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Nanostructures from Single Amino Acid‐Based Molecules: Stability, Fibrillation, Encapsulation, and Fabrication of Silver Nanoparticles
Author(s) -
Koley Pradyot,
Pramanik Animesh
Publication year - 2011
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201101465
Subject(s) - nanostructure , materials science , molecule , nanoparticle , nanorod , nanobiotechnology , curcumin , nanotechnology , tripeptide , peptide , solvent , chemical engineering , combinatorial chemistry , organic chemistry , chemistry , biochemistry , engineering
The small‐sized molecules that have been developed from single hydrophobic amino acids (Phe, Trp, Tyr and Leu) by suitably protecting the –NH 2 and –CO 2 H 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, CaCl 2 , (NH 4 ) 2 SO 4 and N(n‐Bu) 4 Br. 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.