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Although traditional Tibetan medicine is a valuable source for the discovery of novel lead compounds, the isolation of structural analogs from natural sources remains a challenge in the field of separation science. The Tibetan medicine Gentiana szechenyii (GC) is widely to treat various types of inflammation and upper respiratory tract infections. Despite its strong medicinal value, a complex purification process has limited investigations into its chemical composition. Therefore, in this study, a novel off-line two-dimensional supercritical fluid chromatographic (2D-SFC) method was developed and successfully applied to the efficient separation and purification of complex compounds and structural analogs from GS. Initially, the crude GS sample was pretreated using a binary medium-pressure liquid chromatography system to obtain the target fraction (Fr16, 1.0 g). A novel propyl urea and phenyl/tetrazole stationary phases off-line 2D-SFC system was then developed and applied for the separation and purification of Fr16. Consequently, five polyphenolic compounds were successfully isolated with purities of >95%. The obtained results demonstrate the potential of off-line 2D-SFC for maximizing the discovery of novel structural analogs and isomers, thereby providing a theoretical basis for the further exploitation of natural products.
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http://dx.doi.org/10.1002/jssc.70180 | DOI Listing |
Anal Methods
September 2025
Jilin Province Product Quality Supervision and Inspection Institute, Changchun 130103, China.
A method for determination of ten kinds of sweeteners in soybean products by multi-plug filtration cleanup (-PFC) combined with ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The sample was extracted with acetonitrile (containing 1% formic acid), degreased by using -hexane liquid-liquid extraction and purified by solid phase extraction using an -PFC column (Oasis PRiME HLB). The analytes were separated by using a Waters ACQUITY UPLC® BEH C (2.
View Article and Find Full Text PDFMikrochim Acta
September 2025
Department of Public Health Laboratory Sciences, College of Public Health, Hengyang Medical School, University of South China, 28 Changsheng West Road, Hengyang, 421001, Hunan, China.
We systematically evaluated the DNA adsorption and desorption efficiencies of several nanoparticles. Among them, titanium dioxide (TiO₂) nanoparticles (NPs), aluminum oxide (Al₂O₃) NPs, and zinc oxide (ZnO) NPs exhibited strong DNA-binding capacities under mild conditions. However, phosphate-mediated DNA displacement efficiencies varied considerably, with only TiO₂ NPs showing consistently superior performance.
View Article and Find Full Text PDFArch Microbiol
September 2025
División de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Plasmids are fundamental to molecular biology and biotechnology, playing a crucial role in bacterial evolution. Some plasmids are linked to complex cellular dynamics, including pathogenicity islands, antibiotic resistance, and gene mobilization. This study reports the isolation and sequencing of two cryptic plasmids with different electrophoretic mobilities from the Escherichia coli clinical isolate O55.
View Article and Find Full Text PDFBackground: To improve the molecular diagnostic yield for Aspergillus spp. from respiratory samples, we developed and evaluated a new DNA extraction method directly from respiratory samples combined with in-house Aspergillus real-time PCR.
Methods: We developed a method using beads and resin, where a sample is centrifuged to separate the supernatant and pellet.
Mol Ecol Resour
September 2025
Centre for Evolutionary Hologenomics (CEH), Globe Institute, University of Copenhagen, Copenhagen, Denmark.
Global efforts to standardise methodologies benefit greatly from open-source procedures that enable the generation of comparable data. Here, we present a modular, high-throughput nucleic acid extraction protocol standardised within the Earth Hologenome Initiative to generate both genomic and microbial metagenomic data from faecal samples of vertebrates. The procedure enables the purification of either RNA and DNA in separate fractions (DREX1) or as total nucleic acids (DREX2).
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