Whether a drug can effectively bind to its target protein, or how different parts of a virus or a cell interact, depends on processes taking place at the level of individual molecules. Their behaviour is determined not only by their shape, but also by the electrostatic forces acting between them. Understanding how these forces are distributed helps scientists explain why certain molecules attract each other, how they bind and how they interact.This is where the <a target="_blank" rel="noopener noreferrer" href="https://acc.biodata.ceitec.cz/">Atomic Charge Calculator (ACC)</a> comes in. Researchers at Masaryk University have been developing this computational tool for more than a decade. Its third and most advanced generation to date was developed at CEITEC Masaryk University and the Faculty of Science at Masaryk University, in collaboration with the Faculty of Informatics at Masaryk University and Palacký University Olomouc.ACC III calculates the electric charges of individual atoms and visualises their distribution directly within three-dimensional molecular structures. It brings together twenty different calculation methods in a single environment and can work with a wide range of molecules – from small organic compounds to proteins and other large biomolecular structures.A key advantage of Atomic Charge Calculator III is that it combines a broad range of computational methods with ease of access. Basic calculations can be performed directly in a web browser, with no need to install specialised software or register for an account. The resulting charges can be displayed directly on a 3D model of the molecule. For advanced users and large-scale analyses, the platform also supports automated data processing and allows its computational core to be run locally.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CEITEC_Co_pritahuje_molekuly_Nova_generace_nastroje_z_CEITEC_zviditelnuje_sily_mezi_atomy_d32d7bd2cd.jpg" alt="CEITEC/Biological Data Management and Analysis Core Facility: What Attracts Molecules? A New Generation of a CEITEC Tool Makes the Forces Between Atoms Visible: Oseltamivir bound to influenza virus neuraminidase (blue: positive partial charges, red: negative charges). A strong electrostatic interaction occurs between a negatively charged region of the drug and positively charged regions of the protein." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CEITEC_Co_pritahuje_molekuly_Nova_generace_nastroje_z_CEITEC_zviditelnuje_sily_mezi_atomy_d32d7bd2cd.jpg 140w," sizes="100vw" width="1600" height="1786"><h3>Why are scientists interested in the electric charges of atoms?</h3>Electrons are not distributed evenly within molecules. Individual atoms can therefore carry different partial electric charges. These charges play an important role in determining how molecules behave towards their surroundings and towards one another.Positively and negatively charged regions of molecules can attract each other, while regions with the same charge repel each other. The distribution of these charges therefore helps determine which molecules approach each other, how they orient themselves and how strongly they may bind. In biology, this is important, for example, in molecular recognition or when a drug binds to its target protein. Understanding partial charges therefore helps scientists gain insight into the interactions underlying the behaviour of many molecular systems.There is, however, no single universal way to determine partial charges. Different computational methods can produce different values, and the choice of method also depends on how the results will be used. Accurate quantum-chemical calculations can also become very computationally demanding when large numbers of structures are involved. ACC III therefore brings together empirical methods that allow these calculations to be performed more quickly and on a large scale.“From the outset, we designed ACC III to make calculating partial atomic charges as straightforward as possible. Users do not need to install anything or deal with complicated settings – they simply upload a molecule and start the calculation with a single click. The application then suggests suitable methods from the twenty available and can handle both small molecules and large biomolecular structures,” says <a target="_blank" rel="noopener noreferrer" href="https://www.ceitec.eu/tomas-racek-ph-d/u94476?page=publication">Tomáš Raček</a>, who has been developing and maintaining ACC since 2018.<h3>How an antiviral drug binds to an influenza virus protein</h3>The authors demonstrate what charge distribution can reveal using the well-known antiviral drug oseltamivir, marketed as Tamiflu. The drug binds to neuraminidase, a protein of the influenza A virus. ACC III can show directly within the three-dimensional structure where positive and negative partial charges are located and how they contribute to the interaction between the drug and the protein.“The example of oseltamivir clearly shows why it is useful not only to calculate the charges, but also to visualise them directly within the structure. This allows us to see which parts of the two molecules interact electrostatically. The same approach can be used to study many other molecular systems,” explains Tomáš Raček.ACC III is not limited to small molecules. It can also work with proteins and other large biomolecular structures. The authors demonstrate this using a second example: the SARS-CoV-2 pore complex. Coronaviruses form these pores during replication in infected cells and use them to transport viral RNA across membranes. Visualising partial charges helps distinguish the parts of the complex that pass through the non-polar environment of the membrane from its more highly charged regions.<h3>From calculation straight to a 3D model</h3>The new generation of the Atomic Charge Calculator also offers more advanced visualisation. It uses Mol*, which allows calculated charges to be mapped directly onto a three-dimensional structure and explored interactively. A visualisation created using ACC III was also selected for the cover of the special Nucleic Acids Research Web Server Issue. Created by Tomáš Raček, the cover image shows the distribution of partial charges in a membrane protein system.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CEITEC_Co_pritahuje_molekuly_Nova_generace_nastroje_z_CEITEC_zviditelnuje_sily_mezi_atomy_3_85cc310925.jpeg" alt="CEITEC/Oxford University Press: What Attracts Molecules? A New Generation of a CEITEC Tool Makes the Forces Between Atoms Visible: Cover page in Nucleic Acids Research journal." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CEITEC_Co_pritahuje_molekuly_Nova_generace_nastroje_z_CEITEC_zviditelnuje_sily_mezi_atomy_3_85cc310925.jpeg 124w," sizes="100vw" width="1600" height="2011">Results can be downloaded in several standard formats and, for the first time, stored directly in the mmCIF format commonly used for three-dimensional biomolecular structures. Information about the structure and its calculated charges can therefore remain together in a single file and be used by other tools.For researchers who need to process large numbers of structures, ACC III also provides an API and a computational core that can be run locally. The platform can therefore be used both for individual calculations through its web interface and as part of larger automated analyses.<h3>More than a decade of development</h3>Scientists introduced the first Atomic Charge Calculator in 2015, followed by its second generation in 2020. In the meantime, the team also developed specialised tools: PDBCharges for structures from the Protein Data Bank and AlphaCharges for structures from the AlphaFold Database.“The Atomic Charge Calculator was never a one-off project,” says <a target="_blank" rel="noopener noreferrer" href="https://www.ceitec.eu/prof-radka-svobodova-ph-d/u17518?page=publication">Radka Svobodová</a>, Head of the Biological Data Management and Analysis Core Facility at CEITEC Masaryk University. “For more than a decade, we have been continuously developing tools that respond both to new possibilities in structural bioinformatics and to the needs of their users. The third generation combines straightforward web-based use with capabilities that are important for the automated processing of large numbers of molecular structures.”<blockquote>Atomic Charge Calculator III is freely available through its web interface and does not require registration for basic use. Its development was supported by the ELIXIR CZ research infrastructure.</blockquote><h5>The authors presented the new generation of the tool in <a target="_blank" rel="noopener noreferrer" href="https://academic.oup.com/nar/article/54/W1/W211/8662890">Nucleic Acids Research</a>.</h5>

What Attracts Molecules? A New Generation of a CEITEC Tool Makes the Forces Between Atoms Visible 

Not every concentration job can tolerate heat — and not every concentrator that handles heat well can handle cold. <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/2441">Refrigerated centrifugal vacuum concentrators</a> exist for a specific reason: proteins, RNA, enzymes, and synthetic peptides degrade quickly under thermal stress, and standard concentrators that rely on heat alone can compromise sample integrity before evaporation finishes. We compared two of the leading refrigerated systems — the Labconco Refrigerated CentriVap and the <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/2611">Thermo Fisher Refrigerated SpeedVac SRF110</a> — to see how they stack up for labs where sample preservation is non-negotiable.<blockquote><a target="_blank" rel="noopener noreferrer" href="https://explore.organomation.com/labconco-refrigerated-centrivap-vs-thermo-fisher-refrigerated-speedvac">Download the full comparison with pricing here!</a></blockquote><h3>The Problem Refrigeration Actually Solves</h3>It's a detail that gets lost in most spec-sheet comparisons: running a<a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/products?manufacturerItems=540&amp;search=centrivap"> vacuum concentrator </a>without temperature control can cause a sample to over-cool itself. As solvent evaporates under vacuum, the process pulls latent heat from the sample — the same evaporative cooling effect that makes sweat feel cold on skin. For a heat-stable solvent, that's irrelevant. For a temperature-sensitive biomolecule, it can drop the sample low enough to risk unwanted freezing or sublimation mid-run. Labconco's own engineering notes for the Refrigerated CentriVap describe this directly: the unit pairs a refrigeration system with a heater so operators can hold a precise set-point temperature and avoid sublimated samples caused by evaporative cooling. That's the whole reason this product category exists, and it's worth understanding before comparing specs line by line.<h3>Price: A Wider Gap at the High End</h3>The Labconco Refrigerated CentriVap is typically priced around $13,000 USD. The Thermo Fisher SRF110 runs higher, generally $15,000–$17,000 USD, and that's before factoring in the modular kit components — Thermo Fisher sells the SRF110 with a separate vacuum system, rotor, vapor trap, and heat transfer fluid bundled into the total kit price. The price gap between these two refrigerated units is proportionally larger than what we found comparing their non-refrigerated counterparts, which makes the value case for the CentriVap even more pronounced at this tier.<h3>Capacity: The Difference That Matters Most Right Now</h3>This is where the two systems really separate, and it lines up with where lab demand is heading. The Refrigerated CentriVap processes up to 312 samples per run; the SRF110 tops out at 132. Both handle volumes up to 50 mL, so this isn't a volume trade-off the way it was in our earlier comparison — it's a straight throughput advantage for the CentriVap.That gap matters because<a target="_blank" rel="noopener noreferrer" href="https://peptidestaff.com/industry-trends/peptide-therapy-market-forecast-2026/"> peptide-based therapeutics </a>have become one of the fastest-growing classes of drugs in the pharmaceutical industry, and manufacturing capacity — not demand — is widely cited as the primary bottleneck holding the sector back. <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/article/7541">GLP-1 programs</a> in particular are pushing <a target="_blank" rel="noopener noreferrer" href="https://www.bachem.com/knowledge-center/glp-1-demand-for-peptide-manufacturers/">peptide manufacturers</a> toward industrialized, large-scale production platforms rather than one-off batch work. <a target="_blank" rel="noopener noreferrer" href="https://www.organomation.com/">Sample prep equipment</a> sits squarely inside that bottleneck: every purification run, HPLC fraction, and concentration step has to scale alongside the chemistry. A concentrator that processes more than double the samples per run, like the Refrigerated CentriVap, is a meaningfully different proposition for a peptide synthesis or purification lab than it would have been five years ago.<h3>Temperature Range: How Cold You Can Go</h3>The CentriVap's refrigeration reaches as low as -10°C; the SRF110 bottoms out at -4°C. Both units heat up to +100°C. That six-degree gap on the cold end isn't dramatic on paper, but for the most heat-labile peptides and enzymes, the lower floor gives operators more margin before a sample is at risk — particularly during longer runs where evaporative cooling has more time to compound any thermal load on the sample.<h3>Vortex Speed and Mechanical Flexibility</h3>The CentriVap offers an adjustable vortex range from 500 to 1,800 rpm, while the SRF110 runs up to 1,725 rpm. The CentriVap's lower floor is the more useful distinction here — fragile, large, or shear-sensitive samples (think intact proteins or larger peptide constructs) sometimes need to run at reduced rotor speed to avoid mechanical stress, and the CentriVap gives operators that headroom on both ends rather than just a ceiling.<h3>Lid Material: Visibility vs. Durability</h3>The Refrigerated CentriVap uses a glass lid, letting operators see into the chamber during a run. The SRF110 uses an epoxy-coated aluminum lid, which trades visibility for added durability. For labs running visually distinct sample batches — colored buffers, multiple project codes, HPLC fractions pulled at different time points — the ability to glance at the chamber without interrupting a run has real workflow value, especially in a core facility setting where one instrument serves multiple research groups.<h3>What This Means for Core Facilities</h3>Shared instrumentation cores feel throughput and cold-temperature constraints differently than a single-PI lab does. A<a target="_blank" rel="noopener noreferrer" href="https://blog.organomation.com/blog/an-appreciation-for-academic-core-labs"> core running samples from multiple research groups </a>— some doing routine RNA cleanup, others running heat-labile peptide fractions from an HPLC purification step — needs an instrument that won't bottleneck on either axis. The CentriVap's combination of higher per-run capacity and a lower refrigeration floor gives a shared facility more room to serve mixed workloads without forcing every group onto the same conservative settings a less flexible unit would require.<h3>Built for the Same Footprint</h3>Both units are sized for fume hood placement, with the CentriVap measuring 15.0 x 27.2 x 13.9 inches against the SRF110's 16.62 x 25 x 13.75 inches — close enough that floor planning isn't a deciding factor either way. Both carry standard one-year warranties.<h3>The Bottom Line</h3>For labs concentrating proteins, RNA, enzymes, or peptide fractions at scale — particularly anyone supporting peptide therapeutic development, where production capacity is already the limiting factor industry-wide — the Labconco Refrigerated CentriVap's combination of higher throughput, lower cold-temperature floor, and lower price makes it the stronger fit. The SRF110 remains a capable option for labs with smaller batch sizes already standardized on Thermo Fisher's modular vacuum ecosystem.Organomation distributes the full Labconco CentriVap line, including the Refrigerated and Refrigerated Pro models. Contact our team at sales@organomation.com to talk through rotor configuration, cold trap pairing, and throughput planning for your lab.&nbsp;<blockquote><h5><a target="_blank" rel="noopener noreferrer" href="https://explore.organomation.com/labconco-refrigerated-centrivap-vs-thermo-fisher-refrigerated-speedvac">Download the full comparison with pricing here!</a></h5></blockquote>

Refrigerated SpeedVac SRF110 vs. CentriVap - Why Sample Capacity Matters More Than Ever for Peptide and Protein Labs

Our Library never stops expanding. What are the most recent contributions to LabRulezLCMS Library in the week of 14th September 2026? Check out new documents from the field of liquid phase, especially HPLC and LC/MS techniques!<blockquote>👉 <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library">SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT LCMS AND RELATED TECHNIQUES</a></blockquote><blockquote>👉 Need info about different analytical techniques? Peek into <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library">LabRulezGCMS</a> or <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library">LabRulezICPMS</a> libraries.</blockquote>This week we bring you application notes by Agilent Technologies and Waters Corporation and posters by Shimadzu / AOAC and Thermo Fisher Scientific / Metabolomics!<h3>1. Agilent Technologies: Improved Analysis of Intact Proteins and Peptides by Reversed Phase HPLC Using the Altura Ultra Inert PLRP-S 1000 Å Column</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/an_altura_ultrainert_column_HPLC_analysis_5994_9322en_agilent_2b3a542647.pdf">Full PDF for download</a></li></ul>Intact protein analysis by reversed-phase HPLC (RP-LC) plays a vital role in quality control for determining the purity of biotherapeutic proteins and improving the identification and quantification of critical quality attributes (CQAs). When coupled to mass spectrometric detection, it allows several things. First, an accurate molecular weight to be determined; second, the identification of variants containing post‑translational modifications (PTMs) and proteoforms; and third, the antibody-to-drug ratio in the case of antibody drug conjugates (ADCs).1&nbsp;While many RP columns have a silica-based stationary phase to enable broader functionalization, residual acidic silanol groups can interact with basic residues in peptides, proteins, and other biomolecules, resulting in significant peak tailing and loss of chromatographic performance. Polystyrene/divinyl benzene (PS/DVB)-based stationary phases do not contain unintentional adsorption sites. Additionally, larger pore sizes have demonstrated superior chromatographic efficiency through less diffusion restriction into the pore volume and reduction of size exclusion mechanisms, degrading the RP-based selectivity.2&nbsp;Wide-pore columns like the PLRP-S 1000Å provide an exceptional performance with biomolecules, particularly when combined with MS-compatible mobile phase conditions such as formic acid.&nbsp;Even so, some undesirable interactions may be observed when using stainless-steel column hardware. Molecules that possess multiple negative charges (including oligonucleotides, phosphorylated peptides and proteins, and proteins with low isoelectric point in general) may interact with exposed metal ions in stainless-steel column hardware. This can result in the need to "deactivate" new columns by making multiple injections of sample until reproducible results are obtained.&nbsp;This application note demonstrates how the new <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/library?mainauthorItems=10&amp;search=Altura+Ultra+Inert">Altura Ultra Inert </a>PLRP-S 1000 Å column serves as an effective high-performance workhorse in the analysis of large, intact biomolecules. Developed to effectively block nonspecific adsorption during separations, Ultra Inert technology reduced passivation time 15-fold and delivered ~ 10% greater recovery for mAbs and ADCs and up to 100% for smaller biomolecules like GLP-1s and small globular proteins.<h4>Experimental</h4><h5>Instrumentation&nbsp;</h5><ul><li>Agilent 1290 Multicolumn thermostat (G7116B)&nbsp;</li><li>Agilent 1290 Bio multisampler (G7137A)&nbsp;</li><li>Agilent 1290 Bio high-speed pump (G7132A)&nbsp;</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/library?mainauthorItems=10&amp;search=6530">Agilent 6530 Q-TOF MS system</a>&nbsp;</li></ul><h5>Software and data processing&nbsp;</h5><ul><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/library?mainauthorItems=10&amp;search=MassHunter+Workstation">Agilent MassHunter Workstation, version 10.1&nbsp;</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/library?mainauthorItems=10&amp;search=MassHunter+Qualitative+Analysis">Agilent MassHunter Qualitative Analysis software, version&nbsp;B.07&nbsp;</a></li><li>Agilent DAR calculator, version B01.01</li></ul><h4>Conclusion&nbsp;</h4>Intact mass analysis is a critical methodology to determine the purity of biotherapeutics, but due to the chemical complexity of these analytes, nonspecific adsorption from both silica stationary phase and metal column housing can be highly deleterious to separation performance. The Agilent Altura PLRP-S 1000 Å provides a highly robust solution combining the chemical inertness of polystyrene/divinyl benzene stationary phase with the ultra‑inert Altura hardware to dramatically reduce deleterious peak tailing and increase recovery for biotherapeutics. Herein, we see that analyte recovery for both mAbs, ADCs, GLP-1s, and globular proteins are improved versus stainless-steel, while the Altura PLRP-S column is capable of monitoring both quality critical PTMs such as loss of drug payload as well as accurate quantification of ADC DAR.<h3>2. Shimadzu / AOAC: Ambient Ionization Mass Spectrometric Detection of Aroma Released During Gummy Chewing</h3><ul><li>Poster</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/aoac_2026_47_2_34c41f762f.pdf">Full PDF for download</a></li></ul>In recent years, there has been growing interest in evaluating flavor using analytical instrumentation, and retronasal aroma during eating is important. In this study, we proposed an analytical method for measuring retronasal aroma during eating using a single quadrupole mass spectrometer (<a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/library?mainauthorItems=1&amp;search=2050">LCMS-2050</a>) equipped with an ambient ion source (Dark Current Discharge Ionization : DCDI) without pretreatment.<h4>Conclusion</h4>We developed a simple method for evaluating retronasal aroma using a single quadrupole mass spectrometer with an ambient ionization source. Ambient ionization mass spectrometry (DCDI LCMS-2050) can rapidly measure retronasal aroma during eating. Time-resolved visualization reveals texture-dependent differences in aroma release dynamics among grape-flavored gummies. It is also expected to lead to the visualization of the marriage between food and alcohol. This approach may facilitate objective evaluation of flavor release during consumption and support product formulation and sensory science.<h3>3. Thermo Fisher Scientific / Metabolomics: Orbitrap Tribrid Real-Time similarity searching of mzCloud library for guided unknown characterization of tea metabolites</h3><ul><li>Poster</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/po_004849_lsms_rtls_tribrid_apex_small_molecule_metabolomics_po004849_na_en_d0d3156065.pdf">Full PDF for download</a></li></ul>In metabolomics LC-MS data is processed to generate a list of detected compounds with a level of confidence in the identity of each compound based on reference data. This reference data may be spectral data and/or retention time information stored in a library or in silico information generated based on fragmentation rules. These annotated compounds are then used to evaluate biological changes between normal and disease states. One of the major hurdles between collected data and coming to reliable conclusions about the biology is the limited number of standards available to build these libraries. It is common to have hundreds to thousands of compounds detected in a data set that have no library match because there is no commercial standard for that unknown. Instead, there is just an elemental formula and matches from a structure database. These structures can be compared using in silico fragmentation techniques to determine which isomers plausibly match the data. MSn data can help reduce the list of possible matches, but without guidance, ddMS3 may not consistently collect data on the most relevant MS2 fragments to accomplish this.&nbsp;In this work we use Real-Time Library Search (RTLS) in a ddMS3 method to help guide the instrument in real time to collect the most relevant data for confirming structural matches.<h4>Materials and methods</h4><h5>Test method(s)&nbsp;</h5>1 μL aliquots were analyzed using a <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/lcms/products?category=48&amp;manufacturerItems=3&amp;search=gold">Thermo Scientific Hypersil GOLD column</a> on a <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/744">Thermo Scientific Vanquish Horizon UHPLC</a> coupled with a <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/561">Thermo Scientific Orbitrap IQ-X Tribrid mass spectrometer</a> and Thermo Scientific Orbitrap Tribrid Apex Small Molecule mass spectrometer. RTLS was run in similarity mode using the offline version of <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/1764">Thermo Scientific mzCloud library</a>.&nbsp;<h5>Data analysis&nbsp;</h5>Data was processed using Thermo Scientific Freestyle and <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/1759">Compound Discoverer software</a>.<h4>Conclusions&nbsp;</h4>Tea extracts were analyzed using RTLS to find the most similar compound in the offline version of the mzCloud library and trigger MS3 on the highest m/z matching and non-matching fragments. This provided additional information to confirm similarity and provide insight on shared sub-structures to the library compound as well as additional information on the portions of the structure that were unique to the experimental compound.<h3>4. Waters Corporation: The Quantification of Glucagon-like Peptide Receptor Agonists (GLP-1 RAs) in Plasma Extracts Using Capillary UHPLC-MS/MS</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/pdf/720009537_en_0068921516.pdf">Full PDF for download</a></li></ul><div><div><section><div><div><div><div><div><div><h5>Benefits&nbsp;</h5><ul><li>10-fold improvement in sensitivity&nbsp;</li><li>Robust methodology for &gt;500 injections&nbsp;</li><li>Reduced solvent usage&nbsp;</li><li>No need for complex nanospray MS source</li></ul>Obesity represents, perhaps, the largest healthcare challenge, affecting approximately 1.3 billion people globally, contributing to a diverse range of chronic diseases e.g., metabolic, cardiovascular, muscular skeletal, and multiple cancers.1 The rapid growth of obesity and associated global healthcare costs means there is a critical need for safe effective treatments.2 GLP-1 RA initially developed for type 2 diabetes have shown clinical efficacy as weight loss medicines.2 These drugs mimic the action of gut hormones which regulate energy metabolism and appetite by interacting with the hypothalamus, brain stem etc., resulting in weight loss. The success of these GLP-1 RAs is associated with their on-target efficacy and long duration of action,3 e.g., half-life of semaglutide t½ = 160–180 hours3 cf. 1–2 minutes for human GLP-1.4 The long half-life of these GLP-1 RAs results in low, sub ng/mL plasma levels 48–72 hours after dosing, which requires a high sensitivity bioanalytical assay to accurately quantify the plasma concentrations5 and define the PK elimination phase.&nbsp;Tandem quadrupole electrospray ionization (ESI) mass spectrometry, operated in multiple reaction monitoring (MRM) mode, coupled with 2.1 mm ID ultra-high performance liquid chromatography (UHPLC) is the dominant technology platform for quantitative bioanalysis. As next generation GIP/GLP-1 RAs promise to be more potent, resulting in lower dosing levels and plasma levels, there is a need for more sensitive analytical methodologies to support drug metabolism and pharmacokinetics (DMPK) studies. Capillary/nano LC-MS/MS have been extensively employed in proteomics to increase analytical sensitivity and enable small volume analysis.5 This sensitivity increase is derived from a combination of the superior ionization efficiency at low flow rates and analyte concentration due to the smaller column geometry.6 This application note illustrates the use of capillary (300 µm) UHPLC-MS/MS (MRM) to affect 10-fold improvement in GLP-1-RAs peak response in human plasma extracts, and detection limits as low as 20 pg/mL for tirzepatide.<h4>Experimental</h4>Capillary chromatography was performed on an ACQUITY™ M-class Chromatography System connected to a <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/195">Xevo™ TQ-XS Mass Spectrometer</a> (Waters Corporation, Wilmslow, UK) equipped with a microflow probe. Capillary UHPLC separations were performed on an <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/1952">ACQUITY Premier Peptide CSH C18</a>, 300 Å, 1.7 µm, 300 µm x 50 mm Chromatography Column.MS analysis was performed at unit mass resolution using positive ESI at a capillary voltage of 3.0 kV, with a cone voltage of 32 V. The cone gas flow, desolvation gas flow, and desolvation gas temperature were 50 L/h, 300 L/h and 600 °C, respectively. The data were analyzed using <a target="_blank" rel="noopener noreferrer" href="https://labrulez.com/en-us/all/products/1544">waters_connect™ Software</a>, and MRM transitions used to monitored for the MS/MS detection of liraglutide, exenatide, semaglutide and tirzepatide were as follows: liraglutide 938.7 → 1128.4, exenatide 838 → 396, semaglutide 1029.2 → 1238.1, and tirzepatide 1204.2 → 396.2. Data analysis was performed using MS Quan Software.<h4>Conclusion</h4>Bioanalysis plays a critical role in the drug discovery and development processes providing data to support DMPK, safety assessment, pharmacokinetics/pharmacodynamics (PK/PD), and clinical development studies. The development of new, more potent medicines, innovating delivery platforms, micro sampling, and new approach methodologies (e.g., organ on a chip) all require greater levels of analytical sensitivity. Capillary scale UHPLCMS/MS offers the potential to improve bioanalytical detection limits up to 10-fold, without the need for long analysis times and complex operation associated with nano spray LC-MS/MS. Here, the application of capillary (300 µm ID) scale chromatography for the detection of GLP-1 RAs in human plasma extracts at levels as low as 20 pg/mL with robustness over 500 injections was demonstrated.</div></div></div></div></div></div></section></div></div>

News from LabRulezLCMS Library - Week 38, 2026

Article

Product

Application

Science and research

Poster

Since its establishment in 2011, CEITEC has quickly developed into a cutting-edge infrastructure for research which performs highly alongside the best institutes in Europe. Among the main priorities of CEITEC are the promotion of a motivating and dynamic international scientific environment, the provision of state-of-the-art research infrastructure, and the policy of open communication and equal opportunities.

CEITEC

Everything from the world of analytical chemistry in one place. We connect people in solving their problems. At Labrulez you will find all the necessary information easily, quickly and clearly. Stop searching and start finding.

LabRulez

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.

Organomation

Waters Charged Aerosol Detector (CAD)

Waters Charged Aerosol Detector (CAD) enables universal quantitation of non-volatile and semi-volatile compounds independent of UV activity, with wide dynamic range and seamless integration with Empower™ Software.

<h3>Expand Your Detection Range with a Detector Purpose-Built for Empower™ Software</h3>Empower™ Software–based laboratories require detection solutions that are easy to adopt, robust, and capable of accurately quantifying non-volatile and semi-volatile compounds—regardless of chemical structure or UV activity. The Waters Charged Aerosol Detector (CAD) is purposefully engineered to meet these demands, delivering universal, reliable detection fully integrated with Waters chromatography systems and Empower™ or MassLynx™ Software.With a wide dynamic range exceeding four orders of magnitude, the Waters CAD enables simultaneous quantitation of low-level, non-UV-active analytes, along with related impurities and excipients, in a single run—helping laboratories reduce method development time, increase productivity, and improve process control.<h4>Key Benefits</h4><ul><li>Universal detection without UV limitations Detect and quantify non-volatile and semi-volatile compounds independent of chromophore presence.</li><li>Wide dynamic range (&gt;4 orders of magnitude) Confidently quantify trace-level components and major constituents simultaneously.</li><li>Purpose-built for Empower™ Software Seamless integration into regulated workflows with Empower-based qualification and long-term software compatibility.</li><li>Compatible across Waters LC platforms Integrates easily with Alliance™, Arc™, ACQUITY™ Arc, ACQUITY™ H-Class, ACQUITY™ I-Class, and UPLC™ Systems.</li><li>Designed for robustness and ease of use Optimized hardware, simplified maintenance, and enhanced system protection features minimize downtime.</li></ul><h4>Technical Specifications</h4><h5>Detector Performance</h5><ul><li>Detector flow rate: 0.010–2.000 mL/min</li><li>Dynamic range: Greater than four orders of magnitude (four individual power values)</li><li>Sampling rate: Up to 200 Hz</li><li>Number of channels: Four (4), supported by four (4) independent background current channels</li></ul><h5>Temperature Control</h5><ul><li>Evaporation temperature:<ul><li>Ambient (off)</li><li>Controlled range: 10 °C to 100 °C (0.1 °C increments)</li><li>Minimum of 5 °C above ambient</li></ul></li></ul><h5>Gas Requirements</h5><ul><li>Inert gas supply: Nitrogen (recommended) or compressed air</li><li>Inlet pressure: 4.83–5.52 bar (483–552 kPa, 70.0–80.0 psi)</li><li>Gas consumption: Typically ≤ 5 L/min</li></ul><h5>Diagnostics and Monitoring</h5><ul><li>Diagnostic channels include:<ul><li>Nebulizer gas flow and pressure (psi)</li><li>Evaporator temperature (°C)</li><li>Ion trap voltage (V)</li><li>Charger current (µA)</li><li>Mixing chamber temperature (°C)</li></ul></li></ul><h5>Electrical and Physical Specifications</h5><ul><li>Power requirements: 100–240 VAC</li><li>Dimensions:<ul><li>Width: 34.3 cm (13.5 in)</li><li>Height: 20.8 cm (8.2 in)</li><li>Depth: 61.0 cm (24.0 in)</li></ul></li><li>Biocompatible: No</li></ul><h5>Software and System Compatibility</h5><ul><li>Optimized for Empower™ Software and MassLynx™ Software control</li><li>Robust chromatography data system (CDS) communications to minimize downtime</li><li>Backward compatibility to Empower™ 3 Feature Release 4 Service Release 3 (SR3)</li><li>Fully compatible with systems qualification and validation requirements in regulated environments</li></ul><h5>Seamless Method Transfer Across Laboratories</h5>The Waters CAD is designed to simplify method transfer within organizations and across external laboratories. It maintains method simplicity while adding enhanced tools for equivalency and reproducibility, reducing the need for revalidation when transitioning from legacy or third-party CAD solutions.The intuitive ACQUITY™ console control panel enables straightforward operation and simplifies replacement of outdated technology across laboratory networks.<h5>Designed for Ease of Use and Reliability</h5><ul><li>Single filter manifold with push/pull filter replacement</li><li>Easy-to-replace nebulizer for improved serviceability</li><li>Intelligent divert valve automatically sends flow to waste if gas pressure is lost or system errors occur</li><li>Enhanced leak detection and flood protection, safeguarding instruments in the event of CDS communication loss</li></ul><h5>Recommended Use</h5>Accurate quantitation in:<ul><li>HPLC, UHPLC, and UPLC separations</li><li>Preparative and purification workflows</li><li>Pharmaceutical QC and R&amp;D</li><li>Analysis of excipients, lipids, sugars, surfactants, and non-UV-active impurities</li></ul>

Thermo Scientific Transcend Multichannel UHPLC Systems

Thermo Scientific Transcend Multichannel UHPLC Systems are advanced LC-MS systems with a multichannel UHPLC architecture that increase analytical productivity and maximize mass spectrometer utilization without compromising data quality.

Thermo Scientific™ Transcend™ Multichannel UHPLC Systems are advanced LC-MS platforms designed for laboratories that demand higher throughput, improved efficiency, and stronger return on investment. Their multichannel UHPLC architecture connects up to four fully independent LC channels to a single mass spectrometer, dramatically increasing system utilization without compromising data quality.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_8_5f824e5e08.jpg" alt="Thermo Scientific™ Transcend™ Multichannel UHPLC Systems: The Transcend LX systems feature either 2 or 4 (shown) completely independent LC channels." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_8_5f824e5e08.jpg 245w," sizes="100vw" width="955" height="404"><h3>Key benefits</h3><ul><li>Significantly increased LC-MS throughput</li><li>Maximized mass spectrometer utilization</li><li>Maintained sensitivity, selectivity, and robustness</li><li>Reduced operating costs and analysis time</li><li>Scalable configurations tailored to laboratory needs</li></ul><h3>Multichannel UHPLC architecture</h3>Conventional single-channel LC-MS systems process samples sequentially, leaving the mass spectrometer idle during injection, column washing, and equilibration. Transcend systems overcome this limitation by intelligently interleaving injections from multiple LC channels, delivering data to the mass spectrometer only during relevant retention time windows and enabling substantial productivity gains.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_5_ab4093366d.jpg" alt="Thermo Scientific™ Transcend™ Multichannel UHPLC Systems: Injections are interleaved to maximize throughput and mass spectrometer use." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_5_ab4093366d.jpg 169w," sizes="100vw" width="831" height="764"><h3>Vanquish UHPLC platform</h3>Thermo Scientific™ Transcend™ Multichannel UHPLC Systems are built on proven <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products?category=40&amp;manufacturerItems=3&amp;search=vanquish">Thermo Scientific Vanquish UHPLC</a> technology. The Transcend multichannel architecture integrates up to four independent Vanquish-based UHPLC channels into a single LC-MS platform.The Vanquish UHPLC platform provides:<ul><li>high mechanical and operational robustness</li><li>reproducible long-term performance</li><li>precise gradient formation and stable flow control suitable for multichannel operation</li><li>flexible pump configurations (binary or quaternary) tailored to application requirements</li></ul>By combining the Transcend multichannel concept with Vanquish UHPLC technology, laboratories can achieve high throughput without compromising chromatographic performance, sensitivity, or system reliability.<h3>System configurations</h3><ul><li>Transcend LX and VLX Designed for high-throughput LC-MS workflows without on-line sample cleanup<ul><li>2- and 4-channel configurations</li><li>Fully independent LC channels</li></ul></li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_1567f69a93.jpg" alt="Thermo Scientific™ Transcend™ Multichannel UHPLC Systems: Transcend LX UHPLC Systems" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_1567f69a93.jpg 245w," sizes="100vw" width="968" height="500"><ul><li>Transcend TLX Designed for workflows requiring automated on-line sample cleanup<ul><li>1-, 2-, and 4-channel configurations</li><li>Integrated TurboFlow™ technology</li></ul></li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_2_8ac2e32016.jpg" alt="Thermo Scientific™ Transcend™ Multichannel UHPLC Systems: Transcend TLX UHPLC Systems" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_2_8ac2e32016.jpg 245w," sizes="100vw" width="1674" height="523">Each LC channel operates independently, allowing identical methods to run in parallel or multiple methods to be combined within a single system.<h3>On-line sample cleanup with TurboFlow™ technology (TLX)</h3>TurboFlow™ technology enables rapid on-line removal of matrix interferences directly within the LC-MS system, resulting in:<ul><li>Reduced or eliminated manual sample preparation</li><li>Direct injection of complex biological and environmental samples</li><li>Improved sensitivity and reproducibility</li><li>Increased method robustness and simplified workflows</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_3_efccaa3928.jpg" alt="Thermo Scientific™ Transcend™ Multichannel UHPLC Systems: On-line sample cleanup with TurboFlow™ technology (TLX)." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_3_efccaa3928.jpg 245w," sizes="100vw" width="1105" height="556"><h3>System control and software</h3>All system functions are managed by Thermo Scientific™ Aria™ MX software, providing:<ul><li>Control of pumps, valves, gradients, and injection scheduling</li><li>Intuitive multichannel method setup</li><li>Parallel execution of up to four methods</li><li>A user-friendly graphical interface for complex LC-MS workflows</li></ul>Aria MX software is fully compatible with <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/1758">Thermo Scientific™ Xcalibur™</a> and <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products/77">Thermo Scientific™ TraceFinder™</a> software.<h3>Mass spectrometer compatibility</h3>Transcend systems are designed as a flexible LC-MS platform compatible with a broad range of Thermo Fisher Scientific mass spectrometers, including:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products?category=20&amp;manufacturerItems=3&amp;search=tsq">TSQ triple quadrupole systems</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/products?category=134&amp;manufacturerItems=3&amp;search=orbitrap">High-resolution Orbitrap instruments</a></li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_4_fc2c09672b.jpg" alt="Thermo Scientific™ Transcend™ Multichannel UHPLC Systems: Transcend TLX-2 system with a TSQ Altis Plus triple quadrupole mass spectrometer." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_4_fc2c09672b.jpg 245w," sizes="100vw" width="1178" height="646"><h3>Typical application areas</h3><ul><li>Clinical research and bioanalysis</li><li>Pharmaceutical development and quality control</li><li>Toxicology</li><li>Environmental analysis</li><li>High-throughput screening workflows</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_6_db70763211.jpg" alt="Thermo Scientific™ Transcend™ Multichannel UHPLC Systems: Retention time (A) and peak area (B) reproducibility of a high-throughput targeted proteomics assay for quantifying SARS-CoV-2 peptides in clinical research samples across five days. The Transcend TLX-4 UHPLC system was used for on-line sample clean-up and analysis of 500 respiratory tract swab samples per day. (Cardozo, K.H.M., Lebkuchen, A., Okai, G.G. et al. Establishing a mass spectrometry-based system for rapid detection of SARS-CoV-2 in large clinical sample cohorts. Nat Commun 11, 6201 (2020))" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Scientific_Transcend_Multichannel_UHPLC_Systems_6_db70763211.jpg 245w," sizes="100vw" width="1489" height="862">

KNAUER AZURA HTQC UHPLC System

KNAUER AZURA HTQC UHPLC (1240 bar) enables high-throughput QC with parallel analysis and column re-equilibration for faster workflows.

The KNAUER AZURA HTQC UHPLC (1240 bar) is a high-performance UHPLC system designed for high-throughput quality control (QC) where speed, robustness, and reproducibility are essential.The system features a unique concept of parallel analysis and offline column re-equilibration, significantly increasing productivity. With two gradient pumps, one column performs the analytical run while the second is re-equilibrated in backflush mode.This architecture enables:<ul><li>≥30% reduction in cycle time</li><li>increased sample throughput</li><li>column protection from matrix contamination</li><li>consistent retention times</li></ul>It is ideal for pharmaceutical QC laboratories requiring automation and validated workflows.<h4>Key Features</h4><ul><li>UHPLC system up to 1240 bar (124 MPa)</li><li>Dual gradient pumps (HPG + LPG)</li><li>Parallel analysis and column re-equilibration</li><li>Backflush mode for column protection</li><li>≥30% faster analysis cycles</li><li>High flow reproducibility</li><li>Autosampler with cooling</li><li>Column thermostat (Peltier)</li><li>Fully automated modular system</li><li>MS detector compatibility</li></ul><h4>System Configuration</h4>Included components:<ul><li>Eluent tray E 2.1L</li><li>Pump P 8.1L (HPG)</li><li>Pump P 6.1L (LPG)</li><li>Liquid handler LH 8.1 + Robotic Cooler</li><li>Column thermostat CT 2.1</li><li>Column switching &amp; backflush valve</li><li>Accessories and tools</li></ul><h3>Technical Specifications</h3><h4>Pumps</h4><h5>P 8.1L (HPG – analytical pump):</h5><ul><li>Max pressure: 1240 bar</li><li>Flow rate: up to 5 mL/min</li><li>Adaptive pulsation compensation</li><li>Degasser + binary solvent selection</li><li>Low baseline noise</li></ul><h5>P 6.1L (LPG – re-equilibration):</h5><ul><li>Quaternary gradient</li><li>Integrated degasser</li><li>Low dwell volume</li><li>Inline filter</li></ul><h4>Autosampler</h4><h5>LH 8.1:</h5><ul><li>XYZ autosampler</li><li>Capacity: up to 390 samples</li><li>Temperature: 4–40 °C</li><li>Low carryover</li></ul><h4>Column Thermostat</h4><h5>CT 2.1:</h5><ul><li>Peltier controlled</li><li>Above and below ambient operation</li><li>High precision</li></ul><h4>Valve System</h4><ul><li>Column switching + backflush</li><li>Up to 1200 bar</li><li>Parallel column operation</li></ul><h4>Detection</h4><ul><li>Compatible with all HPLC detectors</li><li>Ideal for LC-MS coupling</li></ul><h4>HTQC Concept</h4><ul><li>Independent flow paths (analysis vs re-equilibration)</li><li>Backflush re-equilibration</li><li>Parallel operation</li><li>Increased throughput without compromise</li></ul><h4>Typical Applications</h4><ul><li>Pharmaceutical QC</li><li>Routine validated workflows</li><li>High sample throughput environments</li><li>Reversed-phase HPLC</li></ul>

KNAUER High Precision AZURA P 6.1L HPLC Pump

KNAUER AZURA P 6.1L HPLC pump with up to 1000 bar, precise gradient control, and low pulsation for reliable UHPLC workflows.

The KNAUER AZURA P 6.1L is a high-precision analytical HPLC pump designed for accurate and reproducible solvent delivery in both HPLC and UHPLC applications.The pump combines essential features of a modern pumping system, including low pulsation, high pressure capability, precise gradient formation, and flexible configuration. It is available in both HPG (high-pressure gradient) and LPG (low-pressure gradient) versions, with a flow range up to 50 mL/min.The system uses a dual serial piston mechanism with active pulsation compensation, ensuring excellent flow stability under all conditions. A low-dead-volume microfluidic mixer enables efficient and precise solvent mixing.Different pump heads are available:<ul><li>up to 10 mL/min at 862 bar</li><li>up to 5 mL/min at 1000 bar</li></ul>Optional configurations include biocompatible materials (PEEK, ceramic, titanium) and specialized setups for normal phase applications (e.g., hexane, heptane).<h4>Key Features</h4><ul><li>High-precision analytical HPLC/UHPLC pump</li><li>Pressure up to 1000 bar</li><li>Flow rates up to 50 mL/min</li><li>Dual piston system with low pulsation</li><li>Active pulsation compensation</li><li>HPG and LPG gradient configurations</li><li>Microfluidic mixer (50–600 µl)</li><li>RFID pump head detection</li><li>Optional degasser</li><li>Biocompatible configurations available</li><li>Robust operation with demanding solvents</li></ul><h3>Technical Specifications</h3><h4>Solvent Delivery</h4><ul><li>Pump type: analytical HPLC pump</li><li>Mechanism: dual serial piston</li><li>Flow range: 0.001 – 50 mL/min</li><li>Max pressure: up to 1000 bar</li><li>Flow accuracy: ± 0.25%</li><li>Precision: ≤ 0.04% RSD</li></ul><h4>Gradient</h4><ul><li>Range: 0–100% (0.1% steps)</li><li>HPG accuracy: ± 0.3%</li><li>HPG precision: &lt; 0.1% RSD</li><li>LPG accuracy: ± 0.3% to ± 2%</li><li>LPG precision: &lt; 0.5% RSD</li></ul><h4>Mixing</h4><ul><li>Microfluidic mixer</li><li>Volumes: 50 / 100 / 200 / 400 / 600 µl</li><li>Low dead volume</li></ul><h4>Degasser (optional)</h4><ul><li>2–4 channels</li><li>Max flow: 10 mL/min per channel</li><li>Residual O₂: &lt; 0.5 ppm</li><li>Membrane: fluoropolymer</li></ul><h4>Materials</h4><ul><li>PEEK, Tefzel®, Systec AF</li><li>Optional biocompatible materials (titanium, ceramic)</li></ul><h4>Control &amp; Communication</h4><ul><li>LAN, analog inputs</li><li>Event outputs (TTL, relay)</li><li>Optional mobile control</li><li>RFID pump head detection</li></ul><h4>Operating Conditions</h4><ul><li>Temperature: 4–40 °C</li><li>Humidity: &lt; 90% non-condensing</li></ul><h4>Dimensions &amp; Power</h4><ul><li>Dimensions: 361 × 208 × 523 mm</li><li>Weight: 14.1 kg</li><li>Power supply: 100–240 V, 50–60 Hz</li><li>Power consumption: max 100 W</li></ul>

KNAUER High Precision AZURA P 8.1L UHPLC Pump

KNAUER AZURA P 8.1L UHPLC pump with up to 1240 bar, adaptive pulsation compensation, and high precision for demanding UHPLC applications.

The KNAUER AZURA P 8.1L is a high-performance UHPLC pump designed for ultra-fast and high-resolution chromatographic applications. With a maximum pressure of 1240 bar (124 MPa) and flow rates up to 5 mL/min, it meets the demands of modern UHPLC workflows.The pump features a dual serial piston mechanism combined with adaptive pulsation compensation, which operates independently of flow rate, pressure, and solvent type through real-time monitoring of eluent compressibility and variable piston stroke.Together with KNAUER’s advanced piston drive technology, this results in exceptional flow reproducibility under all operating conditions. High-precision in-house manufacturing ensures long piston seal lifetime and maximum system uptime.<h4>Key Features</h4><ul><li>UHPLC pump up to 1240 bar</li><li>Flow rates up to 5 mL/min</li><li>Dual serial piston system</li><li>Adaptive pulsation compensation</li><li>Excellent flow reproducibility</li><li>HPG gradient capability</li><li>Integrated 4-channel degasser</li><li>RFID pump head detection</li><li>Low baseline noise</li><li>High durability and long lifetime</li><li>Compatible with UHPLC and LC-MS systems</li></ul><h3>Technical Specifications</h3><h4>Solvent Delivery</h4><ul><li>Pump type: analytical UHPLC pump</li><li>Mechanism: dual serial piston</li><li>Max pressure: 1240 bar</li><li>Flow rate: up to 5 mL/min</li><li>Flow accuracy: ± 0.25%</li><li>Precision: ≤ 0.04% RSD</li></ul><h4>Gradient</h4><ul><li>Type: HPG (high-pressure gradient)</li><li>Range: 0–100% (0.1% steps)</li><li>Accuracy: ± 0.3%</li><li>Precision: &lt; 0.1% RSD</li></ul><h4>Degasser</h4><ul><li>Channels: 4</li><li>Max flow: 5 mL/min per channel</li><li>Residual O₂: &lt; 0.5 ppm</li><li>Technology: fluoropolymer membrane</li></ul><h4>Connections</h4><ul><li>Inlet: UNF 1/4-28 (1/8” tubing)</li><li>Outlet: UNF 10-32 (1/16” capillary)</li></ul><h4>Materials</h4><ul><li>PEEK, Tefzel®, Systec AF</li><li>Compatible with most solvents (except HCl and halogenated hydrocarbons)</li></ul><h4>Control &amp; Communication</h4><ul><li>LAN, analog inputs</li><li>Event outputs (TTL, relay)</li><li>Optional mobile control</li><li>RFID pump head detection</li></ul><h4>Safety &amp; Operating Conditions</h4><ul><li>Leak sensor</li><li>Soft start and programmable pressure limits</li><li>Temperature: 4–40 °C</li><li>Humidity: &lt; 90% non-condensing</li></ul><h4>Dimensions &amp; Power</h4><ul><li>Dimensions: 361 × 208 × 523 mm</li><li>Weight: 26.7 kg</li><li>Power supply: 100–240 V, 50–60 Hz</li><li>Power consumption: max 310 W</li></ul>

KNAUER AZURA Autosampler AS 6.1L

KNAUER AZURA AS 6.1L autosampler with up to 768 samples, ultra-low carryover, and fast injection cycles for HPLC/UHPLC workflows.

The KNAUER AZURA® AS 6.1L is a high-performance autosampler designed for automated sample injection in HPLC/UHPLC systems, offering high capacity, precision, and flexibility for both routine and high-throughput applications.The autosampler supports:<ul><li>up to 768 sample positions (microtiter plates)</li><li>up to 108 standard 1.5 mL vials</li></ul>A highly effective internal and external needle wash system minimizes carryover to extremely low levels. The system is also fast, with a complete injection cycle taking less than one minute, including needle washing.Three injection modes are supported:<ul><li>full loop filling (highest precision)</li><li>partial loop filling (variable volumes)</li><li>µl pickup (loss-free injection of small volumes)</li></ul>The integrated ILD™ (Intermediate Loop Decompression) valve ensures accurate high-pressure injections without sample dilution and reduces pressure spikes, protecting the column.<h4>Key Features</h4><ul><li>Autosampler for HPLC/UHPLC systems</li><li>Up to 768 sample positions</li><li>Up to 108 vials (1.5 mL)</li><li>Ultra-low carryover (&lt; 0.0003%)</li><li>Fast injection cycle (&lt; 1 min)</li><li>3 injection modes (full loop, partial loop, µl pickup)</li><li>ILD™ technology for high-pressure injection</li><li>PASA™ (pressure-assisted sample aspiration)</li><li>Optional sample cooling (4–40 °C)</li><li>Missing vial/plate detection</li><li>Supports precolumn derivatization</li></ul><h3>Technical Specifications</h3><h4>Sample Injection</h4><ul><li>Injection volume range: 0.1 µl – 10 mL</li><li>Precision:<ul><li>Full loop: &lt; 0.3% RSD</li><li>Partial loop: &lt; 0.5% RSD</li><li>µl pickup: &lt; 1.0% RSD</li></ul></li><li>Accuracy: 0.2 µl (250 µl syringe)</li></ul><h4>Performance</h4><ul><li>Carryover:<ul><li>&lt; 0.0015% (standard)</li><li>&lt; 0.0003% (extended wash)</li></ul></li><li>Injections per vial: max. 9</li><li>Cycle time:<ul><li>7 s (same vial)</li><li>14 s (different vials)</li><li>&lt; 60 s total</li></ul></li></ul><h4>Capacity &amp; Compatibility</h4><ul><li>Microtiter plates: ANSI SLAS standard</li><li>Max vial/plate height: 47 mm</li></ul><h4>Additional Features</h4><ul><li>Headspace pressure (bubble prevention)</li><li>Precolumn derivatization</li><li>Sample tray cooling (optional, 4–40 °C)</li><li>Vial detection sensor</li></ul><h4>Materials</h4><ul><li>ETFE, PTFE, stainless steel, glass, Vespel</li><li>Wide chemical compatibility</li></ul><h4>Control &amp; Communication</h4><ul><li>LAN / Ethernet</li><li>Analog inputs</li><li>TTL inputs (start, stop, freeze)</li><li>Relay output (alarm, marker)</li></ul><h4>Operating Conditions</h4><ul><li>Temperature: 10–40 °C</li><li>Humidity: 20–80%</li></ul>

KNAUER AZURA CT 2.1 Column Thermostat

KNAUER AZURA CT 2.1 column thermostat with Peltier control (5–85 °C), high stability, and optional eluent pre-heating for precise HPLC separations.

The KNAUER AZURA CT 2.1 is a cost-effective column thermostat designed for precise and stable temperature control in HPLC applications.The instrument uses a microprocessor-controlled Peltier element, enabling both heating and cooling in the range of 5–85 °C. Its high temperature stability allows for programming linear and non-linear temperature gradients, improving separation performance.For advanced applications, the system can be optionally equipped with an eluent pre-heating cartridge, ensuring consistent temperature conditions, improved selectivity, and better peak shapes.Its compact design supports flexible integration and accommodates multiple columns.<h4>Key Features</h4><ul><li>Column thermostat for HPLC applications</li><li>Temperature range 5–85 °C</li><li>Peltier technology (heating and cooling)</li><li>High temperature stability (±0.1 °C)</li><li>Accurate temperature control (±0.2 °C)</li><li>Programmable temperature gradients</li><li>Optional eluent pre-heating</li><li>Supports multiple columns</li><li>Compact and robust design</li><li>Built-in safety features</li></ul><h3>Technical Specifications</h3><h4>Thermostatting</h4><ul><li>Technology: Peltier (heating &amp; cooling)</li><li>Temperature range: 5–85 °C</li><li>Heating/cooling rate: 2 °C/min</li><li>Accuracy: ± 0.2 °C</li><li>Stability: ± 0.1 °C</li><li>Air circulation: fan-assisted bidirectional flow</li></ul><h4>Column Compartment</h4><ul><li>Max number of columns: up to 8</li><li>Max length: 325 mm</li><li>Max diameter: 35 mm</li><li>Compatibility:<ul><li>125 mm × 4.6 mm ID (with precolumn)</li><li>300 mm × 4.6 mm ID</li><li>300 mm × 16 mm ID</li></ul></li></ul><h4>Internal Dimensions</h4><ul><li>90 × 390 × 47 mm</li></ul><h4>Safety</h4><ul><li>Self-check and auto-calibration at startup</li><li>Adjustable shut-off temperature</li><li>Leak sensor with acoustic alarm</li></ul><h4>Control &amp; Communication</h4><ul><li>LAN interface</li><li>Optional Mobile Control (stand-alone operation)</li></ul><h4>Power &amp; Dimensions</h4><ul><li>Power supply: 90–230 V, 50–60 Hz</li><li>Power consumption: 100 W</li><li>Dimensions: 150 × 470 × 310 mm</li><li>Weight: 8.4 kg</li></ul><h4>Optional Accessories</h4><ul><li>Eluent pre-heating cartridge<ul><li>for capillaries 0.1 mm / 0.18 mm ID</li></ul></li></ul>

KNAUER AZURA Valve Unifier VU 4.1

KNAUER AZURA VU 4.1 valve drive enables fast automated valve switching with RFID identification for HPLC/UHPLC systems.

The KNAUER AZURA VU 4.1 Valve Unifier is a compact valve drive unit designed for automated valve switching in HPLC/UHPLC systems. It enables precise and fast control of liquid flow paths, which is essential for applications such as column switching, sample injection, eluent selection, and fractionation.Due to its ultra-fast switching speed, the flow path is interrupted only briefly, significantly reducing pressure spikes and improving system stability.The device uses RFID technology for automatic valve identification, ensuring easy and error-free valve exchange. Integrated GLP data monitoring simplifies maintenance tasks such as rotor seal replacement.The unit can be operated:<ul><li>stand-alone via display</li><li>via software</li><li>through LAN or analog I/O</li></ul>This makes it easy to integrate into almost any LC system.<h4>Key Features</h4><ul><li>Universal valve drive for &gt;40 valve types</li><li>Ultra-fast switching (minimal pressure spikes)</li><li>RFID valve identification</li><li>GLP data monitoring for maintenance</li><li>Standalone operation via display</li><li>Integration into LC systems (LAN, analog, software)</li><li>Compact design</li><li>Easy maintenance and valve exchange</li><li>Flexible use in LC and industrial applications</li></ul><h3>Technical Specifications</h3><h4>Communication &amp; Control</h4><ul><li>Interfaces: LAN, display, terminal strip</li><li>Control:<ul><li>display (stand-alone)</li><li>software</li><li>event control</li></ul></li><li>Inputs:<ul><li>Home</li><li>Backward/Inject</li><li>Forward/Load</li><li>Start</li></ul></li><li>Outputs:<ul><li>Trigger out</li><li>Event output</li></ul></li></ul><h4>Performance &amp; Features</h4><ul><li>Ultra-fast valve switching</li><li>Reduced pressure peaks</li><li>Supports &gt;40 valve types</li><li>RFID valve recognition</li><li>GLP maintenance tracking</li></ul><h4>Operating Conditions</h4><ul><li>Temperature: 4–40 °C</li><li>Humidity: &lt; 90% non-condensing</li></ul><h4>Power &amp; Dimensions</h4><ul><li>Power supply: external 24 V DC</li><li>Power consumption: 65 W</li><li>Dimensions: 80 × 123 × 192 mm</li><li>Weight: 1.9 kg</li></ul><h4>Typical Applications</h4><ul><li>Column switching</li><li>Eluent selection</li><li>Sample injection</li><li>Fraction collection</li><li>LC workflow automation</li><li>Dosing systems in chemical industry</li></ul>

KNAUER AZURA DAD 2.1L Diode Array Detector

KNAUER AZURA® DAD 2.1L is a high-performance diode array detector for HPLC/UHPLC featuring 190–700 nm coverage, LightGuide technology, low drift, and up to 100 Hz data acquisition.

The KNAUER AZURA® DAD 2.1L is a high-performance diode array detector designed for analytical, semi-preparative, and preparative liquid chromatography applications. Combining advanced optical technology, excellent sensitivity, and intuitive operation, the detector offers an affordable solution for demanding HPLC and UHPLC workflows.The detector features a newly developed optical system and intelligent temperature management that ensure maximum sensitivity while minimizing baseline drift. Optional LightGuide flow cells based on total internal reflection technology maximize light throughput and minimize peak dispersion, resulting in superior signal-to-noise performance. An optional fiber-optic adapter allows physical separation of the flow cell from the detector, enhancing safety when handling hazardous, explosive, or toxic compounds.<h3>Key Features</h3><ul><li>High-performance diode array detector for HPLC and UHPLC</li><li>Wavelength range from 190 to 700 nm</li><li>256-diode array with 2 nm pixel pitch</li><li>Advanced optical system with optimized temperature management</li><li>LightGuide flow cell technology for enhanced signal-to-noise ratio</li><li>Wide selection of interchangeable 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, tool-free lamp replacement</li><li>Compatible with ClarityChrom®, OpenLAB®, Chromeleon™, PurityChrom®, and Mobile Control</li><li>LAN and analog connectivity for easy integration into virtually any LC system</li></ul><h3>Technical Specifications</h3><h4>Detection System</h4><ul><li>Detector type: Diode Array Detector (DAD)</li><li>Number of diodes: 256</li><li>Pixel pitch: 2 nm per diode</li><li>Detection channels:<ul><li>8 digital channels</li><li>4 analog channels</li></ul></li><li>Light source: Deuterium lamp with integrated GLP chip</li><li>Wavelength range: 190–700 nm</li><li>Spectral resolution: &lt;10 nm (FWHM)</li><li>Slit width: 7.0 nm</li><li>Wavelength accuracy: ±1 nm</li><li>Wavelength repeatability: ±0.1 nm</li></ul><h4>Performance</h4><ul><li>Noise: ±5 µAU at 254 nm</li><li>Drift: 400 µAU/h at 254 nm</li><li>Linearity: &gt;2.0 AU at 274 nm</li><li>Maximum data rate:<ul><li>100 Hz via LAN</li><li>12.5 Hz via analog output</li></ul></li></ul><h4>Flow Cells</h4><ul><li>Flow cells are not included and must be ordered separately</li><li>Stainless steel and bio-inert configurations available</li><li>Optional LightGuide total-reflection technology</li></ul><h4>Control and Communication</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 control through chromatography data systems</li></ul><h4>GLP Functions</h4><ul><li>Lamp identification</li><li>Lamp operating hours</li><li>Lamp ignition count</li><li>Comprehensive GLP reporting</li></ul><h4>Power and Dimensions</h4><ul><li>Power supply: 100–240 V, 50–60 Hz</li><li>Power consumption: 75 W</li><li>Dimensions (W × H × D): 361 × 158 × 523 mm</li><li>Weight: 12.2 kg</li></ul>

KNAUER AZURA DAD 6.1L Diode Array Detector

KNAUER AZURA® DAD 6.1L is a premium diode array detector with 190–1000 nm coverage, 1024-diode array, Polka-Dot optics, and LightGuide technology for maximum sensitivity.

The KNAUER AZURA® DAD 6.1L is a high-end diode array detector designed for analytical, semi-preparative, preparative, and process liquid chromatography applications. Featuring an extended wavelength range of 190–1000 nm, KNAUER Polka-Dot optical technology, and a 1024-diode array, it delivers exceptional sensitivity, spectral resolution, and baseline stability.The detector combines a high-brightness deuterium lamp and tungsten-halogen lamp to provide seamless UV and visible light detection. Optional LightGuide flow cells based on total internal reflection technology maximize light throughput while minimizing peak dispersion. An optional fiber-optic adapter enables physical separation of the flow cell from the detector, increasing safety when working with hazardous, explosive, or toxic compounds and protecting the detector from potential leaks at high flow rates.<h3>Key Features</h3><ul><li>High-end diode array detector for HPLC, UHPLC, and process chromatography</li><li>Extended wavelength range from 190 to 1000 nm</li><li>1024-diode array with 0.8 nm pixel pitch</li><li>KNAUER Polka-Dot optical technology for maximum sensitivity</li><li>LightGuide flow cell technology for superior signal-to-noise ratio</li><li>Wide range of analytical, semi-preparative, and preparative flow cells</li><li>Optional fiber-optic adapter for remote flow cell positioning</li><li>High-brightness deuterium and halogen lamps</li><li>Internal holmium filter for wavelength verification</li><li>Integrated leak sensor</li><li>Front-access lamp replacement</li><li>Compatible with ClarityChrom®, OpenLAB®, Chromeleon™, PurityChrom®, and Mobile Control</li><li>Suitable for both laboratory and process applications</li></ul><h3>Technical Specifications</h3><h4>Detection System</h4><ul><li>Detector type: Diode Array Detector (DAD)</li><li>Number of diodes: 1024</li><li>Pixel pitch: 0.8 nm per diode</li><li>Detection channels:<ul><li>8 digital channels</li><li>4 analog channels</li></ul></li><li>Light source:<ul><li>High-brightness deuterium lamp</li><li>Tungsten-halogen lamp</li></ul></li><li>Wavelength range: 190–1000 nm</li><li>Spectral resolution: &lt;3.5 nm (FWHM)</li><li>Slit width: 2.5 nm</li><li>Wavelength accuracy: ±1 nm</li><li>Wavelength repeatability: ±0.1 nm</li></ul><h4>Performance</h4><ul><li>Noise: ±3.5 µAU at 254 nm</li><li>Drift: 300 µAU/h at 254 nm</li><li>Linearity: &gt;2.5 AU at 274 nm</li><li>Maximum data rate:<ul><li>100 Hz via LAN</li><li>12.5 Hz via analog output</li></ul></li></ul><h4>Flow Cells</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>Control and Communication</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>GLP Functions</h4><ul><li>Lamp identification</li><li>Lamp operating hours</li><li>Lamp ignition count</li><li>Comprehensive GLP reporting</li></ul><h4>Power and Dimensions</h4><ul><li>Power supply: 100–240 V, 50–60 Hz</li><li>Power consumption: 75 W</li><li>Dimensions (W × H × D): 361 × 158 × 523 mm</li><li>Weight: 13.8 kg</li></ul>

Products focused on HPLC - page 14

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