Fabrication of a dendrimer-modified boronate affinity material for online selective enrichment of cis-diol-containing compounds and its application in determination of nucleosides in urine. Issue 128 (14th December 2015)
- Record Type:
- Journal Article
- Title:
- Fabrication of a dendrimer-modified boronate affinity material for online selective enrichment of cis-diol-containing compounds and its application in determination of nucleosides in urine. Issue 128 (14th December 2015)
- Main Title:
- Fabrication of a dendrimer-modified boronate affinity material for online selective enrichment of cis-diol-containing compounds and its application in determination of nucleosides in urine
- Authors:
- Gao, Li
Du, Jin
Wang, Chaozhan
Wei, Yinmao - Abstract:
- Abstract : A high binding capacity dendrimer-modified boronate affinity material (SiO2 @dBA) was synthesized and coupled with large-volume injection/online column-switching solid phase extraction to facilitate the determination process of cis -diols. Abstract : Boronate adsorbents have been widely used in the extraction of cis -diol-containing molecules, but most do not have efficient capacity due to limited binding sites on their surface. In this work, a high binding capacity dendrimer-modified boronate affinity material (SiO2 @dBA) was synthesized via introducing tris(2-aminoethyl)amine as branching points and using poly(amidoamine) as the main dendrimeric scaffold before modification by boronate groups. The high density of amino groups on the dendrimer supplied a large number of binding sites for modifying boronate groups. Thus the adsorption capacity (676.8 μmol g −1 for catechol, 771.3 μmol g −1 for dopamine, 770.0 μmol g −1 for adrenaline) of SiO2 @dBA was greatly improved. Moreover, when coupled with large-volume injection and online column-switching solid phase extraction, SiO2 @dBA was able to capture cis -diols from 10 000-fold interference and enrichment factors reached up to 497–514, which was 26- to 51-fold higher than those of analogous non-dendrimer materials. Especially, the proposed method exhibited a striking low limit of detection, 0.24 ng mL −1 for cytidine, 0.52 ng mL −1 for uridine, 0.37 ng mL −1 for guanosine, 0.67 ng mL −1 for adenosine. Finally, theAbstract : A high binding capacity dendrimer-modified boronate affinity material (SiO2 @dBA) was synthesized and coupled with large-volume injection/online column-switching solid phase extraction to facilitate the determination process of cis -diols. Abstract : Boronate adsorbents have been widely used in the extraction of cis -diol-containing molecules, but most do not have efficient capacity due to limited binding sites on their surface. In this work, a high binding capacity dendrimer-modified boronate affinity material (SiO2 @dBA) was synthesized via introducing tris(2-aminoethyl)amine as branching points and using poly(amidoamine) as the main dendrimeric scaffold before modification by boronate groups. The high density of amino groups on the dendrimer supplied a large number of binding sites for modifying boronate groups. Thus the adsorption capacity (676.8 μmol g −1 for catechol, 771.3 μmol g −1 for dopamine, 770.0 μmol g −1 for adrenaline) of SiO2 @dBA was greatly improved. Moreover, when coupled with large-volume injection and online column-switching solid phase extraction, SiO2 @dBA was able to capture cis -diols from 10 000-fold interference and enrichment factors reached up to 497–514, which was 26- to 51-fold higher than those of analogous non-dendrimer materials. Especially, the proposed method exhibited a striking low limit of detection, 0.24 ng mL −1 for cytidine, 0.52 ng mL −1 for uridine, 0.37 ng mL −1 for guanosine, 0.67 ng mL −1 for adenosine. Finally, the method was successfully applied to online determination of trace nucleosides in healthy human urine. In conclusion, the prepared adsorbent has potential to effectively enrich a large range of trace cis -diol substances in real samples. … (more)
- Is Part Of:
- RSC advances. Volume 5:Issue 128(2015)
- Journal:
- RSC advances
- Issue:
- Volume 5:Issue 128(2015)
- Issue Display:
- Volume 5, Issue 128 (2015)
- Year:
- 2015
- Volume:
- 5
- Issue:
- 128
- Issue Sort Value:
- 2015-0005-0128-0000
- Page Start:
- 106161
- Page End:
- 106170
- Publication Date:
- 2015-12-14
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ra18443f ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1324.xml