Formation and potential application of micelles composed of biocompatible N-lauroyl-amino acid ionic liquids surfactant

Rahman Md Moshikur, Md Korban Ali, Rie Wakabayashi, Muhammad Moniruzzaman, Masahiro Goto

Research output: Contribution to journalArticlepeer-review

Abstract

Surface-active ionic liquid (SAIL) surfactants have attracted attention as promising alternatives to conventional surfactants because of their tailor-made and tunable properties. SAILs also address the limitations associated with conventional surfactants including toxicity and formation of unstable micelles. Here, we investigated the aggregation behavior of three biocompatible choline N-lauroyl-amino acid (NLAA)-based ILs with different amino acid side chains in aqueous solutions. The micellar behaviors of NLAA-ILs were investigated using surface tensiometry, conductometry, dynamic light scattering (DLS) and transmission electron microscopy (TEM). The critical micellar concentration (CMC) of the NLAA-ILs was found to be 2 to 4-fold lower compared with the conventional surfactant sodium dodecyl sulfate (SDS). The thermodynamic behavior confirmed that the micelle formation of NLAA-ILs was stable, spontaneous and entropy driven at room temperature. DLS and TEM studies revealed that the size and shape of the micelles depended on the presence of an N‑hydrogen group in the head group of the anion. Choline N-lauroyl glycinate ([Cho][NLG]) and dicholine N-lauroyl aspartate ([Cho]2[NLA]) were predominantly produced as unilamellar vesicles in water whereas choline N-lauroyl sarcosinate ([Cho][NLS]) formed small spherical micelles. Importantly, SAIL [Cho][NLG] showed lower toxicity toward mammalian cells compared with the analogous ILs or the conventional surfactant SDS and similar toxicity to the conventional surfactant Tween 80. SAIL [Cho][NLG] was more efficient at forming hydrophobic ion pairs with the macromolecular drug heparin compared with SAIL [Cho][NLS]. These results clearly suggest that the biocompatible NLAA-ILs represent promising potential substitutes for conventional surfactants in various biomedical applications.

Original languageEnglish
Article number114424
JournalJournal of Molecular Liquids
Volume320
DOIs
Publication statusPublished - Dec 15 2020

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Atomic and Molecular Physics, and Optics
  • Condensed Matter Physics
  • Spectroscopy
  • Physical and Theoretical Chemistry
  • Materials Chemistry

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