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.
36 papers labelled “antimicrobials”, newest first.
2026
In 15 critically ill children with multiple organ dysfunction, a population pharmacokinetic model built on volumetric absorptive microsamples found that estimated glomerular filtration rate and age drove cefepime clearance and distribution; the authors take this as showing the method is workable for antimicrobial monitoring in this group.
Cefepime pharmacokinetics in critically ill children with multiple organ dysfunction syndrome using volumetric absorptive microsampling — Amajor et al., Antimicrobial agents and chemotherapy
- blood
- dried
- vams
- pediatric
- tdm
- antimicrobials
2026
This study validated a method requiring only 10 microlitres of serum and found high agreement between fingerstick capillary samples and venous serum for monitoring twelve antibiotics. The results suggest capillary serum sampling is a feasible, minimally invasive alternative that avoids the haematocrit effect associated with whole blood microsampling.
Feasibility verification of fingerstick capillary microsampling replacing venipuncture for therapeutic drug monitoring of 12 antibiotics using a rapid LC-MS/MS assay — Chen et al., Talanta (paywalled)
- blood
- liquid
- capillary
- validation
- venous-agreement
- pediatric
- tdm
- antimicrobials
2026
The study developed and validated a rapid LC-MS/MS method for quantifying cefazolin in capillary whole blood collected via VAMS, plasma, and plasma ultrafiltrate, showing robust performance across matrices and successful application in a pediatric pilot cohort for therapeutic drug monitoring.
Rapid, robust LC-MS/MS quantification of cefazolin in whole blood microsamples, plasma, and plasma ultrafiltrate: Analytical method validation and preliminary clinical application in pediatric population — Kocur et al., Clinica chimica acta; international journal of clinical chemistry (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
- antimicrobials
2026
A UPLC-MS/MS method for linezolid and metabolites in oral fluid and VAMS capillary blood satisfied ICH M10 validation requirements. Linezolid concentrations correlated strongly with venous plasma in both matrices, offering a non‑invasive option for therapeutic drug monitoring, whereas metabolites were systematically underestimated in VAMS and seldom detectable in oral fluid, restricting metabolite measurement.
Simultaneous quantification of linezolid and its metabolites (PNU-142300 and PNU-142586) in oral fluid and capillary blood by UPLC-MS/MS: method validation and clinical application using non-invasive sampling techniques — González-Berdullas et al., Journal of translational medicine (paywalled)
- blood
- saliva
- dried
- capillary
- vams
- validation
- venous-agreement
- tdm
- antimicrobials
- haematocrit
2025
A systematic review found mixed economic evidence for microsampling in therapeutic drug monitoring; one study reported no cost reduction with DBS home-sampling, €688 versus €676, whilst another predicted savings up to 61%. The authors caution that more work is required to assess costs alongside clinical outcomes and optimise logistics for decentralised implementation.
The economic evidence for microsampling to support therapeutic drug monitoring: A systematic review — Carland et al., British Journal of Clinical Pharmacology (paywalled)
- vams
- blood
- economics
- dbs
- tdm
- self-collection
- dried
- antimicrobials
- pediatric
- immunosuppressants
- validation
2025
A quantitative dried blood spot method using only 10 µL of blood successfully quantified six azole antimycotics and showed samples were stable under conditions simulating postal mailing. A formula to convert dried spot results to plasma values was derived, though the authors note this is an in vitro validation and clinical studies are required for translation to patient care.
Simultaneous Quantification of Azole Antimycotics in Quantitative Dried Blood Spots: A Step Toward Home Sampling for Therapeutic Drug Monitoring — Li et al., Therapeutic drug monitoring (paywalled)
- blood
- dried
- dbs
- qdbs
- self-collection
- validation
- tdm
- antimicrobials
2025
This study validated a method for quantifying fluconazole using the Mitra device, demonstrating sufficient accuracy and precision for therapeutic drug monitoring in paediatric patients.
Determination of Fluconazole in Children in Small Blood Volumes Using Volumetric Absorptive Microsampling (VAMS) and Isocratic High-Performance Liquid Chromatography-Ultraviolet (HPLC-UV) Detection — Zimbelmann et al., Pharmaceutics
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
- antimicrobials
2025
The study compared quantitative dried blood spot (qDBS) and volumetric absorptive microsampling (VAMS) devices for measuring ganciclovir levels in capillary blood from pediatric renal transplant recipients. This comparison provides evidence for choosing between microsampling devices in therapeutic drug monitoring, supporting decentralised sampling approaches that reduce patient burden while maintaining analytical accuracy.
The comparison of two volumetric microsampling devices (qDBS and VAMS) for determining ganciclovir levels in capillary blood using the LC-MS/MS technique in pediatric renal transplant recipients — Kocur et al., European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences (paywalled)
- vams
- volumetric
- blood
- qdbs
- tdm
- dried
- antimicrobials
- capillary
- pediatric
- validation
2025
The study found that dried blood spot sampling showed good agreement with plasma concentrations for vancomycin and creatinine, with most differences within 20%, and patients preferred the finger prick method over venepuncture, supporting its use for decentralised therapeutic drug monitoring.
Clinical validation of an innovative dried whole-blood spot method to quantify simultaneously vancomycin and creatinine in adult patients — Hassanzai et al., The Journal of antimicrobial chemotherapy
- blood
- dried
- dbs
- self-collection
- validation
- venous-agreement
- acceptability
- tdm
- antimicrobials
2025
VAMS finger-prick sampling showed moderate agreement with conventional venous sampling for clofazimine, with a systematic 13% lower concentration that can be corrected, and was more cost-effective by about 4.45 USD per sample, supporting its use for routine therapeutic drug monitoring in MDR-TB.
Analytical and clinical validation of a volumetric absorptive microsampling (VAMS) - Ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the analysis of Clofazimine in whole blood — Nugraha et al., Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- venous-agreement
- tdm
- antimicrobials
- economics
2025
Capillary volumetric absorptive microsampling showed significant differences in absolute antibiotic concentrations compared to venous plasma, yet it reliably tracked the pharmacokinetic profiles of amoxicillin, metronidazole, and azithromycin over time. The approach was well accepted by both participants and clinicians, indicating its feasibility for less invasive therapeutic drug monitoring in periodontal clinical trials.
A comparison between venous blood sampling and capillary volumetric absorptive microsampling for antibiotics levels monitoring in individuals with and without periodontal disease — Lazaridi et al., Clinical oral investigations
- blood
- dried
- capillary
- vams
- neoteryx-mitra
- venous-agreement
- acceptability
- tdm
- antimicrobials
2024
The authors validated a VAMS method for ivermectin therapeutic drug monitoring in whole blood, achieving a lower limit of quantification of 1 ng/mL and a linear range of 1–150 ng/mL. By eliminating haematocrit effects that limit dried blood spots, the method supports accurate decentralised sampling for antiparasitic therapy.
Development and validation of ivermectin quantification method in volumetric absorptive microsampling using liquid chromatography-tandem mass spectrometry — Harahap et al., Heliyon
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
- antimicrobials
2024
The authors validated a UPLC-PDA assay for ceftazidime in 10 microlitre dried blood spots collected with the Capitainer device from neonatal patients, achieving accuracy of 90.1 to 104.8 per cent and precision within 11.7 per cent coefficient of variation across a quantification range of 0.5 to 200 micrograms per millilitre, and confirmed the method worked on clinical neonatal samples. This supports microsampling-based therapeutic drug monitoring of an antimicrobial in a vulnerable population where conventional venous blood draws are difficult.
Development and validation of a UPLC-PDA method for quantifying ceftazidime in dried blood spots — Lv et al., Journal of pharmaceutical and biomedical analysis (paywalled)
- blood
- dried
- capillary
- dbs
- validation
- pediatric
- tdm
- antimicrobials
2024
A community survey of 1699 Tanzanian children using dried blood spots found 17.4% had residual antibiotics, with half of those exposed having no reported use, showing microsampling can reveal hidden antibiotic exposure for stewardship programmes.
Prevalence and predictors of residual antibiotics in children's blood in community settings in Tanzania — Lotto et al., Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases (paywalled)
- blood
- dried
- dbs
- pediatric
- antimicrobials
2024
The study developed and validated LC-MS/MS methods for ganciclovir in serum, dried serum spots, and VAMS-Mitra devices. In 80 pediatric renal transplant recipients, VAMS showed interchangeability with serum samples while extending stability to at least 49 days at room temperature, making decentralised therapeutic drug monitoring more feasible for transplant patients.
Assessment of Dried Serum Spots (DSS) and Volumetric-Absorptive Microsampling (VAMS) Techniques in Therapeutic Drug Monitoring of (Val)Ganciclovir-Comparative Study in Analytical and Clinical Practice — Kocur et al., International journal of molecular sciences
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
- antimicrobials
2024
A validated LC-MS method quantified multiple antibiotics from a single volumetric absorptive microsample, with stability up to 90 days for most analytes and minimal haematocrit effect except vancomycin, enabling pharmacokinetic and pharmacodynamic studies in decentralised settings.
Bioanalysis of six antibiotics from volumetric microsamples: a new tool for precision dosing in critically ill children — Takyi-Williams et al., Bioanalysis (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- pediatric
- tdm
- antimicrobials
- haematocrit
2024
A validated high-throughput LC-MS/MS assay for piperaquine from dried blood spots achieved 54-72% recovery with <9% relative standard deviation and a quantification limit of 3 ng/mL, enabling detection for 4-8 weeks post-dose. The method showed minimal haematocrit interference and is suitable for therapeutic drug monitoring of antimalarial treatment in resource-limited settings and pediatric populations.
A high-throughput LC-MS/MS assay for piperaquine from dried blood spots: Improving malaria treatment in resource-limited settings — Blessborn et al., Journal of mass spectrometry and advances in the clinical lab
- blood
- dried
- capillary
- dbs
- validation
- tdm
- antimicrobials
- haematocrit
2024
The authors validated a dried blood spot method for simultaneous measurement of vancomycin and creatinine with a 5.2-minute run time, demonstrating linear ranges suitable for therapeutic drug monitoring. This supports home-based sampling to reduce the burden of clinic visits for patients requiring vancomycin monitoring.
Dried blood spot analysis for the quantification of vancomycin and creatinine using liquid chromatography - tandem mass spectrometry: Method development and validation — Bahmany et al., Clinica chimica acta; international journal of clinical chemistry (paywalled)
- blood
- dried
- dbs
- validation
- tdm
- antimicrobials
2023
In children, VAMS and dried plasma spot voriconazole, posaconazole and isavuconazole correlated with fresh plasma, Spearman 0.82–0.94, and stayed stable at room temperature for at least 14 days: refrigeration-free antifungal TDM in paediatrics.
VAMS and dried plasma spot for antifungal triazole agents (voriconazole, posaconazole, isavuconazole) in pediatric patients by LC-MS/MS — Simeoli et al., J. Pharmaceutical and Biomedical Analysis (paywalled)
- vams
- neoteryx-mitra
- blood
- tdm
- dried
- antimicrobials
- pediatric
2023
Volumetric absorptive microsampling of whole blood did not provide a reliable basis for calculating meropenem plasma concentrations in critically ill children, so a validated low volume plasma method was required for paediatric therapeutic drug monitoring.
Developing a Method for Quantifying Meropenem in Children-Volumetric Adsorptive Microsampling Versus Plasma Sampling — Ramadan et al., Therapeutic drug monitoring (paywalled)
- blood
- dried
- vams
- neoteryx-mitra
- validation
- venous-agreement
- pediatric
- tdm
- antimicrobials
2023
The study developed and validated an HPLC-DAD method for quantifying favipiravir in whole blood collected via VAMS, meeting FDA 2018 guidelines with a lower limit of quantification of 0.5 micrograms per millilitre. This supports the use of VAMS for therapeutic drug monitoring of favipiravir in decentralised settings.
HPLC-DAD quantification of favipiravir in whole blood after extraction from volumetric absorptive microsampling devices — Azzahra Rahmadhani et al., Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
- blood
- dried
- vams
- neoteryx-mitra
- validation
- tdm
- antimicrobials
2023
Researchers developed and validated a UHPLC-MS/MS method for simultaneous quantification of favipiravir and remdesivir from VAMS blood samples, meeting FDA and EMA validation criteria. The method uses simple protein precipitation and supports therapeutic drug monitoring of COVID-19 antivirals in settings where small sample volumes and simplified processing are advantageous.
Development and validation of method for analysis of favipiravir and remdesivir in volumetric absorptive microsampling with ultra high-performance liquid chromatography-tandem mass spectrophotometry — Harahap et al., Frontiers in medicine
- blood
- dried
- vams
- validation
- tdm
- antimicrobials
2023
The study developed and validated a UHPLC-MS/MS method to measure eight antibiotics in quantitative dried blood spots collected from neonates using a capillary microsampling device. This patient-centric approach enables robust pharmacokinetic monitoring in children where blood volume is limited, supporting decentralised therapeutic drug monitoring.
A Validated UHPLC-MS/MS Method to Quantify Eight Antibiotics in Quantitative Dried Blood Spots in Support of Pharmacokinetic Studies in Neonates — Liu et al., Antibiotics
- blood
- dried
- qdbs
- validation
- pediatric
- tdm
- antimicrobials
2021
The honest counterpoint in children: VAMS predicted plasma vancomycin only modestly, venous/arterial VAMS was more accurate than capillary, and 29% of capillary samples were unusable for collection issues: collection technique and training matter as much as the assay.
Comparison of antibiotic sampling techniques: predicting plasma vancomycin from VAMS capillary versus venous/arterial whole blood — Downes et al., Open Forum Infect. Dis.
- vams
- blood
- tdm
- haematocrit
- dried
- antimicrobials
- capillary
- pediatric
- validation
2021
This review summarises liquid chromatography with tandem mass spectrometry assays using dried blood spots and volumetric absorptive microsampling for quantifying antimicrobial drugs in children, highlighting that VAMS reduces haematocrit bias and offers a viable alternative to traditional plasma sampling for therapeutic drug monitoring.
Microsampling Assays for Pharmacokinetic Analysis and Therapeutic Drug Monitoring of Antimicrobial Drugs in Children: A Critical Review — Moorthy et al., Therapeutic drug monitoring (paywalled)
- blood
- dried
- vams
- dbs
- neoteryx-mitra
- validation
- pediatric
- tdm
- antimicrobials
- haematocrit
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
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
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
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
2018
The study found substantial agreement between serum tobramycin and vancomycin concentrations collected from existing peripheral or central venous catheters and those obtained by venipuncture or fingerstick in pediatric patients. This suggests that using a strict flush and waste protocol allows for therapeutic drug monitoring without additional painful needle sticks, thereby improving patient satisfaction.
Therapeutic antibiotic serum concentrations by two blood collection methods within the pediatric patient: A comparative effectiveness trial — Lichliter et al., Journal for specialists in pediatric nursing : JSPN (paywalled)
- blood
- liquid
- capillary
- venous-agreement
- pediatric
- tdm
- antimicrobials
2018
The authors validated a dried blood spot assay for benznidazole that showed strong agreement with plasma concentrations (r²=0.8295) and proved stable at room temperature for more than one year. This microsampling approach enables therapeutic drug monitoring for Chagas disease in decentralised trials and remote settings, including paediatric populations.
Dried Blood Spot Technique-Based Liquid Chromatography-Tandem Mass Spectrometry Method as a Simple Alternative for Benznidazole Pharmacokinetic Assessment — Galindo Bedor et al., Antimicrobial agents and chemotherapy
- blood
- dried
- dbs
- validation
- venous-agreement
- tdm
- antimicrobials
- haematocrit
2016
Miltefosine concentrations measured in dried blood spots showed excellent agreement with plasma (median ratio 0.99, Pearson's r=0.946) in patients with visceral leishmaniasis. The method demonstrated 97% extraction recovery, remained stable for 162 days at 37°C, and performed reliably across haematocrit levels of 20–35%, offering a valid and practical alternative to venous sampling for therapeutic drug monitoring in decentralised settings.
Validation and Clinical Evaluation of a Novel Method To Measure Miltefosine in Leishmaniasis Patients Using Dried Blood Spot Sample Collection — Kip et al., Antimicrobial agents and chemotherapy
- blood
- dried
- dbs
- validation
- venous-agreement
- tdm
- antimicrobials
- haematocrit
2016
The validation of a dried blood spot assay for ceftriaxone achieved a limit of quantification of 0.14 mg/L with strong correlation between DBS-predicted and measured plasma concentrations (r=0.95). The method showed acceptable thermal stability, retaining over 95% of initial concentrations for periods ranging from 14 hours to 11 months. This supports the use of self-collected DBS samples for therapeutic drug monitoring of antimicrobials in remote and resource-poor settings.
Validation and Application of a Dried Blood Spot Ceftriaxone Assay — Page-Sharp et al., Antimicrobial agents and chemotherapy (paywalled)
- blood
- dried
- dbs
- validation
- venous-agreement
- tdm
- antimicrobials
- haematocrit
2014
Parsons et al. validated a quantitative dried blood spot assay for rifapentine that remained stable for 11 weeks at ambient temperature and showed good agreement with plasma concentrations after haematocrit correction, offering a low-volume sampling approach suitable for therapeutic drug monitoring in international and paediatric tuberculosis trials.
Quantification of rifapentine, a potent antituberculosis drug, from dried blood spot samples using liquid chromatographic-tandem mass spectrometric analysis — Parsons et al., Antimicrobial agents and chemotherapy (paywalled)
- blood
- dried
- dbs
- validation
- venous-agreement
- tdm
- antimicrobials
- haematocrit
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