated using an automated SPE platform or an SPE-compatible liquid handling robot.

Considerations

More labour-intensive than the Evaporation Method.
Requires additional consumables, such as suitable SPE materials.
The workflow involves more handling steps and equipment than the Evaporation Method.

Important information


This product information is not sufficient on its own for the correct and safe use of the product. Always consult the current instructions for use, product-specific documentation, safety information and method limitations.


For Research Use Only (RUO). Not for use in diagnostic procedures, clinical decision-making, patient classification, screening or treatment monitoring.

Chromatograms

Technical data

Repeatability
Cortisol (nmol/l) / CV % low control; high control; serum sample 31.055 / 0.9; 519.454 / 0.6; 245.089 / 0.8
Cortisone (nmol/l) / CV % low control; high control; serum sample 7.140 / 2.6; 144.271 / 0.8; 51.623 / 1.3
Dexamethasone (nmol/l) / CV % low control; high control; serum sample 1.142 / 6.2; 26.841 / 2.1; 6.789 / 4.0
Reproducibility
Cortisol (nmol/l) / CV % low control; high control; serum sample 28.835 / 4.4; 506.170 / 2.9; 441.693 / 3.3
Cortisone (nmol/l) / CV % low control; high control; serum sample 6.506 / 5.0; 136.733 / 3.4; 67.408 / 3.6
Dexamethasone (nmol/l) / CV % low control; high control; serum sample 1.029 / 11.3; 26.043 / 5.6; 10.601 /6.0
Limit of Quantification
Cortisol (nmol/l) 0.785
Cortisone (nmol/l) 0.916
Dexamethasone (nmol/l) 0.500
Linearity
Cortisol (nmol/l) 2480
Cortisone (nmol/l) 750
Dexamethasone (nmol/l) 84

Important Notice: The information provided on this website alone is not sufficient for the correct and safe operation of this product. Always refer to the applicable Instructions for Use and accompanying documentation, including any warnings and safety notices.Please note that system-specific conditions may influence results. If you have any questions or require technical support, we encourage you to contact us to discuss your specific setup or requirements. For Research Use Only (RUO). Not for use in diagnostic procedures. Preparation for future IVDR registration is planned.

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9902 SE Appingedam
The Netherlands

info@diagnotix.com +31 (0)596 20 10 62