Fig. 1: Surfactant-guided spatial assembly of nano-architectures. | Nature Communications

Fig. 1: Surfactant-guided spatial assembly of nano-architectures.

From: Surfactant-guided spatial assembly of nano-architectures for molecular profiling of extracellular vesicles

Fig. 1

a Schematics of the surfactant-guided nanoparticle integration. The integration performance is determined by surfactant interactions with MOF constituents and nanoparticles. Specifically, strong interaction between surfactants (polar heads) and MOF constituents drives central incorporation and heterogeneous MOF growth around the incorporated nanoparticles, while weak interaction induces tangential integration and homogeneous MOF growth. Likewise, strong interaction between surfactants (hydrophobic tails) and nanoparticles stabilize nanoparticle dispersion while weak interaction leads to nanoparticle aggregation. Through surfactant matching to tune these interactions, the spatial distribution and organization of nanoparticles within MOF hosts can be precisely controlled. The approach is universal for diverse nanoparticles and MOFs, and enables rapid, aqueous synthesis (in solution and in situ on various substrates). b Schematics and transmission electron micrographs (TEM) of STAR (Au-ZIF-8) assemblies. Left: Tween 20-guided assembly. Nanoparticles are peripherally dispersed with respect to the MOF host. Right: CTAB-guided assembly. Aggregated nanoparticles are centrally encapsulated within the MOF host. Each experiment was repeated three times independently with similar results. Scale bars, 50 nm. c Dual-probe STAR assay for the direct profiling of extracellular vesicle glycans. In the presence of target glycans, the specific binding of lectin-oxidase mediates in situ generation of hydrogen peroxide, which selectively quenches the fluorescence of the peripheral working probes, while leaving the central reference probes in the same assemblies unaffected. d Microfluidic device and smartphone-based optical detection platform. The microfluidic device consists of two channels: a lower channel with in situ-grown STARs and an upper channel with preloaded lectins. Solution mixing between the two channels during assay workflow enables specific targeting and signal generation.

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