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Polymer monoliths are stationary-phase materials for liquid chromatography and solid-phase extraction. Their porous structure, tuneability and simple synthesis enable tailoring to specific analysis requirements in analytical chemistry. Typically, polymer monoliths are used to separate larger biomolecules. Due to their lower binding capacity, the applications of polymer monoliths for the chromatographic separation of small molecules remain limited. However, recent literature has shown that polymer monoliths have the potential for the extraction of small molecules. In this research, butyl methacrylate-co-ethylene glycol dimethacrylate polymer monoliths were synthesized using localized UV polymerization in capillaries. The performance of reversed-phase polymer monoliths in automated in-line solid-phase extraction-mass spectrometry was demonstrated by the analysis of endocannabinoids from neat standard mixes and spiked cell culture media without prior sample preparation. The synthesized monoliths exhibited a binding capacity of 1896 pmol. Furthermore, we showed the repeatability of the monolith synthesis, with a variance in permeability of 19%. The system's stability is demonstrated through the analysis of multiple batches, comparing different monoliths and reusing the same monolith repeatedly, resulting in relative standard deviations (RSDs) below 20% for all extracted compounds. This automated method with hyphenated mass spectrometry improves throughput over previous manual monolithic extractions for small molecules.
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http://dx.doi.org/10.1093/chromsci/bmaf049 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.
Hydrogel-based bioinks are widely adopted in digital light processing (DLP) 3D printing. Modulating their mechanical properties is especially beneficial in biomedical applications, such as directing cell activity toward tissue regeneration and healing. However, in both monolithic and granular hydrogels, the tunability of mechanical properties is limited to parameters such as cross-linking or packing density.
View Article and Find Full Text PDFJ Chromatogr Sci
August 2025
Metabolomics and Analytics Centre, Leiden Academic Centre for Drug Research, Leiden University, Einsteinweg 55 2333CC Leiden, The Netherlands.
Polymer monoliths are stationary-phase materials for liquid chromatography and solid-phase extraction. Their porous structure, tuneability and simple synthesis enable tailoring to specific analysis requirements in analytical chemistry. Typically, polymer monoliths are used to separate larger biomolecules.
View Article and Find Full Text PDFNanoscale Adv
August 2025
School of Engineering, Brown University Providence Rhode Island USA
Electrically conductive hydrogels are of interest as scaffolds for tissue engineering applications involving the growth, implantation, or attachment of electrically active cells. Such hydrogels should exhibit soft mechanics, tunable conductivity to match native tissue, biocompatibility, and biodegradability into non-toxic, clearable species. Common conductors based on metals or polymers can be challenged by insufficient biocompatibility or biodegradability.
View Article and Find Full Text PDFJ Dent
August 2025
Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, UK.
Objective: To assess the impact of different surface pretreatment protocols on the repair bond strength of resin composite to different ceramics.
Study Selection: Laboratory studies reporting (micro-)tensile bond strength of resin composite to full contour/monolithic ceramics following different surface pretreatment methods.
Sources: Electronic databases (MEDLINE via PubMed, EMBASE via Ovid, Web of Science, and Scopus) were searched in October 2024.
Adv Mater
August 2025
Key Laboratory of Fluorine and Silicon for Energy Materials and Chemistry of Ministry of Education, Jiangxi Normal University, 99 Ziyang Avenue, Nanchang, 330022, P. R. China.
Wide-bandgap (WBG) perovskites with tunable bandgaps can be integrated into organic solar cells to construct tandem solar cells (TSCs), enabling the device to exceed the Shockley-Queisser efficiency limit. However, ionic mismatches and crystallization kinetics in WBG perovskites trigger inhomogeneous phase distribution and defects. In this work, a triphenyl phosphate (Tri-PyPA) is utilized to modulate Br/I competitive crystallization and compositional distribution.
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