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Microsampling Publications Library

Dive into our dynamic, ever-growing library of peer-reviewed publications, posters, application notes, and presentations showcasing the full breadth and depth of Trajan microsampling technologies. Discover cutting-edge methods, compelling scientific breakthroughs, and real-world applications spanning a wide range of disciplines.  

Search results are matched to the publication record, including title, abstract, keywords, authors, and other indexed details. All search terms must appear in the record for it to be included in your results.

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BNT162b2, mRNA-1273, and Sputnik V Vaccines Induce Comparable Immune Responses on a Par With Severe Course of COVID-19

Kaznadzey, A.; Tutukina, M.; Bessonova, T.; Kireeva, M.; Mazo, I.
Front Immunol | 2022

This study compared antibody responses induced by the BNT162b2, mRNA-1273, and Sputnik V COVID-19 vaccines with responses after natural infection. All three vaccines generated strong receptor-binding-domain antibodies, while the data also reinforced the importance of completing multi-dose regimens.

Mercury biomonitoring in German adults using volumetric absorptive microsampling

Koutsimpani-Wagner, A.; Quartucci, C.; Rooney, J. P. K.; Bose-O'Reilly, S.; Rakete, S.
Environ Monit Assess | 2022

This study evaluated VAMS with direct mercury analysis for biomonitoring exposure in German adults. The method showed strong accuracy and precision, particularly at higher concentrations, supporting it as a viable alternative to venous blood collection.

A fast screening method for the detection of CERA in dried blood spots

Rocca, A.; Martin, L.; Kuuranne, T.; Ericsson, M.; Marchand, A.; Leuenberger, N.
Drug Test Anal | 2022

Researchers developed a rapid ELISA-based screening method for detecting continuous erythropoietin receptor activator in dried blood spots. The approach detected CERA for up to 20 days after administration and successfully identified the drug in authentic doping-control samples.

MOG analogues to explore the MCT2 pharmacophore, alpha-ketoglutarate biology and cellular effects of N-oxalylglycine

Fets, L.; Bevan, N.; Nunes, P. M.; Campos, S.; Dos Santos, M. S.; Sherriff, E.; MacRae, J. I.; House, D.; Anastasiou, D.
Commun Biol | 2022

Researchers developed MOG analogues to investigate MCT2 transport, α-ketoglutarate biology, and the cellular effects of N-oxalylglycine. Selected compounds retained cellular entry and prolyl-hydroxylase inhibition without inhibiting glutaminolysis or causing cytotoxicity, helping separate the compound’s overlapping biological effects.

Leveraging patient-centric sampling for clinical drug development and decentralized clinical trials: Promise to reality

Maass, K. F.; Barfield, M. D.; Ito, M.; James, C. A.; Kavetska, O.; Kozinn, M.; Kumar, P.; Lepak, M.; Leuthold, L. A.; Li, W.; Mikhailov, D.; Patel, S.; Perez, N. L.; Jackson Rudd, D.; Vakkalagadda, B.; Williams, T. M.; Zha, J.; Zhang, X.; Anderson, M. D.
Clin Transl Sci | 2022

This position paper considers how patient-centric sampling can support clinical drug development and decentralized trials. It outlines potential benefits for participants and sponsors alongside bioanalytical, operational, regulatory, and program-planning requirements.

Characterization of the Population Pharmacokinetics of Moxidectin in Adults Infected with Strongyloides Stercoralis: Support for a Fixed-Dose Treatment Regimen

Smit, C.; Hofmann, D.; Sayasone, S.; Keiser, J.; Pfister, M.
Clin Pharmacokinet | 2022

This study characterized the population pharmacokinetics of moxidectin in adults infected with Strongyloides stercoralis using serial microsamples. Model-based simulations found similar exposure with fixed and weight-based regimens, supporting a simpler fixed-dose approach for large-scale treatment programs.

Application of a Volumetric Absorptive Microsampling (VAMS)-Based Method for the Determination of Paracetamol and Four of its Metabolites as a Tool for Pharmacokinetic Studies in Obese and Non-Obese Patients

Boffel, L.; Delahaye, L.; De Baerdemaeker, L.; Stove, C. P.
Clin Pharmacokinet | 2022

This clinical study evaluated a VAMS-based method for measuring paracetamol and four metabolites in obese and non-obese patients. Finger-prick samples provided results suitable for pharmacokinetic analysis, supporting a less burdensome alternative to conventional venous sampling.

Standardized Workflow for Precise Mid- and High-Throughput Proteomics of Blood Biofluids

Mc Ardle, A.; Binek, A.; Moradian, A.; Chazarin Orgel, B.; Rivas, A.; Washington, K. E.; Phebus, C.; Manalo, D. M.; Go, J.; Venkatraman, V.; Coutelin Johnson, C. W.; Fu, Q.; Cheng, S.; Raedschelders, K.; Fert-Bober, J.; Pennington, S. R.; Murray, C. I.; Van Eyk, J. E.
Clin Chem | 2022

This study established standardized, automated proteomics workflows for naïve plasma, depleted plasma, and dried blood. The high- and mid-throughput approaches produced reproducible protein measurements across a broad dynamic range, supporting scalable biomarker-discovery studies.

Analytical and clinical validation of dried blood spot and volumetric absorptive microsampling for measurement of tacrolimus and creatinine after renal transplantation

Mathew, B. S.; Mathew, S. K.; Aruldhas, B. W.; Prabha, R.; Gangadharan, N.; David, V. G.; Varughese, S.; John, G. T.
Clin Biochem | 2022

This study validated DBS and VAMS methods for simultaneous tacrolimus and creatinine measurement after kidney transplantation. Corrected VAMS results agreed closely with venous samples and supported VAMS as the preferred single-sample option.

Monitoring of Dabrafenib and Trametinib in Serum and Self-Sampled Capillary Blood in Patients with BRAFV600-Mutant Melanoma

Isberner, N.; Gesierich, A.; Balakirouchenane, D.; Schilling, B.; Aghai-Trommeschlaeger, F.; Zimmermann, S.; Kurlbaum, M.; Puszkiel, A.; Blanchet, B.; Klinker, H.; Scherf-Clavel, O.
Cancers (Basel) | 2022

This study evaluated dabrafenib and trametinib exposure and the feasibility of at-home capillary blood sampling in patients with melanoma. Self-sampling was practical, and a conversion model estimated serum pharmacokinetic parameters from microsamples.

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