<p><strong>Although modern agriculture needs to be based on accurate real-time data on soil, plant, and environmental conditions, affordable, sufficiently sensitive, and robust monitoring devices for this purpose are currently missing. According to scientists, low-cost sensors based on new smart materials and printing technologies offer a suitable solution. The results of multidisciplinary research thus far and proposals for the development of these devices have been presented by researchers from Czechia, Great Britain, Spain, and the USA in a review article in the prestigious journal </strong><a target="_blank" rel="noopener noreferrer" href="https://www.nature.com/articles/s41467-026-68778-6#Abs1"><i><strong>Nature Communications</strong></i></a><strong>.</strong></p><p>“<i>Sensor technologies for monitoring plant health are still in their infancy. Only simple sensors capable of monitoring basic parameters such as pH, soil moisture, or temperature are commonly available on the market. However, if farmers are to face current challenges, including climate change, and ensure sufficient food for humanity, they need much more effective tools that will enable them to monitor, for example, various pathogens, including bacteria and fungi. In our opinion, a suitable solution is a combination of new smart materials and printing for the production of inexpensive, durable, and scalable materials</i>,” said the article’s first author, <strong>David Panáček</strong> from CATRIN, who worked on the study during his internship at Imperial College London.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CATRIN_Soucasne_senzory_nestaci_Vedci_navrhuji_novou_cestu_ke_sledovani_zdravi_rostlin_b4014952a3.jpg" alt="CATRIN: David Panáček" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CATRIN_Soucasne_senzory_nestaci_Vedci_navrhuji_novou_cestu_ke_sledovani_zdravi_rostlin_b4014952a3.jpg 208w," sizes="100vw" width="1536" height="1152"></p><p>Sensors for monitoring plant health, for example, lag behind similar devices used in human medicine. According to the authors, advances in materials science, which will enable the development of scalable sensor technologies, play a key role in this potential shift. “<i>Printing techniques, including inkjet printing, screen printing, aerosol printing, 3D printing, and direct laser writing, offer flexible ways to produce flexible sensors, large-area sensors, and sensors integrated directly into plants. The review article summarizes recent advances in printable low-dimensional materials for agricultural sensors, analyzes their physico-chemical properties in relation to sensor performance, and discusses key challenges and future opportunities requiring interdisciplinary integration</i>,” said one of the corresponding authors, <strong>Michal Otyepka</strong>.</p><p>The research brought together materials scientists, chemists, biologists, sensing experts, and printing technology specialists. Materials research and the use of graphene-based smart materials were led by scientists from CATRIN at Palacký University and VŠB-Technical University of Ostrava. Plant biologists from CATRIN contributed their knowledge of plant development, their responses to stress conditions, and the monitoring of their properties. Researchers from Imperial College London took care of the electronics, while representatives from<a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/companies/36"><strong> CEITEC – VUT</strong></a> focused on printing technologies. The team also included leading experts in sensing from the Catalan Institute of Nanoscience and Nanotechnology in Barcelona, and Joseph Wang of the University of California San Diego, the “father of sensing and electrochemistry,” also contributed his extensive knowledge.</p><p>“<i>This is a groundbreaking study on this topic, which has managed to attract some truly big names in their respective fields. Last but not least, the study demonstrates that interdisciplinarity at CATRIN gives rise to completely new and promising research topics, such as plant sensing and its use for studying plant-environment interactions and smart agriculture,</i>” added another corresponding author, <strong>Nuria De Diego</strong>.</p>

Current sensors are not good enough. Scientists propose a new way to monitor plant health

<p><strong>In the week of February 16, the following webinars await you in the field of gas / solid phase and especially Raman, FTIR, GC and GC/MS.</strong></p><blockquote><h4><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinars"><strong>👉 DETAILS AND REGISTRATION IN THE WEBINARS SECTION</strong></a></h4><p><strong>👉 Search and filter in the largest global database</strong> with over <strong>5 000 GC, LC, MS and spectroscopy webinars</strong>.</p></blockquote><div><div><div><div><div><div><h5><strong>1. Agilent Technologies: Small Size, Big Impact – High-Performance Benchtop GC and GC/MS with the Agilent 8850 GC</strong></h5><ul><li>Tu, 17.2.2026 17:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5723">Registration</a></li></ul><p>Discover how the Agilent 8850 GC, compatible with single and triple quadrupole MS, reduces bench space, utilities, and run time while delivering high-performance GC and GC/MS analysis.</p><h5><strong>2. Wasson-ECE Instrumentation: Dynamic Blender</strong></h5><ul><li>Tu, 17.2.2026 21:30 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5745">Registration</a></li></ul><p>Learn how the Dynamic Blender dilutes standards with carrier gas to generate accurate multi-point calibrations from single gas cylinders.</p><h5><strong>3. Waters Corporation: Ask Me Anything About Managing Computerized System Risks to Data Integrity</strong></h5><ul><li>Th, 19.2.2026 17:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5809">Registration</a></li></ul><p>Learn practical strategies for managing computerized system risks in regulated laboratories to protect data integrity, ensure compliance, and avoid regulatory findings.</p></div></div></div></div></div></div>

Webinars LabRulezGCMS Week 08/2026

<p><strong>This laboratory experiment introduces undergraduate chemistry students to headspace GC–MS through a forensic toxicology framework. Students analyze common volatile compounds such as ethanol, isopropanol, acetone, and 1,1-difluoroethane while learning key concepts in gas chromatography, mass spectrometry, calibration, and data evaluation.</strong></p><p>Participants prepare calibrators and controls, quantify ethanol, and assess qualitative analytes in a simulated vitreous humor sample using objective acceptance criteria. Implemented over three semesters with a &gt;92% success rate, the experiment is adaptable to different course levels and resources. Headspace GC–MS offers additional advantages, including minimal sample preparation and reduced instrument maintenance.</p><blockquote><h4><strong>The original article</strong></h4><h4><a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jchemed.5c00118"><strong>Introducing Headspace Gas Chromatography–Mass Spectrometry to Undergraduate Chemistry Students from a Forensic Toxicology Perspective</strong></a></h4><p>Devin C. Baer, and Michele M. Crosby*</p><p>J. Chem. Educ. 2026, 103, 1, 441–448</p><p><a target="_blank" rel="noopener noreferrer" href="https://doi.org/10.1021/acs.jchemed.5c00118">https://doi.org/10.1021/acs.jchemed.5c00118</a></p><h6>licensed under <a target="_blank" rel="noopener noreferrer" href="https://creativecommons.org/licenses/by/4.0/"><strong>CC-BY 4.0</strong></a></h6></blockquote><p><strong>Selected sections from the article follow. Formats and hyperlinks were adapted from the original.</strong></p><div><p>Gas chromatography–mass spectrometry (GC-MS) is widely used across chemistry disciplines, from analysis of biodiesel feedstocks to pesticides residues in vegetables and even two-dimensional GC (GC × GC) such as GC × GC time-of-flight mass spectrometry (GC × GC-TOFMS) in forensic science applications. <a href="javascript:void(0);">(4−6)</a> The two-dimensional GC of the GC × GC-TOFMS can provide more optimized separation of analytes compared to one-dimensional GC and the time-of-flight (TOF) mass analyzer is an alternative to the quadrupole discussed earlier in this section. <a href="javascript:void(0);">(6)</a> In the environmental field, GC-MS can be used to detect pollutants related to microplastics and pesticide residues. <a href="javascript:void(0);">(7,8)</a> GC-MS and GC tandem mass spectrometry (GC-MS/MS) is useful in food safety and quality assurance because of its ability to detect contaminants and assess ingredient quality. <a href="javascript:void(0);">(9,10)</a> GC-MS, including GC × GC-TOFMS and GC-MS/MS, is used in characterization of coal-derived liquids and petroleum exploration. <a href="javascript:void(0);">(11,12)</a> In forensics, these types of instrumentation are used to identify residues, like fire accelerants, explosive residues, or drugs at a crime scene, and to identify drugs, poisons, or other substances in biological samples. <a href="javascript:void(0);">(1,6,13)</a> In summary, a fundamental understanding of GC-MS will lend itself tremendously to any potential career field or discipline that may interest an undergraduate chemistry student.</p><p>In one application of headspace GC-MS, an aliquot of the biological sample is diluted with an internal standard solution and placed in a sealed glass vial. <a href="javascript:void(0);">(1,14)</a> The internal standard solution is a saline-based solution that optimizes the evaporation (sometimes called “salting out”) of the volatile compounds into the headspace portion of the vial, and it contains a compound that is similar in chemical structure to the analyte(s) of interest, The glass vial is heated to separate the volatile compounds from the biological matrix, and a sample of the headspace vapor containing the volatile compound is taken. <a href="javascript:void(0);">(1,14)</a> The concentration of the volatile analyte in the dilute aqueous sample is directly proportional to the concentration of the volatile analyte in the gas phase, or headspace, above the liquid. <a href="javascript:void(0);">(14)</a> Internal standard solution is added to a sample to give an indication of the extraction quality and aids in the concentration determination. The same concentration of the internal standard is added to the calibrators, controls, and case samples in a batch. <a href="javascript:void(0);">(1)</a> The ratio of the analyte response to the internal standard response is the most important factor to consider, not the absolute value of the analyte, in determining the concentration (or the qualitative presence/absence) of the analytes. By using this ratio, students can account for differences in analyte responses due to variables like extraction recovery, matrix effects, and injection volume. <a href="javascript:void(0);">(1,2)</a></p><h4><strong>Relevance to Forensic Toxicology</strong></h4><p>Currently, very few published experiments exist for undergraduates involving forensic toxicology, <a href="javascript:void(0);">(15)</a> and even fewer involve volatile analysis. <a href="javascript:void(0);">(16)</a> Forensic toxicology laboratories routinely analyze samples for the presence of ethanol, methanol, acetone, and isopropanol. <a href="javascript:void(0);">(1)</a> Cases involving driving under the influence (DUI) and homicides are just a few examples targeted by these types of laboratories. <a href="javascript:void(0);">(1,17−20)</a> Ethanol, commonly referred to as alcohol, is the main type of alcohol found in alcoholic beverages and is considered the most commonly encountered substance in forensic toxicology casework. <a href="javascript:void(0);">(1)</a> In the U.S., most states have established a per-se limit for the blood alcohol concentration for drivers of 0.08 g/dL and violating this law could lead to prosecution for driving under the influence. Ethanol is also frequently encountered in post-mortem cases, such as homicides, traffic accidents, and alcohol poisonings. However, it is important to consider when interpreting ethanol concentrations that ethanol can be produced in the body after death by microorganisms breaking down the body. <a href="javascript:void(0);">(1)</a> Certain types of specimens collected after death, such as urine and vitreous humor (clear fluid inside the eye), are more resistant to this phenomenon and can be used to help determine antemortem ethanol consumption versus post-mortem production. <a href="javascript:void(0);">(1)</a> Isopropanol can be found in rubbing alcohol, so it is recommended that a different kind of antiseptic be used to clean the skin before a blood draw for a DUI. Isopropanol can also be found in various household cleaning products. It is also important in post-mortem forensic toxicology as it may be abused by chronic users or accidentally ingested. <a href="javascript:void(0);">(1,19,20)</a> Acetone is important as it is ta product of the metabolism of isopropanol, but it is also produced endogenously. High levels of acetone may be an indication of uncontrolled diabetes, so it is very important in post-mortem casework. <a href="javascript:void(0);">(1,20)</a> Methanol, sometimes known as wood alcohol, can be encountered in forensic toxicology casework, as it is found in improperly distilled alcoholic beverages and many household products. Methanol poisoning can be fatal due to the formation of the metabolite formaldehyde. Furthermore, methanol can be an artifact seen in embalmed specimens. <a href="javascript:void(0);">(1)</a></p><p>While forensic toxicology laboratories use headspace gas chromatography–flame ionization (GC-FID) detection more commonly for the quantitation of volatile compounds, headspace GC-MS is a gold standard for identifying and confirming other types of volatile compounds such as 1,1-difluoroethane (DFE). DFE is commonly found in keyboard cleaners and has the potential for abuse, which is why forensic toxicology laboratories need the ability to detect it. DFE has been detected in driving under the influence cases as it has become anabused inhalant, due to the cheap cost and ease of access. <a href="javascript:void(0);">(17,18)</a></p><p>The University of Tampa possesses a GC-MS equipped with a headspace autosampler; therefore, GC-MS was used rather than GC-FID for this experiment. Furthermore, GC-MS was strategically chosen to give students more practice with complicated data analysis provided by GC-MS in SIM mode. It is important to note that methanol was not chosen as a target for this experiment because of the difficulty in finding enough unique ions without interference from common environmental molecules.</p><h4><strong>Materials and Reagents</strong></h4><p>The following were purchased from Fisher (Hampton, NH): ethanol, acetone, and isopropanol. Endust for Electronics (Buffalo, NY) multi-purpose duster was used for the DFE standard. 20 mL headspace vials and caps were purchased from PerkinElmer (Waltham, MA). A DB-624 column (20 m × 0.18 mm × 1.00 μm) was purchased from Agilent (Santa Clara, CA). The instrument used in this experiment was an <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?mainauthorItems=10&amp;search=6890N"><strong>Agilent 6890N gas chromatograph</strong></a> and <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?mainauthorItems=10&amp;search=5973N"><strong>5973N mass spectrometer</strong></a> (operated in SIM mode) with a Gerstel MPS2 multipurpose autosampler (see <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jchemed.5c00118#tbl1">Table 1</a> for additional instrument parameters). Helium was used as a carrier gas. A 2.5 mL Hamilton CTC and LEAP technologies GC PAL autosampler syringe: gastight was used.</p><h4><strong>Results and Discussion</strong></h4><p>There was a total of 43 students enrolled in the course over 3 semesters with an average grade on the assignment of 83 ± 11%. As part of this assignment, students quantitated ethanol concentrations and qualitatively identified acetone or isopropanol. One student did not complete the assignment as instructed and did not provide appropriate results for the analytes; therefore, the following data were compiled for 42 students unless otherwise stated. Of note, DFE is a recent addition to the experiment and was not used in previous semesters. It has been evaluated and determined to be a suitable qualitative compound for this experiment as an alternative or in addition to acetone and isopropanol. Additional information is provided below as part of the potential modifications to the experiment. It should also be highlighted that this course and thus this experiment are designed to prepare students for a career in forensic science based on feedback and advice from forensic science agencies. It mimics laboratory training and proficiency testing that forensic science analysts must undergo before being approved to conduct casework analyses. Therefore, the success of the experiment was determined by the student’s ability to report accurate results rather than student survey data or feedback.</p><p>The representative retention times are shown in <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jchemed.5c00118#fig1">Figure 1</a> for ethanol, acetone, isopropanol, and <i>tert</i>-butanol (internal standard). DFE was also included in the figure for easy reference. The peak that appears before DFE in <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jchemed.5c00118#fig1">Figure 1</a> represents a small volatile compound that appeared in all samples, including airblanks. If DFE is not used in the experiment, then it is recommended to include a solvent delay of 1 min. The average retention time of ethanol over 3 semesters (<i>n</i> = 42) was 1.60 ± 0.01 min. Acetone’s average retention time was 1.89 ± &lt;0.01 min. Isopropanol’s average retention time was 2.00 ± 0.01 min. The average retention time of <i>tert</i>-butanol was 2.37 ± 0.02 min. See <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jchemed.5c00118#tbl2">Table 2</a> gives a summary of the average retention times for each volatile compound. Of note, the variation of retention time primarily occurred between semesters due to routine annual maintenance. All 42 students’ data passed the calibration acceptance criteria with an average <i>R</i><sup>2</sup> value of the ethanol calibration curve of 0.995 ± 0.004 over 3 semesters (<i>n</i> = 42). <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acs.jchemed.5c00118#fig2">Figure 2</a> shows the chromatograms produced by the SIM analysis of each volatile compound. This figure is an example of one of the components produced in the report generated by students during data processing, where students use these mass spectral data to evaluate and report data.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/J_Chem_Educ_2026_103_1_441_448_Figure_1_Example_total_ion_chromatogram_of_volatile_compounds_and_retention_times_fa3c745c20.jpeg" alt="J. Chem. Educ. 2026, 103, 1, 441–448: Figure 1. Example total ion chromatogram of volatile compounds and retention times." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_J_Chem_Educ_2026_103_1_441_448_Figure_1_Example_total_ion_chromatogram_of_volatile_compounds_and_retention_times_fa3c745c20.jpeg 225w," sizes="100vw" width="1500" height="1041"></p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/J_Chem_Educ_2026_103_1_441_448_Figure_2_Example_SIM_ions_of_each_volatile_compound_fd665d9c8c.jpeg" alt="J. Chem. Educ. 2026, 103, 1, 441–448: Figure 2. Example SIM ions of each volatile compound." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_J_Chem_Educ_2026_103_1_441_448_Figure_2_Example_SIM_ions_of_each_volatile_compound_fd665d9c8c.jpeg 245w," sizes="100vw" width="1500" height="613"></p><h4><strong>Conclusion</strong></h4><p>Students met learning outcomes and gained fundamental instrumental knowledge and hands-on experience through this experiment as they explored the concepts of chromatography and mass spectrometry. While students who completed this experiment had previous experience with GC-MS, this experiment introduced a new way of generating data reports. Students had to explain their conclusions based on these data reports as part of their postlab assignment, which provided firsthand practice of data analysis and communication skills. Trends in student results indicated that the experiment is very robust and reproducible, leading to a high success rate for students. This experiment offers a variety of modifications for instructors based on the number of students, student skill level, and resources available.</p></div>

Introducing Headspace Gas Chromatography–Mass Spectrometry to Undergraduate Chemistry Students from a Forensic Toxicology Perspective

Article

Webinars

Scientific article

Toxicology

Science and research

The Czech Advanced Technology and Research Institute (CATRIN) at Palacký University is a cutting-edge scientific hub dedicated to advancing research in the fields of nanotechnology, biotechnology, and biomedicine. At its core, CATRIN boasts outstanding scientific teams, featuring international researchers. We emphasize interdisciplinarity, foster global collaborations, and work to translate our research findings into practical applications.

CATRIN

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Waters CERTIFIED HPLC Vials

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The glass surface of TruView pH Control LCMS Certified Vials minimizes pH shifts away from the neutral and thus eliminates unwanted reactions and resulting ghost peaks.&nbsp;Ghost peaks are very difficult to troubleshoot.</p><p>Waters TruView pH Control LCMS Certified vials were used to analyze two compounds, drospirenone and lovastatin. The TruView pH Control LCMS Certified Vials show little to no degradant formed over the time tested. Standard glass vials showed considerable degradant formation over the same testing time with irreproducible formation of the degradant across different vials.&nbsp;</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_CERTIFIED_Vials_6_4dc330d849.jpg" alt="Waters CERTIFIED Vials: UV peak areas of lovastatin degradant across replicate vials and different vial types. Error bars indicate standard deviation for the replicate injection peak area." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_CERTIFIED_Vials_6_4dc330d849.jpg 245w," sizes="100vw" width="1024" height="605"></p><div><div><h3><strong>Reducing adsorption starts here</strong></h3><p>Inconsistent analytical results from small molecule analyte adsorption onto the surface of glass vials can be a problem at today’s low analyte concentrations. Some scientists have even experienced total analyte loss with samples stored in vials for an extended time. The vial chemistry, specifically the&nbsp;glass surface, is the major contributor to this problem.</p><p>Polar analytes&nbsp;may adsorb to the glass vial surface by polar-polar interaction and/or ion exchange mechanisms, thereby reducing the overall amount of sample in solution. TruView Certified LCMS Vials&nbsp;reduce this problem dramatically due to a stringent manufacturing process. The process yields a glass surface that has a lower concentration of free ions on the surface.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_CERTIFIED_Vials_8_064003b933.jpg" alt="Waters CERTIFIED Vials: Nortriptyline at 1 ppb concentration in several vials. The tall peak is the initial injection; the smaller peak (overlaid) is the four-hour injection. The first two chromatograms are competitor’s vials. The third chromatogram is for the Waters TruView LCMS Certified vial. " srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_CERTIFIED_Vials_8_064003b933.jpg 245w," sizes="100vw" width="1912" height="1182"></p><div><div><h3><strong>No analyte left behind</strong></h3><p>Instrument development is yielding more sensitive mass spectrometers. With more sensitive instruments, analytes can be detected at pg/mL levels. At these concentrations, understanding adsorption issues is critical for good quantitative results. We tested adsorption loss for the major manufacturers and saw high sample loss across manufacturers and clear and amber glass types – with significantly less loss with Waters TruView Autosampler Vials.</p><h4><strong>Average Analyte Loss</strong></h4><p><strong>Manufacturer: Clear Glass / Amber Glass</strong></p><ul><li><strong>Vendor A</strong>: 55% / 69%</li><li><strong>Vendor B</strong>: 25% / 25%</li><li><strong>Vendor C</strong>: 54% / 74%</li><li><strong>Vendor D</strong>: 18% / 59%</li><li><strong>Vendor E</strong>: 75% / Not tested</li><li><strong>Waters TruView LCMS Certified Vial</strong>: 1% / 6%</li></ul></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div>

Waters Oasis SPE products

Waters Oasis SPE products come in a broad range of sorbents and an array of formats. With Oasis products, you can meet a wide variety of sample preparation needs.

<h4><strong>Faster, cleaner, and simpler SPE starts here</strong></h4><p>Analytical chemists worldwide use SPE to remove interfering matrix compounds and enrich the analyte of interest to ensure the generation of high-quality data.</p><p>Waters Oasis SPE products come in a broad range of sorbents and an array of formats. With Oasis products, you can meet a wide variety of sample preparation needs, from simple and fast sample matrix clean-up to more complex sample preparation challenges.</p><p>Oasis SPE products deliver unmatched purity, consistency, and quality for sample analysis. Along with seven different SPE chemistries, Oasis SPE products use universal to customized protocols to handle your unique sample.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Oasis_SPE_kolonky_2_967d461f2e/Waters-Oasis-SPE-kolonky-2.jpg" alt="Waters: Oasis SPE" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Oasis_SPE_kolonky_2_967d461f2e/thumbnail_Waters-Oasis-SPE-kolonky-2.jpg 245w," sizes="100vw" width="950" height="416"></p><h4><strong>Overview</strong></h4><ul><li>Fully water-wettable sorbents increase reproducibility and enable elimination of condition and equilibration steps</li><li>Co-polymer pH stable from 0–14 with no secondary silanol activity</li><li>Optimal sensitivity for small molecule and therapeutic peptide analysis</li><li>Reduced matrix effects for LC-MS/MS analyses</li><li>Unsurpassed selectivity</li><li>Consistent retention and capacity, yielding the highest SPE recovery</li><li>Reduces variability in analytical results and increases robustness of analysis</li><li><strong>Recommended Use: </strong>For the fastest, cleanest, and simplest approach to SPE-LC-MS/MS method development.</li></ul><h4><strong>Solid-Phase Extraction Chemistries</strong></h4><h5><strong>Oasis PRiME HLB</strong></h5><ul><li>Multi-purpose hydrophilic-lipophilic balanced reversed phase sorbent for acids, bases, and neutrals</li><li>Cleaner samples in fewer steps with simple three-and two-step protocols, no SPE expertise required</li><li>Removes 95% of common matrix interferences, such as proteins, salts, phospholipids, and pigments</li><li>No sorbent conditioning or equilibration steps required</li><li>Faster, more predictable analysis time</li><li>Ideal for reversed-phase SPE clean-up of samples in routine analysis.</li></ul><h5><strong>Oasis PRiME MCX</strong></h5><ul><li>Mixed-mode Cation eXchange sorbent to selectively retain, concentrate and elute basic compounds</li><li>Reversed-phase and ion-exchange functionality for orthogonal sample preparation</li><li>Cleaner samples in fewer steps with simple and fast 3 and 4-step protocols</li><li>Removes 99% of phospholipids from complex sample matrices</li><li>No sorbent conditioning or equilibration steps required</li><li>Faster, more predictable analysis time</li><li>Highly reproducible target analyte recoveries</li><li>Ideal for basic compound specificity while removing matrix interferences in a simple clean-up.</li></ul><h5><strong>Oasis HLB</strong></h5><ul><li>Multi-purpose hydrophilic-lipophilic balanced reversed phase sorbent</li><li>Provides high capacity for acids, bases, and neutrals</li><li>Ideal for ultra-high capacity of very polar compounds.</li></ul><h5><strong>Oasis MCX</strong></h5><ul><li>Mixed-mode Cation eXchange sorbent for bases</li><li>Increased analyte specificity and sensitivity</li><li>Reversed-phase and ion-exchange functionality for orthogonal sample preparation</li><li>Ideal for selective retention of basic analytes.</li></ul><h5><strong>Oasis MAX</strong></h5><ul><li>Mixed-mode Anion eXchange for acids</li><li>Increased analyte specificity and sensitivity</li><li>Reversed-phase and ion-exchange functionality for orthogonal sample preparation</li><li>Ideal for selective retention of acidic analytes.</li></ul><h5><strong>Oasis WAX</strong></h5><ul><li>Weak Anion eXchange mixed-mode sorbent for strong acidic compounds</li><li>Increased analyte specificity and sensitivity</li><li>Reversed-phase and ion-exchange functionality for orthogonal sample preparation</li><li>Ideal for improved retention of strong acidic compounds.</li></ul><h5><strong>Oasis WCX</strong></h5><ul><li>Weak Cation eXchange mixed-mode sorbent for strong basic compounds</li><li>Increased analyte specificity and sensitivity</li><li>Reversed-phase and ion-exchange functionality for orthogonal sample preparation</li><li>Ideal for improved retention of all basic analytes, especially strong bases.</li></ul><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Sorbenty_Oasis_SPE_na_bazi_kopolymeru_Oasis_HLB_c8ffee39b3/Waters-Sorbenty-Oasis-SPE-na-bazi-kopolymeru-Oasis-HLB.png" alt="Waters: Oasis Sorbents" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Sorbenty_Oasis_SPE_na_bazi_kopolymeru_Oasis_HLB_c8ffee39b3/thumbnail_Waters-Sorbenty-Oasis-SPE-na-bazi-kopolymeru-Oasis-HLB.png 211w," sizes="100vw" width="1511" height="1119"></p><h4><strong>Oasis Formats</strong></h4><h5><strong>Oasis μElution Plate</strong></h5><ul><li>Patented μElution plate design</li><li>No evaporation and reconstitution necessary due to elution volumes as low as 25 µL</li><li>Ideal for SPE clean-up and analyte enrichment of small sample volumes</li><li>Compatible with most liquid-handling robotic systems for automated, reliable high-throughput SPE (HT-SPE)</li></ul><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Corporation_Oasis_m_Elution_Plate_aa7e36a4c1.jpg" alt="Waters: Oasis µElution Plate" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Corporation_Oasis_m_Elution_Plate_aa7e36a4c1.jpg 245w," sizes="100vw" width="502" height="260"></p><h5><strong>Oasis 96-Well Sample Extraction Plates</strong></h5><ul><li>Innovative, award-winning two-stage well design</li><li>High throughput and high recovery</li><li>Compatible with most liquid-handling robotic systems for automated, reliable high-throughput SPE (HT-SPE)</li></ul><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Corporation_Oasis_96_Well_Sample_Extraction_Plates_9528d532b9.jpg" alt="Waters: Oasis 96-Well Sample Extraction Plates" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Corporation_Oasis_96_Well_Sample_Extraction_Plates_9528d532b9.jpg 245w," sizes="100vw" width="525" height="329"></p><h5><strong>Oasis Syringe-Barrel Cartridges</strong></h5><ul><li>Ultra-clean syringe barrel and frits</li><li>Available in cartridges ranging from 1 cc to 60 cc</li><li>Flangeless syringe-barrel cartridges available in 1 cc, 3 cc, and 6 cc sizes</li><li>Plus-style cartridges with Luer inlet hub and outlet tip, compatible with hand-held syringes</li></ul><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Corporation_Oasis_Syringe_Barrel_Cartridges_961aa06b8a.jpg" alt="Waters Corporation: Oasis Syringe-Barrel Cartridges" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Corporation_Oasis_Syringe_Barrel_Cartridges_961aa06b8a.jpg 245w," sizes="100vw" width="503" height="311"></p><h5><strong>Oasis Glass Cartridges</strong></h5><ul><li>Ultra-clean glass syringe with Teflon® frit</li><li>For trace level detection and analysis at part-per-trillion (PPT) levels</li><li>Available in 5 cc (200 mg) configuration</li></ul><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Corporation_Oasis_Glass_Cartridges_5e96319c7f.jpg" alt="Waters: Oasis Glass Cartridges" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Corporation_Oasis_Glass_Cartridges_5e96319c7f.jpg 188w," sizes="100vw" width="409" height="339"></p><h5><strong>Oasis On-Line Columns and Cartridges</strong></h5><ul><li>For rugged, reproducible, and ultra-fast on-line analysis</li><li>Wide choice of configurations, particle sizes, and sorbent chemistries</li><li>Available with all six patented Oasis sorbents—PRiME HLB, HLB, MCX, MAX, WCX, and WAX</li><li>High recovery and reproducible results for a wide range of compounds</li><li>Cartridge format for use with Spark Holland Prospekt-2™/Symbiosis™ systems also available</li></ul><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Corporation_Oasis_On_Line_Columns_and_Cartridges_ba02114c92.jpg" alt="Waters: Oasis On-Line Columns and Cartridges" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Corporation_Oasis_On_Line_Columns_and_Cartridges_ba02114c92.jpg 168w," sizes="100vw" width="415" height="386"></p><h4><strong>Sample preparation, improved</strong></h4><p>Improving various aspects of chromatography and mass spectrometry analyses often starts with sample preparation. &nbsp;Solid-phase extraction (SPE) or "liquid-solid phase extraction" is a sample preparation technology that uses particles of chromatographic packing material, usually in a cartridge or 96-well plate format, to chemically separate different analytes and aid in removing matrix components in a sample. &nbsp;</p><p>SPE is a proven sample preparation tool for simple sample matrix removal, including common interferences like proteins, salts, fats and phospholipids. This matrix removal provides many benefits, including matrix effect reduction and an increase in sample concentration and analyte specificity. Matrix removal also significantly simplifies chromatographic complexity by reducing the number of interfering peaks in the LC and reducing signal suppression by providing clean samples for the MS.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Corporation_Oasis_SPE_LC_MS_MS_chromatogram_of_1_pgm_L_of_alprazolam_from_rat_plasma_8b7275b25b.jpg" alt="Waters: Oasis SPE - LC-MS-MS chromatogram of 1 pgmL of alprazolam from rat plasma" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Corporation_Oasis_SPE_LC_MS_MS_chromatogram_of_1_pgm_L_of_alprazolam_from_rat_plasma_8b7275b25b.jpg 169w," sizes="100vw" width="1024" height="946"></p><h4><strong>Get the cleanest extracts with the Oasis 2x4 method</strong></h4><p>Having a variety of tools for method development allows separation scientists to optimize protocols for maximum sensitivity and selectivity. The Oasis 2x4 method for SPE sorbent and protocol selection for acids, bases, and neutrals produces the cleanest extracts – all by eliminating matrix interferences and sample variability. Get the flexibility to extract acids, bases, and neutrals with high SPE recoveries while removing matrix components that may interfere with analysis with our two protocols and four sorbents. By following the simple steps outlined in the Oasis 2x4 method, you can achieve high recoveries and the cleanest extracts.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Oasis_2x4_protokol_pro_vyvoj_metody_c417be9006/Waters-Oasis-2x4-protokol-pro-vyvoj-metody.jpg" alt="Waters: Oasis SPE - Oasis 2 x 4 method development protocol." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Oasis_2x4_protokol_pro_vyvoj_metody_c417be9006/thumbnail_Waters-Oasis-2x4-protokol-pro-vyvoj-metody.jpg 242w," sizes="100vw" width="1519" height="979"></p><h4><strong>Isolate your compounds with the Oasis HLB method</strong></h4><p>Solid-phase extraction (SPE) method development starts with knowledge of the sample matrix—the nature and relative concentration of the analytes of interest and potentially interfering endogenous compounds. The right sorbent and solvents are selected for load, wash, and elute steps, resulting in the creation of rugged, reliable, and selective protocols. The Oasis HLB method is a generic protocol used to isolate a broad range of acidic, basic, and neutral compounds from a wide spectrum of matrices.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Corporation_Oasis_SPE_Generic_Method_Protocol_with_Oasis_HLB_SPE_83d684704d.jpg" alt="Waters: Oasis SPE - Generic Method Protocol with Oasis HLB SPE" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Corporation_Oasis_SPE_Generic_Method_Protocol_with_Oasis_HLB_SPE_83d684704d.jpg 139w," sizes="100vw" width="1024" height="1153"></p><h4><strong>Multiple contaminant analysis with the 2-step pass-through protocol</strong></h4><p>If you are doing multiple residue screening of veterinary drugs, pesticides and mycotoxins in various food matrices, you may be facing a high concentration of organic solvents. With our simple 2-step protocol (pass-through SPE), you can remove matrix interferences quickly if your samples contain a high concentration of organic solvent(s) and concentration and/or salt removal is not required. It can be used as the clean-up method following QuEChERS extraction, saving you significant time compared to the traditional dispersive SPE method - all while achieving superior clean-up.</p><p><strong>To do pass-through SPE, Waters offers 2 convenient and flexible formats:</strong></p><ul><li><strong>Traditional-style cartridges</strong> compatible with vacuum and positive pressure manifolds&nbsp;</li><li><strong>"Plus" style cartridges</strong> that can be used without manifolds when connected to a displacement syringe</li></ul><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Waters_Oasis_SPE_kolonky_3_b4da6242de/Waters-Oasis-SPE-kolonky-3.jpg" alt="Waters: Oasis Plus Light and Plus Short Cartridges for 2-step pass through protocol." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Waters_Oasis_SPE_kolonky_3_b4da6242de/thumbnail_Waters-Oasis-SPE-kolonky-3.jpg 152w," sizes="100vw" width="1308" height="1342"></p>

Products from category Consumables from Waters distributed by Waters Corporation (Europe) - page 1

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