# Research progress in membrane fusion-based hybrid exosomes for drug delivery systems

**Authors:** Anqi Liu, Gang Yang, Yuehua Liu, Tingjiao Liu

PMC · DOI: 10.3389/fbioe.2022.939441 · Frontiers in Bioengineering and Biotechnology · 2022-08-16

## TL;DR

This paper reviews hybrid exosomes made by fusing liposomes and exosomes, which could improve drug delivery with better targeting and biocompatibility.

## Contribution

The paper introduces membrane fusion-based hybrid exosomes as a novel drug delivery system combining the benefits of liposomes and exosomes.

## Key findings

- MFHEs offer high drug loading rates and targeted cellular uptake through surface modification.
- MFHEs have high biocompatibility and low immunogenicity, making them promising for drug delivery.
- The paper summarizes preparation methods and applications of MFHEs in disease treatment and research.

## Abstract

Liposomes are the earliest and most widely used nanoparticles for targeted drug delivery. Exosomes are nanosized membrane-bound particles and important mediators of intercellular communication. Combining liposomes and exosomes using various membrane fusion methods gives rise to a novel potential drug delivery system called membrane fusion-based hybrid exosomes (MFHE). These novel MFHEs not only exhibit potential advantageous features, such as high drug loading rate and targeted cellular uptake via surface modification, but are also endowed with high biocompatibility and low immunogenicity. Here, we provide an overview of MFHEs’ various preparation methods, characterization strategies, and their applications for disease treatment and scientific research.

## Full-text entities

- **Genes:** Hao1 (hydroxyacid oxidase 1, liver) [NCBI Gene 15112] {aka GOX, Gox1, Hao-1}, Cd9 (CD9 antigen) [NCBI Gene 12527] {aka Tspan29}, Cxcr4 (C-X-C motif chemokine receptor 4) [NCBI Gene 12767] {aka CD184, CXC-R4, CXCR-4, Cmkar4, LESTR, PB-CKR}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, Cd47 (CD47 antigen (Rh-related antigen, integrin-associated signal transducer)) [NCBI Gene 16423] {aka 9130415E20Rik, B430305P08Rik, IAP, Itgp}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, MIR497 (microRNA 497) [NCBI Gene 574456] {aka MIRN497, hsa-mir-497, mir-497}
- **Diseases:** CLD (MESH:C536761), ovarian cancer (MESH:D010051), neurological complication (MESH:D002493), crystals (MESH:D000070657), carcinogenesis (MESH:D063646), genetic diseases (MESH:D030342), Tumor (MESH:D009369), fibrosis (MESH:D005355), COVID-19 (MESH:D000086382), myocardial (MESH:D009202), liver fibrosis (MESH:D008103), hyperthermia (MESH:D005334), lung disease (MESH:D008171), fibrotic diseases (MESH:D004194), Diabetic peripheral neuropathy (MESH:D010523), fungal (MESH:D009181), infection (MESH:D007239), nerve damage (MESH:D000080902), hyperglycemia (MESH:D006943), bone loss (MESH:D001847), infarctions (MESH:D007238), cardiac diseases (MESH:D006331), Pulmonary fibrosis (MESH:D011658), toxicity (MESH:D064420)
- **Chemicals:** R837 (MESH:D000077271), clodronate (MESH:D004002), DPPC (MESH:D015060), zirconium (MESH:D015040), docetaxel (MESH:D000077143), PEG 8000 (MESH:C000595216), hydrogen peroxide (MESH:D006861), zirconium-phosphate (MESH:C027006), peptides (MESH:D010455), glucose (MESH:D005947), Doxil (MESH:C506643), polymers (MESH:D011108), CDDP (MESH:D002945), SDS (MESH:D012967), triptolide (MESH:C001899), DPN (MESH:D009243), lipid (MESH:D008055), AF647 (MESH:C569686), ICG (MESH:D007208), Aptamer (-), CCl4 (MESH:D002251), nitrogen (MESH:D009584), 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (MESH:C081581), water (MESH:D014867), PEG (MESH:D011092), phospholipid (MESH:D010743), doxorubicin (MESH:D004317), NIN (MESH:C530716), polypyrrole (MESH:C067635), F (MESH:D005461)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** BALB/c3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184), 293F — Homo sapiens (Human), Transformed cell line (CVCL_6642), J774A.1 — Mus musculus (Mouse), Mouse reticulum cell sarcoma, Cancer cell line (CVCL_0358), NIH-3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594), L-929 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58), Raw 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), CT26 — Mus musculus (Mouse), Mouse colon adenocarcinoma, Cancer cell line (CVCL_7254), SKOV3 — Homo sapiens (Human), Ovarian serous cystadenocarcinoma, Cancer cell line (CVCL_0532), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), SK-Hep1 — Homo sapiens (Human), Liver and intrahepatic bile duct epithelial neoplasm, Cancer cell line (CVCL_0525), HEK293FT — Homo sapiens (Human), Transformed cell line (CVCL_6911)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC9424752/full.md

## References

84 references — full list in the complete paper: https://tomesphere.com/paper/PMC9424752/full.md

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Source: https://tomesphere.com/paper/PMC9424752