Bile salts (BSs) are naturally occurring rigid surfactants with a steroidal skeleton and specific self-assembly and interface behaviors. Using bile salts as precursors, derivatives can be synthesized to obtain molecules with specific functionalities and amphiphilic structure. Modifications on single molecules are normally performed by substituting the least-hindered hydroxyl group on carbon C-3 of the steroidal A ring or at the end of the lateral chain. This leads to monosteroidal rigid building blocks that are often able to self-organize into 1D structures such as tubules, twisted ribbons, and fibrils with helical supramolecular packing. Tubular aggregates are of particular interest, and they are characterized by cross-section inner diameters spanning a wide range of values (3−500 nm). They can form through appealing pH-or temperature-responsive aggregation and in mixtures of bile salt derivatives to provide mixed tubules with tunable charge and size. Other derivatives can be prepared by covalently linking two or more bile salt molecules to provide complex systems such as oligomers, dendrimers, and polymeric materials. The unconventional amphiphilic molecular structure imparts specific features to BSs and derivatives that can be exploited in the formulation of capsules, drug carriers, dispersants, and templates for the synthesis of nanomaterials.
Biocompatible molecules that undergo self-assembly are of high importance in biological and medical applications of nanoscience. Peptides and bile acids are among the most investigated due to their ability to self-organize into many different, often stimuli-sensitive, supramolecular structures. With the aim of preparing molecules mixing the aggregation properties of bile acid and amino acid-based molecules, we report on the synthesis and self-association behavior of two diastereomers obtained by substituting a hydroxyl group of cholic acid with a l-phenylalanine residue. The obtained molecules are amphoteric, and we demonstrate that they show a pH-dependent self-assembly. Both molecules aggregate in globular micelles at high pH, whereas they form tubular superstructures under acid conditions. Unusual narrow nanotubes with outer and inner cross-section diameters of about 6 and 3 nm are formed by the derivatives. The diasteroisomer with α orientation of the substituent forms in addition a wider tubule (17 nm cross-section diameter). The ability to pack in supramolecular tubules is explained in terms of a wedge-shaped bola-form structure of the derivatives. Parallel or antiparallel face-to-face dimers are hypothesized as fundamental building blocks for the formation of the narrow and wide nanotubes, respectively.
An amino acid-substituted bile acid forms tubular aggregates with inner and outer diameters of about 3 and 6 nm. The diameters are unusually small for surfactant self-assembled tubes. The results enhance the spectrum of applications of supramolecular tubules and open up possibilities for investigating a novel class of biological amphiphiles.
Morphology control
and tuning of nanomaterials are crucial to determine
their properties and applications. Solutions based on different synthetic
methodologies have been proposed, and in general they required variation
of several parameters. Here, a new facile and cost-effective bottom-up strategy to control the morphology of mesoporous
silica particles is presented. Specifically, catanionic templating
systems composed of bile acids and CTAB enable the production of submicrometer
MCM-41 particles of various shapes, high porosity, and remarkable
features. The variation of a single component, the bile acid, leads
to the preparation of particles with different morphologies. For instance,
small (<500 nm) well-separated hexagonal platelets and twisted
rods, with tunable aspect ratio and chiral pore channels, were prepared.
Experiments aimed at elucidating the role of the bile acids showed
that the control of shape is due to the specific interactions between
bile acids and CTAB.
Enhanced degradation of mesoporous silica particles in neutral and acidic aqueous solutions was achieved by embedding diimine moieties in the silica network.
Over
the last years, advancements in the use of nanoparticles for
biomedical applications have clearly showcased their potential for
the preparation of improved imaging and drug-delivery systems. However,
compared to the vast number of currently studied nanoparticles for
such applications, only a few successfully translate into clinical
practice. A common “barrier” that prevents nanoparticles
from efficiently delivering their payload to the target site after
administration is related to liver filtering, mainly due to nanoparticle
uptake by macrophages. This work reports the physicochemical and biological
investigation of disulfide-bridged organosilica nanoparticles with
cage-like morphology, OSCs, assessing in detail their bioaccumulation in vivo. The fate of intravenously injected 20 nm OSCs was
investigated in both healthy and tumor-bearing mice. Interestingly,
OSCs exclusively colocalize with hepatic sinusoidal endothelial cells
(LSECs) while avoiding Kupffer-cell uptake (less than 6%) under both
physiological and pathological conditions. Our findings suggest that
organosilica nanocages hold the potential to be used as nanotools
for LSECs modulation, potentially impacting key biological processes
such as tumor cell extravasation and hepatic immunity to invading
metastatic cells or a tolerogenic state in intrahepatic immune cells
in autoimmune diseases.
The introduction of a mannose residue on carbon 3 of lithocholic acid gives rise to an asymmetric and rigid bolaamphiphilic molecule, which self-assembles in water to form elongated tubular aggregates with an outer diameter of about 20 nm. These tubular structures display a temporal evolution, where the average tube diameter decreases with time, which can be followed by time-resolved small-angle X-ray scattering experiments. Cryogenic transmission electron microscopy images collected as a function of time show that at short times after preparation tubular scrolls are formed via the rolling of layers, after which a complex transformation of the scrolls into single-walled tubules takes place. At long time scales, a further evolution occurs where the tubules both elongate and become narrower. The observed self-assembly confirms the tendency of bile acids and their derivatives to form supramolecular aggregates with an ordered packing of the constituent molecules. It also demonstrates that scrolls can be formed as intermediate structures in the self-assembly process of monodisperse single-walled tubules.
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