Sep 2026· Analytical and Bioanalytical Chemistry· 0 citations· 19 references
Medicine
Abstract
Sample preparation in bioanalysis can require significant numbers of (manual) steps and consumables. Such procedures can be bottlenecks regarding cost, throughput, and greenness. This is also the case for analysis of new approach methodologies (NAMs) such as organoids and organ-on-a-chip systems. In this context, approaches tailored for measuring drugs in NAM-related cell culture media (CCM) are being developed. For mass spectrometry-based analysis, automated filtration/filter backflush solid-phase extraction liquid chromatography AFFL-SPE-LC is utilized. Case studies have shown that the "AFFL" platform allows for vast reductions in sample preparation efforts, as the "self-cleaning" filtration features and SPE conditions remove potentially clogging/contaminating materials from samples of biological origin, e.g., the salt and protein content in CCM. Here, broader demonstrations of the AFFL platform's traits for CCM analysis are provided, employing an extended panel of hydrophobic small-molecule drugs. The investigated AFFL platform shows reproducible chromatographic performance, as well as fit-for-purpose inter-matrix and inter-column robustness. Hundred-scale injections can be performed with satisfactory repeatability (e.g., retention time RSDs < 1%), with limited interference from the various CCM matrices investigated. Practical NAM applications are also demonstrated. The approach has clear advantages in greenness, obtaining an AGREE prep score of 0.71, contrasting the < 0.55 scores of more conventional/commercial approaches. The plastic consumable usage of our approach is 28 g/100 samples, a nearly 20-fold improvement over a previously established benchmark (500 g/100 samples). Taken together, these results demonstrate that AFFL provides a robust, low-waste, and scalable LC-MS-based workflow for chemical analysis of NAM-derived samples.
This review provides a thorough investigation into the design and validation of bioanalytical techniques utilizing the AQbD framework, in accordance with ICH rules that delineate GLP and controlled bioanalysis.
A. Sahu, Uttam Prasad Panigrahy, Bikash Ranjan Jena· Drug Metabolism and Bioanaly...· 0 citations
The tightening regulatory landscape for per‑ and polyfluoroalkyl substances (PFAS) has created an urgent demand for robust analytical methods and reliable monitoring data to support risk management and regulatory compliance. Consequently, the analytical demands are increasing, and robust and broadly applicable analytic...
Friederike Lünne, Theresa Zorn, Alexander Köhrer et al.· Angewandte Chemie· 0 citations
The increasing prevalence of polysubstance use and the drawbacks of urine have driven interest in oral fluid (OF) for drugs-of-abuse (DOA) testing. However, OF brings its own analytical challenges including generally lower collection volumes and analyte concentrations, matrix effects and interferents, and the nee...
Christian Grenier, An Q. I. Cheng, Jia He et al.· Clinical Chemistry· 0 citations
Solid-phase microextraction (SPME) with biocompatible coating material is highly compatible with ambient mass spectrometry (AMS), such as direct analysis in real time (DART), for improving sensitivity and reducing matrix effects. However, the practical throughput of SPME−DART-MS remains limited by the mismatch betwee...
Wei Zhou, Marc Driezen, Janusz Pawliszyn· Analytical Chemistry· 0 citations
A plate-based protein precipitation workflow in a scalable, high-throughput format for human plasma and urine demonstrates the suitability of the established protocol for combined MWAS/ExWAS.
Julia Füreder, A. Müller, Giulia Guerra et al.· Analytical Chemistry· 0 citations
A new machine-learning framework aims to improve the success rate of computational protein design while moving away from results that reproduce sequences found in nature.