Robust Polyion Complex Vesicles (PICsomes) under Physiological Conditions Reinforced by Multiple Hydrogen Bond Formation Derived by Guanidinium Groups

Mao Hori, Horacio Cabral, Kazuko Toh, Akihiro Kishimura, Kazunori Kataoka

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Polyion complex vesicles (PICsomes) formed from a self-assembly of an oppositely charged pair of block- and homo-polyelectrolytes have shown exceptional features for functional loading of bioactive agents. Nevertheless, the stability of PICsomes is often jeopardized in a physiological environment, and only PICsomes having chemically cross-linked membranes have endured in harsh in vivo conditions, such as in the bloodstream. Herein, we developed versatile PICsomes aimed to last in in vivo settings by stabilizing their membrane through a combination of ionic and hydrogen bonding, which is widely found in natural proteins as a salt bridge, by controlled introduction of guanidinium groups in the polycation fraction toward concurrent polyion complexation and hydrogen bonding. The guanidinylated PICsomes were successfully assembled under physiological salt conditions, with precise control of their morphology by tuning the guanidinium content, and the ratio of anionic and cationic components. Guanidinylated PICsomes with 100 nm diameter, which are relevant to nanocarrier development, were stable in high urea concentration, at physiological temperature, and under serum incubation, persisting in blood circulation in vivo.

Original languageEnglish
Pages (from-to)4113-4121
Number of pages9
JournalBiomacromolecules
Volume19
Issue number10
DOIs
Publication statusPublished - Oct 8 2018

Fingerprint

Guanidine
Hydrogen bonds
Salts
Membranes
Hemodynamics
Polyelectrolytes
Complexation
Urea
Self assembly
Tuning
Proteins
Temperature
polycations

All Science Journal Classification (ASJC) codes

  • Bioengineering
  • Biomaterials
  • Polymers and Plastics
  • Materials Chemistry

Cite this

Robust Polyion Complex Vesicles (PICsomes) under Physiological Conditions Reinforced by Multiple Hydrogen Bond Formation Derived by Guanidinium Groups. / Hori, Mao; Cabral, Horacio; Toh, Kazuko; Kishimura, Akihiro; Kataoka, Kazunori.

In: Biomacromolecules, Vol. 19, No. 10, 08.10.2018, p. 4113-4121.

Research output: Contribution to journalArticle

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