Literature DB >> 24147867

Direct isolation of flavonoids from plants using ultra-small anatase TiO₂ nanoparticles.

Jasmina Kurepa1, Ryo Nakabayashi, Tatjana Paunesku, Makoto Suzuki, Kazuki Saito, Gayle E Woloschak, Jan A Smalle.   

Abstract

Surface functionalization of nanoparticles has become an important tool for in vivo delivery of bioactive agents to their target sites. Here we describe the reverse strategy, nanoharvesting, in which nanoparticles are used as a tool to isolate bioactive compounds from living cells. Anatase TiO₂ nanoparticles smaller than 20 nm form strong bonds with molecules bearing enediol and especially catechol groups. We show that these nanoparticles enter plant cells, conjugate enediol and catechol group-rich flavonoids in situ, and exit plant cells as flavonoid-nanoparticle conjugates. The source plant tissues remain viable after treatment. As predicted by the surface chemistry of anatase TiO₂ nanoparticles, quercetin-based flavonoids were enriched amongst the nanoharvested flavonoid species. Nanoharvesting eliminates the use of organic solvents, allows spectral identification of the isolated compounds, and opens new avenues for use of nanomaterials for coupled isolation and testing of bioactive properties of plant-synthesized compounds.
© 2013 The Authors The Plant Journal © 2013 John Wiley & Sons Ltd.

Entities:  

Keywords:  Arabidopsis thaliana; anatase TiO2 nanoparticles; catechols; flavonoids; stress; technical advance

Mesh:

Substances:

Year:  2013        PMID: 24147867      PMCID: PMC3935720          DOI: 10.1111/tpj.12361

Source DB:  PubMed          Journal:  Plant J        ISSN: 0960-7412            Impact factor:   6.417


  44 in total

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  13 in total

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7.  Computational study on a puzzle in the biosynthetic pathway of anthocyanin: Why is an enzymatic oxidation/ reduction process required for a simple tautomerization?

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Review 9.  Secondary Metabolites in the Green Synthesis of Metallic Nanoparticles.

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