The Library
1530 papers on microsampling and monitoring, each with a finding paraphrased to our standard and labelled in one vocabulary. Every entry links to a legitimate copy; nothing is copied from an abstract.
Papers 201–261 of 261 labelled “vams”, newest first.
2021
Two feasibility studies assessed low-volume blood sampling for therapeutic drug monitoring. In patients receiving an anti-A therapeutic, drug levels were measured from finger-prick whole blood collected with Neoteryx Mitra and from capillary plasma collected with TASSO OnDemand, and compared with venipuncture samples. The work outlines practical considerations for adopting these patient-centric microsampling methods in decentralised trials and clinical care.
Assessment of low volume sampling technologies: utility in nonclinical and clinical studies — Williams et al., Bioanalysis (paywalled)
- blood
- capillary
- vams
- neoteryx-mitra
- validation
- venous-agreement
- tdm
- biologics
2021
The HPLC-MS/MS assay on dried capillary blood collected with VAMS was linear, precise and stable, and showed strong agreement with liquid venous tacrolimus measurements, supporting its use for therapeutic drug monitoring in transplant recipients.
Volumetric absorptive microsampling for the quantification of tacrolimus in capillary blood by high performance liquid chromatography-tandem mass spectrometry — Tron et al., Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (paywalled)
- blood
- dried
- capillary
- vams
- neoteryx-mitra
- validation
- venous-agreement
- tdm
- immunosuppressants
2020
A review contrasting the formats, framing the haematocrit effect, non-uniform spreading and homogeneity limits of DBS as the problems volumetric sampling is designed to solve.
Opportunities and obstacles for microsampling techniques in bioanalysis: special focus on DBS and VAMS — Londhe & Rajadhyaksha, J. Pharmaceutical and Biomedical Analysis (paywalled)
- vams
- blood
- dbs
- haematocrit
- dried
- validation
2020
A direct DUS-versus-VAMS comparison for 13 steroids on the same urine: VAMS gave better precision and recovery and superior one-year room-temperature stability.
Dried urine microsampling coupled to LC-MS/MS for the analysis of unconjugated anabolic-androgenic steroids — Protti et al., Molecules
- vams
- volumetric
- doping
- dried
- steroids
- toxicology
- hormones
- urine
- validation
2020
Urine VAMS quantified doxycycline with 96–106% accuracy and 31-day room-temperature stability, supporting cold-chain-free adherence monitoring.
A validated VAMS-LC-MS/MS method to quantify doxycycline in urine: monitoring malaria-chemoprophylaxis compliance — Penot, Linard & Taudon, J. Analytical Methods in Chemistry
- vams
- tdm
- dried
- antimicrobials
- urine
- validation
2020
This study validated a method using volumetric absorptive microsampling (VAMS) for therapeutic drug monitoring of antidepressants in whole blood and oral fluid. The method showed good extraction yield (84%), precision (relative standard deviation under 15%), and stability (over 85% after three months), with results agreeing well with conventional sampling. By enabling self-collection at home, VAMS simplifies sampling, improves analyte stability, and reduces costs, making decentralised monitoring of antidepressant treatment feasible.
Whole blood and oral fluid microsampling for the monitoring of patients under treatment with antidepressant drugs — Marasca et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- saliva
- vams
- self-collection
- validation
- tdm
2020
Fingerprick blood collected with Neoteryx Mitra devices showed minimal bias compared to venous sampling for tacrolimus (-5.6%) and creatinine (-6.5%) in renal transplant patients. This validated method could enable home-based therapeutic drug monitoring and kidney function testing, reducing the need for hospital visits.
Assessment of tacrolimus and creatinine concentration collected using Mitra microsampling devices — Marshall et al., Annals of clinical biochemistry (paywalled)
- blood
- capillary
- vams
- neoteryx-mitra
- validation
- venous-agreement
- tdm
- immunosuppressants
2020
The authors developed and validated a VAMS method for quantifying immunosuppressants from venous whole blood using LC-MS/MS with a novel UniSpray ionisation probe. This supports patient-centric microsampling for transplant recipients requiring therapeutic drug monitoring.
Volumetric Absorptive Microsampling (VAMS) for assaying immunosuppressants from venous whole blood by LC-MS/MS using a novel atmospheric pressure ionization probe (UniSpray™) — Paniagua-González et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- vams
- validation
- tdm
- immunosuppressants
2020
The study developed and validated an LC-MS/MS method to measure selumetinib in whole blood collected via VAMS, showing the approach is reliable and stable under various conditions. This supports decentralised therapeutic drug monitoring, particularly in paediatric populations where less invasive sampling is beneficial.
Novel LC-MS/MS method for the determination of selumetinib (AZD6244) in whole blood collected with volumetric absorptive microsampling — Voggu et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
2020
The authors developed and validated high-sensitivity LC-MS/MS methods for tranexamic acid quantification in human whole blood, using either liquid samples or dried samples on volumetric absorptive microsampling devices. The methods performed excellently across clinically relevant concentrations, showed stability for up to one month at +50°C, and were validated with clinical samples, supporting decentralised therapeutic drug monitoring of this antifibrinolytic.
Tranexamic acid quantification in human whole blood using liquid samples or volumetric absorptive microsampling devices — Lamy et al., Bioanalysis (paywalled)
- blood
- liquid
- dried
- vams
- neoteryx-mitra
- validation
- tdm
2020
A VAMS method for measuring gamma-hydroxybutyric acid in blood was fully validated, showing linearity from 0.5 to 200 μg/ml and a lower limit of quantitation of 0.5 μg/ml. The method compared well with conventional plasma analysis in a patient receiving GHB therapy, suggesting microsampling could support decentralised therapeutic drug monitoring for this compound.
Development and validation of volumetric absorptive microsampling coupled with UHPLC-MS/MS for the analysis of gamma-hydroxybutyric acid in human blood — Mohamed et al., Biomedical chromatography : BMC (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
2020
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.
Quantification of testosterone, androstenedione and 17-hydroxyprogesterone in whole blood collected using Mitra microsampling devices — Marshall et al., Annals of clinical biochemistry (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- venous-agreement
- fertility
- hormones
2020
Capillary blood collected by VAMS gave cannabidiol concentrations that agreed strongly with venous plasma (R² 0.93) in five paediatric and young adult patients with Dravet syndrome. This validates VAMS as a less invasive method for therapeutic drug monitoring of cannabidiol, enabling personalised therapy in refractory epilepsy within decentralised settings.
A Volumetric Absorptive Microsampling Technique to Monitor Cannabidiol Levels in Epilepsy Patients — Dubois et al., Frontiers in pharmacology
- blood
- dried
- capillary
- vams
- venous-agreement
- pediatric
- tdm
2020
In children with epilepsy in remote African settings, dried blood microsampling enabled therapeutic drug monitoring but showed most patients had subtherapeutic antiepileptic drug concentrations. Volumetric absorptive microsampling gave inexplicably higher results than dried blood spots, and drug levels did not correlate with seizure control.
Dried Blood Microsampling-Based Therapeutic Drug Monitoring of Antiepileptic Drugs in Children With Nodding Syndrome and Epilepsy in Uganda and the Democratic Republic of the Congo — Velghe et al., Therapeutic drug monitoring (paywalled)
- blood
- dried
- vams
- dbs
- neoteryx-mitra
- pediatric
- tdm
2020
Capillary blood collected with Neoteryx Mitra VAMS microsampling devices can quantify IGF-1 by automated chemiluminescent immunoassay after aqueous extraction. The hormone is stable for at least one month at room temperature, and dried blood concentrations match serum after dilution correction, though capillary samples underestimate high serum values, supporting patient-centric, decentralised endocrine monitoring but requiring population-specific reference ranges.
Volumetric Absorptive Microsampling (VAMS) technology for IGF-1 quantification by automated chemiluminescent immunoassay in dried blood — Marchand et al., Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society (paywalled)
- blood
- dried
- capillary
- vams
- neoteryx-mitra
- validation
- venous-agreement
- hormones
2020
A survey of 39 kidney transplant recipients found that 85% preferred finger prick microsampling over venepuncture and 95% were interested in home self-sampling, highlighting the potential of decentralised blood collection to reduce patient burden and anxiety.
Kidney transplant recipient's perceptions of blood testing through microsampling and venepuncture — Scuderi et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- dbs
- self-collection
- acceptability
2020
The authors developed and validated a volumetric absorptive microsampling assay for vancomycin in whole blood that is suitable for paediatric therapeutic drug monitoring. Vancomycin remained stable in dried VAMS samples for at least 160 days at -78°C, enabling reliable quantification in clinical studies using minimal blood volumes.
A whole blood microsampling assay for vancomycin: development, validation and application for pediatric clinical study — Moorthy et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
- antimicrobials
2020
Capiau et al. developed and validated a VAMS method for cobalt quantitation in whole blood from metal-on-metal prosthesis patients. The method proved accurate (bias ≤4%) and precise (RSD ≤5%), was unaffected by haematocrit, and showed a 0.99 correlation to liquid venous samples; 87% of results satisfied Royal College of Pathologists of Australasia criteria, enabling home-based monitoring of implant wear.
Development, validation and application of an inductively coupled plasma - mass spectrometry method to determine cobalt in metal-on-metal prosthesis patients using volumetric absorptive microsampling — Capiau et al., Talanta (paywalled)
- blood
- dried
- vams
- validation
- venous-agreement
- toxicology
2020
Volumetric absorptive microsampling provides accurate quantification of 16 anti-epileptic drugs within two days of collection, showing less than ten percent deviation from conventional serum sampling and no haematocrit effect across the clinical range. This supports home-based therapeutic drug monitoring for epilepsy patients, though temperature-sensitive drugs require careful storage.
Therapeutic drug monitoring of anti-epileptic drugs - a clinical verification of volumetric absorptive micro sampling — Canisius et al., Clinical chemistry and laboratory medicine (paywalled)
- blood
- vams
- validation
- venous-agreement
- tdm
- haematocrit
2020
A VAMS method for 14 antidepressants, antipsychotics and active metabolites was validated on HPLC-MS and conversion factors from capillary blood to plasma were derived from 49 patient samples using Passing-Bablok and Bland-Altman analysis, enabling routine therapeutic drug monitoring.
Validation and clinical application of a volumetric absorptive microsampling method for 14 psychiatric drugs — Stern et al., Bioanalysis (paywalled)
- blood
- dried
- capillary
- vams
- neoteryx-mitra
- validation
- tdm
2020
The study developed and validated a LC-HRMS method for intact IGF-I from VAMS dried blood according to World Anti-Doping Agency requirements and showed agreement with serum measurements, supporting decentralised sampling for antidoping testing.
Use of capillary dried blood for quantification of intact IGF-I by LC-HRMS for antidoping analysis — Mongongu et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- venous-agreement
- doping
2020
Capillary blood sampling using volumetric absorptive microsampling demonstrated non-significant differences in cannabidiol concentrations compared to venous blood and plasma in pediatric patients treated with Epidiolex. The method requires 30 µL of sample, achieves linear quantification between 1 and 800 µg/L, and ensures analyte stability on VAMS devices for up to four weeks at room temperature.
Cannabidiol Determination on Peripheral Capillary Blood Using a Microsampling Method and Ultra-High-Performance Liquid Chromatography Tandem Mass Spectrometry with On-Line Sample Preparation — Pigliasco et al., Molecules
- blood
- dried
- capillary
- vams
- neoteryx-mitra
- validation
- venous-agreement
- pediatric
- tdm
2020
The Mitra microsampling device showed high clinical concordance with venous blood for tacrolimus (89%) and cyclosporin A (98%) monitoring, with inter- and intra-precision within 11.5% CV and samples stable for up to 7 days at room temperature. Transplant patients preferred collecting capillary samples at home for their immunosuppressant monitoring, supporting decentralised TDM.
Volumetric Microsampling of Capillary Blood Spot vs Whole Blood Sampling for Therapeutic Drug Monitoring of Tacrolimus and Cyclosporin A: Accuracy and Patient Satisfaction — Mbughuni et al., The journal of applied laboratory medicine (paywalled)
- blood
- capillary
- vams
- volumetric
- neoteryx-mitra
- validation
- venous-agreement
- acceptability
- tdm
- immunosuppressants
2020
The authors developed two simple methods to calculate haematocrit from VAMS samples using potassium content, one with aqueous extraction and one with organic extraction, both designed to integrate with existing VAMS assays so that whole-blood results can be converted to serum or plasma values and compared with therapeutic intervals.
Hematocrit prediction in volumetric absorptive microsamples — Capiau & Stove, Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- haematocrit
2020
The study validated a VAMS-based bioanalytical method using the Tasso OnDemand device for the drug gefapixant and demonstrated a mathematical bridging relationship with standard plasma assays, supporting its use in decentralised clinical trials.
Clinical application of volumetric absorptive microsampling to the gefapixant development program — Roadcap et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- venous-agreement
- tdm
2020
The review evaluates microsampling techniques including dried matrix spots, volumetric absorptive microsampling and capillary microsampling for SARS-CoV-2 bioanalytical applications, outlining their respective advantages and disadvantages to guide researchers and clinicians in pandemic-related diagnostics.
Quantitative microsampling for bioanalytical applications related to the SARS-CoV-2 pandemic: Usefulness, benefits and pitfalls — Protti et al., Journal of pharmaceutical and biomedical analysis
- blood
- dried
- vams
- validation
2020
Dried urine spot and volumetric absorptive microsampling methods were validated for quantifying six corticosteroids in 30 μl urine, showing good linearity, extraction yields exceeding 81 percent, and precision within 15 percent relative standard deviation. Analytes remained stable for seven days at room temperature, indicating urine microsampling is viable for remote antidoping control and could support decentralised steroid monitoring.
Microsampling and LC-MS/MS for antidoping testing of glucocorticoids in urine — Protti et al., Bioanalysis (paywalled)
- urine
- dried
- vams
- validation
- hormones
- steroids
- doping
- toxicology
2020
A GC-MS/MS method for anabolic steroids in VAMS dried blood from finger pricking demonstrated good precision, accuracy and stability, with results agreeing with serum specimens. In a testosterone gel administration trial, dried blood total testosterone identified transdermal micro-dosing, with concentrations rising up to ten times baseline at nine hours post-application, supporting decentralised doping screening.
Determination of anabolic steroids in dried blood using microsampling and gas chromatography-tandem mass spectrometry: Application to a testosterone gel administration study — Chang et al., Journal of chromatography. A (paywalled)
- blood
- dried
- vams
- validation
- venous-agreement
- hormones
- doping
2020
Capillary microsampling using the Neoteryx Mitra device predicted tacrolimus AUC with high accuracy and precision compared with venous sampling in renal transplant recipients, with 85% of estimates within ±11.9% error. Patients could self-sample accurately at home, enabling patient-centred therapeutic drug monitoring without extended hospital stays.
Tacrolimus Area Under the Concentration Versus Time Curve Monitoring, Using Home-Based Volumetric Absorptive Capillary Microsampling — Gustavsen et al., Therapeutic drug monitoring (paywalled)
- blood
- capillary
- vams
- neoteryx-mitra
- self-collection
- validation
- venous-agreement
- tdm
- immunosuppressants
2020
The study developed and validated a VAMS-based method for measuring cefepime in small volumes of paediatric blood with high accuracy and precision, enabling less invasive therapeutic drug monitoring in children. This advances decentralised, patient-centric sampling by allowing reliable pharmacokinetic studies without repeated venous draws.
Development and validation of a volumetric absorptive microsampling- liquid chromatography mass spectrometry method for the analysis of cefepime in human whole blood: Application to pediatric pharmacokinetic study — Moorthy et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
- antimicrobials
2020
The review highlights that volumetric absorptive microsampling enables easy, minimally invasive home sampling with room temperature storage and fixed volume accuracy, making it a viable alternative for clinical trials and therapeutic drug monitoring during the COVID-19 pandemic.
Volumetric Absorptive Microsampling as a Sampling Alternative in Clinical Trials and Therapeutic Drug Monitoring During the COVID-19 Pandemic: A Review — Harahap et al., Drug design, development and therapy
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
- dct
- haematocrit
2020
The study validated a VAMS method for cocaine and metabolites in blood and plasma, achieving good extraction yield, precision and accuracy with analyte stability exceeding two months at room temperature. Results from VAMS correlated well with conventional fluid samples, supporting its use for decentralised forensic and toxicological monitoring without venepuncture or cold chain.
Blood and Plasma Volumetric Absorptive Microsampling (VAMS) Coupled to LC-MS/MS for the Forensic Assessment of Cocaine Consumption — Mandrioli et al., Molecules
- blood
- dried
- vams
- neoteryx-mitra
- validation
- doping
- toxicology
2019
Volumetric absorptive capillary microsampling gave reliable tacrolimus measurements throughout the dose interval in renal transplant recipients, with mean biases of -3.1% for mailed samples and -4.2% for direct delivery versus venous blood. Dried microsamples remained stable for one month at ambient temperature, enabling home-based therapeutic drug monitoring with postal shipment.
Tacrolimus Can Be Reliably Measured With Volumetric Absorptive Capillary Microsampling Throughout the Dose Interval in Renal Transplant Recipients — Vethe et al., Therapeutic drug monitoring (paywalled)
- blood
- dried
- capillary
- vams
- validation
- venous-agreement
- tdm
- immunosuppressants
2019
The authors developed and validated an LC-MS/MS assay for THC, CBD and CBN from 20 µL VAMS blood samples with linear calibration curves and inter-day accuracies of 94.4 to 107 per cent, then applied it to a pediatric pharmacokinetic study, demonstrating that patient-centric microsampling can support decentralised therapeutic drug monitoring of cannabinoids in children.
A patient-centric liquid chromatography-tandem mass spectrometry microsampling assay for analysis of cannabinoids in human whole blood: Application to pediatric pharmacokinetic study — Moorthy et al., Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
2019
HPLC-MS/MS methods for midazolam and 1-OH midazolam in wet whole blood and dried blood collected on VAMS were developed and validated, meeting international guideline criteria; a strong correlation between wet and dry concentrations was observed, indicating VAMS is suitable for paediatric clinical studies.
Validation of methods for determining pediatric midazolam using wet whole blood and volumetric absorptive microsampling — Abu-Rabie et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- venous-agreement
- pediatric
- tdm
2019
Volumetric absorptive microsampling (VAMS) using the Neoteryx Mitra device was validated for mitotane therapeutic drug monitoring across 1–50 mg/L, with acceptable haematocrit bias and one-week stability at room temperature. However, comparison with venous plasma showed poor correlation, suggesting home-based VAMS is of limited clinical value for mitotane unless a method-specific target range is established.
A method for the minimally invasive drug monitoring of mitotane by means of volumetric absorptive microsampling for a home-based therapeutic drug monitoring — Friedl et al., Analytical and bioanalytical chemistry (paywalled)
- blood
- dried
- capillary
- vams
- neoteryx-mitra
- validation
- venous-agreement
- tdm
- oncology
2019
The study developed and validated two LC-MS/MS methods for quantifying paracetamol in dried blood and dried cerebrospinal fluid using VAMS, showing acceptable precision and accuracy, limited haematocrit influence, and stability under various storage conditions, thus proving the utility of VAMS for CSF microsampling.
Volumetric absorptive microsampling as an alternative sampling strategy for the determination of paracetamol in blood and cerebrospinal fluid — Delahaye et al., Analytical and bioanalytical chemistry (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- haematocrit
2019
Microsampling with the Neoteryx Mitra device showed acceptable linearity and precision for cyclosporine A, everolimus, sirolimus and tacrolimus, and agreed closely with conventional venous extraction by Deming regression, supporting its use for decentralised immunosuppressant therapeutic drug monitoring.
Feasibility of Immunosuppressant Drug Monitoring by a Microsampling Device — Gruzdys et al., The journal of applied laboratory medicine (paywalled)
- blood
- vams
- neoteryx-mitra
- validation
- venous-agreement
- tdm
- immunosuppressants
2019
In ten healthy volunteers, radiprodil pharmacokinetics measured by Aqua-Cap™ Drummond microsampling closely matched conventional venous blood draws, whereas Mitra™ microsampling gave marginally lower exposure values. Both microsampling methods fell within the accepted bioequivalence range, indicating they could enable patient-centric therapeutic drug monitoring and future paediatric decentralised trials.
A pharmacokinetic study of radiprodil oral suspension in healthy adults comparing conventional venous blood sampling with two microsampling techniques — Sciberras et al., Pharmacology research & perspectives
- blood
- capillary
- vams
- neoteryx-mitra
- validation
- venous-agreement
- pediatric
2019
VAMS capillary blood showed strong agreement with venous serum for measuring anti-influenza antibodies and remained stable for three weeks at room temperature. When volunteers performed finger-stick sampling at home, their results were highly consistent with on-site collection by study personnel.
Application of volumetric absorptive microsampling (VAMS) to measure multidimensional anti-influenza IgG antibodies by the mPlex-Flu assay — Wang et al., Journal of clinical and translational science
- blood
- dried
- capillary
- vams
- neoteryx-mitra
- self-collection
- validation
- venous-agreement
- serology
2019
The VAMS assay quantifies voriconazole and voriconazole N-oxide with linear calibration from 10.0 to 10,000 ng/mL and intra- and inter-day accuracy within 87-102%, enabling accurate and precise therapeutic drug monitoring from a small fixed volume of dried blood.
Development and validation of a volumetric absorptive microsampling assay for analysis of voriconazole and voriconazole N-oxide in human whole blood — Moorthy et al., Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
- antimicrobials
2019
The validated LC-MS/MS method showed similar pharmacokinetic profiles for albendazole and its metabolites across plasma, whole blood, dried blood spots and Mitra microsamples from hookworm-infected adolescents, supporting microsampling for paediatric pharmacokinetic studies. Mitra extraction proved more robust than dried blood spots during validation and is recommended for future albendazole pharmacokinetic work, despite higher albendazole sulfone concentrations observed in both microsampling devices compared with wet matrices.
Pharmacokinetics of Albendazole, Albendazole Sulfoxide, and Albendazole Sulfone Determined from Plasma, Blood, Dried-Blood Spots, and Mitra Samples of Hookworm-Infected Adolescents — Schulz et al., Antimicrobial agents and chemotherapy (paywalled)
- blood
- liquid
- dried
- capillary
- vams
- dbs
- neoteryx-mitra
- validation
- venous-agreement
- pediatric
- tdm
- antimicrobials
2019
The authors validated an LC-MS/MS method for simultaneously measuring vancomycin and creatinine from plasma applied to VAMS devices, reporting acceptable precision and accuracy with both analytes stable for up to two weeks at 45 degrees Celsius, though VAMS concentrations required correction factors to estimate plasma levels. This supports wider access to vancomycin therapeutic drug monitoring in resource-limited settings by enabling ambient transport of dried plasma microsamples.
Simultaneous determination of vancomycin and creatinine in plasma applied to volumetric absorptive microsampling devices using liquid chromatography-tandem mass spectrometry — Andriguetti et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
- antimicrobials
2019
Targeted metabolomics of whole blood using VAMS achieved good recoveries and repeatability (less than 15% RSD) for 36 metabolites, and amino and organic acids remained stable in dried blood for at least four days at room temperature, supporting decentralised microsampling for metabolomics.
Targeted metabolomics of whole blood using volumetric absorptive microsampling — Kok et al., Talanta (paywalled)
- blood
- dried
- vams
- validation
- metabolome
2018
Acetylsalicylic acid concentrations in VAMS samples decrease without a stabilising reagent, whereas whole blood samples remain stable. For decentralised diagnostics, this means stabilisers must be added to VAMS devices before analysis to ensure accurate therapeutic drug monitoring from patient-collected samples.
Quantitative analysis of acetylsalicylic acid in human blood using volumetric absorptive microsampling — Kim et al., Translational and clinical pharmacology
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
2018
Volumetric absorptive microsampling provided acceptable analytical accuracy and precision for atenolol, lisinopril, simvastatin and capillary blood samples without being influenced by haematocrit levels. The VAMS approach demonstrated strong agreement with standard dried blood spot cards in identifying medication adherence among volunteers.
Volumetric absorptive microsampling (VAMS) coupled with high-resolution, accurate-mass (HRAM) mass spectrometry as a simplified alternative to dried blood spot (DBS) analysis for therapeutic drug monitoring of cardiovascular drugs — Tanna et al., Clinical mass spectrometry (paywalled)
- blood
- dried
- vams
- dbs
- neoteryx-mitra
- validation
- tdm
- haematocrit
2018
Volumetric absorptive microsampling provided accurate and precise measurement of key urinary metabolites in alkaptonuria with good recovery and reproducibility, and dried samples compared favourably with liquid specimens, although variable analyte stability may present barriers to routine implementation.
Evaluation of the Mitra microsampling device for use with key urinary metabolites in patients with Alkaptonuria — Taylor et al., Bioanalysis (paywalled)
- urine
- dried
- vams
- neoteryx-mitra
- validation
2018
Capillary C-peptide concentrations measured from dried blood spot and volumetric absorptive microsampling showed strong agreement with reference plasma samples. Both sampling methods maintained stability over 48 hours at room temperature, supporting their utility for remote monitoring of endogenous insulin secretion.
Microsampling Collection Methods for Measurement of C-peptide in Whole Blood — Jones et al., Journal of diabetes science and technology (paywalled)
- blood
- dried
- capillary
- vams
- dbs
- neoteryx-mitra
- validation
- venous-agreement
2018
VAMS recovery relative to DMPK-C depended on the protein, being lower for β-lactoglobulin and myoglobin but higher for cytochrome c and albumin, and haematocrit affected protein quantification from both materials. VAMS showed strong correlation (R² ≥ 0.983), accuracy of 71 to 101 per cent and precision with RSD at or below 20 per cent for six model proteins spiked into blood, supporting its use for decentralised protein analysis with awareness of haematocrit effects.
Volumetric absorptive MicroSampling vs. other blood sampling materials in LC-MS-based protein analysis - preliminary investigations — Andersen et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- haematocrit
2018
A volumetric absorptive microsampling method for quantifying GSKA in human blood was developed and validated. Haematocrit related assay bias was minimised across a 30 to 60 per cent range and all validation parameters met acceptance criteria, indicating the method is suitable for quantitative analysis in decentralised settings.
Drug monitoring by volumetric absorptive microsampling: method development considerations to mitigate hematocrit effects — Fang et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- validation
- tdm
- haematocrit
2017
VAMS microsampling of capillary blood provided accurate measurement of hydroxychloroquine and metabolites in rheumatoid arthritis patients, with results agreeing with venous blood while overcoming dried blood spot limitations of haematocrit bias and inhomogeneity, and offered potential for home self-collection.
Capillary blood collected on volumetric absorptive microsampling (VAMS) device for monitoring hydroxychloroquine in rheumatoid arthritis patients — Qu et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- dried
- capillary
- vams
- dbs
- validation
- venous-agreement
- tdm
2017
Dried VAMS and DBS samples collected at home and analysed after a median of three days showed poor agreement with standard venous or capillary blood for HbA1c monitoring. In contrast, wet VAMS samples analysed immediately demonstrated excellent agreement, indicating that sample drying and delayed analysis compromise reliability for decentralised HbA1c measurement.
Volumetric absorptive microsampling at home as an alternative tool for the monitoring of HbA1c in diabetes patients — Verougstraete et al., Clinical chemistry and laboratory medicine (paywalled)
- blood
- liquid
- dried
- capillary
- vams
- dbs
- self-collection
- validation
- venous-agreement
- acceptability
- pediatric
2017
In breast cancer patients, whole blood microsampling by dried matrix on paper discs and volumetric absorptive microsampling detected a similar number of metabolites with comparable reproducibility and group discrimination to the standard protein precipitation method, supporting their use as simpler alternatives in decentralised metabolomics workflows.
Comparative study on microsampling techniques in metabolic fingerprinting studies applying gas chromatography-MS analysis — Cala & Meesters, Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- metabolome
2017
A miniaturised stable isotope dilution assay using volumetric absorptive microsampling quantified whole blood 5-methyltetrahydrofolic acid from only 10.8 μL with good precision and reproducibility. The dried samples remained stable for three weeks at -20°C, demonstrating VAMS enables accurate folate status screening with minimal blood volume, which is valuable for population and newborn screening programmes.
Assessing Volumetric Absorptive Microsampling Coupled with Stable Isotope Dilution Assay and Liquid Chromatography-Tandem Mass Spectrometry as Potential Diagnostic Tool for Whole Blood 5-Methyltetrahydrofolic Acid — Kopp & Rychlik, Frontiers in nutrition
- blood
- dried
- vams
- neoteryx-mitra
- validation
- biomarkers
2017
VAMS devices collect accurate blood volumes regardless of haematocrit level, but conventional ultrasonication extraction showed reduced drug recovery at higher haematocrit. A new bead-based impact-assisted extraction eliminated this bias, achieving quantitative recovery of naproxen and ritonavir across all haematocrit levels tested.
Volumetric absorptive microsampling combined with impact-assisted extraction for hematocrit effect free assays — Youhnovski et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
- haematocrit
2017
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.
Whole blood microsampling for the quantitation of estetrol without derivatization by liquid chromatography-tandem mass spectrometry — Nys et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
2016
An LC-MS/MS method accurately quantified hydroxyurea from small volumes of dried blood collected on DMPK-C cards and VAMS devices across a linear range of 0.5 to 60 μg/mL with comparable performance. This enables therapeutic drug monitoring and pharmacokinetic assessment in pediatric sickle cell anemia patients using capillary heel- or finger-prick sampling.
Stable-Isotope Dilution HPLC-Electrospray Ionization Tandem Mass Spectrometry Method for Quantifying Hydroxyurea in Dried Blood Samples — Marahatta et al., Clinical chemistry (paywalled)
- blood
- dried
- vams
- dbs
- neoteryx-mitra
- validation
- pediatric
- tdm
2015
VAMS eliminated the variable haematocrit bias seen with DBS, but a residual haematocrit-dependent recovery effect persisted at high haematocrit: the nuance that assays still need per-analyte validation.
Does volumetric absorptive microsampling eliminate the hematocrit bias for caffeine and paraxanthine in dried blood samples? A comparative study — De Kesel, Lambert & Stove, Analytica Chimica Acta (paywalled)
- vams
- blood
- dbs
- haematocrit
- dried
- toxicology
- validation
2015
Combining volumetric absorptive microsampling with phospholipid removal plates reduces matrix effects and delivers high sensitivity for dried blood hepcidin quantification. This method establishes a reliable microsampling protocol to quantify this peptide hormone while mitigating haematocrit bias.
Hepcidin determination in dried blood by microfluidic LC-MS/MS: comparison of DBS and volumetric absorptive microsampling for matrix effect and recovery — Houbart et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- dbs
- neoteryx-mitra
- validation
- hormones
- haematocrit
2015
The authors validated an LC-MS/MS method for quantifying emixustat in whole blood collected by VAMS. The assay performed reliably across the normal adult haematocrit range and the analyte remained stable on the device under ambient, refrigerated, and frozen storage, enabling decentralised therapeutic drug monitoring without plasma separation or cold chain.
Bioanalysis of emixustat (ACU-4429) in whole blood collected with volumetric absorptive microsampling by LC-MS/MS — Miao et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
- haematocrit
2014
The foundational VAMS paper: a fixed ~10 µL is absorbed with under 5% volume variation across a 20–70% haematocrit range, overcoming the area bias and homogeneity problems of the dried blood spot.
Volumetric Absorptive Microsampling: A Dried Sample Collection Technique for Quantitative Bioanalysis — Denniff & Spooner, Analytical Chemistry (paywalled)
- vams
- neoteryx-mitra
- blood
- haematocrit
- dried
- validation
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