DOI > 10.5291/ILL-DATA.9-10-1485

This proposal is publicly available since 07/15/2021

Title

Squalene Nanomedecine: solvent effect in controlling size and internal structure

Abstract

Due to the quick adaptation of microorganisms to chemicals and the shrinking range of drugs available, medicine try to find a way to avoid drug resistance and treatment side effects. In 2016 Couvreur et al. discovered a new prodrug molecule, the Squalene-Gemcitabine, able to self-assemble with liquid crystal structure via squalenoylisation: the nucleoside-like is linked with amide bond to a biocompatible fatty acid the squalenic acid. The prodrug is nanoprecipitated via ouzo effect (solvent-antisolvent mixing). Saha et al. have shown that the nature of the solvent plays a key role in structure stability and nanoparticle size. With a SANS comprehensive characterization, we would like to understand the role of the solvent (polarity, viscosity and water coefficient diffusion) on the nanoformation, to further better control the internal structure and the polydispersity of the particles. Two solvents (acetone and DMSO) and 2 molecules (Squalene-Gemcitabine, Squalene-Deoxycytidine) will be used in different concentrations and ratios.

Experimental Report

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Data Citation

The recommended format for citing this dataset in a research publication is in the following format:

marret; DEME Bruno; GRILLO Isabelle; MULLER Francois and TESTARD. (2016). Squalene Nanomedecine: solvent effect in controlling size and internal structure. Institut Laue-Langevin (ILL) doi:10.5291/ILL-DATA.9-10-1485

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Metadata

Experiment Parameters

  • Environment temperature

    20 and 37
  • Experiment energy

    13A and 6 A
  • Experiment moment

    10-3 to 0.4A-1
  • Experiment res energy

    as on the instrument
  • Experiment res moment

    as on the instrument

Sample Parameters

  • Formula

    • solvent acetone
    • solvent D2O
    • solvent DMSO
    • Gemcitabine-Squalene C36H53F2N3O5
    • Deoxycytidine-Squalene C36H55N3O5
    • Solvent ethanol