Our Library never stops expanding. What are the most recent contributions to LabRulezICPMS Library in the week of 12th January 2026? Check out new documents from the field of spectroscopy/spectrometry and related techniques!<blockquote>👉 <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library">SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT SPECTROSCOPY/SPECTROMETRY RELATED TECHNIQUES</a></blockquote><blockquote>👉 Need info about different analytical techniques? Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library">LabRulezLCMS</a> or <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library">LabRulezGCMS</a> libraries.</blockquote>This week we bring you application notes by Agilent Technologies, Shimadzu, and Waters Corporation and brochure by Thermo Fisher Scientific!<h3>1. Agilent Technologies: Detecting Spice Adulteration with the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=8700+LDIR">Agilent 8700 LDIR</a> Chemical Imaging System</h3>Accelerating adulterant detection in turmeric with IR spectroscopy and imaging&nbsp;<ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_spice_adulteration_8700_ldir_5994_8800en_agilent_235b48c7e6.pdf">Full PDF for download</a></li></ul>Spices are essential components of culinary practices worldwide, valued for their flavor, aroma, and health benefits. However, the intentional or accidental adulteration of spices with cheaper or foreign substances poses significant risks to both food quality and consumer safety. Adulteration practices often aim to increase product volume, enhance visual appeal, or mimic authentic flavors, compromising the integrity of the final product.1Common adulteration practices include substituting genuine plant materials with cheaper or visually similar ones, using inferior plant species or parts, and mixing with fillers such as corn starch, bran, or sawdust. Some products are also adulterated with chemicals to enhance flavor, inorganic substances such as sand, chalk, or red brick powder, or illegal dyes such as Sudan dyes and rhodamine B to intensify&nbsp;color.1–4&nbsp;Current tools for detecting adulteration in herbs and spices face several challenges. Sampling across complex supply chains often lacks consistency, making it difficult to obtain representative samples.5 The chemical and physical complexity of sample matrices, combined with natural variation among species and origins, complicates data interpretation.5&nbsp;In&nbsp;ground or powdered spices, the original plant structures are lost, making it difficult to visually or morphologically identify adulterants, particularly when they are fine or physically similar to the genuine&nbsp;material.6 An <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=8700+LDIR">Agilent 8700 Laser Direct Infrared (LDIR) chemical imaging system</a> (Figure&nbsp;1) was used in this study to detect spice adulteration through the integration of infrared spectroscopy and&nbsp;microscopy<h4>Experimental&nbsp;</h4>Agilent Clarity software: To evaluate the 8700 LDIR's capability in distinguishing genuine spices from common adulterants, a series of pure and adulterated samples were prepared and analyzed using the system's automated Particle Analysis (PA) workflow.<h4>Results and discussion&nbsp;</h4><h5>Identification of pure spices (turmeric)&nbsp;</h5>To verify the 8700 LDIR and the user&nbsp;generated library in identifying particles of varying sizes, shapes, and counts, the pure turmeric sample was analyzed as an "unknown". Turmeric sample identification demonstrated high spectral matching accuracy. Within the selected analysis area, 74&nbsp;particles were detected and 70&nbsp;particles (94.6%) were matched to the turmeric reference spectra in the custom library. Notably, 64 particles achieved Hit Quality Index (HQI) values exceeding 0.8, indicating strong spectral correlation and high confidence in the identification data (Figure 2).<h4>Conclusion&nbsp;</h4>This study demonstrates the suitability of the Agilent 8700 LDIR chemical imaging system with Agilent Clarity software as an effective tool for detecting adulteration in ground spices. Using the automated Particle Analysis (PA) workflow, the system quickly and reliably distinguished turmeric from both organic (corn starch) and inorganic (sand) adulterants based on their distinct IR spectral signatures.&nbsp;Differentiating between chemically similar spices remains challenging due to overlapping IR profiles. However, the 8700 LDIR system's ability to build custom spectral libraries offers flexibility for targeted authentication, allowing laboratories to adapt the system to their evolving analytical needs.&nbsp;A key advantage of the 8700 LDIR method is the speed and simplicity of sample preparation—dry powders can be analyzed directly on low-e slides without solvents or extraction. By combining the high-throughput automated PA workflow with integrated imaging, the 8700 LDIR provides a practical, time-saving solution for routine analysis in food testing&nbsp;laboratories.<h3>2. Shimadzu: Observation of the Automotive Cylindrical Lithium-Ion Battery “4680” Using a Micro-Focus X-ray CT System</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_01_01060_en_5e744626ad.pdf">Full PDF for download</a></li></ul><h4>User Benefits</h4><ul><li>The internal structure of the “4680” cylindrical lithium-ion battery for automotive use, which is a market trend, can be observed nondestructively.&nbsp;</li><li>Electrode placement and bonding condition can be verified, which is useful for product quality inspection.</li></ul>In recent years, with the proliferation of electric vehicles (EVs), the development of high-performance, low-cost automotive batteries has become an urgent priority. Among these, the cylindrical lithium-ion battery “4680” has attracted particular attention. Compared with the conventional “2170,” the “4680” is larger, and its energy density per cell is increased, thereby extending vehicle range. In addition, the adoption of a tab-less structure reduces internal resistance, improving charge/discharge efficiency and thermal management performance, while simplification of the manufacturing process is expected to reduce cost. Owing to these characteristics, the “4680” is drawing attention across both industry and academia as a core technology for next-generation EVs. Meanwhile, lithium-ion batteries are always subject to concerns about the risk of ignition and explosion due to internal short circuits or foreign matter inclusion. Because X-ray CT enables nondestructive testing (NDT) with three-dimensional visualization of internal structures, it is possible to detect fine defects such as electrode misalignment, separator damage, and foreign matter inclusion.&nbsp;This article introduces a case study in which the cylindrical lithium-ion battery “4680” for automotive applications was observed using the microfocus <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=1&amp;search=inspeXio+7000">X-ray CT system inspeXio 7000</a> (Fig. 1).<h4>Conclusion</h4>We presented a case study of imaging the cylindrical lithium-ion battery “4680” using a microfocus X-ray CT system. By nondestructively visualizing its three-dimensional structure, it is possible to obtain important information on the battery’s internal structure, such as the arrangement of electrodes and their bonding state. Thus, X-ray CT is shown to be a powerful tool that contributesto the advancement of battery technology.<h3>3. Thermo Fisher Scientific: MarqMetrix All-In-One X Process Raman Analyzer</h3>Enabling accurate, real-time results for process monitoring in hazardous locations<ul><li>Brochure</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/marqmetrix_all_in_one_x_process_raman_analyzer_ds1339_en_c1739807d2.pdf">Full PDF for download</a></li></ul>The <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2208">Thermo Scientific™ MarqMetrix™ All-In-One X Process Raman Analyzer </a>is a compact, portable spectrometer designed for fast deployment and ease of use. Built for industries where rapid time-to-results is critical, it is designed to be intrinsically and inherently safe for operation within hazardous locations, in such applications as:&nbsp;<ul><li>Midstream and downstream oil &amp; gas operations&nbsp;</li><li>Chemical and polymer applications&nbsp;</li><li>Pharmaceutical development and manufacturing</li></ul><h4>The MarqMetrix All-In-One X Analyzer offers multiple operational advantages:&nbsp;</h4><ul><li>Analysis without sample preparation, delivering Raman spectral results in real time&nbsp;</li><li>Easy setup and deployment by non-spectroscopists&nbsp;</li><li>Intrinsically and inherently safe optical power to robust probes, which can be deployed in hazardous locations: up to ATEX Zone 0 (Europe &amp; Middle East), IECEx (Asia), and Class 1 Div 1 (North America)&nbsp;</li><li>Nondestructive workflows to protect precious samples&nbsp;</li><li>A small footprint for convenient deployment&nbsp;</li><li>Factory calibration for hardware stability and portability&nbsp;</li></ul>The MarqMetrix All-In-One X Process Raman Analyzer is designed for out-of-the-box use, enabling you to be ready in less than 15 minutes to collect highly accurate Raman measurements. Pack this analyzer in a protective case and take it to the point of need; its factory calibration ensures continuous and precise analysis on the go. Easily integrate the MarqMetrix All-In-One X Process Raman Analyzer into your existing process without the need for costly technical expertise. Once implemented, the analyzer enables operators in hazardous locations to make faster, safer, and smarter decisions by delivering real-time compositional insights directly on site.<h3>4. Waters Corporation: Residual Dynabeads Detection with <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2190">Aura+</a></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/720009096_en_aeb7e4288f.pdf">Full PDF for download</a></li></ul>Autologous cell therapies have seen explosive growth as evidenced by the recent landmark FDA approvals of two CAR-T cell therapies, Yescarta® and Kymriah®. 1 Dynabeads™ are commonly used in cell therapy manufacturing process to expand and activate CAR-T cells.2 CD3/CD28 Dynabeads specifically are one of the leading approved GMP expression beads for T cell therapies and are key to achieving the potency required of these novel medicines. Dynabeads are also efficiently removed from the final product to ensure final purity. However, residual CD3/CD28 beads present a significant risk patients’ safety and therefore are generally kept below a widely accepted but not yet regulatory controlled limit of 100 residual beads per 3,000,000 cells.3–4&nbsp;Residual bead analysis is currently performed with manual hemocytometry that uses light microscopy and manual counting. However, manual hemocytometry is prone to human error, which leads to significant bead undercounting because it is incredibly difficult to find and differentiate between Dynabeads and cells in a sample, making residual bead counting one of the most challenging cell therapy lot release assays. Other traditional cell and subvisible analysis tools, including flow cytometers, also undercount beads and cannot differentiate residual Dynabeads from cells and other subvisible particles.&nbsp;In this technical note, we show step-by-step how Aura CL and <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2190">Aura+</a> enable fast, accurate, sensitive, and specific residual Dynabead detection in a concentrated cell therapy product. Powered by backgrounded membrane imaging (BMI) to characterize the entire cell therapy particle population and side illumination membrane imaging (SIMI) to specifically detect Dynabeads, Aura® CL and Aura®+ are the first and only tailored solutions to find and count these hard to detect contaminants.<h4>Conclusion&nbsp;</h4>Analysis of the cell therapy sample on Aura CL or Aura+ begins with the BMI well image, where sharp contrast, high resolution optics provide the landscape to count and size all the particles in your cell therapy product. SIMI imaging, which is run at the same time as BMI, enables the differentiation of biologic vs. non-biologic particles which is essential to this application. Figures 2 and 3 capture how BMI detects all particles present in a cell therapy sample, while SIMI mode selects for particles of higher refractive index contrast. In BMI mode, cells, Dynabeads, and mixtures of the two were all easily visible. However, in SIMI mode, only the residual Dynabeads were detected both in the standard high-throughput 4x mode and in the 10x high magnification mode. This is essential for specific detection of residual Dynabeads given their low abundance in a highly concentrated cell sample as shown in Figure 4. We determined that the limit of quantitation (LOQ) of Dynabeads is &lt;1 bead/well (or 18 beads/mL of sample), well below the hemacytometer residual bead detection rate of 1 bead per 10,000 cells. Additionally, the bead counts in our dilution series exhibited a linear relationship, measuring an R2 of 0.98. Using Aura CL or Aura+ for residual Dynabead detection provides greater accuracy and higher-throughput in counting compared to the cumbersome and error prone currently used methods. Resolving false positive counts can be easily rectified by measuring the particles at higher magnification, where single Dynabeads identity can be confirmed by size. Aura CL and Aura+ deliver the only automated way of measuring single Dynabeads in concentrated cell therapy solutions, while also offering built in orthogonal confirmation through various objectives and light sources.

News from LabRulezICPMS Library - Week 03, 2026

Our Library never stops expanding. What are the most recent contributions to LabRulezICPMS Library in the week of 26th January 2026? Check out new documents from the field of spectroscopy/spectrometry and related techniques!<blockquote>👉 <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library">SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT SPECTROSCOPY/SPECTROMETRY RELATED TECHNIQUES</a></blockquote><blockquote>👉 Need info about different analytical techniques? Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library">LabRulezLCMS</a> or <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library">LabRulezGCMS</a> libraries.</blockquote>This week we bring you application notes by Agilent Technologies, Metrohm and Shimadzu and brochure by Thermo Fisher Scientific!<h3>1. Agilent Technologies: Thin Multilayer Analysis Using the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=8700+LDIR">Agilent 8700 LDIR</a> Chemical Imaging System</h3>Rapid micrometer-scale measurement of layer thickness and composition identification in laminated materials<ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_thin_multilayer_materials_8700_ldir_5994_8799en_agilent_892afacbb6.pdf">Full PDF for download</a></li></ul>Multilayer laminate materials represent a structurally and chemically complex system. They often comprise several distinct polymer layers that are engineered for specific functional roles, despite having total thicknesses of only a few hundred microns. Each layer contributes unique properties such as mechanical strength, barrier performance, or environmental protection, depending on its chemical composition and thickness. Accurate identification and measurement of these thin layers is therefore critical, as defects or deviations in layer thickness can compromise product integrity. Weaknesses can cause failures through damage, potentially resulting in safety issues for the user.Precise mapping and micrometer-scale thickness analysis is essential during the development, quality control, and troubleshooting of multilayer materials. The <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=8700+LDIR">Agilent 8700 Laser Direct Infrared (LDIR) chemical imaging system</a> offers a powerful solution for this application. By combining IR spectroscopy with high-resolution imaging, the system enables chemical identification and visualization of polymer layers with exceptional spatial detail. Enhanced by the intuitive Agilent Clarity software, the 8700 LDIR delivers a fast and effective workflow for multilayer material characterization, addressing key needs in quality assurance, failure analysis, and reverse engineering.&nbsp;<h4>Results and discussion&nbsp;</h4><h5>User-generated spectral library&nbsp;</h5>Following sample preparation, the 8700 LDIR high‑magnification visible camera provided an overview of the laminate structure of sample 1, revealing three distinct layers. The total thickness of the sample and each layer was measured using the Clarity software ruler feature. As shown in Figure 3, the total thickness of sample 1 based on the visible image was measured to be 150 µm (layer 1: 50 µm; layer 2: 50 µm; layer 3: 50 µm). A high‑resolution IR image was then acquired at 1,442 cm–1 with a 1 µm pixel size, enabling detailed visualization of the layer morphology under infrared light (Figure 3).<h4>Conclusion&nbsp;</h4>The Agilent 8700 LDIR chemical imaging system provides a powerful, non-destructive solution for multilayer analysis across diverse applications ranging from food packaging to battery separators. By combining a laminate holder, high-magnification imaging, IR imaging, and line profile spectral collection, the method delivers clear insights into layer thickness, morphology, and material composition. The ability to quickly build custom spectral libraries within the Agilent Clarity software further enhances its utility, especially for identifying unknown materials or contaminants in multilayer&nbsp;materials. The 8700 LDIR multilayer analysis workflow supports both R&amp;D innovation in advanced materials and routine quality assurance across different industries.<h3>2. Metrohm: Almond analysis with near-infrared (NIR) spectroscopy</h3>Multiparameter determination of moisture, fat, and protein<ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_nir_132_download_ab5d492c05.pdf">Full PDF for download</a></li></ul>Almonds are nutritious edible nuts from the almond tree and can be eaten whole or processed in other foods. During processing, quality control (QC) parameters like moisture levels are checked to ensure that the correct percentage is reached before moving on to other stages (e.g., grinding or packaging). When determining almond quality, destructive analytical techniques are helpful but can involve extensive sample preparation and solvent extractions. These traditional techniques are also slow and expensive. Nondestructive near-infrared spectroscopy (NIRS) is a great alternative because it is fast, simple, and cost effective [1]. In this study, almond moisture content (water content), protein content, and fat have been measured using NIRS. NIR spectroscopy offers the rapid and reliable prediction of several quality parameters in seconds without any sample preparation.<h4>EXPERIMENTAL EQUIPMENT&nbsp;</h4>60 samples of ground almonds and 60 samples of whole almonds were measured on a <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=220&amp;search=NIR+Analyzer">Metrohm NIR Analyzer</a>. All measurements were performed in reflection mode (1000–2250 nm) using the large cup accessory. The samples were measured in rotation to collect spectral data from diverse areas. Spectral averaging of signals from several spots helped to reduce sample inhomogeneity. Metrohm software was used for all data acquisition and prediction model development.<h4>CONCLUSION</h4>This Application Note demonstrates that almond protein content analysis, almond fat content analysis, and almond water content (or almond moisture content) analysis can be done with NIRS. NIR spectroscopy offers users a faster, simpler, highly accurate alternative to standard analytical methods for the analysis of ground and whole almonds during processing and final product quality control (Table 1). By using NIRS, all of these parameters can be measured simultaneously without sample preparation, saving time and money.<h3>3. Shimadzu: Technique for Measuring Microplastics Collected on Various Filters Using a Particle Filter Holder</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_01_00976_en_155bd58551.pdf">Full PDF for download</a></li></ul><h4>User Benefits</h4><ul><li>Particle filter holders provide clear microscope images of samples, enabling highly accurate measurements.</li><li>Microplastics can be analyzed accurately and efficiently by using a particle filter holder with a high-speed mapping program and a particle analysis program.</li></ul>Since microplastics (MPs) (with diameters ranging from a few µm up to 5 mm) are widely recognized as an environmental problem in marine environments, Japan’s Ministry of the Environment has issued guidelines for preparation and measuring MPs in environmental surface waters. 1)&nbsp;The guidelines include examples of using a Fourier transform infrared spectrophotometer (FTIR) to identify plastics by the total reflectance measurement method. However, to identify fine MPs, they recommend using instruments like infrared microscopes.&nbsp;In recent years, an increasing number of studies have analyzed fine MPs smaller than 100 µm. Measuring MPs with an infrared microscope requires collecting samples on a filter. Various types of filters can be used for infrared microscopes, each with unique characteristics. But if a filter cannot be held horizontal during drying or measuring, it can develop wrinkles that might decrease measurement accuracy. Therefore, a particle filter (PF) holder was developed that can be placed directly on an infrared microscope stage while holding the filter horizontally. This article describes using the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=1&amp;search=IRXross">IRXross Fourier transform infrared spectrophotometer</a>, an <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=1&amp;search=AIMsight">AIMsight infrared microscope</a> (Fig. 1), and a PF holder to evaluate the properties of various filters and measure a standard sample of MPs.<h4>Example of Measuring MPs&nbsp;</h4>Polystyrene (PS), polyethylene (PE), and polypropylene (PP) particles that fell through a 100 µm mesh were dispersed in purified water. They were then collected by suction filtering through PTFE, Al2O3, Au/PC, and stainless steel filters (Table 1). After collecting the particles, the filters were dried using a PF holder. Fig. 5 shows the filter holder placed in the infrared microscope. Measurement condition settings are indicated in Table 2. The PTFE and Al2O3 filters were measured by the transmission method, whereas the stainless steel and Au/PC filters were measured by the reflection method. For the highspeed mapping program in this measurement, a peak detection range of 3,400 to 2,400 cm-1 was specified for detecting the signal from hydrocarbons (C-H). If there are peaks in that range, the range will be scanned the specified number of times. A tiled image of each filter is shown in Fig. 6. The areas marked with a yellow box were measured. For more information about the high-speed mapping program, refer to <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_01_01001_en_79904665ce.pdf">Application News No. 01-01001-EN</a>.<h4>Conclusion&nbsp;</h4>This article describes using a PF holder to collect fine microplastic particles on various types of filters, and it provides a summary of the characteristics of each filter. Since there are differences in the wavenumber ranges and data acquisition methods for each filter type, users need to understand the individual characteristics of a filter when using it. The results also show that by using a PF holder to hold the filter flat, fine microplastic particles can be conveniently measured with an infrared microscope to obtain clear images and accurate measurements. Furthermore, a highspeed mapping program and particle analysis program can be used to accurately and efficiently analyze microplastics.<h3>4. Thermo Fisher Scientific: Raman at the speed you need - Thermo Scientific DXR3 Raman Family</h3><ul><li>Brochure</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/SS_53191_DXR_3_raman_family_spec_sheet_896bbe523e.pdf">Full PDF for download</a></li></ul>The Thermo Scientific DXR3 Raman Family is a versatile portfolio of Raman spectroscopy instruments designed to deliver high-quality chemical information quickly and reliably across a wide range of applications. Built on a shared, modular platform, the family includes the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2239">DXR3 Raman Microscope</a>, <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2237">DXR3xi Raman Imaging Microscope</a>, and <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2235">DXR3 SmartRaman Spectrometer</a>, enabling users to choose the optimal configuration for point analysis, high-resolution imaging, or bulk sample characterization. All systems emphasize ease of use, reproducibility, and rapid data acquisition, making advanced Raman analysis accessible to both expert spectroscopists and routine laboratory users.The DXR3 Raman Microscope provides research-grade performance with sub-micrometer spatial resolution and intuitive point-and-shoot operation, supporting demanding analytical tasks such as microanalysis, depth profiling, and chemical mapping. For applications requiring fast, high-resolution chemical imaging, the DXR3xi Raman Imaging Microscope delivers exceptional stability, automated feature identification, and rapid image acquisition over both small and large areas. Its advanced EMCCD detector technology and intelligent autofocus significantly reduce experiment time while maintaining high data quality, making it ideal for materials research, pharmaceuticals, and life sciences.The DXR3 SmartRaman Spectrometer is optimized for high-performance bulk sample analysis in busy analytical laboratories. Featuring a large sampling compartment and flexible accessories, it accommodates a wide range of sample formats—from powders and tablets to liquids in bottles or vials. Variable Dynamic Point Sampling (VDPS) technology enables representative averaging over large sample areas, improving reproducibility and reducing sampling bias. Together with multiple excitation laser options and interchangeable gratings, the system supports diverse analytical workflows with minimal maintenance.Across the entire DXR3 family, pre-aligned, user-exchangeable Smart Components, automated alignment and calibration, and powerful OMNIC™ software ensure consistent performance and simplified operation. Extensive microscopy, macro-sampling, and automation options allow systems to be tailored to specific applications, while robust system qualification and diagnostics support long-term reliability. Overall, the DXR3 Raman Family combines speed, flexibility, and analytical confidence, making it a comprehensive solution for modern Raman spectroscopy in research, quality control, and industrial environments.

News from LabRulezICPMS Library - Week 05, 2026

Our Library never stops expanding. What are the most recent contributions to LabRulezICPMS Library in the week of 23rd February 2026? Check out new documents from the field of spectroscopy/spectrometry and related techniques!<blockquote>👉 <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library">SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT SPECTROSCOPY/SPECTROMETRY RELATED TECHNIQUES</a></blockquote><blockquote>👉 Need info about different analytical techniques? Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library">LabRulezLCMS</a> or <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library">LabRulezGCMS</a> libraries.</blockquote>This week we bring you application notes by Agilent Technologies, Metrohm, Shimadzu and Thermo Fisher Scientific!<h3>1. Agilent Technologies: UV-Vis Spectroscopy for Quality Assessment of Paprika as per ASTA Method 20.1</h3>From sample prep to analysis using the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=Cary+3500">Agilent Cary 3500 Multicell UV-Vis</a><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_paprika_uv_vis_cary_5994_8612en_agilent_d903914b39.pdf">Full PDF for download</a></li></ul>Paprika is a widely used spice valued for its deep red color and characteristic flavor, contributing to its prominence in both culinary and commercial applications. As a high‑demand commodity produced from dried capsicum pods, paprika is subject to quality variation and adulteration, which can compromise product authenticity, consumer trust, and regulatory compliance. UV-Visible (UV-Vis) spectroscopy is a rapid, reproducible analytical technique for evaluating paprika quality by quantifying pigment concentration. In paprika, color intensity primarily arises from carotenoid compounds, and is commonly assessed using the ASTA Method 20.11 – a well-established industry standard that commercially grades paprika samples as a numerical ASTA color value.In this application note, we used an <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=Cary+3500">Agilent Cary 3500 Multicell UV-Vis spectrophotometer</a> and <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=UV+Workstation+software">Agilent Cary UV Workstation software</a> to determine the ASTA color value of two commercial paprika samples. The measurements were performed in accordance with ASTA Method 20.1 for the determination of extractable color in capsicums and their&nbsp;oleoresins.<h4>Results and discussion</h4><h5>Paprika samples' analysis&nbsp;</h5>ASTA Method 20.1 measures the color intensity of paprika by extracting pigments with acetone and recording absorbance at 460 nm. The absorbance reading, along with sample weight is then used to calculate the ASTA color value. The ASTA color value is a crucial quality parameter for paprika and other spices, as it indicates the intensity and vibrancy of the red color, which is a key characteristic for consumers and food manufacturers. In this study, the two extracted paprika samples were each measured three times to produce triplicate results (Table 4). Sample 1 had a corrected ASTA color value of approximately 103, and sample 2 had a corrected ASTA color value of approximately 61, indicating a lower color intensity. The corrected ASTA color value was automatically generated in an easy-to-read table of values, and a scan report was automatically exported into a user-defined location.<h4>Conclusion&nbsp;</h4>The Agilent Cary 3500 Multicell UV-Vis spectrophotometer with Agilent Cary UV Workstation software enabled fast, reliable, and standardized quality assessment of paprika samples. Using the well-established industry method, ASTA 20.1, the Cary 3500 system provided precise quantification of carotenoid pigments, supporting grading categorization. The high-throughput multicell design of the Cary 3500 Multicell UV-Vis spectrophotometer allows simultaneous measurement of up to seven samples and a reference, improving efficiency and minimizing variability. The Cary UV Workstation software simplifies data acquisition and analysis with intuitive spectral features such as the End of sequence analysis tool, which can be applied automatically to any scan method, and spectra comparisons through the Load spectrum tool. From sample absorbance measurement to final reporting, the Cary 3500 system eliminated the need for manual data processing or external tools, minimizing complexity and facilitating confidence.<h3>2. Metrohm: NIRS analysis of forages</h3>Multiparameter determination in a few seconds<ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_nir_131_download_2f897ff7f5.pdf">Full PDF for download</a></li></ul>Forages are plants or parts of plants eaten by both livestock and wildlife. Forages provide bulk, help with weight maintenance, and combat several issues [1]. Alfalfa forage is high in protein—well-suited to promote muscle mass in beef cattle or to increase the production of dairy cows [2]. Alfalfa is also commonly used for horse feed. These animals require forages with good palatability along with high digestibility, intake potential, and protein levels, thus increasing the demand for alfalfa and other high-quality feeds. Farmers have responded by producing even higherquality alfalfa in recent years. Since forage quality depends on chemical, biological, and dynamic properties, both measured and calculated methods must be used. Standard alfalfa assays measure neutral detergent fiber (NDF), acid detergent fiber (ADF), crude protein (CP), ash, moisture, and protein. For alfalfa pellets, the mean particle size is also important. Near-infrared spectroscopy (NIRS) offers rapid and reliable prediction of fat, moisture, crude protein, fiber, ash and starch in a few seconds and without sample preparation.<h4>EXPERIMENTAL EQUIPMENT</h4>Samples of alfalfa (including fresh alfalfa, alfalfa pellets, and alfalfa cubes) were analyzed on a <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=220&amp;search=NIR+Analyzer">Metrohm NIR Analyzer</a>. All measurements were performed in reflection mode using the large cup. The samples were measured in rotation to collect spectral data from several areas. Spectral averaging of signals from several spots helped to reduce sample inhomogeneity. The reference values were measured according to ISO norms described at the end of this Application Note. Metrohm software was used for all data acquisition and prediction model development.<h4>CONCLUSION&nbsp;</h4>This Application Note demonstrates the feasibility to determine multiple key parameters of alfalfa forage with NIR spectroscopy. Several analytical methods are usually required to measure key quality parameters for forage (Table 4). NIRS forage analysis enables a highly accurate, cost-effective, and fast alternative.<h3>3. Shimadzu: Analysis of Heavy Metals in Baby Food Using ICP-MS</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_01_01039_en_c563bb1b82.pdf">Full PDF for download</a></li></ul><h4>User Benefits</h4><ul><li>Heavy metals in various baby foods can be analyzed simultaneously with sufficient sensitivity.</li><li>Stable analysis can be performed even for baby foods with high matrix content.</li><li>Using the standard LabSolutions ICPMS rinse function, the time to clean the sample introduction system is minimized, which prevents carryover.</li></ul>Infants’ metabolic pathways are still developing, and because of their lower body weight, they are known to be more susceptible to the effects of harmful substances. In the United States, the Baby Food Safety Act 20211), and in the EU, Commission Regulation (EU) 2023/9152) and Commission Regulation (EU) 2024/19873) require the control of toxic metals contained in baby foods. ICP-MS is suitable for the analysis of trace amounts of toxic metal elements because it can perform multi-element simultaneous analysis with high sensitivity.However, baby foods vary in matrix composition, which raises concerns about non-spectral interferences and long-term stability during ICP-MS analysis. This Application News describes the analysis of five baby foods with different matrices using the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=1&amp;search=ICPMS-2040%2F2050">ICPMS-2040/2050</a> (Fig. 1). Additionally, spike recovery tests and long-term stability were assessed based on the Food and Drug Administration (FDA) Elemental Analysis Manual (EAM) Section 4.74).<h4>Equipment Configuration and Analysis Conditions&nbsp;</h4>The equipment configuration is shown in Table 2. To reduce running costs, a mini-torch with lower argon gas consumption compared to conventional torches was used for analysis. Additionally, to streamline sample preparation, an Online Internal Standard Kit was utilized for online addition.&nbsp;The analysis conditions are detailed in Table 3. After analyzing high-concentration samples, the sample introduction system can influence the analysis values of subsequent samples (carryover). If carryover occurs, re-measurement is necessary, which consumes additional time and samples. With LabSolutions ICPMS, rinse solutions can be set for each sample, enabling effective cleaning in minimal time. Normal cleaning was performed using pure water (Rinse solution 1), and an additional acid rinse solution (Rinse solution 2) was introduced only after high-concentration samples.For example, Table 4 shows the difference in carryover concentration when measuring a blank sample after introducing a sample with a CCV concentration, comparing the case where rinse solution 2 is added for an additional 240 seconds to the case where it is not. Among the elements measured this time, Se and Hg tend to have a higher risk of carryover, but by introducing rinse solution 2, carryover was reduced to below the detection limit. Moreover, even if unexpectedly high-concentration samples are introduced, the Extended Rinsing function allows for automatic additional rinsing (Fig. 3). This eliminates the need to repeatedly check analysis values or to set a uniform cleaning time uniformly, thus reducing the verification effort, the amount of rinse solution required, and the analysis time while preventing carryover.&nbsp;Furthermore, to minimize time spent cleaning the sample introduction system, ProActive Rinsing was used (Fig. 4). When measuring multiple samples, starting the rinse in advance during measurement reduces the measurement time for subsequentsamples.<h4>Conclusion&nbsp;</h4>In this Application News, elemental analysis of baby food was conducted using the ICPMS-2040/2050. We achieved detection limits that met stringent standards. The spike recovery tests yielded good results for all samples with different matrices, confirming the validity of the analysis. Additionally, we analyzed 50 samples of infant formula with a high matrix over approximately six hours and confirmed good stability. The ICPMS-2040/2050 offers high sensitivity, accurate analysis, and good stability. Its Extended Rinsing and ProActive Rinsing functions effectively clean the sample introduction system, preventing carryover. Therefore, the ICPMS-2040/2050 is a suitable instrument for elemental analysis in baby food.<h3>4. Thermo Fisher Scientific: Food protection methods assessed by Surface Enhanced Raman Spectroscopy</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/food_protection_methods_surface_enhanced_raman_spectroscopy_an54670_en_5c5e701389.pdf">Full PDF for download</a></li></ul>Lipid oxidation is a major issue for the meat industry as it can not only affect&nbsp;sensory quality in terms of flavor and odor but can also lead to the formation of toxic compounds such as malondialdehyde (MDA) and cholesterol oxidation products, as well as the accumulation of carbonyls, alcohols and volatile acids. The degree of oxidation depends on various factors such as the type of meat, the fat content, the storage temperature, the availability of oxygen and the type of packaging1, 2. To prevent oxidation, synthetic antioxidants are commonly added to meat products, but consumers are now demanding more natural products3. Several studies have been carried out to evaluate the antioxidant activity of many essential oils or extracts from plants or spices such as rosemary, cinnamon or oregano, and the new trend is to develop innovative packaging by adding these natural antioxidants directly to the packaging materials4–6. These materials, often films, are known as “active packaging” because they enable the controlled release of active agents either on the surface or in the internal atmosphere of the product, or by trapping the radicals responsible for harmful effects on food quality. However, the antioxidant performance of these films must be accurately determined to enable the selection of the right packaging for each foodstuff.&nbsp;Among all the techniques available, Raman spectroscopy is a promising candidate for detecting most molecular species with high specificity and sensitivity, particularly in the presence of Surface-Enhanced Raman Scattering (SERS). Indeed, SERS is a physical phenomenon that occurs in the presence of a rough nano-structured metallic surface that causes the intensification of Raman signals from molecules adsorbed to the surface thanks to the combination of a chemical effect and an electromagnetic effect7 . The metals used are generally gold or silver, which can be prepared by electrochemical roughening, metallic coating, or deposition of nanoparticles (often in a colloidal form). Commercial solutions are available, but many researchers prefer to create their own SERS substrates. The scope of this work is to investigate the potential of a home-made SERS substrate to compare the lipid oxidation over time in ground pork preserved either in a low-density polyethylene (LDPE) conventional packaging or in an active packaging containing oregano extract.<h4>Material and method&nbsp;</h4>Fresh ground pork meat was purchased in bulk from a local supermarket and 22 g samples of meat were placed in 5-cm diameter polystyrene Petri dishes. Each sample was covered with an active film and packed in an LDPE bag under a normal atmosphere. Reference samples were also prepared using conventional LDPE films. All samples were stored in a refrigerator at 5 °C and their lipid extracts were analyzed after 0, 7, 9, 11, 14 and 16 days using a home-made SERS substrate based on silver nanoparticles deposited on a glass Petri dish. A special home-made cooling system was used to perform the analyses at low temperature and SERS spectra were measured at -2 °C on a <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2239">Thermo Scientific™ DXR3 Raman Microscope</a> (Waltham, MA, USA) with a 532 nm laser source, a 900 lines/mm grating covering the 50-3500 cm-1 spectral range and an x10 objective (NA 0.40). The laser power was set at 5&nbsp;mW, and 20 exposures of 30 s each were selected to acquire all data. Thermo Scientific™ OMNIC™ v. 9.2 software was used for data collection and analysis. All the measurements were performed in triplicate. As the decrease in the peak at 1655&nbsp;cm-1 (stretching of C=C bonds from unsaturation) can be attributed to lipid peroxidation, and the 1439 cm-1 (scissoring deformation of CH2) is not affected by it, the area ratio between 1655 cm-1 and 1439 cm-1 bands was calculated to follow the lipid oxidation.<h4>Conclusion&nbsp;</h4>The effectiveness of a home-made SERS substrate coupled with a home-made cooling system was demonstrated for monitoring lipid oxidation in packaged ground pork meat over time. The advantages of this technique are its speed and the minimal sample handling requirements. An improvement factor of the order of 107 over conventional Raman was observed. This study also confirmed the greater efficacy of active packaging containing oregano extracts against lipid oxidation in ground pork, compared to conventional LDPE packaging.

News from LabRulezICPMS Library - Week 09, 2026

Article

Product

Events

Webinars

Application

Academy

Video

Poster

Scientists

Plastics

Environment

Food

Water

Health

Presentation

Scientific article

Interview

Toxicology

Popularization

Science and research

Software

Covid-19

Career

Laboratories

Various

Zaměření

Type of News

Focus

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

LECO Training Course ON/ONH-736/836 Series

LECO Training Course CS-744/844 Series

Pittcon 2026

Boost Your ICP-OES Accuracy

Ride the Tide: Novel NMR Approaches for Peptide Conformation and Kinetics Characterization

Heated Stories: What Differential Scanning Calorimetry Reveals About Petrochemical Materials