Santiago de Frutos

Formation of tubules by p-tert-butylphenylamide derivatives of chenodeoxycholic and ursodeoxycholic acids in aqueous solution.

The formation of tubules by p-tert-butylphenylamide derivatives of chenodeoxycholic and ursodeoxycholic acids in aqueous solution is investigated. The critical aggregation concentrations of the new surfactants are much lower than those of ursodeoxycholate and chenodeoxycholate, indicating the enhanced surfactant properties resulting by the presence of the hydrophobic p-tert-butylphenyl group. The molecular areas at the air-water interface suggest the formation of monolayer films with molecules upright oriented. The shape of the aggregates was investigated by TEM. The main structure present in solution corresponds to tubules. The estimated value for the wall thickness of tubules suggests that a bilayer structure is formed. Host of positively charged latex beads by tubules suggests that their inner and outer surfaces are negatively charged. The acid form of the chenodeoxycholate derivative was recrystallized from toluene and its crystal structure analyzed.

Self-aggregation mechanism of a naphthylamide cationic derivative of cholic acid. From fibers to tubules

The aggregation behavior of a cationic derivative of cholic acid {[3β,5β,7α,12α]-3-(2-naphthoylamino)-7,12-dihydroxycholan-24-triethylamonium iodide} has been studied by surface tension measurements, fluorescence spectroscopy, transmission electronic microscopy (TEM), and circular dichroism. The critical aggregation concentration, the fraction of bound counterions and thermodynamic parameters for the formation of aggregates have been determined, as well as the morphology of the aggregates. TEM images support a consecutive transformation mechanism from fibers to tubules, these having a well-defined geometry and being the only structure observed at the end of the process. Intermediate observed structures are helical ribbons.

Design of dialkyl surfactants from nitrilotriacetic acid as head group

New double-chain surfactants can be designed in which nitrilotriacetic acid plays the role of glycerol in phospholipids. The synthetic methodology is applied to the synthesis of (2-(bis(2-dodecylamino)-2-oxoethyl)amino)acetic acid. This is a symmetric dimeric surfactant but the methodology allows the synthesis of asymmetric double-chain surfactants as well. The Krafft temperature is 16–18 °C. The critical aggregation concentration of the new surfactant (4.76 × 10−5 mol dm−3 in NaOH 0.01 M and 25 °C; surface tension measurements) is two hundred times lower than that for sodium 2-dodecanamidoacetate, which can be considered its monoalkyl surfactant analog, indicating the enhanced surfactant properties resulting from the presence of two hydrophobic alkyl chains. The shape of the aggregates was investigated by transmission electron microscopy. At 40 °C, the main structure present in solution corresponds to vesicles and, from the size distribution of their radii, values of (0.34 ± 0.06)kT and 56.7 ± 2.6 nm were obtained for the effective bending elasticity constant and the spontaneous radius of curvature of vesicles, respectively.

Crystal structure of head-to-head dimers of cholic and deoxycholic acid derivatives with different symmetric bridges.

The crystal structure of three head-to-head dimers (having two cholic acid or deoxycholic acid units) linked at carbon atoms C3 by aromatic or alkyl bridges is studied. An internal coordinates system is necessary for describing the relative orientation in the space of the two bile acid residues. Five angles (three torsion and two common ones) are necessary for defining the relative position of both steroid residues in space. Carbon atoms C3 (which always carries a α-hydroxy group in natural bile acids), and C10 and C13 (which always carry β-methyl groups) of each steroid residue are suitable for this purpose. Furthermore, the distance between each C3 carbon atoms of both steroid residues will allow one to locate the steroids in space. The three dimers selected provide a large range of values for these angles. The packing, hydrogen bond network, and location of guest in the three crystals are discussed.

Diarmed (adamantyl/alkyl) surfactants from nitrilotriacetic acid

The compounds presented here constitute a clear example of molecular biomimetics as their design is inspired on the structure and properties of natural phospholipids. Thus novel double-armed surfactants have been obtained in which nitrilotriacetic acid plays the role of glycerol in phospholipids. The hydrophobic arms are linked to the head group through amide bonds (which is also the case of sphingomyelin): (R1NHCOCH2)(R2NHCOCH2)NCH2CO2H (R1 being CH3(CH2)11, CH3(CH2)17, CH3(CH2)7CHCH(CH2)8, and adamantyl, and R2=adamantyl). The dependence of the surface tension with concentration shows the typical profile of surfactants since a breaking point, which corresponds to the critical aggregation concentration (cac), is observed in all cases. The cac of these diarmed derivatives are about 1-3 orders of magnitude lower than those of classical monoalkyl derivatives used as reference compounds. In contrast to conventional surfactants, reversed trends in cac values and molecular areas at the solution-air interface have been observed. This anomalous behavior is tied to the structure of the surfactants and suggests that long and flexible alkyl chains should self-coil previous to the aggregation or adsorption phenomena. Above cac all compounds form large aggregates, globular in shape, which tend to associate forming giant aggregates.