Abstract

Light-activated liposomes permit site and time-specific drug delivery to ocular and systemic targets. We combined a light activation technology based on indocyanine green with a hyaluronic acid (HA) coating by synthesizing HA–lipid conjugates. HA is an endogenous vitreal polysaccharide and a potential targeting moiety to cluster of differentiation 44 (CD44)-expressing cells. Light-activated drug release from 100 nm HA-coated liposomes was functional in buffer, plasma, and vitreous samples. The HA-coating improved stability in plasma compared to polyethylene glycol (PEG)-coated liposomes. Liposomal protein coronas on HA- and PEG-coated liposomes after dynamic exposure to undiluted human plasma and porcine vitreous samples were hydrophilic and negatively charged, thicker in plasma (~5 nm hard, ~10 nm soft coronas) than in vitreous (~2 nm hard, ~3 nm soft coronas) samples. Their compositions were dependent on liposome formulation and surface charge in plasma but not in vitreous samples. Compared to the PEG coating, the HA-coated liposomes bound more proteins in vitreous samples and enriched proteins related to collagen interactions, possibly explaining their slightly reduced vitreal mobility. The properties of the most abundant proteins did not correlate with liposome size or charge, but included proteins with surfactant and immune system functions in plasma and vitreous samples. The HA-coated light-activated liposomes are a functional and promising alternative for intravenous and ocular drug delivery.
Original languageEnglish
Article number763
JournalPharmaceutics
Volume12
Issue number8
Number of pages24
ISSN1999-4923
DOIs
Publication statusPublished - 12 Aug 2020
MoE publication typeA1 Journal article-refereed

Fields of Science

  • 317 Pharmacy
  • hyaluronic acid
  • liposome
  • drug release
  • light activation
  • stability
  • mobility
  • biocorona
  • INDOCYANINE GREEN
  • BIOMOLECULAR CORONA
  • BIOLOGICAL IDENTITY
  • PROTEIN CORONA
  • PEG
  • NANOPARTICLES
  • DIFFUSION
  • HYDROGELS
  • KINETICS
  • BINDING
  • hyaluronic acid
  • liposome
  • drug release
  • light activation
  • stability
  • mobility
  • biocorona
  • INDOCYANINE GREEN
  • BIOMOLECULAR CORONA
  • BIOLOGICAL IDENTITY
  • PROTEIN CORONA
  • PEG
  • NANOPARTICLES
  • DIFFUSION
  • HYDROGELS
  • KINETICS
  • BINDING

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