Liquid Chromatography (LC/HPLC)

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The Future is 3D
0:35
The Future is 3D
7 months ago
by
Bo Zhang
The History of Slalom Chromatography
0:54
The History of Slalom Chromatography
7 months ago
by
Fabrice Gritti
Addressing Persistent, Mobile, and Toxic Compounds
0:40
Addressing Persistent, Mobile, and Toxic Compounds
8 months ago
by
Kate Jones
Tackling Complex Molecules in the Lab
0:37
Tackling Complex Molecules in the Lab
8 months ago
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Kate Jones
Future Trends in the Laboratory
0:45
Future Trends in the Laboratory
8 months ago
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Kate Jones
Key Application Areas for 2026
0:33
Key Application Areas for 2026
8 months ago
by
Kate Jones
The Future of Column Technology
0:34
The Future of Column Technology
8 months ago
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Kate Jones

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Capillary liquid chromatography (CapLC) offers compelling advantages in sensitivity, solvent reduction, and compatibility with modern mass spectrometry, yet remains underutilized in routine analytical workflows. This article synthesizes expert discussions from a Pittcon 2026 networking session to examine why CapLC adoption has lagged despite decades of development. Key themes include educational gaps, instrumentation limitations, robustness concerns, detection challenges, and supply‑chain constraints. The discussion highlights areas where CapLC already delivers clear value—such as proteomics, oligonucleotide analysis, and high‑throughput screening—and outlines practical pathways for broader adoption through targeted applications, improved instrumentation, and redefined expectations of “routine” chromatography.

Advances in liquid chromatography (LC) address the growing need to analyze complex analytes with higher sensitivity and efficiency. Application-specific column chemistries, optimized system configurations, and improved consumables help mitigate PFAS contamination, metal-sensitive analytes, and solvent-related artifacts. Emerging injection strategies and smart instrumentation aim to enhance data quality and laboratory productivity, demonstrating that optimizing LC methods goes beyond column selection alone.

Μetabolomics enables the comprehensive profiling of small molecules in medicine, plant science, and systems biology. Its true value depends not on the number of detected features but on the reliability of metabolite identification and pathway analysis. Despite well-established guidelines, annotation and definitive identification are often conflated in practice. Simple matches in mass databases are frequently reported as identities, without comparison to standards or chromatographic evidence. This overstatement of confidence compromises validity and risks propagating errors into databases, pathway analyses, and AI-driven workflows. Mass spectrometry (MS) alone is rarely sufficient for identification and orthogonal evidence is essential. Chromatographic retention time is an underused but powerful descriptor reflecting molecular properties. When combined with MS it can provide plausibility checks and form the basis of Level 1 identification. Regulatory frameworks already require such combined criteria in targeted analysis. Systematic use of retention order, retention indices, and prediction models can filter implausible candidates and strengthen identification.

With the global surge in plastic consumption, sustainable recycling has emerged as a cornerstone of environmental stewardship. Polyethylene terephthalate (PET) is a leading player in the recycling revolution, yet ensuring the quality and authenticity of recycled PET (rPET) remains a critical challenge. This article presents a rapid, robust, and quantitative high performance liquid chromatography (HPLC) method for analyzing cyclic oligomers in rPET. This approach aligns with the Japanese Ministry of the Environment guidelines, enabling precise evaluation of rPET quality. The method leverages gradient elution and a practical calibration approach to deliver high throughput and accuracy, supporting the circular economy and the future of sustainable materials.

A quality attribute of Suzuki-Miyura coupling reactions is to measure residual levels of phosphine ligands in the reaction product. Residual phosphine ligands can be present in non-oxidized and oxidized forms. The non-oxidized and oxidized forms have different UV chromophores and can have differing solubility. These differences can preclude accurate and precise quantification. The extent of oxidation is difficult to prevent and control for calibration standards and test materials. This paper describes a method for derivatizing residual phosphines to the oxidized form. The oxidized form is stable and provides a basis for accurate quantification of residual phosphines. This overcomes the challenges for quantifying the non-oxidized and oxidized forms.

Combining silicon micro-nanofabrication technology to create perfectly ordered separation beds on a silicon chip, such as micro-pillar array columns (µPACs), is a powerful innovation in liquid chromatography. This article discusses the numerous possibilities of micro-nanofabrication in the future of analytical chemistry in life science, covering sample preparation, separation science, and detection technologies.

The Chromatographic Society has announced the winners of the Martin Medal and the Silver Jubilee Medal for 2026. Professor Guowang Xu of the Dalian Institute of Chemical Physics in China, has been awarded the Martin Medal, and the Silver Jubilee Medal has been awarded to Professor Bo Zhang of Xiamen University in China.