2017 · Journal of pharmaceutical and biomedical analysis · paywalled
Whole blood microsampling for the quantitation of estetrol without derivatization by liquid chromatography-tandem mass spectrometry
Nys et al.
The finding, in our words
The study developed and validated an LC-MS/MS method for quantitating estetrol from 10–20 µL whole blood collected on volumetric absorptive microsampling devices, demonstrating selectivity, trueness, precision, accuracy and stability without derivatisation, and confirmed performance in murine pharmacokinetic studies; this enables reliable, low-volume microsampling for decentralised pharmacokinetic applications.
A paraphrase to the Library’s standard, never the abstract. The source is one link away and is always the authority.
An LC-MS/MS assay for testosterone, androstenedione and 17-hydroxyprogesterone using Mitra microsampling devices achieved mean recoveries of 102%, 98% and 97% respectively, with limits of quantification of 1–4 nmol/L. This analytical validation demonstrates that volumetric absorptive microsampling can deliver reliable reproductive hormone measurements, supporting its use in decentralised diagnostics.
A liquid chromatography-tandem mass spectrometry method was successfully validated for measuring androstenedione, 17α-hydroxyprogesterone, and 11-ketotestosterone in dried blood samples collected via volumetric absorptive microsampling. The dried samples remained stable at room temperature for up to a week and after postal transit, and plasma concentrations could be reliably estimated from the microsamples when adjusting for haematocrit.
This study compared four dried blood spot devices for glucocorticoid detection, finding that the Mitra VAMS device offered the best combination of analytical recovery and user usability, whilst the HemaXis DB10 showed the least bias compared to whole blood.
The study compared five microsampling devices, including Mitra tips and Tasso-M20, for detecting 27 steroid esters in dried blood by LC-MS/MS, and found that methanol extraction with Girard's reagent P or T provided the best screening sensitivity with detection limits of 0.05 to 1.0 ng/mL, while methoxyamine derivatization was recommended for confirming boldenone and certain testosterone esters. The Tasso-M20 device produced chromatographic interference with methanol extraction that was only partially resolved by using mixed solvents, at the cost of lower recoveries.
The authors validated an LC-HRMS/MS assay for steroids and thyroid hormones in 30 microlitres of capillary blood collected with Neoteryx Mitra VAMS devices, demonstrating storage stability of over 28 days frozen and 14 days at room temperature. Using authentic samples from 50 healthy active adults, the method showed adequate sensitivity to detect the reduced hormone concentrations seen in relative energy deficiency in sport, supporting self-collected VAMS as a practical tool for regular hormone monitoring in athletes.