LCGC (LCGC North America, LCGC Europe, and LCGC Asia Pacific) seeks to uphold the highest standards of editorial ethics.
Peer-reviewed papers are reviewed with the understanding that the work is original and has not previously been published and is not currently under review by another publication.
Scientific method and accuracy: An author’s central obligation is to present an accurate and complete account of the research performed, absolutely avoiding deception and product promotion, including the data collected or used, as well as an objective discussion of the significance of the research. The research report and the data collected should contain sufficient detail and reference to public sources of information to permit a trained professional to reproduce the experimental observations. Fraudulent or knowingly inaccurate statements constitute unethical behavior and are unacceptable.
Originality and plagiarism: The authors should ensure that they have written entirely original works, and if the authors have used the work or words of others, that such use has been appropriately cited or quoted.
Authorship: The co-authors of a paper should be all those persons who have made significant scientific contributions to the work reported and who share responsibility and accountability for the results. Authors should appropriately recognize the contributions of technical staff and data professionals. Other contributions should be indicated in an “Acknowledgments” section.
Using artificial intelligence (AI): Authors may use AI to aid in the production of written articles, video, and audio content. AI-generated content must be thoroughly edited for accuracy and clarity. Authors are required to disclose the use of AI upon submission to LCGC and must include an acknowledgment in the published version.
Disclosure and conflicts of interest: All relationships that could be viewed as presenting a potential conflict of interest must be disclosed by the authors. Submissions from authors who work for manufacturers of analytical instruments or consumables will be considered for publication but must not be promotional. Papers considered promotional will be rejected or sent back to the authors for revision before being resubmitted for reevaluation.
Errors and corrections: When authors discover significant errors or inaccuracies in their own published work, it is their obligation to promptly notify LCGC and cooperate with us to correct the paper in the form of an erratum or to retract the paper. If the editors or publisher learns from a third party that a published work contains a significant error or inaccuracy, then it is the authors’ obligation to promptly correct or retract the paper or provide evidence to the editors of the correctness of the paper.
Handling of unethical publishing behavior: In cases of alleged or proven scientific misconduct, fraudulent publication, or plagiarism, LCGC will take all appropriate measures to clarify the situation and to amend the article in question. This includes the prompt publication of an erratum, clarification, or even the retraction of the affected work. The publisher, together with the editors, shall take reasonable steps to identify and prevent the publication of papers where research misconduct has occurred, and under no circumstances encourage such misconduct or knowingly allow such misconduct to take place.
Copyright and permissions: Authors must obtain written permission to reproduce any copyrighted materials that have appeared elsewhere. Authors must sign a standard license agreement provided by LCGC’s parent company, Informa, confirming that the work is original and does not infringe on any copyrights or other proprietary rights of others, and granting MJH Life Sciences permission to publish and republish the work.
Measuring Procyanidin Concentration in Wines Using UHPLC
January 24th 2025Researchers from the University of Bordeaux (Villenave d'Ornon, France) report the development and validation of a rapid and quantitative analytical method measuring crown procyanidin concentration in red and white wines using ultra-high performance liquid chromatography (UHPLC) coupled with a ultra-high performance liquid chromatography (Q-TOF) mass spectrometer.
The Next Frontier for Mass Spectrometry: Maximizing Ion Utilization
January 20th 2025In this podcast, Daniel DeBord, CTO of MOBILion Systems, describes a new high resolution mass spectrometry approach that promises to increase speed and sensitivity in omics applications. MOBILion recently introduced the PAMAF mode of operation, which stands for parallel accumulation with mobility aligned fragmentation. It substantially increases the fraction of ions used for mass spectrometry analysis by replacing the functionality of the quadrupole with high resolution ion mobility. Listen to learn more about this exciting new development.
The Complexity of Oligonucleotide Separations
January 9th 2025Peter Pellegrinelli, Applications Specialist at Advanced Materials Technology (AMT) explains the complexity of oligonucleotide separations due to the unique chemical properties of these molecules. Issues such as varying length, sequence complexity, and hydrophilic-hydrophobic characteristics make efficient separations difficult. Separation scientists are addressing these challenges by modifying mobile phase compositions, using varying ion-pairing reagents, and exploring alternative separation modes like HILIC and ion-exchange chromatography. Due to these complexities, AMT has introduced the HALO® OLIGO column, which offers high-resolution, fast separations through its innovative Fused-Core® technology and high pH stability. Alongside explaining the new column, Peter looks to the future of these separations and what is next to come.
Testing Solutions for Metals and PFAS in Water
January 22nd 2025When it comes to water analysis, it can be challenging for labs to keep up with ever-changing testing regulations while also executing time-efficient, accurate, and risk-mitigating workflows. To ensure the safety of our water, there are a host of national and international regulators such as the US Environmental Protection Agency (EPA), World Health Organization (WHO), and the European Union (EU) that demand stringent testing methods for drinking water and wastewater. Those methods often call for fast implementation and lengthy processes, as well as high sensitivity and reliable instrumentation. This paper explains how your ICP-MS, ICP-OES, and LC-MS-MS workflows can be optimized for compliance with the latest requirements for water testing set by regulations like US EPA methods 200.8, 6010, 6020, and 537.1, along with ISO 17294-2. It will discuss the challenges faced by regulatory labs to meet requirements and present field-proven tips and tricks for simplified implementation and maximized uptime.