Polysarcosine-Coated liposomes attenuating immune response induction and prolonging blood circulation

J Colloid Interface Sci. 2023 Dec:651:273-283. doi: 10.1016/j.jcis.2023.07.149. Epub 2023 Jul 26.

Abstract

Hypothesis: Liposomes coated with long polysarcosine (PSar) chains at a high density might enable long blood circulation and attenuate accelerated blood clearance (ABC) phenomenon.

Experiments: In this study, we controlled the length (23, 45, 68 mers) and density (5, 10, 15 mol%) of PSar on liposomal coatings and, furthermore, investigated the effects of PSar length and density on the blood circulation time, biodistribution, immune response, and ABC phenomenon induction. Length-controlled PSar-bound lipids (PSar-PEs) were synthesized using a click reaction and inserted into bare liposomes at different combinations of chain lengths and proportions.

Findings: Although all PSar-coated liposomes (PSar-lipos) had similar morphological, physical, and chemical properties, they had different blood circulation times and biodistribution, and exerted varied effects on the immune system. All PSar-lipos with different PSar length and density showed a similar anti-PSar IgM response. Liposomes modified with the longest PSar chain (68 mers) at a high density (15 mol%) showed the longest blood circulation time and, additionally, attenuated ABC phenomenon compared with PEG-lipo. The ex vivo analysis of the biodistribution of liposomes revealed that a thick PSar layer enhanced the blood circulation time of liposomes due to the reduction of the accumulation of liposomes in the liver and spleen. These findings provide new insights into the relationship between IgM expression and ABC phenomenon inhibition.

Keywords: Accelerated Blood Clearance; Anti-PSar IgM; Blood Circulation; Liposome; Polysarcosine; Repeated Administration.

MeSH terms

  • Immunity
  • Immunoglobulin M / metabolism
  • Liposomes* / chemistry
  • Polyethylene Glycols* / chemistry
  • Tissue Distribution

Substances

  • Liposomes
  • Polyethylene Glycols
  • polysarcosine
  • Immunoglobulin M