4.6 Article

Nanoparticle-Based Membrane Assembly and Silicification in Coacervate Microdroplets as a Route to Complex Colloidosomes

Journal

LANGMUIR
Volume 30, Issue 48, Pages 14591-14596

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la503746u

Keywords

-

Funding

  1. ERC Advanced Grant scheme
  2. University of Bristol
  3. Engineering and Physical Sciences Research Council [1100874, EP/L002957/1] Funding Source: researchfish
  4. Natural Environment Research Council [NE/J018325/1] Funding Source: researchfish
  5. EPSRC [EP/L002957/1] Funding Source: UKRI
  6. NERC [NE/J018325/1] Funding Source: UKRI

Ask authors/readers for more resources

The chemical construction of complex colloidosomes consisting of a molecularly crowded polyelectrolyte-enriched interior surrounded by a continuous shell of closely packed silica nanoparticles is studied using optical and fluorescence microscopy, high-resolution X-ray microcomputed tomography, and synchrotron radiation X-ray tomographic microscopy. The colloidosomes are prepared by addition of partially hydrophobic silica nanoparticles to dodecane dispersions of positively or negatively charged coacervate microdroplets consisting of aqueous mixtures of poly(diallyldimethylammonium chloride) (PDDA) and adenosine 5'-triphosphate (ATP) or PDDA and poly(acrylic acid) (PAA), respectively. Interfacial assembly of the nanoparticles produces a polydisperse population of well-defined PDDA/PAA droplets with diameters ranging from 50 to 950 mu m. In contrast, reconstruction of the PDDA/ATP coacervate interior occurs on addition of the silica nanoparticles to produce a nanoparticle-stabilized oil-in-coacervate-in-oil multiphase emulsion. Transfer of the coacervate-containing colloidosomes into water and replication of their internal structure are achieved by addition of tetramethoxysilane, which serves as both a cross-linking and silicification agent to produce mineralized PDDA/PAA or PDDA/ATP microstructures with a uniform solidified texture or multichambered interior, respectively. The integration of colloidosome and coacervate technologies offers a route to a new type of multifunctional microcompartmentalized system based on the membrane-mediated incarceration of molecularly crowded chemical environments.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available