Dual Functionality in Whole Blood Microsampling: Combining Plasma Separation and Immunoaffinity Cleanup for LC-MS Based Targeted Protein Analysis
Mrsa et al.
The finding, in our words
A 3D-printed microsampling device extracted 80% plasma from 20 μL of whole blood while removing more than 93% of hemoglobin interference. The device demonstrated linearity, accuracy and precision suitable for hCG analysis according to EMA guidelines, offering a robust tool for point-of-care diagnostics that enhances analytical sensitivity and specificity.
A paraphrase to the Library’s standard, never the abstract. The source is one link away and is always the authority.
The analysis indicates that dried blood spots and volumetric absorptive microsampling enable minimally invasive monitoring of prohibited substances, with volumetric absorptive microsampling offering improved quantitative reliability over traditional dried spots.
Capillary fingerstick sampling showed high correlation and agreement with venous sampling for serum AMH but with proportional bias, so it may improve access to testing yet should not be considered fully interchangeable without further validation.
Home DBS sampling gave testosterone results that agreed well with venous blood in men on intramuscular testosterone undecanoate, but showed falsely high values in those using topical gel, likely from skin contamination. Patients preferred home collection for its convenience, suggesting DBS is viable for decentralised monitoring of injectable testosterone if patients are taught proper technique.
Earlobe capillary microsampling of 100-250 µL found good agreement with venous draws for progesterone, concordance 0.911, and 17β-estradiol, concordance 0.919, across menstrual cycles, showing suitability for decentralised monitoring. However, participant-reported burden was not assessed, and further validation is required in elite athletes.
In 46 women under hormone monitoring at Columbia University Fertility Center, oestradiol, LH, FSH, progesterone and hCG measured on routine immunoassays from 400 to 600 microlitres of upper-arm capillary blood collected with TAP Micro Select agreed closely with paired venous results for every analyte, with correlation and concordance high throughout. It is the evidence that puts a self-collected sample inside the daily monitoring of an IVF cycle.