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In between molecules and self-assembled fibrillar networks: highly stable nanogel particles from a low molecular weight hydrogelator
The preparation of molecular, non-polymeric nanogels from a low molecular weight hydrogelator is reported. The molecular nanogels are expected to overcome issues associated with the use of polymeric nanogels in biomedicine such as biodegradability, stimuli responsiveness, polydispersity, and batch-t...
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Published in: | Soft matter 2019-04, Vol.15 (17), p.3565-3572 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The preparation of molecular, non-polymeric nanogels from a low molecular weight hydrogelator is reported. The molecular nanogels are expected to overcome issues associated with the use of polymeric nanogels in biomedicine such as biodegradability, stimuli responsiveness, polydispersity, and batch-to-batch reproducibility. Nanogels formed by compound
1
were reproducibly prepared by sonication of a xerogel in PBS, with a total concentration of
ca.
2 mM. The intensity averaged diameter of
ca.
200 nm was determined by DLS. Electron microscopy (TEM and cryo-TEM) showed spherical particles. Light scattering (SALS) indicates that water is the main component of the nanoparticles, and the concentration of
1
in the nanogels is
ca.
3 mg mL
−1
. These particles can be considered to constitute an intermediate state between free molecules and self-assembled fibrillar networks. The nanogels present excellent temporal and thermal stability and accessible hydrophobic domains, as demonstrated by the incorporation of the fluorescent dye Nile Red.
A low molecular weight gelator forms reproducibly nanogel particles with good temporal and thermal stability and they present accessible hydrophobic domains. |
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ISSN: | 1744-683X 1744-6848 |
DOI: | 10.1039/c9sm00252a |