Recent trends in cell membrane-cloaked nanoparticles for therapeutic applications

Methods. 2020 May 1:177:2-14. doi: 10.1016/j.ymeth.2019.12.004. Epub 2019 Dec 24.

Abstract

Synthetic nanoparticles are extensively utilized in various biomedical engineering fields because of their unique physicochemical properties. However, their exogenous characteristics result in synthetic nanosystem invaders that easily induce the passive immune clearance mechanism, thereby increasing the retention effect caused by reticuloendothelial system (RES), resulting in low therapeutic efficacy and toxic effects. Recently, a cell membrane cloaking has been emerging technique as a novel interfacing approach from the biological/immunological perspective. This has been considered as useful technique for improving the performance of synthetic nanocarriers in vivo. By cell membrane cloaking, nanoparticles acquire the biological functions of natural cell membranes due to the presence of membrane-anchored proteins, antigens, and immunological moieties as well as physicochemical property of natural cell membrane. Due to cell membrane cloaking, the derived biological properties and functions of nanoparticles such as their immunosuppressive capability, long circulation time, and disease targeting ability have enhanced their future potential in biomedicine. Here, we review the cell membrane-cloaked nanosystems, highlight their novelty, introduce the preparation and characterization methods with relevant biomedical applications, and describe the prospects for using this novel biomimetic system that was developed from a combination of cell membranes and synthetic nanomaterials.

Keywords: Biomedical applications; Biomimetic; Cell membrane; Nanoparticle; Therapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Atherosclerosis / metabolism
  • Atherosclerosis / pathology
  • Atherosclerosis / therapy*
  • Blood Platelets / chemistry
  • Blood Platelets / metabolism
  • Cell Membrane / chemistry*
  • Cell Membrane / metabolism
  • Disease Models, Animal
  • Drug Delivery Systems / methods*
  • Erythrocytes / chemistry
  • Erythrocytes / metabolism
  • Humans
  • Ischemia / metabolism
  • Ischemia / pathology
  • Ischemia / therapy*
  • Liquid-Liquid Extraction / methods
  • Mice
  • Molecular Mimicry
  • Nanoparticles / chemistry
  • Nanoparticles / metabolism
  • Nanoparticles / therapeutic use*
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Neoplasms / therapy*
  • Polylactic Acid-Polyglycolic Acid Copolymer / chemistry
  • Sonication / methods
  • Stem Cells / chemistry
  • Stem Cells / metabolism
  • T-Lymphocytes / chemistry
  • T-Lymphocytes / metabolism

Substances

  • Polylactic Acid-Polyglycolic Acid Copolymer