Pesticides and biocides are widely used in agriculture, building materials, and urban gardening to control pests and protect crops and public health. While much attention has been paid to pesticide residues in food, water, and outdoor environments, far less is known about their presence inside homes, where people spend the majority of their time. A new RECETOX study published in Indoor Environments addresses this gap by examining pesticides detected in house dust and their relevance for human exposure.&nbsp;The study reveals that Czech household dust commonly contains multiple pesticide residues, highlighting the persistence of both historic and current chemical use indoors. Modern pesticides were detected in 93% of homes, with two fungicides (carbendazim and propiconazole) most frequently found, while compounds related to the long‑banned pesticide DDT were present in dust from all homes, and were at higher levels in homes over 40 years old. Homes located closer to agricultural areas showed higher levels of current‑use pesticides in spring, indicating an influence of nearby farming activities. &nbsp;House dust acts as a sink for chemicals transported indoors from outdoor sources as well as from indoor use. Many pesticides can persist in dust for long periods, leading to continuous exposure in indoor spaces. This is particularly important for young children, who have higher exposure to dust from playing on the floor and mouthing toys and objects. The research underscores that indoor environments are not isolated from their surroundings. Understanding what ends up in house dust is a crucial step toward protecting public health and developing more comprehensive approaches to managing chemical risks in everyday life.&nbsp;<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/RECETOX_Vyzkum_pesticidu_v_domacim_prachu_opomijena_cesta_lidske_expozice_a9a089fd2f.jpg" alt="RECETOX: Pesticides in House Dust: An Overlooked Pathway of Human Exposure" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_RECETOX_Vyzkum_pesticidu_v_domacim_prachu_opomijena_cesta_lidske_expozice_a9a089fd2f.jpg 195w," sizes="100vw" width="738" height="591"><blockquote><h4>Original Article</h4><h4><a target="_blank" rel="noopener noreferrer" href="https://www.sciencedirect.com/science/article/pii/S2950362026000214?via%3Dihub">Legacy and current-use pesticides in indoor settled dust and association with building age and seasonality</a></h4>Paula Marcinekova, Ondřej Mikeš, Simona Rozárka Jílková, Petr Šenk, Jakub Martiník, Jan Böhm, Petra Borilova Linhartova, Lenka Andrýsková, Jana Klánová, Lisa MelymukIndoor Environ., 2026, 3, 100169<a target="_blank" rel="noopener noreferrer" href="https://doi.org/10.1016/j.indenv.2026.100169">https://doi.org/10.1016/j.indenv.2026.100169</a>&nbsp;<h6>licensed under <a target="_blank" rel="noopener noreferrer" href="https://creativecommons.org/licenses/by/4.0/">CC-BY 4.0</a></h6></blockquote><h4>Abstract</h4>Indoor pesticide exposure is increasingly recognized as a significant contributor to pollutant exposure in residential spaces. This study investigates concentrations of legacy organochlorine pesticides (OCPs) and current-use pesticides (CUPs) in settled dust from 116 homes in the Czech Republic, in the context of their seasonal variability, relationships with building characteristics, geospatial factors, and indoor dust bacteriome diversity and composition. CUPs were detected in dust in 93% of homes, with carbendazim (84.5%), propiconazole (49.1%), atrazine (24.1%), and tebuconazole (11.2%) detected most frequently. OCPs were found in all homes. Propiconazole concentrations were significantly higher in homes with adjacent gardens, potentially reflecting its use as a biocide in outdoor building materials. CUP concentrations had clear seasonal trends, with peak levels in spring and summer, corresponding to pesticide application periods, particularly in rural environments. OCP concentrations were substantially higher in houses over 40 years old, indicating the persistence of residues from past indoor uses. While pesticide presence was ubiquitous, exposure estimates for children, under both average and high-exposure scenarios, were well below U.S. EPA reference doses (RfDs) for individual compounds; however, most homes had 3–11 pesticides in dust, raising the possibility of mixture effects. No significant associations, using a Spearman rank correlation matrix, were observed between pesticide concentrations and indoor dust bacteriome diversity and composition. These findings highlight the presence of pesticides in homes, including those in urban areas, driven by both current and historical sources, and reinforce the importance of monitoring to better understand potential exposure pathways.<h4>Instrumentation</h4><h5>1. LC–MS/MS analysis of CUPs</h5><ul><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library?instrumentationItems=27&amp;mainauthorItems=10&amp;search=1290+Series+Gradient">Agilent 1290 Series Gradient HPLC</a></li><li>Columns:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/1701">Phenomenex Luna C18</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library?instrumentationItems=34&amp;mainauthorItems=50&amp;search=SecurityGuard+C18">Phenomenex SecurityGuard C18</a></li></ul></li><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library?mainauthorItems=55&amp;search=QTrap+5500%2B">SCIEX QTrap 5500+</a> (triple quadrupole MS, ESI+)</li></ul><h5>2. GC–MS/MS analysis of OCPs</h5><ul><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?instrumentationItems=1&amp;mainauthorItems=10&amp;search=8890A">Agilent 8890A GC</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?instrumentationItems=19&amp;mainauthorItems=7&amp;search=Rxi-5Sil-MS">Restek Rxi-5Sil-MS capillary column</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?mainauthorItems=10&amp;search=7000D">Agilent 7000D triple quadrupole MS</a></li></ul>

Pesticides in House Dust: An Overlooked Pathway of Human Exposure

This technical note presents a practical troubleshooting strategy for one of the most common issues in liquid chromatography (LC): shifting retention times. The approach is based on a systematic distinction between system-related (physical) and chromatographic (chemical) causes.A key diagnostic parameter used throughout the process is the T₀ (dead time), representing an unretained peak that passes through the column without interaction.<h3>Key Concept: T₀ (Dead Time / Unretained Peak)</h3>T₀ is defined as the retention time of a compound that does not interact with the stationary phase and therefore elutes directly with the mobile phase.<h4>How to Determine T₀</h4>T₀ can be determined experimentally by adding a marker compound to the system:<ul><li>Uracil</li><li>Potassium nitrate</li></ul>These compounds are added to a blank or method and produce a measurable unretained peak used for troubleshooting.<h3>Step 1: Evaluate T₀ Behavior</h3>The first and most important step is to determine whether T₀ is constant or variable.<ul><li>Case A: T₀ is Variable (Shifting) → Indicates a system-related (physical) problem &nbsp;</li><li>Case B: T₀ is Constant → Indicates a chromatographic or chemical problem</li></ul><h3>System-Related Issues (T₀ is Variable)</h3>If T₀ is shifting, the problem is likely related to the LC system hardware or physical parameters. This is especially true when all peaks shift together in the chromatogram.<h3>Possible Causes</h3><ul><li>Incorrect Flow Rate</li><li>Pump Malfunction<ul><li>Inconsistent or unstable flow delivery can cause retention time variability.</li></ul></li><li>Incorrect Column Length<ul><li>Using a column with different dimensions than expected.</li></ul></li><li>Solvent Delivery Issues<ul><li>Empty solvent reservoir (system running dry)</li><li>Blockages or restrictions (e.g., frits, solvent lines)</li></ul></li><li>Tubing or System Volume Changes<ul><li>Changes in tubing configuration</li><li>Differences in system dwell (swell) volume</li></ul></li></ul><h3>Chromatographic / Chemical Issues (T₀ is Constant)</h3>If T₀ remains stable but only specific peaks shift, the issue is likely related to chemistry or column conditions.<h4>Possible Causes</h4><ul><li>Incorrect Stationary Phase<ul><li>Column with same dimensions but different chemistry (e.g., different silica or bonded phase)</li></ul></li><li>Ionizable Analytes Ionizable compounds exist in:<ul><li>Neutral form - More hydrophobic, retained longer on a reversed-phase column</li><li>Ionized form</li></ul>Impact of pH Small pH changes in the mobile phase can significantly affect:<ul><li>Ionization state</li><li>Retention time of specific analytes</li></ul></li><li>Mobile Phase Issues<ul><li>Old solvents</li><li>Evaporation of volatile components</li><li>Changes in composition</li></ul></li><li>4. Temperature Variations<ul><li>Temperature affects analyte–stationary phase interactions</li><li>Even small fluctuations can shift retention times</li></ul></li></ul><h3>Step-by-Step Troubleshooting Workflow</h3><ol><li>Add T₀ Marker<ol><li>Use uracil or potassium nitrate</li></ol></li><li>Monitor T₀<ol><li>Determine whether it is constant or shifting</li></ol></li><li>If T₀ is Variable → Check System<ol><li>Flow rate settings</li><li>Pump performance</li><li>Solvent levels and lines</li><li>Column dimensions</li><li>Tubing and system volume</li></ol></li><li>If T₀ is Constant → Check Chemistry<ol><li>Column phase</li><li>Mobile phase composition and pH</li><li>Solvent quality</li><li>Temperature stability</li><li>Nature of analytes (ionizable vs. non-ionizable)</li></ol></li></ol><h3>Discussion and Practical Insight</h3>This troubleshooting approach simplifies a complex problem by dividing it into two main categories:<ul><li>Physical/system-related</li><li>Chemical/chromatographic</li></ul>The use of T₀ as a diagnostic tool allows rapid identification of the problem origin, reducing unnecessary trial-and-error steps.Particular attention should be paid to ionizable compounds, as they are highly sensitive to pH variations, which can lead to significant and selective retention time shifts.<h3>Conclusion</h3>Retention time shifts in LC can be efficiently diagnosed by evaluating the behavior of the T₀ (unretained peak):<ul><li>Variable T₀ → System issue</li><li>Constant T₀ → Chromatographic/chemical issue</li></ul>By following this structured approach, analysts can quickly narrow down the root cause and implement targeted corrective actions.

Troubleshooting Retention Time Shifts in Liquid Chromatography 

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RECETOX (Research Centre for Toxic Compounds in the Environment) is an independent department of the Faculty of Science of Masaryk University in Brno, which has been established in 1983. RECETOX is focused on the research and education in cross-cutting area of Environment and Health. It addresses interactions among chemicals, environment, and biological systems, including consequences at local, regional, and global levels.

RECETOX - Centrum pro výzkum toxických látek v prostředí

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ARC Solvere Universal HPLC Detector

The Solvere™ is a new LC detector that brings the benefits of the Flame Ionization Detector (FID) to LC. 
Using ARC’s expertise in catalysis and reactor design, a novel method was developed for removing volatile compounds, which allows for the use of both aqueous and organic solvents with the detector. 
Non-volatile components in the sample stream are transformed into the gas phase, converted to methane, and then detected by the FID with a linear range of five orders of magnitude.
ARC Solvere is designed for quantitation of compounds where GC ends with a range up to large 1M+ Da molecules. In addition, Solvere works with a myriad of mobile phases, additives, and gradients, with unprecedented linear range, uniformity and robustness.
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Koncept_detekce_pomoci_HPLC_FID_detektoru_Solvere_1090d61827/ARC-Koncept-detekce-pomoci-HPLC-FID-detektoru-Solvere.jpg" alt="ARC: The concept of HPLC - FID detector Solvere"/>
<h3>Why is it important?</h3>
<ul>
<li>Mobile phases are effectively separated from non-volatile analytes</li>
<li>Analytes are converted into methane for universal FID detection</li>
<li>Compatible with gradients and organic solvents</li>
<li>A variety of molecules such as proteins, peptides, and sugars give a universal carbon response</li>
</ul>
<blockquote>
FOR USE WITH ANY LC MODEL
</blockquote>
<h3>Benefits of the Solvere</h3>
<ul>
<li>Analyte response independent of mobile phase composition</li>
<li>Conversion of analytes to methane for universal FID response</li>
<li>5 orders of magnitude range</li>
<li>~10 ppm LOD</li>
<li>Standalone and automated</li>
</ul>
<h3>Solvere - Universal FID for HPLC</h3>
<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ARC_Ukazka_detekce_Sacharozy_pomoci_Solvere_detektoru_pro_HPLC_21106ae2ae/ARC-Ukazka-detekce-Sacharozy-pomoci-Solvere-detektoru-pro-HPLC.jpg" alt="ARC: Example of Sacharose Analysis Using Solvere Detector for HPLC"/>

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Troubleshooting Retention Time Shifts in Liquid Chromatography

Pesticides in House Dust: An Overlooked Pathway of Human Exposure

News from LabRulezLCMS Library - Week 18, 2026