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C-12 vs C-3 substituted bile salts : An example of the effects of substituent position and orientation on the self-assembly of steroid surfactant isomers

Cautela, Jacopo (author)
Sapienza University of Rome
Severoni, Emilia (author)
Sapienza University of Rome
Redondo-Gómez, Carlos (author)
University of Costa Rica
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di Gregorio, Maria Chiara (author)
Sapienza University of Rome
Del Giudice, Alessandra (author)
Sapienza University of Rome
Sennato, Simona (author)
Sapienza University of Rome
Angelini, Roberta (author)
Sapienza University of Rome
D'Abramo, Marco (author)
Sapienza University of Rome
Schillén, Karin (author)
Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
Galantini, Luciano (author)
Sapienza University of Rome
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 (creator_code:org_t)
Elsevier BV, 2020
2020
English.
In: Colloids and Surfaces B: Biointerfaces. - : Elsevier BV. - 0927-7765. ; 185
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Biomolecule derivatives are transversally used in nanotechnology. Deciphering their aggregation behavior is a crucial issue for the rational design of functional materials. To this end, it is necessary to build libraries of selectively functionalized analogues and infer general rules. In this work we enrich the highly applicative oriented collection of steroid derivatives, by reporting a rare example of C-12 selectively modified bile salt. While nature often exploits such position to encode functions, it is unusual and not trivial to prepare similar analogues in the laboratory. The introduction of a tert-butyl phenyl residue at C-12 provided a molecule with a self-assembly that remarkably switched from rigid pole-like structures to twisted ribbons at a biologically relevant critical temperature (∼25 °C). The system was characterized by microscopy and spectroscopy techniques and compared with the C-3 functionalized analogue. The twisted ribbons generate samples with a gel texture and a viscoelastic response. The parallel analysis of the two systems suggested that the observed thermoresponsive self-assemblies occur at similar critical temperatures and are probably dictated by the nature of the substituent, but involve aggregates with different structures depending on position and orientation of the substituent. This study highlights the self-assembly properties of two appealing thermoresponsive systems. Moreover, it adds fundamental insights hereto missing in the investigations of the relation between self-assembly and structure of synthetic steroids, which are valuable for the rational design of steroidal amphiphiles.

Subject headings

NATURVETENSKAP  -- Kemi -- Materialkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Materials Chemistry (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Bile acid
Hydrogel
Steroid derivatives
Thermoresponsive self-assembly

Publication and Content Type

art (subject category)
ref (subject category)

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