Scalable Platform for Structured and Hybrid Soft Nanocolloids by Continuous Precipitation in a Confined Environment.

Geometrically structured polymer nanocolloids, including Janus nanocolloids, have been widely investigated for their unique properties, which are derived from their anisotropy. Controlled surface decoration with inorganic nanoparticles could induce another level of functionality into structured nanocolloids that could enable applications in fields ranging from rewriteable electronics to biphasic catalysis. Here, we demonstrate flash nanoprecipitation (FNP) as a one-step, scalable process platform for manufacturing hybrid polymer-inorganic nanocolloids in which one phase is selectively decorated with a metal nanocatalyst by tuning the molecular interactions between the feed ingredients during the process. For instance, by modifying the polymer end-group functionality, we document the ability to tune the location of the metal nanocatalyst, including placement at the nanocolloid circumference. Moreover, the addition of molecular additives is shown to transform the Janus nanocolloid structure from spherical to dumbbell or snowman while maintaining the ability to control the nanocatalyst location. In considering the flexibility and continuous nature of the FNP process, it offers an industrial-scale platform for the manufacturing of nanomaterials that are anticipated to impact many technologies.

Combining Precipitation and Vitrification to Control the Number of Surface Patches on Polymer Nanocolloids.

In an effort to incorporate increasingly higher levels of functionality into soft nanoparticles, heterogeneously structured particles stand out as a simple means to enhance functionality by tailoring only particle architecture. Various means exist for the fabrication of particles with specific structural configurations; however, the tunability of particle morphology is still a challenging and often laborious task, especially in self-assembled systems where a single equilibrium configuration dominates. Improved strategies for multipatch particle assembly are therefore needed to allow for the tailoring of particle structure via a single, continuous assembly route. One means of accomplishing this is through kinetic trapping of particle morphologies along the path to the final equilibrium configuration in precipitation-induced, phase-separating polymer blends. Here, we demonstrate this capability by using rapid nanoprecipitation to control the overall size, composition, and patch distribution of soft colloids. In particular, we illustrate that polymer feed concentration, blend ratio, and polymer molecular weight can all serve as functional handles with which to consistently alter particle patch distributions in a self-assembling homopolymer system without redesigning the starting materials. We furthermore delineate the role of polymer vitrification in the determination of particle structure.

Rapid Production of Internally Structured Colloids by Flash Nanoprecipitation of Block Copolymer Blends.

Colloids with internally structured geometries have shown great promise in applications ranging from biosensors to optics to drug delivery, where the internal particle structure is paramount to performance. The growing demand for such nanomaterials necessitates the development of a scalable processing platform for their production. Flash nanoprecipitation (FNP), a rapid and inherently scalable colloid precipitation technology, is used to prepare internally structured colloids from blends of block copolymers and homopolymers. As revealed by a combination of experiments and simulations, colloids prepared from different molecular weight diblock copolymers adopt either an ordered lamellar morphology consisting of concentric shells or a disordered lamellar morphology when chain dynamics are sufficiently slow to prevent defect annealing during solvent exchange. Blends of homopolymer and block copolymer in the feed stream generate more complex internally structured colloids, such as those with hierarchically structured Janus and patchy morphologies, due to additional phase separation and kinetic trapping effects. The ability of the FNP process to generate such a wide range of morphologies using a simple and scalable setup provides a pathway to manufacturing internally structured colloids on an industrial scale.

Nanomedicine as a non-invasive strategy for drug delivery across the blood brain barrier.

The blood brain barrier (BBB) is a major obstacle to drug delivery for diseases of the central nervous system (CNS). This brief review highlights the current invasive and non-invasive technologies available to address this problem. In particular, nanomedicine has shown much promise as a non-invasive strategy due to its drug loading capabilities, ease of targeting to the BBB, and small size. The versatility of this technology in terms of type of drug and imaging agent, carrier material, and targeting mechanism is highlighted in this review. The recent inclusion of imaging agents in the nanocarriers has important consequences for the field of theranostics.

Efficient preparation of size tunable PEGylated gold nanoparticles.

A facile, one-step self-assembly of polymer nanoreactors is reported for the fabrication of uniform PEGylated gold nanoparticles. Nanoreactor assembly occurs within milliseconds and gold nanoparticles are produced within minutes at room temperature. The presented approach enables continuous synthesis of size tunable gold nanoparticles with tailorable surface chemistry.

Directed Assembly of Soft Colloids through Rapid Solvent Exchange.

We studied the directed assembly of soft nanoparticles through rapid micromixing of polymers in solution with a nonsolvent. Both experiments and computer simulations were performed to elucidate the underlying physics and to investigate the role of various process parameters. In particular, we discovered that no external stabilizing agents or charged end groups are required to keep the colloids separated from each other when water is used as the nonsolvent. Furthermore, the size of the nanoparticles can be reliably tuned through the mixing rate and the ratio between polymer solution and nonsolvent. Our results demonstrate that this mechanism is highly promising for the mass fabrication of uniformly sized colloidal particles, using a wide variety of polymeric feed materials.