The small‐sized molecules that have been developed from single hydrophobic amino acids (Phe, Trp, Tyr and Leu) by suitably protecting the –NH2 and –CO2H groups generate diverse nanoscopic structures – such as nanorods, nanofibrils, nanotubes, and nanovesicles – depending upon the protection parameters and solvent polarity. The vesicular structures get disrupted in the presence of various salts, such as KCl, CaCl2, (NH4)2SO4 and N(n‐Bu)4Br. Insertion of unnatural (o/m/p)‐aminobenzoic acids as a protecting group and the lack of conventional peptide bonds in the molecules give the nanostructures proteolytic stability. The nanostructures also show significant thermal stability along with a morphological transformation upon heat treatment. Our in vitro studies reveal that the addition of micromolar concentration “curcumin” significantly reduces the formation of amyloid‐like fibrils. These diverse nanostructures are used as a template for fabricating silver nanoparticles on their outer surfaces as well as in the inner part, followed by calcination in air which helps to obtain a 1D silver nanostructure. Furthermore, the nanovesicles are observed to encapsulate a potent drug (curcumin) and other biologically important molecules, which could be released through salt‐triggered disruption of vesicles.
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Koley et al. (2011) studied this question.
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