Polyamine-guided synthesis of anisotropic, multicompartment microparticles.

ACS Appl Mater Interfaces

Department of Chemical and Biomolecular Engineering, Rice University, 6100 S. Main Street, Houston, TX 77251-1892, USA.

Published: March 2009

Colloidal particles that have nonuniform bulk or surface compositions are of emerging interest because of their potential applications involving advanced chemical storage and delivery and the self-assembly of novel functional materials. Experimental realization of anisotropic particles is much more difficult than that for particles with uniform bulk and surface composition, however. A new wet-chemical synthesis method to anisotropic microparticles is presented. This approach makes convenient use of the unusual observation of a salt-triggered separation of two water-solubilized polyamines into colloidal aggregates with nonuniform polymer composition. The anisotropic structure of these ionically cross-linked aggregates is explained by the difference in surface tensions of the contained single-polymer domains. Contacting the polymer aggregates with silicic acid or 13-nm silica nanoparticles leads to the charge-driven formation of solid or hollow microspheres, respectively. Depending on the poly(lysine)/poly(allylamine) ratio, the nonuniformity of the polymer aggregates translates to surface patches or internal compartments found in the resultant silica/polymer microparticles. Such hybrid materials with their unique structure could serve as a new basis for targeted chemical delivery and controlled release for potential applications in medicine, food, and cosmetics.

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http://dx.doi.org/10.1021/am8001499DOI Listing

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