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Table 2 Summary of artificial exosomes generated by bottom-up approaches

From: Artificial exosomes for translational nanomedicine

Preparation

Particle characterization

Comparison to natural exosomes

Advances

Application

Refs.

Liposomes (PC, CHOL, DSPE-PEG2000, DSPE-PEG-MAL) coupled with MHC peptide complexes

Size by TEM: about 100 nm

NA

Targeted and traceable artificial exosomes

Activate and expand functional antigen-specific T cells

[82]

Liposomes (PC, SM, Chol, DOGS-NTA) bind with APO2L, TRAIL-His10

Size ranged by DLS: 150 –200 nm

NA

Artificial exosomes with improved bioactivity

Effective treatment of antigen-induced arthritis

[83]

Liposomes (PC, SM, Chol, DOGS-NTA-Ni) with inserted recombinant Apo2L, TRAIL

Size ranged by DLS: 150 –200 nm

NA

Artificial exosomes with improved bioactivity

Overcoming Chemoresistance of Human Hematologic Tumor Cells

[84]

Nanoliposome (Cremophor EL, PC, DOPE, DC-Chol) coupled with DEC205 monoclonal antibody

Size by DLS: 81.64 ± 4.25 nm

Zeta potential: 19.8 ± 1.8 mv

NA

Targeted artificial exosomes

High encapsulation efficiency

Specifically transmit antigen to DCs to induce immune responses

[85]

Liposomes (DOPC, SM, Chol, DOPS, DOPE) coated chitosan with embedded Cx43 proteins

Size by DLS: 120 ± 4 nm

Zeta potential: -8 ± 2 mv

Similar size and specific protein marker

High biocompatibility

Effective cytosolic delivery capability

Biomimetic siRNA delivery vehicles

[86]

Liposomes (Chol, PC, SM, Cer) tailored with integrin α6β4

Size by DLS: 113 ± 1

Zeta potential: − 5 ± 2

Similar size, structure and delivery efficiency

Production methodology and regulations

Targeted delivery of therapeutic oligonucleotides to lung cancer

[87]

Liposomes (DMPC, DSPC, DOPC, Chol) and leukocyte membrane proteins

Size by DLS: 122 ± 1.2 nm

Zeta potential: − 14 mv

NA

Large-scale and fast preparation

Stable structure

High drug-loading capacity

Custom-tailored functionality

Targeted tumor therapy

[88]

Liposomes (DMPC, DSPC, DOPC, Chol) and tumor cell membrane proteins

Size by DLS: 115 nm (mean)

Zeta potential: − 45.6 ± 1.0 mV

NA

Large-scale and fast preparation

Multifunction

Stability

Targeted tumor penetration

[89]

Liposomes (DPPC, DSPC, DOPC, Cholesterol) and hybrid cell membrane proteins (tumor cell and red blood cell)

Size by DLS: about 100 nm

Zeta potential: − 17 mv

Similar size and protein markers

Large-scale and fast preparation

Stable structure

High drug-loading capacity

Multifunction

Anti-phagocytosis capability and targeted tumor therapy

[90]

TPE-BPA, CTAB and Fe ions

Size by DLS: less than 100 nm

NA

Fundamental understanding of natural fission–fusion processes of exosomes

Molecular configuration and siRNA delivery

[91]

  1. Cer Ceramide, Chol Cholesterol, CTAB cetyltrimethylammonium bromide, DC Dendritic cells, DC-Chol 3-(N-(N0,N0-dimethylaminoethane)carbamoyl)Cholesterol, DLS dynamic light scattering, DOGS-NTA 1,2-dioleoyl-sn-glycero-3-{[N-(5-amino-1-carboxypentyl)-iminodiacetic acid]succinyl}(nickel salt), DOPC 1,2-dioleoyl-sn-glycero-3-phosphoCholinev DOPE 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine, DOPS 1, 2-dioleoyl-sn-glycero-3-phosphoserine, DPPC 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, DSPC 1,2-distearoyl-sn-glycero-3-phosphocholine, DMPC 1,2-dipalmitoyl-sn-glycero-3-phosphoCholine, DSPE-PEG 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N–[methoxy(polyethylene glycol)2000] , DSPE-PEG-MAL 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[maleimide (polyethylene glycol)-2000], MHC Major histocompatibility complex, NA Not available, PC Phosphatidylcholine, siRNA short interfering RNA, SM sphingomyelin, TEM transmission electron microscope; TRAIL-His10