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


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 TiO? 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 TiO? 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.

SUBMITTER: Kurepa J 

PROVIDER: S-EPMC3935720 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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

Kurepa Jasmina J   Nakabayashi Ryo R   Paunesku Tatjana T   Suzuki Makoto M   Saito Kazuki K   Woloschak Gayle E GE   Smalle Jan A JA  

The Plant journal : for cell and molecular biology 20131129 3


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-r  ...[more]

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