<p><strong>Taťána Gazárková is currently a&nbsp;postdoctoral fellow in the Laboratory of Antibiotic Resistance and Microbial Metabolomics. During her doctoral studies, she focused on chromatography and mass spectrometry. Recently, she was awarded second place in the “Sanofi Prize for Pharmacy 2026” competition.</strong></p><p><strong>Taťána Gazárková </strong>is currently a&nbsp;postdoctoral fellow in the <strong>Laboratory of Antibiotic Resistance and Microbial Metabolomics</strong>. During her doctoral studies, she focused on chromatography and mass spectrometry. Recently, she was awarded second place in the <strong>“Sanofi Prize for Pharmacy 2026” </strong>competition, which is awarded by the<strong> French Embassy in the Czech Republic</strong> for her dissertation – Steroid Analysis Using Modern Chromatographic and Mass Spectrometry Techniques: From Fundamental Studies to Targeted Bioanalytical Applications (supervisor: <strong>Lucie Nováková, Charles University</strong>).&nbsp;</p><h5><strong>What makes this field particularly exciting or unique in your view?</strong></h5><p>What I&nbsp;enjoy about analytical chemistry is that, to a&nbsp;certain extent, it is a&nbsp;kind of detective work. You are often looking for ways to “make the invisible visible”. In other words, extract the information you are interested in from a&nbsp;complex sample and then interpret it correctly. What also appeals to me about bioanalytical chemistry is its interdisciplinary nature. It brings together analytical chemistry, biochemistry, biology and medicine, which means that you need to be able not only to translate a&nbsp;biological or clinical question into a&nbsp;measurable analytical experiment, but also to place the resulting data back into a&nbsp;broader biological context. This combination of different perspectives is probably what I&nbsp;enjoy most about the field. At the same time, there is still plenty of room for fundamental research, ranging from studying analytical techniques themselves and improving them to developing new methodological approaches.</p><h5><strong>How did you end up at the </strong><a target="_blank" rel="noopener noreferrer" href="https://mbu.cas.cz/en/research/laboratory-of-antibiotic-resistance-and-microbial-metabolomics"><strong>Laboratory of Antibiotic Resistance and Microbial Metabolomics</strong></a><strong>, and what project are you currently working on?</strong></h5><p>I came to the Institute of Microbiology through a&nbsp;joint project between<strong> Dr Zdeněk Kameník and Assoc. Prof. Jan Bobek from the First Faculty of Medicine, Charles University</strong>. For me, it was also an opportunity to move from targeted analysis and the study of chromatographic techniques towards untargeted metabolomics and new biological questions.</p><p>In the project, we are trying to identify new biologically active compounds that would be effective, particularly against pathogenic fungi. As a&nbsp;potential source of such compounds, we study streptomycetes, bacteria known for their ability to produce a&nbsp;wide range of biologically active compounds, including many antibiotics that are currently in clinical use. We focus on less-explored host-associated streptomycetes, in which we had already observed antifungal activity in previous experiments. We are especially interested in strains active against Candida albicans whose activity cannot be explained by the presence of a&nbsp;known bioactive compound. These strains may represent an interesting source of novel compounds. We then integrate the results of untargeted metabolomic analyses with genomic analyses, which allows us to obtain a&nbsp;more comprehensive view of the biosynthetic potential of selected strains.</p><h5><strong>You also took part in this year’s Vědafest, a&nbsp;science outreach event for the public. What was it like?</strong></h5><p>I already had some experience with science outreach through events such as Researchers’ Night and the Science Fair at my previous institution, but this year’s Vědafest was still new to me in some ways. This time, I&nbsp;was presenting a&nbsp;field that I&nbsp;myself had entered only relatively recently. It was therefore more challenging to find the right analogies and explain the essence of the topic in a&nbsp;way that was simple, yet precise and scientifically accurate. At the same time, that was exactly what made it inspiring. It forces you to look at your own work from a&nbsp;different perspective. What I&nbsp;enjoyed most was the spontaneity and curiosity of the children, who often came up with questions that would never even occur to an adult.</p><h5><strong>What are the biggest challenges you face on your scientific journey, and what helps you overcome them?</strong></h5><p>One of the greatest, but at the same time most interesting, challenges is, in my view, the uncertainty that is inseparably linked to research. For a&nbsp;long time, you often do not know whether you have taken the right direction in addressing a&nbsp;particular question or whether you will ultimately manage to find that figurative final piece of the puzzle. At the same time, this uncertainty is precisely what makes science exciting for me.</p><p>Another major challenge, particularly in interdisciplinary projects, is communication. It is important from the very formulation of a&nbsp;hypothesis and the planning of experiments through to the interpretation of results, including negative ones, and placing them in a&nbsp;broader context. To some extent, every field has its own language, and finding a&nbsp;common understanding is not always straightforward. Personally, I&nbsp;find it very helpful to be able to discuss problems with colleagues on an ongoing basis, whether individually or during regular laboratory seminars. One of the major strengths of our current group is its interdisciplinary nature, which allows me to look at the same problem from several different perspectives. It is also important for me not to lose my curiosity, because that is ultimately what leads us to ask further questions.</p><h5><strong>What are your plans after completing your PhD?</strong></h5><p>After finishing my PhD, I&nbsp;decided that I&nbsp;do not need to have everything that comes next precisely mapped out straight away. I&nbsp;would like to keep different options open for a&nbsp;while and continue building on my experience in analytical chemistry, while at the same time connecting it with other areas that have a&nbsp;biological or medical relevance. I&nbsp;believe that we can keep learning throughout our lives, so I&nbsp;am quite curious to see where the next stage of my journey will take me.</p><p><i>Thank you for the interview!</i></p>

Interview: What Drew Postdoc Taťána Gazárková to Analytical Chemistry

<p><strong>Per- and polyfluoroalkyl substances (PFAS) have earned the moniker "forever chemicals" due to their extreme persistence in the environment. Their detection is crucial for protecting public health and the environment as these synthetic compounds continue to pose significant challenges worldwide. This comprehensive exploration examines why PFAS detection matters, current detection methods, and future directions in addressing PFAS contamination.</strong></p><h3><strong>Understanding PFAS and Their Health Impacts</strong></h3><p>PFAS are a class of synthetic organic compounds with diverse structures, properties, and uses. Despite their diversity, all PFAS contain perfluoroalkyl moieties that are extremely resistant to environmental and metabolic degradation [1]. This high persistence is a defining characteristic that makes PFAS management particularly challenging.</p><h3><strong>Documented Health Effects</strong></h3><p>Current scientific research has linked PFAS exposure to numerous adverse health outcomes:</p><ul><li>Reproductive effects including decreased fertility and increased high blood pressure in pregnant women [8]</li><li>Developmental effects in children such as low birth weight, accelerated puberty, and behavioral changes [8]</li><li>Reduced immune system function, including decreased vaccine response</li><li>Interference with natural hormones and endocrine disruption</li><li>Increased cholesterol levels and obesity risk</li><li>Increased risk of several cancers, including prostate, kidney, testicular, oral cavity/pharynx, brain, and endocrine cancers [3]</li></ul><p>A 2023 study linked PFAS-contaminated water with up to a <strong>33% increase in cancer incidence</strong> in affected areas [3]. The study compared regions with elevated PFAS levels to cancer data from the National Cancer Institute, finding higher incidences of various cancers after controlling for factors like smoking and obesity.</p><h3><strong>Environmental Persistence and Contamination</strong></h3><p>The extreme persistence of PFAS represents a fundamental concern for environmental management. PFAS are considered the most environmentally persistent substances among organic chemicals [7]. This persistence means that even if all PFAS uses were immediately phased out, existing contamination would continue to affect ecosystems and water supplies for generations.</p><p>A 2023 study at a military fire training site estimated that PFAS contamination will persist for centuries without remediation [7]. The research found that terminal PFAS still exceed regulatory limits by 2000-fold decades after aqueous film-forming foam (AFFF) use ceased, with precursors accounting for around half of the extractable organofluorine across years.</p><h3><strong>Current Detection Methods</strong></h3><h4><strong>EPA Standardized Methods</strong></h4><p>The<strong> Environmental Protection Agency (EPA</strong>) has developed several standardized methods for PFAS detection, each with specific applications and capabilities:</p><h5><strong>EPA Method 533</strong></h5><p><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/epa-533-drying-down-pfas-samples-after-spe"><strong>EPA Method 533</strong></a> focuses on "short chain" PFAS with carbon chain lengths of<strong> C4 to C12</strong>. Released in December 2019, this method complements Method 537.1 and includes several key features:</p><ul><li>Uses isotope dilution quantification approach with extracted internal standards, which reduces overall analytical uncertainty</li><li>Employs weak anion exchange solid phase extraction cartridges as opposed to polystyrene divinylbenzene used in 537.1</li><li>Can analyze 25 PFAS compounds, including additional short-chain PFAS that were not apart of Method 537.1</li><li>Allows for longer holding times: 28 days to extraction and 28 days to analyze (compared to 14 days to extraction in Method 537.1)</li><li>Uses ammonium acetate as a preservative (versus Trisma in Method 537.1) [1]</li></ul><h5><strong>EPA Method 537/537.1</strong></h5><p><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/sample-concentration-epa-method-537-pfas-determination"><strong>EPA Method 537 </strong></a>was first published in 2009 for the determination of 14 PFAS in drinking water [6]. It was later updated to Method 537.1 in 2018 (with editorial updates in 2020) to expand its capabilities:</p><ul><li>Uses<a target="_blank" rel="noopener noreferrer" href="https://www.organomation.com/what-is-solid-phase-extraction-spe"><strong> solid phase extraction (SPE) </strong></a>and<a target="_blank" rel="noopener noreferrer" href="https://www.organomation.com/preparing-samples-for-lc-ms/ms-analysis"><strong> liquid chromatography/tandem mass spectrometry (LC-MS/MS)</strong></a></li><li>Method 537.1 expanded detection to 18 PFAS compounds, including HFPO-DA (one component of GenX technology)</li><li>Utilizes styrene-divinylbenzene (SDVB) media for extraction</li><li>Requires samples to be extracted within 14 days and analyzed within 28 days</li><li>Methanol is used to elute the extracts. This should then be reconstituted with a 96:4 methanol:water mixture [1]</li></ul><p>Together, Methods 533 and 537.1 can detect a total of <strong>29 unique PFAS compounds in drinking water </strong>and are approved for monitoring under the fifth Unregulated Contaminant Monitoring Rule (UCMR 5) and the PFAS National Primary Drinking Water Regulation [1] [3].</p><h5><strong>EPA Method 1633</strong></h5><p><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/preparing-diverse-sample-matrices-for-epa-method-1633"><strong>EPA Method 1633</strong></a>, released in 2024, represents a significant advancement in PFAS analysis:</p><ul><li>Developed for the analysis of <strong>40 PFAS compounds </strong>in various matrices, including surface water, groundwater, wastewater, soil, biosolids, sediment, landfill leachate, and fish tissue</li><li>Expands beyond the drinking water focus of Methods 533 and 537.1</li><li>Provides a standardized approach that may replace modified drinking water methods (i.e., modified EPA 537) that were previously used for non-drinking water matrices [1]</li></ul><h4><strong>Conventional Analytical Techniques</strong></h4><p>The gold standard for PFAS analysis involves chromatographic techniques coupled with mass spectrometry:</p><ul><li>Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) is the most widely used method for PFAS analysis, offering high sensitivity and specificity [1]</li><li>High-Resolution Mass Spectrometry (HRMS) allows for rapid detection and identification of PFAS species at very low concentrations [5]</li></ul><p>These techniques can detect PFAS at parts per trillion (ppt) levels, which is essential given the low concentrations at which PFAS can cause health effects [1]. However, these methods require sophisticated equipment, specialized training, and significant financial resources, making them inaccessible in many regions, particularly in developing countries.</p><h4><strong>Emerging Detection Technologies</strong></h4><p>Several innovative approaches are being developed to address the limitations of conventional methods:</p><ul><li>Electrochemical biosensors using modified electrodes have shown promise for selective PFAS detection with low detection limits [2]</li><li>Surface-Enhanced Raman Spectroscopy (SERS) uses metallic nanoparticles and can be made into a portable method for on-site testing [1]</li><li>Molecular imprinted polymers (MIPs) offer thermal and physical stability, reusability, and low-cost synthesis for PFAS detection [6]</li></ul><p>These emerging technologies aim to provide more accessible, field-deployable, and cost-effective alternatives to traditional laboratory-based methods.</p><h3><strong>Challenges in PFAS Detection</strong></h3><h4><strong>Analytical Challenges</strong></h4><p>Detecting PFAS presents several technical challenges:</p><ul><li>The ubiquity of PFAS in laboratory equipment and accessories can lead to background contamination when measuring at parts-per-trillion levels [1]</li><li>Many components in liquid chromatographs, mass spectrometers, and solid-phase extraction systems contain materials that can leach PFAS compounds [9]</li><li>The vast number of PFAS (thousands of compounds) makes comprehensive detection difficult, as analytical standards are only available for a small subset [1]</li><li>Complex matrices like food and environmental samples require sophisticated sample preparation techniques</li></ul><h4><strong>Global Disparities in Detection Capabilities</strong></h4><p>Access to PFAS detection technology varies significantly worldwide:</p><ul><li>Many developing regions, particularly in Africa, lack adequately equipped laboratories with the necessary instrumentation to detect and measure PFAS</li><li>There is often a scarcity of qualified professionals with experience in PFAS analysis in these regions</li><li>The high cost of acquiring and maintaining sophisticated analytical instruments presents a substantial obstacle to conducting extensive PFAS investigations in resource-limited settings [1]</li><li>Competing priorities such as infectious diseases, poverty, and food security often divert attention and resources from environmental pollutants like PFAS</li></ul><h4><strong>Regulatory Landscape and Compliance</strong></h4><p>The regulatory framework for PFAS is evolving rapidly worldwide:</p><ul><li>The EPA finalized Section 8(a)(7) of the Toxic Substances Control Act in September 2024, requiring manufacturers and importers to report on their use of PFAS since 2011 [10]</li><li>Electronic reporting for PFAS will open on July 11, 2025, with final reporting deadlines in 2026</li><li>Companies must report detailed information including chemical identity, production volumes, industrial and consumer products, worker exposure, and disposal methods [10]</li></ul><p>These regulations are driving demand for more effective and accessible PFAS detection methods to ensure compliance and protect public health.</p><h3><strong>Future Directions in PFAS Detection</strong></h3><h4><strong>Technological Advancements</strong></h4><p>The future of PFAS detection lies in developing more accessible, sensitive, and comprehensive methods:</p><ul><li>Non-targeted screening methods that can identify unknown PFAS compounds without requiring analytical standards for each specific compound</li><li>Total fluorine analysis techniques like Adsorbable Organic Fluorine and Total Oxidizable Precursor Assay that can quantify the presence of fluorine atoms within a sample [1]</li><li>Portable sensors and field-deployable technologies that enable on-site monitoring and rapid response to contamination events</li><li>AI-driven solutions that can improve data analysis and interpretation for complex PFAS mixtures</li></ul><h4><strong>Collaborative Approaches</strong></h4><p>Addressing the global challenge of PFAS detection requires coordinated efforts:</p><ul><li>International partnerships between researchers in developed and developing regions to enhance expertise and capacity building</li><li>Standardization of analytical methods to ensure consistency and comparability of results across different laboratories and regions</li><li>Open data sharing and collaboration across countries to leverage collective knowledge and resources</li><li>Integration of PFAS monitoring into broader environmental and public health surveillance systems</li></ul><h3><strong>Conclusion</strong></h3><p>The detection of PFAS is not merely a technical challenge but a critical public health and environmental imperative [1]. As these "forever chemicals" continue to persist in our environment, developing effective, accessible, and comprehensive detection methods becomes increasingly important. By advancing detection technologies, strengthening regulatory frameworks, and fostering global collaboration, we can better understand, monitor, and ultimately mitigate the impacts of PFAS contamination.</p><p>The EPA's standardized methods (533, 537.1, and 1633) provide crucial tools for monitoring PFAS in various environmental matrices, but continued innovation is needed to address the full spectrum of PFAS compounds and to make detection more accessible globally [1] [6]. The path forward requires sustained investment in research and development, capacity building in resource-limited settings, and a commitment to environmental justice that ensures all communities have access to the tools and information needed to protect themselves from PFAS exposure. Only through such comprehensive approaches can we hope to address the complex challenges posed by these persistent pollutants.</p><p><span>Be sure to check out our other installments of our&nbsp;</span><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/introducing-our-environmental-contaminants-series-making-sense-of-the-alphabet-soup"><span>Environmental Contaminant Series</span></a><span>&nbsp;covering&nbsp;</span><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/the-importance-of-detecting-persistent-organic-pollutants-pops"><span>Persistent Organic Pollutants (POPs)</span></a><span>,&nbsp;</span><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/the-importance-of-detecting-polycyclic-aromatic-hydrocarbons-pahs"><span>Polycyclic Aromatic Hydrocarbons (PAHs)</span></a><span>,&nbsp;</span><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/the-importance-of-detecting-semi-volatile-organic-compounds-svocs"><span>Semi-Volatile Organic Compounds (SVOCs)</span></a><span>, and </span><a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/the-importance-of-detecting-polychlorinated-biphenyls-pcbs"><span>Polychlorinated Biphenyls (PCBs)</span></a><span>.</span></p>

The Importance of Detecting Per- and Polyfluoroalkyl Substances (PFAS)

News from LabRulezLCMS Library - Week 36, 2026

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The Czech Academy of Sciences (CAS) was established by Act No. 283/1992 Coll. as the Czech successor of the former Czechoslovak Academy of Sciences. It is set up as a complex of 54 public research institutions.

Czech Academy of Sciences

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Organomation, founded in 1959, designs and manufactures high-quality nitrogen evaporators and extraction systems. Known for innovation and durability, their lab instruments are used globally for efficient sample preparation with strong customer support.

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KNAUER AZURA MWD 2.1L Multiwavelength Detector

KNAUER AZURA® MWD 2.1L is an 8-channel UV/VIS detector with 190–700 nm coverage, LightGuide technology, high sensitivity, and upgradeability to a DAD system.

<p><strong>The KNAUER AZURA® MWD 2.1L is a sensitive 8-channel UV/VIS multiwavelength detector designed for analytical, semi-preparative, and preparative liquid chromatography. Combining excellent performance, user-friendly operation, and affordability, it provides a versatile solution for routine and advanced LC applications.</strong></p><p>The detector features a newly developed optical unit and intelligent temperature management to ensure maximum sensitivity with minimal baseline drift. Optional LightGuide flow cells based on total internal reflection technology maximize light throughput and minimize peak dispersion, resulting in an optimized signal-to-noise ratio. An optional fiber-optic adapter allows physical separation of the flow cell from the detector, increasing safety when handling hazardous, explosive, or toxic materials.</p><p>The <strong>AZURA® MWD 2.1L</strong> can also be upgraded to a full <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/2423"><strong>AZURA® DAD 2.1L diode array detector</strong></a>, protecting future investments and enabling greater analytical flexibility.</p><h3><strong>Key Features</strong></h3><ul><li>Sensitive <strong>8-channel UV/VIS multiwavelength detector</strong></li><li>Wavelength range<strong> from 190 to 700 nm</strong></li><li>Simultaneous monitoring of <strong>up to 8 digital channels</strong></li><li>LightGuide flow cell technology for improved sensitivity and signal-to-noise ratio</li><li>Intelligent temperature management for minimal baseline drift</li><li>Wide selection of analytical, semi-preparative, and preparative flow cells</li><li>Optional fiber-optic adapter for remote flow cell positioning</li><li>Internal holmium filter for wavelength verification</li><li>Integrated leak sensor</li><li>Front-access lamp replacement</li><li>Upgradeable to the AZURA® DAD 2.1L diode array detector</li><li>Compatible with <strong>ClarityChrom®, OpenLAB®, Chromeleon™, PurityChrom®</strong>, and <strong>Mobile Control</strong></li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detector type: </strong>Multiwavelength Detector (MWD)</li><li><strong>Digital channels: </strong>8</li><li><strong>Analog channels:</strong> 4</li><li><strong>Light source: </strong>Deuterium lamp with integrated GLP chip</li><li><strong>Wavelength range: </strong>190–700 nm</li><li><strong>Spectral resolution: </strong>&lt;10 nm (FWHM)</li><li><strong>Slit width: </strong>7.0 nm</li><li><strong>Wavelength accuracy: </strong>±1 nm</li><li><strong>Wavelength repeatability: </strong>±0.1 nm</li></ul><h4><strong>Performance</strong></h4><ul><li><strong>Noise:</strong> ±5 µAU at 254 nm</li><li><strong>Drift:</strong> 400 µAU/h at 254 nm</li><li><strong>Linearity:</strong> &gt;2.0 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>100 Hz via LAN</li><li>12.5 Hz via analog output</li></ul></li></ul><h4><strong>Flow Cells</strong></h4><ul><li>Flow cells sold separately</li><li>Stainless-steel and bio-inert configurations available</li><li>Optional LightGuide total-reflection technology</li></ul><h4><strong>Control and Communication</strong></h4><ul><li>LAN (RJ-45)</li><li>USB service interface</li><li>Analog inputs and outputs</li><li>Mobile Control stand-alone operation</li><li>Full software integration with chromatography data systems</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp identification</li><li>Lamp operating hours</li><li>Lamp ignition count</li><li>Comprehensive GLP reporting</li></ul><h4><strong>Power and Dimensions</strong></h4><ul><li><strong>Power supply:</strong> 100–240 V, 50–60 Hz</li><li><strong>Power consumption: </strong>75 W</li><li><strong>Dimensions (W × H × D):</strong> 361 × 158 × 523 mm</li><li><strong>Weight:</strong> 12.2 kg</li></ul>

KNAUER AZURA VWD 2.1L Variable Wavelength Detector

Flexible UV/VIS detector with up to four wavelengths, conductivity, temperature, and optional pH monitoring. Ideal for HPLC, FPLC, and purification applications.

<p><strong>The KNAUER AZURA® VWD 2.1L is a versatile variable wavelength detector designed for analytical HPLC, FPLC, and purification applications. Combining UV/VIS detection with optional conductivity, temperature, and pH monitoring, it provides exceptional flexibility for a wide range of chromatographic workflows.</strong></p><p>The detector supports simultaneous monitoring of up to four UV/VIS wavelengths across a broad spectral range from 190 to 900 nm. When equipped with KNAUER’s patented <strong>CombiLight flow cell</strong>, it can simultaneously measure UV absorbance, conductivity, and eluent temperature. An optional pH electrode further extends functionality by enabling real-time pH monitoring during chromatographic separations.</p><h3><strong>Key Features</strong></h3><ul><li>Variable wavelength UV/VIS detector <strong>for analytical HPLC and FPLC</strong></li><li>Simultaneous monitoring of <strong>up to 4 UV/VIS wavelengths</strong></li><li>Broad wavelength range from <strong>190 to 900 nm</strong></li><li>Optional conductivity monitoring up to <strong>1000 mS/cm</strong></li><li>Integrated temperature monitoring</li><li>Optional real-time pH measurement</li><li>Compatible with patented KNAUER CombiLight flow cell technology</li><li>Convertible between flow-cell and fiber-optic configurations</li><li>Internal holmium oxide filter for wavelength verification</li><li>Adjustable leak sensor for enhanced operational safety</li><li>Front-access lamp and flow-cell replacement</li><li>Comprehensive GLP functionality with component recognition</li><li>Suitable for analytical, preparative, and purification workflows</li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detection channels:</strong><ul><li>4 × UV/VIS</li><li>1 × Conductivity</li><li>1 × Temperature</li><li>1 × pH</li></ul></li><li><strong>Wavelength range:</strong> 190–900 nm</li><li><strong>Light source:</strong><ul><li>High-brightness deuterium lamp</li><li>Halogen lamp</li><li>Integrated GLP chip</li></ul></li><li><strong>Flow cell:</strong> Not included</li><li><strong>Optional display:</strong> Mobile Control</li></ul><h4><strong>UV/VIS Performance</strong></h4><ul><li><strong>Spectral bandwidth:</strong> 6 nm (FWHM)</li><li><strong>Wavelength accuracy: </strong>±1.5 nm</li><li><strong>Wavelength precision:</strong> 0.4 nm</li><li><strong>Baseline noise: </strong>±7.5 µAU at 254 nm</li><li><strong>Baseline drift:</strong> 200 µAU/h at 254 nm</li><li><strong>Linearity: </strong>&gt;2.5 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>100 Hz (single UV channel)</li><li>5 Hz (four UV channels)</li></ul></li></ul><h4><strong>Conductivity Monitoring</strong></h4><ul><li><strong>Measurement range: </strong>0.1–1000 mS/cm</li><li><strong>Accuracy:</strong> ±2% or ±0.5 mS/cm (whichever is greater)</li></ul><h4><strong>pH Monitoring</strong></h4><ul><li><strong>Measurement range: </strong>pH 0–14</li><li><strong>Accuracy: </strong>±0.1 pH (between pH 2–12)</li></ul><h4><strong>Temperature Monitoring</strong></h4><ul><li><strong>Measurement range</strong>: 1–99 °C</li><li><strong>Accuracy</strong>: ±1.5 °C (4–40 °C)</li></ul><h4><strong>System Functions</strong></h4><ul><li>Internal holmium oxide filter for wavelength verification</li><li>Adjustable leak sensor</li><li>Automatic integration time</li><li>User-selectable time constants:</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp recognition</li><li>Operating hours tracking</li><li>Light source lifetime monitoring</li><li>Flow-cell recognition</li><li>Detailed GLP reporting</li></ul><h4><strong>Maintenance</strong></h4><ul><li>Front-accessible deuterium lamp</li><li>Front-accessible halogen lamp</li><li>Front-accessible flow cell</li><li>Simplified service procedures</li></ul><h3><strong>Applications</strong></h3><ul><li>Analytical HPLC</li><li>FPLC systems</li><li>Protein purification</li><li>Biopharmaceutical analysis</li><li>Process chromatography</li><li>Preparative chromatography</li><li>Method development</li><li>Quality control laboratories</li><li>UV/VIS monitoring of purification processes</li></ul>

KNAUER AZURA UVD 2.1L UV/VIS Detector

Compact and affordable UV/VIS detector for routine HPLC and fast LC applications, featuring 190–750 nm wavelength range and flexible flow-cell options.

<p><strong>The KNAUER AZURA® UVD 2.1L is a cost-effective UV/VIS detector designed for routine HPLC applications, including fast liquid chromatography methods. Combining reliable performance, compact dimensions, and flexible flow-cell options, it provides an ideal solution for analytical and preparative chromatography laboratories seeking dependable UV detection at an attractive price point.</strong></p><p>The detector utilizes a deuterium lamp covering the wavelength range <strong>from 190 to 750 nm</strong> and offers excellent sensitivity and stability for everyday chromatographic analysis. Its smart mechanical design allows quick and easy access to the flow cell, minimizing maintenance time and maximizing instrument uptime.</p><p>A wide range of interchangeable flow cells is available, including stainless-steel and bio-inert versions suitable for analytical, semi-preparative, and preparative LC applications with <strong>flow rates ranging from 10 μL/min up to 10 L/min</strong>. The detector integrates seamlessly into virtually any LC system through LAN communication, analog I/O, and compatibility with leading chromatography software packages.</p><h3><strong>Key Features</strong></h3><ul><li><strong>Cost-effective UV/VIS detector </strong>for routine HPLC applications</li><li>Suitable for fast LC methods</li><li>Wavelength range <strong>from 190 to 750 nm</strong></li><li>Single-channel variable wavelength detection</li><li><strong>Deuterium lamp </strong>with integrated GLP chip</li><li>Compact and robust instrument design</li><li>Easily accessible flow cell for rapid replacement</li><li>Wide selection of interchangeable flow cells</li><li>Compatible with analytical and preparative LC applications</li><li><strong>Flow rates from 10 μL/min up to 10 L/min</strong></li><li>Integrated leak sensor</li><li>Automatic integration time adjustment</li><li>LAN and analog communication interfaces</li><li>Comprehensive GLP functionality</li><li><strong>Compatible with ClarityChrom®, OpenLAB®, Chromeleon™, ChromGate®, PurityChrom®</strong>, and <strong>Mobile Control</strong></li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detection channels:</strong> 1</li><li><strong>Light source: </strong>Deuterium (D₂) lamp with integrated GLP chip</li><li><strong>Wavelength range:</strong> 190–750 nm</li><li><strong>Spectral bandwidth: </strong>11 nm (FWHM)</li><li><strong>Wavelength accuracy:</strong> ±2.5 nm</li><li><strong>Wavelength precision:</strong> 0.3 nm</li></ul><h4><strong>Performance</strong></h4><ul><li><strong>Noise:</strong> ±15 µAU at 254 nm</li><li><strong>Drift: </strong>300 µAU/h at 254 nm</li><li><strong>Linearity:</strong> &gt;2.0 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>50 Hz via LAN</li><li>20 Hz via analog output</li></ul></li></ul><h4><strong>Flow Cells</strong></h4><ul><li>Flow cells sold separately</li><li>Stainless-steel and bio-inert options available</li><li>Suitable for analytical and preparative chromatography</li><li>Flow rates from 10 μL/min to 10 L/min</li></ul><h4><strong>Communication and Control</strong></h4><ul><li>LAN communication</li><li>Analog input/output</li><li>Mobile Control software</li><li>Event control</li><li>Terminal protocol</li></ul><h4><strong>Inputs</strong></h4><ul><li>Error (IN)</li><li>Start (IN)</li><li>Autozero</li><li>0–10 V Analog (IN)</li></ul><h4><strong>Outputs</strong></h4><ul><li>Events 1–3</li><li>+5 V</li><li>24 V Valve</li></ul><h4><strong>Analog Output</strong></h4><ul><li>1 × 0–5 V scalable</li><li>20-bit resolution</li><li>Adjustable offset</li></ul><h4><strong>Programming Functions</strong></h4><ul><li>Timed wavelength programming</li><li>Event programming</li><li>Fraction valve control</li><li>Wake-up functions</li><li>Up to 9 programs</li><li>Up to 50 program lines</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp recognition</li><li>Operating hours tracking</li><li>Lamp operating hours</li><li>Lamp ignition counter</li><li>Detailed GLP reports</li></ul><h4><strong>Safety and Maintenance</strong></h4><ul><li>Integrated leak sensor</li><li>Easy-access flow cell compartment</li><li>Front-access maintenance</li><li>Minimal downtime for service operations</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li><strong>Operating temperature:</strong> 4–40 °C</li><li><strong>Humidity:</strong> &lt;90% non-condensing</li></ul><h4><strong>Power and Dimensions</strong></h4><ul><li><strong>Power supply: </strong>100–240 V, 50–60 Hz</li><li><strong>Power consumption: </strong>65 W</li><li><strong>Dimensions (W × H × D):</strong> 361 × 158 × 523 mm</li><li><strong>Weight: </strong>5.9 kg</li></ul><h3><strong>Applications</strong></h3><ul><li>Routine HPLC analysis</li><li>Fast LC methods</li><li>Pharmaceutical quality control</li><li>Food and beverage analysis</li><li>Environmental testing</li><li>Chemical analysis</li><li>Preparative liquid chromatography</li><li>Academic and research laboratories</li></ul>

KNAUER AZURA UVD 2.1S UV Detector

Compact single-wavelength UV detector for routine HPLC applications with 190–500 nm range, flexible flow-cell options, and seamless software integration.

<p><strong>The KNAUER AZURA® UVD 2.1S is a compact, cost-effective single-wavelength UV detector designed for routine HPLC applications. Despite its small footprint, it delivers reliable performance and excellent technical specifications, making it one of the most compact HPLC UV detectors available on the market.</strong></p><p>Equipped with a deuterium lamp covering the <strong>wavelength range from 190 to 500 nm</strong>, the detector is suitable for a broad range of analytical chromatography applications. Its intelligent design provides quick access to the flow cell, enabling fast replacement and simplified maintenance. A wide selection of interchangeable flow cells is available, including bio-inert and stainless-steel versions for analytical and preparative LC applications with <strong>flow rates ranging from 10 μL/min up to 10 L/min</strong>.</p><h3><strong>Key Features</strong></h3><ul><li>Compact single-wavelength UV detector for HPLC</li><li>One of the smallest HPLC UV detectors available</li><li>Wavelength range <strong>from 190 to 500 nm</strong></li><li>Deuterium lamp with integrated GLP chip</li><li>Suitable for routine analytical applications</li><li>Compact AZURA® housing design</li><li>Easily accessible flow cell for rapid replacement</li><li>Wide range of interchangeable flow cells available</li><li>Compatible with analytical and preparative LC applications</li><li><strong>Flow rates from 10 μL/min up to 10 L/min</strong></li><li>Stand-alone operation via front panel</li><li><strong>LAN, RS-232</strong>, and analog communication interfaces</li><li>Compatible with major chromatography data systems</li><li>Available as a module for <strong>AZURA® ASM 2.2L</strong></li><li>Low maintenance requirements</li></ul><h3><strong>Technical Specifications</strong></h3><h4><strong>Detection System</strong></h4><ul><li><strong>Detection channels: </strong>1</li><li><strong>Light source:</strong> Deuterium (D₂) lamp with integrated GLP chip</li><li><strong>Wavelength range:</strong> 190–500 nm</li><li><strong>Spectral bandwidth: </strong>13 nm (FWHM)</li><li><strong>Wavelength accuracy: </strong>±3 nm</li><li><strong>Wavelength precision: </strong>0.7 nm</li></ul><h4><strong>Performance</strong></h4><ul><li><strong>Noise:</strong> ±20 µAU at 254 nm</li><li><strong>Drift:</strong> 300 µAU/h at 254 nm</li><li><strong>Linearity:</strong> &gt;2.0 AU at 274 nm</li><li><strong>Maximum data rate:</strong><ul><li>50 Hz via LAN</li><li>20 Hz via analog output</li><li>10 Hz via RS-232</li></ul></li></ul><h4><strong>Flow Cells</strong></h4><ul><li>Flow cells sold separately</li><li>Bio-inert and stainless-steel options available</li><li>Suitable for analytical and preparative chromatography</li><li>Flow rates from 10 μL/min to 10 L/min</li></ul><h4><strong>Communication and Control</strong></h4><ul><li>Front panel operation</li><li>Mobile Control software</li><li>Software control</li><li>Event control</li><li>Analog control</li><li>Terminal protocol</li></ul><h4><strong>Interfaces</strong></h4><ul><li>LAN (RJ-45)</li><li>RS-232 (SUB-D 9)</li><li>Multi-pin connector</li><li>Analog interface (RCA connector)</li></ul><h4><strong>Inputs</strong></h4><ul><li>Autozero</li><li>Start (IN)</li><li>Error (IN/OUT)</li><li>0–10 V Analog Input</li></ul><h4><strong>Outputs</strong></h4><ul><li>Error (OUT/IN)</li></ul><h4><strong>Analog Signals</strong></h4><ul><li>Analog wavelength input: 0–10 V</li><li>Analog output: 1 × ±2.5 V scalable</li><li>Resolution: 20-bit</li></ul><h4><strong>GLP Functions</strong></h4><ul><li>Lamp operating hours monitoring</li></ul><h4><strong>Display</strong></h4><ul><li>LED display</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li><strong>Operating temperature:</strong> 4–40 °C</li><li><strong>Humidity</strong>: &lt;90% non-condensing</li></ul><h4><strong>Power and Dimensions</strong></h4><ul><li><strong>Power supply:</strong><ul><li>Input: 100–240 V</li><li>Output: 24 V DC</li></ul></li><li><strong>Power consumption: </strong>60 W</li><li><strong>Dimensions (W × H × D):</strong> 121 × 129 × 187 mm</li><li><strong>Weight: </strong>1.5 kg</li></ul><h3><strong>Applications</strong></h3><ul><li>Routine HPLC analysis</li><li>Quality control laboratories</li><li>Pharmaceutical analysis</li><li>Food and beverage testing</li><li>Environmental analysis</li><li>Academic research</li><li>Preparative liquid chromatography</li><li>Compact and space-limited laboratory environments</li></ul>

Products from category UV-Vis HPLC detectors distributed by KNAUER - page 1

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