Synthesis of silica-based benzeneboronic acid affinity materials and application as pre-column in coupled-column high-performance liquid chromatography [An article from: Analytica Chimica Acta] Buy on Amazon

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Synthesis of silica-based benzeneboronic acid affinity materials and application as pre-column in coupled-column high-performance liquid chromatography [An article from: Analytica Chimica Acta]

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PublisherElsevier
ISBN / ASINB000PBZTDC
ISBN-13978B000PBZTD2
AvailabilityAvailable for download now
MarketplaceUnited States  🇺🇸

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This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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Three silica-based benzeneboronic acid affinity materials were synthesized by using an m-aminobenzeneboronic acid as the ligand and using three different spacer arms. Under high-pressure, three affinity pre-columns were packed with these materials and the retention of every affinity pre-column with 11 urinary nucleosides was studied. With different spacer arms of boronic acid-substituted silica materials, the absorption to vicinal alcohols (cis-diols) and stability under acidic elution conditions are of great difference. Coupled-column liquid chromatographic methods for the direct analysis of urinary nucleosides were respectively established. As a result, two of three affinity pre-columns showed good chromatographic property in the on-line analysis of urinary nucleosides. The coupled-column system including pre-column I is the best with excellent linearity (R^2>0.995), good recoveries (85.6-96.9%) and reproducibility (R.S.D.: 1.01-4.02%). The pre-column I could at least endure 150 repetitive injections of a 100@mL urinary sample.
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